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Risk factors for colorectal neoplasia in patients with underlying inflammatory bowel disease: A multicenter study

  • Xian Rui Wu
  • , Xiao Bin Zheng
  • , Yan Huang
  • , Qian Cao
  • , Hong Jie Zhang
  • , Ying Lei Miao
  • , Kai Fang Zou
  • , Min Chen
  • , Fa Ming Zhang
  • , Qiao Mei
  • , David Gonzalo
  • , Daniela Allende
  • , Pin Jin Hu
  • , Bo Shen
  • , Xiu Li Liu
  • , Ping Lan

Research output: Contribution to journalArticlepeer-review

Abstract

Background: This study sought to evaluate the risk factors for the development of colitis-associated neoplasia (CAN) in Chinese patients with inflammatory bowel disease (IBD). Methods: IBD patients who developed CAN between 1999 and 2016 were identified from eight medical centers. In addition to initial pathology evaluation, a CAN diagnosis was confirmed by two expert pathologists. Patients with CAN (n ¼ 29) were compared with non-CAN controls (n ¼ 87). Matching was performed for gender and IBD type with a ratio of three controls to one subject. Results: Of the 29 patients with CAN, 8 (27.6%) had colorectal cancer (CRC), 20 (69.0%) had a final diagnosis of low-grade dysplasia and 1 (3.4%) had high-grade dysplasia. Multivariate analysis revealed that an older age at the time of IBD diagnosis and a longer IBD duration were independent risk factors for the development of CAN, with odds ratios of 1.09 [95% confidence interval (CI): 1.04-1.14, P < 0.001] and 1.14 (95% CI: 1.03-1.27, P ¼ 0.013), respectively. Comparison between IBD patients with CRC and those with dysplasia indicated that the former were older at the time of IBD diagnosis (P ¼ 0.012) and had longer IBD durations (P ¼ 0.019). Conclusions: Older age at the time of IBD diagnosis and longer IBD duration were found to be associated with the development of CAN in IBD patients.

Original languageEnglish
Pages (from-to)67-73
Number of pages7
JournalGastroenterology Report
Volume7
Issue number1
DOIs
StatePublished - Feb 1 2019

Keywords

  • Colorectal neoplasia
  • Inflammatory bowel disease
  • Risk factor

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