Skip to main content
World Journal of Gastroenterology logoLink to World Journal of Gastroenterology
. 2003 Jan 15;9(1):99–103. doi: 10.3748/wjg.v9.i1.99

Nested case-control study on the risk factors of colorectal cancer

Kun Chen 1,2,3, Jian Cai 1,2,3, Xi-Yong Liu 1,2,3, Xi-Yuan Ma 1,2,3, Kai-Yan Yao 1,2,3, Shu Zheng 1,2,3
PMCID: PMC4728259  PMID: 12508360

Abstract

AIM: To investigate the risk factors of colon cancer and rectal cancer.

METHODS: A nested case-control study was conducted in a cohort of 64693 subjects who participated in a colorectal cancer screening program from 1989 to 1998 in Jiashan county, Zhejiang, China. 196 cases of colorectal cancer were detected from 1990 to 1998 as the case group and 980 non-colorectal cancer subjects, matched with factors of age, gender, resident location, were randomly selected from the 64693 cohort as controls. By using univariate analysis and mutivariate conditional logistic regression analysis, the odds ratio (OR) and its 95% confidence interval (95%CI) were calculated between colorectal cancer and personal habits, dietary factors, as well as intestinal related symptoms.

RESULTS: The mutivariate analysis results showed that after matched with age, sex and resident location, mucous blood stool history and mixed sources of drinking water were closely associated with colon cancer and rectal cancer, OR values for the mucous blood stool history were 3.508 (95%CI: 1.370-8.985) and 2.139 (95%CI: 1.040-4.402) respectively; for the mixed drinking water sources, 2.387 (95%CI: 1.243-4.587) and 1.951 (95%CI: 1.086-3.506) respectively. All reached the significant level with a P-value less than 0.05.

CONCLUSION: The study suggested that mucous blood stool history and mixed sources of drinking water were the risk factors of colon cancer and rectal cancer. There was no any significant association between dietary habits and the incidence of colorectal cancer.

INTRODUCTION

Colorectal cancer is one of the most common malignant tumors[1-6]. During the past decades, the incidence of colorectal cancer was increased all around the world, more than 500000 cases were diagnosed as colorectal cancer per year. In the east of China, there has been a higher incidence of colorectal cancer. In Jiashan County, the mortality rate of colorectal cancer was the highest among China, which is about 20/100000 per year[7].

The causes of colorectal cancer are generally regarded as two aspects: heredity and environment[8-10]. The former includes family history of cancer, intestinal polyp history, and so on. The later includes particularly dietary habit and physical activity.

Nested Case-Control Study (NCCS), an analytical epidemiological study method, was first presented by Mantel N, an American epidemiologist, in 1973[11], and it was widely used after 1980’s[12-21]. All the subjects in such study are selected from a whole cohort, which is generally called cohort set. Compared with the cohort study, NCCS has the privilege of time-saving, money-saving, and trouble-saving; while compared to case-control study, since the exposure data are collected before the incident of disease, it is certain of the causes and time consequences relationship, and observational bias could be controlled efficiently. All of these characteristics of NCCS are suitable to the study of chronic disease, such as cancer.

There are many reports on the risk factors of colorectal cancer using classical case-control study method, however, few studies used nested case-control study method[22-29]. The purpose of this study is to explore the risk factors of colorectal cancer, providing evidence for the prevention of colorectal cancer.

MATERIALS AND METHODS

Selection of cases and controls

A colorectal cancer screening program beginning on 1st May 1989 and ending on 30th April 1990 was conducted in ten countries which belonged to Jiashan county, Zhejiang province, China, including Weitan town, Yangmiao country, Xiadianmiao country, et al From 75842 eligible subjects aged 30 years and over, 64693 subjects were enrolled as the base cohort set, the respondence rate was 85.3%. Moreover, Jiashan county has founded cancer registration system and colorectal cancer report system, monitoring new cancer cases, including colorectal cancer. The cases in this study, who had participated in the 1989-1990 screening program, were the new colorectal cancer patients reported by Institute of Cancer Research and Prevention of Jiashan county. Up to 1998, the total number was 196 cases. Of which, 151 cases were pathological diagnosed, account for 77.1%, 20 cases were diagnosed in the operation, 10.2%, 23 cases were diagnosed by endoscopy, 11.7%. Under the principle of same-country or town, same-sex, and no more than 3 years age disparity, 980 non-colorectal cancer subjects in the cohort set were selected as controls, resulting the final study subjects of 196 cases and 980 controls.

Contents of the study

The study contents composed of three parts as follow: (1) General characteristics: including age, sex, job types, educational levels, address et al; (2). Personal habits: including dietary habits, drinking water sources, alcohol consumption and cigarette smoking, et al; (3). Symptoms and disease history related with colorectal cancer: including changes of stool status, abdominal operation history, intestinal disease history, asthma history and allergy history, family cancer history, ancylostomiasis history, drug using history, psychic stimulation history, and so on.

