Search tips
Search criteria 


Logo of plosonePLoS OneView this ArticleSubmit to PLoSGet E-mail AlertsContact UsPublic Library of Science (PLoS)
PLoS One. 2010; 5(7): e11636.
Published online 2010 July 16. doi:  10.1371/journal.pone.0011636
PMCID: PMC2905435

Risk Factors for Colorectal Cancer in Patients with Multiple Serrated Polyps: A Cross-Sectional Case Series from Genetics Clinics

Syed A. Aziz, Editor



Patients with multiple serrated polyps are at an increased risk for developing colorectal cancer (CRC). Recent reports have linked cigarette smoking with the subset of CRC that develops from serrated polyps. The aim of this work therefore was to investigate the association between smoking and the risk of CRC in high-risk genetics clinic patients presenting with multiple serrated polyps.

Methods and Findings

We identified 151 Caucasian individuals with multiple serrated polyps including at least 5 outside the rectum, and classified patients into non-smokers, current or former smokers at the time of initial diagnosis of polyposis. Cases were individuals with multiple serrated polyps who presented with CRC. Controls were individuals with multiple serrated polyps and no CRC. Multivariate logistic regression was performed to estimate associations between smoking and CRC with adjustment for age at first presentation, sex and co-existing traditional adenomas, a feature that has been consistently linked with CRC risk in patients with multiple serrated polyps. CRC was present in 56 (37%) individuals at presentation. Patients with at least one adenoma were 4 times more likely to present with CRC compared with patients without adenomas (OR = 4.09; 95%CI 1.27 to 13.14; P = 0.02). For females, the odds of CRC decreased by 90% in current smokers as compared to never smokers (OR = 0.10; 95%CI 0.02 to 0.47; P = 0.004) after adjusting for age and adenomas. For males, there was no relationship between current smoking and CRC. There was no statistical evidence of an association between former smoking and CRC for both sexes.


A decreased odds for CRC was identified in females with multiple serrated polyps who currently smoke, independent of age and the presence of a traditional adenoma. Investigations into the biological basis for these observations could lead to non-smoking-related therapies being developed to decrease the risk of CRC and colectomy in these patients.


Familial non-syndromic colorectal cancer (CRC) constitutes one of the most difficult and diverse patient groups encountered in a genetics clinic, with no apparent germline mutation, an often-indeterminant mode of inheritance, and questions arising as to how to manage the probands, and how to identify which family members are also at risk for CRC. One such condition is hyperplastic polyposis syndrome (HPS), a colorectal polyposis of unknown etiology characterized by the development of multiple serrated polyps in the large intestine. Efforts to define the clinical boundary of HPS have been hampered by heterogeneity of phenotype, with a vast array of polyp numbers, sizes [1], histological subtypes [2], and varying distributions in the colon leading to a set of recognition criteria which are necessarily stringent but which may exclude a significant number of high-risk cases [3]. The clinical significance of HPS is that it is associated with an increased personal and familial risk of CRC [4], [5], [6], [7], and extra-colonic cancers in the wider family setting [8].

Some 10 years ago, Rashid et al suggested that there are at least two phenotypic subtypes of HPS. The first demonstrates numerous hyperplastic polyps which may or may not be large, and such patients have also been described in series by Williams et al [9] and Ferrandez et al [10]. An alternative phenotype of HPS demonstrates fewer polyps than that described above however includes a diversity of polyp types including common hyperplastic polyps, serrated adenomas, sessile serrated adenomas, traditional adenomas, and polyps with mixed elements [1], [11]. This second phenotype of HPS is reported to be more likely to have polyps with diameters exceeding 1cm, dysplastic changes, to involve the proximal colon and to be associated with the presence of CRC [6]. Despite this, estimation of CRC risk in individual patients with HPS remains problematical [12], [13]. That there are at least two forms of HPS has been also suggested by others [14]. The reasons for this phenotypic dichotomy are currently unknown but may involve genetic backgrounds and environmental modifiers.

One environmental modifier may be cigarette smoking. The relationship between serrated neoplasia and smoking has been examined in a number of population-based studies [15], and evidence for an association has emerged for both precursor and malignant lesions in the serrated pathway [16], [17], [18], [19], [20], [21]. Multiple independent studies have shown an identical pattern of higher risk estimates for serrated (hyperplastic) polyps than for adenomas [16], [17], [19] in long-term and current smokers. The highest risks of all were observed when both adenomas and serrated polyps were present [16], [17], [19]. In a meta-analysis of risk factors for serrated polyps, both common and advanced lesions were significantly associated with current cigarette smoking [22]. Consistent with this, several large population-based studies have demonstrated that the CRC subset bearing the molecular signature of serrated neoplasia, namely somatic BRAF mutation, CpG Island Methylator Phenotype (CIMP) and microsatellite instability (MSI) has the highest association with smoking [23] [18], [20]. Given these findings, the authors have explored the effects of cigarette smoking on phenotype and risk of CRC in a large series of high-risk patients with multiple serrated polyps attending genetics clinics. This study presented an opportunity to determine whether cigarette smoking contributed to the increased risk of CRC in these patients.


