Genetic Associations of Anhedonia: Insights into Overlap of Mental and Somatic Disorders.

Consortium psychiatricum Pub Date : 2024-07-06 eCollection Date: 2024-01-01 DOI:10.17816/CP15494
Evgeny Kasyanov, Darya Pinakhina, Aleksandr Rakitko, Ekaterina Vergasova, Danat Yermakovich, Grigoriy Rukavishnikov, Larisa Malyshko, Yaroslav Popov, Elena Kovalenko, Anna Ilinskaya, Anna Kim, Nikolay Plotnikov, Nikolay Neznanov, Valeriy Ilinsky, Aleksandr Kibitov, Galina Mazo
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Abstract

Background: Anhedonia is characterized by a reduced ability to anticipate, experience, and/or learn about pleasure. This phenomenon has a transdiagnostic nature and is one of the key symptoms of mood disorders, schizophrenia, addictions, and somatic conditions.

Aim: To evaluate the genetic architecture of anhedonia and its overlap with other mental disorders and somatic conditions.

Methods: We performed a genome-wide association study of anhedonia on a sample of 4,520 individuals from a Russian non-clinical population. Using the available summary statistics, we calculated polygenic risk scores (PRS) to investigate the genetic relationship between anhedonia and other psychiatric or somatic phenotypes.

Results: No variants with a genome-wide significant association were identified. PRS for major depression, bipolar disorder, and schizophrenia were significantly associated with anhedonia. Conversely, no significant associations were found between PRS for anxiety and anhedonia, which aligns well with existing clinical evidence. None of the PRS for somatic phenotypes attained a significance level after correction for multiple comparisons. A nominal significance for the anhedonia association was determined for omega-3 fatty acids, type 2 diabetes mellitus, and Crohn's disease.

Conclusion: Anhedonia has a complex polygenic architecture, and its presence in somatic diseases or normal conditions may be due to a genetic predisposition to mood disorders or schizophrenia.

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失乐症的遗传关联:洞察精神疾病与躯体疾病的重叠。
背景介绍失乐症的特征是预测、体验和/或学习快乐的能力下降。这种现象具有跨诊断的性质,是情绪障碍、精神分裂症、成瘾和躯体疾病的主要症状之一。目的:评估失乐症的遗传结构及其与其他精神障碍和躯体疾病的重叠:我们对来自俄罗斯非临床人群的 4520 个样本进行了厌世情绪的全基因组关联研究。利用现有的汇总统计数据,我们计算了多基因风险评分(PRS),以研究厌食症与其他精神疾病或躯体疾病表型之间的遗传关系:结果:没有发现具有全基因组显著相关性的变异。重度抑郁症、双相情感障碍和精神分裂症的 PRS 与失乐症显著相关。相反,焦虑症的 PRS 与失乐症之间没有发现明显的关联,这与现有的临床证据非常吻合。在对多重比较进行校正后,躯体表型的 PRS 均未达到显著性水平。欧米伽-3 脂肪酸、2 型糖尿病和克罗恩病与失乐症的关联具有名义显著性:失乐症具有复杂的多基因结构,在躯体疾病或正常情况下出现失乐症可能是由于情绪障碍或精神分裂症的遗传易感性所致。
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