The study aims to describe alterations in the contact activation system during active and inactive ulcerative colitis. Contact activation system measures are compared in a cross sectional (healthy controls vs. active disease) and longitudinal (active diasese vs. inactive disease) fashion.
We include and follow up on 102 adults with active ulcerative colitis. Visits are week 0 (inclusion), 6, 12 and 26 (end of study). We obtain plasma and fecal samples at each visit. Whereas we obtain colonic tissue samples only at inclusion and end of study. Registered data are: * Demographics realate to UC and general wellbeing. * Clinical parametres used for UC evaluation are PRO2, SCCAI, CRP, fecal calprotectin, Mayo endoscopic subscore and Nancy index. * The contact activation system is characterised by FXII, prekallikrein, kallikrein generation, HK, cHK (specific to plasma kallikrein), cHK (specific to tissue kallikrein), C1 inhibitor and Kallistatin. * Polymerized alpha-1-antitrypsin is characterised by the degree of polymerization and the capacity to activate the contact activation system.
Study Type
OBSERVATIONAL
Enrollment
102
Continuous measures of disease activity and activity in the contact activation system.
Department of Medical Gastroenterology, University Hospital of Southern Denmark
Esbjerg, Denmark
Clinical disease activity.
PRO2 score, 0-6 points. A score of one or more defines active disease.
Time frame: End of study (August 28th, 2024)
Endoscopic disease activity.
Mayo endoscopic score, 0-3 points. A score of one or more defines active disease.
Time frame: End of study (August 28th, 2024)
Kallikrein generation
The assay reflects the downstream activation of the contact activation system which allows us to determine the amount of kallikrein generated in each sample.
Time frame: End of study (August 28th, 2024)
Polymerised alpha-1-antitrypsin in participants
A Western blot verifies the present of polymerised alpha-1-antitrypsin.
Time frame: End of study (August 28th, 2024)
Polymerised alpha-1-antitrypsin as an activator of the contact activation system
We add polymerised alpha-1-antitrypsin to our kallikrein generation. If kallikrein is generated the polymers activated the system.
Time frame: End of study (August 28th, 2024)
Localisation of contact activation system components in tissue samples
Immunhistochemical methods locate FXII, PK, cHK (specific to plasma kallikrein and tissue kallikrein), C1 Inhibitor, and Kallistatin in biopsies.
Time frame: End of study (August 28th, 2024)
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