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. 2021 Feb 1;18(2):e1003522. doi: 10.1371/journal.pmed.1003522

Healthy lifestyle, endoscopic screening, and colorectal cancer incidence and mortality in the United States: A nationwide cohort study

Kai Wang 1, Wenjie Ma 2,3, Kana Wu 1,4,5, Shuji Ogino 1,6,7,8, Andrew T Chan 2,3,5,8,9, Edward L Giovannucci 1,4,5, Mingyang Song 1,2,3,4,*
Editor: Frank T Kolligs10
PMCID: PMC7886195  PMID: 33524029

Abstract

Background

Healthy lifestyle and screening represent 2 major approaches to colorectal cancer (CRC) prevention. It remains unknown whether the CRC-preventive benefit of healthy lifestyle differs by endoscopic screening status, and how the combination of healthy lifestyle with endoscopic screening can improve CRC prevention.

Methods and findings

We assessed lifestyle and endoscopic screening biennially among 75,873 women (Nurses’ Health Study, 1988 to 2014) and 42,875 men (Health Professionals Follow-up Study, 1988 to 2014). We defined a healthy lifestyle score based on body mass index, smoking, physical activity, alcohol consumption, and diet. We calculated hazard ratios (HRs) and population-attributable risks (PARs) for CRC incidence and mortality in relation to healthy lifestyle score according to endoscopic screening. Participants’ mean age (standard deviation) at baseline was 54 (8) years. During a median of 26 years (2,827,088 person-years) follow-up, we documented 2,836 incident CRC cases and 1,013 CRC deaths. We found a similar association between healthy lifestyle score and lower CRC incidence among individuals with and without endoscopic screening, with the multivariable HR per one-unit increment of 0.85 (95% CI, 0.80 to 0.90) and 0.85 (95% CI, 0.81 to 0.88), respectively (P-interaction = 0.99). The fraction of CRC cases that might be prevented (PAR) by endoscopic screening alone was 32% (95% CI, 31% to 33%) and increased to 61% (95% CI, 42% to 75%) when combined with healthy lifestyle (score = 5). The corresponding PAR (95% CI) increased from 15% (13% to 16%) to 51% (17% to 74%) for proximal colon cancer and from 47% (45% to 50%) to 75% (61% to 84%) for distal CRC. Results were similar for CRC mortality. A limitation of our study is that our study participants are all health professionals and predominantly whites, which may not be representative of the general population.

Conclusions

Our study suggests that healthy lifestyle is associated with lower CRC incidence and mortality independent of endoscopic screening. An integration of healthy lifestyle with endoscopic screening may substantially enhance prevention for CRC, particularly for proximal colon cancer, compared to endoscopic screening alone.


Kai Wang and colleagues study contributions of healthy lifestyles and endoscopic screening to colorectal cancer outcomes.

Author summary

Why was this study done?

  • Colorectal cancer is the third leading cause of cancer death in both men and women in the United States.

  • Healthy lifestyle and screening represent 2 major approaches to colorectal cancer prevention.

  • Endoscopic screening can detect and remove precancerous lesions, but it remains unknown whether individuals having undergone endoscopic screening can still benefit from healthy lifestyle.

  • It remains to be determined to what extent a combination of healthy lifestyle and endoscopic screening can improve colorectal cancer prevention compared with endoscopic screening alone.

What did the researchers do and find?

  • Using 2 large nationwide cohorts in the US with a median of 26 years of follow-up, we prospectively examined the association of healthy lifestyle with colorectal cancer incidence and mortality among individuals having and not having undergone endoscopic screening separately.

  • We also estimated the proportion of colorectal cancer cases and deaths that are potentially prevented by endoscopic screening alone and by a combination of healthy lifestyle and endoscopic screening.

  • We found a similar association between healthy lifestyle and lower incidence and mortality of colorectal cancer among individuals having and not having undergone endoscopic screening.

  • We also found that an integration of healthy lifestyle with endoscopic screening might substantially enhance the prevention of colorectal cancer and related death compared with endoscopic screening alone, and the increment of the beneficial association was particularly high for proximal colon cancer.

What do these findings mean?

  • Our results indicate that healthy lifestyle is associated with lower colorectal cancer incidence and mortality independent of endoscopic screening status.

  • The evidence highlights the potential of healthy lifestyle to complement endoscopic screening for optimal prevention of colorectal cancer.

  • Our findings highlight the particular merit of an integration of healthy lifestyle and endoscopic screening for prevention of proximal colon cancer, for which endoscopic screening has limited effectiveness.

  • These findings suggest the value of healthy lifestyle for colorectal cancer prevention in settings lacking coverage or capacity of endoscopic screening.

Introduction

Colorectal cancer (CRC) is the third most commonly diagnosed cancer (40.7 per 100,000 population) and the third leading cause of cancer death (14.8 per 100,000 population) in the United States (US) according to the estimates in 2020 [1]. Screening has substantially contributed to the decline in CRC incidence and mortality in elderly Americans during the past 2 decades through detection and removal of precancerous lesions [25]. According to the most recent National Health Interview Survey in 2015, the prevalence of recommendation-consistent CRC screening has increased from 43% in 2005 to 63% in 2015 among US adults aged 50 years and older [6].

Healthy lifestyle practices, including no or quitted smoking, maintaining a healthy body weight, being physically active, limiting alcohol intake, and eating a healthy diet, have been associated with a substantial reduction in CRC incidence and mortality [712]. Compelling data indicate that 20% to 70% of CRC cases and deaths could potentially be prevented by adhering to a healthy lifestyle [1012], highlighting the essential role of healthy lifestyle in CRC prevention. However, adoption and long-term maintenance of healthy lifestyle are challenging, particularly due to the reported “health certificate effect” of CRC screening, in which individuals with negative endoscopic screening may perceive themselves as certified healthy and have reduced incentives for the adoption of healthy lifestyle [1315]. Nevertheless, it is unknown whether healthy lifestyle in individuals having already undergone endoscopic screening remains as beneficial for CRC prevention as those without endoscopic screening. Furthermore, how an integration of healthy lifestyle with endoscopic screening can improve CRC prevention compared with endoscopic screening alone is also an open question. Given the rising use of endoscopic screening, addressing these questions has important clinical and public health significance for improved CRC prevention.

Therefore, in the current study, we assessed the association of healthy lifestyle with CRC incidence and mortality among individuals having and not having undergone endoscopic screening within 2 large cohorts in the US, including the Nurses’ Health Study (NHS) and Health Professionals Follow-up Study (HPFS). We also calculated the population-attributable risks (PARs) for CRC incidence and mortality associated with endoscopic screening alone and a combination of healthy lifestyle and endoscopic screening.

Methods

Study population

The NHS included 121,700 US female nurses aged 30 to 55 years at enrollment in 1976; and the HPFS included 51,529 US male health professionals aged 40 to 75 years at enrollment in 1986 [16,17]. In both cohorts, participants completed a detailed questionnaire about their lifestyle and medical information at baseline, and every 2 years thereafter, with over 90% of follow-up [18]. In the current study, we defined baseline as the year of 1988 for both NHS and HPFS, when we started to collect information of endoscopy. Written informed consent was obtained from all participants. We conducted this study following a prospective analysis proposal (S1 Text). The study protocol was approved by the institutional review board of the Brigham and Women’s Hospital and Harvard T.H. Chan School of Public Health, and those of participating registries as required. This study was reported as per the Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) guideline (S1 Checklist).

Among participants who returned the baseline questionnaires (1988 for both cohorts), we excluded those who had a history of cancer (except nonmelanoma skin cancer), or ulcerative colitis; with a body mass index (BMI) of <18.5 kg/m2; reported implausible energy intakes (<500 or >3,500 kcal/d for women; <800 or >4,200 kcal/d for men); or with missing data on lifestyle exposures or endoscopic screening. After these exclusions, 75,873 women and 42,875 men were included in the analysis (see flowchart in S1 Fig).

Assessment of lifestyle factors

We considered 5 lifestyle factors: BMI, cigarette smoking, physical activity, diet, and alcohol intake. Height, body weight, cigarette smoking, and physical activity were self-reported through biennial questionnaires. Physical activity was assessed by the total hours per week for moderate-to-vigorous intensity activity (including brisk walking) that requires the expenditure of at least 3 metabolic equivalents per hour. Alcohol use and diet were self-reported every 4 years using validated food frequency questionnaires [19,20]. Diet quality was assessed using the 6 dietary recommendations by the World Cancer Research Fund/American Institute for Cancer Research (WCRF/AICR) Third Expert Report released in 2018 for red meat, processed meat, dietary fiber, dairy products, whole grains, and calcium supplement use [21]. To capture long-term exposures and reduce random within-person variation, we calculated cumulative average levels of the exposures. When data on lifestyle factors were missing in a given questionnaire cycle, the last nonmissing observation was carried forward. Detailed information of lifestyle and covariates assessment is provided in S2 Text.

For each of the 5 lifestyle factors, we defined a binary criterion, by which the participants received a score of 1 if they met the criterion and 0 otherwise. The healthy lifestyle comprised a BMI of ≥18.5 and <25.0 kg/m2, never smoking or past smoking with pack-years <5, moderate-to-vigorous intensity activity for ≥30 minutes per day, none-to-moderate alcohol intake (<1 drink [14 g alcohol] per day for women and <2 drinks per day for men), and meeting at least 3 of the 6 dietary recommendations by the WCRF/AICR Third Expert Report 2018. An overall healthy lifestyle score (range, 0 to 5) was then calculated by summing the 5 scores, with a higher score indicating a healthier lifestyle.

Assessment of endoscopic screening

In both cohorts, beginning in 1988 and continuing through 2002, participants were asked biennially whether they had undergone lower gastrointestinal endoscopy and, if so, the reason for the endoscopy. In 2004, we additionally inquired whether the previously reported endoscopies were sigmoidoscopies or colonoscopies. In every cycle thereafter, responses for sigmoidoscopy and colonoscopy were recorded separately. In random samples of participants who reported having negative endoscopy (n = 114 in the NHS and 140 in the HPFS), we collected endoscopic records and observed high concordance rate with self-reported negative endoscopy (97% in the NHS and 100% in the HPFS) [2224].

