2024 Autism Science Review

#1 Families with an existing child with autism have a 20% chance of having another child with autism; this number varies based on the sibling’s gender and the number of autistic children in the family already 
Familial Recurrence of Autism: Updates From the Baby Siblings Research Consortium
PubMed ID: 39011552 

    #2 Many autism-related genes work through a druggable pathway called mTOR.
    Dysregulation of mTOR signaling mediates common neurite and migration defects in both idiopathic and 16p11.2 deletion autism neural precursor cells 
    PubMed ID: 38525876 

      #3 One of the most effective methods for improving  social communication and peer interactions in children is adapted for adults. 
      Adapting the PEERS® for Young Adults Program for Autistic Adults across the Lifespan
      PubMed ID: 39201145 

      #4 A new intervention improves mental health in adolescents and young adults with ASD.  
      Results from a Pilot Randomized Controlled Trial of a Single-Session Growth-Mindset Intervention for Internalizing Symptoms in Autistic Youth
      PubMed ID: 38833031 .

      #5 A new online version of a tool to measure cognitive ability is a promising alternative to in-person assessments for children and adolescents with ASD.
      An Exploration of Online and In-Person Administration of the Kaufman Brief Intelligence Test, Second Edition (KBIT-2) in Children and Adolescents Being Evaluated for Autism Spectrum Disorder
      PubMed ID: 38536637 

      #6 The impact of gastrointestinal issues on behavioral challenges and quality of life in those with profound autism is shared directly with GI doctors. 
      Conference proceedings: Inaugural meeting of the consortium for autism, genetic neurodevelopmental disorders, and digestive diseases
      PubMed ID: 39257288 

      #7 A short screening tool can identify profound autism in adults.
      Toward a functional classification for autism in adulthood
      PubMed ID: 39031157 

      #8 Families of people with profound autism describe specific and unique challenges across their lifespan.
      Profound Autism: An Imperative Diagnosis 
      PubMed ID: 38423722 

      #9 Teachers may overlook autistic school- age females
      Sex Differences and Parent–Teacher Discrepancies in Reports of Autism Traits: Evidence for Camouflaging in a School Setting
      PubMed ID: 39060706 

      #10 Conducting studies in schools reduces racial/ethnic disparities in research.
      Examining race, ethnicity, sex, and gender among autistic youth and their educators who participated in school-based research
      PubMed ID: 39056323 

      Registration is now open for the 11th annual Day of Learning, which will take place at the New York Athletic Club on April 4th!

      2023 was another year of valuable research findings that will improve the lives of individuals on the autism spectrum. Important advances were made in defining autism, measuring who has autism, understanding more about women with autism and identifying genetic mechanisms of resilience. Technology and artificial intelligence (AI) are reducing the time to diagnosis and improving access to early intervention. 

      What is autism?

      This year the community had a lot of conversations on how autism should be defined and diagnosed.

      Autism’s heterogeneity complicates issues relating to research, advocacy, services, supports and medical care. Some experience autism as a debilitating disorder, while others consider it an identity. Many fall in the middle. In 2021, the term “profound autism” was introduced to describe autistic individuals who require 24/7 supports, who are minimally verbal or nonspeaking or who have an IQ under 50. This year, there were several papers that examined this new definition and two editorials that attempted to reconcile the different views around the broad autism spectrum.1,2 Greene and Whitehouse suggest that individual brain differences, originating genetically or as the result of genetic/environmental interactions, lead to an autism diagnosis. That is followed by a “transactional” stage, where a child’s experience with the world molds their later behavior and functioning. This view does not contradict the idea of profound autism but hypothesizes the process by which autistic individuals develop symptoms and features. It also explains the vast heterogeneity across the spectrum, why interventions and supports that are “one size fits all” are not useful and why autism is a distinct category rather than a continuation of typical variation.3

      Who has autism?

      This title was “borrowed” from a 2014 Day of Learning presentation given by Cathy Rice, PhD from the Centers for Disease Control. Even 10 years later, it’s a relevant question.  

      New prevalence numbers for autism were released by the CDC ADDM Network, which has been tracking autism prevalence for the past 20-plus years. This year the CDC reported that the number of 8-year-old children who were diagnosed with autism increased to one in 36, with variability across gender and geographic location.4 Similar data obtained from 4-year-olds show that early identification of ASD is improving, and while racial and ethnic differences still exist in the cohort of 4-year-old children,5 that disparity is reduced by 8 years of age. But while racial disparities are improving, there are still features that differentiate those from different racial backgrounds. For example, intellectual disability is still diagnosed more often in Black children. Girls are also still significantly less likely to be diagnosed than boys at 4 or 8 years of age – a difference that has been consistently demonstrated and warrants further research.   

      This year for the first time, the CDC also measured the prevalence of profound autism using the definition published in the Lancet in 2021 (IQ<50, minimally or nonverbal and requiring round-the-clock supports). The CDC reported that 27.8% of those with ASD meet this definition of profound autism.6 Members of this population are rarely included in research studies. In response, ASF has launched a profound autism pilot grant program specifically devoted to studying this underrepresented and understudied population. 

      The question of “who has autism” is muddled by increased use of social media platforms that circulate inaccurate and misleading information about autism and its features. One study showed that most of the information about autism on TikTok was inaccurate, but that these representations were viewed just as often as were accurate presentations.7 This might explain misunderstandings about autism, what causes it and what can be done to help those with a diagnosis. We will never be able to stop the spread of misinformation on the internet, but families can educate themselves about the science of autism so they know what is true and what is false.

      Rage against the machine

      This year saw an explosion of new technology and artificial intelligence-assisted devices to help diagnose autism.  

      These tools, aka “AI” technologies are being developed to better automate an autism diagnosis in the hopes of decreasing the time families spend on waiting for an evaluation.8 Many of these new AI-based projects have been reviewed elsewhere or described in the ASF Weekly Science podcast.9

      Two such AI tools designed to improve diagnosis use measures of social attention and visual engagement, measuring how much time someone spends looking at social vs. nonsocial scenes. Researchers and clinicians have observed for years that children with autism tend to look less at faces and more at objects in a visual scene, and this knowledge has now been turned into screening and diagnostic tools. Duke University piloted a system called SenseToKnow, and it has shown promising results in pediatric settings.10Another technology, called EarliPoint, moved beyond the pilot stage and received FDA approval after validation for use in identifying children with autism as early as 16 months of age. Both are noninvasive and require a child to spend only a few minutes looking at different stimuli.11,12  They identify children with autism nearly as well as standard assessments, which can take hours to administer and can be costly.   