Investigation methods and quality control

In the 1989-1990 screening investigation, a well-built Investigation Manual as the uniform criteria for inquiring the subjects and filling up the constructed questionnaire was used. All interviewers were trained focusing on the skills of inquiring. No subjects refused to be interviewed except that they were out of towns. For building the database, the questionnaires were coded and put into computer twice to control bias. The data used in this study were taken from this database.

Statistical analysis

Classical analysis methods of case-control study can be used to NCCS data, usually calculating OR value. In this study, Chi-square test was used in the univariate analysis of the data; conditional logistic regression was used in the multivariate analysis. The SPSS 10.0 for windows and the SAS system for windows, version 6.12, were used for completing all the statistical analyses.

RESULTS

General information

In this study, there were 196 cases (84 colon cancer, 112 rectal cancer) and 980 controls. The distribution of age between cases and controls for male and female was shown in Table 1.

Table 1.

The distribution of subjects by age and sex

age male
female
case control case control
30- 3 15 7 35
35- 9 49 3 15
40- 14 69 3 19
45- 11 52 14 66
50- 21 110 14 78
55- 24 114 22 104
60- 11 57 13 63
65- 11 54 3 15
70- 2 10 5 26
75- 2 10 3 14
80- 0 0 1 5
Total 108 540 88 440

The average age of case group was 54.5 ± 10.6 years, while that of the control group was 54.3 ± 10.6 year, there was no statistically significant difference (t = 0.127, P = 0.899). For sex, there was also no difference statistically (χ2 = 0.001, P = 0.979).

Univariate analysis

In order to control the possible confounding bias the age, sex and resident location were matched in the study design. Given that the risk factors of colon cancer might be different from that of rectal cancer, the analysis of the risk factors were separated into colon cancer and rectal cancer, instead of colorectal cancer. The OR and its 95% confidence intervals (95%CI), χ2 and P values in the univariate analysis were showed respectively in Table 2 and Table 3 (the variables showed P > 0.20 were excluded).

Table 2.

Results of univariate analysis for colon cancer (cases n = 84, controls n = 420)

factors OR 95%CI χ2 P
pork eating(y = 1, n = 0) 1.481 0.846 2.593 1.890 0.169
drining mixed water source* (y = 1, n = 0) 2.273 1.255 4.117 7.332 0.007
drining gutter water (y = 1, n = 0) 1.639 0.777 3.457 1.680 0.195
drining well water (y = 1, n = 0) 0.542 0.338 0.870 6.445 0.011
chronic diarrhea history(y = 1, n = 0) 2.018 1.003 4.060 3.871 0.049
constipaton history(y = 1, n = 0) 0.483 0.171 1.363 1.888 0.169
appendicitis history(y = 1, n = 0) 1.697 0.966 2.981 3.386 0.066
appendix operating history(y = 1, n = 0) 1.707 0.873 3.334 2.446 0.118
intestinal polyps history(y = 1, n = 0) 6.503 2.009 21.049 9.762 0.002

*drinking mixed water source refers to the subjects drinking different type of water sources through his/her lifetime, mostly drinking river water and gutter water. So is Table 2, Table 3 and Table 4

Table 3.

Results of univariate analysis for rectal cancer (cases n = 112, controls n = 560)

factors OR 95%CI χ2 P
drining mixed water source (y = 1, n = 0) 2.021 1.170 3.491 6.363 0.011
mucious blood history (y = 1, n = 0) 2.138 1.122 4.072 5.335 0.021
defaecation drug using (y = 1, n = 0) 2.280 0.711 7.312 1.923 0.166
cholecyst excision history (y = 1, n = 0) 2.294 0.715 7.352 1.195 0.163

In Table 2, it was showed that four variables, well water drinking, mixed water source drinking, chronic diarrhea history and intestinal polyp history, were significantly associated with colon cancer (P < 0.05). The factor of appendicitis history showed an OR value close to significant level (P = 0.066). For rectal cancer in Table 3, there were two variables reached the significant level of P = 0.05, which were mixed water source drinking (OR = 2.02) and mucous blood stool history (OR = 2.14).

Mutivariate analysis

The variables showing associations with the risk of colon cancer and rectal cancer at P < 0.15 level were further tested in forward stepwise conditional logistic regression models. The final model consisted of those variables showing a significant association with the risk of colorectal cancer at P < 0.05 level. Results were showed in Table 4 and Table 5 for colon and rectal cancers, respectively.

Table 4.

