Wang M, Kong WJ, Zhang JZ, Lu JJ, Hui WJ, Liu WD, Kang XJ, Gao F. Association of Helicobacter pylori infection with colorectal polyps and malignancy in China. World J Gastrointest Oncol 2020; 12(5): 582-591 [PMID: 32461789 DOI: 10.4251/wjgo.v12.i5.582]
Corresponding Author of This Article
Feng Gao, MD, PhD, Chairman, Professor, Department of Gastroenterology, People’s Hospital of Xinjiang Uygur Autonomous Region, No. 91, Tianchi Road, Tianshan District, Urumqi 830001, Xinjiang Uygur Autonomous Region, China. drxjgf@sina.com
Research Domain of This Article
Oncology
Article-Type of This Article
Retrospective Study
Open-Access Policy of This Article
This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
Author contributions: Wang M and Gao F designed the study; Wang M, Kong WJ and Lu JJ acquired the data and drafted the article; Hui WJ and Liu WD analyzed and interpreted the data; Zhang JZ and Kang XJ revised the article critically for important intellectual content; all the authors approved the version to be published.
Institutional review board statement: This study was reviewed and approved by the Ethics Committee of the People’s Hospital of Xinjiang Uygur Autonomous Region.
Informed consent statement: No consent was required as this was a retrospective study.
Conflict-of-interest statement: All authors declare no conflicts-of-interest related to this article.
Data sharing statement: The datasets collected and/or analyzed during the current study are available from the corresponding author upon reasonable request.
Open-Access: This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
Corresponding author: Feng Gao, MD, PhD, Chairman, Professor, Department of Gastroenterology, People’s Hospital of Xinjiang Uygur Autonomous Region, No. 91, Tianchi Road, Tianshan District, Urumqi 830001, Xinjiang Uygur Autonomous Region, China. drxjgf@sina.com
Received: December 29, 2019 Peer-review started: December 29, 2019 First decision: January 19, 2020 Revised: March 13, 2020 Accepted: March 24, 2020 Article in press: March 24, 2020 Published online: May 15, 2020 Processing time: 136 Days and 19.3 Hours
Abstract
BACKGROUND
Gastric Helicobacter pylori (H. pylori) infection is related to chronic gastritis, gastroduodenal ulcer, and gastric malignancies; whether this infection is related to colorectal polyps and colorectal cancer (CRC), remains debatable.
AIM
To investigate the relationship between gastric H. pylori infection and the risk of colorectal polyps and CRC.
METHODS
We retrospectively analyzed 3872 patients with colorectal polyps who underwent colonoscopy and pathological diagnosis. We also analyzed 304 patients with primary CRC. The characteristics of these patients were compared with those of the control group, which included 2362 patients with the normal intestinal mucosa. All subjects completed a 14C-urea breath test, bidirectional gastrointestinal endoscopy, and a biopsy on the same day. Data on the number, size, location, and pathology of the polyps, the location, and pathology of the CRC, the detection of H. pylori, and the incidence of H. pylori-associated atrophic gastritis or intestinal metaplasia were obtained. A logistic regression model was used to analyze the relationship between gastric infection due to H. pylori, and the incidence of colorectal polyps and CRC.
RESULTS
The prevalence of H. pylori infection was higher in the multiple polyps group than in the solitary polyp group and the control group [95% confidence interval (CI) = 1.02-1.31, P = 0.03; 95%CI: 2.12-2.74, P < 0.001]. The patients with adenomatous polyps had a higher incidence of H. pylori infection than patients with non-adenomatous polyps [59.95% vs 51.75%, adjusted odds ratio (OR) = 1.41, 95%CI: 1.24-1.60, P < 0.01]. Patients with H. pylori-associated atrophic gastritis or intestinal metaplasia were at high risk of CRC (adjusted OR = 3.46, 95%CI: 2.63-4.55, P < 0.01; adjusted OR = 4.86, 95%CI: 3.22-7.34, P < 0.01, respectively). The size and location of the polyps, the histopathological characteristics and the location of CRC were not related to H. pylori infection.
CONCLUSION
Our study demonstrates that the incidence of gastric H. pylori infection and H. pylori-associated atrophic gastritis or intestinal metaplasia elevates the risk of colorectal polyps and CRC.