This cross-sectional study comprised 151 Caucasian patients with multiple serrated polyps (with at least 5 occurring outside the rectum) recruited from genetics clinics in Australia and New Zealand (n = 139) and North America (n = 12) regardless of family history of polyps and cancer. This was done in order to target high-risk patients more likely to be predisposed to serrated polyps whilst simultaneously limiting the chances of recruiting patients with common late-onset distal serrated polyps. Forty-one patients from Australia were participants in the Colon Cancer Family Registry (Colon CFR) [24], 39 were from the Royal Melbourne Hospital Hyperplastic Polyposis Study [25], and the balance of participants were enrolled in the Genetics of Serrated Neoplasia (GSN) study ( through Cancer Care Ontario, Ohio State University Medical Center, the Combined Genetics Clinics of Australia and the Familial GI Cancer Registry of New Zealand. Thirty-six patients from Australia, and 8 from North America have been reported previously [25], [26]. Patients gave written informed consent to participate in research and the study was approved by the HREC of Queensland Institute of Medical Research under the Genetics of Serrated Neoplasia Project (QIMR HREC Protocol P912).


The use of the term serrated polyp in this report encompasses any polyp with serrated glandular architecture [27], and includes hyperplastic or metaplastic polyps, serrated adenoma, sessile serrated adenoma and mixed polyps. Minimum reported polyp count was obtainable from patient records in 120 individuals and in the remaining 31 individuals, polyposis was described as numerous (n = 2), prolific (n = 1) or multiple suggesting hyperplastic polyposis and prompting referral to a genetics clinic (n = 28). Polyposis was categorised into two groups where polyp count was known; moderate (5–79 polyps) and dense (≥80 polyps) [28], and into those fulfilling WHO HPS criterion 3 (>30 polyps throughout the colon) and those with polyp counts between 5 and 30 [3]. Cigarette smoking status of patients at the time of initial diagnosis with polyposis was categorised into 3 groups; never, former and current smokers. Cases were individuals with multiple serrated polyps who presented with at least one CRC at the time of initial diagnosis with polyposis. Controls were individuals with multiple serrated polyps who had not developed CRC at the time of initial diagnosis with polyposis. Index patients were those who presented independent of other family members, and screening cases were diagnosed subsequently to an index case in their respective families.

Polyps and Cancers

Pathology review of polyps was undertaken by a specialist gastrointestinal pathologist (NIW). Twenty-eight CRC were available for analysis and underwent a BRAF V600E somatic mutation test as follows. The somatic T>A mutation at nucleotide 1799 causing the V600E mutation in the BRAF gene was determined using a fluorescent allele specific PCR assay. Briefly, 20–50ng of DNA, extracted from formalin-fixed paraffin-embedded tumour tissue, was amplified in a 25µl reaction containing 100nM each of allele specific primers tagged with differing fluorophores (Mutant Primer (F1): 6-Fam-5′-CAGTGATTTTGGTCTAGCTTCAGA-3′ Wild Type Primer (F2): NED - 5′- TGATTTTGGTCTAGCTACAGT-3′ and a common reverse primer (Reverse Primer (REV): 5′-CTCAATTCTTACCATCCACAAAATG-3′), together with 2.5units of Taq polymerase (Eppendorf), 1× buffer and 200µM of dNTPs. The cycling conditions consisted of an initial denaturation of 95°C for 2mins followed by 35 cycles of 94°C for 30sec, 59°C for 30sec and 65°C for 30sec then a final extension of 65°C for 10mins. After amplification 1µl of the PCR product was added to an 8.7µl mix of HiDi formamide and ROX Genescan 500 size marker (Applied Biosystems, Foster City, CA). The mutant allele (A1799) primer generated a PCR product of 97bp, 3bp larger than the wildtype PCR product after separation on an ABI 3100 genetic analyser. GeneMarker (SoftGenetics) software was used to identify the different size and fluorescent allele PCR products. Positive and negative controls were run in each experiment and 10% of samples were replicated with 100% concordance.

Statistical Analysis

Logistic regressions were performed to estimate odds ratios (ORs) and 95% confidence intervals (95% CIs) for the associations between predictor variables and CRC. Patients with missing data were excluded from the analyses. To estimate the independent effect of cigarette smoking on the risk of CRC, we used multivariable logistic regression models adjusting for potential confounders including age at diagnosis, sex and presence of traditional adenomas. We also tested for interactions between sex and cigarette smoking status in association with CRC. The association between smoking and CRC was estimated separately for males and females. All regression models were compared using the Bayesian Information Criterion [29], [30].

