Sunday, June 20, 2010

Genetic Litany

Chromosome 7q36, engrailed homeobox 2(EN2), the 16p11.2 region, 15q11.2, 15q13.3, 16p13.11; four regions located on 18q (MBD1, TCF4, NETO1, FBXO15); the PON1 gene; MECP2, TM4SF2, TSPAN7, PPP1R3F, PSMD10, MCF2, SLITRK2, GPRASP2, and OPHN1; encoding methyl CpG-binding protein 2; the SHANK2 synaptic scaffolding gene; the 5-HT(2A) receptor gene; neurexin-1 (NRXN1), chromosome 17p13.3, the two genes TUSC5 and YWHAE.

Cell adhesion molecule 1 (CADM1); RELN and GRIK2; MKL2 and SND1; chromosome Xp22.11-p21.2 that encompasses the IL1RAPL1 gene; the GABA receptor gamma 3 (GABRG3); neuroligin (NLGN4X); the FMR1 gene; region 10p14-p15, 7p22.1, the Q6NUR6 gene, JMJD2C gene at 9p24.1, 1p21.1, 6p21.3 and 8q21.13; Mecp2-null microglia; R1117X and R536W; SHANK3 mutations, GABA(A) receptor subunits, ASMT, MTNR1A, MTNR1B; RORA and BCL-2 proteins; DOCK4 microdeletion on 7q31.1, 2q14.3 microdeletion disrupting CNTNAP5; chromosome 2q24.2-->q24.3, telencephalic GABAergic neurons, position 614 of diaphanous homolog 3 (DIAPH3), 22q13.3.

Chromosome 2q37, 4q35.1-35.2, 8p23.2; chromosome 8p and 4q, P-glycoprotein gene (MDR1/ABCB1); glutamate transporter gene SLC1A1, IL1RAPL1 gene mutations, neuroligin mutants; SCAMP5, CLIC4 and PPCDC; fatty acid-binding protein (FABP7), 5-HT transporter gene (HTT, SERT, SLC6A4); proteins neurexin1 and PSD95; Cav3.2 T-type channels, chromosome 7q22-31 region; neuroligin-4 missense mutation; ADRA1A, ARHGEF10, CHRNA2, CHRNA6, CHRNB3, DKK4, DPYSL2, EGR3, FGF17, FGF20, FGFR1, FZD3, LDL, NAT2, NEF3, NRG1, PCM1, PLAT, PPP3CC, SFRP1, VMAT1; SLC18A1, microcephalin 1 gene (MCPH1).

Genetic polymorphisms of cytochrome P450 enzymes, 2p15-16.1, neurobeachin (Nbea); rs1858830 C allele variant, 3q26.31, serotonin receptor 2A gene (HTR2A); 1q42 deletion involving DISC1, DISC2, and TSNAX; alpha4beta 2 nicotinic acetylcholine receptors, adenosine A(2A) receptor gene (ADORA2A) variants; chromosome 1p34.2p34.3, synaptic vesicle gene RIMS3; microdeletions at 17q21.31, linkage loci on chromosomes 7 and 2; 2q37.3 deletion, neuroligin-3 R451C mutation; 2q24-2q31, 7q, 17q11-17q21; synaptic genes NLGN3, NLGN4, and CNTNAP2; dysfunctional ERK and PI3K signaling, ribosomal protein L10 (RPL10) gene, glutamate decarboxylase gene 1 (GAD1) located within chromosome 2q31.

Breakpoints on chromosomes 5 and 18; short arm of chromosome 20, chromosome 20p12.2, serotonin receptor genes HTR1B and HTR2C; genes at 3q25-27, deletion of chromosome 2p25.2, chromosome 10, chromosome 1q21.1; Joubert syndrome gene (AHI1), deletion in 6q16.1, including GPR63 and FUT9; duplication of 8p23.1-8p23.2, NLGN4Y gene, inverted duplication of proximal chromosome 14; SYNGAP1, DLGAP2, X-linked DDX53-PTCHD1 locus; interstitial deletion 9q31.2 to q33.1, methyl-CpG binding protein 1; balanced de novo translocation between chromosomes 2 and 9; contactin 4 (CNTN4), chromosome 2q24-q33 region, PAX6 gene; deletion on 18q12, chromosome 5q31, PTEN, 13q21.

Microdeletions at 7q11.23, chromosomes 1p, 4p, 6q, 7q, 13q, 15q, 16p, 17q, 19q, 22q; FMR1 protein, FOXP2 gene; 2q35 and 8q21.2 breakpoint, sodium channels SCN1A, SCN2A and SCN3A; paternally derived chromosome 13, somatostatin receptor 5 (SSTR5) on chromosome 16p13.3; terminal 11q deletion and a distal 12q duplication, APOE protein, allelic variants of HOXA1/HOXB1; notch4 gene polymorphisms, AVP receptor 1a (AVPR1a), mitochondrial aspartate/glutamate carrier SLC25A12 gene; Arg451Cys-neuroligin-3 mutation, language loci on chromosomes 2, 7, and 13; de novo translocation t(5;18)(q33.1;q12.1), p11.2p12.2.

Mu-opioid receptor gene, chromosome 16p13.3, trisomy 15q25.2-qter; 14q32.3 deletion, autism loci on 17q and 19p, linkage at 17q11-17q21, linkage on 21q and 7q; 3q29 microdeletion, haplotypes in the gene encoding protein kinase c-beta (PRKCB1) on chromosome 16; 6p25.3-22.3, SLC25A12 and CMYA3 gene variants; chromosome 3q25-27, inversion inv(4)(p12-p15.3), partial trisomy of chromosome 8p; locus in 15q14 region, terminal deletion of 4q, duplication at Xp11.22-p11.23; SEMA5A expression Tachykinin 1 (TAC1) gene SNPs, TPH2 and GLO1; biallelic PRODH mutation, recurrent 10q22-q23 deletions, neuropilin-2 (NRP2) gene polymorphisms.

Yes, I know—it might have taken less space to list the genetic features scientists have not implicated in autism's etiology.

Saturday, June 12, 2010

A Different Perspective on a Likely Mirage

One more thought regarding the report recently published in the journal Nature, Functional impact of global rare copy number variation in autism spectrum disorders (Pinto et al., 2010):

If someone wanted to put forth the hypothesis that rare copy number variation has no causal relationship whatsoever to autism, he would be hard pressed to find a more supportive set of evidence than the data supposedly backing the claims being made in (Pinto et al., 2010). Desperate people often see fantastic visions.

A Futuristic Vision

I can see where this co-authorship thing is heading. One day in the not too distant future a paper will appear entitled Today, consisting of a single sentence: “We did some stuff.” The authorship list will comprise the names of the six billion some human inhabitants of this planet, and the paper will be published in the journal Nature, which seems to have a hankering for these things. Everyone can then go about their business of applying for tenure, comfortable in the knowledge it will not be denied.

I hope that day comes soon; in fact, it cannot arrive fast enough. Because then maybe someone—anyone—will finally feel free enough to develop an idea on his own.

Friday, June 11, 2010

How To Talk Like a Modern Scientist

Humans were once curious as to why certain homes had an address of Toledo, Ohio while most homes did not. Modern scientists, attracted by some sizable grants, decided to look into the matter. Here is what a few of them had to say about their findings:

“We compared furniture arrangements of a large set of Toledo homes versus controls and found that if we focused on unusual furniture arrangements (those found in less than 1% of the homes), we could get some interesting and hopefully publishable results. At first we were disappointed to discover that both Toledo and non-Toledo homes were equally likely to have unusual furniture arrangements, but when we cast our statistical eye further we noticed that for unusual furniture arrangements involving television sets (rare televisionic furniture arrangements), Toledo homes were somewhat more likely to have such arrangements than controls. This is a major breakthrough.”

