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Social anxiety disorder (SAD) is a common and debilitating condition marked by intense fear of negative evaluation in social situations. It often co-occurs with other psychiatric disorders, and in particular Autism Spectrum Disorder (ASD). The exact cause of SAD is unclear, though biological, environmental, and genetic factors are believed to contribute. Recent research highlights the involvement of neuropeptides, neurohormones, and immune system components in SAD development, suggesting complex interactions between psychological and biological factors, with a growing focus on inflammation’s role. This study aimed to investigate potential biochemical correlates of SAD in individuals with ASD, their first-degree relatives (BAP group), and healthy controls (HCs), focusing on inflammatory markers, neuropeptides, and growth factors.
Methods
Twenty-four adults with ASD, their relatives, and HCs, for a total of 72 participants, were assessed. Biochemical parameters were analyzed using enzyme-linked immunosorbent assays (ELISA), and social anxiety symptoms were evaluated via the Social Phobia Spectrum—Self Report (SHY-SR) questionnaire.
Results
Individuals with ASD exhibited significantly higher SHY-SR scores compared to the BAP and HCs. Subjects in the ASD group tended to make greater use of anxiolytics in order to improve their social interaction skills. Additionally, a specific pattern of correlation and association was found between biochemical variables and specific SAD symptoms, suggesting a potential role of inflammatory pathways in SAD pathophysiology.
Conclusions
Our results confirm the presence of greater social phobic symptoms in subjects with ASD, and support the hypothesis of a role of the inflammatory cascade in the maintenance of the disorder.
Autism spectrum disorder (ASD) is a lifelong neurodevelopmental condition with substantial functional and societal burden. However, national data on ASD burden remain limited in many middle-income countries, including Jordan.
Aims
This study aimed to quantify temporal trends in the prevalence, incidence and disability burden of ASD in Jordan from 1990 to 2023, using estimates from the Global Burden of Disease (GBD) study 2023.
Method
This population-based longitudinal study used GBD 2023 estimates to quantify the burden of ASD in Jordan from 1990 to 2023. As national epidemiological data are limited, estimates were generated with GBD’s Bayesian meta-regression modelling based on regional covariates. Annual prevalence, incidence and years lived with disability (YLDs) were extracted as counts and rates per 100 000 population with 95% uncertainty intervals, and analysed by age, gender and temporal trends.
Results
Between 1990 and 2023, the burden of ASD in Jordan increased substantially, with estimated point-prevalence cases rising from 23 919 to 97 056, and YLDs increasing from 4541 to 18 399. Point estimates of age-standardised prevalence, incidence and YLD rates increased over time, with consistently higher burdens among males and the highest rates observed in early childhood, particularly ages 2–9 years. However, wide and frequently overlapping 95% uncertainty intervals suggest that temporal changes should be interpreted with caution.
Conclusions
This study describes modelled trends in ASD burden in Jordan from 1990 to 2023, showing an overall increase in prevalence, incidence and disability-related measures. These findings should be interpreted cautiously given the reliance on GBD modelled estimates, but they may support Jordanian and similar countries’ future planning of health services and research priorities.
Recent studies indicate that anxiety is one of the most prevalent mental health challenges faced by children and adolescents diagnosed with autism spectrum disorder (ASD).
Methods:
For young individuals with concurrent Intellectual disability disorder, these rates are projected to be significantly elevated.
Results:
Despite the estimated high prevalence of anxiety among young individuals with co-occurring ASD and intellectual developmental disorder (IDD), significant uncertainty remains in the field about the most effective methods for identifying, diagnosing, and treating anxiety in this distinct group.
Conclusions:
The main objective of this narrative review is to examine the current literature on effective strategies and adjustments for evaluating and treating anxiety in children and adolescents who have co-occurring ASD and IDD, aiming to support professionals engaged with this significantly neglected group.
To explore existing knowledge on autism in medical education and early clinical training, examine the lived experiences of autistic doctors, review relevant National Health Service policies and legal frameworks, and propose a practical framework for improving inclusion. This study comprised a narrative review of the published literature on autism in medical education, foundation training and healthcare settings, supplemented by a positionality statement informed by the author’s clinical experience.
Results
Common barriers include the hidden curriculum of clinical placements, neurotypical templates in communication assessment, sensory demands of clinical environments, significant risks associated with disclosure and inadequate supervisor awareness. Masking imposes substantial psychological costs, including risk of autistic burnout. Legal frameworks exist but are inconsistently applied in practice. The SUPPORT framework is proposed as a structured model: Structured learning environments, Understanding neurodiversity, Predictability, Practical adjustments, Open culture, Relationships and mentorship, and Trainee well-being.
