Evidence map›Paper›PMID 41762477›Full record

ArticlePsychoneuroendocrinology2026

Investigating a biopsychosocial model of depression in autistic youth: The intersection of cortisol and depressive symptoms.

Blythe A Corbett, Trey McGonigle, Nneka Ijeli, Simon Vandekar, Rachael A Muscatello, Sloane Sparks

Abstract read
In one paragraph

Article in Psychoneuroendocrinology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Blythe A CorbettVanderbilt University Medical Center, Department of Psychiatry and Behavioral Sciences, Nashville, TN, United States; Vanderbilt University Medical Center, Vanderbilt Kennedy Center, Nashville, TN, United States; Vanderbilt University, Department of Psychology, Nashville, TN, United States. Electronic address: blythe.corbett@vumc.org.
Trey McGonigleVanderbilt University Medical Center, Department of Biostatistics, Nashville, TN, United States. Electronic address: trey.w.mcgonigle@vumc.org.
Nneka IjeliVanderbilt University Medical Center, Department of Psychiatry and Behavioral Sciences, Nashville, TN, United States. Electronic address: nneka.ijeli@vanderbilt.edu.
Simon VandekarVanderbilt University Medical Center, Department of Biostatistics, Nashville, TN, United States. Electronic address: simon.vandekar@vumc.org.
Rachael A MuscatelloVanderbilt University Medical Center, Department of Psychiatry and Behavioral Sciences, Nashville, TN, United States; Vanderbilt University Medical Center, Vanderbilt Kennedy Center, Nashville, TN, United States. Electronic address: rachael.a.muscatello.1@vumc.org.
Sloane SparksVanderbilt University Medical Center, Department of Psychiatry and Behavioral Sciences, Nashville, TN, United States. Electronic address: n.sloane.sparks@vumc.org.

Funding

Overall: Eunice Kennedy Shriver Intellectual and Developmental Disabilities Research Center at VanderbiltP50HD103537 · NICHD · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Jeffrey L Neul · 2020 to 2026
$10.3M
Examining Stress and Arousal Across Pubertal Development in ASDR01MH111599 · NIMH · VANDERBILT UNIVERSITY MEDICAL CENTER · PI CORBETT, BLYTHE ANNE · 2017 to 2025
$3.9M
Examining Stress and Arousal Across Pubertal Development in ASDRF1MH111599 · NIMH · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Blythe Anne Corbett · 2026 to 2026
$2.3M
NICHD NIH HHS P50 HD103537NIMH NIH HHS R01 MH111599NIMH NIH HHS RF1 MH111599
6 · The paper itself

Abstract

backgroundDepression is a leading mental health concern in adolescents. The maturation of the hypothalamic pituitary adrenal (HPA) axis during adolescence coincides with higher basal cortisol, and elevations in evening cortisol have been associated with depressive symptoms. Autism spectrum disorder (ASD) is differentiated by challenges with socioemotional reciprocity. Research in autistic youth has shown earlier and higher rates of depressive symptoms and elevated evening cortisol. The extent to which cortisol profiles may be linked to depressive symptoms in ASD has not been explored.

methodsParticipants included 244 youth, 140 autistic and 104 neurotypical, aged 10-16 over four years. The Children's Depression Inventory (CDI) 2nd Edition Total T-score assessed depressive symptoms. Salivary morning and evening cortisol collected over three days in the home were log transformed and averaged. We fit a mixed effects model for CDI Total scores with log-transformed cortisol (fit with natural cubic splines) as the main variable of interest, adjusting for diagnosis (ASD or TD), nonlinear age (fit with natural cubic splines), sex, and use of psychotropic medication. We also allowed for diagnosis-by-cortisol and sex-by-cortisol interactions.

resultsThere was a main effect of morning cortisol on the CDI total score (p = 0.028, robust effect size index (RESI) = 0.17), but no main effect for evening cortisol (p = 0.421, RESI=0.00). There was a diagnosis-by-evening cortisol interaction (p = 0.001, RESI = 0.25), but no diagnosis-by-morning cortisol interaction; the ASD CDI scores were flat across evening cortisol values (p = 0.824), however increasing evening cortisol in the interval 0.11-0.80 nmol/L was associated with increasing CDI in the TD group (p = 0.005). We observed a significant morning cortisol by age interaction (p = 0.029, RESI = 0.18).

conclusionsResults replicate previous findings in autism showing higher depressive symptoms, but do not show a clear association with cortisol levels. Elevations in evening cortisol were associated with higher depressive symptoms in neurotypical youth; a link previously found in non-autistic adolescents and adults.

Indexed as

Autism Spectrum DisorderAutistic DisorderDepressionHydrocortisoneAdolescentChildCircadian RhythmFemaleHumansHypothalamo-Hypophyseal SystemMalePituitary-Adrenal SystemSalivaHydrocortisoneAutismCortisolDepressionHPA axis

Identifiers

PMID41762477
PMCPMC12990045

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.