Guptan R C, Thakur V, Malhotra V, Sarin S K
Department of Gastroenterology, GB Pant Hospital, New Delhi, India.
J Gastroenterol Hepatol. 1998 Jul;13(7):675-9. doi: 10.1111/j.1440-1746.1998.tb00712.x.
Approximately 15% of Indian patients with hepatitis B virus (HBV)-related chronic liver disease (CLD) have infection with precore mutant forms. These patients are likely to have an aggressive course. There are equivocal reports of success with interferon therapy of mutant infection in the West. This therapy has not been evaluated in precore mutant-related CLD in Asian Indians. Eighteen patients (mean age 38.2 +/- 12 years, M:F: 17:1) with biopsy proven CLD and precore mutant HBV infection (hepatitis B surface antige (HBsAg) positive, hepatitis B e antigen (HBeAg) negative, anti-HBe positive, HBV-DNA positive) were included. Interferon alpha 2b was given at 3 mIU on alternate days for 4 months. Serology, determination of HBV-DNA (both by dot-blot hybridization and polymerase chain reaction) and liver biopsy were repeated after completion of the therapy. Response to interferon therapy was defined as loss of HBV-DNA by dot-blot hybridization. Thirteen (72.2%) patients responded to the treatment (responders). Mean alanine aminotransferase levels (83 +/- 12 vs 55 +/- 29 IU/L, P < 0.01) and the histological activity index (15 +/- 1.4 vs 12 +/- 1.3, P < 0.01) significantly decreased in the responders compared with initial values. Serum albumin levels also improved at the end of the therapy (3.5 +/- 0.4 g/dL vs 3.8 +/- 0.4 g/dL, P = 0.07). During follow up, seven of the 13 (54%) responders relapsed; cirrhotics relapsed more often than chronic hepatitis patients (P < 0.05). All 18 patients, however, continued to be HBV-DNA positive at the end of follow up. This study concluded that: 1. Interferon therapy is beneficial, albeit to a limited extent, in HBV precore mutant-related chronic liver disease in Asian Indians. 2. It is ineffective in eliminating the mutant HBV infection, which explains the high relapse rate. 3. Prolonged low-dose interferon therapy alone or in combination with newer nucleoside analogues should be evaluated in these patients.
在印度,约15%的乙型肝炎病毒(HBV)相关慢性肝病(CLD)患者感染了前核心区突变型病毒。这些患者的病程可能较为凶险。在西方,关于干扰素治疗突变型感染的疗效报道不一。在亚洲印度人中,尚未对前核心区突变相关CLD患者进行过这种治疗的评估。纳入了18例经活检证实为CLD且感染前核心区突变型HBV的患者(平均年龄38.2±12岁,男:女 = 17:1)(乙肝表面抗原(HBsAg)阳性、乙肝e抗原(HBeAg)阴性、抗-HBe阳性、HBV-DNA阳性)。给予干扰素α2b,剂量为3百万国际单位,隔日一次,共4个月。治疗结束后,重复进行血清学检查、HBV-DNA检测(采用斑点杂交和聚合酶链反应两种方法)以及肝活检。干扰素治疗反应定义为斑点杂交法检测HBV-DNA转阴。13例(72.2%)患者治疗有效(反应者)。与初始值相比,但反应者的平均丙氨酸转氨酶水平(83±12 vs 55±29 IU/L,P<0.01)和组织学活动指数(15±1.4 vs 12±1.3,P<0.01)显著降低。治疗结束时血清白蛋白水平也有所改善(3.5±0.4 g/dL vs 3.8±0.4 g/dL,P = 0.07)。在随访期间,13例反应者中有7例(54%)复发;肝硬化患者比慢性肝炎患者更容易复发(P<0.05)。然而,所有18例患者在随访结束时HBV-DNA仍为阳性。本研究得出以下结论:1. 干扰素治疗对亚洲印度人前核心区突变相关慢性肝病有益,尽管程度有限。2. 它在消除突变型HBV感染方面无效,这解释了高复发率。3. 应在这些患者中评估单独使用或与新型核苷类似物联合使用的延长低剂量干扰素治疗。