A polymorphism in the leptin gene promoter is associated with anemia in patients with HIV disease.

Détails

ID Serval
serval:BIB_6382C64D159D
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
A polymorphism in the leptin gene promoter is associated with anemia in patients with HIV disease.
Périodique
Blood
Auteur⸱e⸱s
Vanasse G.J., Jeong J.Y., Tate J., Bathulapalli H., Anderson D., Steen H., Fleming M., Mattocks K., Telenti A., Fellay J., Justice A.C., Berliner N.
ISSN
1528-0020 (Electronic)
ISSN-L
0006-4971
Statut éditorial
Publié
Date de publication
2011
Volume
118
Numéro
20
Pages
5401-5408
Langue
anglais
Résumé
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.
Pubmed
Web of science
Open Access
Oui
Création de la notice
22/12/2011 11:35
Dernière modification de la notice
20/08/2019 15:20
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