Participants were considered as endoscopically unscreened until the first time they reported undertaking endoscopy for screening purpose and as endoscopically screened thereafter for the remainder of follow-up. Given our focus on screening endoscopy, we stopped updating endoscopy information in mortality analysis once a participant is diagnosed with CRC.

Ascertainment of cases and deaths of CRC

Participants reported CRC diagnoses on each biennial questionnaire. CRC deaths were identified through the National Death Index or reported by family members [25]. For the reported CRC cases or deaths, we obtained medical records to confirm the diagnosis or cause of death by study physicians. When we were unable to obtain medical records (approximately 10% of cases), we linked to the appropriate cancer registry to confirm the diagnosis or death.

We classified CRCs into proximal colon cancers that encompassed those occurring in the cecum, ascending colon, hepatic flexure, and transverse colon; and distal CRCs that encompassed those occurring in the splenic flexure, descending colon, sigmoid colon, rectosigmoid junction, and rectum. We also staged CRC according to the American Joint Committee on Cancer (AJCC) tumor–node–metastasis (TNM) cancer staging system [26].

Statistical analysis

Details about statistical analysis are provided in S2 Text. Participants contributed person-time from return of the baseline questionnaire (1988 for both cohorts) until the date of CRC diagnosis (for CRC incidence analysis only), death, loss to follow-up, or end of the follow-up period (June 30, 2014 for the NHS and January 31, 2014 for the HPFS), whichever came first. We first calculated the age-adjusted CRC incidence and mortality rates by healthy lifestyle score and endoscopic screening status. To account for multiple records per participant and time-varying exposures and covariates, we used an Andersen-Gill data structure with a new record for each 2-year follow-up period. Then, we used time-varying and age-, period-, and cohort-stratified Cox proportional hazards regression models to estimate the multivariable hazard ratios (HRs) and 95% confidence intervals (CIs) for the associations of individual and combined lifestyle factors with CRC incidence and mortality according to endoscopic screening status. We also assessed the associations by anatomical site (proximal colon cancer or distal CRC) and AJCC TNM stage of CRC (TNM 1 and 2 or 3 and 4) using the subtype-stratified Cox proportional cause-specific hazards regression model by the duplication method [27].

To examine the benefit of an integration of healthy lifestyle with endoscopic screening compared to endoscopic screening alone, we calculated the hypothetical PARs [28] and 95% CIs [10] to estimate the proportion of CRC cases and deaths that could have been avoided if all participants in the cohorts had undertaken endoscopic screening and/or maintained healthy lifestyle. To calculate the PARs, we derived the exposure prevalence within our cohorts and used multivariable pooled logistic regression models to calculate the relative risk (RR) [29]. Using the prevalence (Pi) at the exposure category i and the corresponding RR estimates (RRi), we calculated the PAR for healthy lifestyle using the following approximate formula: PAR=Pi(HRi1)Pi(HRi1)+1 [30]. To examine the incremental benefit, we ran the PAR analysis for different definitions of healthy lifestyle (score of ≥2, ≥3, ≥4, or = 5).

In secondary analyses, we calculated the PARs according to family history of CRC (yes and no), regular aspirin use (yes and no), age (≤65, 66–75, and >75 years), and sex (female and male). Because CRC screening is generally recommended for individuals aged 50 to 75 years [6,31], we repeated our analyses among participants aged 50 to 75 years only. To examine whether the results were driven differently by colonoscopic and sigmoidoscopic screenings, we repeated the analyses by only focusing on colonoscopic screening while excluding the person-time counted in the sigmoidoscopic screening group. Due to that we carried forward the status of endoscopic screening since the first time they reported taking endoscopic screening, as a sensitivity analysis, we suspended updating the lifestyle information since the first endoscopic screening and repeated the analysis. In the main analysis, we counted the cycles when no response to endoscopy was recorded (accounting for 11% of all person-time) into the non-screening group, so we repeated the analysis after excluding the cycles as a sensitivity analysis. Because the binary variables could not account for the gradient in CRC risk with more extreme levels of these lifestyle factors, we conducted another sensitivity analysis by calculating an expanded healthy lifestyle score using more refined categorizations for the lifestyle factors. We assigned scores of 1 (least healthy) to 5 (most healthy) to the categories of the lifestyle factors and summed the scores across all 5 factors (range, 5 to 25). We then categorized this expanded score into 6 levels (5 to 10, 11 to 13, 14 to 16, 17 to 19, 20 to 22, and 23 to 25), which were defined as the new healthy lifestyle score (0, 1, 2, 3, 4, and 5). Finally, to examine the benefit of healthy lifestyle for overall health, we assessed mortality due to other causes than CRC. In this analysis, we additionally adjusted for physical exam for disease screening, mammography for breast cancer screening (women only), and prostate-specific antigen testing for prostate cancer screening (men only).

Results

In the 2 cohorts of 118,748 participants with a median of 26 years (2,827,088 person-years) of follow-up, we documented 2,836 incident CRC cases and 1,013 CRC deaths, among which 1,131 cases (40%) and 375 deaths (37%) were of proximal colon cancer, 1,305 cases (46%) and 433 deaths (43%) were of distal colorectal cancer, with the remaining (14% cases and 20% deaths) having no confirmed site information. Overall, 41% and 59% of person-years occurred in the endoscopic screening and non-screening groups, respectively. As shown in Table 1, compared with the non-screening group, the screening group were older, more likely to be male, have family history of CRC, use aspirin, use multivitamins, and have a healthier lifestyle. Within each of the 2 groups, participants with a healthier lifestyle were more likely to be younger, have family history of CRC, and use multivitamins.

Table 1. Age- and sex-standardized characteristics* of study participants according to endoscopic screening status and healthy lifestyle score.

Nonendoscopic screening (1,661,951 person-years, 59%) Endoscopic screening (1,165,137 person-years, 41%)
Healthy lifestyle score Healthy lifestyle score
0 2 4 0 2 4
Person-years (% within group) 40,813 (2) 603,843 (36) 195,339 (12) 25,379 (2) 383,484 (33) 180,278 (15)
Age, years 62.7 61.9 61.2 69.0 68.7 68.7
Male sex, % 38 29 38 44 39 46
White, % 98 96 95 98 95 94
Family history of colorectal cancer, % 12 13 13 19 20 21
Regular aspirin use, % 29 26 25 35 33 32
Current multivitamins use, % 37 39 48 50 51 59
Body mass index, kg/m2 28.3 27.0 23.1 28.2 27.0 23.3
Current smoker, % 30 13 2 13 6 1
Pack-years of smoking 34.8 24.9 12.1 32.4 23.1 11.5
Alcohol intake, g/d 32.3 6.3 4.4 31.8 7.7 5.5
Physical activity, min/d 9.5 15.1 39.2 10.7 17.7 39.7
Dietary intake
    Red meat, serving/d 0.7 0.7 0.5 0.7 0.6 0.4
    Processed meat, serving/d 0.4 0.4 0.2 0.4 0.3 0.2
    Dietary fiber, g/d 14.8 17.5 21.0 16.4 19.3 22.9
    Dairy products, serving/d 2.2 2.3 2.5 2.2 2.2 2.3
    Whole grain, g/d 12.0 17.2 26.4 16.7 22.4 31.4
    Whole grains: total grains in weight 0.2 0.2 0.3 0.3 0.3 0.4
    Calcium supplement, % 35 39 59 41 44 64

* Updated information throughout follow-up was used to calculate the means for continuous variables and percentage for categorical variables. All variables are age- and sex-standardized except person-years, age, and sex.

† Healthy lifestyle score (range, 0–5) was defined as the number of the 5 healthy lifestyle factors: normal body weight (body mass index, ≥18.5 and <25.0 kg/m2), never smoking or past smoking with pack-years <5, moderate-to-vigorous intensity activity for ≥30 minutes per day, none-to-moderate alcohol intake (<1 drink [14 g alcohol]/d for women and <2 drinks/d for men), and meeting at least 3 of the 6 dietary recommendations by the World Cancer Research Fund/American Institute for Cancer Research Third Expert Report 2018, which included red meat <0.5 serving/d, processed meat <0.2 serving/d, dietary fiber ≥30 g/d, dairy products ≥3 servings/d, whole grains ≥48 g/d or account for at least half of total grains, and calcium supplement use.

‡ Among ever smokers only.

Fig 1 shows the associations of healthy lifestyle score with CRC incidence and mortality according to endoscopic screening status. Each unit increment in the healthy lifestyle score was associated with an HR for CRC incidence of 0.85 (95% CI, 0.80 to 0.90) in the screening group and 0.85 (95% CI, 0.81 to 0.88) in the non-screening group (P-interaction = 0.99) (Fig 1A). Compared with participants without endoscopic screening and living a less healthy lifestyle (score = 0), those with screening and a less healthy lifestyle had an HR of CRC incidence of 0.37 (95% CI, 0.24 to 0.56), those without screening but living the healthiest lifestyle (score = 5) had an HR of 0.38 (95% CI, 0.26 to 0.56), those with both screening and a healthiest lifestyle had an HR of 0.14 (95% CI, 0.09 to 0.23). Likewise, the associations of healthy lifestyle score with CRC mortality were also similar among individuals with and without endoscopic screening, with the HR of 0.82 (95% CI, 0.74 to 0.91) and 0.89 (95% CI, 0.82 to 0.96), respectively (P-interaction = 0.27) (Fig 1B). Overall, endoscopic screening was associated with an HR for CRC incidence of 0.53 (95% CI, 0.49 to 0.58) and for CRC mortality of 0.49 (95% CI, 0.43 to 0.56).

Fig 1.

