Rynbrandt D J, Ihrig J, Kleinerman J
Am J Clin Pathol. 1975 Feb;63(2):251-60. doi: 10.1093/ajcp/63.2.251.
Serum trypsin inhibitory capacity determinations are of considerable value in detecting genetically determined types of obstructive pulmonary disease and hepatic disease. These determinations must frequently be followed by determination of protease inhibitor (Pi) phenotype in order to confirm the diagnosis. Piphenotyping has been a specialized and time-consuming procedure, and suggested improvements in the methodology and technics may make it more generally applicable as a clinical laboratory procedure. The prevalence of phenotypes other than MM in a group of 700 control sera from blood donors is reported as a baseline to evaluate typically American populations of mixed ethnic and racial characteristics. There are suggestive differences in prevalences of S and Z genes relating to ethnic stock and racial groups. It is important when comparing the prevalences of S and Z genes in diseasedpopulations to use control groups of similar ethnic and racial compositions. Pi phenotyping is a necessary laboratory procedure in the diagnosis of certain forms of genetically determined chronic obstructive pulmonary disease and hepatic disease. The distributions of all serum protease inhibitory capacity values and those for S and Z Pi phenotypes are shown.
血清胰蛋白酶抑制能力测定在检测遗传性阻塞性肺病和肝病类型方面具有重要价值。为了确诊,这些测定常常需要继之以蛋白酶抑制剂(Pi)表型的测定。Pi表型分型一直是一个专门且耗时的过程,而对方法和技术的改进建议可能会使其更广泛地作为一种临床实验室程序应用。报告了一组来自献血者的700份对照血清中除MM以外的其他表型的患病率,作为评估具有混合种族和民族特征的典型美国人群的基线。在与种族和民族群体相关的S和Z基因患病率方面存在提示性差异。在比较患病群体中S和Z基因的患病率时,使用具有相似种族和民族构成的对照组很重要。Pi表型分型是诊断某些形式的遗传性慢性阻塞性肺病和肝病的必要实验室程序。显示了所有血清蛋白酶抑制能力值以及S和Z Pi表型值的分布情况。