TY - JOUR
T1 - Multivariate genome-wide analysis of stress-related quantitative phenotypes
AU - Schijven, Dick
AU - Geuze, Elbert
AU - Vinkers, Christiaan H.
AU - Pulit, Sara L.
AU - Schür, Remmelt R.
AU - Malgaz, Marie
AU - Bekema, Erwin
AU - Medic, Jelena
AU - van der Kust, Kendrick E.
AU - Veldink, Jan H.
AU - Boks, Marco P.
AU - Vermetten, Eric
AU - Luykx, Jurjen J.
PY - 2019/12
Y1 - 2019/12
N2 - Exposure to traumatic stress increases the odds of developing a broad range of psychiatric conditions. Genetic studies targeting multiple stress-related quantitative phenotypes may shed light on mechanisms underlying vulnerability to psychopathology in the aftermath of stressful events. We applied a multivariate genome-wide association study (GWAS) to a unique military cohort (N = 583) in which we measured biochemical and behavioral phenotypes. The availability of pre- and post-deployment measurements allowed to capture changes in these phenotypes in response to stress. For genome-wide significant loci, we performed functional annotation, phenome-wide analysis and quasi-replication in PTSD case-control GWASs. We discovered one genetic variant reaching genome-wide significant association, surviving permutation and sensitivity analyses (rs10100651, p = 9.9 × 10−9). Functional annotation prioritized the genes INTS8 and TP53INP1. A phenome-wide scan revealed a significant association of these same genes with sleeping problems, hypertension and subjective well-being. Finally, a targeted lookup revealed nominally significant association of rs10100651 in a PTSD case-control GWAS in the UK Biobank (p = 0.02). We provide comprehensive evidence from multiple resources hinting at a role of the highlighted genetic variant in the human stress response, marking the power of multivariate genome-wide analysis of quantitative measures in stress research. Future genetic and functional studies can target this locus to further assess its effects on stress mediation and its possible role in psychopathology or resilience.
AB - Exposure to traumatic stress increases the odds of developing a broad range of psychiatric conditions. Genetic studies targeting multiple stress-related quantitative phenotypes may shed light on mechanisms underlying vulnerability to psychopathology in the aftermath of stressful events. We applied a multivariate genome-wide association study (GWAS) to a unique military cohort (N = 583) in which we measured biochemical and behavioral phenotypes. The availability of pre- and post-deployment measurements allowed to capture changes in these phenotypes in response to stress. For genome-wide significant loci, we performed functional annotation, phenome-wide analysis and quasi-replication in PTSD case-control GWASs. We discovered one genetic variant reaching genome-wide significant association, surviving permutation and sensitivity analyses (rs10100651, p = 9.9 × 10−9). Functional annotation prioritized the genes INTS8 and TP53INP1. A phenome-wide scan revealed a significant association of these same genes with sleeping problems, hypertension and subjective well-being. Finally, a targeted lookup revealed nominally significant association of rs10100651 in a PTSD case-control GWAS in the UK Biobank (p = 0.02). We provide comprehensive evidence from multiple resources hinting at a role of the highlighted genetic variant in the human stress response, marking the power of multivariate genome-wide analysis of quantitative measures in stress research. Future genetic and functional studies can target this locus to further assess its effects on stress mediation and its possible role in psychopathology or resilience.
KW - Deployment
KW - GWAS
KW - Hormone
KW - Quantitative phenotype
KW - Questionnaire
KW - Stress
UR - https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85073076949&origin=inward
UR - https://www.ncbi.nlm.nih.gov/pubmed/31606302
U2 - https://doi.org/10.1016/j.euroneuro.2019.09.012
DO - https://doi.org/10.1016/j.euroneuro.2019.09.012
M3 - Article
C2 - 31606302
SN - 1873-7862
VL - 29
SP - 1354
EP - 1364
JO - European Neuropsychopharmacology
JF - European Neuropsychopharmacology
IS - 12
ER -