Researchers Discover Molecular Difference in Autistic Brains
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The discovery of a molecular difference in autistic brains has sparked a lively debate about the potential implications for treatment and the study's limitations. While some commenters, like GoatInGrey, point out that any treatment would need to address the effects that have already taken place during fetal development, others, such as Hnrobert42 and lez, raise concerns about potential links between vaccines, aluminum, and glutamate receptor development. The discussion is tempered by skeptics like jmward01, who question the study's small sample size (N=32) and the risk of false positives, with ear7h's comment from the original study highlighting the need for further research to understand the findings. As the conversation unfolds, it becomes clear that this research is just the starting point for a much larger conversation about autism and its underlying biology.
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I don't know much about the biochemistry here, I assume this is not something like GABA that can be directly supplemented. But maybe there are precursor nutritional and supplemental substances that can help these people upregulate how much of the glutamate molecule in question the body can produce.
> Reduce receptors. This might suggest a _developmental_ or genetic link. Think of this more like "height" or a particular "facial feature" of a person.
No. This isn't how it works at all. Receptor counts are extremely plastic, able to change within a weeks and in some cases hours. This is how you get drug tolerance.
For now, your best options are ESDM, occupational therapy, modified CBT, ABA, or neurofeedback, depending on your circumstances and presentation. Except for neurofeedback, these are behavioral approaches, so the architectural and neural activity variations aren't directly addressed.
> We want to start creating a developmental story and start understanding whether the things that we’re seeing are the root of autism or a neurological consequence of having had autism your whole life
doi: 10.1016/j.bbi.2015.05.009
Wish I could read the paper.
https://time.com/5175704/andrew-wakefield-vaccine-autism/
Bit rich coming from a sockpuppet account created 57 minutes ago, exclusively commenting on this thread, uncritically addressing it from a very specific angle, isn't it?
However, they did a very large cohort study with hundreds of thousands of subjects. The link completely disappears when genetics are accounted for via sibling pairs.[0]
It took almost two whole minutes of Googling for me to disprove this nonsense. Which shows that RFK did less than 2 minutes worth of research before panicking the world.
[0] https://jamanetwork.com/journals/jama/fullarticle/2817406
Shows how shockingly unaware even researchers are on how broad and nonspecific the diagnosis of autism is...
Were these 16 people hypo or hyper sensitive? Which of their five senses were involved? All? Some? Were some senses hyper and others hypo?
Need to start with categorization and specificity before we can make meaningful progress in research
I'm a dad of two autistic boys who I think would be very different categories. I have friends whose child isn't really autistic, they have a much more rare and specific diagnosis but it's so rare it's hard to get supports so they got him diagnosed as autistic because that criteria is so broad almost anyone can qualify.
Thank you for your work!
The part I take issue with: "lower brain-wide mGlu5 availability may represent a molecular mechanism underlying altered excitatory neurotransmission that has the potential to stratify the heterogeneous autism phenotype."
Seems like the very premise is flawed, though. Searching for a single global identifier for autism would be like if we spent research time trying to find a single global identifier for cancer. Noble effort... Way harder than spending effort on subcategorization into "lung" and "heart" cancers and working on research for detection of those subtypes.
The only good categorization we have in autism now is severity.
The anecdote I always like to share is Temple Grandin.
She was hyper-sensitive to auditory and tactile senses. The cause for this hypersensitivity was cerebellar abnormalities in her brain. Right now, someone who is hypo-sensitive to sound and touch because of different cerebellar development will also be put in the same bucket diagnostically speaking. There's not gonna be any universal way to detect that though...
To quote her directly:
"It would be my number one research priority, but one of the problems we’ve got on studying this, is that one person may have visual sensitivity, another one touch sensitivities, another one, auditory sensitivities. And when you study these, you got to separate them out. You can’t just mix them all together." https://www.sensoryfriendly.net/podcast/understanding-my-aut...
This is more or less not true. If it doesn't hinder a person in any aspect of their life, they don't fit the DSM-V criteria for a diagnosis.
That would be a bit weird though...
The only possible exception I can think of is synaesthesia.
"Deficits are sufficiently severe to cause impairment in personal, family, social, educational, occupational or other important areas of functioning..."
I think that's all an aside, though, if not the ICD (as suggested by another poster) or the DSM definition initially used, which definition is correct?