All statistical tests were two-sided and P-value <0.05 was considered as a significant level of statistical evidence to reject the null hypothesis. All statistical analyses were done using Stata 10.0 [31].


In this analysis, a total of 151 patients diagnosed with multiple serrated polyps were recruited from Australia (n = 89), New Zealand (n = 50), Ohio, USA (n = 11) and Canada (n = 1). CRC was diagnosed in 57 (38%) individuals at presentation. The frequency of patients from Australasia presenting with CRC (37%) was not different significantly from that of North America (42%) (P = 0.8). Baseline characteristics for the study patients are shown in Table 1.

Table 1
Baseline characteristics of participants in the study.

Of all participants, 33% (30/90) of female and 43% (26/61) of male patients presented with at least one CRC. Mean age at diagnosis of polyposis cases with CRC was 52 (standard deviation, SD 15) years ranging from 18 to 85 years while mean age at diagnosis of polyposis in controls (no CRC) was 46 (SD 15) years ranging from 16 to 76 years (P = 0.033). Where site was known, 62% (33/53) of CRC occurred in the proximal colon (P<0.001). Proximal cancer was less frequent in patients under 50 (8/21 or 38%) compared to patients aged 50 and over (25/32 or 78%) (OR = 0.17; 95%CI 0.05 to 0.58; P = 0.005). There was no significant difference between the sexes with respect to the location of the CRC (P = 0.48). Eleven of twenty eight CRC cases (39%) tested positive for somatic BRAF mutation and all 11 were located in the proximal colon. Patients presenting with CRC had significantly higher reported polyp counts (58, SD 55) than did those with no CRC (32, SD 24) (P = 0.002).

A total of 140 patients had at least one polyp reported as an adenoma. Of these, 49 (45%) individuals had CRC. Patients with colorectal adenomas were four times more likely to be diagnosed with CRC compared to patients without adenomas (OR = 4.09; 95%CI 1.27 to 13.14; P = 0.02) after adjusting for age, sex and smoking status (Table 2). Patients with dense polyposis (≥80 polyps) had 5 times increased odds of CRC compared to those with moderate polyposis (5–79 polyps) (OR = 4.31; 95%CI 1.74 to 16.24; P = 0.003). Similarly patients who met WHO HPS criterion 3 were three times more likely to have CRC compared to those who did not (OR = 2.63; 95%CI 1.15 to 6.00; P = 0.02). We found no statistical evidence for increased odds of CRC in patients with advanced serrated polyps (most of which were non-dysplastic sessile serrated adenomas) compared to those without (adjusted OR = 1.15; 95%CI 0.47 to 2.78; P = 0.76). All associations (ORs) were adjusted for age, sex and smoking status (not shown in the tables).

Table 2
Association between smoking, adenoma, sex, age and CRC in patients presenting with multiple serrated polyps.

Of patients diagnosed with CRC, 26 (47%) patients had no history of smoking while 19 (34%) and 10 (20%) patients were former and current smokers respectively. Odds of CRC for former smokers was not statistically different compared to never smokers (OR = 0.71; 95%CI 0.29 to 1.77; P = 0.46) after adjusting for age, sex and adenomas. In addition, there was no statistical difference in the average pack-year exposure between patients with and without CRC (mean pack-years 13.9 vs 14; P = 0.95). We found no significant differences in polyp counts between current smokers and former smokers for either males (mean polyp count 49 vs 41; P = 0.46) or females (41 vs 45; P = 0.74), and between current smokers and never smokers for either males (mean polyp count 49 vs 38; P = 0.36) or females (41 vs 37; P = 0.84).

Current smokers were at 65% decreased odds of CRC compared with never smokers (OR = 0.35; 95%CI 0.14 to 0.88; P = 0.03) after adjusting for age, sex and adenomas. For females, the odds of CRC decreased by 90% in current smokers compared to never smokers (OR = 0.10; 95%CI 0.02 to 0.47; P = 0.004) after adjusting for age and adenomas. For males, there was no statistical evidence for an association between current smoking and CRC (Table 3). The association between current smoking and CRC for male and female HPS cases was statistically different (Interaction between current smoking and sex; P = 0.02). Of all patients in the study, 113/151 (75%) were index patients (those representing the initial diagnosis in each family). When the analysis was confined to index patients, the same pattern of decreased risk in females was observed (OR = 0.11; 95%CI 0.02 to 0.62; P = 0.01). A schematic diagram of the relationship between smoking status at diagnosis and presenting with a CRC is shown in Figure 1, and details of all female patients in the study are given in Table S1.

Figure 1
Schematic diagram of all female patients in the study with CRC and smoking status, showing the decreased odds of presenting with CRC in those currently smoking.
Table 3
Association between cigarette smoking and CRC in multiple serrated polyp patients stratified by sex.


