通过研究 FTO 基因与神经质之间的关联,发现其对主观幸福感和酗酒问题的间接影响

Wenjie Cai, Yvonne Forsell, Catharina Lavebratt, Philippe A. Melas
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引用次数: 0

摘要

脂肪量和肥胖相关(FTO)基因与肥胖之间的关系已得到公认。然而,最近的研究将 FTO 与成瘾表型和多巴胺能信号转导联系起来,从而暗示了更广泛的精神影响。我们通过对 4,756 项全基因组关联研究(GWAS)进行表型关联研究(PheWAS)来探索这一假设,在多重校正显著性水平上确定了 26 个与 FTO 相关的精神特质。这些特征分为四类:药物使用、时间型/睡眠、幸福感和神经质。为了验证这些发现,我们在一个单独的队列中分析了一个功能暗示性 FTO 变体(rs1421085),研究了其对以下方面的影响:(i) 基于酒精使用障碍鉴定测试(AUDIT)的酒精使用情况;(ii) 基于世界卫生组织(WHO)十项幸福指数的主观幸福感;(iii) 基于舍费尔五因素模型(FFM)或卡罗林斯卡人格量表(KSP)的神经质。我们的研究结果证实,rs1421085 与神经质之间存在直接关联,且与年龄、性别、饮酒、体重指数(BMI)和童年逆境无关。有趣的是,虽然没有观察到rs1421085与酒精摄入量的直接关联,但横截面和滞后纵向中介分析发现了rs1421085与问题性饮酒(AUDIT-P)之间的间接关系,而神经质的增加是中介。中介分析还支持 rs1421085 通过神经质增加和体重指数的途径对较低的幸福感产生间接影响。我们的研究首次验证了 FTO 与神经质之间的直接关联。然而,还需要更多的研究来确认 FTO 通过神经质与幸福感和饮酒之间的因果关系。
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Examining the association between the FTO gene and neuroticism reveals indirect effects on subjective well-being and problematic alcohol use
Associations between the fat mass and obesity-associated (FTO) gene and obesity are well-established. However, recent studies have linked FTO to addiction phenotypes and dopaminergic signaling, thus suggesting broader psychiatric implications. We explored this assumption by conducting a phenome-wide association study (PheWAS) across 4,756 genome-wide association studies (GWASs), identifying 26 psychiatric traits associated with FTO at the multiple-corrected significance level. These traits clustered into four categories: substance use, chronotype/sleep, well-being, and neuroticism. To validate these findings, we analyzed a functionally suggestive FTO variant (rs1421085) in a separate cohort, examining its impact on (i) alcohol use based on the Alcohol Use Disorders Identification Test (AUDIT), (ii) subjective well-being based on the WHO (Ten) Well-Being Index, and (iii) neuroticism based on Schafer's Five Factor Model (FFM) or the Karolinska Scales of Personality (KSP). Our results confirmed a direct association between rs1421085 and neuroticism that was independent of age, sex, alcohol use, body mass index (BMI), and childhood adversities. Interestingly, while no direct association with alcohol intake was observed, both cross-sectional and lagged longitudinal mediation analyses uncovered indirect relationships between rs1421085 and problematic alcohol use (AUDIT-P), with increased neuroticism acting as the intermediary. Mediation analyses also supported an indirect effect of rs1421085 on lower well-being through the pathways of increased neuroticism and BMI. Our study is the first to validate a direct association between FTO and neuroticism. However, additional studies are warranted to affirm the causal pathways linking FTO to well-being and alcohol use through neuroticism.
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