Alcohol intake and risk of oesophageal adenocarcinoma: a pooled analysis from the BEACON Consortium
- Neal D Freedman1,
- Liam J Murray2,
- Farin Kamangar1,3,
- Christian C Abnet1,
- Michael B Cook1,
- Olof Nyrén4,
- Weimin Ye4,
- Anna H Wu5,
- Leslie Bernstein6,
- Linda M Brown7,
- Mary H Ward1,
- Nirmala Pandeya8,
- Adele C Green8,
- Alan G Casson9,
- Carol Giffen10,
- Harvey A Risch11,
- Marilie D Gammon12,
- Wong-Ho Chow1,
- Thomas L Vaughan13,
- Douglas A Corley14,
- David C Whiteman8
- 1Division of Cancer Epidemiology and Genetics, National Cancer Institute, NIH, DHHS, Bethesda, Maryland, USA
- 2Centre for Public Health, Queen's University, Belfast, Northern Ireland
- 3Department of Public Health Analysis, School of Community Health and Policy, Morgan State University, Baltimore, Maryland, USA
- 4Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden
- 5Department of Preventive Medicine, Keck School of Medicine, University of Southern California/Norris Comprehensive Cancer Center, Los Angeles, California, USA
- 6Department of Population Sciences, Beckman Research Institute, City of Hope, Duarte, California, USA
- 7RTI International, Rockville, Maryland, USA
- 8Queensland Institute of Medical Research, Brisbane, Australia
- 9Department of Surgery, University of Saskatchewan, Saskatoon SK, Canada
- 10Information Management Services, Silver Spring, Bethesda, Maryland, USA
- 11Department of Epidemiology and Public Health, Yale University School of Medicine, New Haven, Connecticut, USA
- 12Department of Epidemiology, University of North Carolina School of Public Health, Chapel Hill, North Carolina, USA
- 13Program in Epidemiology, Fred Hutchinson Cancer Research Center, Seattle, Washington, USA
- 14Division of Research and Oakland Medical Center, Northern California, Oakland, California, USA
- Correspondence to Dr Neal Freedman, Nutritional Epidemiology Branch, Division of Cancer Epidemiology and Genetics, 6120 Executive Blvd, EPS/320, MSC 7232, Rockville, MD 20852, USA;
- Revised 24 January 2011
- Accepted 25 January 2011
- Published Online First 14 March 2011
Background and aims Alcohol intake is a strong and well established risk factor for oesophageal squamous cell carcinoma (OSCC), but the association with oesophageal adenocarcinoma (OA) or adjacent tumours of the oesophagogastric junction (OGJA), remains unclear. Therefore, the association of alcohol intake with OSCC, OA, and OGJA was determined in nine case–control studies and two cohort studies of the Barrett's Esophagus and Esophageal Adenocarcinoma Consortium (BEACON).
Materials and methods Information was collected on alcohol intake, age, sex, education, body mass index, gastro-oesophageal reflux, and tobacco smoking from each study. Along with 10 854 controls, 1821 OA, and 1837 OGJA, seven studies also collected OSCC cases (n=1016). Study specific ORs and 95% CIs were calculated from multivariate adjusted logistic regression models for alcohol intake in categories compared to non-drinkers. Summary risk estimates were obtained by random effects models.
Results No increase was observed in the risk of OA or OGJA for increasing levels of any of the alcohol intake measures examined. ORs for the highest frequency category (≥7 drinks per day) were 0.97 (95% CI 0.68 to 1.36) for OA and 0.77 (95% CI = 0.54 to 1.10) for OGJA. Suggestive findings linked moderate intake (eg, 0.5 to <1 drink per day) to decreased risk of OA (OR 0.63, 95% CI 0.41 to 0.99) and OGJA (OR 0.78, 95% CI 0.62 to 0.99). In contrast, alcohol intake was strongly associated with increased risk of OSCC (OR for ≥7 drinks per day 9.62, 95% CI 4.26 to 21.71).
Conclusions In contrast to OSCC, higher alcohol consumption was not associated with increased risk of either OA or OGJA. The apparent inverse association observed with moderate alcohol intake should be evaluated in future prospective studies.
- Alcohol drinking
- oesophageal neoplasms
- stomach neoplasms
- gastric cancer
- oesophageal cancer
Significance of this study
What is already known about this topic?
Oesophageal cancer is the sixth leading cause of cancer related mortality worldwide and occurs as two predominant histologic subtypes, oesophageal squamous cell carcinoma and oesophageal adenocarcinoma.
