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血小板源性生长因子D(PDGFD)基因rs7950273多态性与中国汉族人群缺血性脑卒中相关性的研究

A study on the association of rs7950273 polymorphism in the PDGFD with ischaemic stroke in the Chinese Han population.

作者信息

Han Jingjun, Li Huanlian, Wu Deqiang, Zeng Nafen, Wu Zhihua, Cai Longgan, Chen Weiqiang, Zuo Wei, Zhang Yanwei

机构信息

a Department of Thoracic and Cardiovascular Surgery , Guang Dong Medical College FuTian Hospital , Shenzhen , PR China and.

b Key Laboratory of Molecular Biology of Shenzhen, Center for Disease Control and Prevention , Shenzhen , PR China.

出版信息

Ann Hum Biol. 2016;43(1):78-80. doi: 10.3109/03014460.2015.1016552. Epub 2015 Sep 11.

Abstract

BACKGROUND

The association between the platelet-derived growth factor D (PDGFD) gene and atherosclerosis has been widely proven, whereas the relationship between the PDGFD gene and ischaemic stroke remains unconfirmed.

AIM

A case-control study was performed to further evaluate the association of the C → G mutation of rs7950273 in the PDGFD gene with ischaemic stroke (IS) in a Chinese Han population.

SUBJECTS AND METHODS

This study recruited 3033 cases and 2807 controls from general hospitals in the southern, central and northern areas of China. The MGB probe and Taqman 7900HT Sequence Detection System were applied for genotyping.

RESULTS

Genotype was not significantly associated with ischaemic stroke in total. After adjustment for gender, age, BMI, hypertension, diabetes mellitus and smoking, the CG and GG genotypes were still not associated with ischaemic stroke (p = 0.892 and p = 0.582 for CG and GG, respectively).

CONCLUSION

This study suggests that the polymorphism of rs7950273 in the PDGFD gene is not associated with ischaemic stroke in the Chinese Han population. Further studies on the gene-gene and gene-environment interactions for the PDGFD gene and ischaemic stroke are needed.

摘要

背景

血小板衍生生长因子D(PDGFD)基因与动脉粥样硬化之间的关联已得到广泛证实,而PDGFD基因与缺血性卒中之间的关系仍未得到证实。

目的

进行一项病例对照研究,以进一步评估中国汉族人群中PDGFD基因rs7950273的C→G突变与缺血性卒中(IS)的关联。

对象与方法

本研究从中国南部、中部和北部地区的综合医院招募了3033例病例和2807例对照。采用MGB探针和Taqman 7900HT序列检测系统进行基因分型。

结果

总体而言,基因型与缺血性卒中无显著关联。在调整性别、年龄、体重指数、高血压、糖尿病和吸烟因素后,CG和GG基因型仍与缺血性卒中无关联(CG和GG的p值分别为0.892和0.582)。

结论

本研究表明,PDGFD基因rs7950273的多态性与中国汉族人群的缺血性卒中无关联。需要进一步研究PDGFD基因与缺血性卒中的基因-基因和基因-环境相互作用。

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