Role of Diet in Colorectal Cancer Incidence

1Colorectal cancer (CRC) is the third most commonly diagnosed cancer among men and the second most common cancer among women worldwide. The etiology of CRC is multifactorial, with both genetic and environmental factors playing a role. Evidence suggests that modifiable lifestyle factors, including excess adiposity, poor diet, and physical inactivity, play an important role in the occurrence and progression of this disease.,

2Several systematic reviews with meta-analysis of prospective observational studies have summarized evidence for the associations between dietary factors (eg, foods and food groups, beverages, alcohol, macronutrients, and micronutrients) and the incidence of CRC. However, to date, there has been little synthesis of the strength, precision, and quality of this evidence in aggregate. Umbrella reviews provide a structured and critical summary of the evidence and enable the grading of evidence according to specific criteria: sample size, strength and precision of the association, and assessment of the presence of biases.,, The review from the World Cancer Research Fund (WCRF) in partnership with the American Institute for Cancer Research (AICR) provided a summary report based on systematic reviews with dose-response meta-analysis of the association between dietary exposures and CRC. The WCRF/AICR report applied many, but not all, umbrella review criteria for evidence grading and was based on studies published until April 2015. To complement the WCRF/AICR report, we conducted an umbrella review of meta-analyses to provide an updated and unified systematic summary of epidemiological data evaluating the strength of the overall body of evidence investigating the associations between dietary factors and CRC incidence. Furthermore, we expand the review of dietary exposures to some not previously evaluated, such as certain dietary patterns.

3The protocol of this umbrella review has been registered in PROSPERO (CRD42020173636). This study adhered to the Meta-analysis of Observational Studies in Epidemiology (MOOSE) reporting guideline.

4We searched MEDLINE, Embase, and the Cochrane Library from database inception to September 2019 to identify meta-analyses of prospective, observational studies. The search strategy can be found in eTable 1 in the Supplement.

5Two authors (Y.S.L. and T.Y.W.) independently screened titles or abstracts and examined the full text of potentially eligible articles. Discrepancies were resolved by a third reviewer (S.K.V.).

6Studies were included that met the following criteria: (1) meta-analysis of prospective observational studies (ie, cohort design) among adults with multivariable-adjusted summary risk estimates and corresponding 95% CIs that (2) investigated the association of dietary factor(s) with the incidence of CRC. Eligible dietary factors included dietary patterns, prespecified diet quality indices, specific foods, food groups, beverages (including alcohol), macronutrients (ie, carbohydrates, fat, protein), and micronutrients (ie, vitamins, minerals, antioxidants, polyphenols). When more than 1 meta-analysis on the same research question was available, we assessed only the study that included the largest data set, as previously described (eAppendix in the Supplement)., We excluded meta-analyses of studies with other study designs and those with insufficient or inadequate data for quantitative synthesis.

7Data were extracted, and the methodological quality of included meta-analyses was assessed using A Measurement Tool to Assess Systematic Reviews (AMSTAR-2) by 2 authors (Y.S.L. and T.Y.W.) independently and checked by a third author (S.K.V.). For each eligible meta-analysis, we abstracted data at the meta-analysis level (eAppendix in the Supplement). Disagreements were resolved by consensus.

8For each association of diet with CRC, we recalculated the adjusted summary estimates and corresponding 95% CIs with P values using the DerSimonian and Laird random-effects model. Heterogeneity was assessed with the I2 statistic. We estimated the 95% prediction interval (PrI), which evaluates the uncertainty for the effect size that would be anticipated in a new study addressing the identical association. The evidence for small-study effects was assessed by Egger regression asymmetry test. P <.10 was taken as statistical evidence of the presence of small-study effects. We also applied the excess significance test, which evaluates whether the observed number of studies with statistically significant results (positive studies, P ≤.05) differs from the expected number of positive studies, by using a χ2 test. Excess significance bias was set at P ≤.10. The statistical analysis and power calculations were conducted using Stata version 15.0 (StataCorp).

9We graded the quality of the evidence per association generated by a meta-analysis by applying several criteria in concordance with previously published umbrella reviews.,, In brief, associations that presented nominally significant random-effects summary effect sizes (ie, P ≤.05) were graded as convincing (class I), highly suggestive (class II), suggestive (class III), or weak (class IV) evidence (Table 1).