Core tip: This study investigated the association of gastric Helicobacter pylori (H. pylori) infection with the risk of colorectal polyps and colorectal cancer (CRC). The results indicated that patients with H. pylori infection were 2.19 and 3.05 times more likely to develop colorectal polyps and CRC, respectively, than those without H. pylori infection. The prevalence of H. pylori infection was higher in the patient group with multiple polyps and colorectal adenomas than in those with a solitary polyp and non-adenomatous polyps, respectively. Gastric H. pylori infection and H. pylori-associated atrophic gastritis or intestinal metaplasia elevated the risk of colorectal polyps and CRC. Therefore, earlier and frequent colonoscopy is necessary.
Citation: Wang M, Kong WJ, Zhang JZ, Lu JJ, Hui WJ, Liu WD, Kang XJ, Gao F. Association of Helicobacter pylori infection with colorectal polyps and malignancy in China. World J Gastrointest Oncol 2020; 12(5): 582-591
Colorectal cancer (CRC) accounted for 881000 deaths in 2018, representing 9.8% of deaths worldwide. The incidence rate of CRC has increased to the extent that 1.8 million new CRC cases were diagnosed in 2018, according to recent data by the World Health Organization[1]. However, it is difficult to detect CRC early due to the lack of typical clinical symptoms, and 20% of patients who are asymptomatic at diagnosis may manifest with aggressive metastases[2]. The appearance of colorectal polyps and malignancy is a complex process that involves a combination of dietary habits, smoking, drinking and other environmental factors, and genetic susceptibility[3,4]. Colorectal polyps are abnormal protrusions on the surface of the large intestine[5] that are either non-adenomatous or adenomatous polyps. Colorectal adenomatous polyps are considered to be the most important precancerous lesions, developing into CRC through the adenomatous cancer sequence[6]. Therefore, early screening and detection of precancerous lesions can prevent the occurrence and development of CRC[7].
Gastric Helicobacter pylori (H. pylori) infection is a global public health concern, which has infected approximately[8] 50% of the world population, according to recent epidemiological studies[9]. The chronic inflammatory state caused by H. pylori infection is closely related to the occurrence of gastric cancer. H. pylori is listed as a class I carcinogen by the World Health Organization International Agency for Cancer Research[10] and is also involved in the tumorigenesis of extragastric target organs, such as lung cancer, and hepatocellular carcinoma[11]. Previous studies have indicated that gastric H. pylori infection increased the risk of colorectal tumors[12-16]. In contrast, however, several other reports have concluded that gastric H. pylori infection was not correlated with colorectal polyps or CRC[17-21]. Thus, the results of different research studies in different regions vary significantly. Therefore, the present study investigated the relationship between gastric H. pylori infection, colorectal polyps, and CRC in northwestern China. In addition, the study provides answers to questions regarding the necessity for colonoscopy screening in patients with gastric H. pylori infection.
MATERIALS AND METHODS
Study population
We reviewed the consecutive electronic medical records of patients who underwent gastroscopy and colonoscopy at a regional institution from January 2014 to January 2019. The inclusion criteria included: (1) Complete general information (including gender, age, ethnicity, past history, family history, etc.); (2) Age ≥ 18 years; (3) Patients who underwent bidirectional endoscopy (colonoscopy performed immediately after gastroscopy); (4) A clear pathological diagnosis of colorectal polyps or CRC; and (5) Detection of H. pylori infection. Exclusion criteria were as follows: (1) History of gastric cancer, peptic ulcer, and other malignant tumors; (2) Received antibiotics, NSAIDs, proton pump inhibitors or glucocorticoids in the past month; (3) Patients who underwent H. pylori eradication therapy previously, or radiation therapy, chemotherapy, and other specific treatment for tumors; (4) No total colonoscopy or biopsy; (5) Previous history of gastrointestinal surgery; (6) Presence of inflammatory bowel disease, familial adenoma, Gardner’s syndrome (a disease that affects the incidence of CRC); (7) A history of severe systemic disease; (8) A family history of polyposis, and (9) Patients who underwent repeated hospitalizations and a history of endoscopic polyp therapy. All patients provided consent for the study.
