Genome-wide meta-analysis of quantitatively measured generalized anxiety symptoms in individuals of European ancestry
Research output: Contribution to journal › Research article › Contributed › peer-review
Contributors
- Chair of Behavioral Psychotherapy
- Chair of Clinical Psychology and Behavioral Neuroscience
- King's College London (KCL)
- Queensland Institute of Medical Research
- University of Queensland
- Queensland University of Technology
- University of Montreal
- Imperial College London
- University College London
- South London and Maudsley NHS Foundation Trust
- University of Edinburgh
- Lovisenberg Diaconal Hospitaland
- University of Bristol
- Estonian Biocentre
- University of Lausanne
- Humboldt University of Berlin
- Ludwig Maximilian University of Munich
- Karolinska Institutet
- Aarhus University
- University of Groningen
- Dalhousie University
- University of Münster
- University of Utah
- Virginia Commonwealth University
- Örebro University
- University of Greifswald
- Erasmus University Rotterdam
- Massachusetts General Hospital
- University of Mannheim
- University of Marburg
- University of Tartu
- Vrije Universiteit Amsterdam (VU)
- Amsterdam University Medical Centers (UMC)
- Yale University
- University of California at San Diego
- University of Oslo
- University of Würzburg
- German Center for Mental Health (DZPG)
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 (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.
Details
| Original language | English |
|---|---|
| Pages (from-to) | 1594–1608 |
| Number of pages | 15 |
| Journal | Nature human behaviour |
| Volume | 10 |
| Issue number | 8 |
| Publication status | Published - Aug 2026 |
| Peer-reviewed | Yes |
External IDs
| ORCID | /0000-0002-1697-6732/work/219264971 |
|---|---|
| ORCID | /0000-0002-7762-4327/work/219266690 |
| PubMed | 42265330 |