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UMOD 基因启动子区单核苷酸多态性与 CKD 患者发病年龄的关系

白亚玲 徐金升 张文博 张胜雷 张俊霞 崔立文

山东医药Issue(46):5-7,3.
山东医药Issue(46):5-7,3.DOI:10.3969/j.issn.1002-266X.2014.46.002

UMOD 基因启动子区单核苷酸多态性与 CKD 患者发病年龄的关系

Relationship between single nucleotide polymorphisms in UMOD gene promoter region and the age-onset of chronic disease kidney

白亚玲 1徐金升 1张文博 1张胜雷 1张俊霞 1崔立文1

作者信息

  • 1. 河北医科大学第四医院,石家庄050011
  • 折叠

摘要

Abstract

Objective To investigate the relationship between single nucleotide polymorphisms in UMOD gene pro -moter region and the age-onset of chronic kidney disease ( CKD ) .Methods A total of 89 CKD patients ( patient group ) and 104 healthy volunteers ( control group ) were involved in this study .PCR was used to detect the peripheral blood pro-moter region of UMOD gene .The relationship between the polymorphisms in UMOD gene promoter and the age-onset of chronic disease kidney was analyzed .The relationship between the age-onset of CKD and sex, age, smoking history, BMI, mean arterial pressure were analyzed .Results The sequence of -1 617(rs13333226)G polymorphisms in patient group was higher than that in control group (χ2 =4.737, P=0.030).The onset age of CKD patients with rs13333226A was sig-nificantly younger than that of patients with rs13333226G(χ2 =7.902, P=0.005).Single factor analysis showed that the age-onset of CKD patients with BMI >22 was earlier than those with BMI<22(P<0.05).The age-onset of CKD patients with smoking history was earlier than those without smoking history (P<0.05).The SNP of rs13333226 was the independ-ent risk factor for the the age-onset of CKD(OR=0.494,95%CI:0.268~0.913,P<0.05).Conclusions The frequen-cy of rs13333226 G allele was higher in CKD patients .The onset age of CKD patients with rs 13333226 A was significantly earlier.The SNP of rs13333226 was the independent risk factor for the the age-onset of CKD.

关键词

UMOD基因,单核苷酸多态性/慢性肾脏病,发病年龄

Key words

UMOD/singlenueleotide polymorphism/chronic kidney disease/age of onset

分类

医药卫生

引用本文复制引用

白亚玲,徐金升,张文博,张胜雷,张俊霞,崔立文..UMOD 基因启动子区单核苷酸多态性与 CKD 患者发病年龄的关系[J].山东医药,2014,(46):5-7,3.

基金项目

河北省自然科学基金资助项目( H2012206157)。 ()

山东医药

OA北大核心CSTPCD

1002-266X

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