CC BY 4.0 · Journal of Coloproctology 2024; 44(02): e111-e119
DOI: 10.1055/s-0044-1787284
Original Article

The Association between Anthropometric Indicators and Colorectal Polyps and Diverticulosis

Sahar Najafi Mobaraki
1   Department of Gastroenterology, Gastrointestinal and Liver Diseases Research Center, Guilan University of Medical Sciences, Rasht, Iran
,
Farahnaz Joukar
1   Department of Gastroenterology, Gastrointestinal and Liver Diseases Research Center, Guilan University of Medical Sciences, Rasht, Iran
,
Saman Maroufizadeh
2   Department of Biostatistics, School of Health, Guilan University of Medical Sciences, Rasht, Iran
,
Massood Baghaee
1   Department of Gastroenterology, Gastrointestinal and Liver Diseases Research Center, Guilan University of Medical Sciences, Rasht, Iran
3   Department of Internal Medicine, School of Medicine, Razi Hospital, Guilan University of Medical Sciences, Rasht, Iran
,
Mehrnaz Asgharnezhad
1   Department of Gastroenterology, Gastrointestinal and Liver Diseases Research Center, Guilan University of Medical Sciences, Rasht, Iran
,
1   Department of Gastroenterology, Gastrointestinal and Liver Diseases Research Center, Guilan University of Medical Sciences, Rasht, Iran
› Author Affiliations
Funding No funding.
 

Abstract

Introduction Colonic polyps and diverticulosis are common colon findings on colonoscopy. One of the risk factors of colorectal polyps and diverticulosis is the anthropometric index. Therefore, we aimed to investigate the association between the anthropometric index and colorectal findings.

Methods In this cross-sectional study, we included 536 patients referred to Razi Hospital, Rasht, Iran, in 2023 for colonoscopy evaluation. Demographical data, clinical characteristics, and colonoscopy findings were recorded for further analysis. All data were analyzed using SPSS.16 by considering a significant level < 0.05

Results The results showed that 35.4% of the patients had polyps, with the majority having a single polyp. The patient's mean age was 55.94 ± 13.33 years; most were females (54.1%). The most common type of polyp was pedunculated, and most were located in the sigmoid colon. The prevalence of diverticular was 11.4%, most of which were also located in the sigmoid colon. Obesity was significantly associated with an increased risk of polyps, while overweight individuals had a higher risk of diverticula (P < 0.05). Age, rural residence, and low physical activity level were identified as factors associated with an increased risk of polyps and diverticula.

Conclusion The findings suggest that obesity and overweight are risk factors for polyps and diverticula, respectively. Further research is warranted to explore additional factors and develop preventive strategies for colorectal diseases. These results support the need for preventive strategies and screening programs to reduce the risk of future colorectal lesions.


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Introduction

Colorectal polyps and diverticulosis are two common gastrointestinal conditions that affect a significant portion of the population worldwide. Colorectal polyps and diverticulosis are prevalent conditions that impact the gastrointestinal health of individuals across different age groups and geographical locations.[1] Colorectal polyps are abnormal growths that develop on the inner lining of the colon or rectum.[2] While diverticulosis refers to the formation of small pouches in the lining of the large intestine.[3] According to epidemiological studies, the prevalence of colorectal polyps varies widely in the general population.[4] [5] [6] The incidence of diverticulosis increases with age, affecting approximately individuals younger than 40.[7] [8] Colonic diverticulosis in any location may lead to an increased incidence of adenoma and colorectal polyps.[9] [10] [11]

The etiology of colorectal polyps and diverticulosis involves a complex interplay of genetic, environmental, and lifestyle factors. While the exact mechanisms underlying their development are not fully understood, several hypotheses have been proposed. Colorectal polyps may arise from genetic mutations, chronic inflammation, and dietary factors.[12] [13] Anthropometric indicators, waist-to-hip ratio (WHR), and body mass index (BMI) indicators of central adiposity have also been linked to an elevated risk of these colorectal disorders. Abdominal fat accumulation is more metabolically active and associated with higher levels of inflammation and insulin resistance than overall body fat.[14] [15] [16]

On the other hand, diverticulosis is thought to result from increased colonic pressure and structural alterations in the intestinal wall.[17] Factors such as a low-fiber diet, obesity, a sedentary lifestyle, and aging contribute to the development of diverticulosis. Chronic constipation and prolonged straining during bowel movements may also play a role in the formation of diverticular pouches. Obesity, defined as a high BMI, has been consistently associated with an increased risk of both conditions.[18] [19] Excess body weight and abdominal adiposity are thought to promote chronic inflammation, insulin resistance, and hormonal imbalances, which can contribute to developing colorectal polyps and diverticulosis.[20] [21] Obesity and central adiposity play a prominent role in their development, highlighting the importance of maintaining a healthy weight and daily physical activity.[22] [23]

However, further research is needed to elucidate the underlying mechanisms and establish more robust causal relationships. By better understanding the association between anthropometric indicators and colorectal polyps and diverticulosis, healthcare professionals can enhance preventive strategies, early detection, and management of these gastrointestinal disorders; in this regard, we conducted this study to investigate the association between BMI and WHR, and prevalence of colorectal polyp and diverticulosis.


#

Methods

Study Design

This cross-sectional study was conducted on 536 patients referred for colonoscopy evaluation at the Razi Hospital, Rasht, Iran, in 2023. Patients were selected through a convenience sampling method during 2023. The demographical and clinical data of patients, including age, gender, habitat (urban or rural), educational level (illiterate, under diploma, diploma, and with a university degree), history of smoking, alcohol consumption, occupational exposure, family history of colorectal cancer, level of physical activity according to International Physical Activity Questionnaires (IPAQ)[24] as low, middle, and high, BMI as low weight BMI < 18.5 kg/m2), average weight (BMI = 18.5–24.99 kg/m2), overweight (BMI = 25–29.9 kg/m2), and obese (BMI≥30 kg/m2, and WHR as low, normal, and high-risk, were recorded. Moreover, colonoscopy findings included types and numbers of polyps (pedunculated or sessile), size of polyps (<5mm, 5-10 mm, and >10 mm), numbers of diverticula, and location of polyps and diverticula (rectum, sigmoid colon, descending colon, ascending colon, and cecum). Patients with a history of gastrointestinal and other underlying diseases, inflammation, malignancies, and colectomy were excluded from the study. This study was approved by the ethical committee of the Guilan University of Medical Sciences (IR.GUMS.REC.1401.505). All patients gave their consent to participate in the study.


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Statistical Analysis

The variables are number (percentage) and mean ± standard deviation (SD). Chi-square and independent t-tests were performed to assess the association between groups. Moreover, the Cochran-Armitage test was used to compare the studied outcomes in different levels of BMI and WHR in three models (Model 1: Unadjusted, Model 2: Adjusted for age and gender, and Model 3: Adjusted for age, gender, etc.). Logistic regression was applied to evaluate the association between exposure and outcomes. The results were presented as crude odds ratio (OR) and adjusted odds ratio (aOR) with 95% confidence intervals (95% CI). The data was analyzed using SPSS version 16 software, and a significance level of 0.05 was considered.


