Dsm Disorders Disappear in Statistical Clustering of Psychiatric Symptoms (2024)
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A study found that traditional DSM disorders dissolve when psychiatric symptoms are clustered statistically, sparking discussion on the limitations and potential biases of the DSM.
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https://www.ncbi.nlm.nih.gov/books/NBK519711/
Going back to DSM-III TFA has a good link
https://ajp.psychiatryonline.org/doi/full/10.1176/appi.ajp.2...
>This is unproblematic as long as DSM criteria are understood to index rather than constitute psychiatric disorders.
With "index" taken to mean:
>a pragmatic and well-validated way to identify [a] syndrome
I.e. "Do DSM Compress?"
This is probably exacerbated by the closure of mental institutions where you could see in person what the textbook means exactly.
Trying to understand diseases just by the text (and not even considering differential diagnosis) is an exercise in frustration. And I feel more professionals lately are just "Chinesing room" it instead of having actual experience
Fwiw I think it’s patently obvious behaviors can influence people, but in my mind they influence the avenue of expression - they don’t create disorders from scratch. So like e.g. body image would be the underlying disorder, and if it expresses as bulimia or anorexia or cutting could be somewhat “socially contagious”.
What does seem right to me is if you feel fucked up about your body and your attractiveness, how you express that can be influenced by what you see other people doing. But if you feel confident about yourself there is no amount of hanging out with people with eating disorders that will give you one…
If you’d like to link a paper that has informed your understanding, i’d be happy to read it. But telling me to “read up on it” is a weird dodge of a direct question. Have you read up on it?
I have read a little, not a lot - but what i have read makes a case for some influence of social groups but doesn’t make a case for eating disorders being contagious like viruses.
From my anecdotal experience with people I've known, it makes sense that the other symptoms in that spectrum, like bloating and anxiety, could make someone more receptive to unrealistic body standards and "solutions" to achieve those standards and regain control. That's what it's really about: not feeling in control.
I've had video calls with a doc who took maybe 5 minutes at most of hearing subjective experiences to confidently reach a conclusion. I've also had a 45 minute "by the book" DSM-based session where boxes were being ticked... and the questions were f---ing *terrible*, if you pardon my French. "Do you have trouble concentrating" is terribly vague and can always be justified either way. Not to mention, it takes maybe a few moments to "catch on" on how to answer which questions; which seems to be a terrible way of introducing bias into the answers (as also mentioned in the article). Having someone describe their personal life is in many ways much better because it cannot be a rigid yes/no question.
And all this talk is without mentions of other aspects that also need addressing, like the continuous spectrum of many conditions...
My current psychiatrist figured out my main issues after talking to me for 15 minutes. Sent me off to a psychologist back up his assumptions before prescribing anything. Recommended therapists who specialize in the area I needed support in.
The psychologist I went to was great as well (after seeing one that was a terrible). She did a lot of testing (three sittings lasting around two hours) but said the tests were really just to rule out other things. The important part were the conversations.
My life improved tremendously after that.
If you’re focused in particular on getting a diagnosis for something, I’d also recommend reading relevant parts of “Psychopathology and Mental Distress” which is a tomb of a book that aggregates both DSM and ICD diagnostic criteria, but also provides current meta surveys on relevant research, from multiple perspectives. It’s reasonably easy to read but definitely better after getting the basic thinking tools from a proper course on clinical psych.
I mean, it's the same question as "How do I assess whether my plumber or mechanic or electrician knows what they're doing." Sure, sometimes there's an easy, obvious difference, but you can't really know for sure whether or not your electrician is grounding your entire house to your hot-water pipes unless you have enough skill and expertise not to need one. After a point, working with any professional requires a weird blend of faith and of assessment you don't have the expertise to actually do.
Orthogonally, she also had sensitivities to light and epileptic symptoms. She told the doctor this, and the doctor doubled her dose of antidepressants. Just one of many, many stories. I've come to consider the higher-level of medicine quite scientific, but the on-the-ground doctors as unscientific. They mostly don't have time or enough feedback to make good decisions in most cases I've seen. That's a profession that shouldn't work on faith.
Asking you “do you have trouble concentrating?” is lazy (at least, on its own. Asking a patient to perform a self-assessment is not bad medicine necessarily). A doctor should also be evaluating your concentration in other ways.
To be fair, for the practitioner this shouldn't be a question about objective capital-letter Truth, it's one throw of darts representing a self-reported aspect of self-experience and self-perception.