The diagnosis of normal intestinal mucosa, colorectal polyps, CRC, atrophic gastritis, and intestinal metaplasia was mainly based on endoscopic manifestations and histopathological examinations. Pathological diagnoses required confirmation by two pathologists. Referring to the fourth national consensus report on H. pylori infection treatment in 2012[22], H. pylori infection was defined as follows: Positive 14C-urea breath test and/or positive hematoxylin and eosin staining on gastric biopsies.
Study design
All subjects underwent complete colonoscopy and data regarding the location, size, shape, and number of polypoid lesions and the location of tumors were recorded. According to the size of the largest polyp, the patients with colorectal polyps were divided into those with a maximum diameter ≥ 1 cm and those with a maximum diameter ≤ 1 cm. According to the number of polyps, patients with a single polyp were included in the solitary polyp group, and those with ≥ 2 polyps were included in the multiple polyps group. Colorectal polyps and CRC were classified according to the location. The distal colorectum was defined as the anus to the splenic flexure, while the proximal colon was defined as the cecum to the splenic flexure, and patients with multiple lesions on both sides were defined as the whole colon. We divided H. pylori-related gastric disease into atrophy and intestinal metaplasia according to a method described previously[23]. Colorectal polyps including non-adenomatous and adenomatous polyps were considered. The prevalence of gastric H. pylori infection in CRC patients, patients with colorectal polyps, and the control group were compared. In addition, the prevalence of atrophic gastritis or intestinal metaplasia with gastric H. pylori infection among CRC patients, colorectal polyp patients, and the control group was also compared.
Statistical analysis
SPSS 17.0 was used for statistical analysis. Data for continuous variables were expressed as mean ± SD, and categorical data as a ratio or percentage. The t-test was used for data with a normal distribution. For comparisons among multiple groups of means (e.g., sex, BMI), one-way ANOVA was used. If the hypothesis of homogeneity of variance was not satisfied, Welch’s ANOVA was used. In addition, we used the χ2 test to compare categorical variables. A logistic regression model was applied to estimate the correlation between H. pylori infection, colorectal polyps, and CRC. After adjusting for gender and age, we calculated the odds ratio (OR) value and 95% confidence interval (95%CI). All variables with P < 0.05 were considered statistically significant and remained in the final models.
RESULTS
Patient characteristics
In total, 6538 patients were enrolled in our study (Figure 1). The characteristics of the participants are outlined in Table 1. Of these patients, 3872 were confirmed to have colorectal polyps and 304 had CRC by colorectal biopsy, and the remaining 2362 patients who had no abnormalities on colonoscopy, no history of polypectomy, and no clinical symptoms were classified as controls. The patient group with colorectal polyps included 2189 men and 1683 women. Their mean age was 53.01 ± 12.60 years. The patient group with CRC comprised 167 men and 137 women with an average age of 61.26 ± 12.94 years. The control group comprised 1355 men and 1007 women with a mean age of 45.81 ± 13.44 years. There were significant differences in age among the three groups (Welch F = 320.48, P < 0.001). However, there were no significant differences in gender, BMI, smoking, drinking, or family history of CRC among the three groups (P = 0.66; P = 0.06; P = 0.39; P = 0.28; P = 0.16, respectively). All patients underwent gastroscopy on the day of colonoscopy. The main indications for performing gastroscopy and colonoscopy are shown in Table 2.
Table 1 Baseline characteristics of the participants, n (%).
Figure 1 Flowchart of the study participants.
Controls were patients with neither colorectal polyps nor colorectal cancer. CRC: Colorectal cancer; H. pylori: Helicobacter pylori.
Table 2 The main indications for gastroscopy and colonoscopy.