Fig 1

Association of healthy lifestyle score with CRC incidence (panel A) and mortality (panel B) according to endoscopic screening status and the corresponding age-adjusted incidence and mortality rates. Healthy lifestyle score (range, 0–5) was defined as the number of the 5 healthy lifestyle factors: normal body weight (BMI, ≥18.5 and <25.0 kg/m2), never smoking or past smoking with pack-years <5, moderate-to-vigorous intensity activity for ≥30 minutes per day, none-to-moderate alcohol intake (<1 drink [14 g alcohol]/d for women and <2 drinks/d for men), and meeting at least 3 of the 6 dietary recommendations by the WCRF/AICR Third Expert Report 2018, which included red meat <0.5 serving/d, processed meat <0.2 serving/d, dietary fiber ≥30 g/d, dairy products ≥3 servings/d, whole grains ≥48 g/d or account for at least half of total grains, and calcium supplement use. Multivariable Cox proportional hazards regression was used to calculate the HRs and 95% CIs while adjusting for age, calendar period, sex, ethnicity, current multivitamins use, regular aspirin use, family history of CRC, menopausal status and hormone use (women only) in incidence analysis, and, additionally, diagnoses of cardiovascular disease and type 2 diabetes in mortality analysis. Error bars indicate 95% CIs. BMI, body mass index; CI, confidence interval; CRC, colorectal cancer; HR, hazard ratio; pys, person-years; WCRF/AICR, World Cancer Research Fund/American Institute for Cancer Research.

When assessed by anatomical site and TNM stage, the associations remained similar between the screening and non-screening groups for proximal colon cancer (P-interaction = 0.29) and distal CRC (P-interaction = 0.93) (S2 Fig), and TNM 1 and 2 (P-interaction = 0.49) and TNM 3 and 4 CRC (P-interaction = 0.86) (S3 Fig). Similar associations were also found for each of the individual lifestyle factors between the screening and non-screening groups (all P-interaction > 0.10) (S1 and S2 Tables).

We then assessed the combined association of healthy lifestyle and endoscopic screening (Table 2). For CRC incidence, the PAR with endoscopic screening alone was 32% (95% CI, 31% to 33%), increased to 37% (95% CI, 33% to 41%) when combined with a healthy lifestyle score of ≥2, 43% (95% CI, 37% to 48%) with score ≥3, 49% (95% CI, 42% to 55%) with score ≥4, and 61% (95% CI, 42% to 75%) with score = 5. For CRC mortality, the PAR with endoscopic screening alone was 34% (95% CI, 29% to 39%), increased to 38% (95% CI, 30% to 45%), 50% (95% CI, 40% to 59%), and 55% (95% CI, 37% to 69%) when combined with a lifestyle score of ≥2, ≥3, and ≥4, respectively.

Table 2. PAR estimates for CRC incidence and mortality associated with endoscopic screening and healthy lifestyle* separately and in combination.

Exposures Prevalence (%) Age-adjusted rate /100,000 pys % PAR (95% CI)
Colorectal cancer incidence
    Endoscopic screening 41 78 32 (31–33)
    Healthy lifestyle score ≥2 80 92 7 (5–10)
    Healthy lifestyle score ≥3 45 82 16 (12–21)
    Healthy lifestyle score ≥4 17 75 24 (16–31)
    Healthy lifestyle score = 5 3 65 34 (16–49)
    Endoscopic screening and healthy lifestyle score ≥2 34 73 37 (33–41)
    Endoscopic screening and healthy lifestyle score ≥3 20 65 43 (37–48)
    Endoscopic screening and healthy lifestyle score ≥4 8 61 49 (42–55)
    Endoscopic screening and healthy lifestyle score = 5 2 44 61 (42–75)
Colorectal cancer mortality
    Endoscopic screening 41 28 34 (29–39)
    Healthy lifestyle score ≥2 76 33 5 (1–9)
    Healthy lifestyle score ≥3 39 26 20 (11–28)
    Healthy lifestyle score ≥4 13 24 23 (7–38)
    Endoscopic screening and healthy lifestyle score ≥2 32 26 38 (30–45)
    Endoscopic screening and healthy lifestyle score ≥3 17 20 50 (40–59)
    Endoscopic screening and healthy lifestyle score ≥4 6 17 55 (37–69)

CI, confidence interval; CRC, colorectal cancer; PAR, population-attributable risk; pys, person-years; WCRF/AICR, World Cancer Research Fund/American Institute for Cancer Research.

* Healthy lifestyle score (range, 0–5) was defined as the number of the 5 healthy lifestyle factors: normal body weight (body mass index, ≥18.5 and <25.0 kg/m2), never smoking or past smoking with pack-years <5, moderate-to-vigorous intensity activity for ≥30 minutes per day, none-to-moderate alcohol intake (<1 drink [14 g alcohol]/d for women and <2 drinks/d for men), and meeting at least 3 of the 6 dietary recommendations by the WCRF/AICR Third Expert Report 2018, which included red meat <0.5 serving/d, processed meat <0.2 serving/d, dietary fiber ≥30 g/d, dairy products ≥3 servings/d, whole grains ≥48 g/d or account for at least half of total grains, and calcium supplement use.

† PARs and 95% CIs were calculated while adjusting for age, calendar period, sex, ethnicity, current multivitamins use, regular aspirin use, family history of CRC, menopausal status and hormone use (women only) in incidence analysis, and, additionally, diagnoses of cardiovascular disease and type 2 diabetes in mortality analysis.

We also calculated the PARs by CRC subsites (Fig 2) and TNM stage (Fig 3). For incidence of proximal colon cancer, the PAR increased from 15% (95% CI, 13% to 16%) with endoscopic screening alone to 51% (95% CI, 17% to 74%) with the combination of endoscopic screening and healthy lifestyle score of 5. The corresponding PAR for distal CRC increased from 47% (95% CI, 45% to 50%) to 75% (95% CI, 61% to 84%), for TNM 1 and 2 CRC from 27% (95% CI, 26% to 28%) to 52% (95% CI, 31% to 68%), and for TNM 3 and 4 CRC from 37% (95% CI, 33% to 41%) to 68% (95% CI, 45% to 84%). For mortality, combining a healthy lifestyle (score ≥4) with endoscopic screening was associated with an increase in the PAR from 13% (95% CI, 2% to 23%) to 52% (95% CI, 20% to 74%) for proximal colon cancer, and from 49% (95% CI, 42% to 56%) to 65% (95% CI, 48% to 78%) for distal CRC.

Fig 2. PAR estimates for incidence and mortality of proximal colon cancer and distal CRC with endoscopic screening alone and endoscopic screening–healthy lifestyle combination.

Fig 2

Healthy lifestyle score (range, 0–5) was defined as the number of the 5 healthy lifestyle factors: normal body weight (BMI, ≥18.5 and <25.0 kg/m2), never smoking or past smoking with pack-years <5, moderate-to-vigorous intensity activity for ≥30 minutes per day, none-to-moderate alcohol intake (<1 drink [14 g alcohol]/d for women and <2 drinks/d for men), and meeting at least 3 of the 6 dietary recommendations by the WCRF/AICR Third Expert Report 2018, which included red meat <0.5 serving/d, processed meat <0.2 serving/d, dietary fiber ≥30 g/d, dairy products ≥3 servings/d, whole grains ≥48 g/d or account for at least half of total grains, and calcium supplement use. PARs and 95% CIs were calculated while adjusting for age, calendar period, sex, ethnicity, current multivitamins use, regular aspirin use, family history of CRC, menopausal status and hormone use (women only) in incidence analysis, and, additionally, diagnoses of cardiovascular disease and type 2 diabetes in mortality analysis. Error bars indicate 95% CIs. BMI, body mass index; CI, confidence interval; CRC, colorectal cancer; PAR, population-attributable risk; WCRF/AICR, World Cancer Research Fund/American Institute for Cancer Research.

Fig 3. PAR estimates for incidence of CRC by TNM stage (TNM 1 and 2 and 3 and 4) with endoscopic screening alone and endoscopic screening–healthy lifestyle combination.

Fig 3

Healthy lifestyle score (range, 0–5) was defined as the number of the 5 healthy lifestyle factors: normal body weight (BMI, ≥18.5 and <25.0 kg/m2), never smoking or past smoking with pack-years <5, moderate-to-vigorous intensity activity for ≥30 minutes per day, none-to-moderate alcohol intake (<1 drink [14 g alcohol]/d for women and <2 drinks/d for men), and meeting at least 3 of the 6 dietary recommendations by the WCRF/AICR Third Expert Report 2018, which included red meat <0.5 serving/d, processed meat <0.2 serving/d, dietary fiber ≥30 g/d, dairy products ≥3 servings/d, whole grains ≥48 g/d or account for at least half of total grains, and calcium supplement use. PARs and 95% CIs were calculated while adjusting for age, calendar period, sex, ethnicity, current multivitamins use, regular aspirin use, family history of CRC, and menopausal status and hormone use (women only). Error bars indicate 95% CIs. BMI, body mass index; CI, confidence interval; CRC, colorectal cancer; PAR, population-attributable risk; TNM, tumor–node–metastasis; WCRF/AICR, World Cancer Research Fund/American Institute for Cancer Research.

In the stratified analysis, we found that an integration of healthy lifestyle with endoscopic screening was associated with a substantially increased PAR across all the subgroups according to family history of CRC, regular aspirin use, age, and sex (S3 Table). In addition, we found a beneficial association of healthy lifestyle score with mortality due to other causes than CRC in both the endoscopic screening (HR, 0.86 per one-unit increment; 95% CI, 0.85 to 0.88) and non-screening groups (HR, 0.83 per one-unit increment; 95% CI, 0.82 to 0.84) (S4 Fig).

Our results were robust to several sensitivity analyses, including restricting to participants aged 50 to 75 years (S4 Table), defining screening based on colonoscopy only (S5 Table), stopping updating lifestyle information after the first report of endoscopic screening (S6 Table), excluding the person-times when response to endoscopy was missing (S7 Table), and defining the healthy lifestyle score using the 5 lifestyle factors as 5-categorical variables (S5 Fig and S8 Table).