Whereas incidence rates of oesophageal adenocarcinoma have increased rapidly in many western countries over the past three decades, rates of oesophageal squamous cell carcinoma have concurrently declined.
Heavy alcohol consumption is an established cause of oesophageal squamous cell carcinoma, but associations with oesophageal adenocarcinoma have been inconsistent in past studies.
Previous studies of oesophageal adenocarcinoma have been too small to detect modest associations.
What are the new findings?
Heavy alcohol consumption, even consuming seven or more drinks per day, was not associated with increased risk of oesophageal adenocarcinoma in the 11 studies and more than 1800 cases of the Barrett's Esophagus and Esophageal Adenocarcinoma Consortium (BEACON).
Heavy alcohol intake was also not associated with adjacent adenocarcinomas of the oesophagogastric junction.
Modest alcohol consumption appeared to be associated with reduced risk for adenocarcinomas of both the oesophagus and oesophagogastric junction.
How might it impact on clinical practice in the foreseeable future?
These results indicate that heavy alcohol consumption is not a risk factor for adenocarcinomas of the oesophagus and oesophagogastric junction, highlighting substantial differences in the aetiology of oesophageal squamous cell carcinoma and oesophageal adenocarcinoma, the two most common histological types of oesophageal cancer.
Our findings may provide clinicians with further data to address patient queries about the causes of their cancer.
Oesophageal cancer is the sixth leading cause of cancer related mortality worldwide1 and occurs as two predominant histologic subtypes, oesophageal squamous cell carcinoma (OSCC) and oesophageal adenocarcinoma (OA).2 Whereas incidence rates of OA have increased rapidly in many western countries over the past three decades, rates of OSCC have concurrently declined.3
Alcohol intake is a strong and well established risk factor for OSCC.2 4–12 The association of alcohol with OA or adjacent adenocarcinomas overlapping the oesophagogastric junction (OGJA), however, remains unclear. Results have been inconsistent in previous studies,6 7 9 10 12–16 regardless of whether analysed as total alcoholic beverage intake or the individual beverage types of beer, liquor, and wine. Previous studies were limited in size, precluding precise quantification of modest effects and offering limited power to compare associations for OA with OGJA.2 3 17
To overcome these limitations, and to examine possible effect modification by known risk factors, such as sex, body mass index (BMI), gastro-oesophageal reflux disease, or tobacco smoking,2 3 17 18 we performed pooled analyses of the association between alcohol intake with OA and OGJA using data from nine case–control and two cohort studies of the international Barrett's Esophagus and Esophageal Adenocarcinoma Consortium (BEACON).
Analyses included participants from 11 BEACON studies. Population based case–control studies included the Population Health Study,14 the Larynx/Esophagus/Oral cavity (LEO) Study,12 the US Multi-Center Study,7 the nationwide Swedish Esophageal and Cardia Cancer (SECC) study,9 the Los Angeles County Multi-ethnic Case-control Study,16 the Nebraska Health Study II,19 the Nova Scotia Barrett Esophagus Study (NSBES),15 the Factors Influencing the Barrett's Adenocarcinoma Relationship (FINBAR) Study,13 and the nationwide Australian Cancer Study (oesophageal cancer component).10 Analyses also included eligible cases from two prospective cohort studies, the National Institutes of Health-AARP Diet and Health (NIH-AARP) study with follow-up through 2003,6 and the Kaiser-Permanente Multiphasic Health check-up Study with follow-up until 2006.20 We drew nested control sets randomly from the cohorts in a four to one control–case ratio from the NIH-AARP study and in an eight to one ratio from the Kaiser Multiphasic Health check-up Study.
Combining all 11 studies, 4140 cases (2064 OA, 2076 OGJA), and 13 676 controls were available for analysis. Among participants with available data on alcohol intake, we restricted our analyses to white non-Hispanic study participants (3658 cases: 1821 OA, 1837 OGJA; and 10 854 controls) due to low numbers of cases in participants from other ethnic groups (50 black, 112 Hispanic, and 71 other). All studies collected OA cases and 10 studies collected OGJA cases.6 7 9 10 12–14 16 19 20 Seven participating studies also collected OSCC cases,6 7 9 10 12 14 20 for which 1016 cases and 9253 controls were available for analysis.
Study specific case numbers and characteristics are presented in table 1.
Data acquisition was approved by the Institutional Review Board or Research Ethics Committee of each participating institution providing data for the study; permission to participate in the BEACON consortium was also provided by these boards if required by a study's home institution.
