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FTO和TCF7L2基因变异与性早熟。

Genetic variation of FTO and TCF7L2 in premature adrenarche.

作者信息

Lappalainen Saila, Voutilainen Raimo, Utriainen Pauliina, Laakso Markku, Jääskeläinen Jarmo

机构信息

Department of Pediatrics, University of Kuopio and Kuopio University Hospital, FI-70211 Kuopio, Finland.

出版信息

Metabolism. 2009 Sep;58(9):1263-9. doi: 10.1016/j.metabol.2009.03.025. Epub 2009 Jun 18.

Abstract

Premature adrenarche (PA) has been associated with increased body mass index. Our aim was to determine whether the obesity-associated variant at fat mass and obesity gene (FTO) is more frequent in PA subjects. Furthermore, we hypothesized that altered Wnt signaling due to genetic variants at transcription factor 7-like 2 (TCF7L2) could play a role in the polygenic pathogenesis of PA. We genotyped polymorphisms at FTO rs9939609 and at TCF7L2 rs7903146 and rs12255372 in 73 Finnish white prepubertal children with PA and in 97 age- and sex-matched healthy controls. In addition, we investigated the associations of these genetic variations with weight, height, circulating adrenocortical hormone levels, glucose metabolism, lipid profile, and blood pressure. The differences in the minor allele frequencies (MAFs) of rs9939609, rs7903146, and rs12255372 were not statistically significant between the PA and control groups (difference in MAFs [95% confidence interval]: -0.06 [-0.18, 0.05], 0.04 [-0.05, 0.12], and 0.01 [-0.07, 0.10]; P = .3, .4, and .8, respectively). However, the risk allele at TCF7L2 rs7903146 was more frequent in PA subjects than in controls when we restricted the analysis to the subjects with lower weight-for-height than the median of the PA subjects (weight-for-height <108%, corresponding body mass index SD score <0.79; difference in MAFs [95% confidence interval]: 0.12 [-0.001, 0.23]; P = .038). Risk variant at FTO rs9939609 associated with higher weight-for-height in the healthy children (P = .001). In conclusion, the minor variant at FTO rs9939609 seems to play no major role in the increased weight-for-height of PA subjects; but the risk allele at TCF7L2 rs7903146 may have a role in the pathogenesis of PA in lean subjects.

摘要

早熟性肾上腺初现(PA)与体重指数增加有关。我们的目的是确定脂肪量和肥胖基因(FTO)处与肥胖相关的变异在PA受试者中是否更常见。此外,我们推测转录因子7样2(TCF7L2)处的基因变异导致的Wnt信号改变可能在PA的多基因发病机制中起作用。我们对73名患有PA的芬兰白人青春期前儿童以及97名年龄和性别匹配的健康对照者的FTO rs9939609、TCF7L2 rs7903146和rs12255372处的多态性进行了基因分型。此外,我们研究了这些基因变异与体重、身高、循环肾上腺皮质激素水平、葡萄糖代谢、血脂谱和血压之间的关联。PA组和对照组之间rs9939609、rs7903146和rs12255372的次要等位基因频率(MAF)差异无统计学意义(MAF差异[95%置信区间]:-0.06[-0.18,0.05]、0.04[-0.05,0.12]和0.01[-0.07,0.10];P分别为0.3、0.4和0.8)。然而,当我们将分析限制在身高体重低于PA受试者中位数的受试者中时(身高体重<108%,相应的体重指数标准差评分<0.79;MAF差异[95%置信区间]:0.12[-0.001,0.23];P=0.038),PA受试者中TCF7L2 rs7903146的风险等位基因比对照组更常见。FTO rs9939609处的风险变异与健康儿童较高的身高体重相关(P=0.001)。总之,FTO rs9939609处的次要变异似乎在PA受试者身高体重增加中不起主要作用;但TCF7L2 rs7903146的风险等位基因可能在瘦型受试者PA的发病机制中起作用。

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