MTP -493G/T gene polymorphism is associated with steatosis in hepatitis C-infected patients

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 investigate...

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Published inBrazilian journal of medical and biological research Vol. 45; no. 1; pp. 72 - 77
Main Authors Siqueira, E.R.F., Oliveira, C.P.M.S., Correa-Giannella, M.L., Stefano, J.T., Cavaleiro, A.M., Fortes, M.A.H.Z., Muniz, M.T.C., Silva, F.S., Pereira, L.M.M.B., Carrilho, F.J.
Format Journal Article
LanguageEnglish
Published Brazil Sociedade Brasileira de Medicina Tropical 01.01.2012
Associação Brasileira de Divulgação Científica
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ISSN0100-879X
1414-431X
0100-879X
1414-431X
DOI10.1590/S0100-879X2011007500160

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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% of the patients with fibrosis grade 3+4 presented at least one G allele versus 34.3% of the patients with fibrosis grade 1+2 (OR = 1.8; 95%CI = 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%CI = 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.
AbstractList 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% of the patients with fibrosis grade 3+4 presented at least one G allele versus 34.3% of the patients with fibrosis grade 1+2 (OR = 1.8; 95% CI = 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% CI = 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.
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% of the patients with fibrosis grade 3+4 presented at least one G allele versus 34.3% of the patients with fibrosis grade 1+2 (OR = 1.8; 95%CI = 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%CI = 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.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% of the patients with fibrosis grade 3+4 presented at least one G allele versus 34.3% of the patients with fibrosis grade 1+2 (OR = 1.8; 95%CI = 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%CI = 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.
Author Siqueira, E.R.F.
Carrilho, F.J.
Fortes, M.A.H.Z.
Oliveira, C.P.M.S.
Stefano, J.T.
Cavaleiro, A.M.
Muniz, M.T.C.
Pereira, L.M.M.B.
Silva, F.S.
Correa-Giannella, M.L.
AuthorAffiliation Universidade de Pernambuco
Universidade de São Paulo
Instituto do Fígado de Pernambuco
AuthorAffiliation_xml – name: Universidade de São Paulo
– name: Universidade de Pernambuco
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  surname: Siqueira
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  givenname: C.P.M.S.
  surname: Oliveira
  fullname: Oliveira, C.P.M.S.
  organization: Universidade de São Paulo, Brasil
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  surname: Correa-Giannella
  fullname: Correa-Giannella, M.L.
  organization: Universidade de São Paulo, Brasil
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  surname: Stefano
  fullname: Stefano, J.T.
  organization: Universidade de São Paulo, Brasil
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  surname: Carrilho
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  organization: Universidade de São Paulo, Brasil
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Issue 1
Keywords Microsomal transfer protein
Hepatitis C
Fibrosis
Steatosis
Language English
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Snippet The reduction of hepatic microsomal transfer protein (MTP) activity results in fatty liver, worsening hepatic steatosis and fibrosis in chronic hepatitis C...
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StartPage 72
SubjectTerms Adult
Alcoholic beverages
Autoimmune diseases
BIOLOGY
Carrier Proteins - genetics
Disease Progression
Fatty liver
Fatty Liver - genetics
Fatty Liver - metabolism
Fatty Liver - pathology
Female
Fibrosis
Gene polymorphism
Genetic Predisposition to Disease
Genotype
Hemochromatosis
Hepatitis C
Hepatitis C, Chronic - genetics
Hepatitis C, Chronic - metabolism
Hepatitis C, Chronic - pathology
Humans
Male
MEDICINE, RESEARCH & EXPERIMENTAL
Microsomal transfer protein
Polymerase Chain Reaction
Polymorphism, Genetic - genetics
Promoters
Regression analysis
Short Communication
Steatosis
Transcription
Wilson's disease
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Title MTP -493G/T gene polymorphism is associated with steatosis in hepatitis C-infected patients
URI https://www.ncbi.nlm.nih.gov/pubmed/22147193
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