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首页> 外文期刊>Molecular biology reports >Associations of polymorphisms in the candidate genes for Alzheimer's disease BIN1, CLU, CR1 and PICALM with gestational diabetes and impaired glucose tolerance
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Associations of polymorphisms in the candidate genes for Alzheimer's disease BIN1, CLU, CR1 and PICALM with gestational diabetes and impaired glucose tolerance

机译:多态性在阿尔茨海默病Bin1,Clu,Cr1和鼠脊髓中候选基因的关联与妊娠期糖尿病和葡萄糖耐量受损

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摘要

Alzheimer's disease (AD) is the most common type of dementia, with a prevalence that is rising every year. AD is associated with type 2 diabetes mellitus (T2DM) and insulin resistance, and is therefore sometimes called "type 3 diabetes mellitus". The aim of this study was to examine whether the variants of some candidate genes involved in the development of AD, namely BIN1 (rs744373), CLU (rs11136000), CR1 (rs3818361), and PICALM (rs3851179), are related to several disorders of glucose metabolism-gestational diabetes (GDM), T2DM and impaired glucose tolerance (IGT). Our study included 550 women with former GDM and 717 control women, 392 patients with T2DM and 180 non-diabetic controls, and 117 patients with IGT and 630 controls with normal glucose tolerance. Genotyping analysis was performed using specially-designed TaqMan assays. No significant associations of the genetic variants rs744373 in BIN1, rs11136000 in CLU, or rs3818361 in CR1 were found with GDM, T2DM or IGT, but rs3851179 in PICALM was associated with an increased risk of GDM. The frequency of the AD risk-associated C allele was significantly higher in the GDM group compared to controls: OR 1.21; 95% CI (1.03-1.44). This finding was not apparent in T2DM and IGT; conversely, the C allele of the PICALM SNP was protective for IGT: OR 0.67; 95% CI (0.51-0.89). This study demonstrates an association between PICALM rs3851179 and GDM as well as IGT. However, elucidation of the possible role of this gene in the pathogenesis of GDM requires further independent studies.
机译:阿尔茨海默病(AD)是最常见的痴呆类型,每年都有普遍存在的潮流。 AD与2型糖尿病(T2DM)和胰岛素抵抗有关,因此有时称为“3型糖尿病”。本研究的目的是检查参与AD,即BIN1(RS744373),CLU(RS1113660),CR1(RS3818361)和麦克法司(RS3851179)的多种候选基因的变体是否与几种疾病有关葡萄糖新陈代谢 - 妊娠糖尿病(GDM),T2DM和葡萄糖耐量受损(IGT)。我们的研究包括前GDM和717名妇女的550名妇女,392名T2DM和180名非糖尿病对照,117例IGT和630名患者,具有正常葡萄糖耐量。使用专门设计的Taqman测定进行基因分型分析。在CC1,CL1中的BIN1,RS11136000中的遗传变异RS744373没有显着关联,或CR1中的CR1中的RS3818361,但PicalM中的RS3851179与GDM的风险增加有关。与对照组相比,GDM组的AD风险相关的C等位基因的频率显着较高:或1.21; 95%CI(1.03-1.44)。在T2DM和IGT中,这一发现并不明显;相反,婴儿床SNP的C等位基因对IGT:或0.67的保护剂是保护剂; 95%CI(0.51-0.89)。本研究展示了Picalm RS3851179和GDM之间的关联以及IGT。然而,阐明该基因在GDM发病机制中的可能作用需要进一步的独立研究。

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