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2型糖尿病视网膜病变中基质金属蛋白酶-2(MMP-2)基因多态性

MMP-2 gene polymorphisms in type 2 diabetes mellitus diabetic retinopathy.

作者信息

Yang Jie, Fan Xiao-Hui, Guan Yong-Qing, Li Yan, Sun Wei, Yang Xin-Zhi, Liu Rui

机构信息

Department of Ophthalmology, the Fourth Hospital of Hebei Medical University, Shijiazhuang 050011, Hebei Province, China.

出版信息

Int J Ophthalmol. 2010;3(2):137-40. doi: 10.3980/j.issn.2222-3959.2010.02.10. Epub 2010 Jun 18.

Abstract

AIM

To study the association between polymorphisms of the MMP-2 gene and diabetic retinopathy (DR).

METHODS

MMP-2 C-1306T and C-735T SNPs was genotyped by polymerase chain reaction-restrictive fragment length polymorphism (PCR-RFLP) analysis in 151 DR patients and 150 healthy individuals served as control.

RESULTS

There is no significant difference between the patient and control groups in allele or genotype distributions of MMP-2 C-735T (P=0.263 and P=0.248). Also, there is no significant difference between the patient and control in allele of MMP-2 C-1306T (P=0.03). However the result has significant deviation of C/C, C/T, T/T genotypic frequencies between the patient and control groups in MMP-2 C-1306T (P=0.008). We found that subjects with the MMP-2 C-1306T genotype had an overall 2-fold increase in the risk of developing DR [adjusted odds ratio (OR)=2.446; 95% confidence interval (CI)=1.239-4.829] compared with those with the T-1306T or C-1306T genotype. Stratification analysis showed that the MMP-2 -1306C/T and -735C/T SNPs are not associated with the development of NPDR to PDR of DR in North Chinese Han population.

CONCLUSION

MMP-2 C-1306T genotypes may be associated with DR development in the Chinese population. However, there is no relationship between the MMP-2 C-735T genotypes with the development of DR.

摘要

目的

研究基质金属蛋白酶-2(MMP-2)基因多态性与糖尿病视网膜病变(DR)之间的关联。

方法

采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)分析法对151例DR患者和150例健康对照者进行MMP-2 C-1306T和C-735T单核苷酸多态性(SNP)基因分型。

结果

MMP-2 C-735T的等位基因或基因型分布在患者组和对照组之间无显著差异(P=0.263和P=0.248)。此外,MMP-2 C-1306T的等位基因在患者组和对照组之间也无显著差异(P=0.03)。然而,MMP-2 C-1306T的C/C、C/T、T/T基因型频率在患者组和对照组之间存在显著差异(P=0.008)。我们发现,与T-1306T或C-1306T基因型者相比,MMP-2 C-1306T基因型者发生DR的风险总体增加了2倍[校正优势比(OR)=2.446;95%置信区间(CI)=1.239-4.829]。分层分析表明,在中国北方汉族人群中,MMP-2 -1306C/T和-735C/T SNP与DR从非增殖性糖尿病视网膜病变(NPDR)发展为增殖性糖尿病视网膜病变(PDR)无关。

结论

MMP-2 C-1306T基因型可能与中国人群DR的发生有关。然而,MMP-2 C-735T基因型与DR的发生无关。

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