In this cross-sectional series of high-risk patients with multiple serrated polyps, we have shown that the risk of CRC is increased in the presence of a synchronous adenoma, and decreased in females who are current smokers, regardless of age. In contrast, a positive association between smoking and colorectal neoplasia has been consistently reported. Multiple primary reports and meta-analyses have demonstrated that long term and current exposure to cigarette smoke is significantly associated with both colorectal cancer and its precursor lesions [16], [18], [19], [20], [21], [22], [32], [33], [34], [35], [36], [37], [38], [39], [40], [41], [42], [43], [44], [45], [46], [47], [48]. The evidence regarding precursor lesions is particularly strong. In a meta-analysis of 42 independent studies, smoking was significantly associated with adenomatous polyps with an OR of 2.14 (95%CI 1.86–2.46). Risk estimates were higher in studies where the control population had undergone colonoscopy [34], thus supporting an earlier hypothesis proposed by Terry and Neugut [49] that controls need to be screened in order that a more accurate risk estimate be obtained. When serrated polyps are examined, higher risk estimates than for adenomas are obtained, and higher again are the risk estimates from patients with both serrated polyps and adenomas [16], [17], [19].

When the association between smoking and colorectal cancer is analysed, risk estimates are decreased compared to those obtained when studying polyps, a phenomenon known as the smoking paradox. Two reasons for this have been proposed. Firstly that the effect of smoking on polyps may be greatest in small lesions with little malignant potential, and secondly that a longer latency period than the duration of many cohort studies may be required for smoking to exert its effects [34]. Whilst both of these reasons are likely to contribute to the smoking paradox, recent work on molecular sub-typing has demonstrated that smoking is significantly associated with the subset of colorectal cancers which harbor a somatic mutation in BRAF [18], and this may also contribute to the apparent dilution effect of smoking on colorectal cancer as BRAF-mutated cancers comprise only 10% overall. Where CRC were linked to somatic BRAF mutation, the risk was associated with long-term smoking [18].

Despite this evidence, international health-governing bodies such as the office of the US Surgeon General and the International Agency for Research on Cancer (IARC) have deemed this evidence insufficient to establish causality [32]. The major reason for this is that the results may be confounded by factors associated with both smoking and colorectal cancer such as physical activity [50], alcohol consumption [51], and diet [52]. A recent report however addressed both multiple risk factors and long duration of smoking in studying a large cohort of patients where the median duration of smoking was 44 years. The results confirmed that long-term smoking presented the highest risk for colorectal cancer, even after adjusting for multiple covariates known to affect risk [32].

Given the consistent findings from multiple reports that current smoking increases the risk of serrated polyps, and the significant association between smoking and colorectal cancer which develops via the serrated pathway, we studied a group of high-risk patients predisposed to develop multiple serrated polyps with a view to exploring the influence of smoking on the increased CRC risk present in this group of patients. Our results suggest that in patients predisposed to developing multiple serrated polyps, there is no significant association between smoking and an increased risk of presentation with CRC. In a recently-reported analysis of risk factors for serrated polyps, current smokers showed significant increases in risk for both common and advanced serrated polyps particularly in the distal colon [22]. In our study, CRC were more likely to be proximal, suggesting that if the effect of smoking in patients with multiple serrated polyps is to increase the likelihood of left sided polyps, then our findings that smoking overall has no significant effect on CRC development is consistent with this, as left colon serrated polyps are less likely to undergo malignant conversion. Of interest, a previously reported association with distal CRC was confirmed in our study in patients aged under 50 at presentation [25], [28], [53].

An unexpected finding of our study was that current smoking in females reduced the risk of presenting with CRC when compared to never smokers. This result remained significant after adjusting for both age at presentation and adenomas, as patients with a CRC were older at presentation than patients without a malignant lesion, as well as the finding of an increased risk of CRC conferred by at least one traditional adenoma. The two female patients in our study who were currently smoking and who presented with CRC were later-onset, and were among the long-term smokers (>40 years) as well as those with the highest polyp counts (122 and 129 respectively, with pan-colonic polyposis but interestingly concentrated in the recto-sigmoid). In a very recent publication, Walker and colleagues presented a series of 32 patients, predominantly female, with hyperplastic polyposis where 9 currently smoking female patients were described. Of note, three of these 9 patients had CRC and all 3 had recto-sigmoid polyp counts >50 [54]. Therefore it is likely that the females with multiple serrated polyps whose disease is more proximally located are the targets of this observed effect. In addition, the effect on female current smokers, though significant, was not complete, and suggests only a subset with a particular genetic background or who are within a dose-response window, are responding to a component of cigarette smoke, and this fraction will vary among patient cohorts. Polyp counts were significantly higher in patients with CRC in our series, however variances were large thus suggesting an overlapping distribution of cancer risk, and highlighting the complex nature of this condition. The most important risk factor for CRC remained the presence of a co-existing adenomatous lesion [6], [28], [55], the nature of which is a current area of investigation [56]. Of the 4 patients with CRC in whom no traditional adenomas were reported, one demonstrated multiple serrated adenomas (dysplastic serrated polyps). The confirmation that the presence of dysplasia in individuals with multiple serrated polyps is a risk factor for developing CRC will signal to clinicians the need for increased vigilance if continuing colonoscopic surveillance in these individuals and may trigger a discussion regarding surgery if all polyps cannot be removed.