“We discovered novel candidate furniture arrangements that significantly increase the risk of having a Toledo address. This will allow us to develop home decorative intervention strategies and get furniture therapists to front doors much quicker—in some instances preventing homes from ever appearing in Toledo, Ohio.”

“Our results substantiate the importance of unusual furniture arrangements in Toledo homes, and this is likely to change how home decoration is viewed in the Toledo area. Most people in the field believed that Toledo homes shared common furniture arrangements perhaps in just a few rooms. But in fact most Toledo homes are probably decoratively quite unique—each having their own form of furniture arrangement.”

“You and I may have just as many unusual furniture arrangements in our homes, but since they don't involve television sets, we don't live in Toledo, Ohio.”

“Of great significance to us was the finding that in seven of the Toledo homes there was an unusual furniture arrangement involving a Go Mud Hens pennant, whereas this unusual furniture arrangement did not show up in any of the controls. We double checked against a broad population of Canadian homes and confirmed that those also did not have any Go Mud Hens pennants. This is consistent with earlier findings of high risk Toledo furniture arrangements—such as those involving cheap bowling trophies.”

“The findings, to some extent, are not unexpected. These unusual furniture arrangements are turning up in a number of other cities so it is no surprise that they may be involved in Toledo, Ohio as well. How significant they are will await further testing as to how sensitive and specific these furniture arrangements are as well as what percent of Toledo, Ohio is involved.”

“We have been trying to put together a very large jigsaw puzzle without having the benefit of a nice colorful picture on the box. The unusual furniture arrangements are like the edges, you might say, and they give us an idea of what the picture may look like. With these findings, we are starting to find some of the edge pieces, and that may provide us with some sort of framework for looking at how these decorative schemes work in Toledo, Ohio, leading to cartological features and how these might work in collaboration with the geography, thus producing some of the Toledo houses that we can see around us.”

“The exciting thing about the findings of this study is that it highlights fashionable pathways that can be targets for renovation.”

“Even with these findings, we are able to explain only about 10 percent of the homes in Toledo, Ohio. What causes the other 90 percent of Toledo homes to be located where they are is still on the table. Every little victory is important, but it's still amazing how little we know.”

Indeed.

Questions Unasked

One of the advantages of being an outsider to autism science is that I get to ask simple questions. Take for instance autism's latest hullabaloo, the paper recently published in the journal Nature, Functional impact of global rare copy number variation in autism spectrum disorders (Pinto et al., 2010). There are questions about this study that the media will not ask, nor apparently will any of the study's nearly two hundred authors. I, on the other hand, have no such reservation:

  • If particular types of rare copy number variants (CNVs) are only slightly more likely in autistic individuals than in non-autistic individuals (which is what the study indicates), and if the ratio of autistic individuals to non-autistic individuals is approximately 1:99, then aren't the vast majority of instances of these particular CNVs going to be found within the non-autistic population? And if so, how distinctive for autism can these CNVs possibly be?

  • How is it that only the CNVs which are more likely in autistic individuals can produce significant consequence, whereas the hundreds of other CNVs (from both populations) are apparently benign? Is this science—or wishful thinking?

  • How is it that the broad variety of CNVs more likely in autistic individuals (which are apparently the only ones that can produce significant consequence)—how is it that this diverse hodge-podge of CNVs can all lead to the same diagnosable condition? Is this science—or an amazing coincidence?

  • If the purpose of this study was to uncover a genetic signature underlying autism, shouldn't the major conclusion of this study be that there isn't one?

There are reasons that simple questions go unasked, but those reasons seldom have anything to do with the actual results. I have heard the spin being placed on this study in the media, and I have also listened to what the study's authors have had to say, but I can tell you without hesitation that the study's raw data imparts an entirely different story. Let me put it this way: if you are one of the nearly two hundred scientists who has managed to finagle your name onto the authorship list, then the publication of this study is a positive result; otherwise, it is a whole bunch of nothing.

Wednesday, June 9, 2010

The Unique Accomplishment of Laurent Mottron

I have written previously on this blog about the many innovative and original contributions made by Laurent Mottron and the members of his autism research team, but it would appear this time Dr. Mottron has gone and completely outdone himself in the new paper appearing in the journal Nature, Functional impact of global rare copy number variation in autism spectrum disorders (Dalila Pinto, Alistair T. Pagnamenta, Lambertus Klei, Richard Anney, Daniele Merico, Regina Regan, Judith Conroy, Tiago R. Magalhaes, Catarina Correia, Brett S. Abrahams, Joana Almeida, Elena Bacchelli, Gary D. Bader, Anthony J. Bailey, Gillian Baird, Agatino Battaglia, Tom Berney, Nadia Bolshakova, Sven Bolte, Patrick F. Bolton, Thomas Bourgeron, Sean Brennan, Jessica Brian, Susan E. Bryson, Andrew R. Carson, Guillermo Casallo, Jillian Casey, Brian H.Y. Chung, Lynne Cochrane, Christina Corsello, Emily L. Crawford, Andrew Crossett, Cheryl Cytrynbaum, Geraldine Dawson, Maretha de Jonge, Richard Delorme, Irene Drmic, Eftichia Duketis, Frederico Duque, Annette Estes, Penny Farrar, Bridget A. Fernandez, Susan E. Folstein, Eric Fombonne, Christine M. Freitag, John Gilbert, Christopher Gillberg, Joseph T. Glessner, Jeremy Goldberg, Andrew Green, Jonathan Green, Stephen J. Guter, Hakon Hakonarson, Elizabeth A. Heron, Matthew Hill, Richard Holt, Jennifer L. Howe, Gillian Hughes, Vanessa Hus, Roberta Igliozzi, Cecilia Kim, Sabine M. Klauck, Alexander Kolevzon, Olena Korvatska, Vlad Kustanovich, Clara M. Lajonchere, Janine A. Lamb, Magdalena Laskawiec, Marion Leboyer, Ann Le Couteur, Bennett L. Leventhal, Anath C. Lionel, Xiao-Qing Liu, Catherine Lord, Linda Lotspeich, Sabata C. Lund, Elena Maestrini, William Mahoney, Carine Mantoulan, Christian R. Marshall, Helen McConachie, Christopher J. McDougle, Jane McGrath, William M. McMahon, Alison Merikangas, Ohsuke Migita, Nancy J. Minshew, Ghazala K. Mirza, Jeff Munson, Stanley F. Nelson, Carolyn Noakes, Abdul Noor, Gudrun Nygren, Guiomar Oliveira, Katerina Papanikolaou, Jeremy R. Parr, Barbara Parrini, Tara Paton, Andrew Pickles, Marion Pilorge, Joseph Piven, Chris P. Ponting, David J. Posey, Annemarie Poustka, Fritz Poustka, Aparna Prasad, Jiannis Ragoussis, Katy Renshaw, Jessica Rickaby, Wendy Roberts, Kathryn Roeder, Bernadette Roge, Michael L. Rutter, Laura J. Bierut, John P. Rice, Jeff Salt, Katherine Sansom, Daisuke Sato, Ricardo Segurado, Ana F. Sequeira, Lili Senman, Naisha Shah, Val C. Sheffield, Latha Soorya, Ines Sousa, Olaf Stein, Nuala Sykes, Vera Stoppioni, Christina Strawbridge, Raffaella Tancredi, Katherine Tansey, Bhooma Thiruvahindrapduram, Ann P. Thompson, Susanne Thomson, Ana Tryfon, John Tsiantis, Herman Van Engeland, John B. Vincent, Fred Volkmar, Simon Wallace, Kai Wang, Zhouzhi Wang, Thomas H. Wassink, Caleb Webber, Rosanna Weksberg, Kirsty Wing, Kerstin Wittemeyer, Shawn Wood, Jing Wu, Brian L. Yaspan, Danielle Zurawiecki, Lonnie Zwaigenbaum, Joseph D. Buxbaum, Rita M. Cantor, Edwin H. Cook, Hilary Coon, Michael L. Cuccaro, Bernie Devlin, Sean Ennis, Louise Gallagher, Daniel H. Geschwind, Michael Gill, Jonathan L. Haines, Joachim Hallmayer, Judith Miller, Anthony P. Monaco, John I. Nurnberger Jr, Andrew D. Paterson, Margaret A. Pericak-Vance, Gerard D. Schellenberg, Peter Szatmari, Astrid M. Vicente, Veronica J. Vieland, Ellen M. Wijsman, Stephen W. Scherer, James S. Sutcliffe and Catalina Betancur, 2010).

