ArticleThe journal of headache and pain2026
Shared genetic architecture between depression and migraine: a large-scale genome-wide cross-trait analysis.
Article in The journal of headache and pain, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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1 citing paper in PubMed.
- Migraine immune cell gene targets and their relationship to psychiatric disorders.The journal of headache and pain · 2026Article
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14 authors.
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Abstract
backgroundDepression and migraine are highly prevalent neuropsychiatric disorders that frequently co-occur. However, the extent to which they share genetic determinants, particularly for postpartum depression (PPD), an underexplored subtype, remains insufficiently understood.
methodsWe performed a large-scale genome-wide cross-trait analysis using summary statistics for depression phenotypes (overall depression, major depressive disorder [MDD], PPD) and migraine subtypes (migraine, migraine with aura [MA], migraine without aura [MO]). Genetic correlations were estimated using linkage disequilibrium score regression (LDSC) and GNOVA. Pleiotropically associated loci were identified through cross-trait meta-analysis, followed by fine-mapping and colocalization analyses to prioritize potential loci with stronger evidence for shared causal signals. Functional annotation and gene-based analyses were conducted to explore biological relevance. Bidirectional and multivariable Mendelian randomization (MVMR) were applied to assess potential causal relationships.
resultsWe observed significant global and local genetic correlations between depression and migraine (LDSC r
conclusionsDepression and migraine show substantial genetic overlap and exhibit an asymmetric pattern of potential causal relationships, with stronger MR evidence for the depression-to-migraine direction than for the reverse direction. The pleiotropically associated loci provide genomic evidence for future mechanistic and translational investigation across depression and migraine subtypes. The findings also highlight PPD as a genetically related but potentially distinct subtype warranting further investigation.
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