Correlation between H. pylori infection and colorectal polyps
The colonoscopy findings and pathological characteristics of colorectal polyps are shown in Table 3. The prevalence of H. pylori infection in the colorectal polyp group (2134/3872, 55.11%) was higher than that in the control group (890/2362, 37.68%; P < 0.001). Multivariate logistic regression demonstrated that the patients with positive H. pylori infection in the colorectal polyp group had a higher OR after age and gender adjustment (adjusted OR = 2.19, 95%CI: 1.96-2.44, P < 0.001). The prevalence of H. pylori infection was higher in the multiple polyps group than that in the solitary polyp group and the control group (adjusted OR = 1.15, 95%CI: 1.02-1.31, P = 0.03; adjusted OR = 2.41, 95%CI: 2.12-2.74, P < 0.001). The positive rate of H. pylori infection in the adenomatous polyp group (952/1588, 59.95%) was higher than that in the non-adenomatous polyp group (1182/2284, 51.75%, adjusted OR = 1.41, 95%CI = 1.24-1.60, P < 0.001). The same association was found between the adenomatous polyps and control groups (adjusted OR = 2.53, 95%CI: 2.20-2.89, P < 0.001). However, the polyp size and locations were not associated with H. pylori (P = 0.26; P = 0.08). According to the polyp location, the P value of the proximal colon was 0.18, the distal colorectal was 0.23, and the whole colon was 0.51. Furthermore, based on the status of H. pylori infection and histopathological findings of the gastroscopy specimens, we found that the incidence of H. pylori-related atrophic gastritis in the colorectal polyp group was 34.99% (1355/3872), which was higher than that in the control group (541/2362, 22.90%, P < 0.001) (Table 4). H. pylori-associated atrophic gastritis was significantly associated with colorectal polyps compared to that in the control group (adjusted OR = 5.42, 95%CI: 4.67-6.30, P < 0.001). The prevalence of H. pylori-related intestinal metaplasia in the patient group with colorectal polyps was 8.96% (347/3872), which was higher than that in the control group (105/2362, 4.45%) (P < 0.001). Overall, H. pylori-associated intestinal metaplasia status was positively associated with colorectal polyps (adjusted OR = 5.88, 95%CI: 4.60-7.52, P < 0.001).
Table 3 The association between Helicobacter pylori infection, colorectal polyps, and colorectal cancer, compared with the control group.
Parameter
H. pylori positive [n (%)]
H. pylori negative [n (%)]
Adjusted OR (95%CI)
P value
Control group
890 (37.68)
1472 (62.32)
1
Colorectal polyp group
2134 (55.11)
1738 (44.89)
2.19 (1.96-2.44)
< 0.01
Polyp size
≥ 1 cm
529 (56.70)
404 (43.30)
2.33 (1.98-2.74)
< 0.01
< 1 cm
1605 (54.61)
1334 (45.39)
2.15 (1.92-2.41)
< 0.01
Polyp number
Solitary
942 (53.34)
824 (46.66)
1.98 (1.74-2.25)
< 0.01
Multiple
1192 (56.60)
914 (43.40)
2.41 (2.12-2.74)
< 0.01
Polyp histology
Adenomatous polyps
952 (59.95)
636 (40.05)
2.53 (2.20-2.89)
< 0.01
Non-adenomatous polyps
1182 (51.75)
1102 (48.25)
2.00 (1.77-2.26)
< 0.01
Polyp location
Proximal colon
732 (57.28)
546 (42.72)
2.49 (2.15-2.88)
< 0.01
Distal colorectal
1160 (53.51)
1008 (46.49)
1.98 (1.75-2.24)
< 0.01
Whole colon
242 (56.81)
184 (43.19)
2.37 (1.92-2.94)
< 0.01
CRC group
189 (62.17)
115 (37.83)
3.05 (2.33-3.99)
< 0.01
CRC location
Proximal colon
65 (67.01)
32 (32.99)
3.73 (2.39-5.82)
< 0.01
Distal colorectal
124 (59.90)
83 (40.10)
2.79 (2.04-3.81)
< 0.01
Table 4 The association of Helicobacter pylori-associated atrophic gastritis or intestinal metaplasia with colorectal polyps and colorectal cancer, compared with the control group.