There you can see it for yourself, in plain black and white, defying what must have been nearly insurmountable odds—Laurent Mottron has somehow managed to get himself not included in the list of contributing authors. What else can I say—this is clearly a unique accomplishment within the current field of autism research.

Indeed, Dr. Mottron's feat is so unusual and amazing that it leaves me wondering how he possibly could have pulled it off. My suspicion is that Geraldine Dawson, panicked at the thought of perhaps being excluded from the authorship list (which would itself be a unique and amazing event), during her mad, entreating rush to track down the head author must have knocked Dr. Mottron over and rendered him totally unconscious for a considerable period of time, thus leading to his name not appearing on the roll. But little matter. In an accomplishment like this—where one has so definitively set himself apart from all his peers—the means are merely a secondary consideration, the accomplishment is the thing. My heartiest congratulations!

Sunday, June 6, 2010

Memetic Residue

Can we assume that Richard Dawkins has plunged headlong (and superciliously) into his anti-religion career mostly because the biology gig did not work out?

Bright Dissent

I was thinking of fostering an Atheists Against Richard Dawkins movement, but unfortunately, its first commandment would have to be, “Thou shalt not be so fatuous as to foster a movement.”

Saturday, May 29, 2010

The Takeaway from Autism Science

If you cannot conceive the context, and if you have no grasp of the concept, then all the material data in the world will serve only to feed your blindness—even good information turns rancid in the oppressive heat of ignorance.

Friday, May 14, 2010

Linguistics for Autistics

Language is the use of a biologically immediate artifact to represent something not biologically immediate.


Almost any material artifact can serve the purpose of conveying language—gestures, sound, nudges, smears in the mud. The larynx was convenient, but not essential.


Since the locus of language is the external, material world (not the inside of our human skull) language remains open to any life-form. If a species does not use language, it is because that species has nothing to say.


Humans had nothing to say for an incredibly long period of time—this species passed the better part of its existence locked inside its biological immediacy.


What is crucial about language is not its material form, but rather its representational form. That is what connects biological immediacy to conceptual distance.


If you are aware of a pattern, then you are aware of time. If you are aware of symmetry, then you are aware of space. But how do you inform your neighbor?


Among other things, language was a solution to autistic loneliness.


One cannot deceive within one's own biological immediacy. Deception is a consequence of language.


Not only is deception a consequence of language, it is an essential feature of language. The means by which one conveys biologically removed events are also the means by which one conveys biologically removed non-events.


As with nearly every other autism-inspired invention, non-autistics quickly co-opted language for their own use and bent it to their own purpose; and as with nearly every other instance of non-autistic pilferage, the twisted results have been stunningly and humanly prodigious.


Chomsky was doing just fine when he approached linguistics as a branch of logic. He only went awry after he began approaching linguistics as a branch of science.


The underlying structure of language (Chomsky's universal grammar) reflects the structure of the non-biological world: space and time, stasis and change, mass and energy. The underlying structure of language arises from autistic perception.


Language always acts (represents) in the here and now. Persistent forms of language—such as writing—convey the material of language across space and time, but the sending and receiving still occur inside someone's biological immediacy.


Although autistic perception launched human language and gave it its underlying structure, non-autistic perception soon provided a hefty adornment—language gained its biological and social girth practically overnight.


Pronouns are superfluous to language, as is gender—but try convincing the ninety-nine percent who would feel empty without them.


What value is you and I, we and they, he, she and it, when a proper noun would serve just as well? (That is a question asked by someone not strongly attached to the species.)


Small talk is a reminder of this species' former days, when language itself was superfluous. Subtext was once all we had, and all we needed.


Autistic children grow up to a language that has been corrupted—the biological and social adornments constantly throw them off.


Autistic and non-autistic individuals are both exceedingly logical—just not in the same way.


Mathematics, logic, science—these are all salves against deception, and as such belong under the umbrella of language, not the umbrella of the objective world.


An artifact of language can be used to represent language itself, but it is almost never wise to do so. Meta-language is a misuse of the tool.


Language is not an instinct. Even less so is it a human instinct. What most children have an instinct for is to do what other humans do.


There are no language modules inside the human brain, just the magical thinking modules of linguistics professors and cognitive scientists.


Together with self-reflecting mirrors and obsessive masturbators, Steven Pinker reminds us that expansive vision is possible only because cognitively diverse people have the wherewithal to get beyond themselves.

Monday, May 3, 2010

What Self-Constructed Means

Let me be clear: when Harold Doherty uses the latest CDC autism prevalence reports to support his oft-repeated claim that 75-80% of individuals with Autistic Disorder have an intellectual disability, he is fabricating that statistic. The CDC reports show no such thing.

Mr. Doherty “arrives” at his number by taking statistics applied to the entire autism spectrum, then waves his magic wand over the number of Asperger's cases that should be excluded, and voilà, out pops the 75-80% figure. That's a self-constructed (fabricated) statistic.

As I have offered to Mr. Doherty before, he can show me to be wrong (and earn my apology) simply by providing two items—his math and the data he used from the CDC prevalence reports. So far Mr. Doherty has declined to do either. Anyone want to take a guess as to why?

Saturday, May 1, 2010

Autism and Intellectual Disability

Since Harold Doherty can't seem to stop repeating, ad nauseam, his self-constructed statistic about autism and intellectual disability, I thought I would counter with a real story about autism and intellectual disability, one involving some actual facts and one requiring a little more thought and attention than needed for just making up numbers or repeating the made-up numbers of others. This is a story about my own son.


Although I don't think our part of the country is typically included in the biennial CDC autism prevalence reports, if it were, this is the year from which Brian's records would be examined and tallied towards the total—he turns eight in a few months and thus he is part of the 2002 birth cohort to be counted as of 2010. And if Brian's records were to be included as part of that study, they would show him falling under the following two categories: Autistic Disorder and intellectual disability. In other words, in Mr. Doherty's narrow-minded view of the situation, Brian would officially qualify as one of the more dire autism cases—the cases Mr. Doherty wants everyone to focus on exclusively. So let's do just that. Let's focus on Brian's case.

Both those categorizations—Autistic Disorder and intellectual disability—result from the occasion of Brian's official diagnosis, received shortly after his fourth birthday. They are essentially the only evidence in Brian's records that the CDC would have to go on. When receiving his official diagnosis, Brian was given a thorough battery of tests, enough to extend over the course of two days, with the cognitive tests being given near the end of the second day. My wife was actually present with Brian as he was administered those tests, because someone was needed to help keep him seated and to help keep him focused long enough to be given the questions. Thus she was in a perfect position to report on how the entire episode turned out to be something of an unmitigated disaster.

There were several less-than-stellar moments, but the most telling incident came when the examiner asked Brian to count out loud from 1 to 10, to which Brian replied with complete silence and a little more squirming in his chair. After a brief period of time, the examiner repeated the question, to which Brian answered with still more silence and still more squirming, until finally the examiner noted the result on her chart and moved on to the next question. Needless to say, given this and several similar exchanges, Brian's overall cognitive score turned out to be significantly low.

But here's the thing:

This boy, who among other inabilities was being marked as unable to count from 1 to 10 at four years of age, was also the same boy who had been regularly entertaining himself from around the time of his third birthday by counting backwards from 100 to 1—cheerfully, voluntarily, and without mistake.