      Telehealth technologies like As You Are and CanvasDx (CanvasDx was FDA approved last year) are taking advantage of technological advancements to use clinician-coded measures of autism behaviors (like social communication abilities, social interaction, restrictive and repetitive behaviors, and caregiver reports of autistic behavior and impairment) to provide accessible diagnostic services. These are more like traditional assessments, but can be done in more naturalistic settings like the home over the internet. They use mathematical calculations to determine probability of a diagnosis from shorter observations.

      All of these “machine learning” approaches build on existing science around what is known about the early signs of autism, which behavioral features are most salient and what can be done to minimize burden to the family and eliminate diagnostic bias, as well as provide quality assessment services in countries that have few trained experts. The goal is to reduce the unacceptable waitlists to receive an evaluation. Other machine learning approaches are being studied to identify the best method of intervention,13 sleep14 and probability of a genetic diagnosis.15 Based on the number of published research protocols, there are at least four AI-based research studies in progress to improve understanding and prediction of severe and dangerous behaviors.

      These tools were built off the arsenal of scientific discovery in autism that has been established over the past decades. Without many years of eye tracking, brain tissue analysis, genetic discovery and facial expression analysis, developing tools like these would have been impossible. 

      Where are our girls?

      With females four times less likely to receive a diagnosis for various reasons16,  there is a lack of knowledge of the needs of females with autism, also called autistic females at birth.

      In 2023, the Lancet published a list of suggestions for supporting females on the spectrum, ranging from recognizing “female driven” stereotyped behavior to improving employment opportunities that are traditionally focused on male interests. 17 While it is known that factors like camouflaging autistic features may hide a diagnosis, age tends to play a huge role in the features that are displayed by autistic females vs. autistic males, as well as in how these behaviors are interpreted by clinicians.18 While many non-biological hypotheses have been generated to explain the difference in diagnostic prevalence of females vs. males, there are also neurobiological markers which may explain why certain features of autism are different in females, including different activity in certain brain regions during adolescence.19,20 Scientists have been able to dissect different cells from male and female brains to confirm that female cells have a higher rate of mutations in ASD risk genes compared to males.21 Finally, more research this year points to different patterns of brain development, which may explain behavioral differences in autistic females vs. males at birth.19,20,22 Females and males are typically different, and gender disparities in diagnosis are not unique to autism. However, as females with autism are understudied and often overlooked, clinicians and care providers need more tools to help autistic females receive the support they need. 

      How does the autism brain work?

      Understanding of basic neurological processes in autism leads to clues which influence therapeutics.

      Everyone wants to know what the autism brain looks like and how it functions across the lifespan and across genders. By understanding basic neurological processes in the brain, scientists can identify tailored support options and even therapeutics. More studies this year have shown similarities in how areas of the autistic brain connect compared to brains of people with ADHD and bipolar depression. This is additional evidence that autism is part of the bigger spectrum of neurodevelopmental disorders that includes depression, schizophrenia and obsessive-compulsive disorder. It also indicates that, while the autism brain may have a distinct profile, it has many similarities to other conditions and disorders.23

      Therapeutic clues are being identified from circuits and molecular markers in the brain. By studying brain tissue, scientists have found that genes controlling how neurons connect and communicate are dampened in autism, while those affecting inflammation are heightened. This finding has been confirmed in other body tissue24 and model systems.25 The changes suggest that initial overexcitation and overconnectivity of cells in the brain lead to inflammation and potential neurodegeneration. These changes may worsen over time, opening up areas of research not just in childhood but through adulthood.26 One of the genes of interest, GABA, turns cells off and is thought of as a “traffic light,” ensuring that not all the lights are green and that traffic flows safely. Brain tissue studies revealed that a decrease in the number of cells that contain GABA (and thus ensure that cells do not become too excited) is linked to two specific features of ASD: stereotypy and intellectual ability.27 The study of brain tissue and the ability to look directly at the brains of people with autism is only made possible by families who have learned more about the benefits of postmortem brain donation through the Autism BrainNet.

      Finally, new model systems, called assembloids, are also now being used to identify and understand not just the genes associated with autism, but how they function in cells.28 By using assembloids, sometimes referred to as “brains in a dish,” hundreds of different genes can be systematically altered and the functions of the cells examined to determine what those genes do. Using these systems, researchers found that a gene associated with ASD affected the function of a part of the cell called the endoplasmic reticulum, which resulted in abnormal migration, i.e., brain cells did not go to the right places during development.29

      Cha-Cha-Cha-Changes

      Families and individuals experience autism across the lifespan, so why should it just be studied at one time point?

      Longitudinal studies that track individuals over time are rare but critical in developing our understanding of autism trajectories. Studies this year point to at least three groups of trajectories: kids who start off with fewer signs and continue to have relatively fewer support needs; kids who are more impaired and stay relatively stable; and kids whose symptoms worsen over time. Features at 6 months were able to predict outcome at 5-6 years with some (but not absolute) accuracy.30 While some studies point to three or four trajectory “groups,” others show at least six.31   

      Longitudinal studies also indicated that people with autism show higher levels of mental health problems across childhood, predicted by IQ and gender, 32 with girls showing higher levels of depression and anxiety. Higher IQ at age 2 predicted lower levels of attention problems.32 From midlife through early old age, physical health worsened (as expected) but autism symptoms improved, with differences seen between those with and without intellectual disability.33 Other “turning points” or critical windows for change seem to happen in childhood and early adolescence,34 reinforcing that change over time is not linear; there are many peaks and valleys along the way, influenced again by intellectual ability. Females seem to be disproportionately affected by medical and psychiatric issues when transitioning from adolescence into adulthood.35 Future studies should integrate core autism features as well as comorbid conditions36 to better understand the abilities, disabilities and trajectories of those with ASD. 

      Genetics is not always deterministic

      New understanding of the types of gene changes, where they occur in the body and how they influence development can influence the type of treatment a person receives.

