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Braz. j. med. biol. res ; 45(1): 72-77, Jan. 2012. tab
Article in English | LILACS | ID: lil-610549

ABSTRACT

The reduction of hepatic microsomal transfer protein (MTP) activity results in fatty liver, worsening hepatic steatosis and fibrosis in chronic hepatitis C (CHC). The G allele of the MTP gene promoter, -493G/T, has been associated with lower transcriptional activity than the T allele. We investigated this association with metabolic and histological variables in patients with CHC. A total of 174 untreated patients with CHC were genotyped for MTP -493G/T by direct sequencing using PCR. All patients were negative for markers of Wilson’s disease, hemochromatosis and autoimmune diseases and had current and past daily alcohol intake lower than 100 g/week. The sample distribution was in Hardy-Weinberg equilibrium. Among subjects with genotype 1, 56.8 percent of the patients with fibrosis grade 3+4 presented at least one G allele versus 34.3 percent of the patients with fibrosis grade 1+2 (OR = 1.8; 95 percentCI = 1.3-2.3). Logistic regression analysis with steatosis as the dependent variable identified genotypes GG+GT as independent protective factors against steatosis (OR = 0.4, 95 percentCI = 0.2-0.8; P = 0.01). The results suggest that the presence of the G allele of MTP -493G/T associated with lower hepatic MTP expression protects against steatosis in our CHC patients.


Subject(s)
Adult , Female , Humans , Carrier Proteins/genetics , Fatty Liver/genetics , Hepatitis C, Chronic/genetics , Polymorphism, Genetic/genetics , Disease Progression , Fatty Liver/metabolism , Fatty Liver/pathology , Genetic Predisposition to Disease , Genotype , Hepatitis C, Chronic/metabolism , Hepatitis C, Chronic/pathology , Polymerase Chain Reaction
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