Like many autistic children, Brian does not like to sit still for very long, and he does not like to be barraged with an endless stream of questions. Even today, I would be hesitant to predict his performance on an IQ exam, because I'm not sure he would have enough patience to sit all the way through it. But I can tell you this much: anyone who has spent more than an hour with him would laugh hysterically at the notion of him being classified as intellectually disabled. He now reads at the third grade level. He does multiple-digit addition and subtraction. He is eerily adept at logic and probability puzzles. Plus he can talk up a linguistic storm as long as the subject is one that intrigues him (Disney and ceiling fans, for instance, would currently net you at least a ten-minute monologue). There has never been any doubt for those who actually know Brian: he may be highly atypical, but he is also highly intelligent.

Of course, the CDC will never know that.


Administering cognitive tests to any child under the age of about eight is a dubious procedure, but it becomes especially doubtful when applied to autistic children. There are many reasons autistic children will perform poorly and erratically on intelligence tests, with a good number of those reasons having nothing to do with the child's actual level of cognitive skill. If we are going to accumulate valid statistics on the relative intelligence of the autistic population, then the first thing we must do is focus on tests administered at older ages—exactly the opposite of what is currently being done.

And there are other factors to consider. For instance, as Michelle Dawson and her colleagues have been demonstrating, autistic individuals tend to evince a different kind of intelligence than do non-autistic individuals, an intelligence that often leaves behind an erratic trail across the range of standard cognitive tests, but an intelligence which nonetheless remains highly correlated to the types of cognitive skills often valued within the current culture. If we continue to compare autistic intelligence only to the norm, then we are going to continue to overlook many of the more valuable cognitive contributions autistic individuals have to make.

On the other hand, I don't want to be entirely pollyannish about the situation either. Clearly, there are also a significant number of autistic individuals who do experience various kinds and degrees of cognitive difficulty—difficulties that can often extend throughout a lifetime. The reasons for this phenomenon remain poorly understood and are a genuine cause for concern; and indeed, when one surveys the entire landscape of autism and intellectual ability—both the promises and the problems—what emerges is an extremely complex and puzzling picture. Autistic intelligence is different; it is also highly variable. Autistic intelligence is full of intriguing possibilities; it also gives rise to a surfeit of unanswered questions. Whatever else one might say about autism and intelligence, at the very least one must admit that these are fertile grounds for further study and exploration.

And in the end, I think that is what bothers me the most about Mr. Doherty's repetitive fictions. That he makes up his numbers and passes along the concocted platitudes of others—well, that is something I can deal with, because those activities simply mark Mr. Doherty as another nondescript member of the autism advocacy throng. But the facileness—that is what I found so hard to swallow. It can be only pure cognitive laziness that would prompt Mr. Doherty to fabricate statistics, thereby obscuring a wealth of valuable and potentially helpful information about autism and intelligence. And in my opinion, it is that cognitive laziness that needs to be classified as autism's true intellectual disability.

Tuesday, April 27, 2010

Upcoming Schedule

I want to let everyone know that the blog entries here will be somewhat less frequent and more erratically spaced throughout the remainder of 2010. Part of the slowdown can be chalked up to some blog fatigue and of course the ever present demands of parenthood and a full-time job. But the bigger reason is that I want to devote more time to a new project:

What I essentially am going to do is take a subset of these blog posts from the last two years, clean them up, add a few items to them, and reassemble the lot into a more cohesive, publishable-friendly format—probably something along the lines of what I did with Autistic Symphony. My expectation is to have the project completed by the end of the year.

Tuesday, April 13, 2010

ASAN's Reply to My Open Letter

I was tempted to leave the body of this post blank, but let me state more straightforwardly that ASAN has simply chosen not to reply to my open letter regarding the organization's honesty and integrity. That is of course ASAN's right, and nothing unusual need be inferred from its exercising of that right.

For me personally, however, the silence is disappointing. Keep in mind that ASAN, through regular email requests and at no prompting from me, frequently asks for my support, and keep in mind that I have been generally desirous of giving that support. ASAN has done good work in the past—for instance, its rallying of support against the Ransom Notes campaign. And the stated goals of ASAN are ones that, generally speaking, I believe would be beneficial for nearly all autistic individuals.

Nonetheless, I refuse to hold ASAN to any lesser standard than I would hold any other organization that asks for my support, and that includes standards of transparency, honesty and integrity. Speaking bluntly, I have never found ASAN to be a very transparent organization, and as I think this latest incident has demonstrated, ASAN appears to have some work ahead of it if it is going to meet consistently the principles of honesty and integrity.

Going forward, I remain willing to keep an open mind and a tentative eye for ASAN, but that organization needs to realize that if it is going to continue to ask for my support, then in return I am going to seek evidence that it is meeting the highest organizational standards. Lately, that evidence has been very difficult to find.


One final matter: political expediency. I have never myself heard directly from ASAN that it is willing to place political expediency above principles of accuracy and openness, but I have heard far too often from ASAN apologists that various forms of political expediency are at times necessary and valid tactics to be employed against the so-called opposing forces. To that line of reasoning, my reply is unqualified, and it goes like this:

What autistic individuals need more than anything is accurate information, along with acceptance, support and understanding based upon that information. Autistic individuals need accurate information more than they need treatments, more than they need funding, more than they need laws; for without accurate information, all those efforts would be pointless. What autistic individuals do not need is more political and personal expediency. Autistic individuals have suffered a long history of burden from organizations all too happy to practice political and personal expediency at the expense of accurate information—Autism Speaks, DAN, FEAT, Generation Rescue, ASA, the Judge Rotenberg Center—the list goes on and on. Thus it is important to state with unqualified clarity that autistic individuals do not need the burden of suffering from one more such organization—even if that organization happens to be run by autistic individuals.

Tuesday, April 6, 2010

Treasures

On what I hope is a more productive note than my previous entry, I would like to draw attention to a series of posts being made on parenting over at Brett's Waste Blog. These posts generally highlight the value of celebrating what is unique in each child and of encouraging children to pursue individual interests and strengths—no matter how unusual those interests and strengths may seem. Such ideas should be applied to all children of course, but they are particularly important for autistic children, many of whom are not celebrated and not encouraged for being who they are.

One day, I hope to record a few thoughts and observations about my own son. I think I have held back so far simply because I do not have the rhetorical skills to do him justice, but what I can report today is that as he approaches his eighth birthday, he remains both obviously autistic and extraordinarily delightful. In many respects my son serves as the perfect counterexample to those who insist that only intense treatments and early intervention can help an autistic child progress; for having experienced none of these, my son has developed into an individual full of warmth, joy, skill and complexity, an individual with a unique and valuable perspective upon his world. I stand in complete awe of him, and I also stand aghast at the thought of anyone wishing for him to be any other way than the way he actually is.

It is my firm conviction that when we approach autistic children as medical problems in need of being fixed, we end up throwing away one of humanity's greatest treasures.

Wednesday, March 31, 2010

An Open Letter to ASAN Regarding Its Honesty and Integrity

To the Autistic Self Advocacy Network (ASAN):

I would like to request clarification on the matter of the Cat in a Dog's World blog and its affiliation to an ASAN Chapter Director. In particular, I would like to know the following:

  1. Is ASAN aware that ASAN leaders are blogging pseudonymously in support of ASAN and its policies?
  2. Does ASAN condone or encourage this practice?
  3. If ASAN does not condone or encourage this practice, would ASAN be willing to speak out publicly against this practice and remind its leaders that they are expected to conduct themselves with honesty, openness and integrity at all times?

This is not a small matter for ASAN. Undisclosed pseudonymous blogging in support of ASAN and its policies reflects poorly on both the individual and the organization. This practice, to put it quite simply, is dishonest. I am willing to accept that the original intentions were simply a question of poor judgment, but the indications are that the individual involved wishes to continue this practice even after being made aware of its unethical nature. Furthermore, ASAN's silence on the matter makes it unclear if the organization itself understands the consequences of these actions.