Results of multivariate analysis for colon cancer

factors OR 95%CI P
drining mixed source water (y = 1, n = 0) 2.387 1.243 4.587 0.009
mucous blood history (y = 1, n = 0) 3.508 1.370 8.985 0.009

Table 4 and Table 5 illustrated that, at P = 0.05 level, both for colon cancer and rectal cancer, the final logistic regression model comprised two factors: mixed water source drinking and mucous blood stool history.

Table 5.

Results of multivariate analysis for rectal cancer

factors OR 95%CI P
drinking mixed water source (y = 1, n = 0) 1.951 1.086 3.506 0.025
mucous blood history (y = 1, n = 0) 2.139 1.040 4.402 0.039
factors 2.870 1.117 7.371 0.029

DISCUSSION

It is generally believed that colorectal cancer is the combined outcome of heredity and environment[8-10,30]. Despite uncertainties regarding the underlying association between heredity and colorectal cancer, the genetic factors may affect the individual sensitivity to cancer[3,30-37]; many documents had reported that the environmental factors might also influence colorectal cancer[37-46]. On the secondary prevention for colorectal cancer, symptoms and/or disorders of pre-cancer, such as intestinal polyps, ulcerative colitis, should be considered[48,49].

Univariate analysis results of this study showed that drinking well water is a protective factor for colon cancer, OR value was 0.542, (P < 0.05); drinking mixed water, mostly drinking river water and gutter water, was a risk factor both for colon cancer and rectal cancer, OR values were 2.387 (95%CI: 1.247-4.587) and 1.951 (95%CI: 1.086-3.506) in multivariate conditional logistic model, respectively. The association between drinking mixed water and colorectal cancer is consistent with former study. In this study, country subjects account for about 75%, most of the mixed water drinking aggregated in country. In the local country, people usually were drinking river water and well water. It reflects that uncertainty of drinking water source, especially mixed drinking river water and gutting water would increase the incidence of colon cancer and rectal cancer. The findings in this study resembled other study reports[45,50].

Chronic diarrhea, mucous blood stool and constipation history are the pre-clinical symptoms of colorectal cancer[51-54]. This study has found the positive association between mucous blood stool history and colorectal cancer. In final colon cancer logistic model and rectal cancer logistic model, the OR values of mucous blood stool history were 3.508 (95%CI: 1.370-8.985) and 2.139 (95%CI: 1.04-4.402) respectively, both reached statistical significant level. Univariate analysis also showed that, for colon cancer, the OR value of chronic diarrhea history was 2.018 (95%CI: 1.023-4.06), P < 0.05, but did not enter the final logistic regression model.

Intestinal polyp history commonly regarded as a high risk factor for colorectal cancer[55-63]. Although the univariate analysis result showed a positive association between intestinal polyp history and colon cancer, OR = 6.503 (95%CI: 2.009-21.049), P < 0.05, after being matched with age, sex and location, the factor did not enter the final logistic regression model. However, the association between intestinal polyp history and rectal cancer could not reach the significant level even in the univariate analysis.

Although the association between dietary habits and colorectal cancer has been reported[35,38,39,41,43,47,64,65], this study was not able to confirm such a positive association. It was reported that increasing fat while reducing fibrous in diet would increase the incidence of colorectal cancer[66-68]. In this study, after merging the two variables, pork eating and vegetable eating, into one variable by cross-difference method, we got a negative association. Red meat eating, such as fish cooked with soy souse, was reported to be the risk factor of colorectal cancer[69], but the result of this did not agree with that. Moreover, recent reports were not consistent with each other about the association between cigarette smoking and colorectal cancer, nor does the alcohol consumption[69-74]. This study did not find any statistical association between cigarette smoking, nor was alcohol consumption and colorectal cancer.

Nested case control study, namely case control study within cohort, is based on a cohort set. After baseline investigation for the cohort set, including population structure, exposure factors and pertinent factors, the study subjects are divided into two groups: the disease individuals form the case group and the individuals of control group need to be randomly selected from the non-disease subjects. This kind of study can be analyzed statistically as a case-control study. The risk factors found in nested one are certain in cause and time consequence. In addition, the number of case in this study was abundance after ten years of follow-up; the controls were randomly selected from the whole disease-free cohort set and can represent the normal public population well. All of these endue the results with persuasion.

It should be noted that, after ten years of follow-up, some exposure factors may have changed, factors such as dietary habits, drinking water sources, intestinal disease history may be different from the primate investigation. All the changes may discount the preciseness of the conclusion. That the association between dietary habits and colorectal cancer could not be put forward any positive evidence might be explained by such changes.