Patients with HPS as currently defined are at a significantly increased risk of presenting with CRC, and are likely to represent a subset of the population with a particular genetic background [57]. Two large studies of 77 and 126 patients respectively, suggest that the risk of CRC in HPS is approximately 30–40% [28], [58], and coupled with a high background of somatic BRAF mutation (30–40% of CRC arising in HPS have a somatic BRAF mutation) [59], such an elevated risk may simply serve to overwhelm any effect of smoking on BRAF-mutated CRC. In the current report, we found no evidence that current smoking was more likely to be associated with a BRAF-mutated CRC. Of interest, a recent publication has shown that the BRAF-smoking-CRC axis is essentially confined to males [60].

The apparent decrease in CRC risk for currently smoking females is consistent with a biological mechanism akin to that observed in patients with ulcerative colitis which may be operating in a subset of female patients with multiple serrated polyps. The anti-inflammatory effects of smoking in ulcerative colitis are anecdotally well known, and the risk to females of CRC in ulcerative colitis is significantly decreased with respect to males [61]. The results reported here suggest that inflammatory processes may be responsible for neoplastic progression in serrated neoplasia predisposition in a subset of female patients. A risk factor study for serrated polyps has demonstrated that aspirin use decreased the risk of advanced proximal polyps, lending indirect support to this finding [22]. Alternatively, unspecified sex-specific factors related to body mass index (BMI), or hormonal factors, as are seen in the protective effects of smoking on endometrial cancer may be confounding the results reported here. Since no BMI or hormonal data were available for these patients at the time of writing, it is not possible to test this hypothesis. Of interest, decreased risks from current smoking for ASPs have been reported previously from a series of serrated polyp patients with no co-existing CRC or adenomas [62], and this work alludes to possible overlapping mechanisms with the findings of our report. Though cases in that report were not partitioned by sex, another previous report has shown that advanced serrated polyps are more likely to be present in females [63].

The results of our study suggest that current smoking neither accounts for, nor exacerbates, the high risk of CRC in patients predisposed to multiple serrated polyps. Further, in females with multiple serrated polyps, current smoking appears to be associated with a decreased risk of presenting with CRC. Due to the limited numbers in our analysis, our findings may be due to chance. The results of our study may also be influenced by ascertainment status of the patients, but when we reanalyzed our data using only index patients, the results remained significant. Three-quarters of our patients represented the first presentation in their respective families, and 70% of these had no affected relatives with CRC so were referred to the genetics service on the basis of having polyposis. A further effect on the outcomes reported here is that confounders including diet, obesity, physical activity, hormonal status and alcohol intake, may have influenced the results, and further larger studies will be needed to confirm our findings both in high-risk clinics and in the population. Our findings are unlikely to be broadly applicable to sporadic CRC cases as patients with multiple serrated polyps from genetics clinics are likely to have a particular genetic background, however, there may be some overlapping effects [62]. The direct effects of sex hormones alone can be ruled out by the number of females, many of whom are below the age of menopause, who were former or never smokers and who have presented with CRC. The increased proportion of patients with numerous serrated polyps who are current smokers has been noted previously [28], [54], and this observation requires further investigation to determine whether cigarette smoking enhances the phenotype [28], thus bringing it to clinical attention, or is associated with symptom relief in patients with a high polyp burden who therefore continue to smoke.

Importantly, investigations into the biological mechanism for our observation of decreased risk of CRC in females may lead to a CRC-preventive modality for female patients with serrated polyps independent of cigarette smoking and its attendant health risks, and may ultimately lead to a desirable reduction in the incidence of colectomy in the management of high-risk female patients with multiple serrated polyps. In addition, increased surveillance may be required in females when smoking cessation occurs to counteract any potential rebound effect. If this biological mechanism is an anti-inflammatory process, alternative therapies to nicotine could potentially be established in the treatment regimen of female patients with multiple serrated polyps.

Supporting Information

Table S1

Details for all female participants with multiple serrated polyps. FH CRC = family history of CRC; ASP = advanced serrated polyp; AD = adenomas; CRC = presented with CRC at initial diagnosis; y = yes, n = no, u = unknown

(0.21 MB DOC)


The authors acknowledge the contribution of staff and participants in the Genetics of Serrated Neoplasia (GSN) study (, the Familial GI Cancer Registry of New Zealand, the Ohio State University Medical Center, The Jeremy Jass Memorial Pathology Collection, the Colon Cancer Family Registry ( and the Royal Melbourne Hospital.


