Eriksson S, Moestrup T, Hägerstrand I
Acta Med Scand. 1975 Oct;198(4):243-7. doi: 10.1111/j.0954-6820.1975.tb19535.x.
Theoccurrence of PAS-positive, diastase-resistant, inclusion bodies in hepatocytes has been used as a marker of heterozygous (Pi MZ) alpha1-antitrypsin deficiency in order to study the frequency of lung, liver and malignant disease in a consecutive autopsy material from a well defined population. Typical PAS-positive inclusion bodies were found in the liver in 26 (3.7%) of the 700 cases studied. In these 26 subjects both liver (cirrhosis or fibrosis) and lung disease (emphysema) were significantly more prevalent (p less than 0.001) than among PAS-negative controls. The prevalence of malignant disease did not differ between the groups. The results are consistent with the concept that heterozygous (Pi MZ) alpha1-antitrypsin deficiency predisposes to both liver and lung disease but does not influence the survival rate.
肝细胞中出现的PAS阳性、抗淀粉酶、包涵体已被用作杂合子(Pi MZ)α1-抗胰蛋白酶缺乏症的标志物,以便在来自明确人群的连续尸检材料中研究肺、肝和恶性疾病的发生率。在所研究的700例病例中,有26例(3.7%)肝脏中发现典型的PAS阳性包涵体。在这26名受试者中,肝脏疾病(肝硬化或纤维化)和肺部疾病(肺气肿)的发生率均显著高于PAS阴性对照组(p<0.001)。两组之间恶性疾病的发生率没有差异。这些结果与以下概念一致,即杂合子(Pi MZ)α1-抗胰蛋白酶缺乏症易患肝脏和肺部疾病,但不影响生存率。