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Genomic influences on self-reported childhood maltreatment.

Authors :
Dalvie S
Maihofer AX
Coleman JRI
Bradley B
Breen G
Brick LA
Chen CY
Choi KW
Duncan LE
Guffanti G
Haas M
Harnal S
Liberzon I
Nugent NR
Provost AC
Ressler KJ
Torres K
Amstadter AB
Bryn Austin S
Baker DG
Bolger EA
Bryant RA
Calabrese JR
Delahanty DL
Farrer LA
Feeny NC
Flory JD
Forbes D
Galea S
Gautam A
Gelernter J
Hammamieh R
Jett M
Junglen AG
Kaufman ML
Kessler RC
Khan A
Kranzler HR
Lebois LAM
Marmar C
Mavissakalian MR
McFarlane A
Donnell MO
Orcutt HK
Pietrzak RH
Risbrough VB
Roberts AL
Rothbaum AO
Roy-Byrne P
Ruggiero K
Seligowski AV
Sheerin CM
Silove D
Smoller JW
Stein MB
Teicher MH
Ursano RJ
Van Hooff M
Winternitz S
Wolff JD
Yehuda R
Zhao H
Zoellner LA
Stein DJ
Koenen KC
Nievergelt CM
Source :
Translational psychiatry [Transl Psychiatry] 2020 Jan 27; Vol. 10 (1), pp. 38. Date of Electronic Publication: 2020 Jan 27.
Publication Year :
2020

Abstract

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 <superscript>2</superscript> <subscript>snp</subscript> ), (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 <superscript>2</superscript> <subscript>snp</subscript> 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 = 4.35 × 10 <superscript>-8</superscript> , FOXP1; rs10262462, p = 3.24 × 10 <superscript>-8</superscript> , FOXP2) were identified in the discovery dataset but were not replicated in PGC-PTSD. h <superscript>2</superscript> <subscript>snp</subscript> for childhood maltreatment was ~6% and the PRS derived from the UKBB was significantly predictive of childhood maltreatment in PGC-PTSD (r <superscript>2</superscript>  = 0.0025; p = 1.8 × 10 <superscript>-15</superscript> ). The most significant genetic correlation of childhood maltreatment was with depressive symptoms (r <subscript>g</subscript>  = 0.70, p = 4.65 × 10 <superscript>-40</superscript> ), 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.

Details

Language :
English
ISSN :
2158-3188
Volume :
10
Issue :
1
Database :
MEDLINE
Journal :
Translational psychiatry
Publication Type :
Academic Journal
Accession number :
32066696
Full Text :
https://doi.org/10.1038/s41398-020-0706-0