Department of Anthropology, University of Toronto at Mississauga, 3359 Mississauga Road North, Mississauga, ON, Canada, L5L 1C6.
Diabetologia. 2011 Aug;54(8):2038-46. doi: 10.1007/s00125-011-2172-y. Epub 2011 May 15.
AIMS/HYPOTHESIS: We report a genome-wide association study of type 2 diabetes in an admixed sample from Mexico City and describe the results of a meta-analysis of this study and another genome-wide scan in a Mexican-American sample from Starr County, TX, USA. The top signals observed in this meta-analysis were followed up in the Diabetes Genetics Replication and Meta-analysis Consortium (DIAGRAM) and DIAGRAM+ datasets.
We analysed 967 cases and 343 normoglycaemic controls. The samples were genotyped with the Affymetrix Genome-wide Human SNP array 5.0. Associations of genotyped and imputed markers with type 2 diabetes were tested using a missing data likelihood score test. A fixed-effects meta-analysis including 1,804 cases and 780 normoglycaemic controls was carried out by weighting the effect estimates by their inverse variances.
In the meta-analysis of the two Hispanic studies, markers showing suggestive associations (p < 10(-5)) were identified in two known diabetes genes, HNF1A and KCNQ1, as well as in several additional regions. Meta-analysis of the two Hispanic studies and the recent DIAGRAM+ dataset identified genome-wide significant signals (p < 5 × 10(-8)) within or near the genes HNF1A and CDKN2A/CDKN2B, as well as suggestive associations in three additional regions, IGF2BP2, KCNQ1 and the previously unreported C14orf70.
CONCLUSIONS/INTERPRETATION: We observed numerous regions with suggestive associations with type 2 diabetes. Some of these signals correspond to regions described in previous studies. However, many of these regions could not be replicated in the DIAGRAM datasets. It is critical to carry out additional studies in Hispanic and American Indian populations, which have a high prevalence of type 2 diabetes.
目的/假设:我们报告了一项在墨西哥城混合人群中进行的 2 型糖尿病全基因组关联研究,并描述了对这项研究和另一项来自美国得克萨斯州 Starr 县墨西哥裔美国人样本的全基因组扫描的荟萃分析结果。荟萃分析中观察到的最高信号在糖尿病遗传学复制和荟萃分析联盟 (DIAGRAM) 和 DIAGRAM+ 数据集中进行了跟进。
我们分析了 967 例病例和 343 例血糖正常对照者。这些样本用 Affymetrix 全基因组人类 SNP 芯片 5.0 进行基因分型。使用缺失数据似然评分检验检测基因分型和推断标记与 2 型糖尿病的关联。通过按其逆方差加权效应估计值,对包括 1804 例病例和 780 例血糖正常对照者的两个西班牙裔研究进行固定效应荟萃分析。
在对这两项西班牙裔研究的荟萃分析中,在两个已知的糖尿病基因 HNF1A 和 KCNQ1 以及其他几个额外区域中,确定了具有提示性关联(p < 10(-5))的标记。对这两项西班牙裔研究和最近的 DIAGRAM+ 数据集的荟萃分析,在 HNF1A 和 CDKN2A/CDKN2B 基因内或附近,以及在 IGF2BP2、KCNQ1 和以前未报道的 C14orf70 三个额外区域中,确定了全基因组显著信号(p < 5×10(-8))。
结论/解释:我们观察到许多与 2 型糖尿病具有提示性关联的区域。其中一些信号与以前的研究中描述的区域相对应。然而,这些区域中的许多在 DIAGRAM 数据集中无法复制。在具有 2 型糖尿病高发率的西班牙裔和美洲印第安人群中进行额外的研究至关重要。