Sutinen S, Koistinen J, Pääkkö P
Acta Pathol Microbiol Immunol Scand A. 1985 Jul;93(4):183-8. doi: 10.1111/j.1699-0463.1985.tb03938.x.
Pi phenotypes, determined post mortem by isoelectric focusing and immunofixation, emphysema, assessed from inflation fixed specimens and smoking history were correlated in 186 hospital necropsies. It was possible to determine Pi phenotype in 98.4% of the specimens. Phenotype M occurred in 87.5%, MZ in a 8.1%, MS in 2.1% and FM in 0.5%. An expected association was found between smoking and emphysema but not between the Pi phenotypes and emphysema. Thus, while smoking is a major aetiological factor, the Pi MZ heterozygous state does not seem to predispose to structural emphysema. However, the small number of cases did not allow an estimation of the risk of smoking in Pi MZ heterozygous persons compared to those with the normal Pi phenotype.
通过等电聚焦和免疫固定法在尸检后确定Pi表型,从充气固定标本评估肺气肿情况,并将吸烟史与186例医院尸检结果进行关联分析。98.4%的标本能够确定Pi表型。表型M出现的比例为87.5%,MZ为8.1%,MS为2.1%,FM为0.5%。发现吸烟与肺气肿之间存在预期的关联,但Pi表型与肺气肿之间未发现关联。因此,虽然吸烟是主要的病因因素,但Pi MZ杂合状态似乎不会导致结构性肺气肿。然而,病例数量较少,无法估计Pi MZ杂合个体与正常Pi表型个体相比的吸烟风险。