Association of serotonin receptor gene polymorphisms with anorexia nervosa: a systematic review and meta-analysis

Arturo Bevilacqua, Francesca Santini, Daniela La Porta, Silvia Cimino
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Abstract

Purpose

Several studies have investigated the association between anorexia nervosa and polymorphisms of genes regulating serotonin neurotransmission, with a focus on the rs6311 polymorphism of 5-HTR2A. However, inconsistent results of these studies and conflicting conclusions of existing meta-analyses complicate the understanding of a possible association. We have updated these results and evaluated the involvement of other serotonin receptor gene polymorphisms in anorexia nervosa.

Methods

Adhering to PRISMA guidelines, we have searched studies on anorexia nervosa and serotonin-regulating genes published from 1997 to 2022, selected those concerning receptor genes and meta-analyzed the results from twenty candidate gene studies on the 5-HTR2A rs6311 polymorphism and the 5-HTR2C rs6318 polymorphism.

Results

Present analyses reveal an association for the 5-HTR2A rs6311 polymorphism, with G and A alleles, across eighteen studies (2049 patients, 2877 controls; A vs. G allele, Odds Ratio = 1.24; 95% Confidence Interval = 1.06–1.47; p = 0.009). However, after geographic subgrouping, an association emerged only in a Southern European area, involving five studies (722 patients, 773 controls; A vs. G allele, Odds Ratio = 1.82; 95% Confidence Interval = 1.41–2.37; p < 0.00001). No association was observed for the 5-HTR2C rs6318 polymorphism across three studies.

Conclusions

To date, the involvement in the pathophysiology of anorexia nervosa of the 5-HTR2A rs6311 polymorphism appears limited to a specific genetic and/or environmental context, while that of the 5-HTR2C rs6318 polymorphism seems excluded. Genome-wide association studies and epigenetic studies will likely offer deeper insights of genetic and environmental factors possibly contributing to the disorder.

Level of evidence

III Evidence obtained from well-designed cohort or case–control analytic studies.

Clinical trial registration PROSPERO registration number: CRD42021246122.

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血清素受体基因多态性与神经性厌食症的关系:系统回顾与荟萃分析
目的多项研究调查了神经性厌食症与调节血清素神经递质的基因多态性之间的关联,重点是 5-HTR2A 的 rs6311 多态性。然而,这些研究的结果并不一致,现有的荟萃分析得出的结论也相互矛盾,这使得人们对可能存在的关联性的理解变得更加复杂。我们更新了这些结果,并评估了其他血清素受体基因多态性在神经性厌食症中的参与情况。方法根据PRISMA指南,我们检索了1997年至2022年发表的有关神经性厌食症和血清素调节基因的研究,选择了那些与受体基因有关的研究,并对20项候选基因研究中有关5-HTR2A rs6311多态性和5-HTR2C rs6318多态性的结果进行了荟萃分析。结果目前的分析显示,在 18 项研究中,5-HTR2A rs6311 多态性与 G 等位基因和 A 等位基因存在关联(2049 例患者,2877 例对照;A 等位基因与 G 等位基因的比值比 = 1.24;95% 置信区间 = 1.06-1.47;p = 0.009)。然而,在进行地理分组后,只有在南欧地区的五项研究(722 名患者,773 名对照组;A 与 G 等位基因的比值比 = 1.82;95% 置信区间 = 1.41-2.37;p <;0.00001)中出现了关联。结论迄今为止,5-HTR2A rs6311 多态性参与神经性厌食症的病理生理学似乎仅限于特定的遗传和/或环境背景,而 5-HTR2C rs6318 多态性似乎不参与其中。全基因组关联研究和表观遗传学研究可能会对可能导致该疾病的遗传和环境因素有更深入的了解。证据等级III 从设计良好的队列或病例对照分析研究中获得的证据:CRD42021246122。
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来源期刊
CiteScore
6.50
自引率
10.30%
发文量
170
审稿时长
>12 weeks
期刊介绍: Eating and Weight Disorders - Studies on Anorexia, Bulimia and Obesity is a scientific journal whose main purpose is to create an international forum devoted to the several sectors of eating disorders and obesity and the significant relations between them. The journal publishes basic research, clinical and theoretical articles on eating disorders and weight-related problems: anorexia nervosa, bulimia nervosa, subthreshold eating disorders, obesity, atypical patterns of eating behaviour and body weight regulation in clinical and non-clinical populations.
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