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干扰素治疗丙型肝炎疗效相关因素分析 被引量:2

CORRELATIVE FACTOR ANALYSIS OF HEPATITIS C TREATED WITH INTERFERON
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摘要 目的:探讨预测干扰素治疗慢性丙型肝炎(CHC)疗效的临床上适用、简便、易行的指标。方法:对采用干扰素(IFNα-1b)治疗32例CHC临床资料进行观察,包括治疗前后肝功能(ALT、SB、GGT)、抗-HCVOD水平、HCV基因型、HCVRNA、SIL-2R、β2-MG等,治疗结束时有效者为肝功能复常同时HCVRNA阴转,其余反应模式均为无效者。结果:HCV基因型为Ⅲ型患者疗效(5/10)明显高于Ⅱ型(2/19)(P<0.05),有效者治疗前血清抗—HCVOD明显低于无效者(P<0.05),治疗后有效者β2-MG升高水平(3.45±1.08)mg/L明显高于无效者(1.33±0.95)mg/L(P<0.05),而两者治疗前ALT、SB、GGT、IgM、β2-MG患者的年龄无明显差别(P>0.05)。结论:感染HCV基因型,治疗前抗—HCVOD水平及治疗后β2-MG变化对预测IFN治疗CHC疗效有一定参考价值。 Objective:To find clinical suitable,simple and feasible parameters to predict the effect of chronic hepatitis C(CHC) treated with interferon-1b(IFN).Methods:Pre-therapy and post-therapy,some parameters of 32 CHC patients treated with IFN were observed,including their liver functions (ALT,SB,GGT),Anti-HCV OD values,HCV genotypes HCV RNA,SIL-2R,β 2-MG,etc.In the end of therapy,the patients with normal ALT and negative HCV RNA were called responders,others were called non-responders.Results:Respondent rate was higher in HCV Ⅲ(5/10) than in HCV Ⅱ (2/19) (P<0.05);pre-therapy Anti-HCV OD value was lower in responders than in non-responders (P<0.05);post-therapy,elevated values of β 2-MG in responders (3.45±1.08) mg/L were higher than in non-responders (1.33±0.95) mg/L(P<0.05).No significant difference was found in age,the values of ALT,SB,GGT,IgM,β 2-MG pre-therapy (P<0.05).Conclusion:Some parameters such as HCV genotype,pre-therapy Anti-HCV OD value and elevated value of β 2-MG may be useful to predict the effect of CHC treated with IFN.
出处 《医师进修杂志》 1999年第8期16-18,共3页 Journal of Postgraduates of Medicine
关键词 干扰素 丙型肝炎 药物疗法 Interferon\ Chronic hepatitis C\ Correlative therapy factor
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  • 1周建英,张启顺,柳盛.苦参素与干扰素联合治疗慢性乙型肝炎的临床观察[J].中国医药导报,2006,3(17):84-85. 被引量:17
  • 2张顺财,刘厚钰,王吉耀,朱无难,高田昭.丙型肝炎病毒亚型与肝细胞癌关系的研究[J].临床肝胆病杂志,1996,12(3):135-137. 被引量:9
  • 3Shepard CW, Finelli L, Alter MJ. Global epidemiology of hepatitis C virus infection [J]. The Lancet infectious diseases, 2005, 5(9): 558-567.
  • 4Wang YS, Youngster S, Bausch J, et al. Identification of the major positional isomer of pegylated interferon alpha -2b [ J ]. Biochemistry, 2000, 39(35): 10634-106340.
  • 5Nez M, Ros P, Martn-carbonero L, et al. Role of hepatitis C virus genotype in the development of severe transaminase elevation after the introduction of antiretroviral therapy [J]. JAIDS Journal of Acquired Immune Deficiency Syndromes, 2002, 30( 1 ): 65.
  • 6Ofito E. HCV genotype as a predictor of response to interferon therapy in patients with chronic hepatitis C [J]. Nihon rinsho Japanese journal of clinical medicine, 2001, 59(7): 1556.
  • 7Kasahara A, Hayashi N, Hiramatsu N, et al. Ability of prolonged interferon treatment to suppress relapse after cessation of therapy in patients with chronic hepatitis C: a muhicenter randomized controlled trial [ J ]. Hepatology, 1995,21 ( 2 ):291-297.
  • 8Mizokami M, Orito E, Gibo Y, et al. Genotype, serum level of hepatitis C virus RNA and liver histology as predictors of response to interferon α 2α therapy in Japanese patients with chronic hepatitis C [J]. Liver, 1996, 16(1): 23-27.
  • 9Martinot-peignoux M, Marcellin P, Pouteau M, et al. Pretreatment serum hepatitis C virus RNA levels and hepatitis C virus genotype are the main and independent prognostic factors of sustained response to interferon alfa therapy in chronic hepatitis C [J]. Hepatology, 1995, 22(4): 1050-1056.
  • 10Wu YS,Bai JY,Yang CM,et al.Study of HCV genotypes in Wulumuqi [J].Linchuang Neike Zazhi(J Clin Intern Med), 1997:14 (5):265-266.

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