Hepatic fibrosis and serum alpha-fetoprotein (AFP) as predictors of response to HCV treatment and factors associated with serum AFP normalisation after treatment

被引:12
作者
El Raziky, Maissa [1 ]
Attia, Dina [2 ]
El Akel, Wafaa [1 ]
Shaker, Olfat [3 ]
Khatab, Hany [4 ]
Abdo, Shaimaa [5 ]
Elsharkawy, Aisha [1 ]
Esmat, Gamal [1 ]
机构
[1] Cairo Univ, Hepatogastroenterol Dept, Endem Med, Cairo, Egypt
[2] Beni Suef Univ, Hepatogastroenterol Dept, Endem Med, Bani Suwayf, Egypt
[3] Cairo Univ, Dept Clin Biochem, Cairo, Egypt
[4] Cairo Univ, Dept Pathol, Cairo, Egypt
[5] Egyptian Minist Hlth Hosp, Dept Gastroenterol & Hepatol, Cairo, Egypt
关键词
Chronic hepatitis C virus; Hepatic fibrosis; Alpha-fetoprotein; SUSTAINED VIROLOGICAL RESPONSE; C VIRUS; PROGENITOR CELLS; HEPATOCELLULAR-CARCINOMA; ANTIVIRAL THERAPY; LIVER; DIFFERENTIATION; PROLIFERATION; MORBIDITY; RIBAVIRIN;
D O I
10.1016/j.ajg.2013.08.005
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background and study aim: Elevated levels of alpha-fetoprotein (AFP) can be seen in patients with chronic hepatitis C (CHC) and liver cirrhosis without hepatocellular carcinoma and were negatively associated with treatment response. However, factors associated with its changes are not identified. We aimed in this study to verify a cut-off value for AFP as a predictor of response to standard of care (SOC) antiviral therapy in Egyptian chronic hepatitis C virus (HCV)-infected patients and identify factors associated with its changes post treatment. Patients and methods: A total of 175 chronic non-cirrhotic HCV-infected patients were evaluated for baseline serum AFP and liver biopsy were classified according to Ishak scoring system of hepatic fibrosis. All patients were scheduled to receive SOC antiviral therapy for 48 weeks and had been followed up to week 72. Reassessment of AFP and repeated liver biopsy at week 72 were feasible only in 79 patients. Results: High baseline AFP levels were observed in non-respondents (non-sustained virological respondents (non-SVRs)) (P < 0.01); the AFP level decreased in all patients post treatment (P = 0.01), especially in the SVRs (P < 0.01). In multivariate analysis, hepatic fibrosis was a predictor of response to treatment (P = 0.02), while body mass index (BMI) (25-30 kg m(-2)), hepatic activity (A2), hepatic fibrosis stage (F2-F4) and fibrosis improvement were predictors of AFP difference (P = 0.007, 0.01, 0.012, <0.001, 0.030, and 0.018), respectively. The diagnostic performance to predict the HCV treatment response was best by adding both AFP and hepatic fibrosis stage factors; the best cut-off value for AFP was 3.57 ng dl(-1) with 50% sensitivity and 68% specificity with area under the curve (AUC) of 0.55 and for hepatic fibrosis stage was 3, with a sensitivity of 88%, a specificity of 30% with an AUC of 0.58. Conclusion: In chronic HCV-infected patients, serum AFP below 3.57 ng dl(-1) and hepatic fibrosis <= stage 3 are expected to have good response to treatment; BMI (25-30 kg m(-1)), A2, fibrosis >2 and fibrosis improvement predict AFP change post treatment. (C) 2013 Arab Journal of Gastroenterology. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:94 / 98
页数:5
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