Inflammatory polyps occur more frequently in inflammatory bowel disease than other colitis patients

Ulcerative Colitis (UC) and Crohn’s disease (CD) are the two major subtypes of Inflammatory Bowel Diseases (IBD). When patients have symptoms, signs and ileo-colonoscopic findings consistent with idiopathic IBD but cannot be classified clearly as UC or CD, they may be characterized as indeterminate colitis or IBD-Undifferentiated (IBDU) [1]. There are however many other types of colitis that are not consistent with CD, UC or IBDU. These have been referred to as non-IBD/non-infectious colitis (NIC) [2, 3].

The inflammation in UC is usually limited to the mucosal layer. It always involves the rectum, where the highest activity of inflammation is usually found, and in the majority of patients inflammation may extend more proximally in a continuous manner [4]. UC symptoms are typically characterized by chronic bloody diarrhea, tenesmus and abdominal pain.

In CD, the inflammation is transmural, affecting all layers of the gut wall and might involve any part of the gastrointestinal (GI) tract from mouth to anus. CD intestinal lesions show a discontinuous pattern most frequently affecting the terminal ileum and the colon.

About 1.4 million patients in the United States suffer from IBD. In most populations, the incidence of UC is slightly higher than CD. However, it has been observed that in African Americans CD may be more frequent than UC. A recent meta-analysis by Shi et al. reported significant variations in the demographic distribution, familial predisposition, phenotype, and outcomes of IBD between Caucasians, African Americans, Hispanics, and Asians [5]. However, in the study African Americans only made up 1% of the overall study population. Thus, there is a need for studies to understand the specific reason behind this variation in these understudied populations.

Patients with UC, as well as CD, have higher risk of dysplasia, that can be classified either as low grade dysplasia (LGD) or high grade dysplasia (HGD) [6]. African Americans are poorly represented in IBD studies despite the fact that, the population is known to be at a high risk of colonic neoplasia. NIC is a group of non-IBD colitis for which no infectious agent had been identified. Indeed apart from infectious colitis that are triggered by pathogens such as E. coli, Campylobacter and C. difficile, several other types of colitis are known to occur in the absence of such infectious agents [2, 3, 7‐9]. These include ischemic colitis, drug-induced colitis, and radiation colitis [2]. Whether NIC represents a risk factor for the development of colorectal neoplasia is uncertain [10‐13].

In IBD, colorectal neoplasia is thought to generally develop from flat low-grade or high dysplasia, or dysplasia-associated lesions or masses in the colon, now referred to as polypoid dysplasia [14]. This neoplastic transformation is triggered by multiple factors that induce several genetic and epigenetic changes in the colonocytes in a way that favors cells’ proliferation and reduce apoptosis. Dietary factors may be primary agents in such development [15‐17]. In addition, the human colon contains the greatest number of bacteria, with 100-fold more genes than the human host. These bacteria, their toxins and their interaction with diet lead to the production of carcinogenic compounds that might affect the colon mucosa homeostasis [15‐17]. African Americans are also known to have a high incidence of Colorectal cancer (CRC) that is more aggressive than in other populations [18]. Diet, gut microbiota and other factors trigger inflammatory reactions that might facilitate or accompany oncogenic transformation [19, 20]. Indeed, the term Colitis-Associated-Cancers (CAC) has been coined primarily to describe cancers that develop as an extension of persistent chronic inflammatory events usually IBD.

In this study, we investigated the association between IBD/NIC and polyps’ development and location in the predominantly African American population at our institution.

IBD is a chronic relapsing inflammatory disease that is distinguishable from other idiopathic inflammations affecting the gut [26]. IBD involving the colon can predispose to low and high grade dysplasia and ultimately lead to colon cancer [14]. However, there are few studies addressing this issue in AAs, a population at high risk of CRC that is witnessing a spike in IBD cases [27].

Studies show that IBD is more common in whites than other American ethnic minorities [28]. A systematic review done by Afzali et al., showed that the incidence and prevalence of IBD among minorities is increasing. Hispanics and Asians tend to get pancolonic UC [29]. There is often a significant limitation of access to treatment among minorities which predisposes them to poorer outcomes [5] A recent study that evaluated disparities of outcome among hospitalized patients with IBD, revealed that Hispanics have higher mortality when compared to non-Hispanic Whites [30]. AAs have a higher chance of recurrence of CD after surgery [31]and even AAs children have more severe disease when compared to white children [32].

The risk of CRC begins to increase 8 or 10 years after UC diagnosis with risk factors of younger age at diagnosis, longer duration, greater anatomical extent of colonic involvement, degree of inflammation, family history of CRC, and presence of primary sclerosing cholangitis [33]. Here, we analyzed patients with IBD for the presence or absence of colonic polyps. Using the ICD-9 and ICD-10 codes for colitis and a thorough review of clinical, pathological and colonoscopy reports, we identified 70 IBD and 415 NIC cases to evaluate for their correlation with colon polyp development. The two groups of patients showed similar sex distribution. AAs were highly represented in both groups: 73% in the NIC group and 81% in the IBD group. Our institution caters mainly to minority populations with a predominance of AAs. No gender difference between the two groups was noticed. There was a significant age difference between the two groups, IBD patients being younger.