As someone who has designed questionnaires for a public health agency, reading the article made me feel we should've fully randomized the order of appearance of individual questions, including the 'front-matter' stuff like self-reported gender, age, education, marital status.
As someone who got quite upset about a particular questionnaire's formulations at the tender age of 10, I'd now say let's not get too wrought up about this, a questionnaire can be a valid tool but it will also always be a somewhat blunt tool, so let's use it bluntly: don't fret, put your mark into one of those five boxes, move on to the next question, done, over, out. If it's about me then it's about how I feel about it, now, and I can choose to feel extremely good or bad or fairly somewhat well-nigh indifferent about sh*t, just here and now. As the one being questionnaired, I also have the right to lean into the questions and bend the outcome as I see fit. Been there, done that.
That is not always seen as an option for some patients. Having observed a family member take a specific autism questionnaire, I can tell you that as for some people - often exactly the people who should be dianosed - it does not always feel possible to pick an option that to them is wrong.
In said case, they ended up getting diagnosed with autism elsewhere, because that one question on the first questionnaire was one they felt impossible to move past, and so it was never submitted.
Thankfully they had another option that wasn't being gatekept with a broken quesionnaire.
This might not be directly relevant to the article, but I think it's worth mentioning it in the general context of questionnaire design.
The DSM isn’t the source of those question inventories. There are different question sets for different conditions that each have their own source, often a set of researchers or an institution that has put in some work to study and test them. Some of the more obscure question inventories are even paid material that clinicians (or their offices, more accurately) are supposed to license.
I caution against the clinicians who do rapid-fire diagnostics and slap a label on the patient within minutes of talking to them. Some patients like this when the diagnosis matches what they already self-diagnosed or they want to hear, but in these cases some clinicians are just picking up on the hints the patient gave and mirroring it back to them.
This rapid diagnostic method is an easy way to improve your patient satisfaction scores (important for performance measures at some clinics, especially when PE or corporate gets involved) and it’s an obvious way to free up some time in a clinician’s busy day.
There is a growing problem of lazy providers who try to speedrun the diagnosis and send patients on their way with a prescription for something and a request for a follow up appointment. During COVID when controlled substance prescribing rules were loosened for remote appointments there were even pill mills that would advertise for specific diagnoses on TikTok and then incentivize the providers to see as many patients per day and prescribe them all Adderall because it turned them into repeat customers for the recurring prescriptions. There was a whistleblower who revealed that they were measured on their rates of prescribing controlled substances and discouraged from prescribing alternatives with lower abuse/addiction potential even when patients admitted to having drug abuse problems. This is an extreme example but don’t discount the incentive for your provider to shorten your appointment for selfish reasons, not because the patient’s condition is obvious and easy to diagnose accurately within minutes.
My own personal experience with psychologists and psychiatrists, is most of them don’t go by the text of the DSM, they go by the understanding of various disorders they’ve received from their teachers, mentors, supervisors, colleagues-which at times has a rather loose relationship with what the text of the DSM actually says-and once they’ve made their minds up as to what is the correct diagnosis, then-when required for a formal report-they look at the DSM text and work out how to justify their diagnostic decision by relating what the text says to the evidence at hand
Dr. Palmer recommends the ketogenic diet, but not all people need this specific intervention to improve their metabolism. I think the best place to start for most people is simply eliminating their consumption of white flour, or at the least, fortified white flour [2].
Dr. Palmer tweeted about anemia and Vitamin B-12 deficiency [3]. Many patients are prescribed synthroid (T4) for their thyroid, but they often still have all the symptoms of hypothyrodism because their body doesn't activate T4 -> T3. Adding a source of T3 to patients' Synthroid treatment can make a big difference in their behavioral symptoms.
I have a book by some psychiatrists who were active in the 1940's -> 1950's, which is before the first 'psychiatric' medications were released. I didn't know this book was compiled by psychiatrists when I ordered it - I thought it was going to be a general book about the pro-metabolic intervention.
It's unfortunate that the prescription drug industry never figured out why some of their chemicals help with the symptoms labeled 'depression'. The MAOIs were reasonably-effective at helping acutely-depressed people out of bed. Each generation of antidepressants was less effective than the previous, until the SSRI's arrived. Now we're stuck with antidepressants that have always been known to cause people to commit suicide. At least the psychiatrists are now revisiting MAOIs as an option for people who don't respond well to the suicide pills (SSRIs).
Antipsychotics are a tragedy: anti-dopamine drugs make patients feel terrible. The one exception to the anti-treatment received by psychotics is an anti-serotonin drug approved for parkinsons psychosis [4].
