It doesn't apply to all of the spectrum. They only studied adult males with HFA or AS. The patterns that they were looking for are specific to this group (NOT children, or LFA, or MFA, etc). But because of their much improved research design & validity, I'm sure researchers will do copy-cat experiments with other demographics, as well as look for sub groups of etiology in the HFA/AS population. They also need to do life-span studies, which can draw co-relations between socialization effects and neuro-anatomical differences.
I haven't had a chance to do a close reading of the paper yet but so far my biggest peeve is their lack of discussion about the
social biases in their population. They were diagnosed as children & do not have other syndromes (eg fragile X), or LDs, or comorbid psychiatric conditions. Most clinical samples tend to be biased towards white males, in their mid twenties, with upper-middle class urban backgrounds. (Which is actually a major criticism of the DSM in general). So yeah anyone who falls outside of this population only get researched as an afterthought (if at all) and have a much greater chance of getting misdiagnosed.
Neuro-plasticity has been found to continue throughout the life-span so your social environment, health, and personal choices continue to affect your brain structure after childhood. It is possible for identical twins diagnosed with ASDs to be on opposite ends of the spectrum by adulthood. [i.e. same genes + different experiences = variable expression of autism]
A lot of questions need to be asked. How do people who were traumatized with ABA as kids compare to those whose differences were celebrated and respected? Or girls who first presented with anorexia? Or the diverse manifestations of talents? Primary means of interacting with the world (tactile, verbal, visual etc.)? What about common co-morbidities like epilepsy, social anxiety and depression?
They recognized
someof these but not the social variables:
"Future work is thus needed to develop specific classifiers for different developmental stages, autistic subgroups and females with ASD." (p.54)
So yeah, I agree with you guys: there is no way they should use this as a primary diagnostic tool any time soon. It's the typically sensationalistic media that have pushed that idea. The researchers themselves are certainly not advocating this.
*sorry for the ridiculously long post
**If anyone is interested but can't access the actual journal article I can send it over.