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Nature human behaviour · 2026

Genome-wide meta-analysis of quantitatively measured generalized anxiety symptoms in individuals of European ancestry.

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Skelton Megan, Mitchell Brittany L, Assary Elham, Li Danyang, Morneau-Vaillancourt Genevieve, Murphy Alan E, Ter Kuile Abigail R, Wang Rujia, Adams Mark J, Byrne Enda M, Corfield Elizabeth C, Grimes Poppy Z, Hannigan Laurie J, Hu Jihua, Kõiv Kadri, Kwong Alex S F, Papiol Sergi, Pettersen Johanne H, Pistis Giorgio, Castelao Enrique, Strom Nora I, van der Most Peter J, Anxiety Disorders Working Group of the Psychiatric Genomics Consortium, GLAD+ authors, Lifelines Cohort Study, NIHR BioResource, PROTECT-AD Consortium, Andreassen Ole A, Erhardt-Lehmann Angelika, Havdahl Alexandra, Skene Nathan, Verhulst Brad, Weber Heike, Armour Chérie, Ask Helga, Copeland William E, Dannlowski Udo, Deckert Jürgen, Domschke Katharina, Hickie Ian B, Lehto Kelli, Lonsdorf Tina B, Lueken Ulrike, Lupton Michelle K, Medland Sarah E, McIntosh Andrew M, Oldehinkel Albertine J, Preisig Martin, Reif Andreas, Snieder Harold, Walters James T R, Wray Naomi R, Hartman Catharina A, Martin Nicholas G, Hettema John M, Breen Gerome, Coleman Jonathan R I, Eley Thalia C

Аннотация

Anxiety is heritable and exists on a continuum, with symptoms ranging from adaptive threat response to clinical disorder. Here we performed a genome-wide association meta-analysis of generalized anxiety symptom severity in 693,869 individuals of European ancestry from 14 cohorts. We identified 80 independent genome-wide significant variants within 74 loci, 39 of which were newly associated with anxiety. SNP-based heritability was 5.9% (posterior s.d. = 0.15%). Polygenic scores were significantly associated with anxiety symptom severity and disorder in European, African and South Asian ancestry samples (R2 = 1.2-2.9%). Significant genetic correlations (rg) were estimated with mental and physical health traits, including case-control anxiety, neuroticism and depression (rg = 0.71-0.85), irritable bowel syndrome (rg = 0.57), coronary artery disease, endometriosis and migraine (rg = 0.20-0.27). Gene-based and pathway analyses implicated synaptic and axonal processes, with enriched expression in the brain. These findings highlight the discovery power gained from analysing a quantitative trait rather than a case-control phenotype in anxiety genetics.

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