[0] https://www.chrispalmermd.com/ https://twitter.com/ChrisPalmerMD/
[1] https://brainenergy.com/
[2] Flour manufacturers tend to use the cheapest fortifications possible. For example, the type of iron used for fortification is usually simply 'iron shavings', which usually becomes rust by the time it's absorbed.
[3] https://twitter.com/ChrisPalmerMD/status/1903071654328111413
[4] https://pmc.ncbi.nlm.nih.gov/articles/PMC5819716/
None of these hold up under actual studies. It’s the domain of wishful thinking that sadly preys upon people desperate for answers. Some times the placebo effect works for a while, but usually people just end up with a cabinet full of supplement bottles and a history of fad diets with no progress on their condition.
It is easy to test (drink a sugar challenge drink and measure H2 in breath) but as it is time consuming and not profitable rarely done.
I agree with you overall, but interestingly, research really has found a link between lower Vitamin B12/B6/B2 levels and ADHD. Also lower Vitamin D, and delayed circadian rhythm. You certainly can't use supplements as a replacement for stimulants but they may help.
(at which point you'll often notice immunodeficiencies, minor "unexplainable" abnormalities in bloodwork),
and indeed cognitive issues, depression, anxiety, and other more severe brain malfunctions.
but diagnostic names for groupings of common symptoms,
caused by seemingly completely unrelated stuff ranging from childhood trauma, to a staph infection or mercury leak in a tooth root.
> A study of 894 ADHD probands and 1135 of their siblings aged 5–17 years old found a ninefold increased risk of ADHD in siblings of ADHD probands compared with siblings of controls [2]. Adoption studies suggest that the familial factors of ADHD are attributable to genetic factors rather than shared environmental factors [3, 4] with the most recent one reporting rates of ADHD to be greater among biological relatives of non-adopted ADHD children than adoptive relatives of adopted ADHD children. The adoptive relatives had a risk for ADHD like the risk in relatives of control children [4].
> Twin studies rely on the difference between the within-pair similarities of monozygotic (MZ) twin pairs, who are genetically identical, and dizygotic (DZ) twin pairs, who share, on average, 50% of their segregating genes. The mean heritability across 37 twin studies of ADHD or measures of inattentiveness and hyperactivity is 74% (Fig. 1). A similar heritability estimate of around 80% was seen in a study of MZ and DZ twins, full siblings, and maternal and paternal half-siblings [5]. The heritability is similar in males and females and for the inattentive and hyperactive-impulsive components of ADHD [6,7,8].
https://www.nature.com/articles/s41380-018-0070-0
Granted they did have a control for adopted siblings
https://www.psychologytoday.com/gb/blog/looking-in-the-cultu...
"Although many twin studies have been conducted (which is quite an understatement; there are almost 9,000 hits for “twin study” on PubMed!), there have long been critics who argue that they are scientifically worthless."
Smith, Jinkinson. (2020). The debate over twin studies: an overview. http://dx.doi.org/10.22541/au.159674847.78026661
"Because heritability is defined by both genetic and environmental influences, it is not a fixed characteristic of a disease or trait, but a population-specific estimate, analogous to, for example, the mean height, cholesterol level or life expectancy in a population. It also cannot be interpretated at the family or individual level."
Kaprio J. (2012). Twins and the mystery of missing heritability: the contribution of gene-environment interactions. Journal of internal medicine, 272(5), 440–448. https://doi.org/10.1111/j.1365-2796.2012.02587.x
For example, monozygotic twins will always have the same eye color (99+% correlation), while dizygotic twins do not. Thus we can conclude eye color is genetic. Both twins are raised by their respective parents, so it's unlikely parenting is causing this difference in eye-color-correlation.
https://williamjbarry.substack.com/p/the-first-1000-days
https://www.psychologytoday.com/gb/blog/looking-in-the-cultu...
"Although many twin studies have been conducted (which is quite an understatement; there are almost 9,000 hits for “twin study” on PubMed!), there have long been critics who argue that they are scientifically worthless."
Smith, Jinkinson. (2020). The debate over twin studies: an overview. http://dx.doi.org/10.22541/au.159674847.78026661
"Because heritability is defined by both genetic and environmental influences, it is not a fixed characteristic of a disease or trait, but a population-specific estimate, analogous to, for example, the mean height, cholesterol level or life expectancy in a population. It also cannot be interpretated at the family or individual level."