10For each meta-analysis initially graded as showing convincing, highly suggestive, or suggestive evidence, we reexamined the list of adjusted confounding factors at the component study level. We performed a sensitivity analysis by including only adjusted estimates to assess the robustness of the main analysis. Based on the literature, the most consistent potential confounders considered for sensitivity analysis are age, body mass index (BMI), race, sex, and other dietary factors as observed in our umbrella review. Other sensitivity analyses included the omission of small-sized studies (ie, <25th percentile) from those meta-analyses with evidence of small-study effects, as detailed under the heading of statistical analyses and low-quality studies (as defined in each meta-analysis).

11In total, we identified 9954 publications, evaluated 222 full-text articles (2.2%), and included 45 meta-analyses (20.3%),,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,, describing 109 associations in this umbrella review (eFigure in the Supplement). The 177 articles (79.7%) that were excluded and the reasons for their exclusion are provided in eTable 2 in the Supplement. The descriptive characteristics of the 45 eligible meta-analyses,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,, are provided in eTable 3 in the Supplement. The included meta-analyses were published between 2006 and 2019. The median (interquartile range [IQR]) number of studies per meta-analysis was 6 (3-9), and the median (IQR) duration of follow-up was 10.2 (9.3-12.9) years. The median (IQR) meta-analysis sample size was 598 744 (229 046-991 476). The median (IQR) number of cases (ie, incidence of CRC) was 5076 (2673-9355) cases, and the number of cases was greater than 1000 for 99 associations (90.8%).

12The evaluation of methodological quality using AMSTAR-2 (Table 2 and Table 3; eTable 3 in the Supplement) revealed that 2 meta-analyses (4.4%) were of high quality and 15 meta-analyses (33.3%) were of moderate quality. Twenty meta-analyses (44.4%) were of low quality, with the remaining 8 (17.8%) rated as having critically low quality.

13Overall, the 45 meta-analyses described 109 associations, including 794 individual study estimates of CRC incidence associated with dietary exposures. The included meta-analyses provided adjusted summary estimates on the associations between dietary patterns,,,,, (13 associations), food groups,,,,,,,,,,, (23 associations), beverages including alcohol,,,,,,, (12 associations), macronutrients,,,,,,, (18 associations), and micronutrients,,,,,,,,,,,, (43 associations) and the incidence of CRC. Definitions of dietary patterns is provided in the eAppendix in the Supplement.

14A total of 35 of the 109 associations (32.1%) were nominally statistically significant at P ≤.05 (Table 2 and Table 3). Of these, only 7 associations (20.0%) reached statistical significance at P ≤ 1 × 10−6. Overall, 24 significant associations (68.6%) suggested potential protective effects of dietary factors or dietary patterns associated with CRC risk, including adherence to a healthy diet, Mediterranean diet, pesco-vegetarian diet, or semivegetarian diet and higher intakes of dietary fiber, whole grains, legumes, dairy products including yogurt and nonfermented milk, fruits and vegetables, and micronutrients (ie, supplemental and dietary calcium, zinc, magnesium, vitamin A, vitamin B6, folic acid, vitamin D, vitamin E). The remaining significant associations (31.4%) suggested higher risk of CRC with adherence to an unhealthy diet or Western diet and increased intake of alcohol, red meat, processed meat, pork, eggs, and haem iron.

15Seventeen associations (15.6%) had large heterogeneity (I2 > 50%). The 95% PrIs excluded the null value for 8 associations (7.3%). The effect sizes of the largest study were statistically significant at P ≤.05 for 29 associations (26.6%). Small-study effects were found for 11 associations (10.1%), and excess significance bias was not identified. Seventy-four (67.9%) associations without statistical significance at P ≤.05 using random-effects models are presented in eTable 4 in the Supplement.

16Among the 109 associations, 5 (4.6%) were supported by convincing evidence (Table 2 and Table 3). Two of these associations (40.0%), ie, higher vs lower red meat intake (AMSTAR-2, high quality) and heavy alcohol intake (defined as >4 drinks per day compared with those who did not drink or occasionally drank) (AMSTAR-2, moderate quality), were associated with increased risk of CRC. In contrast, convincing evidence was found for 3 inverse associations: higher vs lower intake of total dietary fiber (AMSTAR-2, high quality), calcium (AMSTAR-2, moderate quality), and yogurt (AMSTAR-2, moderate quality) were associated with reduced CRC incidence.

