The Affiliated Qingdao Municipal Hospital of Qingdao University, Qingdao, 266011, China.
Department of Gastroenterology, The Affiliated Qingdao Municipal Hospital of Qingdao University, Qingdao, 266011, China.
Lipids Health Dis. 2019 Aug 31;18(1):165. doi: 10.1186/s12944-019-1108-2.
Present evidences suggested that TRIB1 rs17321515 polymorphism was tightly associated with the increased risk of NAFLD and CHD. CHD is one of the main complications of NAFLD, whether TRIB1 rs17321515 polymorphism could affect the risk of CHD in general population and NAFLD patients in Chinese Han population was remain unknown. The present study was designed to investigate the association between TRIB1 rs17321515 polymorphism and the risk of CHD in general population and NAFLD patients in Chinese Han population, and investigate the effect of TRIB1 rs17321515 polymorphism on serum lipid levels.
TRIB1 rs17321515 gene polymorphism was genotyped using the polymerase chain reaction (PCR) in healthy controls (n = 175), CHD patients (n = 155), NAFLD patients (n = 146), and NAFLD+CHD patients (n = 156). Serum lipid profiles were determined using biochemical methods. Statistical analyses were performed using SPSS 24.0 statistical software.
The TRIB1 rs17321515 AA+GA genotypes were the significant risk factors for the CHD in general population (OR = 1.788; 95% CI: 1.104-2.897; P = 0.018) and in the NAFLD patients (OR = 1.760; 95% CI: 1.071-2.891; P = 0.026). After adjusted for age, gender, and body mass index, the risk for CHD in general population (OR = 1.857; 95% CI: 1.116-3.089; P = 0.017) and NAFLD patients was still significant (OR = 1.723; 95% CI: 1.033-2.873; P = 0.037). In addition, TRIB1 rs17321515 A carriers possess the higher lipid profiles in the included subjects.
TRIB1 rs17321515 AA+GA genotypes were significant associated with the risk of CHD in general population and in NAFLD patients in Chinese Han population. The rs17321515 A allele increases the serum lipid profiles in included subjects.
现有证据表明,TRIB1 rs17321515 多态性与非酒精性脂肪性肝病(NAFLD)和冠心病(CHD)的风险增加密切相关。CHD 是 NAFLD 的主要并发症之一,TRIB1 rs17321515 多态性是否会影响中国汉族人群的 CHD 风险尚不清楚。本研究旨在探讨 TRIB1 rs17321515 多态性与中国汉族人群普通人群和 NAFLD 患者 CHD 风险之间的关系,并探讨 TRIB1 rs17321515 多态性对血清脂质水平的影响。
采用聚合酶链反应(PCR)检测健康对照组(n=175)、CHD 患者(n=155)、NAFLD 患者(n=146)和 NAFLD+CHD 患者(n=156)中 TRIB1 rs17321515 基因多态性。采用生化方法检测血清脂质谱。统计分析采用 SPSS 24.0 统计软件。
TRIB1 rs17321515 AA+GA 基因型是普通人群(OR=1.788;95%CI:1.104-2.897;P=0.018)和 NAFLD 患者(OR=1.760;95%CI:1.071-2.891;P=0.026)发生 CHD 的显著危险因素。经年龄、性别和体重指数校正后,普通人群(OR=1.857;95%CI:1.116-3.089;P=0.017)和 NAFLD 患者的 CHD 发病风险仍显著升高(OR=1.723;95%CI:1.033-2.873;P=0.037)。此外,TRIB1 rs17321515 A 携带者在纳入的受试者中具有更高的血脂谱。
TRIB1 rs17321515 AA+GA 基因型与中国汉族人群普通人群和 NAFLD 患者的 CHD 风险显著相关。rs17321515 A 等位基因增加了纳入受试者的血清脂质谱。