Abstract | BACKGROUND: METHODS: We designed a case-control study including 516 CAD patients and 318 age- and sex-matched control subjects. Using the improved multiplex ligation detection reaction (iMLDR) method, we genotyped two SNPs (rs28765985 and rs7308390) of ACAT-2 gene in all subjects. RESULTS: We found that the genotypes, the dominant model (CC + CT vs TT) and over-dominant model (CT vs CC + TT) of rs28765985 were significantly different between CAD patients and the controls (P=0.027, P=0.012 and P=0.035, respectively). The rs28765985 C allele was associated with a significantly elevated CAD risk [CC/CT vs TT: odds ratio (OR) = 1.48, 95% confidence interval (CI) = 1.02-2.16, P=0.04] after adjustment for confounders. The TC and LDL-C levels were significantly higher in rs28765985 CC/CT genotypes than that in TT genotypes (P<0.05). CONCLUSIONS: Rs28765985 of ACAT-2 gene are associated with CAD in Uygur subjects. Subjects with CC/CT genotype or C allele of rs28765985 were associated with an increased risk of CAD.
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Authors | Yong-Tao Wang, Buamina Maitusong, Yi-Tong Ma, Zhen-Yan Fu, Yi-Ning Yang, Xiang Ma, Xiao-Mei Li, Fen Liu, Bang-Dang Chen |
Journal | Bioscience reports
(Biosci Rep)
Vol. 39
Issue 2
(02 28 2019)
ISSN: 1573-4935 [Electronic] England |
PMID | 30696703
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | © 2019 The Author(s). |
Chemical References |
- Cholesterol, LDL
- Sterol O-Acyltransferase
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Topics |
- Aged
- Case-Control Studies
- China
(ethnology)
- Cholesterol, LDL
(blood)
- Coronary Artery Disease
(blood, genetics)
- Female
- Gene Frequency
- Genetic Predisposition to Disease
- Humans
- Male
- Middle Aged
- Polymorphism, Single Nucleotide
- Sterol O-Acyltransferase
(genetics)
- Sterol O-Acyltransferase 2
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