I look forward to ASAN's reply regarding these questions and concerns.


Respectfully,

Alan Griswold

Saturday, February 20, 2010

The Emergence of Early Behavioral Signs of an Autism Research Disorder

It looks as though I will to need to interrupt my blogging break before it has had much of a chance to begin:

The occasion for this interruption is the online publication of A Prospective Study of the Emergence of Early Behavioral Signs of Autism (Ozonoff et al., 2010). Note that I have recently posted my thoughts regarding a different paper from this same general group of researchers, Play and Developmental Outcomes in Infant Siblings of Children with Autism (Christensen et al., 2010), a paper I generally decried as containing too much researcher bias and too much reliance upon the use of concocted measures. But as luck would have it, Christensen et al. (2010) was apparently only the warm-up act: when it comes to researcher bias and concocted measures, surely nothing can hold a candle to Ozonoff et al. (2010).

And I am starting to worry. Observations of infants and toddlers who are at high risk for autism (because they have older siblings who have already been diagnosed with autism) carry the potential of providing some valuable insight into the nature of the condition; but this will only happen if those observations arrive mostly unfiltered. Based upon what I have seen so far in Christensen et al. (2010) and Ozonoff et al. (2010), and given that a good portion of the research wherewithal directed towards at-risk children has been entrusted to this one tight-knit, rather homogeneous group of researchers, it appears as though these observations are not only going to arrive filtered, they are going to arrive after having been passed through a very distorting lens.

Let me begin by summarizing my complaints and concerns about Ozonoff et al. (2010).

1. The study is based almost entirely on made-up measures—measures designed to give the appearance of science when in fact those measures are not scientific at all. And as if that were not bad enough, those measures are then used, quite falsely, to create the illusion of comparable data, when in fact no such comparison is warranted. The findings of Ozonoff et al. (2010), while not entirely without merit, are based far too much upon a constructed fiction.

2. This particular group of researchers has been displaying a consistent bias in how it regards autism—etiology, preferred treatments, etc.—a bias that is strongly coloring the group's research methodology, and more importantly, is causing the group to overlook and dismiss data that does not fit into its preconceived notions. The findings of Ozonoff et al. (2010), while not entirely without merit, have been rendered needlessly incomplete through researcher bias.

3. For a so-called prospective study, Ozonoff et al. (2010) seems to have had a good portion of its structure retrospectively decided. While this is not sinister in and of itself, given the background of the researchers and given their potential interest in having the findings of these studies turn out in certain ways, it would seem that a greater premium would be placed upon methodological transparency and fair-mindedness. The findings of Ozonoff et al. (2010), while not entirely without merit, raise questions about general approach and about potential conflicts of interest.


Made-up Measures. There is a reason that much of science has been built up around the consistency of the yardstick and stop watch. I realize not all experiments can be conducted with quite the same degree of measurement consistency as is provided by distance and time—including within the field of autism research—and thus some leeway towards the use of broader techniques can at times be tolerated. But that leeway should not extend to complete freedom in making up measurement tools on an as-needed basis.

The measures upon which Ozonoff et al. (2010) relies are spelled out in the section “Measures Used to Track Behavioral Symptom Emergence,” a section surely deserving of a creativity award, but just as surely not deserving of the name science. Although I cannot do justice to the section myself—it really needs to be read to understand just how much measurement construction is actually going on—let me say that in essence it lays out various observer count and judgment statistics that are re-grouped and massaged together into categories freely labeled as face gazes, social smiles and directed vocalizations—“yardsticks” that I doubt have ever been employed in quite this way before, and quite likely will never be used this way again. True, these methods do allow for some crude observational comparisons between autistic and non-autistic individuals at similar ages—and so they are not completely worthless—but think about trying to repeat this experiment. Think about another research group having to train a set of observers to count face gazes or different types of vocalizations in precisely the same way as in Ozonoff et al. (2010), and you will realize there are no legitimate means by which to replicate this study, because the study has been based almost entirely on measures more fuzzy than a cotton ball.

But it gets much worse. Note that these made-up measures are applied to the study subjects at 6 months of age, 12 months, 18 months, 24 months, and 36 months, with the researchers then implying, straight faced, that these measurements can then be directly compared across all these ages. This is just the height of folly! Take face gazes for instance. Think about what might be counted as a face gaze coming from a six month-old, and then think about what might be counted as a face gaze emanating from a 36 month-old. I am not an expert on infants and toddlers, but I do not hesitate to say that the quality and characteristics of a face gaze from a six month-old are not going to be anything like those from a 36 month-old. That does not stop the Ozonoff et al. (2010) researchers, however—not one bit. There you can find them, plotting out these measurements across all ages in the graphs of Figure 1, alongside corresponding conclusions about how autistic and non-autistic children have “gained” or “lost” skills over time; there is never the slightest hint that these across-age comparisons are instead a massive instance of placing 6 month-old apples next to 36 month-old oranges. And if you have the slightest doubt about the non-comparability of face gazes over time, think about how much more absurd are the comparisons of directed vocalizations. These are the summation of nonverbal vocalizations, word verbalizations and phrase verbalizations that can be corresponded to face gazes. But tell me, exactly how many word and phrase verbalizations do we expect from a 6 month-old, and in contrast, how many word and phrase verbalizations might we expect from a 36 month-old? Once again, the so-called directed vocalizations of 6 month-olds are demonstrably nothing like the directed vocalizations of 36 month-olds, and yet the researchers act as though giving these measurements the same name is all that is needed to justify their direct comparison.

This research behavior is inexcusable, because after all it was the Ozonoff et al. (2010) researchers who made up the measures in the first place. They as well as anybody would know that comparing these measurements across child ages is ludicrous, and I would have to seriously question the intelligence or integrity of anyone who would insist on doing so. But note that this is precisely what happens when scientists start relying on measurement schemes that stray too far from objectivity—it is not all that large a step from made-up measures to made-up use of those measures. As I said in my comments regarding Christensen et al. (2010), concocted measures are the calling card of a concocted science.


Researcher Bias. There is never much doubt about where this research group stands in its description of autism. Both Ozonoff et al. (2010) and Christensen et al. (2010) are literally littered with phrases describing autism as a social deficit disorder, one best approached through early intervention directed towards getting autistic children to adopt social behaviors more in line with those of non-autistic children. This philosophy precedes any attempt at observation.

Of course, there is nothing unusual or wrong about researchers having a point of view. But when that point of view colors nearly every aspect of their research methodology, and when that point of view causes the researchers to consistently overlook important pieces of information that do not fit neatly into their preconceived notions, then there is indeed a problem. My comments regarding Christensen et al. (2010) already noted that these researchers' dismissive attitude towards autistic-like behaviors in infants and toddlers has caused them to turn a blind eye to the characteristics of these behaviors, and thus the researchers are overlooking valuable information, namely that early autistic behaviors are indeed quite structured, predictable and purposeful, characteristics that would be obvious to anyone willing to take a closer look. But this theme of willful blindness is continued unabated right through Ozonoff et al. (2010). First, note the influence of the researchers' point of view on research design: all the measures these authors decide to use are directed solely towards their theory of autism as a social deficit disorder—face gazes, social smiles, directed vocalizations, examiner ratings of social engagement. This would be a lovely set of statistics if all we were interested in is what the authors want to tell us, but surely a much broader set of statistics would be more helpful if we what we are interested in is what the infants and toddlers have to tell us.

And then there is the curious case of the unused statistic. The researchers start out by measuring a category called gaze to objects, but note the problem already contained within the description of that measure—“infant's gaze is directed toward an object that the examiner is presenting to the child or to another object visible in the frame”—anyone with even a modicum of understanding about autism could tell you that there is a world of difference between attention paid to an object presented by another person and attention paid to an object through independent motivation. But this research group, so caught up in its social deficit model, fails to untangle that distinction, and when its further efforts to fit this already mangled statistic into its thesis fail to gain significance, the authors decide to drop all further mention of the measure. Thus orientation to objects and structure, potentially one of the more valuable pieces of information that might have been gathered from this study, ends up getting so messed up by researcher bias that there ends up being no information at all. This is clearly a disservice to science, and a disservice to autistic individuals.

