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

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

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Abstract

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 (R  = 1.2-2.9%). Significant genetic correlations (r ) were estimated with mental and physical health traits, including case-control anxiety, neuroticism and depression (r  = 0.71-0.85), irritable bowel syndrome (r  = 0.57), coronary artery disease, endometriosis and migraine (r  = 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.
Original languageEnglish
Number of pages18
JournalNature Human Behaviour
Early online date09 Jun 2026
DOIs
Publication statusEarly online date - 09 Jun 2026

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