Competing Interests: The authors have declared that no competing interests exist.

Funding: This work was supported by grants from the Cancer Council Queensland, the Hicks Foundation in Victoria, and the National Cancer Institute through 1R01CA123010 (Genetics of Serrated Neoplasia) and RFA # CA-95-011 through cooperative agreements with the Australasian Colorectal Cancer Family Registry (U01 CA097735). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.


1. Rashid A, Houlihan PS, Booker S, Petersen GM, Giardiello FM, et al. Phenotypic and molecular characteristics of hyperplastic polyposis. Gastroenterology. 2000;119:323–332. [PubMed]
2. Torlakovic E, Snover DC. Serrated adenomatous polyposis in humans. Gastroenterology. 1996;110:748–755. [PubMed]
3. Burt R, Jass JR. Hyperplastic polyposis. In: Hamilton SR, Aaltonen LA, editors. Pathology and Genetics of Tumours of the Digestive System. Lyon: IARC Press; 2000. pp. 135–136.
4. Hyman NH, Anderson P, Blasyk H. Hyperplastic polyposis and the risk of colorectal cancer. Dis Colon Rectum. 2004;47:2101–2104. [PubMed]
5. Lage P, Cravo M, Sousa R, Chaves P, Salazar M, et al. Management of Portuguese patients with hyperplastic polyposis and screening of at-risk first-degree relatives: a contribution for future guidelines based on a clinical study. Am J Gastroenterol. 2004;99:1779–1784. [PubMed]
6. Leggett BA, Devereaux B, Biden K, Searle J, Young J, et al. Hyperplastic polyposis: association with colorectal cancer. Am J Surg Pathol. 2001;25:177–184. [PubMed]
7. Yeoman A, Young J, Arnold J, Jass J, Parry S. Hyperplastic polyposis in the New Zealand population: a condition associated with increased colorectal cancer risk and European ancestry. N Z Med J. 2007;120:U2827. [PubMed]
8. Jarrar AM, Church JM, Fay S, Kalady MF. Is the phenotype mixed or mistaken? Hereditary nonpolyposis colorectal cancer and hyperplastic polyposis syndrome. Dis Colon Rectum. 2009;52:1949–1955. [PubMed]
9. Williams GT, Arthur JF, Bussey HJR, Morson BC. Metaplastic polyps and polyposis of the colorectum. Histopathology. 1980;4:155–170. [PubMed]
10. Ferrandez A, Samowitz W, DiSario JA, Burt RW. Phenotypic characteristics and risk of cancer development in hyperplastic polyposis: case series and literature review. Am J Gastroenterol. 2004;99:2012–2018. [PubMed]
11. Renaut AJ, Douglas PR, Newstead GL. Hyperplastic polyposis of the colon and rectum. Colorectal Dis. 2002;4:213–215. [PubMed]
12. Jass JR. Gastrointestinal polyposes: clinical, pathological and molecular features. Gastroenterol Clin North Am. 2007;36:viii. [PubMed]
13. Jass JR. Colorectal Polyposes: from phenotype to diagnosis. Pathology Research and Practice. 2008;204:431–47. [PubMed]
14. Burt RW, Samowitz WS. Serrated adenomatous polyposis: A new syndrome? Gastroenterology. 1996;110:950–952. [PubMed]
15. Young J. Serrated neoplasia of the colorectum and cigarette smoking. Gastroenterology. 2008;135:323–324. [PubMed]
16. Ji BT, Weissfeld JL, Chow WH, Huang WY, Schoen RE, et al. Tobacco smoking and colorectal hyperplastic and adenomatous polyps. Cancer Epidemiol Biomarkers Prev. 2006;15:897–901. [PubMed]
17. Morimoto L, Newcomb P, Ulrich C, Bostick R, Lais C, et al. Risk factors for hyperplastic and adenomatous polyps: evidence for malignant potential? Cancer Epidemiol Biomarkers Prev. 2002;11:1012–1018. [PubMed]
18. Samowitz WS, Albertsen H, Sweeney C, Herrick J, Caan BJ, et al. Association of smoking, CpG island methylator phenotype, and V600E BRAF mutations in colon cancer. J Natl Cancer Inst. 2006;98:1731–1738. [PubMed]
19. Shrubsole MJ, Wu H, Ness RM, Shyr Y, Smalley WE, et al. Alcohol Drinking, Cigarette Smoking, and Risk of Colorectal Adenomatous and Hyperplastic Polyps. Am J Epidemiol 2008 [PubMed]
20. Slattery ML, Curtin K, Anderson K, Ma KN, Ballard L, et al. Associations between cigarette smoking, lifestyle factors, and microsatellite instability in colon tumors. J Natl Cancer Inst. 2000;92:1831–1836. [PubMed]
