Molecular PsychiatryGeneticsPeer-reviewed journal article
A major role for common genetic variation in anxiety disorders
Kirstin Lee PurvesiD, Jonathan R. I. ColemaniD, Sandra Melanie MeieriD, Christopher RayneriD, Katrina A. S. DavisiD, Rosa CheesmaniD, Marie Bækvad‐HanseniD, Anders Dupont BørglumiD, Shing Wan Cho, Jürgen DeckertiD, Héléna A. GaspariD, Jonas Bybjerg‐GrauholmiD, John M. HettemaiD, Matthew H. HotopfiD, DAVID MICHAEL HOUGAARDiD, Christopher HübeliD, Carol KaniD, Andrew Mark McIntoshiD, Ole N MorsiD, Preben Bo MortenseniD, Merete NordentoftiD, Thomas Mears WergeiD, Kristin K. NicodemusiD, Manuel MattheiseniD, Gerome D. BreeniD, Thalia Catherine EleyiD
Abstract
Anxiety disorders are common, complex psychiatric disorders with twin heritabilities of 30-60%. We conducted a genome-wide association study of Lifetime Anxiety Disorder (n = 83 565) and an additional Current Anxiety Symptoms (n= 77 125) analysis. The liability scale common variant heritability estimate for Lifetime Anxiety Disorder was 26%, and for Current Anxiety Symptoms was 31%. Five novel genome-wide significant loci were identified including an intergenic region on chromosome 9 that has previously been associated with neuroticism, and a locus overlapping the BDNF receptor gene, NTRK2. Anxiety showed significant genetic correlations with depression and insomnia as well as coronary artery disease, mirroring findings from epidemiological studies. We conclude that common genetic variation accounts for a substantive proportion of the genetic architecture underlying anxiety.
- organism: human
- assay: GWAS summary statistics
- research focus: GWAS / association mapping
- approach: statistical model
- Citations
- 426
- FWCI
- 26.13
- Field percentile
- top 1%
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