Footnotes

Supported by the National Natural Science Foundation of China, No. 30170828

Edited by Zhao M

References

  • 1.Zhang YL, Zhang ZS, Wu BP, Zhou DY. Early diagnosis for colorectal cancer in China. World J Gastroenterol. 2002;8:21–25. doi: 10.3748/wjg.v8.i1.21. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.Thiis-Evensen E, Hoff GS, Sauar J, Majak BM, Vatn MH. Flexible sigmoidoscopy or colonoscopy as a screening modality for colorectal adenomas in older age groups Findings in a cohort of the normal population aged 63-72 years. Gut. 1999;45:834–839. doi: 10.1136/gut.45.6.834. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Colonna M, Grosclaude P, Faivre J, Revzani A, Arveux P, Chaplain G, Tretarre B, Launoy G, Lesec'h JM, Raverdy N, et al. Cancer registry data based estimation of regional cancer incidence: application to breast and colorectal cancer in French administrative regions. J Epidemiol Community Health. 1999;53:558–564. doi: 10.1136/jech.53.9.558. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Smalley W, Ray WA, Daugherty J, Griffin MR. Use of nonsteroidal anti-inflammatory drugs and incidence of colorectal cancer: a population-based study. Arch Intern Med. 1999;159:161–166. doi: 10.1001/archinte.159.2.161. [DOI] [PubMed] [Google Scholar]
  • 5.Soliman AS, Smith MA, Cooper SP, Ismail K, Khaled H, Ismail S, McPherson RS, Seifeldin IA, Bondy ML. Serum organochlorine pesticide levels in patients with colorectal cancer in Egypt. Arch Environ Health. 1997;52:409–415. doi: 10.1080/00039899709602219. [DOI] [PubMed] [Google Scholar]
  • 6.Kee F, Wilson R, Currie S, Sloan J, Houston R, Rowlands B, Moorehead J. Socioeconomic circumstances and the risk of bowel cancer in Northern Ireland. J Epidemiol Community Health. 1996;50:640–644. doi: 10.1136/jech.50.6.640. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Liu X, Zheng S, Chen K, Ma X, Zhou L, Yu H, Yao K, Chen K, Cai S, Zhang S. [Randomized controlled trial of sequence mass screening program for colorectal cancer] Zhonghua Liuxing Bingxue Zazhi. 2000;21:430–433. [PubMed] [Google Scholar]
  • 8.Haile RW, Siegmund KD, Gauderman WJ, Thomas DC. Study-design issues in the development of the University of Southern California Consortium's Colorectal Cancer Family Registry. J Natl Cancer Inst Monogr. 1999;(26):89–93. doi: 10.1093/oxfordjournals.jncimonographs.a024231. [DOI] [PubMed] [Google Scholar]
  • 9.Campbell T. Colorectal cancer. Part 1: Epidemiology, aetiology, screening and diagnosis. Prof Nurse. 1999;14:869–874. [PubMed] [Google Scholar]
  • 10.Coughlin SS, Miller DS. Public health perspectives on testing for colorectal cancer susceptibility genes. Am J Prev Med. 1999;16:99–104. doi: 10.1016/s0749-3797(98)00137-8. [DOI] [PubMed] [Google Scholar]
  • 11.Mantel N. Synthetic retrospective studies and related topics. Biometrics. 1973;29:479–486. [PubMed] [Google Scholar]
  • 12.Hellard ME, Sinclair MI, Fairley CK, Andrews RM, Bailey M, Black J, Dharmage SC, Kirk MD. An outbreak of cryptosporidiosis in an urban swimming pool: why are such outbreaks difficult to detect. Aust N Z J Public Health. 2000;24:272–275. doi: 10.1111/j.1467-842x.2000.tb01567.x. [DOI] [PubMed] [Google Scholar]
  • 13.McDonald AD, McDonald JC, Rando RJ, Hughes JM, Weill H. Cohort mortality study of North American industrial sand workers. I. Mortality from lung cancer, silicosis and other causes. Ann Occup Hyg. 2001;45:193–199. [PubMed] [Google Scholar]
  • 14.Coker AL, Gerasimova T, King MR, Jackson KL, Pirisi L. High-risk HPVs and risk of cervical neoplasia: a nested case-control study. Exp Mol Pathol. 2001;70:90–95. doi: 10.1006/exmp.2000.2350. [DOI] [PubMed] [Google Scholar]
