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胰岛素信号转导通路相关基因多态性与阿尔茨海默病的关系

郑南 赵和丹 田华伟 王金龙 黄通 李小玲 周国强 刘盛元

新医学2017,Vol.48Issue(8):550-554,5.
新医学2017,Vol.48Issue(8):550-554,5.DOI:10.3969/j.issn.0253-9802.2017.08.008

胰岛素信号转导通路相关基因多态性与阿尔茨海默病的关系

Relationship between insulin signal transduction pathway-associated gene polymorphism and Alzheimer disease

郑南 1赵和丹 2田华伟 1王金龙 2黄通 3李小玲 1周国强 1刘盛元3

作者信息

  • 1. 518033 深圳,中山大学附属第八医院
  • 2. 314500 嘉兴,嘉兴市康慈医院心理科
  • 3. 518030 深圳,深圳市南山区慢性病防治院慢性病防控中心
  • 折叠

摘要

Abstract

Objective To investigate the relationship between insulin signal transduction pathway-associated gene phosphatidylinositol 3 kinase (PI3K) polymorphism and Alzheimer disease (AD).Methods In this study, 231 AD patients(AD group) and 231 healthy subjects (healthy control group) were recruited.Peripheral venous blood sampling was collected for DNA detection.The gene polymorphism of PI3K was detected by PCR and single nucleotide polymorphism sequencing.The serum level of PI3K protein was measured by enzyme linked immunosorbent assay (ELISA).The PI3K genotype, allele distribution and PI3K protein level were statistically compared between two groups.The relationship between PI3K polymorphism rs3730087 and expression level of PI3K protein was analyzed.Results The genotype and allele of PI3K polymorphism reference IDPIK3R1 rs3730087 and the PI3K protein level significantly differed between the AD and healthy control groups (P<0.05).The expression levels of PI3K protein with varying gene polymorphisms significantly differed between TT and TC (P=0.004), TT and CC in the AD group (P=0.016), TT and TC(P=0.001), TT and CC(P=0.022)in the healthy control group.Conclusions The insulin signal transduction pathway-associated gene PI3K polymorphism exerts certain effect upon AD.PIK3R1 rs3730087 (T>C) increases the risk of AD.

关键词

基因多态性/胰岛素信号/阿尔兹海默病/转导通路

Key words

Gene polymorphism/Insulin signal/Alzheimer disease/Transduction pathway

引用本文复制引用

郑南,赵和丹,田华伟,王金龙,黄通,李小玲,周国强,刘盛元..胰岛素信号转导通路相关基因多态性与阿尔茨海默病的关系[J].新医学,2017,48(8):550-554,5.

基金项目

广东省医学科研基金资助项目(A2015387) (A2015387)

新医学

OACSTPCD

0253-9802

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