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#

Results

The frequency of demographical data and clinical characteristics of the patients referred for colonoscopy have been illustrated in [Table 1]. According to the results, the patient's mean age, BMI, and WHR were 55.94 ± 13.33 years, 27.59 ± 4.99 kg/m2, and 0.92 ± 0.07, respectively. Most of the studied population were aged upper 60, female gender, under diploma, urban residents with high BMI (overweight and obese), high-risk WHR, and low physical activity levels.

Table 1

Frequency of demographical data and clinical characteristics of patients referred for colonoscopy (n = 536)

Variables

Frequency (%)

Age

(year)

≤40

71 (13.2)

41-50

84 (15.7)

51-60

169 (31.5)

60<

212 (39.6)

Gender

Male

246 (45.9)

Female

290 (54.1)

Educational level

Illiterate

106 (19.8)

Under diploma

267 (49.8)

Diploma

122 (22.8)

University degree

41 (7.6)

Habitat

Urban

359 (67.0)

Rural

177 (33.0)

BMI

(kg/m2)

18.5<

12 (2.2)

18.5≤BMI < 25

164 (30.6)

25≤BMI < 30

195 (36.4)

30≤

165 (30.8)

WHR

Low-risk

189 (35.3)

Normal-risk

98 (18.3)

High-risk

249 (46.5)

Physical activity

Low

364 (67.9)

Middle

153 (28.5)

High

19 (3.5)

Smoking

Yes

48 (9.0)

No

488 (91.0)

Alcohol consumption

Yes

7 (1.3)

No

529 (98.7)

Occupational exposure

Yes

27 (4.9)

No

509 (95.1)

Family history of colorectal cancer

Yes

84 (15.7)

No

452 (84.3)

Number of polyps

One

137 (25.6)

Two

35 (6.5)

Three

14 (2.6)

Four

4 (0.7)

Types of polyp

(Among 265 detected polyps)

Pedunculated

240 (90.6)

Sessile

25 (9.4)

Size of polyps

(Among 265 detected polyps)

< 5mm

32 (12.1)

5-10 mm

159 (60.0)

>10mm

74 (27.9)

Location of polyp

(Among 265 detected polyps)

Rectum

52 (19.6)

Sigmoid colon

63 (23.8)

Descending colon

36 (13.6)

Transvers colon

54 (20.4)

Ascending colon

49 (18.5)

Cecum

11 (4.2)

Number of diverticula

In one location

32 (6.0)

In two location

10 (1.9)

In three location

8 (1.5)

In four location

11 (2.1)

Location of diverticula

(Among 120 locations of diverticula)

Rectum

0 (0.0)

Sigmoid colon

38 (31.7)

Descending colon

29 924.2)

Transvers colon

23 (19.2)

Ascending colon

27 (22.5)

Cecum

3 (2.5)

Abbreviatoins: BMI, Body mass index; WHR, Waist -hip circumstance.


Of 536 participants, 290 (54.1%) were females, and 190 (35.4%) patients had polyps; 72.1%, 18.4%, 7.4%, and 2.1% had one, two, three, and four polyps, respectively. Among 265 detected polyps, most were pedunculated, measured >10 mm, with the location in the sigmoid colon. The frequency of 11.4% (n = 61) in patients. Among them, 52.5%, 16.4%, 13.1%, and 18.0% had diverticula in one, two, three, and four locations, respectively, most located in the sigmoid colon.

The results of the Cochrane-Armitage test in three models illustrated that in models 1 and 2, polyps' OR significantly increased in obese individuals (P < 0.05). In all three models, the OR of diverticula was significantly increased in overweight individuals (P < 0.05). The chance of developing polyps was significantly associated with high-risk WHR in model 2 (P < 0.05). At the same time, no association was observed between the WHR and the chance of developing diverticula in all three models (P > 0.05) ([Table 2]).

Table 2

Cochran-Armitage trend evaluation for the association between BMI and WHR with the chance of developing colorectal polyps and diverticulosis in patients referred for colonoscopy

Variables

Chance of developing

Model 1

Model 2

Model 3

(95% CI) OR

P value

(95% CI) OR

P value

(95% CI) OR

P value

Polyp

BMI

<25

31.2

1 (ref)

25≤BMI < 30

33.8

1.13 (0.73-1.74)

0.594

1.12 (0.72-1.75)

0.612

1.11 (0.070-1.78)

0.651

30≤

41.9

1.58(1.01-2.47)

0.043

1.62 (1.03-2.56)

0.037

1.44 (0.89-2.33)

0.140

WHR

Low-risk

31.7

1 (ref)

Moderate-risk

36.7

1.2 (0.75-2.08)

0.396

1.47 (0.86-2.52)

0.158

1.49 (0.85-2.62)

0.165

High-risk

37.8

1.30 (0.87-1.94)

0.193

2.06 (1.11-3.81)

0.021

1.87 (0.98-3.57)

0.056̀

Diverticula

BMI

<25

6.8

1 (ref)

25≤BMI < 30

14.9

2.39 (1.18-4.84)

0.016

2.51 (1.22-5.15)

0.012

2.32 (1.10-4.91)

0.028

30≤

12.1

1.89 (0.89-3.99)

0.097

2.02 (0.94-4.35)

0.074

1.83 (0.83-4.04)

0.137

WHR

Low-risk

11.1

1 (ref)

Normal-risk

16.3

1.56 (0.77-3.15)

0.214

1.68 (0.80-3.50)

0.168

1.83 (0.85-3.92)

0.423

High-risk

9.6

0.85 (0.46-1.58)

0.615

0.84 (0.35-2.02)

0.698

0.80 (0.32-2.03)

0.643

P value < 0.05 as a significant level; OR: crude odds ratio; CI: confidence interval; BMI: Body mass index; WHR: Waist -hip circumstance; Model 1: Unadjusted model; Model 2: Model adjusted for age and gender; Model 3: Model adjusted for demographical data and clinical characteristics.


According to [Table 3], the prevalence of polyp significantly increased with increasing age and BMI, and it is also higher in rural residents and patients with lower physical activity (P < 0.05). Patients with high-risk WHR represented a higher frequency of polyps, but no statistically significant differences were observed (P > 0.05). The mean age of patients with and without polyps was 58.92 ± 11.93 and 54.31 ± 13.78 years, respectively, significantly different among the two groups (P < 0.001). The mean BMI in patients with and without polyp was 28.51 ± 5.21 and 27.08 ± 4.80 kg/m2, respectively, significantly different among the two studied groups (P = 0.002). Also, the mean of WHR in patients with and without polyp was 0.92 ± 0.07 and 0.91 ± 0.07, respectively, which represented no statistically significant difference among the two groups (P = 0.086).