Clinical implications
Autistic doctors bring valuable strengths to clinical practice. The barriers they face during the transition from medical school to clinical practice are documented and preventable. Despite legal protections and growing awareness of neurodiversity, National Health Service training frameworks do not consistently address the needs of autistic clinicians. The SUPPORT framework provides a practical, low-resource approach to addressing these barriers, with implementation requiring greater awareness and institutional commitment. These findings identify the need for medical training to move past recognition of neurodiversity and towards creating clinical environments in which autistic doctors can thrive.
Early diagnosis of autism spectrum disorder (ASD) remains a significant challenge due to the time-consuming and subjective nature of traditional diagnostic methods. This study proposes a reliability-oriented hybrid deep learning framework that provides a low-cost, scalable, non-invasive, and AI-assisted pre-screening tool for early ASD risk indication and referral support.
Methods:
The proposed system integrates two independent deep learning architectures: (1) a ResNet18 model optimized with 10-fold cross-validation using static periocular image data, and (2) a multi-CNN facial image classification ensemble combining ResNet50, EfficientNet-B0, and DenseNet121 architectures. The periocular pathway uses the fine-tuned ResNet18 fully connected softmax layer as its decision boundary. The facial pathway uses weighted probabilistic averaging, and the two subsystem outputs are subsequently combined through an OR-based reliability fusion rule. Additionally, explainable artificial intelligence (Grad-CAM) was employed to visualize decision-relevant regions.
Results:
The static periocular ResNet18 model achieved a sensitivity of 90%, while the multi-CNN facial classification ensemble reached a sensitivity of 87.1% and an AUC of 0.948. Under the conditional-independence assumption, OR-based reliability fusion yielded an analytically estimated system-level sensitivity of 0.9871, corresponding to a joint false-negative probability of approximately 1.29%.
Conclusions:
The developed hybrid model is positioned as an AI-assisted pre-screening and early-referral support tool, not as a replacement for clinical evaluation. By combining reliability-oriented parallel fusion with explainable AI, the system supports clinical transparency and offers a scalable pathway for early ASD risk indication.
Problematic teacher–pupil relationships (TPR) affect children’s educational outcomes and mental health, particularly for children with psychiatric disorders and neurodevelopmental conditions, yet few population-based studies have explored this association.
Aims
To estimate the association between problematic TPRs and psychiatric disorder classifications including neurodevelopmental conditions and poor mental health, and whether this varied by informant.
Method
A cross-sectional analysis of the Mental Health in Children and Young People 2017 survey (n = 6634) was performed. Mental health was assessed using the Strengths and Difficulties Questionnaire, whereas classification of psychiatric disorders, including neurodevelopmental conditions, was assessed using the Development and Well-Being Assessment. TPR quality was evaluated through reports from parents and children (aged >11 years). Bivariable and multivariable regression analyses were stratified by age (5–10 years, n = 3509; 11–16 years, n = 3010), controlling for covariates. Multiple imputation was used to address missing data.
Data-set information: NatCen Social Research (2024), Mental Health in Children and Young People 2017, UK Data Service, SN 8467.
Results
Problematic TPRs were associated with increased odds of any psychiatric disorder in children aged 5–10 years (adjusted odds ratio = 4.80, 95% CI: 2.74–8.40) and 11–16 years (adjusted odds ratio = 4.07, 95% CI: 2.76–6.01). Strengths and Difficulties Questionnaire total difficulties scores were higher by 4.26 points (95% CI: 3.09–5.42) and 3.93 points (95% CI: 3.04–4.83) for children aged 5–10 and 11–16 years, respectively. Problematic TPRs were also associated with attention-deficit hyperactivity disorder, with no significant differences between informant types. Teacher recognition of poor mental health did not moderate these associations.
Conclusions
These findings support the importance of TPRs in school policy and of supporting teachers to foster positive relationships in schools.
Despite growing recognition as a public health concern, the burden of autism spectrum disorder (ASD) in Ethiopia remains poorly characterised owing to limited diagnostic capacity and epidemiological data, hampering evidence-based policy and intervention planning.
Aims
This study aimed to quantify the longitudinal burden of ASD in the Ethiopian paediatric population from 1990 to 2023 and project future trends to 2050 to inform national health strategies.
