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抗线粒体抗体阳性但碱性磷酸酶正常:这是原发性胆汁性肝硬化吗?

Positive antimitochondrial antibody but normal alkaline phosphatase: is this primary biliary cirrhosis?

作者信息

Mitchison H C, Bassendine M F, Hendrick A, Bennett M K, Bird G, Watson A J, James O F

出版信息

Hepatology. 1986 Nov-Dec;6(6):1279-84. doi: 10.1002/hep.1840060609.

Abstract

Twenty-nine patients with a positive antimitochondrial antibody titer greater than or equal to 1/40, who were detected during screening for other autoimmune disease, are described who had a normal serum bilirubin, alkaline phosphatase and transaminase and who had no symptoms of liver disease at presentation. Liver biopsies in 12 of the 29 fulfilled diagnostic criteria for primary biliary cirrhosis; a further 12 were consistent with primary biliary cirrhosis, but only 2 were normal. There was a high incidence of other autoantibodies and autoimmune diseases, especially thyroid antibodies and disorders. Sixteen of these patients have been followed for over 4 years since diagnosis (mean = 6 years, range = 4 to 9 years) and for a mean of 8.7 years since initial detection of the antimitochondrial antibody (range = 4 to 13). Five of 16 developed symptoms suggestive of primary biliary cirrhosis, and 11 of 16 developed elevation of alkaline phosphatase. The antimitochondrial antibody activity in these patients was in the same IgG subclasses (predominantly IgG1 and IgG3) as that seen in a group of 23 patients with clinically, biochemically and histologically advanced primary biliary cirrhosis. All showed the same abnormalities on quantitative estimation of the total IgG subclasses in serum; relative excess of IgG3 and, to a lesser extent, IgG2 was exhibited. It is concluded that, in this study, the finding of an antimitochondrial antibody titer greater than or equal to 1/40 is strongly suggestive of primary biliary cirrhosis even in the absence of symptoms and the presence of a normal alkaline phosphatase.

摘要

29例抗线粒体抗体滴度大于或等于1/40且呈阳性的患者,这些患者是在筛查其他自身免疫性疾病时被检测到的,其血清胆红素、碱性磷酸酶和转氨酶正常,就诊时无肝病症状。29例患者中有12例肝脏活检符合原发性胆汁性肝硬化的诊断标准;另有12例符合原发性胆汁性肝硬化,但只有2例正常。其他自身抗体和自身免疫性疾病的发生率很高,尤其是甲状腺抗体和疾病。自诊断以来,其中16例患者已随访4年以上(平均6年,范围4至9年),自最初检测到抗线粒体抗体以来平均随访8.7年(范围4至13年)。16例中有5例出现提示原发性胆汁性肝硬化的症状,16例中有11例碱性磷酸酶升高。这些患者的抗线粒体抗体活性与一组23例临床、生化和组织学上处于晚期原发性胆汁性肝硬化患者的抗线粒体抗体活性属于相同的IgG亚类(主要是IgG1和IgG3)。血清总IgG亚类定量评估显示所有患者均有相同异常;表现为IgG3相对过量,IgG2在较小程度上也过量。结论是,在本研究中,即使没有症状且碱性磷酸酶正常,抗线粒体抗体滴度大于或等于1/40的发现也强烈提示原发性胆汁性肝硬化。

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