Discussion

In 2 large prospective cohorts, we found that adherence to a healthy lifestyle was associated with a similar risk reduction of CRC incidence and mortality among individuals with and without endoscopic screening. Our results suggest that approximately 32% of CRC cases and 34% of CRC deaths could potentially be prevented by endoscopic screening alone and, when combined with the 5 healthy lifestyle factors, these figures increased to 61% and 55%, respectively. Moreover, the incremental benefit was particularly strong for proximal colon cancer (PAR increased from 15% to 51% for incidence, and from 13% to 52% for mortality). These findings indicate that adherence to healthy lifestyle confers a substantial benefit for reduction of CRC incidence and mortality independent of endoscopic screening and that integrating healthy lifestyle with endoscopic screening may substantially enhance CRC prevention.

Screening is the cornerstone of CRC prevention, and endoscopic screening has been shown to confer a persisting protection against CRC for up to 15 to 17 years [32,33]. In the current study, we found that endoscopic screening was associated with an HR for CRC incidence of 0.53 and for CRC mortality of 0.49, consistent with our prior findings [33] and other studies [34,35]. Over the years, despite an overall increase in the uptake of endoscopic screening, substantial disparity remains in the US [36,37]. On the other hand, although the importance of lifestyle and diet for CRC prevention has been increasingly recognized [12], it remains unclear whether adherence to healthy lifestyle in individuals having already undertaken endoscopic screening remains as beneficial for CRC prevention as in those without endoscopic screening. To the best of our knowledge, the current study represents the first effort to answer that question and to comprehensively quantify the joint beneficial association of healthy lifestyle and endoscopic screening with CRC prevention.

Although precancerous lesions can be detected and removed through endoscopic screening, the benefit is far from perfect, due to procedural (e.g., poor bowel preparation, difficulty in accessing the proximal colon) and lesion-related reasons (e.g., missed/incomplete resection of serrated polyps). On the other hand, lifestyle modification, as a primary prevention approach for CRC, operates through various biological pathways, including reduction in hyperinsulinemia and systemic inflammation, and modulation of gene expression and the gut microbiota [3842]. Therefore, given the independent pathways through which healthy lifestyle and endoscopic screening exert protection against CRC, it is not surprising that we observed a similar CRC-preventive association of adherence to healthy lifestyle in individuals with and without endoscopic screening.

Our findings have important clinical and public health implications. First, we provide empirical evidence for the independent associations of healthy lifestyle and endoscopic screening with lower CRC incidence and mortality. Despite the protection of endoscopic screening against CRC [32,33], the fact that healthy lifestyle may be associated with a further increased CRC prevention highlights the need to promote healthy lifestyle to optimize CRC prevention. Second, we observed a higher increment in the beneficial association for proximal colon cancer when integrating healthy lifestyle with endoscopic screening. Given the rising incidence of proximal colon cancer and the diminished benefit of endoscopy in preventing these tumors [33], our results suggest that an emphasis on healthy lifestyle may help address these limitations. Third, our findings highlight the merit of healthy lifestyle for CRC prevention in settings lacking coverage or capacity for endoscopic screening [43,44]. For example, compared to individuals with no endoscopic screening or healthy lifestyle, those with the 5 healthy lifestyle practices but remain unscreened might have a 62% reduction in CRC risk (HR, 0.38; 95% CI, 0.26 to 0.56), which was very close to that (63%) among individuals only undertaking endoscopic screening but still living a less healthy lifestyle (HR, 0.37; 95% CI, 0.24 to 0.56). Fourth, we noted a more general benefit of healthy lifestyle than endoscopic screening for other outcomes than CRC. We found that each increment in the number of healthy lifestyle practices was associated with 14% to 17% reduction in mortality due to other causes than CRC. However, no such benefit was observed for endoscopic screening. Nevertheless, given the challenges in undertaking and maintaining healthy lifestyle practices (only 3% of our study population had all 5 healthy lifestyle factors), screening should still serve as an unshakable cornerstone for CRC prevention.

Our study has several strengths, including the large sample size, long-term follow-up, repeated assessments of lifestyle factors and endoscopic screening, and detailed information on potential confounders. Also, several limitations should be noted. First, the information of lifestyle factors and endoscopic screening was self-reported and thus subject to measurement error. However, the accuracy of these self-reported data within our cohorts has been well documented (see S2 Text) [2224,33,45,46]. Second, we used a less stringent threshold to define healthy lifestyle due to the low prevalence of healthy lifestyle. For example, we included past smoking with pack-years <5 in the nonsmoking group and defined healthy lifestyle as a score of ≥4 rather than 5 in CRC mortality analysis. Thus, the PAR for healthy lifestyle may have been underestimated. Third, our study participants are all health professionals and predominantly whites, thereby limiting the generalizability of our findings, particularly given that individuals with a healthier lifestyle are more likely to undertake screening. However, it is unlikely that the biological effect of healthy lifestyle would substantially differ between health professionals and the general population. On the other hand, given the generally healthier lifestyle profiles of health professionals, we may have underestimated the benefit of lifestyle in the general population. Additionally, we lacked data on other screening modalities than endoscopy and were thus unable to examine their influence on our results.

In conclusion, our study suggests that adherence to healthy lifestyle is associated with substantial reduction in CRC incidence and mortality independent of endoscopic screening. Integration of healthy lifestyle with endoscopic screening may improve prevention of CRC, particularly proximal colon cancer, compared to endoscopic screening alone.

Supporting information

S1 Checklist. Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) checklist.

(DOCX)

S1 Fig. Flowchart of study participants.

(TIF)

S2 Fig

Association of healthy lifestyle score with incidence of proximal colon cancer (panel A) and distal colorectal cancer (panel B) according to endoscopic screening status and the corresponding age-adjusted incidence rates. Healthy lifestyle score (range, 0–5) was defined as the number of the 5 healthy lifestyle factors: normal body weight (BMI, ≥18.5 and <25.0 kg/m2), never smoking or past smoking with pack-years <5, moderate-to-vigorous intensity activity for ≥30 minutes per day, none-to-moderate alcohol intake (<1 drink [14 g alcohol]/d for women and <2 drinks/d for men), and meeting at least 3 of the 6 dietary recommendations by the WCRF/AICR Third Expert Report 2018, which included red meat <0.5 serving/d, processed meat <0.2 serving/d, dietary fiber ≥30 g/d, dairy products ≥3 servings/d, whole grains ≥48 g/d or account for at least half of total grains, and calcium supplement use. Multivariable Cox proportional hazards regression was used to calculate the HRs and 95% CIs while adjusting for age, calendar period, sex, ethnicity, current multivitamins use, regular aspirin use, family history of CRC, and menopausal status and hormone use (women only). P-heterogeneity = 0.175 among unscreened participants and 0.349 among screened participants. BMI, body mass index; CI, confidence interval; CRC, colorectal cancer; HR, hazard ratio; pys, person-years; WCRF/AICR, World Cancer Research Fund/American Institute for Cancer Research.

(TIF)

S3 Fig

Association of healthy lifestyle score with incidence of CRC by TNM stage (panel A: TNM 1 and 2; panel B: TNM 3 and 4) according to endoscopic screening status. Healthy lifestyle score (range, 0–5) was defined as the number of the 5 healthy lifestyle factors: normal body weight (BMI, ≥18.5 and <25.0 kg/m2), never smoking or past smoking with pack-years <5, moderate-to-vigorous intensity activity for ≥30 minutes per day, none-to-moderate alcohol intake (<1 drink [14 g alcohol]/d for women and <2 drinks/d for men), and meeting at least 3 of the 6 dietary recommendations by the WCRF/AICR Third Expert Report 2018, which included red meat <0.5 serving/d, processed meat <0.2 serving/d, dietary fiber ≥30 g/d, dairy products ≥3 servings/d, whole grains ≥48 g/d or account for at least half of total grains, and calcium supplement use. Multivariable Cox proportional hazards regression was used to calculate the HRs and 95% CIs while adjusting for age, calendar period, sex, ethnicity, current multivitamins use, regular aspirin use, family history of CRC, and menopausal status and hormone use (women only). BMI, body mass index; CI, confidence interval; CRC, colorectal cancer; HR, hazard ratio; TNM, tumor–node–metastasis; WCRF/AICR, World Cancer Research Fund/American Institute for Cancer Research.

(TIF)

S4 Fig. Association of healthy lifestyle score with mortality due to other causes than CRC according to endoscopic screening status.

Healthy lifestyle score (range, 0–5) was defined as the number of the 5 healthy lifestyle factors: normal body weight (BMI, ≥18.5 and <25.0 kg/m2), never smoking or past smoking with pack-years <5, moderate-to-vigorous intensity activity for ≥30 minutes per day, none-to-moderate alcohol intake (<1 drink [14 g alcohol]/d for women and <2 drinks/d for men), and meeting at least 3 of the 6 dietary recommendations by the WCRF/AICR Third Expert Report 2018, which included red meat <0.5 serving/d, processed meat <0.2 serving/d, dietary fiber ≥30 g/d, dairy products ≥3 servings/d, whole grains ≥48 g/d or account for at least half of total grains, and calcium supplement use. Multivariable Cox proportional hazards regression was used to calculate the HRs and 95% CIs while adjusting for age, calendar period, sex, ethnicity, current multivitamins use, regular aspirin use, family history of CRC, menopausal status and hormone use (women only), diagnoses of cardiovascular disease and type 2 diabetes, physical exam for disease screening, mammography for breast cancer screening (women only), and prostate-specific antigen testing for prostate cancer screening (men only). BMI, body mass index; CI, confidence interval; CRC, colorectal cancer; HR, hazard ratio; WCRF/AICR, World Cancer Research Fund/American Institute for Cancer Research.

(TIF)

S5 Fig. Association of healthy lifestyle score with CRC incidence according to endoscopic screening status when healthy lifestyle score was defined by the five 5-categorical lifestyle factors.

