Literature DB >> 20029176

The Association of African Ancestry and elevated creatinine in the Coronary Artery Risk Development in Young Adults (CARDIA) Study.

Carmen A Peralta1, Neil Risch, Feng Lin, Michael G Shlipak, Alex Reiner, Elad Ziv, Hua Tang, David Siscovick, Kirsten Bibbins-Domingo.   

Abstract

Whether genetic factors account for differences in early kidney disease among blacks in a young healthy population is not well known. We evaluated the association of self-reported race and genetic African ancestry with elevated creatinine (> or =1.3 mg/dl for men, > or =1.1 mg/dl for women) among 3,113 black and white participants in the Coronary Artery Risk Development in Young Adults (CARDIA) study, ages 38-50 years. We estimated individual African ancestry using 42 ancestry informative markers. Blacks were more likely to have elevated creatinine than whites, and this effect was more pronounced in men: adjusted odds ratio (AOR) for black versus white men = 7.03, 4.15-11.91; AOR for women = 2.40, 1.15-5.02. Higher African ancestry was independently associated with elevated creatinine among black men (AOR = 1.53,1.08-2.16 per SD increase in African ancestry), but not women. A graded increase in odds of elevated creatinine by African Ancestry was observed among black men compared with white men: AOR = 4.27 (2.26-10.06) for black men with 40-70% African ancestry; AOR = 8.09 (4.19-15.61) for black men with 70-80% African ancestry; AOR = 9.05 (4.81-17.02) for black men with >80% African ancestry. Genetic factors common to African ancestry may be associated with increased risk of early kidney dysfunction in a young, healthy population, particularly among black men. 2009 S. Karger AG, Basel.

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Year:  2009        PMID: 20029176      PMCID: PMC3487144          DOI: 10.1159/000268955

Source DB:  PubMed          Journal:  Am J Nephrol        ISSN: 0250-8095            Impact factor:   3.754


  39 in total

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2.  Mice with disrupted BK channel beta1 subunit gene feature abnormal Ca(2+) spark/STOC coupling and elevated blood pressure.

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3.  Informativeness of genetic markers for inference of ancestry.

Authors:  Noah A Rosenberg; Lei M Li; Ryk Ward; Jonathan K Pritchard
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Review 4.  Human population structure and genetic association studies.

Authors:  Elad Ziv; Esteban González Burchard
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5.  Inference of population structure using multilocus genotype data: linked loci and correlated allele frequencies.

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6.  Genetic structure of human populations.

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7.  Genomewide linkage analysis to serum creatinine, GFR, and creatinine clearance in a community-based population: the Framingham Heart Study.

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Journal:  Hum Genet       Date:  2003-02-11       Impact factor: 4.132

9.  Racial differences in early-onset renal disease among young adults: the coronary artery risk development in young adults (CARDIA) study.

Authors:  Catherine O Stehman-Breen; Daniel Gillen; Michael Steffes; David R Jacobs; Cora E Lewis; Catarina I Kiefe; David Siscovick
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10.  Racial differences in the progression from chronic renal insufficiency to end-stage renal disease in the United States.

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Journal:  J Am Soc Nephrol       Date:  2003-11       Impact factor: 10.121

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4.  The FDA Metformin Label Change and Racial and Sex Disparities in Metformin Prescription among Patients with CKD.

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Review 5.  Addressing the global burden of chronic kidney disease through clinical and translational research.

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6.  Effect of Genetic African Ancestry on eGFR and Kidney Disease.

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7.  Human genetics. The genetics of Mexico recapitulates Native American substructure and affects biomedical traits.

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8.  An ancestry-based approach for detecting interactions.

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9.  Racial and Ethnic Disparities in Graft and Recipient Survival in Elderly Kidney Transplant Recipients.

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10.  Separate and Unequal: Race-Based Algorithms and Implications for Nephrology.

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