      There has been great debate over the utility of genetic research in ASD, including the roles of different types of gene mutations in functioning and outcome. Even among rare genetic syndromes associated with autism, there is great heterogeneity in features both within a diagnosis,37,38 and across disorders.39 So how deterministic are single gene mutations associated with autism? Recently, Rolland and colleagues demonstrated that some individuals who had rare genetic mutations did not qualify for a diagnosis,40  sparking debate about resilience to genetic mutations. Is it social environment, epigenetic factors, gender or other genes in the background that are conferring protection? 

      Recent evidence suggests that assortative mating may explain rare genetic variants in children with rare genetic forms of autism.41 The phenotypic similarities of the biological parents have only before been hypothesized for common variation, but this new work suggests a role for rare variation as well. In addition, those with rare genetic mutations and ASD are also more likely to have common variants, each with their own distinct influence on brain development and autism behaviors. This is consistent with a liability threshold model, where family members who may share genetic risk factors do not have a diagnosis, but where the rare genetic and common genetic variants add to a broad continuum of traits. In some of these cases, it can lead to a diagnosis.42 More genetic research will help identify how rare and common gene variants interact, how they lead to an autism diagnosis, what neural mechanisms are involved and whether and how the genes lead to other outcomes besides autism.

      Sometimes it’s not all about the autism

      Comorbidites of autism often are life-threatening and impair quality of life. There are some solutions. 

      Comorbid medical and psychiatric issues are a prescient issue in the autism community because individuals with ASD experience a higher burden of these disorders and conditions.43 There is an enduring recognition that comorbidities of autism can be severe, impair daily life and, in the case of catatonia and seizures, even be fatal. Some features associated with these comorbidities can be explained by etiological factors like family history and preterm birth.43 Many genes that are related to autism have multiple functions all over the body, including the GI system, leading to GI distress and dysfunction with an autism diagnosis.44 Identification of these genes has led to potential therapies.45-47 Most comorbidities are present across the lifespan, while some improve over time.48

      The unspoken heroes of autism families: siblings!

      Siblings have a unique relationship that lasts an entire life. Who knows you better than your sister or brother?

      Research shows that nonautistic siblings of people with autism are at higher risk for psychiatric and neurodevelopmental disorders compared to the general population. A thorough review of the literature published this year indicates a decreased quality of life and sense of well-being in non-autistic siblings. This varied by age, sibling relationship and other factors, but was found to be consistent across studies.49 There is not yet enough research to draw any conclusion about psychopathology in siblings, although depression was detected in some small studies.50 A new intervention incorporating cognitive behavioral therapy, positive psychology and stress management showed promise in increasing resilience to adverse events as well as promoting improved coping around stressful events in siblings.51

      The presence of a typically developing sibling has a beneficial effect on a multitude of outcomes for their autistic brother or sister, although differences in ages, sibling relationships and presence of challenging behaviors influenced the strength of the findings.52 The IQ of the autistic sibling and the presence of externalizing behaviors significantly influenced conflict between siblings. Instances where the proband had an intellectual disability showed the lowest level of conflict, while instances where the proband was prone to aggression resulted in the highest levels of conflict.53

      Final thoughts

      After a diagnosis, the first task is to find appropriate services, supports and interventions. But what works in one person does not necessarily work in another.

      The goal of autism research is to help individuals with autism and their families lead their best lives. The rise of personalized medicine will improve opportunities to deliver the right treatments to the right person at the right time. Gene-first studies are identifying treatments that are targeted at underlying biological causes in individuals with monogenic forms of autism. Longitudinal studies can identify critical windows for intervention. AI-driven technologies are being developed to improve diagnosis and mitigate symptoms.12 Comprehensive meta-analyses continue to reinforce the benefits of behavioral and developmental interventions for core features of autism. 54 And studies continue to confirm that “earlier is better” when it comes to intervention. For example, a new randomized clinical trial confirmed that 18-to-24-month-old children who received more intensive, individualized forms of intervention showed greater gains in language, social communication and self-help than those who received intervention later.55 Another study showed that those with better baseline adaptive skills had such strong responses to early intervention that their diagnosis was no longer evident by school age, suggesting this may influence response to intervention.56 Research this year also demonstrated that meaningful gains in language can be made in autistic children who are non-speaking through behavioral and naturalistic developmental interventions,57 as well as confirming that early intervention saves costs in the long term.58,59 No single intervention is going to support everyone across the autism spectrum equally, but it is clear that access to early, evidence-based intervention to help children live their best lives possible is imperative for child health and development.

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      26.       Zhang P, Omanska A, Ander BP, Gandal MJ, Stamova B, Schumann CM. Neuron-specific transcriptomic signatures indicate neuroinflammation and altered neuronal activity in ASD temporal cortex. Proc Natl Acad Sci U S A 2023; 120(10): e2206758120.

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      29.       Meng X, Yao D, Imaizumi K, et al. Assembloid CRISPR screens reveal impact of disease genes in human neurodevelopment. Nature 2023; 622(7982): 359-66.

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      51.       Kuhlthau KA, Traeger L, Luberto CM, et al. Resiliency Intervention for Siblings of Children With Autism Spectrum Disorder: A Randomized Pilot Trial. Acad Pediatr 2023; 23(6): 1187-95.

      52.       Cuskelly M, Gilmore L, Rayner C, Girkin F, Mulvihill A, Slaughter V. The impacts of typically developing siblings on the developmental outcomes of children with disability: A scoping review. Res Dev Disabil 2023; 140: 104574.

      53.       Rixon L, Hastings RP, Kovshoff H, Bailey T. Short Report: Outcomes for siblings associated with sub-groups of autistic children with intellectual disability identified by latent profile analysis. Res Dev Disabil2022; 130: 104337.

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      56.       Harstad E, Hanson E, Brewster SJ, et al. Persistence of Autism Spectrum Disorder From Early Childhood Through School Age. JAMA Pediatr 2023; 177(11): 1197-205.

      57.       Kasari C, Shire S, Shih W, Landa R, Levato L, Smith T. Spoken language outcomes in limited language preschoolers with autism and global developmental delay: RCT of early intervention approaches. Autism Res 2023; 16(6): 1236-46.

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      59.       Segal L, Green J, Twizeyemariya A, et al. Estimated Therapy Costs and Downstream Cost Consequences of iBASIS-Video Interaction to Promote Positive Parenting Intervention vs Usual Care Among Children Displaying Early Behavioral Signs of Autism in Australia. JAMA Netw Open 2023; 6(4): e235847.

      May 26, 2023 — News and autism updates from ASF, the Autism Science Foundation.

