Department of Biochemistry, Wake Forest University School of Medicine, Winston-Salem, NC 27157-1053, USA.
Hum Genet. 2010 Aug;128(2):195-204. doi: 10.1007/s00439-010-0842-3. Epub 2010 Jun 8.
African Americans have increased susceptibility to non-diabetic (non-DM) forms of end-stage renal disease (ESRD) and extensive evidence supports a genetic contribution. A genome-wide association study (GWAS) using pooled DNA was performed in 1,000 African Americans to detect associated genes. DNA from 500 non-DM ESRD cases and 500 non-nephropathy controls was quantified using gel electrophoresis and spectrophotometric analysis and pools of 50 case and 50 control DNA samples were created. DNA pools were genotyped in duplicate on the Illumina HumanHap550-Duo BeadChip. Normalization methods were developed and applied to array intensity values to reduce inter-array variance. Allele frequencies were calculated from normalized channel intensities and compared between case and control pools. Three SNPs had p values of <1.0E-6: rs4462445 (ch 13), rs4821469 (ch 22) and rs8077346 (ch 17). After normalization, top scoring SNPs (n = 65) were genotyped individually in 464 of the original cases and 478 of the controls, with replication in 336 non-DM ESRD cases and 363 non-nephropathy controls. Sixteen SNPs were associated with non-DM ESRD (p < 7.7E-4, Bonferroni corrected). Twelve of these SNPs are in or near the MYH9 gene. The four non-MYH9 SNPs that were associated with non-DM ESRD in the pooled samples were not associated in the replication set. Five SNPs that were modestly associated in the pooled samples were more strongly associated in the replication and/or combined samples. This is the first GWAS for non-DM ESRD in African Americans using pooled DNA. We demonstrate strong association between non-DM ESRD in African Americans with MYH9, and have identified additional candidate loci.
非裔美国人易患非糖尿病(非 DM)终末期肾病(ESRD),大量证据支持遗传因素的作用。本研究采用汇集 DNA 的全基因组关联研究(GWAS),在 1000 名非裔美国人中检测相关基因。采用凝胶电泳和分光光度分析对 500 例非 DM ESRD 病例和 500 例非肾病对照的 DNA 进行定量,并创建 50 例病例和 50 例对照 DNA 样本池。将 DNA 池在 Illumina HumanHap550-Duo BeadChip 上进行双重基因分型。开发并应用了标准化方法来降低数组间的变异性。从归一化通道强度中计算等位基因频率,并比较病例和对照池之间的等位基因频率。三个 SNP 的 p 值均<1.0E-6:rs4462445(ch 13)、rs4821469(ch 22)和 rs8077346(ch 17)。归一化后,对 65 个得分最高的 SNP 进行个体基因分型,在最初的 464 例病例和 478 例对照中进行了验证,并在 336 例非 DM ESRD 病例和 363 例非肾病对照中进行了复制。有 16 个 SNP 与非 DM ESRD 相关(p<7.7E-4,Bonferroni 校正)。其中 12 个 SNP 位于或靠近 MYH9 基因。在汇集样本中与非 DM ESRD 相关的四个非 MYH9 SNP 在复制集不相关。在汇集样本中中度相关的五个 SNP 在复制和/或合并样本中相关性更强。这是第一项使用汇集 DNA 对非裔美国人非 DM ESRD 的 GWAS。我们证明了非裔美国人非 DM ESRD 与 MYH9 之间的强烈关联,并确定了其他候选基因座。