Table 3

Comparison of the demographical and clinical characteristics in terms of the prevalence of polyps and diverticula in patients referred for colonoscopy

Variables

Patients with polyp

n (%)

Patients without polyp

n (%)

P value

P for trend

Patients with diverticula

n (%)

Patients without diverticula

n (%)

P value

P for trend

Age

(year)

≤40

13 (6.8)

58 (16.8)

0.002

<0.001

3 (4.9)

68 (14.3)

0.014

0.001

41-50

28 (14.7)

56 (16.2)

5 (8.2)

79 (16.6)

51-60

58 (30.5)

111 (32.1)

19 (31.1)

150 (31.6)

60<

91 (47.9)

121 (35.0)

34 (55.7)

178 (37.5)

Gender

Male

91 (47.9)

155 (44.8)

0.491

31 (50.8)

215 (45.3)

0.412

Female

99 (52.1)

191 (55.2)

30 (49.2)

260 (54.7)

Educational status

Illiterate

41 (21.6)

65 (18.8)

0.805

0.851

17 (27.9)

89 (18.7)

0.346

0.099

Under diploma

91 (47.9)

176 (50.9)

29 (47.5)

238 (50.1)

Diploma

42 (22.1)

80 (23.1)

12 (19.7)

110 (23.2)

University degree

16 (8.4)

25 (7.2)

3 (4.9)

38 (8.0)

Habitat

Urban

112 (58.9)

247 (71.4)

0.003

40 (65.5)

319 (67.2)

0.804

Rural

78 (41.1)

99 (28.9)

21 (34.4)

156 (32.8)

BMI

(kg/m2)

<25

55 (28.9)

121 (35.0)

0.105

0.043

12 (19.7)

164 (34.5)

0.048

0.115

25≤BMI < 30

66 (34.7)

129 (37.3)

29 (47.5)

166 (34.9)

30≤

69 (36.3)

96 (27.7)

20 (32.8)

145 (30.5)

WHR

Low-risk

60 (31.6)

129 (37.3)

0.411

0.200

21 (34.4)

168 (35.4)

0.208

0.562

Moderate-risk

36 (18.9)

62 (17.9)

16 (26.2)

82 (17.3)

High-risk

94 (49.5)

155 (44.8)

24 (39.3)

225 (47.4)

Physical activity

Low

133 (70.0)

231 (66.8)

0.020

0.110

47 (77.0)

317 (66.7)

0.245

0.095

Middle

56 (29.5)

97 (28.0)

13 (21.3)

140 (29.5)

High

1 (0.5)

18 (5.2)

1 (1.6)

18 (3.8)

History of smoking

Yes

11 (5.8)

37 (10.7)

0.057

3 (4.9)

45 (9.5)

0.241

No

179 (94.2)

309 (89.3)

58 (95.1)

430 (90.5)

Alcohol consumption

Yes

2 (1.1)

5 (1.4)

0.702

0 (0.0)

7 (1.5)

1

No

188 (98.9)

341 (98.6)

61 (100.0)

468 (98.5)

Occupational exposure

Yes

11 (5.8)

15 (341)

0.453

3 (4.9)

23 (4.8)

0.979

No

179 (94.2)

331 (95.7)

58 (95.1)

452 (95.2)

Family history of colorectal cancer

Yes

27 (14.2)

57 (16.5)

0.490

3 (4.9)

81 (17.1)

0.014

No

163 (85.8)

289 (83.5)

58 (95.1)

394 (82.9)

Chi-square and independent t-test were used to calculate the association; P-value < 0.05 was considered a significant level; P for trend was calculated using Cochran-Armitage test; BMI: Body mass index; WHR: Waist-hip circumstance.


The diverticula's prevalence significantly increased with age and BMI (P < 0.05). Moreover, the frequency of diverticula decreased by increasing physical activity, but no statistically significant differences were reported (P > 0.05). This prevalence in patients with a family history of colorectal cancer was significantly lower than in patients without (P < 0.05). The mean age of patients with and without diverticula was 61.97 ± 11.87 and 55.17 ± 13.32 years, respectively, significantly different among the two groups (P < 0.001). The mean BMI in patients with and without diverticula was 28.57 ± 4.45 and 27.46 ± 5.05 kg/m2, respectively, illustrating a statistically non-significant difference among the two groups (P = 0.104). Also, the mean of WHR in patients with and without diverticula was 0.92 ± 0.07, which was similar (P = 0.541).

The chance of having diverticulosis in patients with a family history of colorectal cancer was lower than in patients without a family history (P = 0.05). The results showed that upper age had a higher chance of developing diverticulitis (P < 0.05). The chance of getting polyps increased with age, BMI, university degree, rural residents, and low physical activity. The chance of getting polyps in patients with low physical activity was higher compared to patients with moderate and high physical activity levels [Table 4].

Table 4

Multiple and univariable logistic regression analysis (adjusted) to identify independent factors related to the incidence of polyp and diverticula in patients referred for colonoscopy.

Variables

Polyp

Diverticula

Univariable logistic regression

Multivariable logistic regression

Univariable logistic regression

Multivariable logistic regression

(95% CI) OR

P value

(95% CI) OR

P value

(95% CI) OR

P value

(95% CI) OR

P value

Age (year)

1.03 (1.01-1.04)

<0.001

1.03 (1.01-1.05)

<0.01

1.04 (1.02-1.07)

<0.001

1.04 (1.02-1.07)

0.001

Gender

Male

1 (ref)

Female

0.88 (0.62-1.26)

0.491

0.59 (0.32-1.08)

0.086

0.80 (0.47-1.36)

0.413

1.03 (0.4-2.38)

0.937

Educational status

Illustrated

1 (ref)

Under diploma

0.82 (0.51-1.31)

0.403

1.06 (0.64-1.76)

0.824

0.64 (0.33-1.22)

0.173

0.75 (0.37-1.54)

0.438

Diploma

0.83 (0.48-1.43)

0.506

1.38 (0.75-2.56)

0.305

0.57 (0.26-1.26)

0.165

0.86 (0.35-2.08)

0.732

University degree

1.01 (0.48-2.13)

0.969

2.69 (1.14-6.38)

0.025

0.41 (0.11-1.49)

0.178

0.73 (0.18-2.94)

0.653

Habitat

Urban

1 (ref)

Rural

1.74 (1.20-2.52)

0.004

2 .00 (1.33-3.02)

<0.001

1.07 (0.61-1.88)

0.804

0.94 (0.51-1.72)

0.831

Mean of BMI (kg/m2)

1.06 (1.02-1.10)

0.002

1.05 (1.01-1.09)

0.011

1.04 (0.99-1.10)

0.105

1.04 (0.98-1.10)

0.159

WHR

Low-risk

1 (ref)

Moderate-risk

1.25 (0.75-2.08)

0.396

1.49 (0.85-2.62)

0.165

1.56 (0.77-3.15)

0.214

1.81 (0.84-3.87)