Each study provided a questionnaire, study methods, and a de-identified dataset including information on alcohol consumption, age, sex, BMI (weight divided by height squared, in kg/m2), education, gastro-oesophageal reflux, tobacco smoking, and study centre (for multicentre studies).7 12 14 We compared the data provided by each study with published data; any apparent inconsistencies were resolved with the study investigators.
Though all studies included questions on typical alcohol intake, the method of assessment and the wording of questions differed across studies. Seven studies assessed alcohol intake by interviewer administered questionnaire,7 9 12 14–16 19 one study used a paper questionnaire,20 two studies used computer based questionnaires,9 13 and two studies administered questionnaires by mail.6 10 Typical adult alcohol intake was assessed by six studies,7 12 14–16 19 whereas one study assessed alcohol drinking at the age intervals of 20 to <30 years, 30 to <50 years, and ≥50 years10; for this study the average of these data was used for the pooled analysis. In these seven studies,7 10 12 14–16 19 the non-drinking category was restricted to life-long never drinkers. The remaining four studies assessed typical alcohol intake at a specific timepoint: 20 years9 or 5 years before interview,13 or in the past 12 months for the two cohort studies.6 20 In these four studies,6 9 13 20 therefore, non-drinkers were those who were not drinking at the reference timepoint. One of these four studies assessed alcohol intake in categories (non-drinker, 0 to <3, 3 to <6, 6 to <9, ≥9 drinks per day).20 For each category in this study, we assigned the median alcohol intake within the stated ranges of other BEACON studies.
Alcohol intake across studies was standardised to a single drink of 14 g of ethanol (one 12 ounce (350 ml) beer, 5 ounce (150 ml) glass of wine, or 1.5 ounces (44 ml) of liquor). Intakes of beer, wine, and liquor were available separately for 10 studies.6 7 9 10 12–16 19 Duration of alcohol drinking was available for seven studies (table 1).7 10 12 14–16 19
Risk estimates were adjusted for known and suspected risk factors for OA and OGJA, namely age (years: <50, 50 to <60, 60 to <70, ≥70), total cigarette smoking exposure (pack-years: 0, >0 to <15, 15 to <30, 30 to <45, ≥45), BMI (<25, 25 to <30, ≥30), gastro-oesophageal reflux status (yes vs no), and study centre (for multicentre studies). For education, we used study specific variables. Data on gastro-oesophageal reflux were available for five studies.7 9 10 13 16 Because one study did not collect information on the age at smoking initiation at study baseline,6 we estimated duration by subtracting the median age at smoking initiation in a subset of the cohort (17 years) from current age or for former smokers the age at smoking cessation. This duration variable was then used to calculate pack-years. All other variables were available for all studies.
We analysed alcohol intake in categories. Study specific relative risk (RR) estimates were estimated by logistic regression models in Stata 10.0 and then pooled using random effects models.21 Results for fixed effect models were similar (data not shown). Heterogeneity between studies was assessed by the I2 statistic.22 Heterogeneity that can be explained by chance is indicated by an I2 of 0%. Values of p<0.05 were considered significant and all tests were two-sided.
Total alcohol exposure was assessed by drink-years, created by multiplying years of alcohol drinking in lifetime by typical drinks per day. Linear trend tests were also assessed in random effects models. In each study, we fitted a trend variable with the median intake per alcohol category; pooled results were then obtained by random effects meta-analysis of the study specific risk estimates. Risk estimates for beer, wine, and liquor used non-drinkers of any alcohol type as the referent and were adjusted for categories of total alcohol intake in order to investigate beverage specific effects independent of ethanol content. As a sensitivity analysis, we examined risk estimates that were unadjusted for total alcohol intake and results were similar. We also stratified analyses by categories of sex, BMI, gastro-oesophageal reflux, and cigarette smoking to identify potential modifiers of an association with alcohol intake.
Details on study design and assessment of alcohol use are shown in table 1. Alcohol use among controls ranged from a median of 0.1 drinks per day in the Nebraska study to 1.2 drinks per day in the FINBAR study.
Table 2 provides odd ratios (ORs) for frequency (drinks per day), duration (years) and drink-years of alcohol intake, relative to non-drinking. Overall, RR estimates had low to moderate heterogeneity with a majority of I2 below 40%. Not even the highest amount of alcohol intake (≥7 drinks per day) was associated with increased risk of OA (OR 0.97, 95% CI 0.68 to 1.36) or OGJA (OR 0.77, 95% CI 0.54 to 1.10). No evidence for a dose–response for either end point was observed and tests for linear trend were not statistically significant (OA: p=0.21; OGJA: p=0.88). Relative to non-drinkers, ORs for most categories of intake were <1.
