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. 2007 Oct;133(4):1099-105; quiz 1340-1.
doi: 10.1053/j.gastro.2007.08.001. Epub 2007 Aug 2.

Histologic inflammation is a risk factor for progression to colorectal neoplasia in ulcerative colitis: a cohort study

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Histologic inflammation is a risk factor for progression to colorectal neoplasia in ulcerative colitis: a cohort study

Roopali Bansal Gupta et al. Gastroenterology. 2007 Oct.

Abstract

Background & aims: Although inflammation is presumed to contribute to colonic neoplasia in ulcerative colitis (UC), few studies have directly examined this relationship. Our aim was to determine whether severity of microscopic inflammation over time is an independent risk factor for neoplastic progression in UC.

Methods: A cohort of patients with UC undergoing regular endoscopic surveillance for dysplasia was studied. Degree of inflammation at each biopsy site had been graded as part of routine clinical care using a highly reproducible histologic activity index. Progression to neoplasia was analyzed in proportional hazards models with inflammation summarized in 3 different ways and each included as a time-changing covariate: (1) mean inflammatory score (IS-mean), (2) binary inflammatory score (IS-bin), and (3) maximum inflammatory score (IS-max). Potential confounders were analyzed in univariate testing and, when significant, in a multivariable model.

Results: Of 418 patients who met inclusion criteria, 15 progressed to advanced neoplasia (high-grade dysplasia or colorectal cancer), and 65 progressed to any neoplasia (low-grade dysplasia, high-grade dysplasia, or colorectal cancer). Univariate analysis demonstrated significant relationships between histologic inflammation over time and progression to advanced neoplasia (hazard ration (HR), 3.0; 95% CI: 1.4-6.3 for IS-mean; HR, 3.4; 95% CI: 1.1-10.4 for IS-bin; and HR, 2.2; 95% CI: 1.2-4.2 for IS-max). This association was maintained in multivariable proportional hazards analysis.

Conclusions: The severity of microscopic inflammation over time is an independent risk factor for developing advanced colorectal neoplasia among patients with long-standing UC.

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Figures

Figure 1
Figure 1
Histological Activity Index
  1. Inactive colitis with no cryptitis or crypt abscesses; HAI=0.

  2. Mildly active colitis with one crypt abscess (arrow); HAI=1

  3. Moderately active colitis with cryptitis involving >50% of crypts (arrows); HAI=2.

  4. Severely active colitis with ulceration; HAI=3.

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References

    1. Itzkowitz SH, Harpaz N. Diagnosis and management of dysplasia in patients with inflammatory bowel diseases. Gastroenterology. 2004;126:1634–48. - PubMed
    1. Eaden JA, Abrams KR, Mayberry JF. The risk of colorectal cancer in ulcerative colitis: a meta-analysis. Gut. 2001;48:526–35. - PMC - PubMed
    1. Ekbom A, Helmick C, Zack M, Adami HO. Ulcerative colitis and colorectal cancer. A population-based study. N Engl J Med. 1990;323:1228–33. - PubMed
    1. Connell WR, Lennard-Jones JE, Williams CB, Talbot IC, Price AB, Wilkinson KH. Factors affecting the outcome of endoscopic surveillance for cancer in ulcerative colitis [see comments] Gastroenterology. 1994;107:934–44. - PubMed
    1. Lynch DA, Lobo AJ, Sobala GM, Dixon MF, Axon AT. Failure of colonoscopic surveillance in ulcerative colitis [see comments] Gut. 1993;34:1075–80. - PMC - PubMed

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