OP, I think, is clearly harkening back to a previous post on HN (article at: https://www.psychiatrymargins.com/p/autisms-confusing-cousin...) by a professional discussing that the public often misunderstands and ignores key aspects of the definition. This seems rather a bit like you pointing out laypeople might read and not understand what they got out of the POSIX.1-2024 spec.
Mu. If it was confirmed, but not "confirmed by laboratory criteria according to country definitions and requirements", then they do not meet the diagnostic criteria (interpreted literally). Suppose, for instance, that there was a procedural error that might have messed up the diagnosis (so is forbidden by regulation), but in this case didn't mess up the diagnosis.
I can produce as many of these literally-correct, deliberate misinterpretations as you like. They have no bearing on actual medical practice.
> which definition is correct?
Which definition of "carbon atom" is correct? Our definitions have, for 200 years, been sufficient to distinguish "carbon atom" from "not carbon atom", but those definitions have changed significantly in that time. Autism is that category into which autistic people fall, and into which allistic people do not fall, which is distinguished from several other categories with which it is often confused. (The ICD-11 spends way more words on distinguishing autism from OCD, Tourette's, schizophrenia, etc than on defining it directly.)
So the definition is perfectly correct, assuming you know what "clinical stages" there are.
> Are you a trained psychologist?
seems a bit confrontational, unless you yourself are a trained psychologist, in which case it would seem fitting to volunteer those credentials along with this challenge.
Now, needless to say, this is not how anyone actually thinks about psychiatric or psychological issues in practice, especially with conditions such as autism, and just highlights the relative absurdity of some of the diagnostic metrics, practices and definitions.
What we tend to do is tie the diagnosis of autism to the individual identity and assume that it is a consistent category and applicative diagnosis that stays with a person over time because it is biological. We know, of course, that this is despite not having any working biological test for it, and diagnosing it via environmental and behavioural contexts. And don't even get me started on tying in diagnosis of aspergers/autistic individuals with broadly differing abilities and performance metrics on a range of metrics under the one condition such that the non-verbals and low-functioning side of neurotypicals get lumped in with the high iq and hyper-verbal high-functioning aspergers as having the same related condition even though neurotypicals are closer to the non-verbals and low-iqs on the same metrics and scores.
The entire field and classification system, along with the popular way of thinking about the condition is, if i might editorialise, an absolute mess.
Firstly a fish without legs objectively does not have legs, but we do not necessarily call it disabled, even though it clearly lacks a facility.
Secondly, the autism spectrum disorders are, as I previously mentioned, not obviously just about deficits of behaviours or functions but also can take in extended and exceptional abilities in some areas and greater sensitivities rather than deficits or lack of an ability, so it is not clear that the entire diagnosis can be defined by deficits or lacking things. The high functioning and Asperger's type diagnosis is not about a universal deficit diagnosis and we do not generally call neuro-typical humans disabled because they lack prodigious activity or interest in math, language, or other subjects, even though that can also objectively be measured and called a deficit.
To get an Asperger's diagnosis under the DSM-IV you needed deficits, too. "Disorder" is in the title of the thing, if something isn't conceptualized as a disorder it isn't in there.
https://www.kennedykrieger.org/stories/interactive-autism-ne...
Adults have been socialised to mask the more problematic behaviours, and they can also be unaware that what they're doing is masking: they can believe that everyone struggles like that.
Why do we care so much about objective evidence? Because of prohibition. Prescribing stimulants isn't illegal because it is difficult to diagnose ADHD. It's difficult to diagnose ADHD for the very same reason it's illegal to prescribe stimulants: our society values prohibition of drugs over actual healthcare. An ADHD diagnosis implies a compromise of prohibition, so our society has structured the means to that diagnosis accordingly.
Experts in the field estimate a very high incidence of undiagnosed ADHD in adults. During the height of the COVID-19 epidemic, telehealth services were made significantly more available, which lead to a huge spike in adult ADHD diagnoses. Instead of reacting to that by making healthcare more ADHD accessible, our society backslid; lamenting telehealth providers as "pill mills", and generating a medication shortage out of thin air.
That may be true for ADHD, but autism diagnoses don't "unlock" any particular prescription medication, so I don't think that can be the whole story.
That can certainly be a syndrome, but the official DSM definition of autism is not based on those criteria.
Clinical autism tends to be much harsher in its presentation.
Society punishes us severely for not being able to see the difference between red and green, to use that metaphor. And they seem to expect that if they punished us just a little harder, we would suddenly become normal. Thats the big problem.
