Yang Qian, Yin Rui-Xing, Zhou Yi-Jiang, Cao Xiao-Li, Guo Tao, Chen Wu-Xian
Department of Cardiology, Institute of Cardiovascular Diseases, the First Affiliated Hospital, Guangxi Medical University, 22 Shuangyong Road, Nanning, 530021, Guangxi, People's Republic of China.
Lipids Health Dis. 2015 Jul 25;14:79. doi: 10.1186/s12944-015-0078-2.
The v-maf avian musculoaponeurotic fibrosarcoma oncogene homolog B gene (MAFB) has been associated with serum lipid levels in the Eurpean population, but little is known about such association in the Chinese population or in atherosclerosis-related patients. Therefore, the purpose of the present study was to assess the association of the single nucleotide polymorphisms (SNPs) in the MAFB and serum lipid levels and the risk of coronary artery disease (CAD) and ischemic stroke (IS) in the Chinese population.
A total of 1,065 unrelated patients (CAD, 525 and IS, 540) and 539 healthy controls were recruited in this study. Genotypes of the MAFB rs2902940 and rs6102059 SNPs were determined by the Snapshot technology platform.
The rs2902940AA genotype was associated with an increased risk of CAD (adjusted OR = 1.63, 95% CI = 1.07-2.48, P = 0.023) and IS (adjusted OR = 1.69, 95% CI = 1.09-2.61, P = 0.017). The rs2902940GA/AA genotypes were also associated with an increased risk of CAD (adjusted OR = 1.56, 95% CI = 1.04-2.32, P = 0.030 for GA/AA vs. GG) and IS (adjusted OR = 1.72, 95% CI = 1.14-2.60, P = 0.010 for GA/AA vs. GG). Significant interactions were observed only in those with higher body mass index (BMI), hypertension and diabetes (P < 0.05). The subjects with rs2902940GA/AA genotypes in controls had lower serum ApoAI levels than the subjects with GG genotype (P = 0.024).
The rs2902940A allele carriers in the MAFB conferred a decreased serum ApoAI level in controls and an increased risk of CAD and IS. The rs2902940GA/AA genotypes interacted with higher BMI, hypertension and diabetes to contribute the risk of CAD and IS.
v-maf禽肌纤维肉瘤致癌基因同源物B基因(MAFB)与欧洲人群的血脂水平有关,但在中国人群或动脉粥样硬化相关患者中,对此类关联知之甚少。因此,本研究的目的是评估中国人群中MAFB单核苷酸多态性(SNP)与血脂水平以及冠状动脉疾病(CAD)和缺血性卒中(IS)风险之间的关联。
本研究共招募了1065名无亲缘关系的患者(CAD患者525名,IS患者540名)和539名健康对照者。通过Snapshot技术平台测定MAFB rs2902940和rs6102059 SNP的基因型。
rs2902940AA基因型与CAD风险增加相关(校正OR = 1.63,95%CI = 1.07 - 2.48,P = 0.023)和IS风险增加相关(校正OR = 1.69,95%CI = 1.09 - 2.61,P = 0.017)。rs2902940GA/AA基因型也与CAD风险增加相关(校正OR = 1.56,95%CI = 1.04 - 2.32,GA/AA与GG相比P = 0.030)和IS风险增加相关(校正OR = 1.72,95%CI = 1.14 - 2.60,GA/AA与GG相比P = 0.010)。仅在体重指数(BMI)较高、患有高血压和糖尿病的人群中观察到显著的相互作用(P < 0.05)。对照组中携带rs2902940GA/AA基因型的受试者血清载脂蛋白A1(ApoAI)水平低于携带GG基因型的受试者(P = 0.024)。
MAFB中rs2902940A等位基因携带者在对照组中血清ApoAI水平降低,且CAD和IS风险增加。rs2902940GA/AA基因型与较高的BMI、高血压和糖尿病相互作用,增加了CAD和IS的风险。