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儿童静息代谢率相关基因变异与超重/肥胖风险:一项为期3年的队列研究。

RMR-Related Gene Variation on the Risk of Overweight/Obesity in Children: A 3-Year Panel Study.

作者信息

Lee Myoungsook, Lee Yunkyoung, Kang Inhae, Shin Jieun, Sorn Sungbin R

机构信息

Department of Food & Nutrition, and Research Institute of Obesity Sciences, Sungshin Women's University, Seoul 01133, Korea.

Department of Food & Nutrition, and Interdisciplinary Graduate Program in Advanced Convergence Technology and Science, Jeju National University, Jeju 63243, Korea.

出版信息

J Pers Med. 2021 Feb 2;11(2):91. doi: 10.3390/jpm11020091.

Abstract

From a pilot GWAS, seven SNPs were significantly associated with resting metabolic rate (RMR) in obese children aged 8-9 years. The aim of this study was to investigate how RMR-linked variation affected obesity in Korean children. With the follow-up students (77.9%) in the 3-year panel study, the changes of the variables associated with obesity (such as anthropometrics, blood biochemistry, and dietary intake) were collected. After the SNPs were screened by Affymetrix Genome-Wide Human SNP array 6.0, the genotyping of the seven SNPs was performed via SNaPshot assay. As the prevalence of obesity (≥85th percentile) increased from 19.4% to 25.5%, the rates of change of the variables RMR, body mass index (BMI), waist circumference (WC), systolic blood pressure (SBP), and dietary intake (energy and carbohydrate intakes) increased. The rate of overweight/obesity was higher in all mutant alleles of the seven SNPs than it was in the matched children without mutant alleles. However, over the 3-year study period, RMRs were only significantly increased by the mutants of two single nucleotide polymorphisms (SNPs), rs996229 and rs756942, mainly related to male overweight/obesity as both WC and SBP levels increased. In the mutants of two of the SNPs, the odds ratio of overweight/obesity risk was six times higher in the highest tercile of fat intake and SBP than those of the lowest tercile. For personalized medicine to prevent pediatric obesity, SBP, WC, and dietary fat intake should be observed, particularly if boys have mutants of SNPs, rs9916229, or rs756942.

摘要

在一项针对8至9岁肥胖儿童的全基因组关联研究(GWAS)试点中,七个单核苷酸多态性(SNPs)与静息代谢率(RMR)显著相关。本研究旨在调查RMR相关变异如何影响韩国儿童的肥胖情况。在为期3年的队列研究中,对随访学生(77.9%)收集了与肥胖相关的变量变化(如人体测量学、血液生化和饮食摄入)。通过Affymetrix全基因组人类SNP阵列6.0筛选SNPs后,通过SNaPshot分析对这七个SNPs进行基因分型。随着肥胖患病率(≥第85百分位数)从19.4%增至25.5%,RMR、体重指数(BMI)、腰围(WC)、收缩压(SBP)和饮食摄入(能量和碳水化合物摄入)等变量的变化率上升。七个SNPs的所有突变等位基因的超重/肥胖率均高于无突变等位基因的匹配儿童。然而,在为期3年的研究期间,只有两个单核苷酸多态性(SNPs),即rs996229和rs756942的突变体使RMR显著增加,这两个突变体主要与男性超重/肥胖相关,因为WC和SBP水平均升高。在其中两个SNPs的突变体中,脂肪摄入和SBP最高三分位数的超重/肥胖风险优势比是最低三分位数的六倍。为了通过个性化医疗预防儿童肥胖,应监测SBP、WC和饮食脂肪摄入,特别是当男孩有SNPs,rs9916229或rs756942的突变体时。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7450/7913067/099ce99ac42f/jpm-11-00091-g001.jpg

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