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A Quantitative Trait Locus on 7q31 for the Changes in Plasma Insulin in Response to Exercise Training: The HERITAGE Family Study

机译:7q31定量特征位点对运动训练后血浆胰岛素变化的影响:HERITAGE家庭研究

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摘要

Several genome-wide linkage scans have been carried out to identify quantitative trait loci for type 2 diabetes and related metabolic phenotypes. However, no previous linkage scans have focused on the response to exercise training of relevant metabolic traits. We performed a genome-wide linkage scan for baseline fasting glucose, insulin, and C-peptide and their responses to a 20-week exercise training program in nondiabetic white and black men and women from the HERITAGE Family Study. In SIBPAL linkage analyses, the maximum number of sibpairs available was 344 and 93 for baseline phenotypes and 300 and 72 for exercise training response phenotypes in whites and blacks, respectively. A total of 509 markers with an average spacing of 6.0 Mb were used. The strongest linkage was found for the changes in fasting insulin in response to exercise training with a marker in the leptin gene on 7q31 (empirical multipoint P = 0.0004) in whites. In blacks, the strongest linkage was observed for baseline fasting glucose on 12q13-q14 (empirical multipoint P = 0.0006). These regions harbor several potential candidate genes. The present findings may be important in identifying individuals at increased risk of developing type 2 diabetes and who are most likely to benefit from a physically active lifestyle.
机译:已经进行了几次全基因组连锁扫描,以鉴定2型糖尿病和相关代谢表型的定量性状基因座。但是,以前的连锁扫描都没有集中于对相关代谢性状的运动训练的反应。我们对来自HERITAGE家庭研究的非糖尿病白人和黑人进行了全基因组连锁扫描,以检测基线空腹血糖,胰岛素和C肽及其对20周运动训练计划的反应。在SIBPAL连锁分析中,白人和黑人的基准表型可用最大同胞对分别为344和93,运动训练反应表型分别为300和72。总共使用了509个标记,平均间隔为6.0 Mb。发现白人对7q31时瘦素基因中的标记物进行运动训练后,空腹胰岛素的变化之间存在最强的联系(经验多点P = 0.0004)。在黑人中,基线空腹血糖在12q13-q14上观察到最强的连锁(经验多点P = 0.0006)。这些区域包含几个潜在的候选基因。目前的发现对于识别罹患2型糖尿病的风险增加且最有可能从体育锻炼中受益的个体可能很重要。

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