Genome-wide association meta-analysis of eating behavior traits revealed one susceptibility locus for emotional eating.

IF 10.4 1区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Manon Muntaner, Katrin Horn, Blandine de Lauzon-Guillain, Muriel Tafflet, Teemu Palviainen, Kirsi H Pietiläinen, Guiomar Masip, Braxton D Mitchell, Christian Couture, Marie-Claude Vohl, Janne Pott, Philippe Amouyel, Monique Romon, Louis Perusse, Nanette Steinle, Jaakko Kaprio, Barbara Heude, Anke Tönjes, Peter Kovacs, Markus Scholz, Aline Meirhaeghe
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Abstract

In order to identify new and genome-wide significant loci for eating behavior traits (cognitive restraint, uncontrolled eating and emotional eating), we conducted a meta-GWAS with seven studies of European ancestry (n = 11,250). Eating behavior was assessed using the Three-Factor Eating Questionnaire. Genotype effects of single studies were estimated using additive models adjusting for age, sex, BMI, and principal components and single study results were combined by fixed-effect meta-analysis.For cognitive restraint and uncontrolled eating, no genome-wide significant association could be detected. For emotional eating, one genomic region on chromosome 5 comprising two polymorphisms attained genome-wide significance (P = 4.0×10-8 for rs6877636 and P = 3.2×10-8 for rs6897090). The minor alleles were associated with higher emotional eating scores (β=0.093 ± 0.017), with a similar direction of effect in each study. Both SNPs, in near perfect linkage disequilibrium, mapped to RP11-24P24.1, a processed pseudogene of ornithine decarboxylase 1 (ODC1). Enrichment analysis revealed a significant overlap between genome-wide BMI-associated variants and nominal emotional eating variants, supporting the hypothesis that shared genetic factors may influence both eating behavior traits and obesity risk. Finally, we observed a number of interesting associations reaching suggestive significance (P < 10-6) involving BMI candidate genes, including a suggestive association between FTO variants and cognitive restraint (rs9922708, β = 0.069, P = 5.9×10-7).In conclusion, our meta-GWAS identified for the first time a robust chromosomal region associated with emotional eating in seven studies. Given that emotional eating strongly influences body weight but is often stigmatized, recognizing genetic susceptibility to certain eating behaviors may help reduce stigma and alleviate guilt.

Abstract Image

饮食行为特征的全基因组关联荟萃分析揭示了情绪化饮食的一个易感性位点。
为了确定饮食行为特征(认知约束、不受控制的饮食和情绪性饮食)的新的和全基因组重要位点,我们对7项欧洲血统研究(n = 11,250)进行了meta-GWAS。饮食行为采用三因素饮食问卷进行评估。使用调整年龄、性别、BMI和主成分的加性模型估计单个研究的基因型效应,并通过固定效应荟萃分析合并单个研究结果。对于认知限制和不受控制的饮食,没有发现全基因组的显著关联。对于情绪化进食,5号染色体上包含两个多态性的一个基因组区域达到了全基因组显著性(rs6877636和rs6897090的P = 4.0×10-8和P = 3.2×10-8)。次要等位基因与较高的情绪性进食得分相关(β=0.093±0.017),各研究的影响方向相似。在接近完美的连锁不平衡中,这两个snp都定位于RP11-24P24.1,一个鸟氨酸脱羧酶1 (ODC1)的加工假基因。富集分析显示,全基因组bmi相关变异和名义情绪性饮食变异之间存在显著重叠,支持了共享遗传因素可能影响饮食行为特征和肥胖风险的假设。最后,我们观察到一些涉及BMI候选基因的有趣关联,具有暗示意义(P -6),包括FTO变异与认知约束之间的暗示关联(rs9922708, β = 0.069, P = 5.9×10-7)。总之,我们的meta-GWAS在七项研究中首次发现了一个与情绪化进食相关的强大染色体区域。考虑到情绪性饮食对体重的影响很大,但往往被认为是耻辱,认识到某些饮食行为的遗传易感性可能有助于减少耻辱和减轻内疚感。
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来源期刊
Molecular Psychiatry
Molecular Psychiatry 医学-精神病学
CiteScore
20.50
自引率
4.50%
发文量
459
审稿时长
4-8 weeks
期刊介绍: Molecular Psychiatry focuses on publishing research that aims to uncover the biological mechanisms behind psychiatric disorders and their treatment. The journal emphasizes studies that bridge pre-clinical and clinical research, covering cellular, molecular, integrative, clinical, imaging, and psychopharmacology levels.
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