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魁北克家族研究中瘦素及瘦素受体基因多态性与静息代谢率和呼吸商的关系

Polymorphisms in the leptin and leptin receptor genes in relation to resting metabolic rate and respiratory quotient in the Québec Family Study.

作者信息

Loos R J F, Rankinen T, Chagnon Y, Tremblay A, Pérusse L, Bouchard C

机构信息

Human Genomics Laboratory, Pennington Biomedical Research Center, Baton Rouge, LA 70808, USA.

出版信息

Int J Obes (Lond). 2006 Jan;30(1):183-90. doi: 10.1038/sj.ijo.0803127.

Abstract

BACKGROUND

Leptin (LEP) is an endocrine hormone that participates in many metabolic pathways, including those associated with the central regulation of energy homeostasis.

OBJECTIVE

We examined the associations between polymorphisms in the LEP and leptin receptor (LEPR) genes and resting metabolic rate (RMR) and respiratory quotient (RQ) in the Quebec Family Study.

METHODS AND SUBJECTS

Three polymorphisms in LEPR (K109R, Q223R and K656N) and one in LEP (19A > G) were genotyped in 678 subjects. RMR, RQ at rest and RQ while sitting, standing and walking at 4.5 km/h (RQ45) were adjusted for age, sex, fat mass and fat-free mass.

RESULTS

RQ45 was associated with the LEPR-K109R (P = 0.004) and Q223R (P = 0.03) polymorphisms, and RMR showed association with the LEPR-K656N polymorphism (P = 0.006). For the LEP-19A > G polymorphism, no significant associations were observed. However, LEP-A19A homozygotes who were carriers of the LEPR N656 allele had a significantly lower RQ45 compared to other genotype combinations (P for interaction=0.003).

CONCLUSION

These findings suggest that DNA sequence variation in the LEPR gene contributes to human variation in RMR and in the relative rates of substrate oxidation during low-intensity exercise in steady state but not in a resting state.

摘要

背景

瘦素(LEP)是一种内分泌激素,参与多种代谢途径,包括与能量稳态中枢调节相关的途径。

目的

在魁北克家庭研究中,我们研究了LEP和瘦素受体(LEPR)基因多态性与静息代谢率(RMR)和呼吸商(RQ)之间的关联。

方法与研究对象

对678名研究对象进行LEPR基因的3种多态性(K109R、Q223R和K656N)以及LEP基因的1种多态性(19A>G)的基因分型。对静息时的RMR、RQ以及以4.5公里/小时速度坐、站和行走时的RQ(RQ45)进行年龄、性别、脂肪量和去脂体重的校正。

结果

RQ45与LEPR-K109R(P=0.004)和Q223R(P=0.03)多态性相关,RMR与LEPR-K656N多态性相关(P=0.006)。对于LEP-19A>G多态性,未观察到显著关联。然而,与其他基因型组合相比,携带LEPR N656等位基因的LEP-A19A纯合子的RQ45显著更低(交互作用P=0.003)。

结论

这些发现表明,LEPR基因中的DNA序列变异导致了人类在静息状态下RMR以及稳态低强度运动期间底物氧化相对速率的个体差异,但在静息状态下不存在这种差异。

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