Kaprio J. (2012). Twins and the mystery of missing heritability: the contribution of gene-environment interactions. Journal of internal medicine, 272(5), 440–448. https://doi.org/10.1111/j.1365-2796.2012.02587.x
Cecil, C. A. M., & Nigg, J. T. (2022). Epigenetics and ADHD: Reflections on Current Knowledge, Research Priorities and Translational Potential. Molecular diagnosis & therapy, 26(6), 581–606. https://doi.org/10.1007/s40291-022-00609-y
"The convincing evidence for genes as risk factors for ADHD does not exclude the environment as a source of etiology. The fact that twin estimates of heritability are less than 100% asserts quite strongly that environmental factors must be involved. ADHD’s heritability is high, and that estimate encompasses gene by environment interaction. Thus, it is possible that such interactions will account for much of ADHD’s etiology. Environmental risk factors likely work through epigenetic mechanisms, which have barely been studied in ADHD [148]. The importance of the environment can also be seen in the fact that, as for other complex genetic disorders, much of ADHD’s heritability is explained by SNPs in regulatory regions rather than coding regions [149]."
Faraone, S. V., & Larsson, H. (2019). Genetics of attention deficit hyperactivity disorder. Molecular psychiatry, 24(4), 562–575. https://doi.org/10.1038/s41380-018-0070-0
To be clear, ADHD, despite having "disorder" in the name, is actually a syndrome: a complex of symptoms that, when recognized together, indicate that a certain set of interventional treatments will likely be applicable.
Diagnosing someone with a syndrome does not indicate any knowledge is available on the cause (etiology) of the symptoms. Many different things can cause the same set of symptoms. But if a certain treatment ameliorates anything qualifying as that syndrome, regardless of the upstream cause, then the diagnosis of the syndrome (and so the existence of the syndrome as a concept) is useful, even if it's not informative.
The DSM actually covers two very different categories of what we might call "mental" illnesses: neurocognitive illnesses, and neuroendocrine (or neurohormonal) illnesses.
Neurocognitive illnesses — structural problems with the brain or its cells (think Parkinson's Disease, or ALS, or Lewy Body dementia) — are usually traceable to specific etiologies, as each one usually has either a very unique presentation of signs and symptoms, or has unique markers that can be assayed/biopsied for.
Neuroendocrine illnesses, on the other hand, are almost always syndromes. Many different upstream problems (genetic, toxic, nutritive, auto-immune, etc) can potentially cause the same small menagerie of messenger-chemicals to get out of whack, and due to this, many different upstream problems end up looking like the same few "templates" of symptoms. If you can put the particular out-of-whack messenger-chemicals back into whack with drugs that do that, then you've fixed the symptoms — which doesn't fix the upstream problem (if it even can be fixed), but does fully compensate downstream for the upstream problem.
If so, and if this view is really prevalent in psychiatry, somehow it's completely lost on the general public and media.
This is not in contradiction to something being syndrome. Plus patients usually do not understand and do not have to understand technical nuts and bolts of whatever issues they have.
You cant require people to talk in clunky language qualifying every single nuance each time they speak about issues or diagnoses they have. You would just render them unable to express what they need to express.
> If so, and if this view is really prevalent in psychiatry, somehow it's completely lost on the general public and media.
General public and media are completely lost on eating disorders, OCD, psychosis and pretty much any other psychiatric/psychological problem. They are equally lost on AI, HIV and economic policy.
If I feel sad all the time, it is not a behavior. It is a feeling. If I am forgetting a lot, it is a brain function too, not a behavior. Behavior can be used to mitigate the disordered brain, it can be result of it, it can be completely intendent of it.
Behavior can be something positive or neutral. Eating is behavior, giving a gift is a behavior.
You may be losing things often because your place is a complete mess. You may not keep attention in conversations because you spend all your time playing video games and cant relate to anybody, or because regular people simply bore you and you need to find your own crowd.
These kind of explanations are far different than "My brain is inherently and permanently incapable of 'proper executive function'. and the REASON Im like xyz is because of ADHD". Take a look at /r/ADHD if you get a chance. I saw a top thread that read "Does anyone else have trouble keeping eye contact during sex?" with everyone going "wow me too! I didnt know this was an adhd thing!"
Also your example is kinda dumb! You don't have to have Alzheimers to be forgetful, it's actually quite common. But if you post "anyone else here keep forgetting things?" on r/Alzheimers obviously people on there are going to be like "yeah me too".