And then you meet the next person, who has not yet tortured and broken you, so they again do not believe that you "don't have the intel", and you get to go through it all over again.
The worst part is when you start believing for yourself that they're right, that you're holding back, and that it's all your fault for not giving them what they want.
The only people who take the DSM seriously are insurance agents and charlatans.
There is some underlying reality to what autism is, even if we do not have a good understanding of it; and even if turns out to be multiple unrelated things that happen to have similar symptoms.
Of the people with those actual conditions, it seems entirely plausible that some will not be hindered.
The authors of the DSM-V needed to create a diagnostic criteria for a condition that they do not understand, and for which no objective test is known. Further, their objective was designing something useful in a clinical setting. Giving those constraints, saying "if it is not a problem, we don't care about it" is entirely reasonable; despite not being reflective of the underlying reality.
To a first approximation, the DSM is about what a majority thinks is wrong. Sometimes this is pretty close to universal. Sometimes it isn't: https://en.wikipedia.org/wiki/Homosexuality_in_the_DSM
This study suggests that there are several different things called "autism". That's because "autism" as a term is not about some underlying reality, but a bucket that a bunch of people get tossed when some medical professionals see them as similar. And they come to the attention of those medical professionals because those people either say they have a problem or are called a problem by others.
But a problem with a person is always about a person in a context. Blue-eyed people are hindered by their eyes in bright light. Do we call that a genetic disease and look for cures? Not here, because there are enough "normal" people with blue eyes. But if it was just 1 in 20,000 people with blue eyes, it'd surely be treated as a disease.
Or we could imagine a "Height Deficiency Syndrome" characterized by inability to reach the top shelves in a normal house. With an effort, we could surely cure this impactful genetic problem through early application of hormones and the use of new CRISPR-related technologies. Or we could look at it as normal human variation which only "hinders" people because of how our society is set up to cater to "normal" people.
But we thankfully now have a term for that sort of nonsense: medicalization of deviance.
1. "Normal" people with a level of glutamate receptors at 10, say, on a scale I'm inventing for this example
2. "Autistic" (according to the DSM) people with a level of, say, 5, who are hindered by the effects of being at this level
3. "A little bit autistic" people at a level of, say, 8, who aren't hindered and don't meet the DSM criteria, but in fact actually benefit from the effects of being at this level
Some "normals" might then want to inhibit their glutamate receptors somewhat to get the benefits of being at an 8 or a 9 on my made-up scale.
Just like with ADHD it's likely that medication will at best have limited effectiveness and many side effects.
You're confusing the autism spectrum itself with Autism Spectrum Disorder. Autism Spectrum Disorder indeed has to do with social/etc difficulties. The autism spectrum itself on the other paw is a physical, quantifiable difference in neural architecture. Autistic people think differently whether they are diagnosed with Autism Spectrum Disorder or not.
https://www.verywellhealth.com/broad-autism-phenotype-117279...
The autism in this study is ASD. This study doesn't have that much to say about people who don't qualify for a diagnosis, since they would not have qualified to take part in it.
But yes, if you are saying ASD (and not autism itself, as the article suggests) is by definition a hindrance, I would be inclined to agree with you, for the reasons you've outlined.
BAP, I think, comes from heritability studies of people who are related to diagnosed people but do not themselves qualify as autistic, ie they are more likely to have traits associated with ASD despite not being diagnosable.
But here there’s a basic design flaw. This is a study of 16 ASD cases and 16 neurotypical controls. Small sample sizes like this require careful matching. The problem: the autistic subjects are 100% White but controls are 37.5% White. That imbalance can’t be waved away with statistics or Jedi mind tricks. Recruiting matched neurotypicals would have been straightforward.
One other issue is high heterogeneity within the two groups. In their Figure 1 (sorry behind a paywall), 4 - 6 of the autistic individuals have low mGlu5 levels across all regions. Two or three neurotypicals have high levels. Are these distributions actually normal, or are subgroups driving effects? It would help to know whether the participants’ GRM5 genotypes were informative wrt these subgroups. They weren’t checked.
So we might be able to make all the non-autistic people autistic? What would the world be like if everyone was mildly autistic?
My impression is this article and research that generalizes across the entire spectrum is not very useful.
Secondly, there are perverse consequences in brain chemistry and signalling: flooding a brain deficient in glutamate processing receptors with glutamate may not help, it may overload pathways and cause hindrance, not compensation.