It is easy to see what one wants to see, but the trick in science is to overcome this tendency long enough to see instead as broadly as one can. Ozonoff et al. (2010) does not rise to the level of that standard.


Questions about Approach. Although Ozonoff et al. (2010) does not spell out its overall approach in great detail or with much clarity, one can still piece together enough information from its pages to realize that what was prospective about this study was the gathering of much raw data from a rather large group of participants, while what was retrospective about this study was the harvesting of subsets of this data—as well as subsets of participants—from the initial study group. Of course, this approach raises some key questions about the timing and purpose of various study technique decisions, but these questions go largely unanswered.

I would not mention this but for the fact it must be realized that the circumstances of these at-risk infant studies, as well as the circumstances of the researchers who have been entrusted to conduct them, by necessity invite greater scrutiny. Lists of researchers given the means to conduct at-risk infant studies reveal a consistent and like-minded set of names: names such as S. Rogers, S. Ozonoff, M. Sigman and G. Dawson are associated with these studies again and again. These are researchers who are close colleagues, and who have built careers around a similar social-deficit view of autism, and who are holding mostly high-paying positions at organizations that espouse nearly identical views of autism, and who have been associated with a self-promoted and perhaps proprietary intervention technique (the Early Start Denver Model); so I do not think I am revealing any state secrets in suggesting that this group of researchers might have a vested interest in having the results of their at-risk infant studies turn out in a certain way. There is nothing necessarily sinister in this, and I certainly do not see any evidence of fraudulent results, but under these circumstances, and given the rather narrow focus of both study methodology and study results we have been seeing so far from this group, I think some healthy skepticism and a polite call for greater transparency are certainly warranted.

And I would also think the autism research community might want to reconsider the wisdom of entrusting such a new and potentially valuable line of research to such an homogeneous-minded set of researchers. While there is no easy way to eliminate conflicts of interest entirely from the autism research community, at the very least, if we had some competing interests engaged in conducting some of these studies, we might be more successful in broadening our view.


Allow me to borrow a page from these researchers' storybook and suggest that early diagnosis of their autism research disorder is actually a good thing, because it opens the door to some early intervention. The intervention need not be all that intensive in this case—I think some straightforward occupational therapy will do. For instance, we might try a few sessions where when the researchers attempt to invent novel and fuzzy measures by which to conduct their studies, they are immediately re-directed to consider measures a bit more objective, broadly scoped and possibly repeatable. When the researchers begin to perseverate on their biases, we might present them with a series of PECS cards, for instance, that demonstrate how data and information can get easily overlooked when scientists walk around with blinders on. And when the researchers insist on arranging their studies to suit only their particular interests, we might enroll them in some structured play dates—friendship classes, if you will—opportunities for these researchers to practice taking turns, sharing, playing by the rules, opportunities to experience the good feeling that comes from allowing others to express their interests too.

I am half tempted to package this form of intervention and market it under a catchy phrase—say, the Early Start Indianapolis Model. But of course I know I would never get away with such a scheme, everyone would see at once through my ruse. After all, I am only suggesting that these researchers associated with Ozonoff et al. (2010) and Christensen et al. (2010) merely follow what has actually been available to them all along, merely follow the well understood principles of logic, mathematics and science.



Ozonoff, S., Iosif, A., Baguio, F., Cook, I.C., Moore Hill, M., Hutman, T., Rogers, S.J., Rozga, A., Sangha, S., Sigman, M., Steinfeld, M.B., & Young, G.S. (2010). A Prospective Study of the Emergence of Early Behavioral Signs of Autism Journal of the American Academy of Child & Adolescent Psychiatry DOI: 10.1016/j.jaac.2009.11.009

Christensen, L., Hutman, T., Rozga, A., Young, G.S., Ozonoff, S., Rogers, S.J., Baker, B., & Sigman, M. (2010). Play and Developmental Outcomes in Infant Siblings of Children with Autism Journal of Autism and Developmental Disorders DOI: 10.1007/s10803-010-0941-y



Sunday, February 14, 2010

Early Spring Break

It's time to recharge my batteries, so I'm going to be taking another break from blogging—probably until around early April or so. Feel free to check back then.

Saturday, February 6, 2010

The Autistic Perceptual Difference

I want to draw your attention to a paper recently published online in the Journal of Autism and Developmental Disorders: Play and Developmental Outcomes in Infant Siblings of Children with Autism (Christensen, Hutman, Rozga, Young, Ozonoff, Rogers, Baker, Sigman, 2010; hereafter referred to as PDO). There is much I might criticize about this paper—for instance, its prejudicial insistence on describing everything autistic as an impairment, and also its abundant use of pseudo measures to create the veneer of science (that is, an observer “counting” the number of functional play activities in a four minute session is not the same thing as measuring the distance from Mars to Neptune, no matter how much statistical massaging is applied thereafter—concocted measures are the calling card of a concocted science). In truth, however, these criticisms would apply to almost every instance of current autism research, so they do not of themselves distinguish the paper. What does distinguish the paper is that after one filters out all the fuzzy science, and after one overlooks all the prejudicial assumptions emanating from the paper's authors, the residue that remains still provides some useful insight into the nature of autism, including strong evidence for what I believe to be the nearest thing we currently have to that much sought-after prize, an actual cause of autism. Since the paper's authors have preemptively blinded themselves to these fertile possibilities (because of their prejudicial insistence on seeing everything autistic as an impairment), allow me to step in and try to shed a more productive light on their work.



The study described in PDO centers on observational data of infant siblings of autistic children, alongside similar observational data of non-autistic controls. Since a fair portion of these infant siblings will later be recognized as autistic themselves, these observations allow for a relatively large number of comparisons of autistic and non-autistic behaviors at early ages, well before outside interventions and influences begin to obscure the source of such behaviors. This particular study observed children at the age of eighteen months, and although both autistic and non-autistic behaviors are fairly limited at this age, it is not unreasonable to assume that whatever behaviors do exist at eighteen months, they are for the most part naturally and spontaneously derived.

To cut to the chase, a major finding from PDO is that the infant siblings who will eventually be identified as autistic are observed to display fewer functional play behaviors and more non-functional repetitive play behaviors than do non-autistic controls. The terms “functional” and “non-functional” are unfortunate choices (I will have more to say about these terms later), but within the context of PDO, it becomes apparent that the term “functional” is intended to describe play activity that is considered “appropriate” vis-a-vis the activities and expectations of other humans, and thus another, less prejudicial way of describing this particular finding is to say that non-autistic children engage more frequently in human-centric or human-derived play behaviors, whereas autistic children tend to engage, relatively speaking, in more object-centric or object-repetitive behaviors. Indeed, when the authors get around to discussing the observed differences between autistic and non-autistic behaviors at eighteen months of age, they concentrate precisely on this people versus non-people aspect of perception and activity. The authors' own words:

Examination of the subtypes of functional play revealed that the ASD [autistic] sibling group showed fewer self-directed and other-directed play behaviors than the TD [typically developing] controls. However, the ASD sibling group did not show fewer object-directed functional play acts. This finding is of particular interest because it suggests that children with ASD may not understand people as potential recipients of a play action and/or are not motivated to direct play behaviors to people (self or other) even before many of them are diagnosed.

