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乙型肝炎病毒基因型及e抗原状态对聚乙二醇干扰素抗病毒疗效的影响 被引量:5

Influences of the genotypes of HBV and HBeAg regarding their response to PEG-IFN in chronic hepatitis B patients
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摘要 目的探讨乙型肝炎病毒(HBV)不同基因型及乙型肝炎e抗原(HBeAg)对聚乙二醇干扰素治疗慢性乙型肝炎(CHB)应答率的影响。方法采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP) 方法,分析42例用聚乙二醇干扰素治疗的CHB患者基因型及HBeAg不同状态时对抗病毒治疗的影响。结果不同基因型对聚乙二醇干扰素的应笞率不同,B基因型的持续应答率为66.7%(12/18),C基因型持续应答率为27.3%(3/11)。HBeAg阴性患者的持续应答率为87.5%(7/8),HBeAg阳性患者为38.1%(8/21), P<0.05。结论HBV基因型及HBeAg的不同状态是预测聚乙二醇干扰素疗效的重要因素,且后者比前者的意义更大。 Objective To study the effects of genotypes of HBV and HBeAg on the response to PEG-mterferon alpha (PEG-IFN) in chronic hepatitis B (CHB) patients. Methods PCR-RFLP and S gene sequencing were conducted in 42 CHB patients. Results The sustained response (SR) rates were 66.7% in genotype B and 27.3% in genotype C group. The P value was 0.039 by the Pearson Chi-square test, while it was 0.06 by the Fisher's exact test. The results suggested a trend that patients with genotype B HBV compared to genotype C had better SR to PEG-IFN therapy, although the difference was not significant. Results also showed that SR rate in patients with HBeAg-negative CHB (7/8 87.5%) was significantly higher than that in HBe+ CHB patients (8/21 38.1%, P < 0.05). Conclusion Our results indicate that HBV genotype and HBeAg, especially the later, are main factors for predicting PEG-IFN therapy response in CHB patients.
出处 《中华肝脏病杂志》 CAS CSCD 北大核心 2005年第7期488-490,共3页 Chinese Journal of Hepatology
关键词 乙型肝炎 病毒基因型 e抗原状态 聚乙二醇 干扰素Α 抗病毒疗法 HBeAg 聚合酶链反应 Hepatitis B virus Genotype Interferon alpha Polymerase chain reaction
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  • 1中华医学会传染病与,寄生虫病学分会,肝病学分会.病毒性肝炎防治方案[J].中华肝脏病杂志,2000,8(6):324-329. 被引量:14017
  • 2阎丽,侯金林,郭亚兵,王战会,林裕龙,骆抗先.乙型肝炎病毒基因型S基因PCR-RFLP分型方法的建立[J].中华传染病杂志,2001,19(4):224-228. 被引量:77
  • 3Schiefke I, Klecker C, Maier M, et al. Sequential combination therapy of HBe antigen-negative/virus-DNA-positive chronic hepatitis B with famciclovir or lamivudine and interferon-alpha-2a. Liver Int,2004, 24: 98-104.
  • 4Orito E, Mizokami M, Sakugawa H, et al. A case-control study for clinical molecular biological differences between hepatitis B viruses of genotype B and C. Hepatology, 2001, 33: 218-223.

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