21. Slattery ML, Curtin K, Sweeney C, Levin TR, Potter J, et al. Diet and lifestyle factor associations with CpG island methylator phenotype and BRAF mutations in colon cancer. Int J Cancer. 2007;120:656–663. [PubMed]
22. Wallace K, Grau MV, Ahnen D, Snover DC, Robertson DJ, et al. The association of lifestyle and dietary factors with the risk for serrated polyps of the colorectum. Cancer Epidemiol Biomarkers Prev. 2009;18:2310–2317. [PubMed]
23. Weisenberger DJ, Siegmund KD, Campan M, Young J, Long TI, et al. CpG island methylator phenotype underlies sporadic microsatellite instability and is tightly associated with BRAF mutation in colorectal cancer. Nat Genet. 2006;38:787–793. [PubMed]
24. Newcomb PA, Baron J, Cotterchio M, Gallinger S, Grove J, et al. Colon Cancer Family Registry: an international resource for studies of the genetic epidemiology of colon cancer. Cancer Epidemiol Biomarkers Prev. 2007;16:2331–2343. [PubMed]
25. Chow E, Lipton L, Lynch E, D'Souza R, Aragona C, et al. Hyperplastic polyposis syndrome: phenotypic presentations and the role of MBD4 and MYH. Gastroenterology. 2006;131:30–39. [PubMed]
26. Sweet K, Willis J, Zhou XP, Gallione C, Sawada T, et al. Molecular classification of patients with unexplained hamartomatous and hyperplastic polyposis. Jama. 2005;294:2465–2473. [PubMed]
27. Jass JR. Serrated adenoma of the colorectum and the DNA-methylator phenotype. Nature Clinical Practice. 2005;2:398–405. [PubMed]
28. Buchanan D, Sweet K, Drini M, Jenkins M, Win A, et al. Phenotypic Diversity in Patients with Multiple Serrated Polyps: A Genetics Clinic Study. 2010. International Journal of Colorectal Disease In Press 15th January 2010. [PMC free article] [PubMed]
29. Millar P. BIC: Stata module to evaluate the statistical significance of variables in a model: Statistical Software Components S449507 2005
30. Schwarz G. Estimating the Dimension of a Model. The Annals of Statistics. 1978;6:461–464.
31. StataCorp. Stata Statistical Software: Release 10. . 10 ed. 2007. College Station, TX.
32. Hannan LM, Jacobs EJ, Thun MJ. The association between cigarette smoking and risk of colorectal cancer in a large prospective cohort from the United States. Cancer Epidemiol Biomarkers Prev. 2009;18:3362–3367. [PubMed]
33. Peppone LJ, Mahoney MC, Cummings KM, Michalek AM, Reid ME, et al. Colorectal cancer occurs earlier in those exposed to tobacco smoke: implications for screening. J Cancer Res Clin Oncol 2008 [PMC free article] [PubMed]
34. Botteri E, Iodice S, Raimondi S, Maisonneuve P, Lowenfels AB. Cigarette smoking and adenomatous polyps: a meta-analysis. Gastroenterology. 2008;134:388–395. [PubMed]
35. Abrams JA, Terry MB, Neugut AI. Cigarette smoking and the colorectal adenoma-carcinoma sequence. Gastroenterology. 2008;134:617–619. [PubMed]
36. Widome R, Forster JL, Hannan PJ, Perry CL. Longitudinal patterns of youth access to cigarettes and smoking progression: Minnesota Adolescent Community Cohort (MACC) study (2000–2003). Prev Med. 2007;45:442–446. [PMC free article] [PubMed]
37. Paskett ED, Reeves KW, Rohan TE, Allison MA, Williams CD, et al. Association between cigarette smoking and colorectal cancer in the Women's Health Initiative. J Natl Cancer Inst. 2007;99:1729–1735. [PubMed]
38. Luchtenborg M, Le Marchand L. Tobacco smoking increases risk of colorectal cancer. Hawaii Med J. 2007;66:139. [PubMed]
39. Gupta C, Pabla M, Malani AK. Smoking and DNA mismatch repair polymorphisms in colorectal polyps and cancer. Am J Gastroenterol. 2007;102:211. [PubMed]
40. Buc E, Kwiatkowski F, Alves A, Panis Y, Mantion G, et al. Tobacco smoking: a factor of early onset of colorectal cancer. Dis Colon Rectum. 2006;49:1893–1896. [PubMed]
41. Anderson JC, Messina C. Smoking and risk for colorectal cancer. Arch Intern Med. 2006;166:1669–1670; author reply 1671. [PubMed]
42. Luchtenborg M, Weijenberg MP, Kampman E, van Muijen GN, Roemen GM, et al. Cigarette smoking and colorectal cancer: APC mutations, hMLH1 expression, and GSTM1 and GSTT1 polymorphisms. Am J Epidemiol. 2005;161:806–815. [PubMed]