0.129

High-risk

1.30 (0.87-1.94)

0.193

1.87 (0.98-3.57)

0.056

0.85 (0.46-1.8)

0.615

0.80 (0.32-2.01)

0.631

Physical activity

High

1 (ref)

Middle

10.39 (1.35-79.95)

0.025

10.43 (1.29-84.32)

0.028

1.67 (0.21-13.54)

0.630

1.28 (0.14-11.44)

0.828

Low

10.36 (1.37-78.51)

0.024

10.06 (1.27-80.08)

0.029

2.67 (0.35-20.46)

0.345

2.23 (0.26-19.13)

0.463

History of smoking

Yes

0.51 (0.26-1.03)

0.061

0.48 (0.22-1.07)

0.073

0.49 (0.15-1.64)

0.250

0.44 (0.12-1.57)

0.205

Alcohol consumption

Yes

0.73 (0.14-3.078)

0.703

1.53 (0.19-12.37)

0.692

-

Occupational exposure

Yes

1.36 (0.61-3.01)

0.455

1.58 (0.65-3.80)

0.310

1.02 (0.30-3.49)

0.979

1.11 (0.30-4.17)

0.873

Family history of colorectal cancer

Yes

0.84 (0.51-1.38)

0.491

0.90 (0.53-1.52)

0.689

0.25 (0.08-0.82)

0.022

0.27 (0.08-0.90)

0.032

P value < 0.05 as a significant level; OR: crude odds ratio; CI: confidence interval; BMI: Body mass index; WHR: Waist-hip circumstance; Model 1: Unadjusted model; Model 2: Model adjusted for age and gender; Model 3: Model adjusted for demographical data and clinical characteristics.



#

Discussion

The incidence of diverticulosis and colorectal polyps is increasing rapidly worldwide.[25] [26] [27] Previous studies have shown that using colonoscopy to screen for colorectal lesions may help the prevention of malignancy and can reduce colorectal cancer-related deaths by approximately 60 percent.[28] [29] We performed this study to assess the prevalence and risk factors for the presence and development of colorectal polyps and diverticula. In the cross-sectional study, polyps and diverticula were 35.4% and 11.4%, respectively, indicating a higher prevalence of these lesions than previous studies in the same regional population from 2006 to 2009.[30] These increases are likely the result of an aging population and lifestyle changes and follow trends reported in other developing countries. The frequency of diverticulosis and colorectal polyps in our cohort is consistent with previous studies, showing an increase in frequency with the aging of the patient population.[4] [31] [32]

The prevalence of polyps and diverticula is higher in some populations and lower in others, which may be influenced by factors like different age groups, changes in diet and lifestyle habits, quality of equipment, or colonoscopy techniques that cause different detection rates over time.[32] [33] [34] The proportion of patients with polyps and diverticula increased with age, which suggested that age is a significant risk factor for both disorders.[35] Compared to our findings, other studies have shown that these lesions increase with age.[32] [36] The chance for colorectal polyps was higher in obese people, so the chance of developing polyps increased with increasing BMI. Previous studies have shown an association between BMI and colorectal polyps,[4] [19] [37] but not exclusively.[4] [38]

In this study, polyp prevalence was not statistically significantly associated with WHR, but the chance of polyp development increased with high-risk WHR. Bai et al. demonstrated an association between WHR and conventional adenomas or serrated polyps.[39] Another study has indicated that men with a higher BMI and WHR are associated with an increased risk of hyperplastic polyps, adenomas, and the occurrence of both types of polyps.[40] The prevalence of colorectal diverticula was higher in overweight people, so the chance of the development of polyps increased with increasing BMI. Prior studies found that Obesity has been associated with an increased risk of colonic diverticulosis.[41] [42]

Peery et al. established that obesity (BMI >30) significantly increased the risk of colonic diverticulosis in women but not men.[43] Beyond BMI, limited evidence suggests that visceral fat may play a significant role in the pathogenesis of diverticulitis.[44] [45] [46] However, it is unclear whether WHR concerns diverticulitis in women. Unlike other studies,[47] [48] we found that the prevalence and risk of diverticula were unrelated to WHR. In contrast to a study, that showed that the associations between WHR and diverticulitis remained essentially unchanged upon further adjustment of BMI in males,[44] Ma et al. showed that when BMI and WHR were determined together, WHR appeared to play a role in determining diverticulitis in overweight or obese women.[47]

Contrary to the Fu et al. study,[49] in which people with a lower level of education had a higher risk of polyps, in this study, people with a level of university education had a higher risk of developing colorectal polyps. Perhaps one of the reasons for this result is that people with higher education have more knowledge about diseases and their prevention, and therefore they do medical screenings more often. The current study also demonstrated that rural people have a higher risk of getting polyps. Previous literature reported that Hispanics living in urban areas are less likely to develop adenomatous polyps, which supports our findings.[50] [51] [52] Medical awareness, access to specialists, and non-adherence to cancer screening recommendations are more likely in rural residents. We observed the expected inverse trend between the chance risk of the polyp and the high level of physical activity. This association is consistent with other studies investigating the protective properties of physical activity and colonic polyps.[53] [54] The mechanism of this effect is unknown, but it can lead to decreased insulin levels, systemic inflammation, and abdominal obesity.[53] [55]

Finally, similar to other studies,[56] [57] [58] we indicated that patients with a positive family history of diverticulitis are at higher risk for diverticulitis. This phenomenon might be explained by the fact that some genes, such as LAMB4, TNFSF15, ARHGAP15, ANO1, ELN, and SPINT2, play known roles in processes logically related to diverticulitis, including inflammation, intestinal transport, intestinal motility, and extracellular matrix formation.[59] [60] Our study failed to show the effect of other risk factors of colorectal lesions that need further investigation.


#

Limitation

One of the limitations of this study is its cross-sectional nature. The limited geographic indications for colonoscopy do not allow any clear conclusions to be drawn, especially considering the lack of comparative studies in this region and Iran.


#

Conclusion

Our study indicated that colorectal polyps and diverticula are prevalent north of IRAN. Age and BMI were significantly associated with the presence and development of polyps and diverticula. The incidence of colorectal polyps was also influenced by high-risk WHR, university degree, living in rural and low physical activity. In addition, a family history of colorectal cancer affects the risk of diverticulosis development. Due to the possible precursor lesions of colorectal cancer, more attention should be paid to risk factors for colorectal polyps and diverticula to prevent and treat this spectrum of diseases.


#

Declarations


#
#

Consent for Publication

Not applicable.

Authors' Contributions

FJ, SNM, and FMGH participated in the research design. MA and SM participated in writing the first draft. SM and MB participated in the performance of the research and analytic tools. SNM, SM, and FJ participated in data analysis. All authors reviewed and confirmed the final manuscript.


Availability of Data and Materials

The study protocol and the datasets analyzed are available from the corresponding author upon request.