      Read about what ASF presented and discovered for autism updates at INSAR 2023.

      Autism Does Not Mean The Same Thing to Every Person

      This was a theme throughout INSAR. For some, autism is an identity, others a condition, and others a disorder. Everyone with autism is different, genetically, sociologically, demographically.  What is true of one person, even one autistic person, is not true of another. Everyone’s voice matters, but we should be doing better about including autistic voices in scientific research.

      Some voices from the autism community have expressed concerns about the scientific study of autism. One roundtable discussion group of neurodiverse autistic people centered around the feeling that genetic studies will be used to eliminate people with autism. These feelings linger despite genetic studies having the clearly defined purpose of helping with autism diagnosis and treatment.

      There is so much to learn from the study of genetics. Like the community itself, autism is diverse and complex. Genetic studies have helped doctors be able to recommend treatments for families with autism. The largest genetic study to date found insights into some of the biological complexities involved in autism, which can help develop new approaches to diagnosis and treatment.

      As ASF Chief Science Officer Dr. Alycia Halladay said on her ASF podcast, we need to work together as a community with interactions that are not solely based in fear and anger. We can be careful about how genetics is used. But we don’t need to stop science from being done. There are a multitude of conditions that are autism. There are so many discoveries to be made that will help with diagnosis and treatment. More studies are required, not less.

      ASF INSAR 2023 Get More People Involved in Autism Science

      Improve Accessibility for Participants in Autism Research

      Minimally verbal or intellectually disabled people are being excluded from autism research. One of the INSAR panels seeking to address this problem was “Breaking Down Barriers to Research for Children with Genetic Disorders, Intellectual Disability or Communication Challenges.“

      The goal of the panel was to share methods of helping participants to ensure families can complete the assessments to help their children. The chair, Dr. Carol Wilkinson, used a Swiss cheese analogy to show that participation can’t always follow a straight line. For example, some families get started but circumstances prevent them from finishing. Or they can’t get to the clinic to start. Or they complete biological assessments but then they can’t collect IQ.

      So what are the recommendations to help improve research participation from families?

      • Be flexible. Tests and protocols likely will need to be adapted for each participant. Many children on the spectrum have sensory issues. Some have challenging behaviors. Others may not understand what they have to do to participate. Researchers should look at the the difference in developmental level ratio against chronological age. In other words, don’t assume what participants can or can’t do based on their age. Skip unnecessary and non-applicable material as needed.
      • Meet them where they are at. Collect data in the most naturalistic setting where the participant feels most comfortable. Even if it means leaving your own comfortable place. Dr. Caitlin Hudac from the University of South Carolina shared how she spent 92 days on the road, collecting data from families within their own surroundings.
      • Use a personalized approach. Get as much information about your participant(s) ahead of time as possible. Examples: what’s their favorite toy, game, snack, etc.? Getting to know the people involved in research helps the family participate and improves the quality of data.
      • Plan for remote. It’s not always feasible to meet in-person with families during research. But that’s not the only way to do assessments or collect data. Dr. Karen Chenausky completed many parts of her research over Zoom, including language assessments, parent-child interactions, and motor tasks. She was able to protect the participants’ privacy and use a free downloadable app that parents used to measure language.

      Autism and Aging

      Internationally renowned expert Patricia Howlin from Kings College London talked about adulthood with autism. She has studied autism from birth to adulthood, seen autistic kids grow to be adults, and has used a unique longitudinal study design to address what happens to autistic kids as they get old. Unfortunately, there have not been enough studies in this area, the existing studies are designed differently, and not enough people are in each study.

      We still need multiple approaches, but people with autism as they age don’t have nearly the amount of information about them as those young children. That should change. The dynamics and needs of people aging with autism are as a varied as the spectrum itself. Additional studies should be expanded with the goal of determining precise and diverse definitions of quality of life for autistic people as they age.

      Autism in Females

      Girls are an underserved community in autism that needs more support and better diagnostics. This was made clear through multiple presentations at INSAR. To partially illustrate, this video from SPARK for Autism shows some of the needs specific to women and girls.

      Studies show higher burdens of rare genes and common genes associated with ASD and non-diagnosed family members like mothers or sisters.  This includes a South Korea study which replicated other studies with samples from around the world. There are many other traits unique to females with autism that warrant further study, including what’s called the “female protective effect” which theorizes that women and girls are better able to tolerate known genetic mutations. Multiple studies support this theory. It may help explain autism being less common among females.

      Research has also shown that females with ASD are diagnosed later and tend to have a lower IQ.  But a couple of subsets of children deserve a closer look to investigate what may be part of the female protective effect. These children either showed autistic traits early in life but then didn’t meet autism criteria later, or they met autism criteria in toddlerhood but didn’t meet the diagnostic threshold at a later school age. Girls in the first group (early life autistic traits that didn’t increase with age) showed poorer language ability. Girls from the second subset (those who missed the early diagnosis) had better language and less pronounced autism features but more problems in peer relationships. Are either of these related to the female protective effect? We don’t have a clear answer yet.

      Utilize The Autistic Community to Broaden Perspective

      How do we work with the autistic community to conduct science that is important but at the same time communicate the importance of that science? One of INSAR’s advocate panels talked about what should be done and not done using Spectrum10k as an example.  After backlash and concerns about the study design and principal investigators, the study’s leaders went back to the drawing board. They created and documented a new process. It was made for those that believe in genetics research as well as those in the community that are fearful of it.

      While there is no exact recipe, including the autism community in research should be mandatory and based on the following principles:

      • Trustworthiness; everything should be transparent, clear, and balanced.
      • Autistic-led and based on community priorities, not just the loudest voices on social media.
      • Include a diversity of voices and use engagement methods that are accessible. Provide physical and language accommodations as needed, such as type to text.
      • Ensure that something gets done, not just talked about, as part of the consultation.

      Autism science and research should benefit the larger community. Including a broad range of perspectives is critical.

      INSAR Videos On-Demand

      Videos from INSAR plenary sessions will be available starting June 5. This on-demand content will only be available until July 10 but is free to INSAR members. INSAR Membership reopens June 1.

      May 4, 2023 — News and autism updates from ASF, the Autism Science Foundation. Read about profound autism updates, see what’s happening at INSAR 2023, and watch the highlights video from ASF’s 2023 Day of Learning.

