Literature DB >> 20466664

Association of polymorphisms in the klotho gene with severity of non-diabetic ESRD in African Americans.

Meredith A Bostrom1, Pamela J Hicks, Lingyi Lu, Carl D Langefeld, Barry I Freedman, Donald W Bowden.   

Abstract

BACKGROUND: Non-diabetic forms of nephropathy commonly lead to end-stage renal disease (non-DM ESRD). Previous studies have demonstrated that African Americans are more susceptible to non-DM ESRD compared to other ethnic groups, and this risk has a strong genetic component. A genome-wide scan for ESRD in African American families enriched for non-DM ESRD showed evidence for linkage in chromosome 13q33.3, and a candidate gene in this region, klotho, was selected for a detailed analysis in a follow-up case-control association study.
METHODS: Thirty-four single-nucleotide polymorphisms (SNPs) in the klotho gene were genotyped in 317 unrelated African American non-DM ESRD cases and 354 non-nephropathy controls, including 12 SNPs identified by re-sequencing a region around exon 4.
RESULTS: Two SNPs demonstrated modest admixture-adjusted evidence of association with non-DM ESRD, rs650439 (P = 0.013, recessive model) and rs643780 (P = 0.017, recessive model), while rs17643698 approached significance (P = 0.0953, two degrees of freedom test). Eight of the most significant SNPs were tested for replication in a second case-control collection (557 African American non-DM ESRD cases and 187 controls), and there was no evidence of association in replicate cases and controls; nor when the samples were combined for a total of 874 non-DM cases and 541 controls. Cox proportional hazards models were computed to test for association between polymorphisms in klotho and age at onset of ESRD. A three-SNP haplotype, rs526906, rs525014 and rs571118 (T/T/A), was associated with age of onset of ESRD [P = 0.007, recessive model; hazard ratio (HR) = 0.70]. Subjects homozygous for this haplotype had a mean 4 years later onset of ESRD, suggesting a slower disease progression. HapMap subjects homozygous for this haplotype had increased expression of klotho, further supporting a protective role of this variant in ESRD.
CONCLUSION: We conclude that three SNPs in intron 1 of the klotho gene are associated with delayed age at onset of non-DM ESRD in African Americans.

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Year:  2010        PMID: 20466664      PMCID: PMC2948839          DOI: 10.1093/ndt/gfq214

Source DB:  PubMed          Journal:  Nephrol Dial Transplant        ISSN: 0931-0509            Impact factor:   5.992


  27 in total

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2.  Association of polymorphisms of the androgen receptor and klotho genes with bone mineral density in Japanese women.

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Review 3.  Klotho in chronic kidney disease--what's new?

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4.  Severely reduced production of klotho in human chronic renal failure kidney.

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5.  Identification of podocin (NPHS2) gene mutations in African Americans with nondiabetic end-stage renal disease.

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9.  Polymorphisms in the non-muscle myosin heavy chain 9 gene (MYH9) are strongly associated with end-stage renal disease historically attributed to hypertension in African Americans.

Authors:  Barry I Freedman; Pamela J Hicks; Meredith A Bostrom; Mary E Cunningham; Yongmei Liu; Jasmin Divers; Jeffrey B Kopp; Cheryl A Winkler; George W Nelson; Carl D Langefeld; Donald W Bowden
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Journal:  Lancet Neurol       Date:  2007-05       Impact factor: 44.182

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1.  Lack of association of Klotho gene variants with valvular and vascular calcification in Caucasians: a candidate gene study of the Framingham Offspring Cohort.

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Journal:  Nephrol Dial Transplant       Date:  2011-05-12       Impact factor: 5.992

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6.  Influence of Klotho gene polymorphisms on vascular gene expression and its relationship to cardiovascular disease.

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