肥胖症:从遗传和基因组角度探讨其与大脑功能的联系

IF 9.6 1区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Molecular Psychiatry Pub Date : 2024-09-05 DOI:10.1038/s41380-024-02737-9
Sadia Saeed, Amélie Bonnefond, Philippe Froguel
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引用次数: 0

摘要

肥胖症是一个不断升级的全球健康负担,对医疗和经济产生深远影响。传统观点认为,肥胖症是一种 "纯粹 "的代谢紊乱,其特点是卡路里消耗和能量消耗之间的不平衡。然而,目前的知识认识到,罕见或常见的遗传因素与神经发育和精神异常的出现之间存在着错综复杂的相互作用,这些因素有利于肥胖症的发生,而这些表型又受到生活方式等环境因素的调节。三十年的人类基因研究揭示了导致严重早发性单基因肥胖症的 20 个基因,以及与常见多基因肥胖症相关的约 1000 个基因位点,其中大部分在大脑中表达,这表明肥胖症是一种神经和精神疾病。因此,应更好地认识肥胖与大脑功能的关系。在此背景下,本综述试图通过阐明肥胖与神经发育和精神功能障碍的遗传决定因素来拓宽目前的研究视角。我们详细研究了最新的遗传学发现,并将其与肥胖症相关的临床和行为表型联系起来。这包括多基因肥胖症是如何受到无数基因变异的影响,从而影响与成瘾和奖赏相关的大脑区域,并将其与单基因肥胖症区分开来。此外,还探讨了非综合征和综合征单基因肥胖之间的连续性,并提供了神经发育和认知评估方面的证据。此外,还讨论了针对这些遗传机制的当前治疗方法,这些方法可改善临床疗效和认知优势。总之,这篇综述证实了肥胖症的遗传基础,肯定了肥胖症是一种神经系统疾病,可能对神经发育和精神状况有更广泛的影响。它强调了遗传学、基因组学和神经生物学的交汇点前景广阔,是开发治疗肥胖症及其相关神经疾病的定制医疗方法的基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Obesity: exploring its connection to brain function through genetic and genomic perspectives

Obesity represents an escalating global health burden with profound medical and economic impacts. The conventional perspective on obesity revolves around its classification as a “pure” metabolic disorder, marked by an imbalance between calorie consumption and energy expenditure. Present knowledge, however, recognizes the intricate interaction of rare or frequent genetic factors that favor the development of obesity, together with the emergence of neurodevelopmental and mental abnormalities, phenotypes that are modulated by environmental factors such as lifestyle. Thirty years of human genetic research has unveiled >20 genes, causing severe early-onset monogenic obesity and ~1000 loci associated with common polygenic obesity, most of those expressed in the brain, depicting obesity as a neurological and mental condition. Therefore, obesity’s association with brain function should be better recognized. In this context, this review seeks to broaden the current perspective by elucidating the genetic determinants that contribute to both obesity and neurodevelopmental and mental dysfunctions. We conduct a detailed examination of recent genetic findings, correlating them with clinical and behavioral phenotypes associated with obesity. This includes how polygenic obesity, influenced by a myriad of genetic variants, impacts brain regions associated with addiction and reward, differentiating it from monogenic forms. The continuum between non-syndromic and syndromic monogenic obesity, with evidence from neurodevelopmental and cognitive assessments, is also addressed. Current therapeutic approaches that target these genetic mechanisms, yielding improved clinical outcomes and cognitive advantages, are discussed. To sum up, this review corroborates the genetic underpinnings of obesity, affirming its classification as a neurological disorder that may have broader implications for neurodevelopmental and mental conditions. It highlights the promising intersection of genetics, genomics, and neurobiology as a foundation for developing tailored medical approaches to treat obesity and its related neurological aspects.

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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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