Ethics Approval and Consent to Participate

This study was approved by the ethical committee of the Guilan University of Medical Sciences (IR.GUMS.REC.1401.505). All patients gave their consent to participate in the study.


Competing Interests

The authors declare that they have no competing interests in this work.


  • References

  • 1 Viscido A, Ciccone F, Vernia F. et al. Association of Colonic Diverticula with Colorectal Adenomas and Cancer. Medicina (Kaunas) 2021; 57 (02) 108 PubMed
  • 2 Meseeha MAM. Colon Polyps. In Treasure Island (FL):. StatPearls Publishing;; Available at: https://www.ncbi.nlm.nih.gov/books/NBK430761/
  • 3 Nallapeta NS, Farooq U. PKD [Updated 2023 A 16]. IS. Diverticulosis [Internet]. StatPearls Publishing; 2023 . Available at: https://www.ncbi.nlm.nih.gov/books/NBK430771/
  • 4 Pan J, Cen L, Xu L. et al. Prevalence and risk factors for colorectal polyps in a Chinese population: a retrospective study. Sci Rep 2020; 10 (01) 6974
  • 5 Levin B, Lieberman DA, McFarland B. et al; American Cancer Society Colorectal Cancer Advisory Group, US Multi-Society Task Force, American College of Radiology Colon Cancer Committee. Screening and surveillance for the early detection of colorectal cancer and adenomatous polyps, 2008: a joint guideline from the American Cancer Society, the US Multi-Society Task Force on Colorectal Cancer, and the American College of Radiology. Gastroenterology 2008; 134 (05) 1570-1595
  • 6 Kazem Shahmoradi M, Soleimaninejad M, Sharifian M. Evaluation of colonoscopy data for colorectal polyps and associated histopathological findings. Ann Med Surg (Lond) 2020; 57: 7-10 https://www.sciencedirect.com/science/article/pii/S2049080120301904 [Internet]
  • 7 Weizman AV, Nguyen GC. Diverticular disease: epidemiology and management. Can J Gastroenterol 2011; 25 (07) 385-389
  • 8 Yang F, Lin L, Jiang X, Lv H, Sun C. Increasing Diverticulosis in an Aging Population: A Colonoscopy-Based Study of 5-Year Trends in 26 463 Patients in Northern China. Med Sci Monit 2018; 24: 2825-2831
  • 9 Ray J, Zidong Z, Yuan J, Quan M, Hachem C. The relationship between colon polyps and colonic diverticulosis: a retrospective review. Ann Gastroenterol 2023; 36 (03) 314-320
  • 10 Gohil VB, Patrie JT, Shami VM. et al. Colonic diverticulosis is associated with an increased adenoma detection rate in patients undergoing first-time screening colonoscopy. J Interv Gastroenterol 2012; 2 (02) 70-75
  • 11 Abu Baker F, Z'cruz De La Garza JA, Mari A. et al. Colorectal Cancer and Polyps in Diverticulosis Patients: A 10-Year Retrospective Study in 13680 Patients. Gastroenterol Res Pract 2019; 2019: 2507848
  • 12 Miulescu AM. Colonic Diverticulosis. Is there a Genetic Component?. Maedica. Romania 2020; 15: 105-110 PubMed
  • 13 Barbaro MR, Cremon C, Fuschi D. et al. Pathophysiology of Diverticular Disease: From Diverticula Formation to Symptom Generation. Int J Mol Sci 2022;23(12):
  • 14 Ramadas Jr A, Kandiah M, Zarida H, Yunus Gul AG, Faizal JA. Obesity and risk of colorectal adenomatous polyps: a case-control study in hospital kuala lumpur. Malays J Nutr 2009; 15 (01) 1-10
  • 15 Shih C-W, Chen Y-H, Chen W-L. Percentage of body fat is associated with increased risk of diverticulosis: A cross sectional study. PLoS One 2022; 17 (03) e0264746
  • 16 Luu HN, Tran MT, Nguyen MV-T. et al. Association between body mass index and colorectal adenomas: Findings from a case-control study in Vietnam. Int J Cancer 2021; 149 (11) 1898-1909 . Available at: https://doi.org/10.1002/ijc.33757
  • 17 Matrana MR, Margolin DA. Epidemiology and pathophysiology of diverticular disease. Clin Colon Rectal Surg 2009; 22 (03) 141-146
  • 18 Lee TH, Setty PT, Parthasarathy G. et al. Aging, Obesity, and the Incidence of Diverticulitis: A Population-Based Study. Mayo Clin Proc 2018; 93 (09) 1256-1265
  • 19 Salimian S, Habibi M, Sehat M, Hajian A. Obesity and incidence of colorectal polyps: a case-controlled study. Ann Med Surg (Lond) 2023; 85 (02) 306-310
  • 20 Böhm SK. Excessive Body Weight and Diverticular Disease. Visc Med 2021; 37 (05) 372-382
  • 21 Jamal Talabani A, Lydersen S, Ness-Jensen E, Endreseth BH, Edna T-H. Risk factors of admission for acute colonic diverticulitis in a population-based cohort study: The North Trondelag Health Study, Norway. World J Gastroenterol 2016; 22 (48) 10663-10672
  • 22 Aune D, Sen A, Leitzmann MF, Norat T, Tonstad S, Vatten LJ. Body mass index and physical activity and the risk of diverticular disease: a systematic review and meta-analysis of prospective studies. Eur J Nutr 2017; 56 (08) 2423-2438
  • 23 Rosemar A, Angerås U, Rosengren A. Body mass index and diverticular disease: a 28-year follow-up study in men. Dis Colon Rectum 2008; 51 (04) 450-455
  • 24 Booth M. Assessment of physical activity: an international perspective. Res Q Exerc Sport 2000; 71 (Suppl. 02) 114-120
  • 25 Jemal A, Bray F, Center MM, Ferlay J, Ward E, Forman D. Global cancer statistics. CA Cancer J Clin 2011; 61 (02) 69-90
  • 26 Tursi A. Diverticulosis today: unfashionable and still under-researched. Therap Adv Gastroenterol 2016; 9 (02) 213-228
  • 27 Wong MCS, Huang J, Huang JLW. et al. Global prevalence of colorectal neoplasia: a systematic review and meta-analysis. Clin Gastroenterol Hepatol 2020; 18 (03) 553-561.e10
  • 28 Dolatkhah R, Somi MH, Bonyadi MJ, Asvadi Kermani I, Farassati F, Dastgiri S. Colorectal cancer in iran: molecular epidemiology and screening strategies. J Cancer Epidemiol 2015; 2015: 643020
  • 29 Zauber AG. The impact of screening on colorectal cancer mortality and incidence: has it really made a difference?. Dig Dis Sci 2015; 60 (03) 681-691