If a small sample effect turns out to be indicative of a larger property, and if it's shown to be causal and if remeditation involves boosting blood borne glutamate or precursors is 3 stacked IF.
(Not a scientist, not a biologist)
Why not consider the opposite, that the most beneficial quantity of glutamate receptors could be somewhere below the typical amount? If that were true, then we could try to help others reduce their glutamate receptor level to become healthier and more successful (and a little more autistic).
If we found, say, an association between a lower level of neurological characteristic X and concert-level piano skill, then those who aspire to play that instrument at an elite level might try to decrease X. The fact that most of us are rubbish piano players would not be evidence that lower levels of X are harmful, but very much the opposite.
However there are people with severe autism that makes it more or less impossible for them to communicate with other people or live independently. If these people could have their life improved it might make huge difference to them and their families.
Simply put they didn't even touch the keeners, nonverbalists, the piss-in-your-pants, or the perpetual 1 year old autistics. They went after people who previously would be called "Aspergers syndrome".
But everything cognitive seems to be called 'autism spectrum disorder' these days.
Secondly, someone has medical power of attorney over the non-functional autistics. And in reality, they are the ones at most need of (almost passive) study to help them. Us high functioning autistics dont need anywhere near the help.. And we have no way to know an Aspergers and traditional autism are even similar, other than the spectrum brigade keeps adding more and more under 'autism'.
Simply put, guardian says yes to do a single scan a year, and I see no problem with it. More than 1 a year, and we start getting into potential damage. Maybe with some pie-in-the-sky-IRB whatif situation, sure. But 1 scan/yr has no demonstrable damage.
So what I wrote should be read with a "if it is held to be a condition which deserved remediation or avoidance of it's manifestation" attached.
Something in the brain development has gone off course - and by the time you see the early symptoms, it has been off course for a while already. Early interventions help considerably, but you might have to intervene extremely early, before any clinical symptoms show, to prevent it. Even if you knew exactly how to spot the risk so early on and what to do to intervene, which, we really don't.
It may make the difference between "needs a caretaker" and a mere "struggles in life". But it's not going to negate all of the damage.
Gene therapies I have little hope for. Maybe something there may help. But the impression I get is that it's less of a "fix biochemical deficits" issue, and more of an "unwire and rewire existing neural circuits" issue. We have no fucking clue on how to do that. And to sidestep that, you'd have to intervene early - as early as "remove genetic predispositions in an embryo".
The ones who drew the short straw? They would die without a caretaker to take care of them.
Even among the less severely affected: I'm sure there are people who don't mind being autistic, and I'm also sure that there are people who "don't mind being autistic". The difference between the two being: if there somehow was an easy cure, the former wouldn't go for it, but the latter would jump at the possibility. Because their "don't mind" was never anything more cope. Same as what happened to body positivity in the face of Ozempic.
After digging into it, the hypothesis holds. Most autistic people win this lottery you speak of.
Roughly 25–35% of diagnosed autistic people require substantial, ongoing support (e.g., daily assistance, supervised living, or full-time caregiving).
About 30–40% have co-occurring intellectual disability, which strongly correlates with higher support needs.
Roughly 60–75% do not have intellectual disability. Many in this group: Live independently or semi-independently. Work (often underemployed). Mask heavily and are diagnosed late—or never diagnosed.
Probably not. Because self-selection is doing its work. Out of 10 autistic people you know, ~0 are going to be in the "supervised living" category. They exist - you just don't see them.
Anyway, the core assertion holds. The framing and thinking of autism as a disorder of a brain that developed wrong is out-dated and incorrect. We could also frame the neurotypical brain as "wrong" for modern society because it evolved to ensure the survival of humans who needed to be primed and ready to fight or flee at all times.
Better to examine the differences rather than focus on winners and losers and right and wrong.
It's not very helpful to say if someone has been run down by a car that they just have different highway experiences than people who were not run down by cars. Their difference is a significant problem, because they have been run down by a car and it hurts.
More that their brain developed differently and the highway system is incompatible with that difference.
The highway system can and should change just as we individuals can and should try to change our minds in areas where it makes sense to do so.
So if people discuss the getting run down by car problem level the people who have an "I'm different" problem level feel as if they are being insulted, and if people discuss the "I'm different" problem level the people who care for the people who have been run down by cars feel like... well, insulted would probably be the least of it.