Although PDO's science behind the above statement is far from precise, nonetheless, on a crudely observational level, the authors are actually onto something here; indeed, the above statement crystallizes perhaps the most useful aspect of their study. With it, PDO becomes yet another instance in a growing body of evidence, much of it dealing with children at a very young age, that demonstrates the fundamental, early-observable distinction between autistic and non-autistic individuals, namely that each group perceptually focuses on an entirely different class of sensory targets. Non-autistic individuals focus primarily on humans and human-centric activities, whereas autistic individuals focus primarily on objects and activities that are non-biological and non human-centric but that are often rich in concepts such as pattern, structure, symmetry and form. For another much-publicized example of this phenomenon, see the study Two-Year-Olds with Autism Orient to Non-Social Contingencies Rather than Biological Motion (Klin, Lin, Gorrindo, Ramsay, Jones, 2009), which demonstrates that two year-old non-autistic children focus primarily on point light displays that depict biological motion, whereas two year-old autistic children focus primarily on point light displays that depict some form of non-biological pattern.

This repeatedly observable distinction between autistic and non-autistic perception and behavior is so important and so significant that I believe it needs to be highlighted and given a name. Therefore, let me dub it the autistic perceptual difference and let me define it in the following way:

Non-autistic individuals perceptually orient primarily to humans and to human-related activities, whereas autistic individuals do not.

There are several items to note about this definition of the autistic perceptual difference. In the first place, the autistic perceptual difference is not the same thing as a social deficit model of autism. A social deficit model of autism would imply that autistic individuals readily perceive other humans—just as non-autistic individuals do—but that autistic individuals, through a neurological defect or some other mechanism, are somehow unable to respond correctly to social inputs or to social situations. I will not go into detail here about the paucity of evidence in support of the social deficit model of autism, but I would note that the mere fact many autistic individuals do mature to the point of being quite capable and quite sophisticated in social circumstances later in life is enough all by itself to make the idea of an inherent social deficit highly improbable. By contrast, the definition of the autistic perceptual difference implies no such deficit—it posits only the perceptual distinction. All the autistic behaviors commonly portrayed by autism researchers as social shortcomings are in fact behaviors that can be expected—that is to say, they are behaviors that are quite healthy within the context of autistic perception. Autistic social behaviors are simply the natural response arising from a form of perception that does not spontaneously orient to the other members of the species.

A second point to note about the definition of the autistic perceptual difference is that it also provides an affirmative description of non-autistic perception. This is an area conspicuously absent in the current state of autism research. Although considerable research dollars are spent and considerable ink is spilled on describing what is presumably wrong about autistic individuals, scarcely one penny is deployed or one drop of ink is applied to describing what is supposedly right about non-autistic individuals. Or to put it more fundamentally, no one ever bothers to address the question, what makes non-autistic individuals non-autistic? The definition of the autistic perceptual difference provides an answer to that question in a fundamental way, by highlighting the species-specific focus of non-autistic perception, and it should be noted that while this species-specific focus aligns non-autistic individuals with the perceptions and behaviors of the remainder of the animal kingdom, oddly enough it leaves non-autistic individuals somewhat atypical with respect to the current state of civilization and mankind. It is my belief that a wealth of anthropological information is just waiting to be gleaned from the contrast and blending of our respective knowledge about autistic and non-autistic forms of perception, and at any rate, there can be no question autism research will never arrive at an accurate, comprehensive and meaningful description of the nature of autism without also arriving at a correspondingly accurate, comprehensive and meaningful description of the nature of non-autism. The autistic perceptual difference provides an excellent place from which to begin that investigation.

The final thing to note about the definition of the autistic perceptual difference is that it states the primary characteristic of autistic perception. The other observable characteristics—such as the tendency towards repetition, and the natural attraction towards objects and activities embodying pattern, structure, etc.—these remaining observable characteristics, although they follow immediately and necessarily from the lack of a human-specific orientation, they must still be described, technically speaking, as secondary characteristics. What is happening here is that because autistic individuals do not have a species-specific focus to serve for cognitive grounding (as is the case for non-autistic individuals), autistic individuals find themselves in the near grip of a sensory chaos, and must overcome this chaos by engaging with the few features in their sensory environment that inherently stand out. When we reflect upon what kinds of features in a sensory environment would inherently stand out from the remainder, we are led immediately to those features rich in concepts such as symmetry and pattern. And viewed in this light we quickly realize that autistic behaviors—repetitive, structure-focused, symmetry-intense—are once again the expected behaviors arising from their particular form of perception. Far from being deficit driven, such behaviors are indeed quite healthy and quite necessary under the given circumstances of the autistic perceptual difference.

It is possible that one day advances in neuroscience, genetics, or some yet-unknown field will uncover a material cause of autism. Nonetheless, it must be admitted that today, currently—despite all the self-congratulatory press releases and despite Geraldine Dawson's annual pompom efforts—despite all this, the autism research community's current efforts towards uncovering a specified material cause of autism still stands at essentially square zero. The autistic perceptual difference is of course not a material cause of autism; but it is, as far as I can tell, the most fundamental piece of information we currently possess regarding autism, and thus stands as the closest thing we currently have to an actual explanation for autistic characteristics. As more and more studies are performed and published regarding autistic children at extremely young ages, my prediction is that the autistic perceptual difference will continue to emerge as the one consistent thread running throughout all those studies. Strip away their concocted science, strip away their researchers' preconceived notions, strip away the medical community's insistence that autism must be a devastating medical disorder, and what will remain in paper after paper is the same observable fact: non-autistic individuals perceptually orient primarily to humans and to human-related activities, whereas autistic individuals do not. Within that unfolding body of evidence can be found a deep and wonderful scientific story that is badly in need of being told; now if we can only get the researchers compiling that evidence to drop their prejudices for just a moment, and open their eyes.



Let me conclude by discussing in greater detail PDO's usage of the terms “functional” and “non-functional” to describe various types of observed play activity in very young children.

At one point in their paper, the authors do offer some examples to help explain their employment of these terms, noting for instance that a child who puts a toy spoon to the mouth of a doll would be counted as performing a functional play activity because that activity is considered “appropriate” with regard to the functional use of a spoon, whereas a child who repeatedly puts various items into and out of a pot would be counted as engaging in a non-functional repetitive play activity, since such activity does not coincide with the expected usage of a pot. I would have preferred, however, if the authors had stuck with the example of the doll and toy spoon when explaining non-functional play activity, noting for instance that if a child were to line up these items into a regular pattern—say, spoon doll spoon doll—that child would be counted as engaging in a repetitive non-functional play activity, just as with the example of the pot. By keeping the context of their contrasting examples more homogeneous, the authors would have revealed more clearly that their usage of the terms “functional” and “non-functional” has far more to do with their own preconceived judgments of these various play activities, rather than having anything to do with the inherent value of the activities themselves.

Think about it. From the perspective of an eighteen month-old child, the functional value of the many activities possible with a doll and toy spoon must seem rather arbitrary, and indeed would be arbitrary if not for one thing, namely that the “feeding” activity is clearly a human-centric activity. An eighteen month-old child who performs such activities is doing so because he or she has seen other humans make similar motions with a doll and toy spoon (quite likely) or has begun to match human actions with real spoons to the feigned actions with toys (perhaps less likely at eighteen months, but still conceivable). Therefore, what actually makes these activities “functional”—both in the eyes of the child and in the judgments of the researchers—is their human-specific nature. But does it follow therefore that only human-specific activities are functional? And is it wise to describe other classes of play activity as “non-functional”?

Note that the so-called non-functional play activity of autistic children is not random activity. If play activity actually were the result of some kind of impairment, then what we might expect to observe is play activity that is highly chaotic or unstructured in nature; but the play activity of autistic children is anything but. Repetition itself belies the notion of chaotic behavior, since repetition is the embodiment of temporal pattern, and when we consider the nature of activities such as lining up toys, spinning objects and selves, staring at ceiling fans, running back and forth in repeated patterns, flapping arms over and over, etc., we realize that far from being random or chaotic, such activities center almost exclusively on concepts rich in pattern, structure, symmetry and form. While it is true that autistic play activities are generally repetitious, object-oriented and non human-centric, it is not therefore true that such activities are “impaired” or “non-functional,” and to insist on saying so is to admit to having turned a blind eye to what these activities actually consist of. The researchers in PDO need to be reminded that their task was to observe autistic play activities, not prejudge them.

