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胰腺功能不全患儿的粪便糜蛋白酶水平

Fecal chymotrypsin levels in children with pancreatic insufficiency.

作者信息

de Pedro C, Codoceo R, Vazquez P, Hernanz A

出版信息

Clin Biochem. 1986 Dec;19(6):338-40. doi: 10.1016/s0009-9120(86)80006-6.

Abstract

The fecal chymotrypsin (FC) levels in samples collected over 24 h were determined by a new commercial colorimetric method from Boehringer Mannheim in 82 children suffering from various pancreatic disorders. The patients were divided into 4 groups, in accordance with the following etiologies: cystic fibrosis of the pancreas (CFP), chronic severe hepatic disorders (CSH), primary malabsorption syndrome (PMS) and malnutrition due to nondigestive causes (M). The control group comprised 48 children of similar ages. The 24th FC levels as U/g (mean +/- SD) were: 34 +/- 6 in the control group, 2 +/- 2 in the CFP group, 15 +/- 6 in the M group, 19 +/- 9 in the CSH group and 43 +/- 13 in the PMS group. The differences between the CFP patients and all the other groups were statistically significant. These results indicate that the FC levels may be suitable as a diagnostic indication of CFP and capable of differentiating between this disorder and other causes of pancreatic insufficiency.

摘要

采用勃林格曼海姆公司新的比色法,对82例患有各种胰腺疾病的儿童24小时内采集的粪便样本中的胰凝乳蛋白酶(FC)水平进行了测定。根据以下病因将患者分为4组:胰腺囊性纤维化(CFP)、慢性严重肝脏疾病(CSH)、原发性吸收不良综合征(PMS)和非消化性原因导致的营养不良(M)。对照组包括48名年龄相仿的儿童。以U/g为单位(均值±标准差)的第24小时FC水平分别为:对照组34±6,CFP组2±2,M组15±6,CSH组19±9,PMS组43±13。CFP患者与所有其他组之间的差异具有统计学意义。这些结果表明,FC水平可能适合作为CFP的诊断指标,并且能够区分这种疾病与其他胰腺功能不全的原因。

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