The five 5-categorical lifestyle factors included BMI (18.5–24.9, 25.0–27.4, 27.5–29.5, 30.0–34.9, and ≥35.0 kg/m2; scored 5–1, respectively), smoking (never, past smoking with pack-years <5, past smoking with pack-years ≥5, current smoker with pack-years <20, and current smoker with pack-years ≥20; scored 5–1, respectively), physical activity (moderate-to-vigorous intensity activity for 0, 0.1–0.9, 1.0–3.4, 3.5–5.9, and ≥6 hours per week; scored 1–5, respectively), alcohol intake (0, 0.1–13.9, 14–20.9, 21–27.9, and ≥28 g/d; scored 5–1, respectively), and number of the 6 healthy dietary components recommendations by the WCRF/AICR Third Expert Report 2018 (0–1, 2, 3, 4, and 5–6; scored 1–5, respectively). The 6 healthy dietary components included red meat <0.5 serving/d, processed meat <0.2 serving/d, dietary fiber ≥30 g/d, dairy products ≥3 servings/d, whole grains ≥48 g/d or account for at least half of total grains, and calcium supplement use. Sum of the 5 scores (range, 5–25) was then categorical into 5 levels (5–10, 11–13, 14–16, 17–19, 20–22, and 23–25). These 5 levels were defined as the new healthy lifestyle score (0, 1, 2, 3, 4, and 5). Multivariable Cox proportional hazards regression was used to calculate the HRs and 95% CIs while adjusting for age, calendar period, sex, ethnicity, current multivitamins use, regular aspirin use, family history of CRC, and menopausal status and hormone use (women only). Error bars indicate 95% CIs. BMI, body mass index; CI, confidence interval; CRC, colorectal cancer; HR, hazard ratio; WCRF/AICR, World Cancer Research Fund/American Institute for Cancer Research.

(TIF)

S1 Table. Associations of individual lifestyle factors with CRC incidence and mortality according to endoscopic screening status.

(DOCX)

S2 Table. Associations of individual lifestyle factors with incidence of proximal colon cancer and distal CRC according to endoscopic screening status.

(DOCX)

S3 Table. PAR estimates for CRC incidence and mortality with endoscopic screening alone and endoscopic screening–healthy lifestyle combination and the corresponding age-adjusted prevalence, stratified by family history of CRC, regular aspirin use, age, and sex.

(DOCX)

S4 Table. PAR estimates for CRC incidence and mortality with endoscopic screening and healthy lifestyle separately and in combination among the participants aged 50–75 years.

(DOCX)

S5 Table. PAR estimates for CRC incidence and mortality with colonoscopic screening and healthy lifestyle separately and in combination.

(DOCX)

S6 Table. PAR estimates for CRC incidence and mortality with endoscopic screening and healthy lifestyle separately and in combination when we stopped updating lifestyle information after the first endoscopic screening.

(DOCX)

S7 Table. PAR estimates for CRC incidence and mortality with endoscopic screening and healthy lifestyle separately and in combination when we excluded the person-time when response to endoscopy was missing.

(DOCX)

S8 Table. PAR estimates for CRC incidence with endoscopic screening and healthy lifestyle separately and in combination when healthy lifestyle score was defined by the five 5-categorical lifestyle factors.

(DOCX)

S1 Text. Prospective analysis proposal.

(DOCX)

S2 Text. Detailed assessment and statistical analysis.

(DOCX)

Acknowledgments

The authors thank the participants and staff of the NHS and the HPFS for their continued contributions, as well as the following state cancer registries for their help: Alabama, Arizona, Arkansas, California, Colorado, Connecticut, Delaware, Florida, Georgia, Idaho, Illinois, Indiana, Iowa, Kentucky, Louisiana, Maine, Maryland, Massachusetts, Michigan, Nebraska, New Hampshire, New Jersey, New York, North Carolina, North Dakota, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, Tennessee, Texas, Virginia, Washington, and Wyoming. The authors assume full responsibility for analyses and interpretation of these data.

Abbreviations

AJCC

American Joint Committee on Cancer

BMI

body mass index

CRC

colorectal cancer

HPFS

Health Professionals Follow-up Study

HR

hazard ratio

NHS

Nurses’ Health Study

PAR

population-attributable risk

RR

relative risk

STROBE

Strengthening the Reporting of Observational Studies in Epidemiology

TNM

tumor–node–metastasis

WCRF/AICR

World Cancer Research Fund/American Institute for Cancer Research

Data Availability

Because of the sensitive nature of the data collected for this study, requests to access the dataset from qualified researchers trained in human subject confidentiality protocols may be sent to Brigham and Women's/Harvard Cohorts at https://docs.google.com/forms/d/e/1FAIpQLScAPV23ZIBpkk9CyEJ1OcFJjMol9elKEpLYnPu7g3PgBL57XA/viewform.

Funding Statement

This work was supported by the American Cancer Society Mentored Research Scholar Grant (MRSG-17-220-01 - NEC to M.S.); by the U.S. National Institutes of Health (NIH) grants [P01 CA87969 to M.J. Stampfer; U01 CA186107 to M.J. Stampfer; P01 CA55075, to W.C. Willett; UM1 CA167552 to W.C. Willett; U01 CA167552 to L.A. Mucci and W.C. Willett; K24 DK098311, R01 CA137178, R01 CA202704, R01 CA176726, to A.T.C.; K99 CA215314 and R00 CA215314 to M.S.; R35 CA197735 and R01 CA151993 to S.O.]. Dr. Chan is a Stuart and Suzanne Steele MGH Research Scholar. The funders had no role in design and conduct of the study; collection, management, analysis and interpretation of the data; preparation, review, or approval of the manuscript; and decision to submit the manuscript for publication.

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Decision Letter 0

Adya Misra

4 Aug 2020

Dear Dr Song,

Thank you for submitting your manuscript entitled "Healthy lifestyle, endoscopic screening, and colorectal cancer incidence and mortality in the US: a nationwide cohort study" for consideration by PLOS Medicine.

Your manuscript has now been evaluated by the PLOS Medicine editorial staff [as well as by an academic editor with relevant expertise] and I am writing to let you know that we would like to send your submission out for external peer review.

However, before we can send your manuscript to reviewers, we need you to complete your submission by providing the metadata that is required for full assessment. To this end, please login to Editorial Manager where you will find the paper in the 'Submissions Needing Revisions' folder on your homepage. Please click 'Revise Submission' from the Action Links and complete all additional questions in the submission questionnaire.

Please re-submit your manuscript within two working days, i.e. by .

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Once your full submission is complete, your paper will undergo a series of checks in preparation for peer review. Once your manuscript has passed all checks it will be sent out for review.

Feel free to email us at plosmedicine@plos.org if you have any queries relating to your submission.

Kind regards,

Adya Misra, PhD,

Senior Editor

PLOS Medicine

Decision Letter 1

Emma Veitch

27 Aug 2020

Dear Dr. Song,

Thank you very much for submitting your manuscript "Healthy lifestyle, endoscopic screening, and colorectal cancer incidence and mortality in the US: a nationwide cohort study" (PMEDICINE-D-20-03426R1) for consideration at PLOS Medicine.

Your paper was evaluated by a senior editor and discussed among all the editors here. It was also discussed with an academic editor with relevant expertise, and sent to independent reviewers, including a statistical reviewer. The reviews are appended at the bottom of this email and any accompanying reviewer attachments can be seen via the link below:

[LINK]

In light of these reviews, I am afraid that we will not be able to accept the manuscript for publication in the journal in its current form, but we would like to consider a revised version that addresses the reviewers' and editors' comments. Obviously we cannot make any decision about publication until we have seen the revised manuscript and your response, and we plan to seek re-review by one or more of the reviewers.

In revising the manuscript for further consideration, your revisions should address the specific points made by each reviewer and the editors. Please also check the guidelines for revised papers at http://journals.plos.org/plosmedicine/s/revising-your-manuscript for any that apply to your paper. In your rebuttal letter you should indicate your response to the reviewers' and editors' comments, the changes you have made in the manuscript, and include either an excerpt of the revised text or the location (eg: page and line number) where each change can be found. Please submit a clean version of the paper as the main article file; a version with changes marked should be uploaded as a marked up manuscript.

In addition, we request that you upload any figures associated with your paper as individual TIF or EPS files with 300dpi resolution at resubmission; please read our figure guidelines for more information on our requirements: http://journals.plos.org/plosmedicine/s/figures. While revising your submission, please upload your figure files to the PACE digital diagnostic tool, https://pacev2.apexcovantage.com/. PACE helps ensure that figures meet PLOS requirements. To use PACE, you must first register as a user. Then, login and navigate to the UPLOAD tab, where you will find detailed instructions on how to use the tool. If you encounter any issues or have any questions when using PACE, please email us at PLOSMedicine@plos.org.

We expect to receive your revised manuscript by Sep 17 2020 11:59PM. Please email us (plosmedicine@plos.org) if you have any questions or concerns.

***Please note while forming your response, if your article is accepted, you may have the opportunity to make the peer review history publicly available. The record will include editor decision letters (with reviews) and your responses to reviewer comments. If eligible, we will contact you to opt in or out.***

We ask every co-author listed on the manuscript to fill in a contributing author statement, making sure to declare all competing interests. If any of the co-authors have not filled in the statement, we will remind them to do so when the paper is revised. If all statements are not completed in a timely fashion this could hold up the re-review process. If new competing interests are declared later in the revision process, this may also hold up the submission. Should there be a problem getting one of your co-authors to fill in a statement we will be in contact. YOU MUST NOT ADD OR REMOVE AUTHORS UNLESS YOU HAVE ALERTED THE EDITOR HANDLING THE MANUSCRIPT TO THE CHANGE AND THEY SPECIFICALLY HAVE AGREED TO IT. You can see our competing interests policy here: http://journals.plos.org/plosmedicine/s/competing-interests.

Please use the following link to submit the revised manuscript:

https://www.editorialmanager.com/pmedicine/

Your article can be found in the "Submissions Needing Revision" folder.

To enhance the reproducibility of your results, we recommend that you deposit your laboratory protocols in protocols.io, where a protocol can be assigned its own identifier (DOI) such that it can be cited independently in the future. For instructions see http://journals.plos.org/plosmedicine/s/submission-guidelines#loc-methods.

