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Factors affecting plasma postheparin diamine oxidase activity
J S Thompson1, D A Burnett, W P Vaughan
1Department of Surgery, University of Nebraska Medical Center, Omaha 68198-3280.
Digestive Diseases and Sciences
|November 1, 1991
Summary
Plasma diamine oxidase (DAO) activity is lower in Crohn's disease (CD) patients. DAO activity responds to therapy and recurrence, suggesting its potential for monitoring CD patients.
Area of Science:
- Gastroenterology
- Biochemistry
- Clinical Medicine
Background:
- Plasma postheparin diamine oxidase (DAO) activity is explored as a marker for intestinal disorders.
- The precise mechanisms behind reduced plasma DAO activity in Crohn's disease (CD) remain unclear.
- Understanding factors influencing DAO activity is crucial for its clinical application in CD.
Purpose of the Study:
- To investigate the impact of disease extent, location, prior surgery, and therapy on plasma DAO activity in CD patients.
- To correlate plasma DAO activity with disease severity measured by the Crohn's Disease Activity Index (CDAI).
Main Methods:
- Measured plasma postheparin DAO activity in 37 CD patients and 30 healthy volunteers.
- Assessed disease extent (small bowel and colon), location, history of resection, and current therapy.
- Compared DAO activity between patient groups and correlated it with CDAI.
Main Results:
- CD patients exhibited significantly lower DAO activity compared to controls, with higher CDAI.
- No direct correlation was found between DAO activity and CDAI.
- Effective therapy increased DAO activity and decreased CDAI; recurrence showed the opposite trend.
- DAO activity was not influenced by the extent or location of small bowel or colonic disease, nor by prior enterectomy or colectomy.
Conclusions:
- Plasma DAO activity is altered in CD and responds predictably to therapeutic interventions and disease recurrence.
- DAO activity may serve as a valuable tool for monitoring individual CD patient progress.
- The lack of correlation with disease extent/location suggests DAO activity is not solely dependent on enterocyte mass.