      Profound Autism Article from the Child Mind Institute

      “The term profound is not meant to demean anyone or label anyone as a lost cause,” said ASF President Alison Singer. “Just the opposite. The whole idea of creating this nomenclature is so we are better prepared to meet the needs of this population and not pretend they don’t exist.”

       “The main purpose was to call attention to the fact that these kids and adults exist, and that they do need different services,” said Catherine Lord, PhD, the co-chair of the Lancet Commission. 

      Read the full story: https://childmind.org/article/what-is-profound-autism/

      INSAR 2023

      ASF President Alison Singer and Chief Science Officer Dr. Alycia Halladay are in Stockholm this week as attendees and presenters for the 2023 International Society of Autism Research annual meeting. More highlights to come soon!

      2023 Day of Learning Highlights

      Watch a video recap of the 2023 Day of Learning. You can watch all the presentations from every speaker on our YouTube channel.

      April 26, 2023 — News and autism updates from ASF, the Autism Science Foundation.

      Profound Autism Alliance Caregivers Connected Meeting with Judith Ursitti

      Profound Autism Alliance Hosts Virtual Caregivers Connected Meeting

      Judith Ursitti, co-founder of the Profound Autism Alliance, and ECHO autism panelists invite caregivers of profoundly autistic individuals to the first virtual Caregivers Connected meeting on April 27, 2023. The one-hour event will start at 2:00 PM EST. Join up in a supportive, empowering online environment with other caregivers and family of people with profound autism.

      Sign up here to receive the Zoom link before the event.

      The Profound Autism Alliance is committed to the recognition of the unique challenges that people with profound autism and intellectual disability experience. Their mission is to improve health and connection through inclusive research and focused advocacy that will result in meaningful services and supports for people with profound autism. Judith Ursitti and her daughter Amy Ursitti received the 2023 Caryn Schwartzman Spirit Award from ASF at the 2023 Day of Learning.

      autism updates Alycia Halladay comments on Duke University discontinuing its EAP for children with ASD

      ASF CSO Dr. Alycia Halladay on Duke University Discontinuing EAP

      As reported by Vice, Duke University recently discontinued its expanded access program (EAP) to unproven stem cell and cord blood treatments for children with autism. Parents of autistic children had been paying for expensive, unproven treatments based on stem cell and blood cord treatments at Duke.

      ASF’s Dr. Alycia Halladay contributed to Vice’s article, pointing out the lack of evidence supporting stem cell therapies as a safe or effective treatment for autism. ASF also worked with the International Society of Stem Cell Research to make the FDA aware of the issues surrounding the EAP.

      Read the full article here.

      ASF 2023 Day of Learning 10th annual

      All 2023 Day of Learning Videos Now Available

      Missed the Day of Learning? Watch the recordings now for updates on cutting edge research and discussions about the future of autism science!

      Written by staff and the SAB of the Autism Science Foundation

      COVID Recovery Was Slow, But Scientific Progress Continues

      After two grueling pandemic years, 2022 saw a return to quasi-normalcy in both the world at large and in the world of autism research. Although the pandemic was incredibly challenging for autism families and researchers, the pivot to telehealth led to advances in online autism diagnoses, mental health supports, and interventions that will likely benefit autistic people across the globe for years to come.

      Autism scientists working in diverse areas of research made important strides this year and continued to gain valuable insights into every facet of autism. They also identified more effective ways to support people on the spectrum. Researchers developed a better understanding of the unique needs and priorities of specific groups of autistic people, better-defined links between biological mechanisms and behavior, and disparities in autism diagnosis and treatment.

      This work was only possible because of families like yours: You actively participated in important research studies. You agreed to have your data shared with others. You donated. You advocated. Your U.S. tax dollars supported $100 million of NIH grants funded in 2022

      Autism science simply cannot progress without your continued partnership. Earlier this year, ASF launched a “Participate in Research” directory to match families with research studies that meet your needs and interests. Many of these studies offer compensation, and can also provide valuable information and resources to aid your family member. The goal is to use the information gleaned from research to improve the real lives of real people, both now and in the future.

      Here’s a little bit of what 2022 taught us.

      Early identification leads to earlier diagnosis, but diagnosis happens at all ages

      • Developmental milestones are skills that most children reach at a certain age and are used by healthcare providers to track progress. This year, the CDC updated these milestones to track what 75% of children can do by certain ages, rather than 50%, causing some pushback. In addition, the CDC added new time points as well as markers that might predict an autism diagnosis.1
      • In autism, reaching developmental milestones can be delayed from months to years. Delays are often more severe and variable in those with co-occurring intellectual disability and a rare genetic variant. New research reinforced the need to focus on milestones and the importance of early intervention.: If you notice your infant is struggling with new skills, tell your healthcare provider.2
      • Language skills in infants are an important predictor of an ASD diagnosis. Recent work from the ASF-supported Baby Siblings Research Consortium (BSRC) showed that maternal education levels and early gestures are important predictors of these language skills, suggesting markers for intervention.3
      • Researchers have suggested that early behaviors that are predictive of a later diagnosis may be part of a larger “developmental cascade,” where, for example, the trajectory from laying to sitting to language may be disrupted. These are intertwined behavioral and neurobiological networks that affect how a person with autism functions.4
      • There are now multiple biomarkers under investigation. Some are better than others at not just autism diagnosis, but the response to intervention.5 In the future, they can be used to promote earlier diagnosis and more objective measures of the effectiveness of interventions.
      Key takeaways: Parents and clinicians should monitor developmental milestones early in life. Early signs are not a substitute for a diagnosis, but some supports and interventions can be provided that allow for an improvement of trajectories across the lifespan.

      Parent-mediated interventions and training – they work!

      • A review of 30 studies showed promising results from parent-mediated interventions, but improvements in studies are still needed.6
      • Parent-mediated interventions can be used for teaching everything from core autism symptoms to self-care like tooth brushing.7
      • Autism interventions can and should be customized to culture and race.8,9
      • Some parent-mediated interventions have been tested successfully in a hybrid format, leading the way for others to investigate their effect on parent and child outcomes.10
      • While some have suggested parents only recognize the weaknesses in their children, recent research strongly notes that parents know their child’s strengths and use those strengths to help support their family.  Educators also note these strengths in the classroom.11,12
      • Siblings play an important role in the outcome of autistic individuals, while they also experience unique challenges themselves.13,14
      Key takeaways: Parents and caregivers often feel helpless when they are concerned about their child’s development and are facing long waiting lists for services. New research shows that providing support is beneficial for both the parents and the child outcome, and elevates strengths while mitigating support challenges. Further research should continue to explore the role of sibling relationships and support.