Please ensure that the paper adheres to the PLOS Data Availability Policy (see http://journals.plos.org/plosmedicine/s/data-availability), which requires that all data underlying the study's findings be provided in a repository or as Supporting Information. For data residing with a third party, authors are required to provide instructions with contact information for obtaining the data. PLOS journals do not allow statements supported by "data not shown" or "unpublished results." For such statements, authors must provide supporting data or cite public sources that include it.

We look forward to receiving your revised manuscript.

Sincerely,

Emma Veitch, PhD

PLOS Medicine

On behalf of Clare Stone, PhD, Acting Chief Editor,

PLOS Medicine

plosmedicine.org

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Requests from the editors:

*Please structure your abstract using the PLOS Medicine headings (Background, Methods and Findings, Conclusions - "methods and findings" is a single subsection).

*In the last sentence of the Abstract Methods and Findings section, please describe the main limitation(s) of the study's methodology.

*In the abstract conclusions, the text currently reads "Healthy lifestyle may reduce CRC incidence and mortality independent of

endoscopic screening", but this assumes that the effect sizes seen in the main analyses represent causal effects, and given the study design we can't assume this. It would be better in the abstract to use more moderate language and to present the findings consistently as associations - in the main discussion you can then go on to say that, if those effects were causal then the implications might mean (xyz...), but this conclusion shouldn't be leapt to.

*Please use the following style for the author summary - https://journals.plos.org/plosmedicine/s/revising-your-manuscript#loc-author-summary - this should use bullets and the headers need to be different. See also an example, https://journals.plos.org/plosmedicine/article?id=10.1371/journal.pmed.1002416

*We'd suggest ensuring that the study is reported according to the STROBE guideline; when doing so, please include the completed STROBE checklist as Supporting Information. Please add the following statement, or similar, to the Methods: "This study is reported as per the Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) guideline (S1 Checklist)." The STROBE guideline can be found here: http://www.equator-network.org/reporting-guidelines/strobe/. When completing the checklist, please use section and paragraph numbers, rather than page numbers.

*Did your study have a prospective protocol or analysis plan? Please state this (either way) early in the Methods section.

a) If a prospective analysis plan (from your funding proposal, IRB or other ethics committee submission, study protocol, or other planning document written before analyzing the data) was used in designing the study, please include the relevant prospectively written document with your revised manuscript as a Supporting Information file to be published alongside your study, and cite it in the Methods section. A legend for this file should be included at the end of your manuscript.

b) If no such document exists, please make sure that the Methods section transparently describes when analyses were planned, and when/why any data-driven changes to analyses took place.

c) In either case, changes in the analysis-- including those made in response to peer review comments-- should be identified as such in the Methods section of the paper, with rationale.

*In the discussion section, as noted above for the abstract, some of the language should be moderated so it doesn't assume causal effects. Eg, "Approximately 32% of CRC cases and 34% of CRC deaths could potentially be prevented by endoscopic screening alone" - this could be presented later, but with the caveat that these estimates are based on assuming the effect size seen in your analyses are entirely reflective of a "true" causal effect (which may not be true). The discussion in general should be careful about where it uses causal language and it would be better to ensure the main part of the discussion presents the findings as associations, only going on later to discuss the implications **if these associations are indeed causal**.

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Comments from the reviewers:

Reviewer #1: I confine my remarks to statistical aspects of this paper. The general approach is OK but I have a number of issues to resolve before I can recommend publication.

First, quoting a "per unit" estimate is misleading, as the trend in both groups was non-linear (and nonlinear in different ways).

Second, the interaction term added is not adequate, as it does not address the above. Consider CRC incidence (as shown in fig 1A). If the factor of 0.85 was correct, then the nonscreened group would have HRs of 1, 0.85, 0.72, 0.61, 0.52 and 0.44; while the screened group would have values of 0.37 0.31, 0.27 0.23 0.19 amd 0.16. These are not accurate (and the two lines are not parallel)

Third, it's an interesting question whether the appropriate measure for reduction in risk is the ratio or the difference. Reducing a large risk by (say) 15% is not the same as reducing a small risk by 15%.

More specific points: On p. 5 at the top, give a rate of CRC death per person, not just "3rd highest"

Also on p. 5, the huge range of risk reduction for liefestyle (20 to 70%) makes these claims less credible (at least to me).

p. 7 Please define "metabolic equivalents"

p. 7 I'm not altogether happy with the way the lifestyle factor was computed. Dichotomoizing risk factors is kind of silly. People don't go from "normal" to "high" risk when they cross some threshold. E.g., for BMI (a very flawed measure of obesity) you aren't fine at 24.9 and then high risk at 25.1. Also, 31 minutes of exercise is not dramatically different from 29 minutes. It would be better to develop a measure of risk that left all measures continuouis (and maybe nonllinear).eith based on data or based on literature.

p 10 How was the "per unit" number calculated, given that there were 5 different logistic regressions run for each group?

Peter Flom

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Reviewer #2: Wang and colleagues address an important topic- the associations between screening and/or healthy lifestyles and the risk of colorectal cancer incidence and mortality, using the Nurses health Study and Health professionals follow-up study, two large, important cohorts that have been sources for many important observational studies. They found that the protective effects of screening and health lifestyle (based on a healthy lifestyle score) were independently associated with lower risks of CRC incidence and mortality. These findings are important and timely. The study is well-executed and the supplementary analyses helpful. I would make a few suggestions to better put them in context:

1) I would ask that the language be changed to highlight these are associations, not interventions or trials: For example, instead of concluding: "Healthy lifestyle may reduce CRC incidence and mortality independent of endoscopic screening." I would suggest "Healthy lifestyle is associated with lower CRC incidence and mortality independent of endoscopic screening." Similarly, saying "First, we provide empirical evidence for the substantial benefit of lifestyle modification, independent of endoscopic screening, for improved CRC prevention." is probably less accurate than "First, we provide empirical evidence for the independent association of healthy behaviors and endoscopic screening with lower CRC incidence."

2) It would be helpful to discuss the rationale for turning the actual, sometimes linear measures included in the healthy lifestyle score into dichotomized scores. Giving the same weight to 3 drinks per day and 10 drinks per day, for example, seems to underweight extreme scores.

3) What is the relationship between the lifestyle score and all-cause mortality? I am assuming the the effects go beyond that of CRC.

4) The discussion talks about "lifestyle modification" which is an intervention framing, but I think it is important to reiterate the associations are with given levels of healthy behaviors moreso than the results of chnages in those behaviors. This framing is important because while both screening and healthy lifestyles are associated with less incidence and mortality, the effort required to achieve the protective levels of lifestyle (medium to high intensity counseling interventions) may be considerably greater than those required to get endoscopic screening (a discrete event).

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Reviewer #3: From non-randomized studies on colonoscopy screening as well as from randomized studies on sigmoidoscopy and FOBT studies we have learned that endoscopic screening is a sufficient tool to reduce incidence and mortality from colorectal cancer. Furthermore, epidemiologigal studies have identified various life style associated risk factors for colorectal cancer, including BMI, smoking, nutrition. Probably up to 50% of colorectal cancers could be prevented by a healthy life style. Whereas both a healthy life style and screening can reduce the colorectal cancer burden and both are recommended by various national and international guidelines, it is so far not known whether individuals undergoing screening colonoscopy can further reduce their colorectal cancer risk by maintaining a healthy life style.

Wang et al. provide an answer to this important question in their study. Based on the analysis of well-known and thoroughly studied cohorts, the nurses health study and the health professionals follow-up study, they are able to demonstrate that the reduction of colorectal cancer incidence and mortality by maintaining a healthy life style is independent of participating in colonoscopy screening. Furthermore, individuals who undergo colonoscopy and follow a healthy life style are able to further reduce their colon cancer risk. Therefore, the recommendation will be to participate in bowel screening and to maintain a healthy lifestyle in oder to minimize risk. To the best of my knowledge, this ist he first study to provide this evidence.

The study is well designed, the analyzes have been properly performed and the manuscipt is well written. I only have some minor issues:

1. Is there data available on the adenomatous polyp count / size in the colonoscopies? If yes, is there a difference regarding life style? I would expect that a healthy life style is associated with a lower polyp count.

2. Were the colonoscopies primary screening colonoscopies? Or did some patients have sigmoidoscopies or FOB testing before with a finding that resulted in referral to secondary screening by colonoscopy? How did you include negative screening by sigmoidoscopy or negative FOBT screening in your analysis? Somebody having negative sigmoidoscopy and/or negative FOBT every other year has undergone screening that will also reduce the risk of a diagnosis of colorectal cancer and will usually not undergo colonoscopy. If data on FOBT screening is available, data for sigmoidoscopies is obviously available, it would be important to study the group with no screening at all as the unscreened group currently comprises no screeing at all + screening other than colonoscopy.

3. How did authors account for changes in life style, e.g. unhealthy lifestyle in the beginning of the study and changing to a healthier diet over time?

4. Was there a difference in Duke`s or UICC staging of the cancers diagnosed between groups? As a stage shift towards lower stages by screening is known, it could be speculated that the group with screening + healthy diet not only has less cancers but also cancers at earlier stages.

5. Was there a difference in risk of a colon cancer diagnosis between individuals receiving one or more negative screening colonoscopies over time?

6. Page 8: Participants were considered as endoscopically unscreened until the first time they reported undertaking endoscopy for screening purpose and as endoscopically screened thereafter… How did authors account for diagnostic colonoscopies performed for complaints that did not provide any pathologies? A person undergoing colonoscopy for other reason than screening with no significant findings will usually not undergo screening colonoscopy within the next couple of years.

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Any attachments provided with reviews can be seen via the following link:

[LINK]

Decision Letter 2

Adya Misra

23 Nov 2020

Dear Dr. Song,

Thank you very much for submitting your manuscript "Healthy lifestyle, endoscopic screening, and colorectal cancer incidence and mortality in the US: a nationwide cohort study" (PMEDICINE-D-20-03426R2) for consideration at PLOS Medicine.