  • 15.Josefsson AM, Magnusson PK, Ylitalo N, Sørensen P, Qwarforth-Tubbin P, Andersen PK, Melbye M, Adami HO, Gyllensten UB. Viral load of human papilloma virus 16 as a determinant for development of cervical carcinoma in situ: a nested case-control study. Lancet. 2000;355:2189–2193. doi: 10.1016/S0140-6736(00)02401-6. [DOI] [PubMed] [Google Scholar]
  • 16.Akre O, Lipworth L, Tretli S, Linde A, Engstrand L, Adami HO, Melbye M, Andersen A, Ekbom A. Epstein-Barr virus and cytomegalovirus in relation to testicular-cancer risk: a nested case-control study. Int J Cancer. 1999;82:1–5. doi: 10.1002/(sici)1097-0215(19990702)82:1<1::aid-ijc1>3.0.co;2-l. [DOI] [PubMed] [Google Scholar]
  • 17.Del Amo J, Petruckevitch A, Phillips AN, De Cock KM, Stephenson J, Desmond N, Hanscheid T, Low N, Newell A, Obasi A, et al. Risk factors for tuberculosis in patients with AIDS in London: a case-control study. Int J Tuberc Lung Dis. 1999;3:12–17. [PubMed] [Google Scholar]
  • 18.Mathews WC, Caperna J, Toerner JG, Barber RE, Morgenstern H. Neutropenia is a risk factor for gram-negative bacillus bacteremia in human immunodeficiency virus-infected patients: results of a nested case-control study. Am J Epidemiol. 1998;148:1175–1183. doi: 10.1093/oxfordjournals.aje.a009606. [DOI] [PubMed] [Google Scholar]
  • 19.Wideroff L, Potischman N, Glass AG, Greer CE, Manos MM, Scott DR, Burk RD, Sherman ME, Wacholder S, Schiffman M. A nested case-control study of dietary factors and the risk of incident cytological abnormalities of the cervix. Nutr Cancer. 1998;30:130–136. doi: 10.1080/01635589809514652. [DOI] [PubMed] [Google Scholar]
  • 20.Deacon JM, Evans CD, Yule R, Desai M, Binns W, Taylor C, Peto J. Sexual behaviour and smoking as determinants of cervical HPV infection and of CIN3 among those infected: a case-control study nested within the Manchester cohort. Br J Cancer. 2000;83:1565–1572. doi: 10.1054/bjoc.2000.1523. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Ylitalo N, Sørensen P, Josefsson AM, Magnusson PK, Andersen PK, Pontén J, Adami HO, Gyllensten UB, Melbye M. Consistent high viral load of human papillomavirus 16 and risk of cervical carcinoma in situ: a nested case-control study. Lancet. 2000;355:2194–2198. doi: 10.1016/S0140-6736(00)02402-8. [DOI] [PubMed] [Google Scholar]
  • 22.García Rodríguez LA, Huerta-Alvarez C. Reduced incidence of colorectal adenoma among long-term users of nonsteroidal antiinflammatory drugs: a pooled analysis of published studies and a new population-based study. Epidemiology. 2000;11:376–381. doi: 10.1097/00001648-200007000-00003. [DOI] [PubMed] [Google Scholar]
  • 23.Knekt P, Hakulinen T, Leino A, Heliövaara M, Reunanen A, Stevens R. Serum albumin and colorectal cancer risk. Eur J Clin Nutr. 2000;54:460–462. doi: 10.1038/sj.ejcn.1600997. [DOI] [PubMed] [Google Scholar]
  • 24.Bertario L, Russo A, Crosignani P, Sala P, Spinelli P, Pizzetti P, Andreola S, Berrino F. Reducing colorectal cancer mortality by repeated faecal occult blood test: a nested case-control study. Eur J Cancer. 1999;35:973–977. doi: 10.1016/s0959-8049(99)00062-3. [DOI] [PubMed] [Google Scholar]
  • 25.Collet JP, Sharpe C, Belzile E, Boivin JF, Hanley J, Abenhaim L. Colorectal cancer prevention by non-steroidal anti-inflammatory drugs: effects of dosage and timing. Br J Cancer. 1999;81:62–68. doi: 10.1038/sj.bjc.6690651. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Kato I, Dnistrian AM, Schwartz M, Toniolo P, Koenig K, Shore RE, Akhmedkhanov A, Zeleniuch-Jacquotte A, Riboli E. Serum folate, homocysteine and colorectal cancer risk in women: a nested case-control study. Br J Cancer. 1999;79:1917–1922. doi: 10.1038/sj.bjc.6690305. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27.Kato I, Dnistrian AM, Schwartz M, Toniolo P, Koenig K, Shore RE, Zeleniuch-Jacquotte A, Akhmedkhanov A, Riboli E. Iron intake, body iron stores and colorectal cancer risk in women: a nested case-control study. Int J Cancer. 1999;80:693–698. doi: 10.1002/(sici)1097-0215(19990301)80:5<693::aid-ijc11>3.0.co;2-g. [DOI] [PubMed] [Google Scholar]
