Prediction of sustained virologic responses to combination therapy of pegylated interferon-alpha and ribavirin in patients with chronic hepatitis C infection

被引:22
作者
Ismail, Mona H. [1 ]
机构
[1] Univ Dammam, King Fahd Hosp Univ, Coll Med, Dept Internal Med,Div Gastroenterol, Al Khobar, Saudi Arabia
关键词
Chronic hepatitis C; Saudi; sustained virologic response; treatment response predictors;
D O I
10.4103/2230-8229.108182
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Background and Aim: Hepatitis C virus (HCV) infection is a major health problem worldwide. Genotype-4 is the most common genotype in Saudi Arabia. The response to treatment with pegylated interferon-a combined with ribavirin in chronic HCV infection varies. This study aimed at investigating the pre- and on-treatment predictors of sustained virologic response (SVR) in patients with chronic hepatitis C (CHC) infection. Patients and Methods: Clinical data of 48 patients with CHC treated with standard HCV antiviral combination therapy, between January 2005 and December 2010, at a Saudi University hospital, were retrospectively reviewed for age, sex, body mass index, liver enzymes, HCV-RNA viral load, liver biopsy, and response to treatment. The primary end point was SVR defined as undetectable HCV-RNA by polymerase chain reaction (PCR) 24 weeks after the end of treatment. Univariable logistic regression was used to explore the association between the different variables and SVR. These independent predictors of SVR were then analyzed with multivariable logistic regression analysis. Results: Of the 48 treated patients, 25 (52%) were females and 27 (56%) were Saudi. The mean age was 43 years (43 +/- 10 years). Twenty-four (50%) had genotype-4, and 26 (54%) had liver biopsy. The overall SVR rate was 75% (36/ 48) and was 83.3% (20/24) among genotype-4 patients. Baseline factors associated with SVR identified by univariate logistic regression were genotype-4 and early viral response (EVR), defined as a drop of >= 2 log in serum HCV viral load after 12 weeks of initiation of combination therapy (P = 0.001). However, in stepwise regression analysis, the independent factor associated with the effect of antiviral therapy was genotype-4. When on-treatment variables were included, EVR (P = 0.003) and low baseline viral load (P = 0.048) were highly predictive of SVR. Conclusions: Of our HCV-treated patients, 75% had SVR. HCV genotype-4, EVR, and low baseline viral load were predictive of SVR.
引用
收藏
页码:35 / 40
页数:6
相关论文
共 28 条
  • [1] Predictors of sustained virologic response in hepatitis C genotype 4: beyond the usual suspects
    Abdo, Ayman A.
    Sanai, Faisal M.
    [J]. ANNALS OF SAUDI MEDICINE, 2009, 29 (01) : 1 - 3
  • [2] Steatosis accelerates the progression of liver damage of chronic hepatitis C patients and correlates with specific HCV genotype and visceral obesity
    Adinolfi, LE
    Gambardella, M
    Andreana, A
    Tripodi, MF
    Utili, R
    Ruggiero, G
    [J]. HEPATOLOGY, 2001, 33 (06) : 1358 - 1364
  • [3] Predictors of sustained virological response to a 48-week course of pegylated interferon alfa-2a and ribavirin in patients infected with hepatitis C virus genotype 4
    Al Ashgar, Hamad
    Helmy, Ahmed
    Khan, Mohamed Q.
    Al Kahtani, Khalid
    Al Quaiz, Mohammed
    Rezeig, Mohammed
    Kagevi, Ingvar
    Alshehri, Abdullah
    Al Kalbani, Abdullah
    Al Swat, Khalid
    Dahab, Salim
    Elkum, Naser
    Al Fadda, Mohammed
    [J]. ANNALS OF SAUDI MEDICINE, 2009, 29 (01) : 4 - 14
  • [4] Hepatitis C virus genotypes in patients with chronic liver disease and haemodialysis patients from Saudi Arabia
    AlFaleh, FZ
    Huraib, S
    Sbeih, F
    AlKarawi, M
    AlRashed, R
    AlMofleh, IA
    Sougiyyah, M
    Shaheen, M
    Ramia, S
    [J]. JOURNAL OF VIRAL HEPATITIS, 1995, 2 (06) : 293 - 296
  • [5] Peginterferon α-2b plus ribavirin compared with interferon α-2b plus ribavirin for initial treatment of chronic hepatitis C in Saudi patients commonly infected with genotype 4
    Alfaleh, FZ
    Hadad, Q
    Khuroo, MS
    Aljumah, A
    Algamedi, A
    Alashgar, H
    Al-Ahdal, MN
    Mayet, I
    Khan, MQ
    Kessie, G
    [J]. LIVER INTERNATIONAL, 2004, 24 (06) : 568 - 574
  • [6] Predictors of response of US veterans to treatment for the hepatitis C virus
    Backus, Lisa I.
    Boothroyd, Derek B.
    Phillips, Barbara R.
    Mole, Larry A.
    [J]. HEPATOLOGY, 2007, 46 (01) : 37 - 47
  • [7] BEDOSSA P, 1994, HEPATOLOGY, V20, P15
  • [8] Steatosis and chronic hepatitis C: analysis of fibrosis and stellate cell activation
    Clouston, AD
    Jonsson, JR
    Purdie, DM
    Macdonald, GA
    Pandeya, N
    Shorthouse, C
    Powell, EE
    [J]. JOURNAL OF HEPATOLOGY, 2001, 34 (02) : 314 - 320
  • [9] Effects of interferon treatment response on liver complications of chronic hepatitis C: 9-year follow-up study
    Coverdale, SA
    Khan, MH
    Byth, K
    Lin, R
    Weltman, M
    George, J
    Samarasinghe, D
    Liddle, C
    Kench, JG
    Crewe, E
    Farrell, GC
    [J]. AMERICAN JOURNAL OF GASTROENTEROLOGY, 2004, 99 (04) : 636 - 644
  • [10] De Filippi F, 2003, J BIOL REG HOMEOS AG, V17, P133