      The brain has a distinct “signature” and sensory issues are on the front line

      • One type of immune cell of the brain called the microglia has been known to affect cell communication, shape, and number. Researchers have now determined when and where these cells are expressed during development, laying the foundation for research into a critical brain cell type.17
      • The greatest differences in gene expression in the brain are in sensory areas like the visual cortex.15 This may explain the almost universal problems in sensory processing that autistic individuals experience, and why sensory problems are so common in ASD.18
      • The visual area, specifically the occipital cortex, was also enlarged at young ages, more so in kids who have siblings with a diagnosis, demonstrating that genetic heritability plays a role in brain activity involved in sensory processing in families.19
      • A new marker of sensory processing was detected: differences in the activity of a neurotransmitter called GABA. GABA commonly slows down the activity of brain cells, which is important when they are too active, indicating this neurotransmitter is critical for sensory processing. Changing the activity of GABA neurons can alleviate sensory problems in autistic individuals.20
      • In addition, changes in the thickness of different cortical regions may influence sensory responses, depending on whether there is overstimulation or understimulation.21
      • Another brain region called the amygdala may relate to anxiety in autistic people. Certain areas of the amygdala are different in size,22 and can explain variability in anxiety.23  There is also disruption in connectivity from the amygdala to outside regions,24 which may also explain how anxiety interacts with autism features.
      • Rather than examining one autism feature at a time, it seems that ability to make gains or show potential for change over time is correlated to differences in brain structure. Markers of change over time are also linked to genes associated with ASD.25 Targets of intervention based on biological markers may need to focus on sensitivity to change rather than a specific number on an instrument per se.
      • The use of biological tools has increased this year. These tools include induced pluripotent stem cells (IPSCs) and organoids that are based on cells from individuals with different forms of ASD. Studies have looked at different types of autism (idiopathic and genetically-based) and identified creation of new brain cells as a common biological mechanism.26 New studies also used novel tools to improve the validity of these cell-based systems.27
      • Animal models can be used to identify mechanisms by which genes and environmental factors exert their influence over behavior. Right now, there are hundreds of animal models of ASD, but not all of them are used appropriately to understand ASD. The ability of the model to recapitulate both the biology and behavior involved in ASD is essential.28
      Key takeaways: While different brain regions are specialized in their function, they interconnect and turn on and off in synchrony. Researchers need better models of human neurobiology, including better animal models, to understand the core and associated autism features, from sensory dysfunction to GI issues. If you want to learn more about research involving the brains of people with autism, sign up for more information at Autism BrainNet.

      Genetic markers start to explain phenotype

      • The presence of rare genetic variants and common variants tend to funnel people into groups defined by intellectual disability (ID) or high educational attainment.29,30 Scientists have identified and characterized two major types of genetic variation associated with ASD. Rare genetic variants are commonly associated with lower cognitive function and profound autism, but that is not always the case.31  Even with hundreds of thousands of samples, scientists have still not found a direct gene – outcome linkage.  However, genetics are still important.  Genetic findings can help identify specific needs leading to appropriate supports.
      • Certain types of gene mutations can explain associations with features like psychosis,32 as well as obesity and depression.33
      • Five new variants were identified that are not linked to intellectual or developmental disability (IDD), but are linked to other neuropsychiatric issues besides ASD.31,34 Therefore, rare ASD or DD gene mutations usually lead to some sort of deleterious outcome.
      • There is a significant overlap between ASD genes and genes associated with developmental disorders in general. Researchers suggest that autism specificity may be the result of when the gene is expressed. For example, in developmental disorders, genes are expressed in progenitor cells while in ASD they may be expressed in developing neurons.35 
      • Other studies have not found any ASD-specific gene, they show linkage to neurodevelopmental problems in general, and can be grouped based on what cells are affected.35
      • There are shared pathways between ASD and other neuropsychiatric disorders.36 
      • Studies have shown linkages between epilepsy, ASD and ADHD.37
      Key takeaways: Genetic markers associated with ASD are also associated with other developmental conditions like ADHD and intellectual disability, as well as comorbid conditions like obesity. Two major types of genetic markers, rare and common variations, may represent biomarkers of two different phenotypes, but there is overlap, and rare and common variants are likely mixed in most people. Genetic research is important for a better understanding of ASD and the development of individualized approaches for supports.

      But genetics doesn’t tell it all

      • Parental genetics and environmental factors are intertwined on a biological level. Genes associated with depression in parents are also linked to ASD.38
      • Maternal immune infections are an established risk factor for ASD. However, the genetics of children with and without maternal immune challenges during pregnancy are different.39
      • Studies in Norway offer a unique perspective of gestational exposures by banking blood taken mid-pregnancy during usual obstetrical visits. One study has shown that certain cytokines, or markers of immune activity, are elevated during pregnancy in both boys and girls with autism, particularly in girls. It’s unclear what role these cytokines play collectively or individually, or where they came from in the first place.40
      • Where you live can affect the role of genes vs. environment, evidenced by environmental factors playing a bigger role in heritability in certain areas of Sweden and the U.K.41
      • Genetics and the environment clearly interact when it comes to the influence of an ASD diagnosis. For example, pesticide exposure exacerbated the effects of the autism CHD8 gene on rodent behavior.42
      • The role of environmental factors may depend not just on a diagnosis but on specific autism traits.43
      • Given that autism is likely part of a larger developmental disorder spectrum, regulation of toxic chemicals which are harmful to development must be expanded.44
      Key takeaways: The role of environmental factors in ASD has often been disassociated with genetics when it should be integrated into the understanding of autism’s causes, behavioral features, and interventions.