For example, participants who reported typically drinking 0.5 to <1 drink per day had lower risk of both OA (OR 0.63, 95% CI 0.41 to 0.99) and OGJA (OR 0.78, 95% CI 0.62 to 0.99). Risk estimates from the seven participating studies7 10 12 14–16 19 which restricted the non-drinking referent category to lifetime never drinkers were similar to the four participating studies that could not make this restriction (figures 1 and 2). To increase power, we also looked at a combined end point which included both OA and OGJA cases. Alcohol intake was not associated with increased risk of this combined end point either (OR for ≥7 drinks per day 0.86, 95% CI 0.66 to 1.11; I2=12%).
We observed evidence for a modest inverse association between years of alcohol drinking and OA and OGJA, with p values for linear trends of 0.02 and 0.003, respectively. Relative to never drinking, ORs for drinking for ≥50 years were 0.71 (95% CI 0.48 to 1.05) for OA and 0.64 (95% CI 0.46 to 0.89) for OGJA. Overall, results for drink-years, reflecting duration of alcohol drinking and typical drinks per day, were null with little evidence for a dose–response association. The p value for linear trend was not significant for each end point. Yet relative to never drinking, there was evidence for a non-linear association. For example, the OR for 25 to <50 drink-years was 0.66 for OA and 0.79 for OGJA, whereas the corresponding ORs for >200 to <300 drink-years were 1.04 and 0.98, respectively.
In order to distinguish possible effects of individual types of alcoholic beverages from a possible generic effect of ethanol, we examined ORs for categories of beer, liquor, and wine consumption after adjustment for total alcohol intake (table 3). Beer intake had an apparent inverse association with OA and OGJA risk, though the p value for linear trend was not significant for either OA (p=0.12) or OGJA (p=0.06). Associations for liquor intake centred around unity, whereas there was suggestive evidence for a non-linear association with wine.
Relative to non-drinking, the OR for drinking 0.5 to <1 drink of wine per day was 0.59 (95% CI 0.39 to 0.88) for OA and 0.64 (95% CI 0.45 to 0.90) for OGJA. In the highest category of wine intake (≥3 drinks per day), the OR was 1.49 (95% CI 0.80 to 2.78) for OA and 1.18 (95% CI 0.51 to 2.72) for OGJA.
Next, we examined the association of alcohol (drinks per day) with cancer risk separately in men and women and by stratum of gastro-oesophageal reflux, BMI, and tobacco smoking (supplementary tables 1 and 2). Risk estimates generally appeared similar and 95% CIs overlapped across most strata. One exception was an increased risk for OA (OR 4.25, 95% CI 1.60 to 11.30, 14 cases; p for linear trend=0.13) among women drinking ≥3 alcoholic beverages per day, but no evidence for OGJA (OR 0.99, 95% CI 0.41 to 2.35, 11 cases; p for linear trend=0.90). No such patterns were observed in men.
In contrast to results for OA and OGJA, we observed a strong dose–response association between alcohol intake and OSCC among the seven BEACON studies which also included OSCC cases (table 4). Relative to non-drinking, the OR for drinking ≥7 drinks per day was 9.62 (95% CI 4.26 to 21.71; p for linear trend <0.0001).
In this large pooled analysis of over 15 000 participants in 11 studies of the BEACON consortium, we found no evidence for an association between higher alcohol intake and increased risk of OA or OGJA. Indeed, risks among alcohol drinkers tended to be below those among non-drinkers, albeit mostly statistically non-significant. We found no evidence that any particular type of beverage (beer, liquor, or wine) was especially associated with increased or decreased cancer risk. Further, we exploited the large numbers of cases and controls in the BEACON dataset to examine associations by stratum of sex, gastro-oesophageal reflux disease, cigarette smoking, and BMI. Of the examined strata, alcohol intake was associated with increased OA risk in just one, women who drank ≥3 drinks per day. Given that the category comprised only 14 cases, the p for linear trend was not significant, and no association was observed with less intake, with OGJA, or in men, we conclude that this single association is most likely a chance finding.
Our results for OA and OGJA stand in remarkable contrast to results for OSCC in this and previously published studies.2 4–12 The OSCC results, generated from the same studies as the OA and OGJA results, should allay concerns about non-differential misclassification of alcohol intake, recall bias, and reverse causation as explanations for our null findings. Associations between other environmental risk factors and oesophageal cancer have also been shown to vary by histologic type. For example, higher BMI is a consistent risk factor for OA but not OSCC risk.23 Cigarette smoking is a risk factor for both tumour sites, though the magnitude of the association appears greater for OSCC than OA.6 7 9 11 12 24 Distinct associations between Helicobacter pylori infection and OSCC and OA risk have also been observed.25 Together with opposing incidence trends over time,3 these results indicate distinct aetiologies for OSCC and OA.