H. pylori-associated atrophic gastritis [n (%)]
Adjusted OR (95%CI)
P value
H. pylori-associated intestinal metaplasia [n (%)]
Adjusted OR (95%CI)
P value
Control group
541 (22.90)
1
105 (4.45)
1
Colorectal polyp group
1355 (34.99)
5.42 (4.67-6.30)
< 0.01
347 (8.96)
5.88 (4.60-7.52)
< 0.01
CRC group
144 (47.37)
3.46 (2.63-4.55)
< 0.01
55 (18.09)
4.86 (3.22-7.34)
< 0.01
Correlation between H. pylori infection and CRC
The prevalence of H. pylori infection in the CRC group (189/304, 62.17%) was higher than that in the control group (890/2362, 37.68%) (P < 0.001). After adjustment for age and gender, multivariate logistic regression demonstrated that the patients with positive H. pylori infection in the CRC group had a higher OR (adjusted OR = 3.05, 95%CI: 2.33-3.99, P < 0.001) and among 304 patients with CRC, 270 cases had adenocarcinoma, including 167 cases with H. pylori infection (61.85%); 11 cases had neuroendocrine tumors, including 7 cases with H. pylori infection (63.64%); 14 cases had intramucosal cancer, including 9 cases with H. pylori infection (64.29%); 9 cases had signet ring cell cancer, including 6 cases with H. pylori infection (66.67%). The histopathological findings of CRC were not related to H. pylori (P > 0.05). Moreover, the χ2 test showed that CRC location was not correlated with H. pylori infection (P = 0.62). Compared to the control group, both H. pylori-related atrophic gastritis and intestinal metaplasia significantly increased the risk of CRC (adjusted OR = 3.46, 95%CI: 2.63-4.55, P < 0.001; adjusted OR = 4.86, 95%CI: 3.22-7.34, P < 0.001) (Table 2).
DISCUSSION
H. pylori infection plays an important role in the pathogenesis of gastrointestinal diseases[24]. However, whether gastric H. pylori infection increases the risk of colorectal polyps and CRC has been debated in various studies. This could be related to differences in the dietary habits of the study population, the patient population susceptible H. pylori, study sample size, and other factors. The H. pylori infection rate in China is more than 50%[25]. The relationship between gastric H. pylori infection and colorectal polyps and CRC in Northwest China is unclear; thus, we conducted this study. Some studies have shown that gender and age are related to H. pylori infection, colorectal polyps, and CRC[12,26]. Therefore, we conducted a multifactorial logistic regression analysis after adjusting for those factors. No significant differences in BMI, smoking, drinking, or family history of CRC among the subjects were found.
The results showed that the increase in H. pylori infection rate was positively correlated with the increase in colonic polyp incidence, polyp number, and malignancy, suggesting that H. pylori infection might be a risk factor for colorectal polyps and tumors. Patients with H. pylori infection are 2.19 times more likely to develop colorectal polyps and 3.05 times more likely to develop CRC than those who do not have H. pylori infection. Additionally, we found that the incidence of H. pylori infection coexisting with atrophic gastritis or intestinal metaplasia was higher in patients with colorectal polyps and CRC than in the control group. There was a significant correlation between H. pylori-associated gastropathy and colorectal adenomatous polyps or CRC. These results are consistent with those of previous studies[26,27]. A large-scale population-based study by Sonnenberg et al[28] also supports this argument. However, another study found no significant relationship between H. pylori infection and CRC. This may have been due to the broader age range and the limited number of patients[29].
There are a few plausible theories to explain the distribution of colorectal polyps and CRC and its association with H. pylori infection. Hong et al[30] found that gastric H. pylori infection was positively associated with an increased risk of proximal colorectal adenomatous polyps. Zhang et al[31] found that H. pylori infection mainly increased the risk of distal CRC. However, our study illustrates that gastric H. pylori infection could increase the risk in both proximal and distal colorectal neoplasms, which was consistent with the study by Inoue et al[32,33]. H. pylori infection causes microbiological changes in the digestive tract, increases the production of bile acids, causes DNA damage and activation, plays an important role in the proximal colonic mucosa, and increases the risk of proximal colonic polyps and malignancy[34]. Preclinical models have demonstrated that increased gastrin secretion caused by H. pylori infection has a mitogenic effect and selectively acts on the distal colon, thereby increasing the risk of distal colon polyps and malignancy[35]. These mechanisms may work synergistically. In addition, in our study, no significant differences were found among CRC patients with different pathological types and the prevalence of H. pylori infection. This may be because the most prevalent type of CRC is adenocarcinoma; however, studies with a larger sample size are needed to confirm this hypothesis.
The mechanism by which gastric H. pylori infection increases the incidence of colorectal polyps and CRC is not clear. Some studies have shown that gastrin gene expression is up-regulated in both colorectal polyps and CRC[36,37], and H. pylori infection can cause hypergastrinemia. Gastrin acts on gastrointestinal epithelial cells and can promote the formation of COX-2, which affects the occurrence, development, invasion, and metastasis of colorectal neoplasia[38]. Gastrin can also induce colonic mucosal cell proliferation to promote the development of CRC[39]. Moreover, from the perspective of gastrointestinal microecology, chronic gastritis caused by long-term H. pylori infection can lead to massive glandular atrophy and decreased gastric acid secretion. Low gastric acid may adversely affect the intestinal flora, cause bacterial overgrowth, colonic disorders, and colorectal carcinogenesis[40,41]. In addition, H. pylori infection may cause damage to colorectal epithelium through the chronic inflammatory response mediated by inflammatory factors such as interleukin-8[42].