Looked at without prejudice, autistic play activities are seen to be functional in at least two very critical aspects. In the first place, autistic play activities are functional towards the development of autistic cognition. As we have already noted, without primary perception of species-specific influences, autistic individuals must obtain their cognitive grounding through their engagement with the few elements in their sensory environment that inherently stand out from the remainder, elements humanity has now come to recognize through the concepts of pattern, symmetry, structure and form. Viewed in this light, autistic play activities are seen as not only essential, but indeed healthy towards the developmental progress appropriate for an autistic form of perception, and another prediction I will readily make is that when all is said and done, it will come to be recognized that it is the lack of understanding towards these autistic perceptual and cognitive needs—along with the many mindless attempts to intervene and thwart such needs—that accounts for the large majority of poor outcomes in autistic individuals.

Just as importantly, autistic play activities are functional in another, much broader sense, one that the scientific community has sadly ignored through the present day, but one that is literally stunning in its overall size, scope and impact.

Humanity currently faces an outstanding riddle regarding the origin and nature of its sudden transformation from biologically limited primate to collective architect of landscapes now thoroughly drenched in such concepts as abstraction, symmetry, pattern and form. The irrational bleatings of the sociobiologists notwithstanding, no plausible explanation has yet to be offered as to the source of this sudden transformation. But in point of fact, the source of that transformation actually exists right before our very eyes. If you are in need of an example, I would note that several instances could have been found engaged in the four-minute play sessions of the PDO study.

Whereas no material cause for autism has yet to be uncovered, the material cause of humanity's remarkable cultural transformation exists in abundance all around us, exists in the embodiment of a form of cognition that focuses primarily on the non-biological concepts of pattern, structure, symmetry and form—the distinguishing hallmarks of modern civilization, and the distinguishing hallmarks of autistic perception. The atypical play activity of autistic children is indeed functional, functional in a way we have hardly begun to conceive.

Saturday, January 30, 2010

One More Session

At first, he might even cooperate—
Longing for praise and uncertain yet
As to the nature of this new game,
He leaps forward with beaming curiosity.
You begin touting his sudden progress.

Later, after he has recognized
This falsely structured hour
As yet one more attempt
To pound square pegs into round holes,
You begin searching for a new therapy.

Saturday, January 23, 2010

Fossilization

You cannot create literature as a professional writer. You cannot discover breakthrough knowledge as a professional scientist. And you cannot inspire mankind as a professional philosopher.

When we take our most treasured enterprises and transform them into commodities, we destroy all their merit. We now have millions of writers, but no brilliant words. We now have millions of scientists, but no useful insight. We now have millions of philosophers, but no courageous wisdom.

Academia has fossilized humanity's worth.

Friday, January 15, 2010

A New Approach to Covering the Costs of Autism Research Publication

I would like to propose a new approach to paying for the costs of autism research publication. Instead of having subscribers pay for access to autism research journals, a much better solution would be to have contributors pay for the right to publish in autism research journals.

This idea might at first appear to be somewhat counterintuitive, but it has one obvious advantage over the current approach: the new approach does a much better job of matching costs to benefits. For example, readers of autism research journals, who currently receive nothing of value for their enterprise, would no longer be charged for the privilege, providing in this case a perfect match of expense and gain. At the same time, those who get published in autism research journals—and thereby gain access to doctoral degrees, tenured positions, editorial appointments, government committees and of course additional funding—would be obliged to provide some recompense for these many benefits, thereby helping to keep the system going.

But I believe I can do this excellent idea even one better.

Instead of charging a flat fee for the publication of an autism research article, a much more effective approach would be to charge an exponentially increasing scale based upon the number of co-authors listed on each paper. A one-author article, for instance—which, after all, does have some chance of providing valuable insights into the nature of autism—might be published for just a nominal amount, or perhaps even for free. Adding a second author, however, would require the contribution of, let us say, an additional two thousand dollars to the final invoice, and adding a third author would augment the overall fee by a further four thousand dollars, adding a fourth author would cost an additional eight thousand dollars, and so on.

Under this proposal—and given the size of some co-author lists I have seen on recent autism articles—a few lucky journals might find themselves able to cover an entire decade's worth of expense through the publication of a single article alone. However, let me be clear on this—I do not recommend the booking of outlandish profits under such circumstances: the majority of revenue gathered in excess of reasonable costs should be returned immediately to supporting governmental agencies, for the express purpose of retiring national debts.

Another feature that might be added to my proposal—a slight improvement, if you will—is to require a surcharge for the inclusion of any co-authors who possess high name recognition or who have reached a certain standard of publication profligacy. That is to say, for each S. Baron-Cohen, G. Dawson, or F. Volkmar pasted onto the end of any given co-author list, this would add, oh let us say, an additional fifty thousand dollars to the final publishing fee. Now it is true that if this supplemental S. Baron-Cohen, G. Dawson, or F. Volkmar happens to be the tenth author “contributing” to the given paper, then that additional name, under the scale described above, would already be setting back the paper to the tune of a half million dollars or so, and thus tacking on an additional fifty thousand dollars might seem like overdoing it a bit. But keep in mind that the value in this new approach is to match costs to benefits, and we all know how much a career (not to mention, the peer review prospects) can be enhanced by association with that one special “colleague.” If perhaps this final feature of my proposal does seem a bit too controversial, might I suggest employing it on a trial basis at first, in just a few select journals, until the feature's true benefit becomes more apparent.

I of course have some additional revenue-raising suggestions, ones based upon the number of citations employed in each article—in particular, citations of the authors' own prior work—but I would prefer to keep such suggestions on the back burner for now; I do not want to overload the system all at once with too much cash. After an appropriate investment plan has been put in place at each journal, along with all the necessary safeguards, maybe then consideration can be given to some of these more advanced techniques.


Now I know what you must be thinking. You must be thinking that if this new approach is so obviously beneficial, then why has someone from the autism research community not already suggested it. I admit to feeling a bit sheepish about having to make this proposal myself, being an outsider and all, but I would note that there are many circumstances in life in which those who are part of a community are so attached to that community they cannot easily take a step back and gain helpful perspective. Quite often—let us be honest here for once—people are simply standing too close to the problem to recognize its solution.

Saturday, January 9, 2010

Beasts

Evolution is a delicate description.
Bordering on the tautological,
It requires nuanced reflection
Upon time, environment and biological dynamics
To see its process unfolding as physical necessity,
And not deductive creed.

Thus when lumbering, blustery giants
Such as Dawkins and Pinker barge in,
One is reminded of stubbly-thumbed oafs
Who destroy posthaste every delicacy they touch.
No subtlety. No discretion. Just
The ponderous pounding of their shiny new toy
Again and again and again.

It is that trait,
This barbarous, incontinent bashing
Of Darwin's dangerous idea
Against every surface they meet,
That betrays their vulnerability—
Like beasts,
They have not reflected upon evolution at all.

Thursday, December 31, 2009

Scientific Advancement

I agree with Michelle Dawson's assessment that the editorial board of the proposed journal Autism Insights is dubious in nature and bad news for autistic individuals, and I expect its actions will be motivated far more by personal interests and personal agendas than by any desire to advance the science.

But my question is: how would this differ from the editorial board of any other autism-related journal?


In fact, it is revealing that assessments in autism science have now devolved mostly into questions of scientific reputation, for when you are faced with a discipline in which practically no one is advancing the science in any meaningful way, reputation becomes the only thing left to argue.

Nonetheless, scientific reputation is only a pseudo measure. Playing by the rules and convincing others to recognize you for having played by the rules does nothing to promote understanding—to promote autism insight, if you will—and it certainly does not qualify as good news for autistic individuals.

Good science spinning its wheels travels no farther than bad science prowling at random.

Scientific Accumulation

A million trivial results do not add up to something significant; they add up to triviality.