  • 28.Karlén P, Kornfeld D, Broström O, Löfberg R, Persson PG, Ekbom A. Is colonoscopic surveillance reducing colorectal cancer mortality in ulcerative colitis A population based case control study. Gut. 1998;42:711–714. doi: 10.1136/gut.42.5.711. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.Meijer GA, Baak JP, Talbot IC, Atkin WS, Meuwissen SG. Predicting the risk of metachronous colorectal cancer in patients with rectosigmoid adenoma using quantitative pathological features. A case-control study. J Pathol. 1998;184:63–70. doi: 10.1002/(SICI)1096-9896(199801)184:1<63::AID-PATH974>3.0.CO;2-D. [DOI] [PubMed] [Google Scholar]
  • 30.Hemminki K, Lönnstedt I, Vaittinen P, Lichtenstein P. Estimation of genetic and environmental components in colorectal and lung cancer and melanoma. Genet Epidemiol. 2001;20:107–116. doi: 10.1002/1098-2272(200101)20:1<107::AID-GEPI9>3.0.CO;2-4. [DOI] [PubMed] [Google Scholar]
  • 31.Chapman PD, Burn J. Genetic predictive testing for bowel cancer predisposition: the impact on the individual. Cytogenet Cell Genet. 1999;86:118–124. doi: 10.1159/000015363. [DOI] [PubMed] [Google Scholar]
  • 32.Thorson AG, Knezetic JA, Lynch HT. A century of progress in hereditary nonpolyposis colorectal cancer (Lynch syndrome) Dis Colon Rectum. 1999;42:1–9. doi: 10.1007/BF02235175. [DOI] [PubMed] [Google Scholar]
  • 33.Briskey EN, Pamies RJ. Colorectal cancer: update on recent advances and their impact on screening protocols. J Natl Med Assoc. 2000;92:222–230. [PMC free article] [PubMed] [Google Scholar]
  • 34.Lichtenstein P, Holm NV, Verkasalo PK, Iliadou A, Kaprio J, Koskenvuo M, Pukkala E, Skytthe A, Hemminki K. Environmental and heritable factors in the causation of cancer--analyses of cohorts of twins from Sweden, Denmark, and Finland. N Engl J Med. 2000;343:78–85. doi: 10.1056/NEJM200007133430201. [DOI] [PubMed] [Google Scholar]
  • 35.Marchand LL. Combined influence of genetic and dietary factors on colorectal cancer incidence in Japanese Americans. J Natl Cancer Inst Monogr. 1999;(26):101–105. doi: 10.1093/oxfordjournals.jncimonographs.a024220. [DOI] [PubMed] [Google Scholar]
  • 36.Bonaïti-Pellié C. Genetic risk factors in colorectal cancer. Eur J Cancer Prev. 1999;8 Suppl 1:S27–S32. [PubMed] [Google Scholar]
  • 37.Ponz de Leon M, Pedroni M, Benatti P, Percesepe A, Rossi G, Genuardi M, Roncucci L. Epidemiologic and genetic factor in colorectal cancer: development of cancer in dizygotic twins in a family with Lynch syndrome. Ital J Gastroenterol Hepatol. 1999;31:218–222. [PubMed] [Google Scholar]
  • 38.Prichard PJ, Tjandra JJ. Colorectal cancer. Med J Aust. 1998;169:493–498. [PubMed] [Google Scholar]
  • 39.Rafter J, Glinghammar B. Interactions between the environment and genes in the colon. Eur J Cancer Prev. 1998;7 Suppl 2:S69–S74. doi: 10.1097/00008469-199805000-00011. [DOI] [PubMed] [Google Scholar]
  • 40.Gandhi SK, Reynolds MW, Boyer JG, Goldstein JL. Recurrence and malignancy rates in a benign colorectal neoplasm patient cohort: results of a 5-year analysis in a managed care environment. Am J Gastroenterol. 2001;96:2761–2767. doi: 10.1111/j.1572-0241.2001.04137.x. [DOI] [PubMed] [Google Scholar]
  • 41.Ritenbaugh C. Diet and prevention of colorectal cancer. Curr Oncol Rep. 2000;2:225–233. doi: 10.1007/s11912-000-0072-2. [DOI] [PubMed] [Google Scholar]
  • 42.Park JG, Park YJ, Wijnen JT, Vasen HF. Gene-environment interaction in hereditary nonpolyposis colorectal cancer with implications for diagnosis and genetic testing. Int J Cancer. 1999;82:516–519. doi: 10.1002/(sici)1097-0215(19990812)82:4<516::aid-ijc8>3.0.co;2-u. [DOI] [PubMed] [Google Scholar]
