Autonomic and hormonal biomarkers in individuals with autism spectrum disorders and developmental or intellectual delay: A systematic PRISMA review.
Vidal-Zaborski Olivia, Merino Diane, Fernandez Arnaud, Mercery Mégane, Herbreteau Louise, Askenazy Florence, Zuluaga Maria A, Ismailova Esma, Douet-Vannucci Vanessa, Thümmler Susanne
What this study means for families
This research looked at stress responses in autistic children who also have intellectual disabilities. Studies found these children often have overactive stress systems - their bodies stay in 'high alert' mode and don't calm down properly after stressful situations. Their stress hormones also work differently than typical children. Better heart rate patterns were linked to better social skills.
However, the research quality was limited, so we need more studies to fully understand these stress patterns.
Summary by AutismInsights from published abstract. This is not a substitute for reading the original paper.
Research summary
This systematic review examined autonomic nervous system and stress hormone biomarkers in individuals with autism spectrum disorder (ASD) who also have global developmental delay or intellectual disability. Analysis of 34 studies involving approximately 1,160 individuals (mean age 10.7 years) revealed consistent patterns of autonomic hyperarousal, including sympathetic nervous system overactivation and reduced parasympathetic tone. Stress hormone findings were mixed, showing both low cortisol levels and disrupted feedback mechanisms. Better respiratory sinus arrhythmia was associated with improved social adaptation.
However, study quality was generally low due to small sample sizes and methodological variability, limiting the strength of conclusions about physiological stress responses in this vulnerable population.
Summary by AutismInsights from published abstract. This is not a substitute for reading the original paper.
Key findings
- 1
Individuals with ASD and developmental delay showed sympathetic hyperactivation and reduced parasympathetic tone
Confidence: moderateRelevance: Indicates chronic stress state requiring targeted interventions - 2
Respiratory sinus arrhythmia was positively associated with social adaptation
Confidence: moderateRelevance: Heart rate variability may serve as biomarker for social functioning - 3
HPA axis findings were mixed, showing both hypoactivation and feedback dysfunction
Confidence: limitedRelevance: Suggests complex stress hormone dysregulation requiring individualized assessment - 4
ASD symptom severity was more consistently associated with physiological profiles than IQ
Confidence: moderateRelevance: Autism characteristics may be better predictors of stress responses than cognitive ability
Summary by AutismInsights from published abstract. This is not a substitute for reading the original paper.
Clinical implications
Findings suggest individuals with ASD and developmental delay experience chronic physiological stress requiring targeted stress management interventions. Respiratory sinus arrhythmia may serve as a useful biomarker for monitoring intervention effectiveness and social adaptation progress in clinical practice.
Summary by AutismInsights from published abstract. This is not a substitute for reading the original paper.
Limitations
Most studies had low certainty due to small sample sizes, high methodological variability, and heterogeneity in populations and protocols. Few studies specifically targeted ASD with developmental delay profiles. No meta-analysis could be performed due to high heterogeneity between studies.
Summary by AutismInsights from published abstract. This is not a substitute for reading the original paper.
Original abstract
Individuals with autism spectrum disorder (ASD) and co-occurring global developmental delay or intellectual disability (GDD-ID) are highly vulnerable to stress, but a very small amount of research is being conducted at the physiological level. This review aims to identify and synthesize studies examining autonomic nervous system (ANS) and hypothalamic-pituitary-adrenal (HPA) axis biomarkers in such populations. The review followed PRISMA 2020 guidelines (Pages et al., 2021) and the inclusion criteria encompassed peer-reviewed studies published in English that reported direct physiological biomarker measurements (e.g., heart rate variability, electrodermal activity, cortisol) in individuals with ASD and documented GDD-ID (IQ < 75 and/or developmental delay). Exclusion criteria included studies involving animals, pharmacological interventions, or solely behavioural outcomes.
The literature search was conducted across four databases: PubMed, Scopus, Web of Science, and OpenAlex (last search: April 2025). Two reviewers independently screened publications, assessed bias (JBI) and evaluated the certainty (GRADE). No meta-analysis was performed due to high heterogeneity. The protocol was registered on PROSPERO (CRD420251025329).
Thirty-four studies (n ≈ 1160 individuals with ASD; mean age: 10.7 years) were included. ANS studies reported that ASD individuals had a sympathetic hyperactivation, a reduced parasympathetic tone (low respiratory sinus arrhythmia), and a delayed recovery after stress. HPA findings were mixed, showing both hypoactivation (low cortisol) and feedback dysfunction (e.g., Dexamethasone non-suppression) in those individuals. Respiratory sinus arrhythmia (RSA) was positively associated with social adaptation.
Age-related physiological maturation appeared atypical. ASD's symptom severity was more consistently positively associated with physiological profiles than IQ. Clear evidence was limited since most studies had low certainty due to small sample sizes, variability and heterogeneity in methods, populations, and task relevance. Only few recent studies targeted ASD-GDD-ID profiles.
Individuals with ASD and GDD-ID exhibit autonomic hyperarousal and altered HPA regulation, suggesting reduced physiological flexibility. However, strong discrepancies exist among studies, and hereby, more inclusive and adapted protocols are needed to better characterise this physiological profile.
Evidence Grade
limited
Grade assigned by AutismInsights based on study type and published abstract.
Study Details
- Type
- Systematic Review
- Journal
- Neuroscience and biobehavioral reviews
- Year
- 2026
- PMID
- 41314363
- DOI
- 10.1016/j.neubiorev.2025.106496
MeSH Terms