Method
Using Global Burden of Disease (GBD) 2023 data, we estimated ASD prevalence, incidence and disability-adjusted life-years (DALYs) among Ethiopian children and adolescents. Trends were analysed using joinpoint regression and future burden was forecast to 2050 using autoregressive integrated moving average (ARIMA) modelling.
Results
Between 1990 and 2023, ASD prevalence increased by 155%, from 271 805 to 693 644 cases. Correspondingly, the age-standardised prevalence rate increased from 950 to 1185 cases per 100 000 population. Although annual incident cases nearly doubled (from 24 576 to 47 274), the age-standardised incidence rate declined slightly from 86 to 81 cases per 100 000. DALYs increased by 162% to 134 386 in 2023, while the age-standardised DALY rate increased from 179 to 230 per 100 000. Projections to 2050 suggest that the overall ASD burden will persist, with a stable incidence rate but an increasing DALY rate.
Conclusions
Nearly 700 000 Ethiopian children and adolescents were living with ASD in 2023. The significant increases in prevalence and DALYs over three decades underscore the urgent need for a comprehensive national strategy, including enhanced diagnostic infrastructure and early intervention programmes.
As perinatal medical care has improved, the most prevalent aftermath of preterm birth has shifted to developmental and behavioral deficits without motor disabilities. Compared to individuals born at term, individuals born preterm, particularly those born before 32 weeks’ gestational age, have poorer cognition, executive function, attention span, processing speed, language skills, and academic outcomes. They are at elevated risk for developing behavioral and emotional conditions, including attention deficit hyperactivity disorder, anxiety, autism, depression and mood disorder. Individuals born preterm have long-term differences in brain structure. Interventions for individuals are critical, beginning in early years.
Neurodevelopmental disorder traits are associated with a range of psychosocial difficulties, yet the longitudinal processes linking these traits to mental health remain insufficiently explored. This study examined developmental associations among autism spectrum disorder (ASD) traits, attention-deficit/hyperactivity disorder (ADHD) traits, social maladjustment, and mental health from childhood through adolescence.
Methods
Longitudinal data were drawn from 9,619 students across 11 grade cohorts in mainstream classrooms. Cross-lagged structural equation modeling was used to estimate independent longitudinal associations among ASD traits, ADHD traits, social maladjustment, and mental health, while controlling for confounding factors. ASD and ADHD traits were modeled simultaneously to clarify their unique developmental patterns.
Results
ASD traits were consistently associated with later internalizing problems and peer difficulties. ADHD traits were associated with later internalizing and externalizing problems, as well as academic challenges and strained teacher–parent relationships. These associations differed by trait type, suggesting distinct developmental pathways. Several bidirectional associations also emerged: poorer mental health was associated with subsequent social maladjustment, which was subsequently linked to persistent developmental difficulties.
Conclusions
The findings indicate that social maladjustment is involved in the longitudinal associations between developmental disorder traits and mental health and may shape developmental trajectories. These results highlight the need for comprehensive support approaches that consider peer relationships, learning environments, and family–school relationships.
The shorter lifespan and increased prevalence of physical and psychiatric comorbidities in autistic people is a challenge for mental health. There is a high risk of suicide-related behaviors in autism, which are related to mental health issues, social isolation, and other factors. Here we aimed to systematically review the evidence on risk and protective factors of suicidal behaviors in autistic people. Electronic datasets (PubMed, Scopus, Web of Science, and PsycInfo) were searched for empirical articles on the risk and protective factors for suicide in autism. The PRISMA guidelines were followed, and a series of inclusion and exclusion criteria were applied to the retrieved data. This review included 19 studies reporting multiple risk factors associated with suicide-related behaviors. Noteworthy contributors among these factors include psychiatric comorbidities, bullying, cyberbullying, teacher harassment, and cognitive functions. The evidence for protective factors is limited; however, social relationships are highlighted. Identifying risk and protective factors is paramount for detecting early warning signs and enabling the prevention and intervention of suicidal behavior. Our review identified key sociodemographic, clinical, and cognitive risk factors to take into account as alarm-signs when identifying suicidal behaviors in autism.
Catatonia remains under-recognised in many low- and middle-income countries, particularly in transition-age youth (15–25 years). This is especially relevant in parts of Central Asia, where diagnostic traditions have historically emphasised schizophrenia. Drawing on clinical observations and existing literature, this paper highlights how limited recognition of adult autism and catatonia may contribute to diagnostic uncertainty and missed treatment opportunities. Catatonia is frequently treatable yet insufficiently incorporated into psychiatric training and service development in resource-limited settings. Strengthening of diagnostic precision, training in catatonia assessment and research in transition-age populations would represent achievable steps towards improving mental health in low- and middle-income country settings.