  • 43.Jansen MC, Bueno-de-Mesquita HB, Buzina R, Fidanza F, Menotti A, Blackburn H, Nissinen AM, Kok FJ, Kromhout D. Dietary fiber and plant foods in relation to colorectal cancer mortality: the Seven Countries Study. Int J Cancer. 1999;81:174–179. doi: 10.1002/(sici)1097-0215(19990412)81:2<174::aid-ijc2>3.0.co;2-#. [DOI] [PubMed] [Google Scholar]
  • 44.Gertig DM, Hunter DJ. Genes and environment in the etiology of colorectal cancer. Semin Cancer Biol. 1998;8:285–298. doi: 10.1006/scbi.1998.0078. [DOI] [PubMed] [Google Scholar]
  • 45.Gulis G, Fitz O, Wittgruber J, Suchanová G. Colorectal cancer and environmental pollution. Cent Eur J Public Health. 1998;6:188–191. [PubMed] [Google Scholar]
  • 46.van Kranen HJ, van Iersel PW, Rijnkels JM, Beems DB, Alink GM, van Kreijl CF. Effects of dietary fat and a vegetable-fruit mixture on the development of intestinal neoplasia in the ApcMin mouse. Carcinogenesis. 1998;19:1597–1601. doi: 10.1093/carcin/19.9.1597. [DOI] [PubMed] [Google Scholar]
  • 47.Kenji T, Hedio O, Yasuharu O, Iwao Y, Tomohiro S, Katsuya Y, Kiichi M, Shigeru T, Hideki A. [Dietary factors and prevention of colon cancer] Nihon Geka Gakkai Zasshi. 1998;99:368–372. [PubMed] [Google Scholar]
  • 48.Charalambopoulos A, Syrigos KN, Ho JL, Murday VA, Leicester RJ. Colonoscopy in symptomatic patients with positive family history of colorectal cancer. Anticancer Res. 2000;20:1991–1994. [PubMed] [Google Scholar]
  • 49.Winawer SJ. Natural history of colorectal cancer. Am J Med. 1999;106:3S–6S; discussion 50S-51S. doi: 10.1016/s0002-9343(98)00338-6. [DOI] [PubMed] [Google Scholar]
  • 50.Wang ZQ, He J, Chen W, Chen Y, Zhou TS, Lin YC. Relationship between different sources of drinking water, water quality improvement and gastric cancer mortality in Changle County-A retrospective-cohort study in high incidence area. World J Gastroenterol. 1998;4:45–47. doi: 10.3748/wjg.v4.i1.45. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 51.Martínez Martínez L, López Santamaría M, Prieto Bozano G, Molina Arias M, Jiménez Alvarez C, Tovar Larrucea JA. [Diagnosis and therapeutic options in chronic idiopathic intestinal pseudo-obstruction: review of 16 cases] Cir Pediatr. 1999;12:71–74. [PubMed] [Google Scholar]
  • 52.Browning SM. Constipation, diarrhea, and irritable bowel syndrome. Prim Care. 1999;26:113–139. doi: 10.1016/s0095-4543(05)70105-6. [DOI] [PubMed] [Google Scholar]
  • 53.Ho KY, Kang JY, Seow A. Prevalence of gastrointestinal symptoms in a multiracial Asian population, with particular reference to reflux-type symptoms. Am J Gastroenterol. 1998;93:1816–1822. doi: 10.1111/j.1572-0241.1998.00526.x. [DOI] [PubMed] [Google Scholar]
  • 54.Iacono G, Cavataio F, Montalto G, Florena A, Tumminello M, Soresi M, Notarbartolo A, Carroccio A. Intolerance of cow's milk and chronic constipation in children. N Engl J Med. 1998;339:1100–1104. doi: 10.1056/NEJM199810153391602. [DOI] [PubMed] [Google Scholar]
  • 55.Lal G, Ash C, Hay K, Redston M, Kwong E, Hancock B, Mak T, Kargman S, Evans JF, Gallinger S. Suppression of intestinal polyps in Msh2-deficient and non-Msh2-deficient multiple intestinal neoplasia mice by a specific cyclooxygenase-2 inhibitor and by a dual cyclooxygenase-1/2 inhibitor. Cancer Res. 2001;61:6131–6136. [PubMed] [Google Scholar]
  • 56.Rex DK. Surveillance colonoscopy following resection of colorectal polyps and cancer. Can J Gastroenterol. 2001;15:57–59. doi: 10.1155/2001/751657. [DOI] [PubMed] [Google Scholar]
  • 57.Anderson J. Clinical practice guidelines. Review of the recommendations for colorectal screening. Geriatrics. 2000;55:67–73; quiz 74. [PubMed] [Google Scholar]
  • 58.Katsumata T, Igarashi M, Kobayashi K, Sada M, Yokoyama K, Saigenji K. [Usefulness of endoscopic polypectomy in early colorectal cancer] Nihon Geka Gakkai Zasshi. 1999;100:782–786. [PubMed] [Google Scholar]
  • 59.Tobi M. Polyps as biomarkers for colorectal neoplasia. Front Biosci. 1999;4:D329–D338. doi: 10.2741/tobi. [DOI] [PubMed] [Google Scholar]