  • 30 Joukar F, Majd SK, Fani A, Nazari N, Mansour-Ghanaei F. Colonoscopy outcome in north of Iran (Guilan): 2006-2009. Int J Clin Exp Med 2012; 5 (04) 321-325
  • 31 Wang F-W, Chuang H-Y, Tu M-S. et al. Prevalence and risk factors of asymptomatic colorectal diverticulosis in Taiwan. BMC Gastroenterol 2015; 15: 40
  • 32 Wong ER, Idris F, Chong CF, Telisinghe PU, Tan J, Chong VH. Diverticular disease and colorectal neoplasms: Association between left sided diverticular disease with colorectal cancers and right sided with colonic polyps. Asian Pac J Cancer Prev 2016; 17 (05) 2401-2405
  • 33 Azzam N, Aljebreen AM, Alharbi O, Almadi MA. Prevalence and clinical features of colonic diverticulosis in a Middle Eastern population. World J Gastrointest Endosc 2013; 5 (08) 391-397
  • 34 Peery AF, Keku TO, Martin CF. et al. Distribution and characteristics of colonic diverticula in a United States screening population. Clin Gastroenterol Hepatol 2016; 14 (07) 980-985.e1
  • 35 Jeong SJ, Lee J, Kim E. et al. Prevalence and risk of colorectal polyps among the Korean population under 50 years. Medicine (Baltimore) 2022; 101 (27) e29493
  • 36 Faucheron JL, Roblin X, Bichard P, Heluwaert F. The prevalence of right-sided colonic diverticulosis and diverticular haemorrhage. Colorectal Dis 2013; 15 (05) e266-e270
  • 37 He X, Wu K, Ogino S, Giovannucci EL, Chan AT, Song M. Association between risk factors for colorectal cancer and risk of serrated polyps and conventional adenomas. Gastroenterology 2018; 155 (02) 355-373.e18
  • 38 Lieberman DA, Prindiville S, Weiss DG, Willett W. VA Cooperative Study Group 380. Risk factors for advanced colonic neoplasia and hyperplastic polyps in asymptomatic individuals. JAMA 2003; 290 (22) 2959-2967
  • 39 Bai H, Xu Z, Li J. et al. Independent and joint associations of general and abdominal obesity with the risk of conventional adenomas and serrated polyps: A large population-based study in East Asia. Int J Cancer 2023; 153 (01) 54-63
  • 40 Morimoto LM, Newcomb PA, Ulrich CM, Bostick RM, Lais CJ, Potter JD. Risk factors for hyperplastic and adenomatous polyps: evidence for malignant potential?. Cancer Epidemiol Biomarkers Prev 2002; 11 (10 Pt 1): 1012-1018
  • 41 Mashayekhi R, Bellavance DR, Chin SM. et al. Obesity, but not physical activity, is associated with higher prevalence of asymptomatic diverticulosis. Clin Gastroenterol Hepatol 2018; 16 (04) 586-587
  • 42 Wijarnpreecha K, Ahuja W, Chesdachai S. et al. Obesity and the risk of colonic diverticulosis: a meta-analysis. Dis Colon Rectum 2018; 61 (04) 476-483
  • 43 Peery AF, Keil A, Jicha K, Galanko JA, Sandler RS. Association of obesity with colonic diverticulosis in women. Clin Gastroenterol Hepatol 2020; 18 (01) 107-114.e1
  • 44 Strate LL, Liu YL, Aldoori WH, Syngal S, Giovannucci EL. Obesity increases the risks of diverticulitis and diverticular bleeding. Gastroenterology 2009; 136 (01) 115-12 -2.e1
  • 45 Yamada E, Ohkubo H, Higurashi T. et al. Visceral obesity as a risk factor for left-sided diverticulitis in Japan: a multicenter retrospective study. Gut Liver 2013; 7 (05) 532-538
  • 46 Docimo Jr S, Lee Y, Chatani P, Rogers AM, Lacqua F. Visceral to subcutaneous fat ratio predicts acuity of diverticulitis. Surg Endosc 2017; 31 (07) 2808-2812
  • 47 Ma W, Jovani M, Liu P-H. et al. Association between obesity and weight change and risk of diverticulitis in women. Gastroenterology 2018; 155 (01) 58-66.e4
  • 48 Bae HJ, Kim ST, Hong SG. et al. Risk factors for asymptomatic colon diverticulosis. Korean J Gastroenterol 2019; 74 (03) 142-148
  • 49 Fu Z, Shrubsole MJ, Smalley WE. et al. Lifestyle factors and their combined impact on the risk of colorectal polyps. Am J Epidemiol 2012; 176 (09) 766-776
  • 50 Orsak G, Allen CM, Sorensen W, McGaha P. Risk of colorectal polyps and malignancies among predominantly rural hispanics. J Immigr Minor Health 2019; 21 (05) 931-937
  • 51 Zheng XE, Li T, Lipka S. et al. Location-dependent ethnic differences in the risk of colorectal adenoma: a retrospective multiethnic study. J Clin Gastroenterol 2014; 48 (01) e1-e7
  • 52 Patel S, Lipka S, Shen H. et al. The association of H. pylori and colorectal adenoma: does it exist in the US Hispanic population?. J Gastrointest Oncol 2014; 5 (06) 463-468
  • 53 Sanchez NF, Stierman B, Saab S, Mahajan D, Yeung H, Francois F. Physical activity reduces risk for colon polyps in a multiethnic colorectal cancer screening population. BMC Res Notes 2012; 5 (01) 312
  • 54 Wolin KY, Yan Y, Colditz GA. Physical activity and risk of colon adenoma: a meta-analysis. Br J Cancer 2011; 104 (05) 882-885
  • 55 Zhang S, Zhang J, Kim Y, Zhang W. Prevalence of colorectal polyps based on cardiorespiratory fitness, muscle strength, health behavior, and abdominal obesity in asymptomatic elderly. In: Healthcare. Multidisciplinary Digital Publishing Institute; 2021. . bl 1400
  • 56 Strate LL, Morris AM. Epidemiology, pathophysiology, and treatment of diverticulitis. Gastroenterology 2019; 156 (05) 1282-1298.e1
  • 57 Londono E, Chugh A. Risk Factors and Management of Diverticulitis. Annals of Advanced Biomedical Sciences 2023; 6 (01) 194
  • 58 Almalki T, Garfinkle R, Kmiotek E. et al. Family history is associated with recurrent diverticulitis after an episode of diverticulitis managed nonoperatively. Dis Colon Rectum 2020; 63 (07) 944-954
  • 59 Koprowski MA, Affleck A, Tsikitis VL. Emerging evidence and recent controversies in diverticulitis: a 5-year review. Ann Gastroenterol 2022; 35 (01) 8-16
  • 60 Maguire LH. Genetic Risk Factors for Diverticular Disease-Emerging Evidence. J Gastrointest Surg 2020; 24 (10) 2314-2317

