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Meta-Analysis
. 2018 Aug;28(4):66-70.
doi: 10.1097/YPG.0000000000000201.

Shared genetic etiology between alcohol dependence and major depressive disorder

Affiliations
Meta-Analysis

Shared genetic etiology between alcohol dependence and major depressive disorder

Jerome C Foo et al. Psychiatr Genet. 2018 Aug.

Abstract

The clinical comorbidity of alcohol dependence (AD) and major depressive disorder (MDD) is well established, whereas genetic factors influencing co-occurrence remain unclear. A recent study using polygenic risk scores (PRS) calculated based on the first-wave Psychiatric Genomics Consortium MDD meta-analysis (PGC-MDD1) suggests a modest shared genetic contribution to MDD and AD. Using a (~10 fold) larger discovery sample, we calculated PRS based on the second wave (PGC-MDD2) of results, in a severe AD case–control target sample. We found significant associations between AD disease status and MDD-PRS derived from both PGC-MDD2 (most informative P-threshold=1.0, P=0.00063, R2=0.533%) and PGC-MDD1 (P-threshold=0.2, P=0.00014, R2=0.663%) meta-analyses; the larger discovery sample did not yield additional predictive power. In contrast, calculating PRS in a MDD target sample yielded increased power when using PGC-MDD2 (P-threshold=1.0, P=0.000038, R2=1.34%) versus PGC-MDD1 (P-threshold=1.0, P=0.0013, R2=0.81%). Furthermore, when calculating PGC-MDD2 PRS in a subsample of patients with AD recruited explicitly excluding comorbid MDD, significant associations were still found (n=331; P-threshold=1.0, P=0.042, R2=0.398%). Meanwhile, in the subset of patients in which MDD was not the explicit exclusion criteria, PRS predicted more variance (n=999; P-threshold=1.0, P=0.0003, R2=0.693%). Our findings replicate the reported genetic overlap between AD and MDD and also suggest the need for improved, rigorous phenotyping to identify true shared cross-disorder genetic factors. Larger target samples are needed to reduce noise and take advantage of increasing discovery sample size.

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Figures

Fig. 1
Fig. 1
Polygenic risk score model fit. (a) GESGA target sample based on PGC-MDD2 (n=59 265 cases; n=112 092 controls); (b) PGC-MDD1 (n=8148 cases; n=7955 controls) discovery samples; (c) BoMa-MDD target sample based on PGC-MDD2 and (d) PGC-MDD1; and inset (e) non-PREDICT (left) and PREDICT (right) GESGA target subsamples based on PGC-MDD2. MDD, major depressive disorder; PGC, Psychiatric Genomics Consortium. #P<0.10; 1*P<0.05; 2*P<0.01; 3*P<0.001; 4*P<0.0001; 5*P<0.00001.

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References

    1. Andersen AM, Pietrzak RH, Kranzler HR, Ma L, Zhou H, Liu X, et al. (2017). Polygenic scores for major depressive disorder and risk of alcohol dependence. JAMA Psychiatry 74:1153–1160. - PMC - PubMed
    1. Bulik-Sullivan B, Finucane HK, Anttila V, Gusev A, Day FR, Loh PR, et al. (2015). An atlas of genetic correlations across human diseases and traits. Nat Genet 47:1236–1241. - PMC - PubMed
    1. Crum RM, Green KM, Storr CL, Chan YF, Ialongo N, Stuart EA, Anthony JC. (2008). Depressed mood in childhood and subsequent alcohol use through adolescence and young adulthood. Arch Gen Psychiatry 65:702–712. - PMC - PubMed
    1. Davey Smith G, Hemani G. (2014). Mendelian randomization: genetic anchors for causal inference in epidemiological studies. Hum Mol Genet 23:R89–R98. - PMC - PubMed
    1. Edwards AC, Aliev F, Bierut LJ, Bucholz KK, Edenberg H, Hesselbrock V, et al. (2012). Genome-wide association study of comorbid depressive syndrome and alcohol dependence. Psychiatr Genet 22:31–41. - PMC - PubMed

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