Metabolism of the colonic mucosa of patients with ulcerative colitis (UC; n=31) and Crohn's disease (CD; n=26) and normal mucosa (control, n=26) was investigated using in vitro high-resolution proton magnetic resonance spectroscopy. Of the 31 UC patients, 20 were in the active phase and 11 were in t
Similarity in the metabolic profile in macroscopically involved and un-involved colonic mucosa in patients with inflammatory bowel disease: an in vitro proton (1H) MR spectroscopy study
โ Scribed by Uma Sharma; Rajiv R. Singh; Vineet Ahuja; Govind K. Makharia; Naranamangalam R. Jagannathan
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- English
- Weight
- 772 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0730-725X
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โฆ Synopsis
Background:
The histological extent of inflammatory bowel disease (ibd) is greater than that evident by colonoscopic evaluation. we hypothesized that metabolic profile in macroscopically un-involved colonic mucosa in ibd is similar to that of controls with healthy colon. we thus assessed the differences in metabolic profile in macroscopically involved and un-involved colonic mucosa of ibd patients to further substantiate the extent of disease.
Patients and methods:
Colonic mucosal biopsies were obtained and snap frozen from both the macroscopically un-involved and involved colonic mucosa of ibd patients and macroscopically normal colonic mucosa of controls and were subjected to in-vitro high-resolution proton ((1)h) magnetic resonance (mr) spectroscopy and the concentrations of metabolites were determined.
Results:
Thirty-two metabolites were assigned in the proton mr spectrum of colonic mucosa of ibd patients. the concentrations of amino acids (isoleucine, leucine, valine, arginine, lysine, glutamine/glutamate, alanine), membrane metabolites (choline, glycerophosphorylcholine/phosphorylcholine), glycolytic product (lactate) and short chain fatty acid (formate) were significantly lower while significantly high level of glucose were observed in the macroscopically un-involved colonic mucosa of ibd patients compared to the macroscopically normal mucosa of controls. there was no significant difference in the concentrations of metabolites in macroscopically involved and un-involved colonic mucosa of ibd patients.
Conclusions:
The metabolic profile in macroscopically un-involved colonic mucosa of ibd patients is similar to that of macroscopically involved mucosa but different from colonic mucosa of controls. this suggests that even macroscopically un-involved colonic mucosa is metabolically abnormal and may explain the increase in extent of disease with time.
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