      Biological sex plays a role

      • Studies replicated this year showed that females with autism have a higher burden of rare genetic mutations. In addition, research is demonstrating that females with an autism diagnosis also show a higher level of “common” variations.29,45
      • The effect of higher levels of common variation in females extends to even undiagnosed members of ASD-impacted families, demonstrating that females carrying ASD genetic variation are resilient.45
      • The two above studies implicate an important role of the female protective effect but do not explain all of the differences in diagnosis.46
      • Some scientists have wondered if biases in instruments used to inform a diagnosis play a role in the sex difference. One study used a mathematical algorithm to eliminate the difference in M:F diagnostic differences, but still, females show different behavioral profiles. This further reiterates that instruments should be used to inform, not make a diagnosis, and that autism is more than a yes or no diagnosis. 47
      • Clinicians may miss an autism diagnosis in females because of camouflage. Females are also more likely to camouflage, which means they (consciously or unconsciously) pretend to fit in as a typically-developing girl. This leads to lower quality of life.48
      •  Intellectual disability plays a bigger role in autism features in girls vs. boys.49
      •  New genetic mutations involving the X chromosome were identified – and these mutations are more likely to occur in females.35
      • Sex differences in brain region size can be attributed to gene expression patterns. In other words, brain differences in males and females with ASD are due, in part, to underlying genetics.50
      Key takeaways: Females with ASD show different biological and behavioral profiles and are understudied in research and underserved in the community. Future research should aim to include more females to better understand their unique needs and provide targeted support.

      It’s still not over, but families are in a better place than a year ago

      Autistic Girl on Computer
      • Despite a rocky start at the height of the pandemic in 2020 and 2021, opportunities to receive autism diagnoses, mental health supports, and interventions via telehealth have been improved, and polished, and are not only acceptable to families and clinicians but are effective.51-57
      • Families and clinicians were happier with remote diagnosis and evaluation when the diagnosis was clear; in cases where there was some ambiguity, it caused frustration.58,59
      • While many families and individuals experienced a mental health decline during the pandemic, some exhibited resiliency under social distancing guidelines.60 The differences could be due to the degree to which services were lost, coping styles, and pre-existing mental health attributes.61
      Key takeaways: Autism families suffered during the pandemic, but it also allowed for new approaches to be developed that may ultimately improve practice – including hybrid clinical services, holistic family support, and more comprehensive diagnostic practices.

      It’s not all about the ASD

      • Individuals with ASD experience higher levels of anxiety, GI issues, epilepsy, and other developmental disorders like ADHD compared to those without a diagnosis.
      • While not a core autism symptom, anxiety is linked to insistence on sameness in toddlers with ASD, which indicates a similar underlying mechanism.62
      • Gastrointestinal issues plague people with autism, and there are few options for treatment. The gastrointestinal microbiome has been a target for intervention for autism symptoms, although studies are still ongoing.63 GI issues were the focus of a major NIH-funded meeting this year.
      • Suicide risk is higher in ASD. 64
      • Sleep problems, while mostly studied in children, are now shown to follow kids into adolescence and adulthood.65
      • There is a high degree of overlap in the brain activity profiles between ADHD and ASD kids. Differences are mostly seen when symptom severity is accounted for. ADHD and ASD show more similarities in the brain than differences.66
      • Behavioral profiles between ADHD and ASD are also similar.67
      • Mental health concerns are present in adolescents and adults with ASD with cognitive inflexibility strongly linked to compromised mental health.68,69 Cognitive inflexibility, which is different than cognitive ability, is how someone shifts their attention from one thing to another based on what is going on around them. This may be a focus for future mental health interventions.
      • Unfortunately there are no strong individual-level predictors in childhood of mental health issues in adults, but some factors that may lead to better mental health are better living skills and higher IQ.70
      Key takeaways: Outside the core features of autism listed in the DSM5, individuals experience a wide range of associated features, ranging from psychiatric issues to medical comorbidities. For many individuals, these associated features are highly debilitating.

      Biases in underserved communities are getting more attention

      • A recent analysis showed a reduction of the disparities in the age of ASD diagnosis for Black and Hispanic children over the last four years, but a difference still exists.71
      • This is likely due to provider bias, but not necessarily diagnostic instrument biases. The standard diagnostic tools are not biased toward race or sex.72
      •  Lessons learned from the pandemic reiterate the need for intense community engagement, flexibility, and an understanding that a holistic approach – rather than one focused on ASD – is necessary for working with underserved communities73,74.
      • A culturally-adapted parent training program delivered by Black providers was effective in the Black community and could be a model for future engagement efforts.8
      • Only 25% of intervention studies report the ethnic and racial makeup of their participants,75 indicating that researchers need to do a better job of deliberately including racial and ethnic minorities, recruiting them as research leads and coordinators, and including them on boards for scientific review.76
      • Low socioeconomic status contributes to social and communication deficits in young children with ASD.77
      Key takeaways: Racial and ethnic biases are still pervasive in autism research and diagnosis, and we need a holistic approach to support families in all aspects of their lives beyond just autism symptoms. Scientists must continue to focus on the deliberate inclusion of these groups in both research and career training to better serve all individuals with autism.

      On a final note, there has been a lot of debate this year about the language used to describe autism. 78-81 There is a diversity of experiences with autism and likely to be a diversity of perspectives. Families and scientists should use scientifically accurate terms to best describe the wide range of autistic people and their symptoms.82  What that is may differ from person to person, and situation to situation, which means context and preference need to be considered as well.

      References

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      2.         Kuo SS, van der Merwe C, Fu JM, et al. Developmental Variability in Autism Across 17 000 Autistic Individuals and 4000 Siblings Without an Autism Diagnosis: Comparisons by Cohort, Intellectual Disability, Genetic Etiology, and Age at Diagnosis. JAMA Pediatr 2022; 176(9): 915-23.

      3.         Pecukonis M, Young GS, Brian J, et al. Early predictors of language skills at 3 years of age vary based on diagnostic outcome: A baby siblings research consortium study. Autism Res 2022; 15(7): 1324-35.

      4.         Bradshaw J, Schwichtenberg AJ, Iverson JM. Capturing the complexity of autism: Applying a developmental cascades framework. Child Dev Perspect 2022; 16(1): 18-26.

      5.         Webb SJ, Naples AJ, Levin AR, et al. The Autism Biomarkers Consortium for Clinical Trials: Initial Evaluation of a Battery of Candidate EEG Biomarkers. Am J Psychiatry 2022: appiajp21050485.

      6.         Conrad CE, Rimestad ML, Rohde JF, et al. Parent-Mediated Interventions for Children and Adolescents With Autism Spectrum Disorders: A Systematic Review and Meta-Analysis. Front Psychiatry 2021; 12: 773604.

