Suppr超能文献

非糖尿病性终末期肾病的候选基因在非裔美国人中的全基因组关联研究:使用 pooled DNA 进行研究。

Candidate genes for non-diabetic ESRD in African Americans: a genome-wide association study using pooled DNA.

机构信息

Department of Biochemistry, Wake Forest University School of Medicine, Winston-Salem, NC 27157-1053, USA.

出版信息

Hum Genet. 2010 Aug;128(2):195-204. doi: 10.1007/s00439-010-0842-3. Epub 2010 Jun 8.

Abstract

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.

摘要

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。

相似文献

1
Candidate genes for non-diabetic ESRD in African Americans: a genome-wide association study using pooled DNA.
Hum Genet. 2010 Aug;128(2):195-204. doi: 10.1007/s00439-010-0842-3. Epub 2010 Jun 8.
2
A genome-wide association study for diabetic nephropathy genes in African Americans.
Kidney Int. 2011 Mar;79(5):563-72. doi: 10.1038/ki.2010.467. Epub 2010 Dec 8.
3
Relevance of the ACTN4 gene in African-Americans with non-diabetic end-stage renal disease.
Am J Nephrol. 2012;36(3):252-60. doi: 10.1159/000342205. Epub 2012 Sep 4.
4
Association of polymorphisms in the klotho gene with severity of non-diabetic ESRD in African Americans.
Nephrol Dial Transplant. 2010 Oct;25(10):3348-55. doi: 10.1093/ndt/gfq214. Epub 2010 Apr 22.
6
Differential effects of MYH9 and APOL1 risk variants on FRMD3 Association with Diabetic ESRD in African Americans.
PLoS Genet. 2011 Jun;7(6):e1002150. doi: 10.1371/journal.pgen.1002150. Epub 2011 Jun 16.
7
Association Analysis of the Cubilin (CUBN) and Megalin (LRP2) Genes with ESRD in African Americans.
Clin J Am Soc Nephrol. 2016 Jun 6;11(6):1034-1043. doi: 10.2215/CJN.12971215. Epub 2016 May 19.
9
Sickle cell trait is not independently associated with susceptibility to end-stage renal disease in African Americans.
Kidney Int. 2011 Dec;80(12):1339-43. doi: 10.1038/ki.2011.286. Epub 2011 Aug 17.
10
The influence of carnosinase gene polymorphisms on diabetic nephropathy risk in African-Americans.
Hum Genet. 2009 Aug;126(2):265-75. doi: 10.1007/s00439-009-0667-0. Epub 2009 Apr 17.

引用本文的文献

1
Genetic susceptibility of hypertension-induced kidney disease.
Physiol Rep. 2021 Jan;9(1):e14688. doi: 10.14814/phy2.14688.
2
Mechanisms of Injury in APOL1-associated Kidney Disease.
Transplantation. 2019 Mar;103(3):487-492. doi: 10.1097/TP.0000000000002509.
3
Genomic approaches in the search for molecular biomarkers in chronic kidney disease.
J Transl Med. 2018 Oct 25;16(1):292. doi: 10.1186/s12967-018-1664-7.
8
Genome-Wide Association of CKD Progression: The Chronic Renal Insufficiency Cohort Study.
J Am Soc Nephrol. 2017 Mar;28(3):923-934. doi: 10.1681/ASN.2015101152. Epub 2016 Oct 11.
9
Multicentric Genome-Wide Association Study for Primary Spontaneous Pneumothorax.
PLoS One. 2016 May 20;11(5):e0156103. doi: 10.1371/journal.pone.0156103. eCollection 2016.
10
Genetic Variants Underlying Risk of Intracranial Aneurysms: Insights from a GWAS in Portugal.
PLoS One. 2015 Jul 17;10(7):e0133422. doi: 10.1371/journal.pone.0133422. eCollection 2015.

本文引用的文献

5
MYH9 is a major-effect risk gene for focal segmental glomerulosclerosis.
Nat Genet. 2008 Oct;40(10):1175-84. doi: 10.1038/ng.226. Epub 2008 Sep 14.
6
MYH9 is associated with nondiabetic end-stage renal disease in African Americans.
Nat Genet. 2008 Oct;40(10):1185-92. doi: 10.1038/ng.232. Epub 2008 Sep 14.
8
Association analysis of the ephrin-B2 gene in African-Americans with end-stage renal disease.
Am J Nephrol. 2008;28(6):914-20. doi: 10.1159/000141934. Epub 2008 Jun 26.
10
A genome-wide association study in 574 schizophrenia trios using DNA pooling.
Mol Psychiatry. 2009 Aug;14(8):796-803. doi: 10.1038/mp.2008.33. Epub 2008 Mar 11.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验