The early diagnosis of CRC is relatively difficult. During the development of CRC, the normal mucosa develops into an adenoma and then to adenocarcinoma. This process provides opportunities for early detection and intervention of CRC. Early diagnosis and resection of colonic polyps can reduce the morbidity and mortality of CRC[43]. Further studies with regard to pathogenic mechanisms should be continued, which can help to develop relevant prevention and early detection strategies.
Some studies found that only the current situation of H. pylori infection could stimulate the immune response, thus inducing or perpetuating chronic inflammation of the gastrointestinal tract[44,45]. The strength of our study was that histopathological results and the 14C-urea breath test were used to determine H. pylori. A histopathological examination has high specificity and sensitivity in the diagnosis of gastric pathological changes and H. pylori infection. However, histopathological examination and the 14C-urea breath test can only diagnose the current infection of H. pylori, compared with the serological tests, which do not distinguish current or past infections. Therefore, our study explains the current relationship between H. pylori infection, colorectal polyps, and CRC more accurately. In addition, our sample size was relatively large, which is an advantage of this study.
Our study also has several limitations. First, we did not consider the possible effect of the duration of H. pylori infection on colorectal polyps and CRC. Secondly, we did not consider other confounding factors, such as constipation, eating habits, and metabolic syndrome. Thirdly, this was a single-center study. More investigation through prospective multicenter studies with large sample sizes should be conducted.
In conclusion, this study showed that gastric H. pylori infection and H. pylori-related gastric atrophic or intestinal metaplasia increased the risk of colorectal polyps and CRC. Early colonoscopy screening and surveillance is necessary to reduce the risk of colonic polyps and CRC in patients with H. pylori infection. Further investigation is required to understand whether the eradication of gastric H. pylori can reduce the occurrence of colorectal polyps and CRC.
ARTICLE HIGHLIGHTS
Research background
Gastric Helicobacter pylori (H. pylori) infection is a global public health problem. It is associated with chronic gastritis, gastroduodenal ulcer and gastric malignancies. The relationship between H. pylori infection and the risk of colorectal polyps and colorectal cancer (CRC) has also received extensive attention in recent years.
Research motivation
There is still no clear conclusion regarding the relationship between gastric H. pylori infection and the risk of colorectal polyps and CRC.
Research objectives
Our main purpose was to investigate the correlation between gastric H. pylori infection and the risk of colorectal polyps and CRC, which is essential for the early screening and detection of colorectal precancerous lesions.
Research methods
A retrospective analysis of 6538 patients who underwent colonoscopy was conducted. The patients were divided into three groups: The CRC group, colorectal polyps group, and the control group. All subjects completed a 14C-urea breath test, bidirectional gastrointestinal endoscopy, and a biopsy on the same day. The characteristics of gastrointestinal endoscopy, pathology of gastritis, polyps and CRC, and the detection of H. pylori in the three groups were analyzed.
Research results
Patients with H. pylori infection were 2.19 times more likely to develop colorectal polyps and 3.05 times more likely to develop CRC than those who did not have H. pylori infection. The prevalence of H. pylori infection was higher in the multiple polyps group than in the solitary polyp group, and was also higher in the adenomatous polyps group than in the non-adenomatous polyps group. Additionally, we found that the incidence of H. pylori infection coexisting with atrophic gastritis or intestinal metaplasia was higher in patients with colorectal polyps and CRC than in the control group. The size and location of polyps, the histopathological characteristics and the location of CRC were not related to H. pylori infection.
Research conclusions
The incidence of colonic polyps and CRC in patients with gastric H. pylori infection and H. pylori-associated atrophic gastritis or intestinal metaplasia was significantly higher than that in the normal population. Early and frequent colonoscopy is necessary to reduce the risk of colonic polyps and CRC in patients with H. pylori infection. The mechanism by which gastric H. pylori infection increases the incidence of colorectal polyps and CRC should be further studied.
