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The Unpredictable Chronic Mild Stress Protocol for Inducing Anhedonia in Mice
Published on: October 24, 2018
Genetic interactions with stressful environments in depression and addiction
Margit Burmeister1, Srijan Sen2
1Computational Medicine & Bioinformatics and a Research Professor in the Michigan Neuroscience Institute, University of Michigan, Ann Arbor, MI, USA. She also holds appointments as Professor of Psychiatry and Professor of Human Genetics. She received her doctorate from the Ruprecht Karl University of Heidelberg in Germany for work at the European Molecular Biology Laboratory. She trained as a postdoctoral fellow at the University of California in San Francisco. She has held visiting Professorships at the Max Planck Institute for Molecular Genetics in Berlin, Shanghai Jiao Tong University, China, the Weizmann Institute of Science, Israel, the University of Heidelberg and the Chinese University of Hong Kong in Shenzhen, China.
Abstract:
Stress is the most important proximal precipitant of depression, yet most large genome-wide association studies (GWAS) do not include stress as a variable. Here, we review how gene × environment (G × E) interaction might impede the discovery of genetic factors, discuss two examples of G × E interaction in depression and addiction, studies incorporating high-stress environments, as well as upcoming waves of genome-wide environment interaction studies (GWEIS). We discuss recent studies which have shown that genetic distributions can be affected by social factors such as migrations and socioeconomic background. These distinctions are not just academic but have practical consequences. Owing to interaction with the environment, genetic predispositions to depression should not be viewed as unmodifiable destiny. Patients may genetically differ not just in their response to drugs, as in the now well-recognised field of pharmacogenetics, but also in how they react to stressful environments and how they are affected by behavioural therapies.
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