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血管紧张素转换酶2基因G8790A多态性:与2型糖尿病合并脑卒中之关联

The ACE2 G8790A Polymorphism: Involvement in Type 2 Diabetes Mellitus Combined with Cerebral Stroke.

作者信息

Wu Yan-Hui, Li Jia-Ying, Wang Chi, Zhang Li-Mei, Qiao Hong

机构信息

Department of Endocrinology, The Second Affiliated Hospital of Harbin Medical University, Harbin, China.

出版信息

J Clin Lab Anal. 2017 Mar;31(2). doi: 10.1002/jcla.22033. Epub 2016 Aug 8.

Abstract

BACKGROUND

We aimed to investigate the correlations between ACE2 polymorphisms and type 2 diabetes mellitus (T2DM) combined with cerebral stroke (CS).

METHODS

A total of 346 patients treated or hospitalized in our hospital were enrolled, including 181 cases without cerebrovascular complications (T2DM group) and 165 cases combined with CS (T2DM + CS group); 284 healthy individuals were selected as the control group. PCR-RFLP and ELISA were used to analyze ACE2 G8790A polymorphisms and serum ACE2 levels, respectively.

RESULTS

Significant differences were observed in the genotype/allele frequency of ACE2 G8790A between the T2DM + CS and control groups, and the T2DM and T2DM + CS groups, and in the genotype frequency of ACE2 G8790A between the T2DM and the control groups. The A allele may increase the risk of T2DM combined with CS. The AA genotype may also increase the risk of T2DM combined with CS (OR = 3.733, 95%CI = 2.069-6.738; OR = 3.597, 95%CI = 1.884-6.867). Serum ACE2 levels showed statistically significant differences among the groups. Systolic pressure and diastolic pressure were protective factors of T2DM combined with CS.

CONCLUSION

The ACE2 G8790A polymorphism in T2DM patients was correlated with CS, and the A allele might be a risk factor of T2DM combined with CS.

摘要

背景

我们旨在研究血管紧张素转换酶2(ACE2)基因多态性与2型糖尿病(T2DM)合并脑卒(CS)之间的相关性。

方法

共纳入我院治疗或住院的346例患者,其中无脑血管并发症的181例(T2DM组),合并CS的165例(T2DM + CS组);选取284例健康个体作为对照组。分别采用聚合酶链反应-限制性片段长度多态性分析(PCR-RFLP)和酶联免疫吸附测定(ELISA)检测ACE2 G8790A基因多态性和血清ACE2水平。

结果

T2DM + CS组与对照组、T2DM组与T2DM + CS组之间ACE2 G8790A的基因型/等位基因频率存在显著差异,T2DM组与对照组之间ACE2 G8790A的基因型频率存在显著差异。A等位基因可能增加T2DM合并CS的风险。AA基因型也可能增加T2DM合并CS的风险(比值比[OR] = 3.733,95%置信区间[CI] = 2.069 - 6.738;OR = 3.597,95%CI = 1.884 - 6.867)。各组血清ACE2水平差异有统计学意义。收缩压和舒张压是T2DM合并CS的保护因素。

结论

T2DM患者的ACE2 G8790A基因多态性与CS相关,A等位基因可能是T2DM合并CS的危险因素。

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