Evaluation of IGF-2/ApaI polymorphism in pregnant women infected with human immunodeficiency virus type 1 taking antiretroviral drugs


Autoria(s): MARCOLIN, Alessandra C.; DUARTE, Geraldo; QUINTANA, Silvana M.; ARAUJO, Francielle M.; BEITUNE, Patricia El; GONCALVES, Carla V.; RAMOS, Ester S.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

19/10/2012

19/10/2012

2009

Resumo

Objective: Studies carried Out to assess the effects of antiretroviral drugs (ARV) in HIV-1 infected pregnant women have demonstrated carbohydrate intolerance. Some reports also refer to the effect of disturbances in the expression of the insulin-like growth factor (IGF) system on pancreas beta-cell function in humans and IGF-2/ApaI polymorphisms have been associated with obesity and features of the metabolic syndromes. in the present study, we tested the association between IGF-2/ApaI genotype and hyperglycemia in HIV-1 infected pregnant women receiving ARV. Design: We studied IGF-2/ApaI polymorphism in 87 healthy pregnant women, 43 HIV-1 infected pregnant women taking ARV with hyperglycemia during pregnancy, and 43 HIV-1-negative pregnant women with gestational diabetes. Blood samples were obtained for DNA extraction, PCR and genotyping. Data were analyzed statistically by the Kolmogorov-Smirnov normality, ANOVA and chi-square tests. Results: There were no significant differences in genotype frequency among the three groups analyzed. Considering the HIV-1-infected pregnant women, there were no significant differences in genotype frequency between the zidovudine group and the triple antiretroviral treatment group. There were no significant differences in allele frequencies among the groups evaluated. Non-white pregnant women tended to present the GG genotypes compared to white pregnant women. Conclusion: These results contribute to a better understanding of metabolic glycemic disorders in HIV-1 infected pregnant women using ARV, showing that IGF-2/ApaI polymorphisms are not responsible as a single Causative factor of glycemic alterations. These data indicate that other variables should be studied in order to explain these glycemic abnormalities. (C) 2009 Elsevier Ltd. All rights reserved.

CAPES

Identificador

GROWTH HORMONE & IGF RESEARCH, v.19, n.6, p.513-516, 2009

1096-6374

http://producao.usp.br/handle/BDPI/24885

10.1016/j.ghir.2009.05.003

http://dx.doi.org/10.1016/j.ghir.2009.05.003

Idioma(s)

eng

Publicador

CHURCHILL LIVINGSTONE

Relação

Growth Hormone & Igf Research

Direitos

restrictedAccess

Copyright CHURCHILL LIVINGSTONE

Palavras-Chave #Pregnancy #HIV-1 #IGF-2 #Antiretroviral drugs #Hyperglycemia #TO-CHILD TRANSMISSION #APAL POLYMORPHISM #GENE VARIANTS #IGF2 #GROWTH #METABOLISM #THERAPY #WEIGHT #HIV-1 #Cell Biology #Endocrinology & Metabolism
Tipo

article

original article

publishedVersion