Exploring the Genetic Overlap Between Metabolic Traits and Anorexia Nervosa

IF 4 Q2 NEUROSCIENCES
Danielle M. Adams , Murray J. Cairns
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引用次数: 0

Abstract

Background

Anorexia nervosa (AN) is an eating disorder with complex biology that remains largely uncharacterized. Recent genome-wide association studies have identified genetic associations between metabolic traits and AN that may relate to the underlying pathophysiology of the condition. Moreover, observational studies have identified evidence of dysregulated metabolic traits in AN, with emerging evidence suggesting that some of these findings are also observed in weight-restored individuals. While there is evidence for putative shared genetic factors linking metabolic traits and AN, the biology underpinning these genetic relationships has not been thoroughly investigated.

Methods

To further explore shared genetic architecture between metabolic traits and AN with regional specificity, we investigated spatially localized genetic correlation and Bayesian colocalization between 6 metabolic traits (body mass index, high-density lipoprotein, leptin, fasting insulin, insulin resistance, and type 2 diabetes) (n = 30,931–659,316) and AN (n = 72,517).

Results

Significant local genetic correlation was identified across 60 regions, between genetic liability to AN and one of the 6 metabolic traits, after Benjamini-Hochberg correction. Three of these regions showed strong evidence of colocalization with a shared variant (posterior probability > 0.8), indicating potential functional mechanisms related to the trait associations for high-density lipoprotein and body mass index.

Conclusions

Using evidence of local genetic correlation and colocalization, we found independent regions of the genome that may determine the genome-wide genetic correlation between metabolic traits and AN and identified specific shared genes which may assist with our mechanistic understanding of the inherent biological link between AN and metabolites.
探讨代谢特征与神经性厌食症之间的遗传重叠。
背景:神经性厌食症(AN)是一种具有复杂生物学特征的进食障碍,在很大程度上仍未被描述。最近的全基因组关联研究已经确定了代谢性状和AN之间的遗传关联,这可能与该疾病的潜在病理生理有关。此外,观察性研究已经发现了AN中代谢特征失调的证据,新出现的证据表明,这些发现中的一些也存在于体重恢复的个体中。虽然有证据表明代谢性状和AN之间存在共同的遗传因素,但支撑这些遗传关系的生物学尚未得到彻底研究。方法:为了进一步探索代谢性状与AN之间具有区域特异性的共同遗传结构,我们研究了6个代谢性状(体重指数、高密度脂蛋白、瘦素、空腹胰岛素、胰岛素抵抗和2型糖尿病)(n = 30,931-659,316)与AN (n = 72,517)之间的空间定位遗传相关性和贝叶斯共定位。结果:经Benjamini-Hochberg校正后,在60个区域中发现了AN遗传倾向与6个代谢性状中的一个之间存在显著的局部遗传相关性。其中3个区域显示出具有共同变异的共定位(后验概率> 0.8),这表明高密度脂蛋白和体重指数的性状关联的潜在功能机制。结论:利用局部遗传相关和共定位的证据,我们发现了基因组的独立区域,这些区域可能决定了代谢性状与AN之间的全基因组遗传相关性,并鉴定了特定的共享基因,这可能有助于我们对AN与代谢物之间内在生物学联系的机制理解。
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来源期刊
Biological psychiatry global open science
Biological psychiatry global open science Psychiatry and Mental Health
CiteScore
4.00
自引率
0.00%
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审稿时长
91 days
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