Address for correspondence

Fariborz Mansour-Ghanaei, MD, AGAF
Department of Gastroenterology, Gastrointestinal and Liver Diseases Research Center, Guilan University of Medical Sciences, Rasht, Iran Razi Hospital
Sardar-Jangle Ave., P.O. Box: 41448-95655, Rasht
Iran   

Publication History

Received: 26 November 2023

Accepted: 09 April 2024

Article published online:
06 June 2024

© 2024. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution 4.0 International License, permitting copying and reproduction so long as the original work is given appropriate credit (https://creativecommons.org/licenses/by/4.0/)

Thieme Revinter Publicações Ltda.
Rua do Matoso 170, Rio de Janeiro, RJ, CEP 20270-135, Brazil

  • References

  • 1 Viscido A, Ciccone F, Vernia F. et al. Association of Colonic Diverticula with Colorectal Adenomas and Cancer. Medicina (Kaunas) 2021; 57 (02) 108 PubMed
  • 2 Meseeha MAM. Colon Polyps. In Treasure Island (FL):. StatPearls Publishing;; Available at: https://www.ncbi.nlm.nih.gov/books/NBK430761/
  • 3 Nallapeta NS, Farooq U. PKD [Updated 2023 A 16]. IS. Diverticulosis [Internet]. StatPearls Publishing; 2023 . Available at: https://www.ncbi.nlm.nih.gov/books/NBK430771/
  • 4 Pan J, Cen L, Xu L. et al. Prevalence and risk factors for colorectal polyps in a Chinese population: a retrospective study. Sci Rep 2020; 10 (01) 6974
  • 5 Levin B, Lieberman DA, McFarland B. et al; American Cancer Society Colorectal Cancer Advisory Group, US Multi-Society Task Force, American College of Radiology Colon Cancer Committee. Screening and surveillance for the early detection of colorectal cancer and adenomatous polyps, 2008: a joint guideline from the American Cancer Society, the US Multi-Society Task Force on Colorectal Cancer, and the American College of Radiology. Gastroenterology 2008; 134 (05) 1570-1595
  • 6 Kazem Shahmoradi M, Soleimaninejad M, Sharifian M. Evaluation of colonoscopy data for colorectal polyps and associated histopathological findings. Ann Med Surg (Lond) 2020; 57: 7-10 https://www.sciencedirect.com/science/article/pii/S2049080120301904 [Internet]
  • 7 Weizman AV, Nguyen GC. Diverticular disease: epidemiology and management. Can J Gastroenterol 2011; 25 (07) 385-389
  • 8 Yang F, Lin L, Jiang X, Lv H, Sun C. Increasing Diverticulosis in an Aging Population: A Colonoscopy-Based Study of 5-Year Trends in 26 463 Patients in Northern China. Med Sci Monit 2018; 24: 2825-2831
  • 9 Ray J, Zidong Z, Yuan J, Quan M, Hachem C. The relationship between colon polyps and colonic diverticulosis: a retrospective review. Ann Gastroenterol 2023; 36 (03) 314-320
  • 10 Gohil VB, Patrie JT, Shami VM. et al. Colonic diverticulosis is associated with an increased adenoma detection rate in patients undergoing first-time screening colonoscopy. J Interv Gastroenterol 2012; 2 (02) 70-75
  • 11 Abu Baker F, Z'cruz De La Garza JA, Mari A. et al. Colorectal Cancer and Polyps in Diverticulosis Patients: A 10-Year Retrospective Study in 13680 Patients. Gastroenterol Res Pract 2019; 2019: 2507848
  • 12 Miulescu AM. Colonic Diverticulosis. Is there a Genetic Component?. Maedica. Romania 2020; 15: 105-110 PubMed
  • 13 Barbaro MR, Cremon C, Fuschi D. et al. Pathophysiology of Diverticular Disease: From Diverticula Formation to Symptom Generation. Int J Mol Sci 2022;23(12):
  • 14 Ramadas Jr A, Kandiah M, Zarida H, Yunus Gul AG, Faizal JA. Obesity and risk of colorectal adenomatous polyps: a case-control study in hospital kuala lumpur. Malays J Nutr 2009; 15 (01) 1-10
  • 15 Shih C-W, Chen Y-H, Chen W-L. Percentage of body fat is associated with increased risk of diverticulosis: A cross sectional study. PLoS One 2022; 17 (03) e0264746
  • 16 Luu HN, Tran MT, Nguyen MV-T. et al. Association between body mass index and colorectal adenomas: Findings from a case-control study in Vietnam. Int J Cancer 2021; 149 (11) 1898-1909 . Available at: https://doi.org/10.1002/ijc.33757
  • 17 Matrana MR, Margolin DA. Epidemiology and pathophysiology of diverticular disease. Clin Colon Rectal Surg 2009; 22 (03) 141-146
  • 18 Lee TH, Setty PT, Parthasarathy G. et al. Aging, Obesity, and the Incidence of Diverticulitis: A Population-Based Study. Mayo Clin Proc 2018; 93 (09) 1256-1265
  • 19 Salimian S, Habibi M, Sehat M, Hajian A. Obesity and incidence of colorectal polyps: a case-controlled study. Ann Med Surg (Lond) 2023; 85 (02) 306-310
  • 20 Böhm SK. Excessive Body Weight and Diverticular Disease. Visc Med 2021; 37 (05) 372-382
  • 21 Jamal Talabani A, Lydersen S, Ness-Jensen E, Endreseth BH, Edna T-H. Risk factors of admission for acute colonic diverticulitis in a population-based cohort study: The North Trondelag Health Study, Norway. World J Gastroenterol 2016; 22 (48) 10663-10672
  • 22 Aune D, Sen A, Leitzmann MF, Norat T, Tonstad S, Vatten LJ. Body mass index and physical activity and the risk of diverticular disease: a systematic review and meta-analysis of prospective studies. Eur J Nutr 2017; 56 (08) 2423-2438
  • 23 Rosemar A, Angerås U, Rosengren A. Body mass index and diverticular disease: a 28-year follow-up study in men. Dis Colon Rectum 2008; 51 (04) 450-455
  • 24 Booth M. Assessment of physical activity: an international perspective. Res Q Exerc Sport 2000; 71 (Suppl. 02) 114-120
  • 25 Jemal A, Bray F, Center MM, Ferlay J, Ward E, Forman D. Global cancer statistics. CA Cancer J Clin 2011; 61 (02) 69-90
  • 26 Tursi A. Diverticulosis today: unfashionable and still under-researched. Therap Adv Gastroenterol 2016; 9 (02) 213-228
  • 27 Wong MCS, Huang J, Huang JLW. et al. Global prevalence of colorectal neoplasia: a systematic review and meta-analysis. Clin Gastroenterol Hepatol 2020; 18 (03) 553-561.e10
  • 28 Dolatkhah R, Somi MH, Bonyadi MJ, Asvadi Kermani I, Farassati F, Dastgiri S. Colorectal cancer in iran: molecular epidemiology and screening strategies. J Cancer Epidemiol 2015; 2015: 643020
