Journal
TRANSLATIONAL PSYCHIATRY
Volume 10, Issue 1, Pages -Publisher
SPRINGERNATURE
DOI: 10.1038/s41398-020-0706-0
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Funding
- Cohen Veterans Bioscience
- NIMH/U.S. Army Medical Research and Materiel Command [R01MH106595]
- One Mind
- Stanley Center for Psychiatric Genetics at the Broad Institute of MIT and Harvard
- [5U01MH109539]
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Childhood maltreatment is highly prevalent and serves as a risk factor for mental and physical disorders. Self-reported childhood maltreatment appears heritable, but the specific genetic influences on this phenotype are largely unknown. The aims of this study were to (1) identify genetic variation associated with self-reported childhood maltreatment, (2) estimate SNP-based heritability (h(snp)(2)), (3) assess predictive value of polygenic risk scores (PRS) for childhood maltreatment, and (4) quantify genetic overlap of childhood maltreatment with mental and physical health-related phenotypes, and condition the top hits from our analyses when such overlap is present. Genome-wide association analysis for childhood maltreatment was undertaken, using a discovery sample from the UK Biobank (UKBB) (n=124,000) and a replication sample from the Psychiatric Genomics Consortium-posttraumatic stress disorder group (PGC-PTSD) (n=26,290). h(snp)(2) for childhood maltreatment and genetic correlations with mental/physical health traits were calculated using linkage disequilibrium score regression. PRS was calculated using PRSice and mtCOJO was used to perform conditional analysis. Two genome-wide significant loci associated with childhood maltreatment (rs142346759, p=4.35x10(-8), FOXP1; rs10262462, p=3.24x10(-8), FOXP2) were identified in the discovery dataset but were not replicated in PGC-PTSD. h(snp)(2) for childhood maltreatment was 6% and the PRS derived from the UKBB was significantly predictive of childhood maltreatment in PGC-PTSD (r(2)=0.0025; p=1.8x10(-15)). The most significant genetic correlation of childhood maltreatment was with depressive symptoms (r(g)=0.70, p=4.65x10(-40)), although we show evidence that our top hits may be specific to childhood maltreatment. This is the first large-scale genetic study to identify specific variants associated with self-reported childhood maltreatment. Speculatively, FOXP genes might influence externalizing traits and so be relevant to childhood maltreatment. Alternatively, these variants may be associated with a greater likelihood of reporting maltreatment. A clearer understanding of the genetic relationships of childhood maltreatment, including particular abuse subtypes, with a range of phenotypes, may ultimately be useful in in developing targeted treatment and prevention strategies.
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