The UK is experiencing increasing demand for autism assessments, placing severe pressure on the National Health Service (NHS) and private services. Policy responses remain unproven and cost-driven adaptations have compromised quality of some assessments. This risks misdiagnosis, inappropriate support and growing demand for reassessments, potentially creating greater long-term burden for individuals and services alike.
Neuroimaging research in autism often excludes individuals with co-occurring intellectual impairment or minimally verbal status, limiting the generalisability of findings. Understanding magnetic resonance imaging (MRI) scan success predictors in a representative autistic sample is crucial for equitable research.
Aims
This study identified factors predicting successful brain MRI acquisition and data quality in diverse autistic individuals, focusing on including those with intellectual impairment or minimally verbal status.
Method
A total of 122 participants (83 autistic individuals (27 with intellectual impairment, 19 with minimally verbal status) and 39 typically developing controls) received multi-modal brain MRI scans (including structural, resting-state functional and diffusion MRI). Scan success, assessed using both binary criteria and quantitative data-quality metrics, was related to participant characteristics.
Results
Although overall scan success was high, specific factors differentiated success within subgroups. Key factors contributing to scan success included age, non-verbal intelligence and attention-deficit hyperactivity disorder (ADHD) symptoms. Older participants, those with fewer ADHD symptoms and those with higher non-verbal intelligence were more likely to achieve successful scans, regardless of autism diagnosis. Higher data quality, particularly in structural and functional MRI, was associated with higher intelligence, better adaptive functioning, fewer autistic and ADHD symptoms, and fewer behavioural problems.
Conclusions
Identifying these factors is key to designing more inclusive and effective neuroimaging protocols. This work paves the way for more comprehensive research into the neurobiology of the full autism spectrum, and offers insights for improving the clinical MRI experience for autistic individuals with diverse support needs. Individualised strategies may also be useful in clinical settings, helping to improve the experience of MRI scanning for autistic individuals.
Comprehension of wh-questions often poses challenges for children with autism spectrum disorder (ASD) in wh-movement languages like English. However, it remains unclear whether wh-in situ languages like Mandarin present similar difficulties. Moreover, the present study explores potential differences in comprehension between Mandarin subject and object wh-questions. We hypothesize a subject wh-question advantage, given that Mandarin object wh-questions exhibit a longer dependency than subject wh-questions. If confirmed, it would support that Mandarin wh-questions involve covert movement. Using eye-movement measures of the intermodal preferential looking (IPL) paradigm, this study investigates the comprehension of matrix subject and object wh-questions in Mandarin-speaking children with ASD (N = 35, mean age = 60.94 months) compared to their typically developing (TD) peers (N = 38, mean age = 29.66 months), matched on expressive vocabulary levels. The results showed that children in the TD group comprehended both subject and object wh-questions. However, in the ASD group, children comprehended only subject wh-questions. Overall, Mandarin-speaking children with ASD exhibited weaker comprehension of wh-questions than their TD counterparts, with particular difficulty processing object wh-questions. The subject-over-object advantage in wh-questions among Mandarin-speaking children with ASD suggests that they were sensitive to the longer dependency involved in object wh-questions. These findings support the involvement of covert movement in Mandarin wh-questions.
This Element provides a broad overview of autism spectrum disorder from early childhood through adolescence. The Element reviews high-impact areas of research relevant to young children, including the shifting diagnostic conceptualizations of autism, current best practices related to screening and diagnosis, our understanding of factors that increase the likelihood of receiving an autism diagnosis, the overlap between autism and other co-occurring conditions, and related contemporary approaches to supports and interventions for young children. The discussion of these topics addresses measurement of outcomes, reproducibility, and methodological rigor. By focusing on these methodological gaps and progress, future directions for research in each of these areas is highlighted.
The study examines the influence of bilingual experience, age and verbal working memory (WM) on the comprehension of passive voice by 116 typically developing (TD) and 65 autistic children aged 3 to 13, who were tested in their societal languages, German or French. Some children were mainly exposed to the societal language while some children were also exposed to other languages. We adopt a continuous approach to bilingual experience and operationalize it as a balance of cumulative exposure, measured through entropy scores. We found that the comprehension of passive voice improved with age in both groups, and higher verbal WM predicted better performance in autistic but not TD children. Although autistic children were less accurate than TD children, bilingual experience did not contribute to the differences between the two groups. These findings suggest that bilingualism has no detrimental effect on the comprehension of complex syntactic structures in autistic children.
