Apolipoprotein B-associated cholesterol is a determinant of treatment outcome in patients with chronic hepatitis C virus infection receiving anti-viral agents interferon-alpha and ribavirin
Autor: | Dermot Neely, D. A. Price, Geoffrey L. Toms, P.T. Donaldson, M. L. Schmid, Margaret F. Bassendine, David Sheridan |
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Rok vydání: | 2009 |
Předmět: |
Apolipoprotein E
Adult Male medicine.medical_specialty Very low-density lipoprotein Apolipoprotein B Hepatitis C virus Blood lipids medicine.disease_cause Gastroenterology Antiviral Agents chemistry.chemical_compound Predictive Value of Tests Internal medicine Ribavirin medicine Humans Pharmacology (medical) Apolipoproteins B Retrospective Studies Hepatology biology business.industry Cholesterol nutritional and metabolic diseases Interferon-alpha Hepatitis C Hepatitis C Chronic Middle Aged medicine.disease Treatment Outcome chemistry Immunology Multivariate Analysis biology.protein lipids (amino acids peptides and proteins) Female business Lipoprotein |
Zdroj: | Alimentary pharmacologytherapeutics. 29(12) |
ISSN: | 1365-2036 |
Popis: | Summary Background Hepatitis C virus (HCV) co-opts very-low-density lipoprotein (VLDL) pathways for replication, secretion and entry into hepatocytes and associates with apolipoprotein B (apoB) in plasma. Each VLDL contains apoB-100 and variable amounts of apolipoproteins E and C, cholesterol and triglycerides. Aim To determine whether baseline lipid levels predicted treatment outcome. Methods Retrospective analysis was performed of 250 chronic hepatitis C (CHC) patients who had received anti-viral agents interferon-alpha and ribavirin; 165 had a sustained virological response (SVR). Pre- and post-treatment nonfasting lipid profiles were measured and non-high-density lipoprotein (non-HDL) cholesterol (i.e. apoB-associated) was calculated. Binary logistic regression analysis assessed factors independently associated with treatment outcome. Results There was an independent association between higher apoB-associated cholesterol (non-HDL-C) and increased odds of SVR (odds ratio 2.09, P = 0.042). In multivariate analysis, non-HDL-C was significantly lower in HCV genotype 3 (g3) than genotype 1 (P = 0.007); this was reversible upon eradication of HCVg3 (pre-treatment non-HDL-C = 2.8 mmol/L, SVR = 3.6 mmol/L, P |
Databáze: | OpenAIRE |
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