Oral administration of a chymotrypsin-labile peptide--a new test of exocrine pancreatic function in man (PFT)
One gram N-benzoyl-L-tyrosyl PABA was orally administered to 24 controls, 15 patients with chronic exocrine pancreatic disease, 13 patients after an attack of acute pancreatitis, two patients with gluten-sensitive enteropathy, and 10 patients with biliary tract disease, peptic ulcer, or other pathol...
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Published in: | Gut Vol. 17; no. 1; pp. 27 - 32 |
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Main Authors: | , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
England
BMJ Publishing Group Ltd and British Society of Gastroenterology
01-01-1976
BMJ Publishing Group LTD |
Subjects: | |
Online Access: | Get full text |
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Summary: | One gram N-benzoyl-L-tyrosyl PABA was orally administered to 24 controls, 15 patients with chronic exocrine pancreatic disease, 13 patients after an attack of acute pancreatitis, two patients with gluten-sensitive enteropathy, and 10 patients with biliary tract disease, peptic ulcer, or other pathology of the gastrointestinal tract. In the presence of chymotrypsin, PABA is split from the peptide and excreted in the urine. The amount of PABA excreted serves as a parameter of exocrine pancreatic function. In 51 patients, exocrine pancreatic secretion was also assessed by the Lundh test. In the control group a mean of 59-6 +/- 12-2% (mean +/- 2 SD) of the peptide-PABA was excreted over a period of six hours. PABA excretion in exocrine pancreatic deficiency was significantly less (P less than 0.001) than in controls. With one exception no overlap of data was noted. In the group with exocrine pancreatic deficiency, a significant relationship was shown between the PFT and the Lundh test. Reproducibility in duplicate test was excellent. The present data justify further investigations of this procedure as a possible new oral test of exocrine pancreatic function. |
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Bibliography: | href:gutjnl-17-27.pdf istex:4926DFD5AB878E8EC245810FBCF5C6724C6BDACD local:gutjnl;17/1/27 PMID:1269977 ark:/67375/NVC-4V203C6M-W ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0017-5749 1468-3288 1458-3288 |
DOI: | 10.1136/gut.17.1.27 |