In other words people with mental illnesses/conditions/disorders/syndromes doubt their own diagnosis, because sometimes it "just feels like an adorably tiresome behavioral `oh you` that everyone laughs at", and other times the wolves are howling inside and suddenly you understand every and all kinds of disability, escapism, compulsion, and serial killers, as you are trying to cancel plans, make up excuses, ask for help, while - by definition - fail to do any and all of those as a headwind of hurt hurls heavy and hopeless.
I just want to know whether my issues are normal and I'm gaslighting myself into thinking I'm broken or a loser, or if my specific issues are actually falling outside the norm. This way I know what treatment modalities might help, and which literature I can peruse instead of wasting my time reading up productivity advice meant for neurotypical people that will try to solve the wrong issue for me and just make me feel worse.
There’s advice for people.
Sometimes it will help you, and sometimes it won’t.
Regardless of the number of people it helped and didn’t help, and what labels apply to them.
You can be stuck for decades, as I was, taking advice that won’t work for you, until you figure out that you can get a medical solution that instantly enables all of those pieces of advice becoming usable.
It is not a coincidence that those pieces of advice weren’t working, they were never going to work unless preceded by medical help.
Many people pre diagnosis suffer the equivalent of taking years of running advice and wondering why the stay behind before noticing they’re missing a leg and it won’t work until they get prosthetics.
That’s not true, of course. You are not relegated to a category of defunct by simply existing without a leg. You can learn to get by without it — many do — and you can learn to excel without it.
When you exclude yourself based on blankets of labels, you miss good advice. Much advice about “running” has little to do with having 2 legs: Breathing, clothing, hydration, nutrition, time of day. Pacing advice can even apply when you run with an implement.
For some people this is their entire reality, having to fight against categorizations that split them into complete ability and disability.
For some others, they don’t even know there’s a fight to be had. They give up before knowing they had any chance at all.
It’s troubling for something like ADHD, where a constellation of symptoms are possible and some do not apply to you personally.
You can’t read because you have ADHD? It may be true. It may also be true that you have been forced to read things you’re not interested in, something rendered practically impossible by this disorder, and someone has labeled you as a non-reader due to your differences. It may also be true that you haven’t discovered Terry Pratchett, and you’re actually quite the reader with the right material.
For some even more others, they feel able with their medication and useless without. Luckily for them, their medication lasts all day, medication shortages do not exist, and their psychiatrist will always prescribe their medications forever.
The sarcasm there is unwarranted. Need for a treatment, when it exists, is orthogonal to its convenience. If you need an organ transplant to live, you need it regardless of whether you have donors and hospitals available or whether the lifelong meds they require can run dry at some point.
As for your larger point, to be clear, I understand the idea you’re trying to convey. Diagnoses can be limiting for some people either internally (limiting self perception) or by external judgement.
I don’t deny that, what I’m saying is that I feel you’re (probably unintentionally) falling into a different extreme that is just as damaging to others, which is to deny the need or convenience of treatment for those for which _there is no successful alternative_.
Shutting down a person through a label is harmful, dismissing their limitations because that would be labelling is harmful as well.
For the point of advice, advice can and will be harmful when it assumes realities that don’t apply to you.
To leave the analogy aside and give actual examples, methods to keep organization and accountability like checkboxes or diaries will not only be failed tries to those who need meds, but also reinforce a feeling of inadequacy as the user now feels lacking in discipline to commit to the method. Lack of self steem and negative self perception (lazy, messy, uncaring, etc) is a way too common comorbility with ADHD for a reason.
In short: no-one "has" ADHD. We just decided that people on the lower end of the spectrum in the "ability to concentrate" trait deserve a bit of a boost from otherwise illegal drugs to function in the society. Being in this lower end is called "having ADHD".
I would also challenge his premise about boring monotonous work is ill suited for humans, hence the ones with ADHD are people who can't do it (as good as others). ADHD people can do boring monotonous work for hours, month after month, and often not even struggle with that. On the other hand some banal easy (and short!) tasks, which won't even register as a task for normal human, will leave ADHD person in shambles, unable to even think about it.
There is lots of bad shit going in on the ADHD brain, it is certainly not just "20% worse concentration" debuff.
It does not logically follow that different symptoms -> different causes.
(Fire can cause smoke, heat, soot, etc. Depending on the wind and other conditions, only some of them may be observable.)
One root cause can manifest in different ways depending on interactions with other factors.
The genetic basis for ADHD is well studied and points to a single set of core causes.
Surely then, each of the symptoms (precieved, subjective symptoms) at that, can exist without ADHD.