I have definite feelings about this exchange on autism, which are being hashed out reasonably without my input. But the Ozempic reference is super interesting. I hope some smart person looks into that particular "correction" vs. "coping" dichotomy at some point in the future.
There seems to be a point of contention amongst the terminology for anybody with autism. Someone with autism might not see themselves as having a disorder. But there are certainly very high needs autistic individuals. Apply a whole spectrum of people as being "developed wrong" and you can start to see ableist language.
I appreciated your metaphor about cars on a highway -- and that there's something wrong with the highway, not the car. I thought it was really simple and clear and I think I got the point you were trying to make. And even if it the highway isn't wrong (it was made for cars after all), we should at least extend it to support many types of transportation.
IMHO, our understanding of autism, specifically, and neural development of the brain, in general, is rudimentary at best. It's too soon to conclude it's incurable.
There is no consensus that autism is like this, but a lot of evidence points that way.
We'd need at least a generational leap in neuroscience to be able to pull off something like that. It's not a "laws of physics prevent you" level of impossible - we just don't have a clue of how would we even to begin approaching something like that.
For example, humans clearly have a window for learning their native language. It just happens, and it's nearly magical. But humans can learn non-native languages after that window slams shut. We vary in our ability to do that, but if it matters, most can pick up useful conversational and reading skills.
I agree it's a matter of research. I think we've barely begun to scratch the surface of what's possible.
If people find it easier to learn and apply the workarounds than to learn the thing itself, then, clearly, something prevents them from just learning the thing itself. Behavioral interventions being generally more successful the earlier you do them lines up with that too.
Maybe there are "low hanging fruits", simple interventions that work well that we are yet to discover. But it's not like no one went looking. And the fact that we are yet to find them weights against it.
Neurotypical does not imply “normal” it only means prevalent - completely different.
Yes, autism sucks _in the contemporary environment_ - we are perhaps better suited for neanderthal / hunter gatherer environment.
However, implying that I should be “cured” for having no interest in NT dynamics and suffer by many of NT byproducts (e.g. noise) puts you up there with Mengle in my book.
If you admit that "autism sucks in the contemporary environment", then, it's pretty clear that there would be people that have it and would want to be rid of it - if only they had that option. Currently, the options they have are "seethe" and "cope" - not a good place to be in. This alone would be enough of reason to look for a cure.
And then there are all the people who lose the "autism lottery" - and end up on assisted living for the rest of their lives. The short straw is really short - you could try an "autism is not a disorder" speech on them, but, not all of them are capable of communicating.
This, too, would be a reason in itself to look for a cure to autism. Unfortunately, what was discovered so far makes an easy solution extremely unlikely.
You would not want to boost glutamate. It's the opposite. You want to reduce glutamate and/or increase GABA. The problem is overexcitation, not underexcitation.
The reason the number of receptors might be low in the first place is downregulation from too much glutamate.
Example: I'm autistic and learn inside-out, building larger new concepts out of smaller existing ones; Asperger's on the other paw, learns outside-in, breaking down larger existing concepts into smaller new ones; both are part of the "autism spectrum", but differ very fundamentally.
[0]: https://www.medrxiv.org/content/10.1101/2024.08.15.24312078v...
This is a really interesting observation - can you expand on this a bit more, please? How did you first notice this distinction?
When, for example, learning a new concept in math or physics, what would outside-in look like vs inside out? Would you characterise neurotypical learning in one way or the other?
A year or two ago I interacted with someone with Asperger's, and since that very rarely happens I hit a sort of uncanny valley with the way they wrote to me, because their writing gave me a lot of neurotypical vibes, but at the same time seemed a lot more logical and structured than actual neurotypical writing. They seemed to be building their writing and ideas out of logical tokens and constructs in an evidently autistic way, but so much of their writing looked neurotypical.
It was sort of like Scratch blocks, where they learned general templates for sentences and paragraphs from neurotypicals, and then substituted entire phrases at a time within them to achieve the desired communication. So while their templates and phrases were learned mostly from neurotypicals, the structure of their communication and usage of it still had a sort of logical system to it.
They remembered concepts by the phrases that had been used to explain it to them in the past, and reused those phrases verbatim, slotting them into the templates wholesale. They didn't fully parse everything like I do, they only broke things down as needed to create new logical tokens for new concepts. It's very interesting and fascinating. I mostly only know the one experience I've had, since I didn't get to speak to them again, but I've started to see it absolutely everywhere since.
