Longitudinal prediction of adolescent depression from environmental and polygenic risk scores

Understanding adolescent depression risk is vital for mitigating its long-term adverse effects. Though polygenic risk scores (PRS) explain increasing proportions of heritable risk, environmental risk remains challenging to quantify, hindering prediction. Existing prediction models often examine environmental risk in isolation, and vary in the number of predictors examined (between 8-800 + ), limiting generalisability. Here, we develop a model predicting adolescent depression symptoms (depRS) from a review of key environmental risk factors and assess depRS and PRS prediction of major depressive disorder (MDD) at 2-year follow-up. Using data from the Adolescent Brain Cognitive Development study (N = 9 797; 47% female), we generated PRS in European, African, American Admixed and East Asian ancestries from a recent trans-ancestry genome-wide study of MDD. We trained depRS to predict parent-reported depression symptoms at 2-year follow-up (age 11-13) from baseline predictors (age 9-11), using Elastic Net regression with 10-fold cross-validation for variable selection. The final depRS model included 12 predictors and explained 12.3% of overall variance. Parental depression, witnessing domestic violence, sleep duration and dieting emerged as top predictors of depression symptoms. depRS showed better-than-chance classification of parent- (AUC = 0.69 [0.66-0.73]) and youth self-reported MDD (AUC = 0.67 [0.64-0.71]), outperforming PRS classification of parent-reported MDD (AUC = 0.64 [0.60-0.68]). Combining depRS and PRS maximised accuracy for both outcomes (Parent AUC = 0.71 [0.68-0.75]; Youth AUC = 0.70 [0.66-0.73]). Though external validation of depRS across geographically and gender diverse cohorts is needed to assess generalisability, findings highlight sleep and dieting as potential targets for mitigating risk and demonstrate the utility of genetic scores in models predicting adolescent depression.

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Publication Details

Journal
Molecular Psychiatry
Published
2026-11-01
DOI
https://doi.org/10.1038/s41380-026-03934-4
Citations
1
Primary Topic
Genetic Associations and Epidemiology
Type
article
Field-Weighted Citation Impact
3.90

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article

Longitudinal prediction of adolescent depression from environmental and polygenic risk scores

Poppy Zenzi Grimes, Alex S. F. Kwong, Stephen M. Lawrie, Heather Clare Whalley et al.
1 citations
Molecular Psychiatry
Genetic Associations and Epidemiology
3.90
article

Longitudinal prediction of adolescent depression from environmental and polygenic risk scores

Poppy Zenzi Grimes, Alex S. F. Kwong, Stephen M. Lawrie, Heather Clare Whalley, Eileen Y. Xu
article en
1 citations

Abstract

Understanding adolescent depression risk is vital for mitigating its long-term adverse effects. Though polygenic risk scores (PRS) explain increasing proportions of heritable risk, environmental risk remains challenging to quantify, hindering prediction. Existing prediction models often examine environmental risk in isolation, and vary in the number of predictors examined (between 8-800 + ), limiting generalisability. Here, we develop a model predicting adolescent depression symptoms (depRS) from a review of key environmental risk factors and assess depRS and PRS prediction of major depressive disorder (MDD) at 2-year follow-up. Using data from the Adolescent Brain Cognitive Development study (N = 9 797; 47% female), we generated PRS in European, African, American Admixed and East Asian ancestries from a recent trans-ancestry genome-wide study of MDD. We trained depRS to predict parent-reported depression symptoms at 2-year follow-up (age 11-13) from baseline predictors (age 9-11), using Elastic Net regression with 10-fold cross-validation for variable selection. The final depRS model included 12 predictors and explained 12.3% of overall variance. Parental depression, witnessing domestic violence, sleep duration and dieting emerged as top predictors of depression symptoms. depRS showed better-than-chance classification of parent- (AUC = 0.69 [0.66-0.73]) and youth self-reported MDD (AUC = 0.67 [0.64-0.71]), outperforming PRS classification of parent-reported MDD (AUC = 0.64 [0.60-0.68]). Combining depRS and PRS maximised accuracy for both outcomes (Parent AUC = 0.71 [0.68-0.75]; Youth AUC = 0.70 [0.66-0.73]). Though external validation of depRS across geographically and gender diverse cohorts is needed to assess generalisability, findings highlight sleep and dieting as potential targets for mitigating risk and demonstrate the utility of genetic scores in models predicting adolescent depression.

Molecular Psychiatry
Manchester Metropolitan University (GB), QIMR Berghofer Medical Research Institute (AU), University of Bristol (GB), MRC Integrative Epidemiology Unit (GB), University of Edinburgh (GB)
Wellcome Trust, University of Edinburgh, National Institutes of Health, Medical Research Council, National Institute of Mental Health, National Institute on Drug Abuse
Good health and well-being
Openalex Percentile: Top 14%
Genetic Associations and Epidemiology
3.90
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