Autism spectrum disorder (ASD) is a population-scale condition with life-course health consequences, yet nutrition support remains inconsistently embedded in routine pathways. Food selectivity is common in ASD and is associated with restricted dietary variety, nutritional imbalance, gastrointestinal morbidity and cardiometabolic vulnerability. Current responses are predominantly clinic-and family-centred and are difficult to scale equitably. This commentary argues that institutional food services (schools, day-care and residential settings) are an underused public health platform to improve inclusion and accountability through sensory-accessible, nutritionally adequate meals. Because these services are commissioned, standardised and audited, sensory accessibility can be operationalised via procurement specifications and quality indicators, enabling benchmarking across sites. Evidence from sensory-informed menu adaptation and implementation work suggests feasibility within routine operations and supports evaluation using system-relevant outcomes (acceptability, nutritional adequacy, waste, feasibility and maintenance). Three policy actions are proposed: embed sensory accessibility in institutional standards, integrate nutrition across sectors and fund scale-up using implementation science.
This study investigated mental health diagnoses in autistic adults to determine whether there were any sex differences in presentation. Autistic adults attending the neurodevelopmental service at Surrey and Borders Partnership NHS Foundation Trust were included.
Results
As part of a service audit, 150 random adults (75 males and females) were selected and their case notes were reviewed. Mental health diagnoses were common: 36% had current suicidal ideation, 20% had attempted suicide, 40% had a past or current diagnosis of anxiety and 62% had a past or current diagnosis of depression. There were more women diagnosed with an eating disorder (9% female, 0% male) and with a historical suicide attempt (21% female, 9% male). However, using a Holm–Bonferroni correction, there were no statistically significant sex differences between mental health diagnoses. Among both sexes, a significant number had been exposed to prenatal and early childhood trauma, nearly 10% had experienced physical trauma, abuse, neglect or assault, and nearly a third had been through parental separation.
Clinical implications
This demonstrates that autistic people presenting to a National Health Service diagnostic clinic are more at risk of experiencing trauma, which subsequently increases their risk of mental illness, alongside any neurological predisposition.
The increasing recognition of neurodivergent conditions in healthcare settings in general highlights the necessity for better understanding and management in neuropsychiatric settings. This study aims to investigate the prevalence and co-occurrence of neurodivergent conditions and traits among patients with neuropsychiatric conditions. A descriptive quantitative cross-sectional study was conducted at a tertiary neuropsychiatric clinic. Participants included 166 consecutive patients, assessed using the Comprehensive Autistic Trait Inventory (CATI) and the Adult ADHD Self-Report Scale (ASRS, version 1.1), with demographic characteristics considered.
Results
In our final analysed cohort (n = 79), among patients with functional neurological disorder (FND) 11% had a confirmed diagnosis of adult spectrum disorder (ASD), 17% were believed to have undiagnosed ASD and 55% exhibited clinically significant ASD traits on the CATI tool. Additionally, 13% had a confirmed diagnosis of attention-deficit hyperactivity disorder (ADHD), 25% were believed to have undiagnosed ADHD and 67% exhibited clinically significant ADHD traits on the ASRS tool.
Clinical implications
The findings indicate a higher than expected prevalence of neurodivergent conditions in people with FND. Enhanced early identification and tailored treatment approaches are likely to be crucial for improving clinical outcomes and patient experiences in neuropsychiatric settings.
Crisis Resolution Teams (CRTs) are being piloted in Ireland as community-based, intensive, short-term services providing rapid intervention for individuals experiencing acute mental health crises. This perspective highlights a group over-represented in emergency care pathways: autistic adults without intellectual disability. For many autistic adults, crises can emerge from burnout, transition pressures and sensory or communication overload, often presenting with heightened distress or suicidality. In systems with limited onward pathways, brief-episode crisis care can become part of a cycle of repeated contacts, with limited scope to address enduring neurodevelopmental needs. We outline pragmatic adaptations: autism-informed workforce education; proactive crisis and safety planning; clear crisis service boundaries with connected pathways for ongoing support; and cross-sector coordination across health and social services. Embedding lived-experience and data capture in learning-sites can drive improvement. Aligned with the Crisis Resolution Service Model of Care and autism policy, these steps can improve safety, equity and continuity of care.