Plenty of engineering blogs, for example, share that sort of tokenized writing style, like for instance this one I recently noticed: https://www.righto.com/2024/12/this-die-photo-of-pentium-sho...
Hi, I'm the author of that blog. Can you tell me more about what you mean by a "tokenized writing style"? One confounding factor is that I have a PhD, so I was trained for many years to write in a formalized, academic style. Also, I deliberately put a lot of "signpost" phrases in my posts, since I'm writing about complex subjects and want to avoid readers getting lost.
I generally do the same thing when I'm learning something, and I have to fully understand a concept and then attack the concrete applications of the concept. But I've also learned how to go the other way when I need to because much of the technical writing I encounter is written for people who need a lot of examples but don't follow abstract concepts. So I've internalized building up the abstract concept from the concrete examples.
I believe it is both. You can go against your brain's coding with some extra work; somewhat like an adapter, I suppose. Your brain just still is coded a certain way natively.
> or example, what you're describing is basically typical of how Keirsey describes concrete versus abstract reasoning in Please Understand Me. And it could be kind of alienating to be the one abstract reasoner in a group of concrete reasoners and if you believe his statistics it's kind of likely that you'll find yourself in that situation a lot because you gravitate toward the abstract rather than the concrete/operational aspects of a concept.
This is very interesting. I've never heard of concrete/abstract reasoners before, but that does sound similar to what I've described. Thank you for the book.
> much of the technical writing I encounter is written for people who need a lot of examples but don't follow abstract concepts.
Yes! I love using examples to illustrate applications of an abstract concept, but I always explain the concept first. When the concept isn't explained first, I am sad. :(
> So I've internalized building up the abstract concept from the concrete examples.
I believe you may be better at it than I :)
Reading from what you have written - that is part of my experience, though I don't think that it has anything to do with being Aspergers or even being on a spectrum, but being alone a lot and educating myself a lot - that basically is what "smart people" in general are doing - including NT. Yes, there are a lot of people that do not actively learn, but that can apply to Aspergers as well as NT. That is not the reason for differences.
Just to save space and not to create another comment - "four phenotypes" are not new attempt to classify. To me it looks like rewording - before there was already quite clear distinction between Aspergers and Aspergers&ADHD combination - both of them are part of "high functioning autism", and they behave wildly differently(people with Aspergers&ADHD part might not be recognized as "weird" but even as NT - by other people). They were all part of spectrum anyway. And from reading the paper it seems, that they have made 2 other types for what was "low functioning" autism. Apparently putting them all in ASD was not helping for bureaucracy - especially when it comes down to finances - it is quite important in Trumps USA and might be also for other countries.
People do often use the terms interchangeably, but that's not how I use it. I use Asperger's to refer to a specific place on the autism spectrum; I don't think there's a better term I can use right now. That place is as opposed to the three other phenotypes. I don't claim to know for absolute certain that the four phenotypes are correct, but I do believe strongly in the idea, because my lived experience appears to match with it closely. It has helped me understand others better, for sure. (Or at least to believe that I do)
I say I don't have Asperger's because I seem to function differently than others who do have it. When I encounter it, I find it interesting, because it's clearly different than how I function and that makes me curious. That makes me think I don't have it, because if I did, then surely I would be able to study myself to learn more about it, yet so far I can only speculate about how my experience must be different.
> Reading from what you have written - that is part of my experience, though I don't think that it has anything to do with being Aspergers or even being on a spectrum, but being alone a lot and educating myself a lot - that basically is what "smart people" in general are doing - including NT. Yes, there are a lot of people that do not actively learn, but that can apply to Aspergers as well as NT. That is not the reason for differences.
Of course neurotypical and neurodivergent people alike can educate themselves and learn. The difference is in how they learn, and what type of learning is most effective for them. Even among autistics, the most effective or natural style of learning can greatly differ. This is also why many schools have entirely different classes for autistic people, because the style of learning that works best for neurotypicals may not be as effective for an autistic person.
What I think has to do with Asperger's is in the type of knowledge that is most useful to you, and the style of learning that is most useful to you. I don't actually know this for sure, but I believe that for any given concept, you would probably use different aspects than I would to understand it. That means if I told you everything that I believe is most essential to my own understanding of something you don't understand yet, you still might not get it, because you might have different requirements to understand that thing, and you might find different things most essential to that understanding.
