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Effect of TRIB1 Variant on Lipid Profile and Coronary Artery Disease: A Systematic Review and Meta-Analysis
被引:2
|作者:
Wei, Baozhu
[1
,2
]
Liu, Yang
[3
]
Li, Hang
[4
]
Peng, Yuanyuan
[1
]
Luo, Zhi
[1
]
机构:
[1] Zhongnan Hosp Wuhan Univ, Wuhan Univ, Dept Cardiol, Wuhan, Peoples R China
[2] Wuhan Univ, Inst Myocardial Injury & Repair, Wuhan, Peoples R China
[3] China Resources & WISCO Gen Hosp, Dept Endocrinol, Wuhan, Peoples R China
[4] Zhongnan Hosp Wuhan Univ, Wuhan Univ, Dept Geratol, Wuhan, Peoples R China
关键词:
GENOME-WIDE ASSOCIATION;
DENSITY-LIPOPROTEIN CHOLESTEROL;
REGULATES HEPATIC LIPOGENESIS;
TRIGLYCERIDES;
RISK;
D O I:
10.1155/2023/4444708
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Background. Emerging evidence indicates tribbles homolog 1 (Trib1) protein may be involved in lipid metabolism regulation and coronary artery disease (CAD) pathogenesis. However, whether TRIB1 gene variants affect lipid levels and CAD remains elusive, this study is aimed at clarifying the effect of TRIB1 variants on lipid profile and CAD. Methods. By searching PubMed and Cochrane databases for studies published before December 18, 2022, a total of 108,831 individuals were included for the analysis. Results. The outcomes of the analysis on all individuals showed that the A allele carriers of rs17321515 and rs2954029 variants had higher low-density lipoprotein cholesterol (LDL-C) and total cholesterol (TC) levels than the noncarriers. Consistently, a higher CAD risk was observed in the A allele carriers. Subgroup analysis indicated that increased LDL-C, TC, and CAD risk were observed in Asian population. Conclusions. Variants of TRIB1 (i.e., rs17321515 and rs2954029) may serve as causal genetic markers for dyslipidemia and CAD in Asian population.
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页数:9
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