Please use this identifier to cite or link to this item:
Title: Interleukin-1 beta and interleukin-6 gene polymorphisms are associated with manifestations of sickle cell anemia
Authors: Vicari, Perla [UNIFESP]
Adegoke, Samuel A. [UNIFESP]
Mazzotti, Diego Robles [UNIFESP]
Cancado, Rodolfo Delfini
Eiko Nogutti, Maria Aparecida [UNIFESP]
Figueiredo, Maria Stella [UNIFESP]
Universidade Federal de São Paulo (UNIFESP)
Fac Ciencias Med Santa Casa São Paulo
Keywords: Sickle cell anemia
Genetic polymorphism
Issue Date: 1-Mar-2015
Publisher: Elsevier B.V.
Citation: Blood Cells Molecules and Diseases. San Diego: Academic Press Inc Elsevier Science, v. 54, n. 3, p. 244-249, 2015.
Abstract: Sickle cell anemia (SCA), a disorder characterized by both acute and chronic inflammation, exhibits substantial phenotypic variability. Interleukin-1 beta (IL-1 beta) and IL-6 are important in acute and chronic diseases, and their single nucleotide polymorphisms (SNPs) have been considered as predictors of prognosis in several inflammatory conditions. This study aims at exploring possible association of IL-1 beta and IL-6 SNPs as potential genetic modifiers and or predictors of SCA clinical and laboratory phenotypes. This cross-sectional study involved 107 SCA patients and 110 age, sex and ethnicity-matched healthy individuals. the SNPs were identified by PCR-RFLP for IL-1 beta (-511C>T and + 3954C>T) and IL-6 (-597G>A and -174G>C) genes. Associations between these SNPs and the clinical and laboratory profiles of patients with SCA were then determined. Allelic and genotypic frequencies of IL-1 beta, and IL-6 SNPs between patients with SCA and controls were similar and followed HWE. IL-1 beta +3954C>T SNP was associated with increased risk of osteonecrosis, elevated pulmonary arterial pressure and lower absolute reticulocyte count, while IL-6 - 597G > A was associated with higher likelihood of retinopathy and leg ulcer. These data indicate that IL-1 beta and IL-6 gene SNPs are associated with SCA complications among Brazilian patients and may act as genetic predictors of SCA clinical heterogeneity. (C) 2014 Elsevier Inc. All rights reserved.
ISSN: 1079-9796
Other Identifiers:
Appears in Collections:Em verificação - Geral

Files in This Item:
There are no files associated with this item.

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.