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涉及MTNR1B基因rs10830963变异与体重减轻的基因-基因相互作用和基因-饮食相互作用。

Gene-Gene Interplay and Gene-Diet Interactions Involving the MTNR1B rs10830963 Variant with Body Weight Loss.

作者信息

Goni Leticia, Cuervo Marta, Milagro Fermin I, Martínez J Alfredo

机构信息

Department of Nutrition, Food Sciences and Physiology, University of Navarra, Pamplona, Spain.

出版信息

J Nutrigenet Nutrigenomics. 2014;7(4-6):232-42. doi: 10.1159/000380951. Epub 2015 Apr 10.

Abstract

BACKGROUND/AIMS: Investigation of the genetic makeup may facilitate the implementation of more personalized nutritional interventions. The aims were to examine whether the rs10830963 MTNR1B polymorphism affects weight loss in response to a hypocaloric diet and to find potential gene-gene interplays and gene-diet interactions.

METHODS

167 subjects enrolled in a personalized nutritional intervention for weight loss (3-6 weeks) were examined for anthropometric measurements, dietary habits and physical activity at baseline and at the first follow-up visit. Three polymorphisms, which have previously been associated with body weight regulation, rs10830963 (MTNR1B), rs9939609 (FTO) and rs17782313 (MC4R), were analyzed using the Luminex® 100/200™ System.

RESULTS

After adjusting for covariates, females with the rs10830963 CG/GG genotype showed lower weight loss than those with the CC genotype. In the total population, carriers of variant alleles of both FTO and MC4R showed a significant association with MTNR1B and weight loss outcome. Moreover, among women, higher total protein and animal protein intakes were associated with a lower weight loss in G allele carriers of the MTNR1B variant.

CONCLUSIONS

Our data evidenced that rs10830963 MTNR1B polymorphism could be associated with individual differences in weight loss induced by a hypocaloric diet. This association was influenced by FTO and MC4R loci and modified by baseline protein intake.

摘要

背景/目的:对基因组成的研究可能有助于实施更具个性化的营养干预措施。本研究旨在探讨rs10830963 MTNR1B基因多态性是否会影响低热量饮食后的体重减轻情况,并寻找潜在的基因-基因相互作用和基因-饮食相互作用。

方法

对167名参加为期3至6周的个性化减肥营养干预的受试者在基线和首次随访时进行人体测量、饮食习惯和身体活动情况检查。使用Luminex® 100/200™系统分析了此前与体重调节相关的三个多态性位点,即rs10830963(MTNR1B)、rs9939609(FTO)和rs17782313(MC4R)。

结果

在调整协变量后,rs10830963 CG/GG基因型的女性体重减轻幅度低于CC基因型的女性。在总体人群中,FTO和MC4R的变异等位基因携带者与MTNR1B及体重减轻结果存在显著关联。此外,在女性中,MTNR1B变异的G等位基因携带者摄入较高的总蛋白和动物蛋白与较低的体重减轻幅度相关。

结论

我们的数据表明,rs10830963 MTNR1B基因多态性可能与低热量饮食引起的体重减轻个体差异有关。这种关联受FTO和MC4R基因座影响,并因基线蛋白摄入量而改变。

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