Evidence of causal effect of major depression on alcohol dependence: findings from the psychiatric genomics consortium

Year: 2019

Type: article

Abstract: ABSTRACT Background Despite established clinical associations among major depression (MD), alcohol dependence (AD), and alcohol consumption (AC), the nature of the causal relationship between them is not completely understood. Methods This study was conducted using genome-wide data from the Psychiatric Genomics Consortium (MD: 135,458 cases and 344,901 controls; AD: 10,206 cases and 28,480 controls) and UK Biobank (AC-Frequency: from “daily or almost daily” to “never”, 438,308 individuals; AC-Quantity: total units of alcohol per week, 307,098 individuals). Linkage disequilibrium score regression and Mendelian Randomization (MR) analyses were applied to investigate shared genetic mechanisms (horizontal pleiotropy) and causal relationships (mediated pleiotropy) among these traits. Outcomes Positive genetic correlation was observed between MD and AD (rg MD-AD =+0.47, P =6.6×10 -10 ). AC-Quantity showed positive genetic correlation with both AD (rg AD-AC-Quantity =+0.75, P =1.8×10 -14 ) and MD (rg MD-AC-Quantity =+0.14, P =2.9×10 -7 ), while there was negative correlation of AC-Frequency with MD (rg MD-AC-Frequency =-0.17, P =1.5×10 -10 ) and a non-significant result with AD. MR analyses confirmed the presence of pleiotropy among these traits. However, the MD-AD results reflect a mediated-pleiotropy mechanism (i.e., causal relationship) with a causal role of MD on AD (beta=0.28, P =1.29×10 -6 ) that does not appear to be biased by confounding such as horizontal pleiotropy. No evidence of reverse causation was observed as the AD genetic instrument did not show a causal effect on MD. Interpretation Results support a causal role for MD on AD based on genetic datasets including thousands of individuals. Understanding mechanisms underlying MD-AD comorbidity not only addresses important public health concerns but also has the potential to facilitate prevention and intervention efforts. Funding National Institute of Mental Health and National Institute on Drug Abuse. Putting data into context Evidence before this study We searched PubMed up to August 24, 2018, for research studies that investigated causality among alcohol-and depression related phenotypes using Mendelian randomization approaches. We used the search terms “alcohol” AND “depression” AND “Mendelian Randomization”. No restrictions were applied to language, date, or article type. Ten articles were retrieved, but only two were focused on alcohol consumption and depression-related traits. The studies were based on genetic variants in alcohol dehydrogenase ( ADH ) genes only, did not find evidence for a causal effect of alcohol consumption on depression phenotypes, with one study finding a causal effect of alcohol consumption on alcoholism. Both studies noted that future studies are needed with increased sample sizes and clinically derived phenotypes. To our knowledge, no previous study has applied two-sample Mendelian randomization to investigate causal relationships between alcohol dependence and major depression. Twin studies show genetic factors influence susceptibility to MD, AD, and alcohol consumption. Differently from observational approaches where several studies have investigated the relationship between alcohol-and depression-related phenotypes, very limited use of molecular genetic data has been applied to investigate this issue. Additionally, the use of genetic information has been shown to be less biased by confounders and reverse causation than observation data. However, genetic approaches, like Mendelian randomization, require large sample sizes to be informative. Added value of this study In this study, we used genome-wide data from the Psychiatric Genomic Consortium and UK Biobank, which include information regarding hundred thousands of individuals, to test the presence of shared genetic mechanisms and causal relationships among major depression, alcohol dependence, and alcohol consumption. The results support a causal influence of MD on AD, while alcohol consumption showed shared genetic mechanisms with respect to both major depression and alcohol dependence. Implications of all the available evidence Given the significant morbidity and mortality associated with MD, AD, and the comorbid condition, understanding mechanisms underlying these associations not only address important public health concerns but also has the potential to facilitate prevention and intervention efforts.

Source: Psychological Medicine

DOI: 10.1017/s0033291719000667

Institutions: Yale University, VA Connecticut Healthcare System, Virginia Commonwealth University, QIMR Berghofer Medical Research Institute, University of Edinburgh, Heidelberg University, Central Institute of Mental Health, Medizinische Fakultät Mannheim, VCU Massey Comprehensive Cancer Center, Amsterdam Public Health, Vrije Universiteit Amsterdam, Washington University in St. Louis, Indiana University Indianapolis, Indiana University School of Medicine, King's College London, University of North Carolina at Chapel Hill, Karolinska Institutet, The University of Queensland, Institute for Molecular Bioscience

Language: English

Topic: Genetic Associations and Epidemiology

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: green

Funders: American Foundation for Suicide Prevention, South London and Maudsley NHS Foundation Trust, National Institute for Health and Care Research, Department of Health and Social Care, King's College London, Vrije Universiteit Amsterdam, Nederlandse Organisatie voor Wetenschappelijk Onderzoek, National Institutes of Health, Medical Research Council, National Institute on Alcohol Abuse and Alcoholism, National Institute on Aging, National Institute of Mental Health, National Institute on Drug Abuse

OpenAlex ID: W2952677689