A polymorphism in the leptin gene promoter is associated with anemia in patients with HIV disease.
Data(s) |
2011
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Resumo |
To study factors associated with anemia and its effect on survival in HIV-infected persons treated with modern combined antiretroviral therapy (cART), we characterized the prevalence of anemia in the Veterans Aging Cohort Study (VACS) and used a candidate gene approach to identify proinflammatory gene single nucleotide polymorphisms (SNPs) associated with anemia in HIV disease. The study comprised 1597 HIV(+) and 865 HIV(-) VACS subjects with DNA, blood, and annotated clinical data available for analysis. Anemia was defined according to World Health Organization criteria (hemoglobin < 13 g/dL and < 12 g/dL in men and women, respectively). The prevalence of anemia in HIV(+) and HIV(-) subjects was 23.1% and 12.9%, respectively. Independent of HIV status, anemia was present in 23.4% and 8% in blacks and whites, respectively. Analysis of our candidate genes revealed that the leptin -2548 G/A SNP was associated with anemia in HIV(+), but not HIV(-), patients, with the AA and AG genotypes significantly predicting anemia (P < .003 and P < .039, respectively, logistic regression). This association was replicated in an independent cohort of HIV(+) women. Our study provides novel insight into the association between genetic variability in the leptin gene and anemia in HIV(+) individuals. |
Identificador |
http://serval.unil.ch/?id=serval:BIB_6382C64D159D isbn:1528-0020 (Electronic) pmid:21926355 doi:10.1182/blood-2011-06-362194 isiid:000297265400009 |
Idioma(s) |
en |
Fonte |
Blood, vol. 118, no. 20, pp. 5401-5408 |
Tipo |
info:eu-repo/semantics/article article |