Your paper was evaluated by a senior editor and discussed among all the editors here. It was also discussed with an academic editor with relevant expertise, and sent to independent reviewers, including a statistical reviewer. The reviews are appended at the bottom of this email and any accompanying reviewer attachments can be seen via the link below:

[LINK]

In light of these reviews, I am afraid that we will not be able to accept the manuscript for publication in the journal in its current form, but we would like to consider a revised version that addresses the reviewers' and editors' comments. Obviously we cannot make any decision about publication until we have seen the revised manuscript and your response, and we plan to seek re-review by one or more of the reviewers.

In revising the manuscript for further consideration, your revisions should address the specific points made by each reviewer and the editors. Please also check the guidelines for revised papers at http://journals.plos.org/plosmedicine/s/revising-your-manuscript for any that apply to your paper. In your rebuttal letter you should indicate your response to the reviewers' and editors' comments, the changes you have made in the manuscript, and include either an excerpt of the revised text or the location (eg: page and line number) where each change can be found. Please submit a clean version of the paper as the main article file; a version with changes marked should be uploaded as a marked up manuscript.

In addition, we request that you upload any figures associated with your paper as individual TIF or EPS files with 300dpi resolution at resubmission; please read our figure guidelines for more information on our requirements: http://journals.plos.org/plosmedicine/s/figures. While revising your submission, please upload your figure files to the PACE digital diagnostic tool, https://pacev2.apexcovantage.com/. PACE helps ensure that figures meet PLOS requirements. To use PACE, you must first register as a user. Then, login and navigate to the UPLOAD tab, where you will find detailed instructions on how to use the tool. If you encounter any issues or have any questions when using PACE, please email us at PLOSMedicine@plos.org.

We expect to receive your revised manuscript by Dec 14 2020 11:59PM. Please email us (plosmedicine@plos.org) if you have any questions or concerns.

***Please note while forming your response, if your article is accepted, you may have the opportunity to make the peer review history publicly available. The record will include editor decision letters (with reviews) and your responses to reviewer comments. If eligible, we will contact you to opt in or out.***

We ask every co-author listed on the manuscript to fill in a contributing author statement, making sure to declare all competing interests. If any of the co-authors have not filled in the statement, we will remind them to do so when the paper is revised. If all statements are not completed in a timely fashion this could hold up the re-review process. If new competing interests are declared later in the revision process, this may also hold up the submission. Should there be a problem getting one of your co-authors to fill in a statement we will be in contact. YOU MUST NOT ADD OR REMOVE AUTHORS UNLESS YOU HAVE ALERTED THE EDITOR HANDLING THE MANUSCRIPT TO THE CHANGE AND THEY SPECIFICALLY HAVE AGREED TO IT. You can see our competing interests policy here: http://journals.plos.org/plosmedicine/s/competing-interests.

Please use the following link to submit the revised manuscript:

https://www.editorialmanager.com/pmedicine/

Your article can be found in the "Submissions Needing Revision" folder.

To enhance the reproducibility of your results, we recommend that you deposit your laboratory protocols in protocols.io, where a protocol can be assigned its own identifier (DOI) such that it can be cited independently in the future. For instructions see http://journals.plos.org/plosmedicine/s/submission-guidelines#loc-methods.

Please ensure that the paper adheres to the PLOS Data Availability Policy (see http://journals.plos.org/plosmedicine/s/data-availability), which requires that all data underlying the study's findings be provided in a repository or as Supporting Information. For data residing with a third party, authors are required to provide instructions with contact information for obtaining the data. PLOS journals do not allow statements supported by "data not shown" or "unpublished results." For such statements, authors must provide supporting data or cite public sources that include it.

We look forward to receiving your revised manuscript.

Sincerely,

Adya Misra, PhD

Senior Editor

PLOS Medicine

plosmedicine.org

-----------------------------------------------------------

Requests from the editors:

Please compare the spline fit and linear fit as suggested by Ref1 in order to check what the differences are and if they are of practical importance rather than statistical significance. Please look at the reduction in error between the two models and then judge whether it is big enough to make the more complex spline model worth the effort.

Please add "our results indicate" or "our study suggests" in order to tone down the language throughout.

Please avoid implying a causal relationship between healthy lifestyle, endoscopic screening and colorectal cancer as this is an observational study

Please introduce all acronyms on first view. For instance the study cohorts are mentioned in the methods but it is not clear what the "NHS" stands for, for example.

Please add participant demographics in the abstract

Comments from the reviewers:

Reviewer #1: The authors have addressed most of my concerns. The remaining issue is about the splines.

I checked "proceed without recommendation" because what to do depends on non-statistical issues.

Here is the statistics part:

The authors tested a cubic spline for statistical significance and found it was not significant. But the p value of a test for linearity is not really the point. P values, in general, are problematic (see the American Statistical Ass'n Statement https://medium.com/@peterflom/some-thoughts-on-9-11-4f746ae9bdcb) and, here, as often, the real issue is effect size. That is, are the curves shown in the figure in their response to me straight or not?

The same effect size will be significant with more subjects. The key issue is whether it is meaningful and important.

And that's a non-statistical question. It depends on whether the difference between a straight line estimate and a spline estimate is "worth it" in terms of complexity.

One way to help answer this question is to see how well the two models do - how much does the spline model reduce the error? Is it enough that people in the field will care?

Peter Flom

Reviewer #3: The revised version of the manuscript has been strongly improved. My questions have been sufficiently answered.

Any attachments provided with reviews can be seen via the following link:

[LINK]

Decision Letter 3

Adya Misra

8 Dec 2020

Dear Dr. Song,

Thank you very much for re-submitting your manuscript "Healthy lifestyle, endoscopic screening, and colorectal cancer incidence and mortality in the US: a nationwide cohort study" (PMEDICINE-D-20-03426R3) for review by PLOS Medicine.

I have discussed the paper with my colleagues and the academic editor and it was also seen again by xxx reviewers. I am pleased to say that provided the remaining editorial and production issues are dealt with we are planning to accept the paper for publication in the journal.

The remaining issues that need to be addressed are listed at the end of this email. Any accompanying reviewer attachments can be seen via the link below. Please take these into account before resubmitting your manuscript:

[LINK]

***Please note while forming your response, if your article is accepted, you may have the opportunity to make the peer review history publicly available. The record will include editor decision letters (with reviews) and your responses to reviewer comments. If eligible, we will contact you to opt in or out.***

In revising the manuscript for further consideration here, please ensure you address the specific points made by each reviewer and the editors. In your rebuttal letter you should indicate your response to the reviewers' and editors' comments and the changes you have made in the manuscript. Please submit a clean version of the paper as the main article file. A version with changes marked must also be uploaded as a marked up manuscript file.

Please also check the guidelines for revised papers at http://journals.plos.org/plosmedicine/s/revising-your-manuscript for any that apply to your paper. If you haven't already, we ask that you provide a short, non-technical Author Summary of your research to make findings accessible to a wide audience that includes both scientists and non-scientists. The Author Summary should immediately follow the Abstract in your revised manuscript. This text is subject to editorial change and should be distinct from the scientific abstract.

We expect to receive your revised manuscript within 1 week. Please email us (plosmedicine@plos.org) if you have any questions or concerns.

We ask every co-author listed on the manuscript to fill in a contributing author statement. If any of the co-authors have not filled in the statement, we will remind them to do so when the paper is revised. If all statements are not completed in a timely fashion this could hold up the re-review process. Should there be a problem getting one of your co-authors to fill in a statement we will be in contact. YOU MUST NOT ADD OR REMOVE AUTHORS UNLESS YOU HAVE ALERTED THE EDITOR HANDLING THE MANUSCRIPT TO THE CHANGE AND THEY SPECIFICALLY HAVE AGREED TO IT.

Please ensure that the paper adheres to the PLOS Data Availability Policy (see http://journals.plos.org/plosmedicine/s/data-availability), which requires that all data underlying the study's findings be provided in a repository or as Supporting Information. For data residing with a third party, authors are required to provide instructions with contact information for obtaining the data. PLOS journals do not allow statements supported by "data not shown" or "unpublished results." For such statements, authors must provide supporting data or cite public sources that include it.

Please note, when your manuscript is accepted, an uncorrected proof of your manuscript will be published online ahead of the final version, unless you've already opted out via the online submission form. If, for any reason, you do not want an earlier version of your manuscript published online or are unsure if you have already indicated as such, please let the journal staff know immediately at plosmedicine@plos.org.

If you have any questions in the meantime, please contact me or the journal staff on plosmedicine@plos.org.  

We look forward to receiving the revised manuscript by Dec 15 2020 11:59PM.   

Sincerely,

Adya Misra, PhD

Senior Editor 

PLOS Medicine

plosmedicine.org

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Requests from Editors:

Please revise to "United States" in the title

Please capitalise "W" in whites

Page 6- paragraph 2 suggest revising “high quality diet” as it is currently ambiguous

Page 7 suggest removing “prospectively”

Please add citations to or copies of the questionnaires used in both NHS and HPFS cohorts

Page 12 Results 1st paragraph should say “multivitamins”

Page 16- please remove "remarkable"

Discussion-I suggest removing all iterations of “causal” as this is an observational study. In addition, I suggest removing the speculation about biological pathways linking healthy lifestyle and CRC incidence.

Late in the paper you note that colonoscopy can include removal of CRC precursors. Please mention this as a possible basis for the preventive effect in the author summary and/or introduction. I assume there are no data on this.

Please remove funding and conflicts of interest information from the main text. These should be provided in the relevant sections of the article submission form.

Presumably, those less likely to be screened are less likely to have a healthy lifestyle - please mention this as a possible limitation?

Discussion- please avoid labels like “unhealthy lifestyle” I suggest replacing with less healthy lifestyle or similar

STROBE checklist- some information appears to be missing, for example page 3

Comments from Reviewers:

Reviewer #1: The authors have addressed my concerns and I now recommend publication

Peter Flom

Any attachments provided with reviews can be seen via the following link:

[LINK]

Decision Letter 4

Richard Turner

15 Dec 2020

Dear Dr Song, 

On behalf of my colleagues and the Academic Editor, Dr Kolligs, I am pleased to inform you that we have agreed to publish your manuscript "Healthy lifestyle, endoscopic screening, and colorectal cancer incidence and mortality in the United States: a nationwide cohort study" (PMEDICINE-D-20-03426R4) in PLOS Medicine.

