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Association of methylenetetrahydrofolate reductase (MTHFR) rs1801133 (677C>T) gene polymorphism with ischemic stroke risk in different populations: An updated meta-analysis
被引:12
作者:
Zhao, Lili
[1
]
Li, Tao
[1
]
Dang, Meijuan
[1
]
Li, Ye
[1
]
Fan, Hong
[1
]
Hao, Qian
[2
]
Song, Dingli
[3
]
Lu, Jialiang
[1
]
Lu, Ziwei
[1
]
Jian, Yating
[1
]
Wang, Heying
[1
]
Wang, Xiaoya
[1
]
Wu, Yulun
[1
]
Zhang, Guilian
[1
]
机构:
[1] Xi An Jiao Tong Univ, Dept Neurol, Affiliated Hosp 2, Xian, Peoples R China
[2] Xi An Jiao Tong Univ, Dept Oncol, Affiliated Hosp 2, Xian, Peoples R China
[3] Xi An Jiao Tong Univ, Dept Thorac Surg, Affiliated Hosp 1, Xian, Peoples R China
基金:
中国国家自然科学基金;
关键词:
polymorphism;
ischemic stroke;
meta-analysis;
risk;
MTHFR rs1801133 (677C > T);
FACTOR-V-LEIDEN;
C677T POLYMORPHISM;
5,10-METHYLENETETRAHYDROFOLATE REDUCTASE;
HOMOCYSTEINE LEVELS;
HEMORRHAGIC STROKE;
PUBLICATION BIAS;
T-ALLELE;
MUTATIONS;
YOUNG;
DISEASE;
D O I:
10.3389/fgene.2022.1021423
中图分类号:
Q3 [遗传学];
学科分类号:
071007 ;
090102 ;
摘要:
Background: Recently, increasing evidence has implicated methylenetetrahydrofolate reductase (MTHFR) gene mutation as a risk factor for ischemic stroke (IS) in the general population. However, studies have been inconclusive and lack evidence on specific populations. We aim to determine whether the rs1801133 (NC_000001.11 (MTHFR):g. 677C > T (p.Ala222Val) variant, we termed as MTHFR rs1801133 (677 C > T), is linked to an increased risk of IS in different age groups and ancestry groups.Methods: The literature relevant to our study was found by searching the PubMed, Cochrane Library, Web of Science, EMBASE, and CNKI databases. A random effect model analysis was used to calculate the pooled odds ratio (OR) and 95% confidence interval (CI) to evaluate any possible association. We conducted a subgroup analysis based on the age and ancestry groups of the included populations.Results: As of March 2022, 1,925 citations had been identified in electronic databases, of which 96 studies involving 34,814 subjects met our eligibility criteria. A strong link was found between IS and the MTHFR gene rs1801133 (677C > T) polymorphism in all genetic models [dominant genetic model (OR = 1.47; 95%CI = 1.33-1.61; p < 0.001), recessive genetic model (OR = 1.52; 95%CI = 1.36-1.71; p < 0.001), heterozygous model (OR = 1.36; 95%CI = 1.24-1.48; p < 0.001), homozygous model (OR = 1.82; 95%CI = 1.58-2.11; p < 0.001), and T allelic genetic model (OR = 1.37; 95%CI = 1.27-1.48; p < 0.001)]. Further subgroup analyses indicated that the MTHFR rs1801133 (677C > T) variant may increase the risk of IS in Asian, Hispanic, or Latin population, middle-aged, and elderly populations (p < 0.001).Conclusion: Our results implied that mutation of the T allele of MTHFR rs1801133 (677C > T) could be a risk factor for IS. A significant association was found among Asian, Hispanic, or Latin population, middle-aged, and elderly people.
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