17Two associations (1.8%) had highly suggestive evidence of an association between diet and incidence of CRC (Table 2 and Table 3). Higher intake of total dairy products (eg, milk, cheese, yogurt) (AMSTAR-2, high quality) was associated with significant CRC risk reduction compared with lower intake. However, a moderate intake of alcohol (defined as >1-3 drinks but not more than 4 per day) (AMSTAR-2, moderate quality) was associated with an increase in the incidence of CRC compared with 0 drinks or occasionally drinking.

18Suggestive evidence for the association of diet or dietary patterns with reduced risk of CRC was found for 8 associations (7.3%), including adherence to the Mediterranean diet, adherence to a healthy diet, adherence to a pesco-vegetarian diet, adherence to a semivegetarian diet, and intake of whole grains, nonfermented milk, and supplemental calcium (Table 3). However, there was suggestive evidence that 2 exposures (adherence to the Western diet and intake of processed meat) were associated with increased risk of CRC in adults (Table 2). The remaining associations, with either weak evidence (18 [16.5%]) or no evidence (74 [67.9%]) are provided in Table 2, Table 3, and eTable 4 in the Supplement.

19Results from sensitivity analyses are reported in eTable 5 in the Supplement. Among convincing associations for increased risk of CRC, only alcohol exposure showed evidence for small-study effects. Removal of small studies from the alcohol analysis did not modify the evidence rating. When excluding low-quality studies and those that did not adjust for important potential confounders, both the association of alcohol intake and red meat intake with CRC retained their evidence ratings. For inverse associations, all retained the class I rank following sensitivity analyses. A summary of all sensitivity analyses is presented in Table 4.

20We included 45 published meta-analyses, which comprised 109 adjusted summary risk estimates for the associations of dietary factors with CRC incidence. We found that few of the 35 statistically significant associations (ie, positive associations of 4 drinks/d and red meat with the incidence of CRC and inverse associations of higher intake of dietary fiber, calcium, and yogurt with the incidence of CRC) were supported by convincing evidence in the main and sensitivity analyses. Suggestive evidence exists for an inverse association of a healthy dietary pattern, Mediterranean diet, pesco-vegetarian diet, and semivegetarian diet and intake of whole grains, total dairy products, and supplemental calcium with CRC incidence. Suggestive evidence also exists for positive associations between higher intakes of processed meat and a moderate intake of alcohol (>1-3 drinks/d) and the incidence of CRC.

21The continuous update project (CUP) report by the WCRF in partnership with the AICR conducted a comprehensive review including meta-analyses to draw conclusions about the roles of diet, nutrition, and physical activity in cancer prevention and survival. Although the WCRF/AICR report provides rigorous estimates for the association of diet with CRC incidence, their criteria for study inclusion and grading of evidence differed from the current umbrella review (eTable 6 in the Supplement). The current umbrella review widened the scope of dietary exposure evaluation to include dietary patterns, in particular, providing evidence to support following a Mediterranean diet or overall dietary patterns that exclude red meat (ie, semivegetarian and pesco-vegetarian diets). In addition, yogurt, which was not evaluated as a discrete exposure in the WCRF/AICR CUP report, was identified as being associated with reduced risk of CRC.

22Our findings largely support existing cancer prevention dietary guidance regarding increasing consumption of dietary fiber and dairy products and limiting intake of red meat and alcoholic beverages.,,, However, we did not find convincing evidence to support limiting consumption of processed meat for CRC prevention. Our results confirmed the positive association of processed meat products with CRC; however, its credibility was suggestive. We did not measure dose-response associations owing to data limitations. However, we examined the summary effect size estimate for concordance regarding the direction of association and level of statistical significance to other eligible meta-analyses reporting the same association (eTable 7 in the Supplement). Findings were concordant with our primary analysis regarding magnitude and direction of the association. Nonetheless, proposed biological mechanisms are highly plausible and the associations have been consistent across studies, with coherence between findings in humans and preclinical studies, providing support for a causal relationship. It has to be noted that the criteria in this article did not explicitly account for biologic plausibility as part of the determination for association.