  • 60.Gruber M, Lance P. Colorectal cancer detection and screening. Lippincotts Prim Care Pract. 1998;2:369–376; quiz 377-378. [PubMed] [Google Scholar]
  • 61.Kennedy BP, Soravia C, Moffat J, Xia L, Hiruki T, Collins S, Gallinger S, Bapat B. Overexpression of the nonpancreatic secretory group II PLA2 messenger RNA and protein in colorectal adenomas from familial adenomatous polyposis patients. Cancer Res. 1998;58:500–503. [PubMed] [Google Scholar]
  • 62.Luo YQ, Ma LS, Zhao YL, Wu KC, Pan BR, Zhang XY. Expression of proliferating cell nuclear antigen in polyps from large intestine. World J Gastroenterol. 1999;5:160–164. doi: 10.3748/wjg.v5.i2.160. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 63.Steindorf K, Tobiasz-Adamczyk B, Popiela T, Jedrychowski W, Penar A, Matyja A, Wahrendorf J. Combined risk assessment of physical activity and dietary habits on the development of colorectal cancer. A hospital-based case-control study in Poland. Eur J Cancer Prev. 2000;9:309–316. doi: 10.1097/00008469-200010000-00004. [DOI] [PubMed] [Google Scholar]
  • 64.Negri E, Franceschi S, Parpinel M, La Vecchia C. Fiber intake and risk of colorectal cancer. Cancer Epidemiol Biomarkers Prev. 1998;7:667–671. [PubMed] [Google Scholar]
  • 65.Järvinen R, Knekt P, Hakulinen T, Rissanen H, Heliövaara M. Dietary fat, cholesterol and colorectal cancer in a prospective study. Br J Cancer. 2001;85:357–361. doi: 10.1054/bjoc.2001.1906. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 66.Franceschi S, Favero A. The role of energy and fat in cancers of the breast and colon-rectum in a southern European population. Ann Oncol. 1999;10 Suppl 6:61–63. [PubMed] [Google Scholar]
  • 67.Rieger MA, Parlesak A, Pool-Zobel BL, Rechkemmer G, Bode C. A diet high in fat and meat but low in dietary fibre increases the genotoxic potential of 'faecal water'. Carcinogenesis. 1999;20:2311–2316. doi: 10.1093/carcin/20.12.2311. [DOI] [PubMed] [Google Scholar]
  • 68.Giovannucci E. An updated review of the epidemiological evidence that cigarette smoking increases risk of colorectal cancer. Cancer Epidemiol Biomarkers Prev. 2001;10:725–731. [PubMed] [Google Scholar]
  • 69.Gertig DM, Stampfer M, Haiman C, Hennekens CH, Kelsey K, Hunter DJ. Glutathione S-transferase GSTM1 and GSTT1 polymorphisms and colorectal cancer risk: a prospective study. Cancer Epidemiol Biomarkers Prev. 1998;7:1001–1005. [PubMed] [Google Scholar]
  • 70.Terry P, Ekbom A, Lichtenstein P, Feychting M, Wolk A. Long-term tobacco smoking and colorectal cancer in a prospective cohort study. Int J Cancer. 2001;91:585–587. doi: 10.1002/1097-0215(200002)9999:9999<::aid-ijc1086>3.0.co;2-h. [DOI] [PubMed] [Google Scholar]
  • 71.Chao A, Thun MJ, Jacobs EJ, Henley SJ, Rodriguez C, Calle EE. Cigarette smoking and colorectal cancer mortality in the cancer prevention study II. J Natl Cancer Inst. 2000;92:1888–1896. doi: 10.1093/jnci/92.23.1888. [DOI] [PubMed] [Google Scholar]
  • 72.Yoshioka M, Katoh T, Nakano M, Takasawa S, Nagata N, Itoh H. Glutathione S-transferase (GST) M1, T1, P1, N-acetyltransferase (NAT) 1 and 2 genetic polymorphisms and susceptibility to colorectal cancer. J UOEH. 1999;21:133–147. doi: 10.7888/juoeh.21.133. [DOI] [PubMed] [Google Scholar]
  • 73.Sinha R, Chow WH, Kulldorff M, Denobile J, Butler J, Garcia-Closas M, Weil R, Hoover RN, Rothman N. Well-done, grilled red meat increases the risk of colorectal adenomas. Cancer Res. 1999;59:4320–4324. [PubMed] [Google Scholar]
  • 74.Neugut AI, Rosenberg DJ, Ahsan H, Jacobson JS, Wahid N, Hagan M, Rahman MI, Khan ZR, Chen L, Pablos-Mendez A, et al. Association between coronary heart disease and cancers of the breast, prostate, and colon. Cancer Epidemiol Biomarkers Prev. 1998;7:869–873. [PubMed] [Google Scholar]

Articles from World Journal of Gastroenterology are provided here courtesy of Baishideng Publishing Group Inc

RESOURCES