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通过抑制试验测定囊性纤维化患者的血清异淀粉酶活性。

Serum isoamylase activities in cystic fibrosis patients, determined by an inhibitory assay.

作者信息

Maillie A J, Vaccaro M I, Calvo E L, Ruiz J A, Emiliani R, Pivetta O H

出版信息

Scand J Gastroenterol. 1986 Oct;21(8):941-4. doi: 10.3109/00365528608996399.

Abstract

Serum isoamylase activities were determined in patients with either cystic fibrosis (CF) or celiac disease and in age-matched healthy children by means of an inhibitory assay suitable for routine application. The percentage pancreatic isoamylase (PIA) activity was significantly decreased in CF patients when compared with that of patients with celiac disease. Cystic fibrosis patients with steatorrhea had lower absolute values of PIA activity and higher values of salivary isoenzyme activity than control individuals. There was no overlapping between values obtained from CF patients and either celiac patients or healthy individuals. These results suggest that determination of PIA activity may be a useful adjunct test for the diagnosis of CF in patients with steatorrhea.

摘要

采用适合常规应用的抑制试验,测定了囊性纤维化(CF)患者、乳糜泻患者以及年龄匹配的健康儿童的血清异淀粉酶活性。与乳糜泻患者相比,CF患者的胰腺异淀粉酶(PIA)活性百分比显著降低。有脂肪泻的CF患者的PIA活性绝对值低于对照组,唾液同工酶活性值高于对照组。CF患者与乳糜泻患者或健康个体的检测值没有重叠。这些结果表明,测定PIA活性可能是诊断有脂肪泻的CF患者的一项有用的辅助检查。

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