So my question is, how do you know I simply dont have multiple completely independent things that together present the 6 symptoms? Even if we are to agree its a genetic condition, the diagnosis of sny particular individual isnt based on genes so theres room for criticism of the diagnostic process
If the DSM isnt what defines ADHD, what is?
ADHD diagnosis requires "onset" before age 14, yet there is such a thing as acquired ADHD (due to brain damage).
And of course the genes don't change during the latter, nor did they change when the age of onset criteria was raised from 12.
And even though both autism and ADHD was described more than a 100 (and 200) years ago it took a long time for AuDHD to be noticed. (2013)
The maps we have are bad, the territory is treacherous, and even if we assume the genes are unchanging the environment they find themselves in does seemingly faster and faster.
Any ADHD diagnosis includes checking for any other mental or physical issue that could explain the symptoms. Any when anything else is ruled out AND it can be established that the person always struggled with those symptoms (ideally that they were present in childhood) will you get a diagnosis.
Furthermore we know that ADHD has a genetic link. You have a 40% chance to have it when your parent has it. While we don't know every detail about how ADHD develops, we know it is something you are born with.
I am so sick that people pretend that ADHD is some vague concept. No, it is vague for you because you are ignorant about it.
Yes, ADHD can show up very differently in people. Which is not surprising because people happen to be different. Covid-19 can have widely different symptoms between people, doesn't mean it is not real.
As an ADHD person when I interact with other with ADHD people, yes there are huge differences but there is always a shared understanding. I never have the feeling the person has a completely different thing. There is always shared understanding.
To me this begs the question of whether the DSM authors might actually know something real and useful that the data don’t show. For example that anhedonia often progresses to suicidality even though the two might not coexist in the same person often. (Doesn’t sound right to me, but that’s how I read the article.) I think it’s plausible that the direct implication of this research is actually wrong. The obvious conclusion is that the DSM is full of it and doesn’t match real people’s experiences. But I suspect it might be that the DSM captures useful correlations and progressions that this method didn’t collect. Perhaps because the data here are from a single point in time, not a progression.
I think the most obvious conclusion is not that the DSM is bunk, but that some of things it groups together might be better to group separately. The real question of course is which grouping corresponds better to the group responding the same way to a similar intervention. After all the point diagnosing is to put people into groups so we can learn from the patterns of similar people to figure out better treatments.
It’s like going to the doctor and getting an HIV diagnosis because you’ve got a runny nose.
With actual doctors, they will take blood work, perform tests to find the actual virus, bacteria or other cause.
They find the cause, not just a list of symptoms.
Psychology and psychiatry is only now starting to actually research causes.
In the end, a diagnosis only helps the patient if it enables a treatment, hopefully an effective one. If you have a cluster of symptoms with two possible causes, and there is no difference in the care for the patient, what's the point of further differential diagnosis?
Many of the mental illnesses are of course bad, but in an evolutionary perspective it makes sense that we have these variations in a population, to optimise adaptation.
> It relies only on self-reported symptoms, and features requiring clinician observation are missing; symptoms are decontextualized (e.g., insomnia due to substance withdrawal isn’t differentiated from insomnia due to anxiety); all symptoms were assessed using a 12-month time scale, even though different symptom patterns exist at different time scales.
In particular, I’m not sure how this would identify somebody with the traditional schizophrenia + anosognosia combo, which requires another person to help diagnose.
Hierarchies don't exist. Nothing in nature is organized in trees (data structures), not even actual trees (the other kind). Organization, relationships, form directed graphs (or the continuous domain equivalent). Hierarchies are deceptively simple because they planarize, meaning you can draw them on paper without crossing lines, or introducing indirect references. But that's often as deceiving as it is helpful.
Think of the "tree of life" - there is no one tree of life, its shape depends on which aspects of phenotype or genotype you select and organize around. Think of corporations and governments - you can either accept there's a lot of "dotted lines" in the org chart, turning it into a dense DAG, or never understand why people do what they do. And so here, it's also quite apparent there are correlations cutting across the proposed hierarchy, clearly visible even on Figure 2 - the one that urges us to disregard the left-to-right ordering of the constructs.
I mean, the researchers are likely perfectly aware of this. My worry is that 90%+ of the insight of the proposed model will get lost in final planarization into a hierarchy that gets into the next DSM.
This study is a very good step in the right direction. The other direction is more quantitative methods such as measuring the brain waves response to a retinal laser flash to detect mental disorders (look it up, it's real)
https://www.nimh.nih.gov/research/research-funded-by-nimh/rd...
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