Research perspectives
This study demonstrates that early colonoscopy screening and surveillance are necessary to reduce the risk of colonic polyps and CRC in patients with H. pylori infection. The future direction of research is to evaluate whether the eradication of gastric H. pylori can reduce the occurrence of colorectal polyps and CRC. Large-scale and long-term follow-up investigations are needed.
Senore C, Giovo I, Ribaldone DG, Ciancio A, Cassoni P, Arrigoni A, Fracchia M, Silvani M, Segnan N, Saracco GM. Management of Pt1 tumours removed by endoscopy during colorectal cancer screening: Outcome and treatment quality indicators.Eur J Surg Oncol. 2018;44:1873-1879.
[PubMed] [DOI][Cited in This Article: ][Cited by in Crossref: 11][Cited by in F6Publishing: 10][Article Influence: 1.7][Reference Citation Analysis (0)]
Lee JY, Park HW, Choi JY, Lee JS, Koo JE, Chung EJ, Chang HS, Choe J, Yang DH, Myung SJ, Jung HY, Yang SK, Byeon JS. Helicobacter pylori Infection with Atrophic Gastritis Is an Independent Risk Factor for Advanced Colonic Neoplasm.Gut Liver. 2016;10:902-909.
[PubMed] [DOI][Cited in This Article: ][Cited by in Crossref: 17][Cited by in F6Publishing: 19][Article Influence: 2.7][Reference Citation Analysis (0)]
Patel S, Lipka S, Shen H, Barnowsky A, Silpe J, Mosdale J, Pan Q, Fridlyand S, Bhavsar A, Abraham A, Viswanathan P, Mustacchia P, Krishnamachari B. The association of H. pylori and colorectal adenoma: does it exist in the US Hispanic population?J Gastrointest Oncol. 2014;5:463-468.
[PubMed] [DOI][Cited in This Article: ][Cited by in F6Publishing: 14][Reference Citation Analysis (0)]
Limburg PJ, Stolzenberg-Solomon RZ, Colbert LH, Perez-Perez GI, Blaser MJ, Taylor PR, Virtamo J, Albanes D. Helicobacter pylori seropositivity and colorectal cancer risk: a prospective study of male smokers.Cancer Epidemiol Biomarkers Prev. 2002;11:1095-1099.
[PubMed] [DOI][Cited in This Article: ]
Liu WZ, Xie Y, Cheng H, Lv NH, Hu FL, Zhang WD, Zhou LY, Chen Y, Zeng ZR, Wang CW, Xiao SD, Pan GZ, Hu PJ. The fourth national consensus report on the treatment of Helicobacter pylori infection.Zhonghua Xiaohua Zazhi. 2012;32:655-661.
[PubMed] [DOI][Cited in This Article: ]
Inoue I, Mukoubayashi C, Yoshimura N, Niwa T, Deguchi H, Watanabe M, Enomoto S, Maekita T, Ueda K, Iguchi M, Yanaoka K, Tamai H, Arii K, Oka M, Fujishiro M, Takeshita T, Iwane M, Mohara O, Ichinose M. Elevated risk of colorectal adenoma with Helicobacter pylori-related chronic gastritis: a population-based case-control study.Int J Cancer. 2011;129:2704-2711.
[PubMed] [DOI][Cited in This Article: ][Cited by in Crossref: 45][Cited by in F6Publishing: 52][Article Influence: 4.0][Reference Citation Analysis (0)]
Finley GG, Koski RA, Melhem MF, Pipas JM, Meisler AI. Expression of the gastrin gene in the normal human colon and colorectal adenocarcinoma.Cancer Res. 1993;53:2919-2926.
[PubMed] [DOI][Cited in This Article: ]
Kountouras J, Kapetanakis N, Zavos C, Polyzos SA, Kouklakis G, Venizelos I, Nikolaidou C, Tzilves D, Paikos D, Katsinelos P, Giouleme O, Soufleris K. Active Helicobacter pylori infection is associated with colorectal mucosa-adenomatous polyp--early and advanced adenocarcinoma sequence.Scand J Gastroenterol. 2014;49:381-382.
[PubMed] [DOI][Cited in This Article: ][Cited by in Crossref: 2][Cited by in F6Publishing: 2][Article Influence: 0.2][Reference Citation Analysis (0)]
