Cheema Amanpreet K, Li Tan, Liuzzi Juan P, Zarini Gustavo G, Dorak Mehmet T, Huffman Fatma G
Department of Dietetics and Nutrition, Robert Stempel College of Public Health, Florida International University, 11200 SW 8th Street, Miami, FL 33199, USA.
Department of Biostatistics, Robert Stempel College of Public Health, Florida International University, 11200 SW 8th Street, Miami, FL 33199, USA.
J Diabetes Res. 2015;2015:921274. doi: 10.1155/2015/921274. Epub 2015 Apr 21.
The aim of this study was to assess the differences in correlation of PPARGC1A polymorphisms with type 2 diabetes (T2D) risk in adults of African origins: African Americans and Haitian Americans. The case-control study consisted of >30 years old, self-identified Haitian Americans (n = 110 cases and n = 116 controls) and African Americans (n = 124 cases and n = 122 controls) living in South Florida with and without T2D. Adjusted logistic regression indicated that both SNP rs7656250 (OR = 0.22, P = 0.005) and rs4235308 (OR = 0.42, P = 0.026) showed protective association with T2D in Haitian Americans. In African Americans, however, rs4235308 showed significant risk association with T2D (OR = 2.53, P = 0.028). After stratification with sex, in Haitian Americans, both rs4235308 (OR = 0.38, P = 0.026) and rs7656250 (OR = 0.23, P = 0.006) showed protective association with T2D in females whereas in African American males rs7656250 had statistically significant protective effect on T2D (OR = 0.37, P = 0.043). The trends observed for genetic association of PPARGC1A SNPs, rs4235308, and rs7656250 for T2D between Haitian Americans and African Americans point out differences in Black race and warrant replicative study with larger sample size.
本研究的目的是评估过氧化物酶体增殖物激活受体γ共激活因子1α(PPARGC1A)基因多态性与非洲裔成年人2型糖尿病(T2D)风险之间的相关性差异,这些非洲裔成年人包括非裔美国人和海地裔美国人。这项病例对照研究纳入了居住在南佛罗里达州、年龄大于30岁、自我认定为海地裔美国人(110例病例和116例对照)以及非裔美国人(124例病例和122例对照),他们患有或未患有T2D。调整后的逻辑回归分析表明,单核苷酸多态性(SNP)rs7656250(比值比[OR]=0.22,P=0.005)和rs4235308(OR=0.42,P=0.026)在海地裔美国人中均显示出与T2D的保护性关联。然而,在非裔美国人中,rs4235308显示出与T2D的显著风险关联(OR=2.53,P=0.028)。按性别分层后,在海地裔美国人中,rs4235308(OR=0.38,P=0.026)和rs7656250(OR=0.23,P=0.006)在女性中均显示出与T2D的保护性关联,而在非裔美国男性中,rs7656250对T2D具有统计学显著的保护作用(OR=0.37,P=0.043)。在海地裔美国人和非裔美国人中观察到的PPARGC1A基因SNP rs4235308和rs7656250与T2D的遗传关联趋势指出了黑人种族之间的差异,需要进行更大样本量的重复研究。