CRC can develop either from an adenoma or from dysplasia developing from extended and long-lasting colitis. Another important factor of colorectal carcinogenesis is the age of the patients. Unlike the adenoma to carcinoma sequence seen in sporadic CRC patients, IBD patients likely develop carcinoma from an inflammation background [34‐36]. Indeed, the prevalence of inflammatory polyps was statistically higher in IBD patients when compared to NIC patients (55% vs. 12%, p = 0.007).

Most inflammatory polyps do not have malignant potential. After adjusting for age, sex and race, odds ratios of IBD for inflammatory polyps was 6.0 (p = 0.016) among patients with polyps. The higher rate of inflammatory polyps in IBD patients might also be the normal consequence of the chronic nature of these types of colitis as opposed to NIC. In IBD, chronic active long-lasting inflammation is a risk factor for the development of CRC [37].

NIC patients seem to have a lower risk. The non-statistical difference but still observed trend (p=0.08) in the greater rate of adenomatous polyps in IBD vs. NIC patients may be due to the low number of patients included in the study, the different duration of colitis, the different ages of patients, or the different immune and molecular mechanisms of inflammation in these two groups of colitis.

The IBD population in our study was at least 12 years younger than the NIC population (38 vs. 50 years) and much younger than the recommended colorectal cancer screening age guideline of 50 years. In general, it is known that it takes at least 8–10 years for dysplasia to start to appear in IBD patients greater than that expected and guidelines recommend that patients start to have surveillance colonoscopies after this time period. The only exceptions are patients with primary sclerosing cholangitis (PSC) where annual CRC screening is to being at IBD diagnosis and there is some evidence that the risk may be earlier in patients with onset of IBD greater than 50 years [38, 39]. In patients with IBD who were followed for more than 30 years, the CRC incidence was as high as 20% and 8% for UC and CD, respectively [26-28]. Our IBD sub-group analysis revealed that more polyps were present in the UC group when compared to CD (27% vs. 5%, p = 0.0001) which correlates with the higher vigilance and shorter follow-ups more often employed for UC than CD patients.

The extent, severity and duration of each colitis event may determine neoplastic transformation potential. Indeed, Abu Rashed et al. reported two cases where giant obstructive polyps were displayed in a 20 year old UC patient within 1 year of diagnosis and in a 71 year old asymptomatic CD colitis case as a result of the long exposure time and duration of colitis [40].

The limitations of this study include that it is retrospective, and it lacks some clinical data in IBD patients such as duration of disease and drugs taken during the course of the disease. The age of onset of IBD in our patients was not known. Prospective studies involving both IBD and NIC with a longer time of follow up, possibly for decades are needed to clarify the role of chronic active inflammation, as well as inflammatory and non-inflammatory polyps, in the development of CRC.

Even though we did not have a large number of Caucasians in our study population, our literature comparison of the prevalence of polyps in Caucasian with IBD versus AAs was comparable in one study [22], less when compared to Dixon et al. [21] and more compared to Lacucci et al. [25]. The study by Lee et al. involved 1484 patient with IBD. There were no control groups for comparison as the purpose of the study was to determine the prevalence and character of polyps. The prevalence of adenomatous polyps was 4.3% as compared to serrated polyps which was 1.4% (p < 0.001). The study design by Dixon et al. was similar to our study, although it only focused on distal adenomas found during flexible sigmoidoscopy and colonoscopy. The prevalence of distal polyps was 2.8% (p = 0.03). The lower prevalence of adenomas is likely due to the fact that only left sided adenomas were evaluated. The study by Lacucci et al. was a cohort study which followed IBD patients for 14 years. There was no control arm in this study. The higher prevalence of polyps in this study is likely attributed to the longer period of follow up of patients.

Our study showed that inflammatory polyps are more common in patients with IBD when compared to patients with other types of colitis. There were also more polyps detected in UC than CD patients. These polyps tend to develop in the same area as the colitis. The prevalence of adenomatous polyps (mostly polypoid masses with adenomatous features), although by frequency greater in IBD vs. NIC, was not statistically different. However, the numbers were limited and our study suggests that it may be valuable to examine a larger sample size to address this important question. Most studies report that inflammation plays a role in colorectal carcinogenesis, and this may include prevalence / incidence of adenomas. In IBD patients, neoplastic development occurs through a pathway where chronic inflammation seems to be the primary trigger and consistent player/stressor in the path to cancer. IBD patients with long duration of active disease need to be monitored through short interval surveillance colonoscopy as recommended in the guidelines. It is unclear if AAs need to be examined at shorter intervals. This should be a focus of future studies given their increased risk of CRC in this population.