43. Toyomura K, Yamaguchi K, Kawamoto H, Tabata S, Shimizu E, et al. Relation of cigarette smoking and alcohol use to colorectal adenomas by subsite: the self-defense forces health study. Cancer Sci. 2004;95:72–76. [PubMed]
44. Giovannucci E. Should smokers be considered a high-risk group for colorectal cancer? Dig Liver Dis. 2004;36:643–645. [PubMed]
45. Colditz GA, Yaus KP. Smoking causes colon carcinoma. Cancer. 2004;100:223–224. [PubMed]
46. Colangelo LA, Gapstur SM, Gann PH, Dyer AR. Cigarette smoking and colorectal carcinoma mortality in a cohort with long-term follow-up. Cancer. 2004;100:288–293. [PubMed]
47. Limburg PJ, Vierkant RA, Cerhan JR, Yang P, Lazovich D, et al. Cigarette smoking and colorectal cancer: long-term, subsite-specific risks in a cohort study of postmenopausal women. Clin Gastroenterol Hepatol. 2003;1:202–210. [PubMed]
48. Anderson JC, Attam R, Alpern Z, Messina CR, Hubbard P, et al. Prevalence of colorectal neoplasia in smokers. Am J Gastroenterol. 2003;98:2777–2783. [PubMed]
49. Terry MB, Neugut AI. Cigarette smoking and the colorectal adenoma-carcinoma sequence: a hypothesis to explain the paradox. Am J Epidemiol. 1998;147:903–910. [PubMed]
50. Trost SG, Owen N, Bauman AE, Sallis JF, Brown W. Correlates of adults' participation in physical activity: review and update. Med Sci Sports Exerc. 2002;34:1996–2001. [PubMed]
51. Strine TW, Okoro CA, Chapman DP, Balluz LS, Ford ES, et al. Health-related quality of life and health risk behaviors among smokers. Am J Prev Med. 2005;28:182–187. [PubMed]
52. Morabia A, Wynder EL. Dietary habits of smokers, people who never smoked, and exsmokers. Am J Clin Nutr. 1990;52:933–937. [PubMed]
53. Yantiss RK, Goodarzi M, Zhou XK, Rennert H, Pirog EC, et al. Clinical, pathologic, and molecular features of early-onset colorectal carcinoma. Am J Surg Pathol. 2009;33:572–582. [PubMed]
54. Walker RG, Landmann JK, Hewett DG, Worthley DL, Buttenshaw RL, et al. Hyperplastic Polyposis Syndrome Is Associated With Cigarette Smoking, Which May Be a Modifiable Risk Factor. Am J Gastroenterol 2010 [PubMed]
55. Rubio CA, Stemme S, Jaramillo E, Lindblom A. Hyperplastic polyposis coli syndrome and colorectal carcinoma. Endoscopy. 2006;38:266–270. [PubMed]
56. Pai RK, Mackinnon AC, Joseph L, Noffsinger A, Hart J. Identification of Histologically Distinct Conventional Adenomas that Arise Predominately in Patients With Sessile Serrated Adenomas. Am J Surg Pathol [PubMed]
57. Young J, Jass JR. The case for a genetic predisposition to serrated neoplasia in the colorectum: hypothesis and review of the literature. Cancer Epidemiol Biomarkers Prev. 2006;15:1778–1784. [PubMed]
58. Boparai KS, Mathus-Vliegen EM, Koornstra JJ, Nagengast FM, van Leerdam M, et al. Increased colorectal cancer risk during follow-up in patients with hyperplastic polyposis syndrome: a multicentre cohort study. Gut 2009 [PubMed]
59. Beach R, Chan AO, Wu TT, White JA, Morris JS, et al. BRAF mutations in aberrant crypt foci and hyperplastic polyposis. Am J Pathol. 2005;166:1069–1075. [PubMed]
60. Rozek LS, Herron CM, Greenson JK, Moreno V, Capella G, et al. Smoking, gender, and ethnicity predict somatic BRAF mutations in colorectal cancer. Cancer Epidemiol Biomarkers Prev. 2010;19:838–843. [PMC free article] [PubMed]
61. Soderlund S, Granath F, Brostrom O, Karlen P, Lofberg R, et al. Inflammatory Bowel Disease Confers a Lower Risk of Colorectal Cancer to Females Than to Males. Gastroenterology [PubMed]
62. Huang C, Farraye F, Shepherd C, Yang S, O'Brien MJ. A Case-Control Study of the Risk Factors for Advanced Serrated Polyps. Gastroenterology. 2008;134:A606 (T2038).
63. Spring KJ, Zhao ZZ, Karamatic R, Walsh MD, Whitehall VL, et al. High prevalence of sessile serrated adenomas with BRAF mutations: a prospective study of patients undergoing colonoscopy. Gastroenterology. 2006;131:1400–1407. [PubMed]

Articles from PLoS ONE are provided here courtesy of Public Library of Science