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 in | Brazilian journal of medical and biological research Vol. 45; no. 1; pp. 72 - 77 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
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Brazil
Sociedade Brasileira de Medicina Tropical
01.01.2012
Associação Brasileira de Divulgação Científica |
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ISSN | 0100-879X 1414-431X 0100-879X 1414-431X |
DOI | 10.1590/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. |
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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 – name: Instituto do Fígado de Pernambuco |
Author_xml | – sequence: 1 givenname: E.R.F. surname: Siqueira fullname: Siqueira, E.R.F. organization: Universidade de São Paulo, Brasil; Universidade de Pernambuco, Brasil; Universidade de Pernambuco, Brasil – sequence: 2 givenname: C.P.M.S. surname: Oliveira fullname: Oliveira, C.P.M.S. organization: Universidade de São Paulo, Brasil – sequence: 3 givenname: M.L. surname: Correa-Giannella fullname: Correa-Giannella, M.L. organization: Universidade de São Paulo, Brasil – sequence: 4 givenname: J.T. surname: Stefano fullname: Stefano, J.T. organization: Universidade de São Paulo, Brasil – sequence: 5 givenname: A.M. surname: Cavaleiro fullname: Cavaleiro, A.M. organization: Universidade de São Paulo, Brasil – sequence: 6 givenname: M.A.H.Z. surname: Fortes fullname: Fortes, M.A.H.Z. organization: Universidade de São Paulo, Brasil – sequence: 7 givenname: M.T.C. surname: Muniz fullname: Muniz, M.T.C. organization: Universidade de Pernambuco, Brasil – sequence: 8 givenname: F.S. surname: Silva fullname: Silva, F.S. organization: Universidade de Pernambuco, Brasil – sequence: 9 givenname: L.M.M.B. surname: Pereira fullname: Pereira, L.M.M.B. organization: Universidade de Pernambuco, Brasil; Instituto do Fígado de Pernambuco, Brasil – sequence: 10 givenname: F.J. surname: Carrilho fullname: Carrilho, F.J. organization: Universidade de São Paulo, Brasil |
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Keywords | Microsomal transfer protein Hepatitis C Fibrosis Steatosis |
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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 |
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