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Upstream Stimulatory Factor 1 基因的 rs3737787 多态性与尼日利亚人群的血脂表型相关。

Polymorphism rs3737787 of Upstream Stimulatory Factor 1 gene is associated with serum lipid phenotype in Nigerian population.

机构信息

Department of Biochemistry, Faculty of Basic Medical Sciences, University of Lagos, Nigeria.

Department of Biochemistry, Faculty of Basic Medical Sciences, University of Lagos, Nigeria.

出版信息

Mol Cell Probes. 2021 Feb;55:101687. doi: 10.1016/j.mcp.2020.101687. Epub 2020 Dec 8.

Abstract

Serum lipid profile which is determined by genotype-phenotype relationship plays a significant role in the development of cardiovascular disease. Upstream stimulatory factor 1 (USF1), has been reported to be associated with serum lipid levels in different population, hence, this study investigated the association of variants in USF1 with serum lipid profile in adults in Lagos state, Nigeria. We genotyped rs3737787 (11235C > T) and rs550376620 (10488G > A) with PCR-RFLP in 384 participants and we used logistic regression to assess the association of these variants with serum lipid levels. The minor allele frequency observed in 10488G > A in both case and control groups was 5% while the minor allele of 11235C > T was observed to be more frequent in the control when compared to the dyslipidemic subjects (24% vs 12%; p = 1.84e-05). Levels of total cholesterol, triglycerides, and LDL-c in dyslipidemic subjects with CC genotype of 11235C > T were significantly higher compared to CT and TT genotypes (p < 0.001; p < 0.0001 and p < 0.0001 respectively). Logistic regression with adjustment for age, gender and BMI, showed that the minor allele carriers of 11235C > T have a reduced risk of dyslipidemia (Odds ratio: 0. 0.043, 95% confidence interval (CI): (0.006-0.331, p = 0.002). Our findings revealed that rs3737787 is associated with lipid phenotype in Nigerian population.

摘要

血清脂质谱由基因型-表型关系决定,在心血管疾病的发展中起着重要作用。上游刺激因子 1(USF1)已被报道与不同人群的血清脂质水平相关,因此,本研究调查了尼日利亚拉各斯州成年人中 USF1 变异与血清脂质谱的关联。我们使用 PCR-RFLP 技术对 384 名参与者进行了 rs3737787(11235C>T)和 rs550376620(10488G>A)的基因分型,并使用逻辑回归评估了这些变异与血清脂质水平的关联。在病例组和对照组中,10488G>A 的次要等位基因频率均为 5%,而 11235C>T 的次要等位基因在对照组中比血脂异常组更为常见(24%比 12%;p=1.84e-05)。与 CT 和 TT 基因型相比,携带 11235C>T 的 CC 基因型的血脂异常患者的总胆固醇、甘油三酯和 LDL-c 水平显著升高(p<0.001;p<0.0001 和 p<0.0001 分别)。在调整年龄、性别和 BMI 后进行的逻辑回归显示,11235C>T 的次要等位基因携带者患血脂异常的风险降低(比值比:0.043,95%置信区间(CI):(0.006-0.331,p=0.002)。我们的研究结果表明,rs3737787 与尼日利亚人群的脂质表型有关。

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