Impact of genetic polymorphisms associated with nonalcoholic fatty liver disease on HIV-infected individuals.

 

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Impact of genetic polymorphisms associated with nonalcoholic disease on HIV-infected individuals.

AIDS. 2015 Sep 24;29(15):1927-35

Authors: Macias J, Rivero-Juarez A, Neukam K, Tellez F, Merino D, Frias M, Merchante N, Rivero A, Pineda JA, Real LM, HEPAVIR study group

Abstract
OBJECTIVE: Fatty liver disease (FLD) is frequently observed in HIV-infected patients and a cause of advanced liver disease. Genetic factors could play a role in determining risk for FLD development in those patients. The aim of this study was to evaluate the association of those single nucleotide polymorphisms (SNPs) previously found to be related to nonalcoholic FLD by genome-wide association analyses in the general population with the presence of FLD, including , in HIV-infected individuals.
DESIGN: This is a transversal study.
METHODS: A total of 431 HIV-infected patients were included in this study. All of them underwent a transient elastography with the controlled attenuation parameter examination and were genotyped for 19 selected SNPs. A controlled attenuation parameter value higher than 238 dB/m was selected to define the presence of FLD. Elevated alanine aminotransferase levels and presence of FLD was considered as a surrogate marker of steatohepatitis.
RESULTS: A total of 179 (41.5%) individuals showed FLD, including 122 (28.3%) with steatohepatitis. The rs12743824 and rs738491 SNPs were independently associated with FLD and steatohepatitis, respectively. For rs12743824, among 252 individuals without FLD, 182 (72.2%) were A-allele carriers vs. 111 (62%) of 179 patients with this disease (multivariate P = 0.006; adjusted odds ratio = 0.51; 95% confidence interval = 0.33-0.83). For rs738491, 20 (16.4%) of 122 patients with steatohepatitis were TT carriers vs. 18 (5.8%) of 309 patients without this condition (multivariate P = 0.005; adjusted odds ratio = 2.94; 95% confidence interval = 1.39-6.20).
CONCLUSION: LPPR4 and SAMM50 allelic variants are independent risk factors for FLD and steatohepatitis development, respectively, in HIV-infected individuals.

PMID: 26352879 [PubMed – in process]

http://www.ncbi.nlm.nih.gov/pubmed/26352879?dopt=Abstract

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