Of course, in some ways this is true for everyone, for example if my most essential pieces of knowledge relate to or build upon other of my knowledge that you also do not have. But in other ways this is only true across different neurotypes, such as Asperger's and neurotypical, or Asperger's and another type of autism, because generally each phenotype appears to share a largely similar type of logical structure. For Asperger's it appears to be those nested tokens, for myself it seems to be a linear stream of thought or reasoning, for some of my friends it appears to be based on context and metadata, and for others of my friends it appears to be based on emotions and lore (sort of hard to explain). That makes four, and every single autistic person I know or encounter seems to fit into one of those boxes. Sometimes it takes longer to tell for sure, but I believe that I eventually always can.
> Just to save space and not to create another comment - "four phenotypes" are not new attempt to classify. To me it looks like rewording - before there was already quite clear distinction between Aspergers and Aspergers&ADHD combination - both of them are part of "high functioning autism", and they behave wildly differently(people with Aspergers&ADHD part might not be recognized as "weird" but even as NT - by other people). They were all part of spectrum anyway. And from reading the paper it seems, that they have made 2 other types for what was "low functioning" autism. Apparently putting them all in ASD was not helping for bureaucracy - especially when it comes down to finances - it is quite important in Trumps USA and might be also for other countries.
It's entirely possible that Asperger's without ADHD is, well, Asperger's, while Asperger's with ADHD is actually not Asperger's, and is rather another autism phenotype instead. To be honest, I've never heard of Asperger's + ADHD, while I've heard of ADHD for all three of the other types, so maybe that's the difference you are observing. I can't know for sure though.
I believe low-functioning autistics may happen to have brain defects or severe trauma or something else that disables them. I don't believe they are fundamentally different from other autistics in terms of the phenotype. I believe that a lot of the time, whether someone is called low-functioning is based primarily on how well they are able to function and how much support they need, and not really specific indicators that would indicate phenotype. Similar to how the criteria for ASD can diagnose autism, but not specifically Asperger's or specifically my type. I know that all four of the phenotypes certainly can be high-functioning, so that leads me to believe that low-functioning may be on top of that, and not a separate category altogether.
I don't think Trump has anything to do with this -- in fact he has been trying to shut down government benefits for autism (and for other things he views as a disability), so it's hard for me to believe that he cares about better classifying them when he seems to want them dead.
To me this just sounds like the interaction of autism with other variances in neurotype. You can also reasonably categorise non-autistic people into people who learn outside-in and those who learn inside-out.
Inside-out versus outside-in also doesn't really have to do with the order of learning. I could very easily learn the basic details of an overall system before I start diving into the details. Black boxes are very common for me to avoid going too deep into research or reverse-engineering rabbitholes (or to paper over an inability for me to learn more about inner workings). It has to do with the structure of learning. For me to model something as a black box, I'll accept that, though there may be parts inside it, I don't need to care how they're implemented. For someone with Asperger's to model something as a black box ... I imagine they already do that by default.
Neurons specifically increase / decrease receptor density in response to environmental factors, eg: use of SSRI's. Any excess of neurotransmitter would likely lead to reduction in receptor density as part of the response. So the story can be as much about an excess of neurotransmitter as it is about depletion of the receptor.
Perhaps the main story here is they can use EEGs as a proxy for measuring this effect so they don't need to put people through PET scans to do wider studies.
It's somewhat comparable to using a handheld magnifying glass on petri dishes and making broad claims about virus morphology. EEG is great, but I'm not sure I buy the methodology in this case. You need a huge N and much better experimental design and absolutely zero hype unless or until you show results with scientific rigor.
This sort of clickbait almost makes me view this type of research as a flavor of pseudo-science. The framing is misleading at best, but the full throated embrace of the clickbait and hype machine is awful.
It's funding bait, narrative manipulation, etc, and it'll either be part of something replicated and justified with much better experiments, or it'll just fade away into oblivion, with no repercussions for any involved should the outcome not actually benefit anyone or anything. There's not even a negative incentive, mGlu5 and "imbalance" claims have been made for decades, and they keep circling the questions but don't ever seem to actually "do" real science.
[1] "The findings support the idea that an imbalance of excitatory and inhibitory signals in the brain could be contributing to traits associated with autism, the researchers say." https://medicine.yale.edu/news-article/molecular-difference-...
[2] "Converging evidence from diverse studies suggests that atypical brain connectivity in autism affects in distinct ways short- and long-range cortical pathways, disrupting neural communication and the balance of excitation and inhibition." https://doi.org/10.3934/Neuroscience.2025031