Wirth H P, Zala G, Meyenberger C, Ammann R
Departement für Innere Medizin, Universitätsspital Zürich.
Schweiz Med Wochenschr. 1995 Apr 15;125(15):750-4.
Antimitochondrial antibodies are of considerable importance for the diagnosis of primary biliary cirrhosis. Several subtypes of antimitochondrial antibodies have been identified and the pattern has been associated with prognosis of the disease in the long term course. 22 patients with primary biliary cirrhosis (19 female, 3 male; age 29-66, mean 49 years) were examined for the occurrence of the subtypes of antimitochondrial antibodies anti M2, anti M4 and anti M9. Diagnosis of primary biliary cirrhosis was based on elevated cholestatic enzymes, antimitochondrial antibodies, histology and exclusion of other chronic liver disease in all patients and elevated serum IgM concentration in 18/22 patients. Most patients were included in a study protocol of the Swiss Association for the Study of the Liver and treated with 10 mg/kg/day oral ursodeoxycholic acid. According to the subtype pattern of antimitochondrial antibodies, patients were divided into 4 groups A to D (A: anti M2-, anti M4-, anti M9+; B: anti M2+, anti M4-, anti M9+; C: anti M2+, anti M4-, anti M9- and D: anti M2+, anti M4+, anti M9-). The groups were compared with respect to the prognostically relevant parameters age, bilirubin, albumin, prothrombin time and peripheral edema, as well as the occurrence of granulomas in liver biopsy, galactose elimination capacity and response to treatment with ursodeoxycholic acid during one year. Treatment response was expressed as decrease of the serum concentration of IgM, GPT, alkaline phosphatase, gamma glutamyl transpeptidase and bilirubin. No significant differences between the four groups were found with respect to the prognostically relevant parameters, histology and galactose elimination capacity at study entry.(ABSTRACT TRUNCATED AT 250 WORDS)
抗线粒体抗体对原发性胆汁性肝硬化的诊断具有重要意义。已鉴定出抗线粒体抗体的几种亚型,其模式与该疾病长期病程的预后相关。对22例原发性胆汁性肝硬化患者(19例女性,3例男性;年龄29 - 66岁,平均49岁)进行了抗线粒体抗体M2、M4和M9亚型出现情况的检查。原发性胆汁性肝硬化的诊断基于所有患者胆汁淤积酶升高、抗线粒体抗体、组织学检查以及排除其他慢性肝病,18/22例患者血清IgM浓度升高。大多数患者纳入了瑞士肝脏研究协会的研究方案,接受每日10 mg/kg口服熊去氧胆酸治疗。根据抗线粒体抗体的亚型模式,患者分为A至D四组(A组:抗M2 - 、抗M4 - 、抗M9 + ;B组:抗M2 + 、抗M4 - 、抗M9 + ;C组:抗M2 + 、抗M4 - 、抗M9 - ;D组:抗M2 + 、抗M4 + 、抗M9 - )。比较了四组在预后相关参数年龄、胆红素、白蛋白、凝血酶原时间和外周水肿方面的情况,以及肝活检中肉芽肿的出现情况、半乳糖清除能力和一年中熊去氧胆酸治疗的反应。治疗反应以IgM、谷丙转氨酶、碱性磷酸酶、γ - 谷氨酰转肽酶和胆红素血清浓度的降低来表示。在研究开始时,四组在预后相关参数、组织学和半乳糖清除能力方面未发现显著差异。(摘要截短于250字)