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儿童肥胖中基质金属蛋白酶2(MMP2)启动子多态性的分析

Analysis of MMP2 promoter polymorphisms in childhood obesity.

作者信息

Morgan Angharad R, Han Dug Yeo, Thompson John Md, Mitchell Edwin A, Ferguson Lynnette R

机构信息

Discipline of Nutrition, FMHS, The University of Auckland, New Zealand.

出版信息

BMC Res Notes. 2011 Jul 21;4:253. doi: 10.1186/1756-0500-4-253.

Abstract

BACKGROUND

Several lines of evidence suggest a possible functional role of Matrix metalloproteinase -2 (MMP-2) in obesity. The aim of this study was to evaluate the role of MMP-2 promoter polymorphisms in percentage body fat (PBF) as a measure of childhood obesity in a New Zealand population.

FINDINGS

546 samples from the Auckland Birthweight Collaborative (ABC) study were genotyped for the three MMP-2 promoter SNPs -1306 C/T (rs243865), -1575G/A (rs243866) and -790 T/G (rs243864) using the Sequenom genotyping platform. The results demonstrated that an MMP-2 promoter haplotype is associated with PBF in New Zealand 7 year old children.

CONCLUSION

We have previously determined that environmental factors are associated with differences in PBF in this study group, and now we have demonstrated a possible genetic contribution.

摘要

背景

多项证据表明基质金属蛋白酶-2(MMP-2)在肥胖中可能具有功能性作用。本研究的目的是评估MMP-2启动子多态性在新西兰人群中作为儿童肥胖指标的体脂百分比(PBF)中的作用。

研究结果

使用Sequenom基因分型平台对奥克兰出生体重协作研究(ABC)的546份样本进行了三种MMP-2启动子单核苷酸多态性-1306 C/T(rs243865)、-1575G/A(rs243866)和-790 T/G(rs243864) 的基因分型。结果表明,一种MMP-2启动子单倍型与新西兰7岁儿童的PBF相关。

结论

我们之前已确定环境因素与该研究组中PBF的差异相关,现在我们证明了可能存在的遗传因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9eea/3154167/5784674cc093/1756-0500-4-253-1.jpg

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