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Published on: June 15, 2018
Association Between Serological Markers and Crohn's Disease Activity
Zunirah Ahmed1, Michael Lysek2, Nan Zhang3
1Department of Medicine, University of Alabama at Birmingham Montgomery, AL 36116, USA.
Insights
High anti-CBir1 IgG levels in Crohn's disease (CD) patients correlate with increased disease activity. Further research is needed to determine if routine testing for this marker can predict a more active clinical course in CD.
Area of Science:
- Gastroenterology
- Immunology
- Clinical Medicine
Background:
- Crohn's disease (CD) is a type of inflammatory bowel disease (IBD).
- Serological markers are being investigated for their potential to predict disease activity in CD.
- Understanding predictors of CD activity is crucial for patient management.
Purpose of the Study:
- To investigate the association between six specific serological markers and Crohn's disease activity.
- To determine if baseline levels of these antibodies can predict the rate of active clinical disease.
Main Methods:
- Retrospective cohort study of adults with CD followed for at least 1 year.
- Baseline measurement of six serological markers: ASCA-IgA, ASCA-IgG, anti-OmpC IgA, anti-CBir1 IgG, anti-A4Fla2 IgG, and anti-FlaX IgG.
- Poisson regression analysis to assess the relationship between baseline markers and active disease rate.
Main Results:
- High baseline anti-CBir1 IgG levels were significantly associated with a doubled likelihood of active CD (IRR 2.06, P = 0.0032) after adjusting for covariates.
- A high A4Fla2 IgG level showed a trend towards association with active CD in unadjusted analysis, but this was not significant after adjustment.
- The other four antibodies did not demonstrate predictive value for clinical course.
Conclusions:
- Elevated anti-CBir1 IgG levels at baseline are linked to a higher probability of active Crohn's disease.
- Further investigation is required to ascertain the clinical utility of routine anti-CBir1 IgG testing for predicting CD activity.
Background:
The aim was to study the association between six serological markers and Crohn's disease (CD) activity at an inflammatory bowel disease (IBD) referral center.
Methods:
We designed a retrospective cohort study using adults (> 18 years) with CD followed for at least 1 year at University of Alabama at Birmingham. Baseline serological markers ASCA-IgA, ASCA-IgG, anti-OmpC IgA, anti-CBir1 IgG, anti-A4Fla2 IgG and anti-FlaX IgG were drawn at initial visit. Poisson regression was used to assess the longitudinal relationship between these markers drawn at baseline and rate of active clinical disease during follow-up.
Results:
Each marker, from 135 patients, was categorized into high vs. low. A Poisson regression model adjusted for age, gender, race, duration of disease, obesity, proton pump inhibitor; steroid and thiopurine use, and disease location demonstrated that CD patients with high anti-CBir1 IgG at baseline were approximately twice more likely to have active clinical disease (incidence rate ratio (IRR) 2.06, 95% confidence interval (CI) 1.28 - 3.33, P = 0.0032). The unadjusted Poisson regression model for A4Fla2 IgG antibody level did suggest that a high A4Fla2 IgG at baseline was associated with a higher likelihood of active CD (IRR 1.64, 95% CI 1.07, 2.53, P = 0.0238) which however, upon adjustment based on effect size, was not significant. The other four antibodies did not appear to predict clinical course.
Conclusions:
High levels of anti-CBir1 IgG appear to be associated with a greater likelihood of active CD. Whether routine baseline testing for anti-CBir1 IgG to predict a more active clinical course is warranted needs more research.
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