  • 29 Zauber AG. The impact of screening on colorectal cancer mortality and incidence: has it really made a difference?. Dig Dis Sci 2015; 60 (03) 681-691
  • 30 Joukar F, Majd SK, Fani A, Nazari N, Mansour-Ghanaei F. Colonoscopy outcome in north of Iran (Guilan): 2006-2009. Int J Clin Exp Med 2012; 5 (04) 321-325
  • 31 Wang F-W, Chuang H-Y, Tu M-S. et al. Prevalence and risk factors of asymptomatic colorectal diverticulosis in Taiwan. BMC Gastroenterol 2015; 15: 40
  • 32 Wong ER, Idris F, Chong CF, Telisinghe PU, Tan J, Chong VH. Diverticular disease and colorectal neoplasms: Association between left sided diverticular disease with colorectal cancers and right sided with colonic polyps. Asian Pac J Cancer Prev 2016; 17 (05) 2401-2405
  • 33 Azzam N, Aljebreen AM, Alharbi O, Almadi MA. Prevalence and clinical features of colonic diverticulosis in a Middle Eastern population. World J Gastrointest Endosc 2013; 5 (08) 391-397
  • 34 Peery AF, Keku TO, Martin CF. et al. Distribution and characteristics of colonic diverticula in a United States screening population. Clin Gastroenterol Hepatol 2016; 14 (07) 980-985.e1
  • 35 Jeong SJ, Lee J, Kim E. et al. Prevalence and risk of colorectal polyps among the Korean population under 50 years. Medicine (Baltimore) 2022; 101 (27) e29493
  • 36 Faucheron JL, Roblin X, Bichard P, Heluwaert F. The prevalence of right-sided colonic diverticulosis and diverticular haemorrhage. Colorectal Dis 2013; 15 (05) e266-e270
  • 37 He X, Wu K, Ogino S, Giovannucci EL, Chan AT, Song M. Association between risk factors for colorectal cancer and risk of serrated polyps and conventional adenomas. Gastroenterology 2018; 155 (02) 355-373.e18
  • 38 Lieberman DA, Prindiville S, Weiss DG, Willett W. VA Cooperative Study Group 380. Risk factors for advanced colonic neoplasia and hyperplastic polyps in asymptomatic individuals. JAMA 2003; 290 (22) 2959-2967
  • 39 Bai H, Xu Z, Li J. et al. Independent and joint associations of general and abdominal obesity with the risk of conventional adenomas and serrated polyps: A large population-based study in East Asia. Int J Cancer 2023; 153 (01) 54-63
  • 40 Morimoto LM, Newcomb PA, Ulrich CM, Bostick RM, Lais CJ, Potter JD. Risk factors for hyperplastic and adenomatous polyps: evidence for malignant potential?. Cancer Epidemiol Biomarkers Prev 2002; 11 (10 Pt 1): 1012-1018
  • 41 Mashayekhi R, Bellavance DR, Chin SM. et al. Obesity, but not physical activity, is associated with higher prevalence of asymptomatic diverticulosis. Clin Gastroenterol Hepatol 2018; 16 (04) 586-587
  • 42 Wijarnpreecha K, Ahuja W, Chesdachai S. et al. Obesity and the risk of colonic diverticulosis: a meta-analysis. Dis Colon Rectum 2018; 61 (04) 476-483
  • 43 Peery AF, Keil A, Jicha K, Galanko JA, Sandler RS. Association of obesity with colonic diverticulosis in women. Clin Gastroenterol Hepatol 2020; 18 (01) 107-114.e1
  • 44 Strate LL, Liu YL, Aldoori WH, Syngal S, Giovannucci EL. Obesity increases the risks of diverticulitis and diverticular bleeding. Gastroenterology 2009; 136 (01) 115-12 -2.e1
  • 45 Yamada E, Ohkubo H, Higurashi T. et al. Visceral obesity as a risk factor for left-sided diverticulitis in Japan: a multicenter retrospective study. Gut Liver 2013; 7 (05) 532-538
  • 46 Docimo Jr S, Lee Y, Chatani P, Rogers AM, Lacqua F. Visceral to subcutaneous fat ratio predicts acuity of diverticulitis. Surg Endosc 2017; 31 (07) 2808-2812
  • 47 Ma W, Jovani M, Liu P-H. et al. Association between obesity and weight change and risk of diverticulitis in women. Gastroenterology 2018; 155 (01) 58-66.e4
  • 48 Bae HJ, Kim ST, Hong SG. et al. Risk factors for asymptomatic colon diverticulosis. Korean J Gastroenterol 2019; 74 (03) 142-148
  • 49 Fu Z, Shrubsole MJ, Smalley WE. et al. Lifestyle factors and their combined impact on the risk of colorectal polyps. Am J Epidemiol 2012; 176 (09) 766-776
  • 50 Orsak G, Allen CM, Sorensen W, McGaha P. Risk of colorectal polyps and malignancies among predominantly rural hispanics. J Immigr Minor Health 2019; 21 (05) 931-937
  • 51 Zheng XE, Li T, Lipka S. et al. Location-dependent ethnic differences in the risk of colorectal adenoma: a retrospective multiethnic study. J Clin Gastroenterol 2014; 48 (01) e1-e7
  • 52 Patel S, Lipka S, Shen H. et al. The association of H. pylori and colorectal adenoma: does it exist in the US Hispanic population?. J Gastrointest Oncol 2014; 5 (06) 463-468
  • 53 Sanchez NF, Stierman B, Saab S, Mahajan D, Yeung H, Francois F. Physical activity reduces risk for colon polyps in a multiethnic colorectal cancer screening population. BMC Res Notes 2012; 5 (01) 312
  • 54 Wolin KY, Yan Y, Colditz GA. Physical activity and risk of colon adenoma: a meta-analysis. Br J Cancer 2011; 104 (05) 882-885
  • 55 Zhang S, Zhang J, Kim Y, Zhang W. Prevalence of colorectal polyps based on cardiorespiratory fitness, muscle strength, health behavior, and abdominal obesity in asymptomatic elderly. In: Healthcare. Multidisciplinary Digital Publishing Institute; 2021. . bl 1400
  • 56 Strate LL, Morris AM. Epidemiology, pathophysiology, and treatment of diverticulitis. Gastroenterology 2019; 156 (05) 1282-1298.e1
  • 57 Londono E, Chugh A. Risk Factors and Management of Diverticulitis. Annals of Advanced Biomedical Sciences 2023; 6 (01) 194
  • 58 Almalki T, Garfinkle R, Kmiotek E. et al. Family history is associated with recurrent diverticulitis after an episode of diverticulitis managed nonoperatively. Dis Colon Rectum 2020; 63 (07) 944-954
  • 59 Koprowski MA, Affleck A, Tsikitis VL. Emerging evidence and recent controversies in diverticulitis: a 5-year review. Ann Gastroenterol 2022; 35 (01) 8-16
  • 60 Maguire LH. Genetic Risk Factors for Diverticular Disease-Emerging Evidence. J Gastrointest Surg 2020; 24 (10) 2314-2317