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      Association of ABCB1 genetic variants with renal function in Africans and in Caucasians

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          Abstract

          Background

          The P-glycoprotein, encoded by the ABCB1 gene, is expressed in human endothelial and mesangial cells, which contribute to control renal plasma flow and glomerular filtration rate. We investigated the association of ABCB1 variants with renal function in African and Caucasian subjects.

          Methods

          In Africans (290 subjects from 62 pedigrees), we genotyped the 2677G>T and 3435 C>T ABCB1 polymorphisms. Glomerular filtration rate (GFR) was measured using inulin clearance and effective renal plasma flow (ERPF) using para-aminohippurate clearance. In Caucasians (5382 unrelated subjects), we analyzed 30 SNPs located within and around ABCB1, using data from the Affymetrix 500 K chip. GFR was estimated using the simplified Modification of the Diet in Renal Disease (MDRD) and Cockcroft-Gault equations.

          Results

          In Africans, compared to the reference genotype (GG or CC), each copy of the 2677T and 3435T allele was associated, respectively, with: GFR higher by 10.6 ± 2.9 ( P < 0.001) and 4.4 ± 2.3 ( P = 0.06) mL/min; ERPF higher by 47.5 ± 11.6 ( P < 0.001) and 28.1 ± 10.5 ( P = 0.007) mL/min; and renal resistances lower by 0.016 ± 0.004 ( P < 0.001) and 0.011 ± 0.004 ( P = 0.004) mm Hg/mL/min. In Caucasians, we identified 3 polymorphisms in the ABCB1 gene that were strongly associated with all estimates of GFR (smallest P value = 0.0006, overall P = 0.014 after multiple testing correction).

          Conclusion

          Variants of the ABCB1 gene were associated with renal function in both Africans and Caucasians and may therefore confer susceptibility to nephropathy in humans. If confirmed in other studies, these results point toward a new candidate gene for nephropathy in humans.

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          Most cited references33

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          Prediction of creatinine clearance from serum creatinine.

          A formula has been developed to predict creatinine clearance (Ccr) from serum creatinine (Scr) in adult males: (see article)(15% less in females). Derivation included the relationship found between age and 24-hour creatinine excretion/kg in 249 patients aged 18-92. Values for Ccr were predicted by this formula and four other methods and the results compared with the means of two 24-hour Ccr's measured in 236 patients. The above formula gave a correlation coefficient between predicted and mean measured Ccr's of 0.83; on average, the difference predicted and mean measured values was no greater than that between paired clearances. Factors for age and body weight must be included for reasonable prediction.
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            Functional polymorphisms of the human multidrug-resistance gene: multiple sequence variations and correlation of one allele with P-glycoprotein expression and activity in vivo.

            To evaluate whether alterations in the multidrug-resistance (MDR)-1 gene correlate with intestinal MDR-1 expression and uptake of orally administered P-glycoprotein (PGP) substrates, we analyzed the MDR-1 sequence in 21 volunteers whose PGP expression and function in the duodenum had been determined by Western blots and quantitative immunohistology (n = 21) or by plasma concentrations after orally administered digoxin (n = 8 + 14). We observed a significant correlation of a polymorphism in exon 26 (C3435T) of MDR-1 with expression levels and function of MDR-1. Individuals homozygous for this polymorphism had significantly lower duodenal MDR-1 expression and the highest digoxin plasma levels. Homozygosity for this variant was observed in 24% of our sample population (n = 188). This polymorphism is expected to affect the absorption and tissue concentrations of numerous other substrates of MDR-1.
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              Cellular localization of the multidrug-resistance gene product P-glycoprotein in normal human tissues.

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                Author and article information

                Journal
                BMC Med Genomics
                BMC Medical Genomics
                BioMed Central
                1755-8794
                2008
                2 June 2008
                : 1
                : 21
                Affiliations
                [1 ]University Institute of Social and Preventive Medicine (IUMSP), Centre Hospitalier Universitaire Vaudois and University of Lausanne, Bugnon 17, Lausanne, Switzerland
                [2 ]Unit of Biochemistry and Clinical Psychopharmacology, Center for Psychiatric Neurosciences, Department of Psychiatry, Centre Hospitalier Universitaire Vaudois and University of Lausanne Lausanne, Switzerland
                [3 ]Division of Nephrology, Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland
                [4 ]Department of Medical Genetics, University of Lausanne, Lausanne, Switzerland
                [5 ]Swiss Institute of Bioinformatics, Lausanne, Switzerland
                [6 ]Department of Medicine, Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland
                [7 ]Ministry of Health, Victoria, Seychelles
                [8 ]Department of Epidemiology and Biostatistics, Case Western Reserve University, Cleveland (OH), USA
                [9 ]Service of Medical Genetics, Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland
                [10 ]Division of Genetics, GlaxoSmithKline, Philadelphia, Pennsylvania, USA
                Article
                1755-8794-1-21
                10.1186/1755-8794-1-21
                2424071
                18518969
                0f81af16-a1f8-4d12-ac6e-1475bc50ae91
                Copyright © 2008 Bochud et al; licensee BioMed Central Ltd.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 25 February 2008
                : 2 June 2008
                Categories
                Research Article

                Genetics
                Genetics

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