Before your manuscript can be formally accepted you will need to complete some formatting changes, which you will receive in a follow up email. Please be aware that it may take several days for you to receive this email; during this time no action is required by you. Once you have received these formatting requests, please note that your manuscript will not be scheduled for publication until you have made the required changes.

In the meantime, please log into Editorial Manager at http://www.editorialmanager.com/pmedicine/, click the "Update My Information" link at the top of the page, and update your user information to ensure an efficient production process. 

PRESS

We frequently collaborate with press offices. If your institution or institutions have a press office, please notify them about your upcoming paper at this point, to enable them to help maximise its impact. If the press office is planning to promote your findings, we would be grateful if they could coordinate with medicinepress@plos.org. If you have not yet opted out of the early version process, we ask that you notify us immediately of any press plans so that we may do so on your behalf.

We also ask that you take this opportunity to read our Embargo Policy regarding the discussion, promotion and media coverage of work that is yet to be published by PLOS. As your manuscript is not yet published, it is bound by the conditions of our Embargo Policy. Please be aware that this policy is in place both to ensure that any press coverage of your article is fully substantiated and to provide a direct link between such coverage and the published work. For full details of our Embargo Policy, please visit http://www.plos.org/about/media-inquiries/embargo-policy/.

Thank you again for submitting to PLOS Medicine. We look forward to publishing your paper. 

Sincerely, 

Richard Turner, PhD 

Senior Editor, PLOS Medicine

rturner@plos.org

Associated Data

    This section collects any data citations, data availability statements, or supplementary materials included in this article.

    Supplementary Materials

    S1 Checklist. Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) checklist.

    (DOCX)

    S1 Fig. Flowchart of study participants.

    (TIF)

    S2 Fig

    Association of healthy lifestyle score with incidence of proximal colon cancer (panel A) and distal colorectal cancer (panel B) according to endoscopic screening status and the corresponding age-adjusted incidence rates. Healthy lifestyle score (range, 0–5) was defined as the number of the 5 healthy lifestyle factors: normal body weight (BMI, ≥18.5 and <25.0 kg/m2), never smoking or past smoking with pack-years <5, moderate-to-vigorous intensity activity for ≥30 minutes per day, none-to-moderate alcohol intake (<1 drink [14 g alcohol]/d for women and <2 drinks/d for men), and meeting at least 3 of the 6 dietary recommendations by the WCRF/AICR Third Expert Report 2018, which included red meat <0.5 serving/d, processed meat <0.2 serving/d, dietary fiber ≥30 g/d, dairy products ≥3 servings/d, whole grains ≥48 g/d or account for at least half of total grains, and calcium supplement use. Multivariable Cox proportional hazards regression was used to calculate the HRs and 95% CIs while adjusting for age, calendar period, sex, ethnicity, current multivitamins use, regular aspirin use, family history of CRC, and menopausal status and hormone use (women only). P-heterogeneity = 0.175 among unscreened participants and 0.349 among screened participants. BMI, body mass index; CI, confidence interval; CRC, colorectal cancer; HR, hazard ratio; pys, person-years; WCRF/AICR, World Cancer Research Fund/American Institute for Cancer Research.

    (TIF)

    S3 Fig

    Association of healthy lifestyle score with incidence of CRC by TNM stage (panel A: TNM 1 and 2; panel B: TNM 3 and 4) according to endoscopic screening status. Healthy lifestyle score (range, 0–5) was defined as the number of the 5 healthy lifestyle factors: normal body weight (BMI, ≥18.5 and <25.0 kg/m2), never smoking or past smoking with pack-years <5, moderate-to-vigorous intensity activity for ≥30 minutes per day, none-to-moderate alcohol intake (<1 drink [14 g alcohol]/d for women and <2 drinks/d for men), and meeting at least 3 of the 6 dietary recommendations by the WCRF/AICR Third Expert Report 2018, which included red meat <0.5 serving/d, processed meat <0.2 serving/d, dietary fiber ≥30 g/d, dairy products ≥3 servings/d, whole grains ≥48 g/d or account for at least half of total grains, and calcium supplement use. Multivariable Cox proportional hazards regression was used to calculate the HRs and 95% CIs while adjusting for age, calendar period, sex, ethnicity, current multivitamins use, regular aspirin use, family history of CRC, and menopausal status and hormone use (women only). BMI, body mass index; CI, confidence interval; CRC, colorectal cancer; HR, hazard ratio; TNM, tumor–node–metastasis; WCRF/AICR, World Cancer Research Fund/American Institute for Cancer Research.

    (TIF)

    S4 Fig. Association of healthy lifestyle score with mortality due to other causes than CRC according to endoscopic screening status.

    Healthy lifestyle score (range, 0–5) was defined as the number of the 5 healthy lifestyle factors: normal body weight (BMI, ≥18.5 and <25.0 kg/m2), never smoking or past smoking with pack-years <5, moderate-to-vigorous intensity activity for ≥30 minutes per day, none-to-moderate alcohol intake (<1 drink [14 g alcohol]/d for women and <2 drinks/d for men), and meeting at least 3 of the 6 dietary recommendations by the WCRF/AICR Third Expert Report 2018, which included red meat <0.5 serving/d, processed meat <0.2 serving/d, dietary fiber ≥30 g/d, dairy products ≥3 servings/d, whole grains ≥48 g/d or account for at least half of total grains, and calcium supplement use. Multivariable Cox proportional hazards regression was used to calculate the HRs and 95% CIs while adjusting for age, calendar period, sex, ethnicity, current multivitamins use, regular aspirin use, family history of CRC, menopausal status and hormone use (women only), diagnoses of cardiovascular disease and type 2 diabetes, physical exam for disease screening, mammography for breast cancer screening (women only), and prostate-specific antigen testing for prostate cancer screening (men only). BMI, body mass index; CI, confidence interval; CRC, colorectal cancer; HR, hazard ratio; WCRF/AICR, World Cancer Research Fund/American Institute for Cancer Research.

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    S5 Fig. Association of healthy lifestyle score with CRC incidence according to endoscopic screening status when healthy lifestyle score was defined by the five 5-categorical lifestyle factors.

    The five 5-categorical lifestyle factors included BMI (18.5–24.9, 25.0–27.4, 27.5–29.5, 30.0–34.9, and ≥35.0 kg/m2; scored 5–1, respectively), smoking (never, past smoking with pack-years <5, past smoking with pack-years ≥5, current smoker with pack-years <20, and current smoker with pack-years ≥20; scored 5–1, respectively), physical activity (moderate-to-vigorous intensity activity for 0, 0.1–0.9, 1.0–3.4, 3.5–5.9, and ≥6 hours per week; scored 1–5, respectively), alcohol intake (0, 0.1–13.9, 14–20.9, 21–27.9, and ≥28 g/d; scored 5–1, respectively), and number of the 6 healthy dietary components recommendations by the WCRF/AICR Third Expert Report 2018 (0–1, 2, 3, 4, and 5–6; scored 1–5, respectively). The 6 healthy dietary components included red meat <0.5 serving/d, processed meat <0.2 serving/d, dietary fiber ≥30 g/d, dairy products ≥3 servings/d, whole grains ≥48 g/d or account for at least half of total grains, and calcium supplement use. Sum of the 5 scores (range, 5–25) was then categorical into 5 levels (5–10, 11–13, 14–16, 17–19, 20–22, and 23–25). These 5 levels were defined as the new healthy lifestyle score (0, 1, 2, 3, 4, and 5). Multivariable Cox proportional hazards regression was used to calculate the HRs and 95% CIs while adjusting for age, calendar period, sex, ethnicity, current multivitamins use, regular aspirin use, family history of CRC, and menopausal status and hormone use (women only). Error bars indicate 95% CIs. BMI, body mass index; CI, confidence interval; CRC, colorectal cancer; HR, hazard ratio; WCRF/AICR, World Cancer Research Fund/American Institute for Cancer Research.

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    S1 Table. Associations of individual lifestyle factors with CRC incidence and mortality according to endoscopic screening status.

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    S2 Table. Associations of individual lifestyle factors with incidence of proximal colon cancer and distal CRC according to endoscopic screening status.

    (DOCX)

    S3 Table. PAR estimates for CRC incidence and mortality with endoscopic screening alone and endoscopic screening–healthy lifestyle combination and the corresponding age-adjusted prevalence, stratified by family history of CRC, regular aspirin use, age, and sex.

    (DOCX)

    S4 Table. PAR estimates for CRC incidence and mortality with endoscopic screening and healthy lifestyle separately and in combination among the participants aged 50–75 years.

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    S5 Table. PAR estimates for CRC incidence and mortality with colonoscopic screening and healthy lifestyle separately and in combination.

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    S6 Table. PAR estimates for CRC incidence and mortality with endoscopic screening and healthy lifestyle separately and in combination when we stopped updating lifestyle information after the first endoscopic screening.

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    S7 Table. PAR estimates for CRC incidence and mortality with endoscopic screening and healthy lifestyle separately and in combination when we excluded the person-time when response to endoscopy was missing.

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    S8 Table. PAR estimates for CRC incidence with endoscopic screening and healthy lifestyle separately and in combination when healthy lifestyle score was defined by the five 5-categorical lifestyle factors.

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    S1 Text. Prospective analysis proposal.

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    S2 Text. Detailed assessment and statistical analysis.

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    Data Availability Statement

    Because of the sensitive nature of the data collected for this study, requests to access the dataset from qualified researchers trained in human subject confidentiality protocols may be sent to Brigham and Women's/Harvard Cohorts at https://docs.google.com/forms/d/e/1FAIpQLScAPV23ZIBpkk9CyEJ1OcFJjMol9elKEpLYnPu7g3PgBL57XA/viewform.


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