      7.         Fenning RM, Butter EM, Macklin EA, et al. Parent Training for Dental Care in Underserved Children With Autism: A Randomized Controlled Trial. Pediatrics 2022; 149(5).

      8.         Kaiser K, Villalobos ME, Locke J, Iruka IU, Proctor C, Boyd B. A culturally grounded autism parent training program with Black parents. Autism 2022; 26(3): 716-26.

      9.         Rivera-Figueroa K, Marfo NYA, Eigsti IM. Parental Perceptions of Autism Spectrum Disorder in Latinx and Black Sociocultural Contexts: A Systematic Review. Am J Intellect Dev Disabil 2022; 127(1): 42-63.

      10.       Brian J, Solish A, Dowds E, et al. “Going Mobile”-increasing the reach of parent-mediated intervention for toddlers with ASD via group-based and virtual delivery. J Autism Dev Disord 2022; 52(12): 5207-20.

      11.       Mirenda P, Zaidman-Zait A, Cost KT, et al. Educators Describe the “Best Things” About Students with Autism at School. J Autism Dev Disord 2022.

      12.       Wilkinson E, Vo LTV, London Z, Wilson S, Bal VH. Parent-Reported Strengths and Positive Qualities of Adolescents and Adults with Autism Spectrum Disorder and/or Intellectual Disability. J Autism Dev Disord 2022; 52(12): 5471-82.

      13.       Rosen NE, Schiltz HK, Lord C. Sibling Influences on Trajectories of Maladaptive Behaviors in Autism. J Clin Med 2022; 11(18).

      14.       Mokoena N, Kern A. Experiences of siblings to children with autism spectrum disorder. Front Psychiatry 2022; 13: 959117.

      15.       Gandal MJ, Haney JR, Wamsley B, et al. Broad transcriptomic dysregulation occurs across the cerebral cortex in ASD. Nature 2022; 611(7936): 532-9.

      16.       Chen Y, Dai J, Tang L, et al. Neuroimmune transcriptome changes in patient brains of psychiatric and neurological disorders. Mol Psychiatry 2022.

      17.       Menassa DA, Muntslag TAO, Martin-Estebane M, et al. The spatiotemporal dynamics of microglia across the human lifespan. Dev Cell 2022; 57(17): 2127-39 e6.

      18.       Wiggins LD, Tian LH, Rubenstein E, et al. Features that best define the heterogeneity and homogeneity of autism in preschool-age children: A multisite case-control analysis replicated across two independent samples. Autism Res 2022; 15(3): 539-50.

      19.       Girault JB, Donovan K, Hawks Z, et al. Infant Visual Brain Development and Inherited Genetic Liability in Autism. Am J Psychiatry 2022; 179(8): 573-85.

      20.       Huang Q, Pereira AC, Velthuis H, et al. GABA(B) receptor modulation of visual sensory processing in adults with and without autism spectrum disorder. Sci Transl Med 2022; 14(626): eabg7859.

      21.       Habata K, Cheong Y, Kamiya T, et al. Relationship between sensory characteristics and cortical thickness/volume in autism spectrum disorders. Transl Psychiatry 2021; 11(1): 616.

      22.       Seguin D, Pac S, Wang J, et al. Amygdala subnuclei volumes and anxiety behaviors in children and adolescents with autism spectrum disorder, attention deficit hyperactivity disorder, and obsessive-compulsive disorder. Hum Brain Mapp 2022; 43(16): 4805-16.

      23.       Andrews DS, Aksman L, Kerns CM, et al. Association of Amygdala Development With Different Forms of Anxiety in Autism Spectrum Disorder. Biol Psychiatry 2022; 91(11): 977-87.

      24.       Lee JK, Andrews DS, Ozturk A, et al. Altered Development of Amygdala-Connected Brain Regions in Males and Females with Autism. J Neurosci 2022; 42(31): 6145-55.

      25.       Pretzsch CM, Schafer T, Lombardo MV, et al. Neurobiological Correlates of Change in Adaptive Behavior in Autism. Am J Psychiatry 2022; 179(5): 336-49.

      26.       Connacher R, Williams M, Prem S, et al. Autism NPCs from both idiopathic and CNV 16p11.2 deletion patients exhibit dysregulation of proliferation and mitogenic responses. Stem Cell Reports 2022; 17(6): 1380-94.

      27.       Revah O, Gore F, Kelley KW, et al. Maturation and circuit integration of transplanted human cortical organoids. Nature 2022; 610(7931): 319-26.

      28.       Silverman JL, Thurm A, Ethridge SB, et al. Reconsidering animal models used to study autism spectrum disorder: Current state and optimizing future. Genes Brain Behav 2022; 21(5): e12803.

      29.       Antaki D, Guevara J, Maihofer AX, et al. A phenotypic spectrum of autism is attributable to the combined effects of rare variants, polygenic risk and sex. Nature Genetics 2022; 54(9): 1284-92.

      30.       Warrier V, Zhang X, Reed P, et al. Genetic correlates of phenotypic heterogeneity in autism. Nature Genetics 2022; 54(9): 1293-304.

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      This week’s podcast explores the question about whether or not it is beneficial or just confusing to teach your child with autism multiple languages, or suppress the use of more than one language at home. Turns out, being bilingual helps with executive functioning (or those with preserved executive functioning can be bilingual), language, and provides benefits in verbal IQ depending on SES. In other words, it’s not harmful, it can be helpful, and those who choose to speak two languages at home should continue to do so if they feel that it is enhancing their child’s learning. Listen to the podcast here and find more information in the links below:

      https://pubmed.ncbi.nlm.nih.gov/35102760/

      https://pubmed.ncbi.nlm.nih.gov/34813032/

      https://pubmed.ncbi.nlm.nih.gov/36222993/

      You heard it in the news this week, and we discuss it on this week’s ASF podcast. Can you make little brains in a dish then make them better by providing them a real structured live neural environment? Can these organoids integrate with a live brain and be functional in vivo? The answers are: yes! Learn more from a new study published this week. Also, what the h**l is genetic confounding and how can it address many of the controversies of genetic vs. the environment? Sometimes genes that predispose to a disorder also predispose to environmental factors leading to that disorder. There is always room for both. Listen to the podcast here and below are the links as promised:

      https://www.fhi.no/en/studies/moba/

      https://pubmed.ncbi.nlm.nih.gov/35793100/

      https://www.nature.com/articles/s41586-022-05277-w