Van Thiel D H, Caraceni P, Molloy P J, Hassanein T, Kania R J, Gurakar A, Friedlander L
Oklahoma Transplant Institute, Baptist Medical Center of Oklahoma, Oklahoma City 73112, USA.
J Hepatol. 1995 Nov;23(5):503-8. doi: 10.1016/0168-8278(95)80054-9.
BACKGROUND/AIMS: Interferon is the only approved therapy for chronic hepatitis occurring as a consequence of an infection with the hepatitis C virus. Because interferon is expensive, has a large number of untoward effects and its efficacy is not guaranteed, many physicians limit their use of this therapy to those with histologically advanced but not end-stage cirrhotic disease. Moreover, most cases are biopsied only after 6 months or more of abnormal alanine aminotransferase levels have been documented. The rationale for this approach to patients with hepatitis C virus infection has not been demonstrated.
In the present study, a total of 37 patients with alanine aminotransferase levels < 1.5 upper limits of normal (59 IU/l or less) who were HCV-RNA positive by reverse transcriptase polymerase chain reaction, were selected for interferon treatment, having been identified as having hepatitis C virus disease as the result of a screening Ab-HCV test confirmed with a positive radio immune blotting assay. Once identified, each subject underwent a percutaneous liver biopsy and was tested for the presence of HBsAg, Ab-HBs and HBV-DNA. All liver biopsies were read and graded according to the criteria of Knodell et al. Each subject was treated with interferon a2b at a dose of 5 MU administered daily until a response was achieved (a minimum period of 6 months) or until a full year had elapsed. A response was defined as HCV-RNA negativity in serum on three consecutive monthly determinations. The study population consisted of 21 males and 16 females ranging in age from 17 to 72 years (mean 46.7 +/- 2.2 years). Their mean serum alanine aminotransferase level at the initiation of therapy was 37.5 +/- 2.1 IU/l with a range of 10-59 (normal values being 40 IU/l or less). 54% of the subjects were presumed to have acquired their hepatitis C virus infection as a result of a blood transfusion; 32% as a result of prior intravenous drug abuse; and 13% had no identifiable risk factor for hepatitis C virus. Despite having normal or near normal serum alanine aminotransferase levels, 9 subjects had chronic persistent hepatitis, 13 had chronic active hepatitis and 15 had chronic active hepatitis + cirrhosis documented by histopathologic assessment of their liver biopsies.
An interferon response was achieved in 5/9 with chronic persistent hepatitis, 11/13 with chronic active hepatitis and 8/15 with chronic active hepatitis + cirrhosis for an overall response rate of 65%.
This study has demonstrated that individuals who: 1) are hepatitis C virus positive with serum alanine aminotransferase levels < 1.5 x upper limits of normal can have histologically advanced liver disease; 2) can respond to interferon therapy defined as clearance of detectable HCV-RNA in serum; and, 3) should be considered for interferon treatment.
背景/目的:干扰素是唯一被批准用于治疗丙型肝炎病毒感染所致慢性肝炎的疗法。由于干扰素价格昂贵、有大量不良反应且疗效无法保证,许多医生仅将这种疗法用于组织学上病变进展但尚未发展至终末期肝硬化的患者。此外,大多数病例仅在丙氨酸转氨酶水平异常记录达6个月或更长时间后才进行活检。这种针对丙型肝炎病毒感染患者的治疗方法的理论依据尚未得到证实。
在本研究中,共有37例丙氨酸转氨酶水平低于正常上限1.5倍(59 IU/L或更低)、经逆转录聚合酶链反应检测HCV-RNA呈阳性的患者被选入干扰素治疗组,这些患者经筛查抗-HCV检测呈阳性,并经放射免疫印迹法检测确认患有丙型肝炎病毒疾病。一经确诊,每位受试者均接受经皮肝活检,并检测HBsAg、抗-HBs和HBV-DNA的存在情况。所有肝活检标本均按照Knodell等人的标准进行解读和分级。每位受试者接受剂量为5 MU的干扰素α2b治疗,每日给药,直至出现反应(最短疗程6个月)或满一年。反应定义为连续三个月每月血清HCV-RNA呈阴性。研究人群包括21名男性和16名女性,年龄在17至72岁之间(平均46.7±2.2岁)。他们治疗开始时的平均血清丙氨酸转氨酶水平为37.5±2.1 IU/L,范围为10至59(正常值为40 IU/L或更低)。54%的受试者被推测因输血感染丙型肝炎病毒;32%因既往静脉药物滥用感染;13%无明确的丙型肝炎病毒危险因素。尽管血清丙氨酸转氨酶水平正常或接近正常,但通过肝活检的组织病理学评估,9名受试者患有慢性持续性肝炎,13名患有慢性活动性肝炎,15名患有慢性活动性肝炎+肝硬化。
5/9的慢性持续性肝炎患者、11/13的慢性活动性肝炎患者和8/15的慢性活动性肝炎+肝硬化患者出现了干扰素反应,总体反应率为65%。
本研究表明,具备以下条件的个体:1)血清丙氨酸转氨酶水平低于正常上限1.5倍且丙型肝炎病毒呈阳性,可能患有组织学上病变进展的肝病;2)对定义为血清中可检测到的HCV-RNA清除的干扰素治疗有反应;3)应考虑接受干扰素治疗。