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The susceptibility of SERPINE1 rs1799889 SNP in diabetic vascular complications: a meta-analysis of fifty-one case-control studies
被引:2
作者:
Chen, JingYi
[1
,2
]
Zhai, ChuanNan
[3
]
Wang, ZhiQian
[4
]
Li, Rui
[5
]
Wu, WenJing
[2
]
Hou, Kai
[3
]
Alzogool, Mohammad
[1
,2
]
Wang, Yan
[1
,2
]
Cong, HongLiang
[3
]
机构:
[1] NanKai Univ, Sch Med, Weijin Rd 94, Tianjin 300071, Peoples R China
[2] Tianjin Eye Hosp, Tianjin Eye Inst, Tianjin Key Lab Ophthalmol & Visual Sci, Gansu Rd 4, Tianjin 300020, Peoples R China
[3] Tianjin Chest Hosp, Dept Cardiol, Taierzhuang South Rd 291, Tianjin 300350, Peoples R China
[4] 4th Peoples Hosp Shenyang, Shenyang Eye Inst, Dept Optometry, 20 Huanghe South Ave, Shenyang 110031, Liaoning, Peoples R China
[5] Tianjin GongAn Hosp, Nanjing Rd 78, Tianjin 300042, Peoples R China
基金:
中国国家自然科学基金;
关键词:
SERPINE1;
rs1799889;
4G;
5G polymorphism;
Plasminogen activator inhibitor 1;
Diabetes;
Diabetic vascular disease;
PLASMINOGEN-ACTIVATOR INHIBITOR-1;
ANGIOTENSIN-CONVERTING ENZYME;
4G/5G POLYMORPHISM;
GENE POLYMORPHISMS;
PAI-1;
GENE;
PROMOTER POLYMORPHISM;
RISK;
ASSOCIATION;
INSULIN;
TYPE-1;
D O I:
10.1186/s12902-021-00837-z
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Background The serine protease inhibitor-1 (SERPINE1) rs1799889 single nucleotide polymorphism (SNP) has been constantly associated with diabetes mellitus (DM) and its vascular complications. The aim of this meta-analysis was to evaluate this association with combined evidences. Methods The systematic search was performed for studies published up to March 2021 which assess the associations between SERPINE1 rs1799889 SNP and the risks of DM, diabetic retinopathy (DR), diabetic cardiovascular disease (CVD) and diabetic nephropathy (DN). Only case-control studies were identified, and the linkage between SERPINE1 rs1799889 polymorphism and diabetic vascular risks were evaluated using genetic models. Results 51 comparisons were enrolled. The results revealed a significant association with diabetes risk in overall population (allelic: OR = 1.34, 95 % CI = 1.14-1.57, homozygous: OR = 1.66, 95 % CI = 1.23-2.14, heterozygous: OR = 1.35, 95 % CI = 1.08-1.69, dominant: OR = 1.49, 95 % CI = 1.18-1.88, recessive: OR = 1.30, 95 % CI = 1.06-1.59) as well as in Asian descents (allelic: OR = 1.45, 95 % CI = 1.16-1.82, homozygous: OR = 1.88, 95 % CI = 1.29-2.75, heterozygous: OR = 1.47, 95 % CI = 1.08-2.00, dominant: OR = 1.64, 95 % CI = 1.21-2.24, recessive: OR = 1.46, 95 % CI = 1.09-1.96). A significant association was observed with DR risk (homozygous: OR = 1.25, 95 % CI = 1.01-1.56, recessive: OR = 1.20, 95 % CI = 1.01-1.43) for overall population, as for the European subgroup (homozygous: OR = 1.32, 95 % CI = 1.02-1.72, recessive: OR = 1.38, 95 % CI = 1.11-1.71). A significant association were shown with DN risk for overall population (allelic: OR = 1.48, 95 % CI = 1.15-1.90, homozygous: OR = 1.92, 95 % CI = 1.26-2.95, dominant: OR = 1.41, 95 % CI = 1.01-1.97, recessive: OR = 1.78, 95 % CI = 1.27-2.51) and for Asian subgroup (allelic: OR = 1.70, 95 % CI = 1.17-2.47, homozygous: OR = 2.46, 95 % CI = 1.30-4.66, recessive: OR = 2.24, 95 % CI = 1.40-3.59) after ethnicity stratification. No obvious association was implied with overall diabetic CVD risk in any genetic models, or after ethnicity stratification. Conclusions SERPINE1 rs1799889 4G polymorphism may outstand for serving as a genetic synergistic factor in overall DM and DN populations, positively for individuals with Asian descent. The association of SERPINE1 rs1799889 SNP and DR or diabetic CVD risks was not revealed.
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页数:18
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