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.

Insights

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.