23Although we found convincing evidence that a higher intake of dietary fiber was associated with reduced risk of CRC, the evidence for different sources of fiber remains low. We observed a suggestive inverse association between whole grains and CRC incidence. Fiber derived from whole grains is accompanied by micronutrients, such as folate, that have demonstrated associations with CRC, but less evidence supports a role in carcinogenesis for other fiber sources (eg, vegetables, fruit, and legumes). We observed a weak inverse association between fruit and vegetable consumption and CRC incidence. Fruit and vegetables are abundant sources not only of fiber, but also of micro- and macronutrients with antitumor properties; thus, they are plausible targets for dietary prevention. Although plausible and consistent, the associations of fruit and vegetable intake with CRC were also reported as weak in the WCRF/AICR reports,, which noted differences in association according to sex as well as nonlinear associations that may attenuate summary estimates.

24Our findings convincingly highlight dietary calcium and yogurt as associated with reduced risk of CRC incidence. Findings for cheese and milk were null and weak, respectively. We also found suggestive evidence for lower CRC risk with higher intakes of supplemental calcium. These findings are complementary given that all dietary factors are sources of calcium, which binds to unconjugated bile acids and free fatty acids in the colonic lumen to minimize their toxic effects. Whether dietary calcium is a causal factor in CRC prevention is difficult to determine given that other correlated constituents (eg, fortified vitamin D) could account for the observations. The high fat content of cheese and cream may hinder their protective associations, possibly by increasing bile acid and fatty acid excretion in the colonic lumen. Other nutrients or bioactive compounds in dairy products, such as lactoferrin or generation of butyrate, may also play a role. The biologic plausibility of yogurt’s associations with reduced risk of CRC stems from the presence of lactic acid–producing bacteria (Lactobacillus bulgaricus and Streptococcus thermophilus) that are purported to reduce levels of carcinogens such as nitroreductase, fecal-activated bacterial enzymes, and soluble fecal bile acids.,, Yogurt intake has been shown to reduce the risk of colorectal adenomas with high malignant potential independent of calcium and nonyogurt dairy intake. Its protective association could also be mediated through its calcium content and modulated by the gut microbiome.

25Selected meta-analyses provide suggestive evidence that supports the adoption of an overall healthy dietary pattern, Mediterranean diet, pesco-vegetarian diet, and semivegetarian diet to prevent CRC, in contrast with Western dietary patterns that are associated with increased CRC risk. Overall dietary pattern accounts for the totality of dietary components in combination and their synergistic or antagonistic influence on human metabolism and disease. Prudent dietary patterns, characterized by higher intakes of vegetables, fruit, whole grains, and low-fat dairy products and lower intakes of alcohol and meat products, are often accompanied by a healthier lifestyle; the converse is true for Western-type dietary patterns. Hence, the suggestive association observed for these dietary behaviors could be influenced by the totality of a healthy or unhealthy lifestyle, in addition to combination(s) of protective or harmful dietary factors.

26This study has limitations. A possible limitation of our review was exclusion of dose-response meta-analyses because the data needed for predictive interval estimation and assessment of small study and excess significant bias effects were not available in those articles. Randomized clinical trials, which account for confounding by design, are scarce in research on associations between diet and cancer owing to cost, the long follow-up time required for cancer end points, and ethical concerns. Consequently, we restricted the current umbrella review to meta-analyses of prospective observational studies. Some forms of bias, such as recall bias owing to self-reported diet, are possible but likely to be nondifferential, which would attenuate the observed associations. We generated estimates of publication bias by assessing small-study effects using the Egger test. However, the Egger test is not recommended with the inclusion of less than 10 studies. Although the small-study effect was indicated for only 11 meta-analyses (10.1%), among these 4 (36.4%) included 5 to 10 studies and 2 (18.2%) included less than 5 studies. However, we were unable to perform alternate tests, such as the Peters test, because this required cases and noncases for each level of exposure, and this information was largely lacking in the meta-analyses. Thus, more research is needed to investigate the associations based on small numbers of included studies. A further limitation is that we did not conduct subgroup analysis (eg, by sex, age group, or location of cancer, such as colon or rectum) because of the lack of data for grading the quality of evidence for most of the exposures. Dietary associations with CRC may differ according to sex and tumor location, as was highlighted by the WCRF/AICR reports.,

27The findings of this study support existing recommendations for diet in the primary prevention of CRC, emphasizing higher intakes of dietary fiber, calcium, and yogurt and lower intakes of red meat and alcohol. Emerging evidence supports a possible role for overall dietary patterns that, in totality, emphasize habitually consuming fruits, vegetables, grains, and low-fat dairy and reducing red meat and alcohol intake. More research is needed on specific foods for which evidence remains suggestive, including other dairy products, whole grains, processed meat, and specific dietary patterns.