Evidence map›Paper›PMID 41135260›Full record

ArticlePediatric neurology2025

Do Common Genetic Factors Underlie Comorbidity Between Migraine and Major Depressive Disorder in Youth?

Alison K Merikangas, Laura M Schultz, Kosha Ruparel, Tarannum Lateef, Raquel E Gur, Laura Almasy

Abstract read
In one paragraph

Article in Pediatric neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

1 citing paper in PubMed.

  1. Review
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.

Alison K MerikangasDepartment of Biomedical and Health Informatics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania; Department of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania; Lifespan Brain Institute of the Children's Hospital of Philadelphia and the University of Pennsylvania, Philadelphia, Pennsylvania. Electronic address: amerikangas@gmail.com.
Laura M SchultzDepartment of Biomedical and Health Informatics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania; Lifespan Brain Institute of the Children's Hospital of Philadelphia and the University of Pennsylvania, Philadelphia, Pennsylvania.
Kosha RuparelLifespan Brain Institute of the Children's Hospital of Philadelphia and the University of Pennsylvania, Philadelphia, Pennsylvania; Department of Psychiatry, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Tarannum LateefDepartment of Neurology, Children's National Health System, George Washington University School of Medicine, Washington, District of Columbia; Genetic Epidemiology Research Branch, Intramural Research Program, National Institute of Mental Health, Bethesda, Maryland.
Raquel E GurLifespan Brain Institute of the Children's Hospital of Philadelphia and the University of Pennsylvania, Philadelphia, Pennsylvania; Department of Psychiatry, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Laura AlmasyDepartment of Biomedical and Health Informatics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania; Department of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania; Lifespan Brain Institute of the Children's Hospital of Philadelphia and the University of Pennsylvania, Philadelphia, Pennsylvania.

Funding

Phenotypic Diversity in COVID-19UL1TR001878 · NCATS · UNIVERSITY OF PENNSYLVANIA · PI FITZGERALD, GARRET A · 2016 to 2025
$102.4M
Neurodevelopmental Genomics: Trajectories of Complex PhenotypesRC2MH089983 · NIMH · UNIVERSITY OF PENNSYLVANIA · PI GUR, RAQUEL E · 2009 to 2011
$14.3M
2/2 Neurodevelopmental Genomics: Trajectories of Complex PhenotypesRC2MH089924 · NIMH · CHILDREN'S HOSP OF PHILADELPHIA · PI HAKONARSON, HAKON · 2009 to 2011
$10.7M
Large-Scale Evaluation of the Effect of Rare Genetic Variants on Psychiatric Symptoms and Cognitive AbilityU01MH119690 · NIMH · BOSTON CHILDREN'S HOSPITAL · PI ALMASY, LAURA A., GLAHN, DAVID C · 2019 to 2023
$5.9M
NCATS NIH HHS UL1 TR001878NIMH NIH HHS RC2 MH089924NIMH NIH HHS RC2 MH089983NIMH NIH HHS U01 MH119690
6 · The paper itself

Abstract

backgroundMigraine and major depressive disorder (MDD) are common, recurring conditions with comorbidity documented in clinical and community samples of both adults and youth. However, the etiology remains unknown. This study aims to (1) examine the prevalence and association between migraine and MDD in a large, diverse youth sample; (2) assess whether polygenic scores (PGSs) from adult genome-wide association studies are associated with these disorders in youth; and (3) evaluate shared genetic susceptibility underlying migraine-depression comorbidity.

methodsThe sample includes 8496 youth from the Philadelphia Neurodevelopmental Cohort (5239 of European-like Ancestry [EA]). Mental disorders and migraine were assessed using structured diagnostic tools aligned with Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition and International Classification of Headache Disorders. In the EA subset, PGS from adult genome-wide association studies were used to examine genetic associations.

resultsIn cross-sectional analyses, 7% of youth met migraine criteria and 12.5% met MDD criteria. Rates were similar across self-reported races. Migraine and depression were significantly associated (odds ratio = 2.05, P < 0.001). There were significant associations between the PGS for migraine and depression with those disorders in EA youth, but no cross-disorder genetic associations emerged.

conclusionsThis is the first study to examine the genetic architecture of comorbid migraine and mood disorders in a large youth sample. PGS from adults were associated with migraine and depression in youth, but the lack of cross-disorder associations suggests limited shared genetic pathways. Future studies should include prospective data to examine potential mechanisms for migraine-depression comorbidity.

Indexed as

Genetic Predisposition to DiseaseMajor Depressive DisorderMigraine DisordersAdolescentChildCohort StudiesComorbidityCross-Sectional StudiesFemaleGenome-Wide Association StudyHumansMaleMultifactorial InheritancePrevalenceYoung AdultComorbidityDepressionMigraine disordersPolygenic scoreYouth

Identifiers

PMID41135260
PMCPMC12674002

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.