In our study, the association with alcohol intake was generally similar for OA and OGJA. It is difficult to distinguish these sites clinically,26 and whether the aetiology of these sites are similar or different is unclear. Whereas OAs were defined in our study as those above the oesophagogastric junction, OGJAs were more heterogeneous and included tumours overlapping the junction. Even so, results were generally similar for both end points and only modest heterogeneity was observed between studies which used distinct diagnostic criteria. Together, these data provide little evidence for an association between alcohol intake and increased risk of tumours either proximal or overlapping the oesophagogastric junction.
We observed suggestive evidence that modest alcohol drinking, particularly <1 drink per day, might be associated with reduced OA and OGJA risk. Such findings may be due to chance, particularly as multiple comparisons were made. As in all observational studies, the observed inverse association with modest alcohol drinking may also reflect additional unknown or poorly measured confounders. For example, moderate alcohol drinking could be associated with aspects of a healthy lifestyle, such that the observed association reflects confounding. In our study, similar results were observed in smokers and in participants with a BMI between 18.5 and <25 and those with a BMI ≥25. Yet, other aspects of a healthy lifestyle could still be responsible for these findings.
Inverse associations may also reflect recall bias or reverse causality as nine of the 11 studies participating in BEACON had a case–control design. Patients diagnosed with cancer may alter their alcohol intake or their report of it. In addition, individuals with undetected tumours or their precursor conditions, such as gastro-oesophageal reflux, might avoid alcohol because it provokes symptoms. Supporting this hypothesis, reflux symptoms have been shown to be associated with less alcohol intake in past studies.13
Of the two participating prospective cohorts, results from the NIH-AARP Diet and Health study6 and the Kaiser-Permanente Multiphasic Health check-up Study20 showed little evidence for an inverse association (figures 1 and 2). Published results from two other cohorts are mixed. Risk estimates for OA were 1.17 (95% CI 0.69–1.98) for drinking up to 5 g (∼1/3 a drink) per day and 0.91 (95% CI 0.51–1.60) for 5–<15 g (∼1 drink) per day relative to non-drinking in the Netherlands Cohort Study.11 In the Million Women Study, risk estimates were 0.78 (95% CI 0.61–0.99) for drinking ≤2 drinks per week relative to not drinking.27 Future prospective studies are needed.
Alternatively, inverse associations with moderate alcohol drinking may reflect contamination of the non-drinking referent group with formerly heavy drinkers. However, we found no evidence for increased cancer risk with higher alcohol intake in our study, even among those drinking ≥7 drinks per day, so contamination with heavy drinkers would not alter the associations in this manner. Furthermore, seven studies restricted the non-drinking category to those who reported never drinking alcohol.7 10 12 14–16 19 Inverse associations with modest alcohol drinking persisted in these seven studies (figures 1 and 2).
It is also possible that these results reflect a true association. For example, ethanol intake may have beneficial effects on insulin resistance or values of serum lipids and lipoproteins,28 which might be important for OA and OGJA risk. Also, wine,29 and to some extent beer,30 are thought to contain antioxidants which could affect cancer risk. Intriguingly, similar results have been observed for alcohol intake in two recent studies of Barrett's oesophagus,13 31 a precursor of OA.
One striking aspect of OA and OGJA epidemiology is the profoundly higher incidence in men relative to women.3 As such, previous studies have had little power to examine the association of alcohol with OA and OGJA in men and women separately. In sex stratified analyses, we generally found comparable results between men and women, with the exception of OA risk among women drinking ≥3 drinks per day. As there were just 14 OA cases in this group, this result may be due to chance variation. Either way, since men typically drink more alcoholic beverages than women, our results suggest differences in alcohol use are very unlikely to explain differences in the incidence of these cancers between men and women.
Strengths of our study include its large size, inclusion of both population based case–control and cohort studies, inclusion of both histologic types of oesophageal cancer and adjacent adenocarcinomas of the oesophagogastric junction, and adjustment for major OA risk factors. We defined variables for alcohol intake in the same way for each study. Furthermore, risk estimates from each study were adjusted for a standard set of covariates. We also investigated risk estimate heterogeneity between studies. Alcohol intake was comprehensively assessed, with analyses of drinks per day, duration, drink-years, and beverage types. Furthermore, we exploited the large dataset to examine possible differences by major risk factors, including BMI, cigarette smoking, and gastro-oesophageal reflux disease. Finally, we found similar risk estimates in studies performed in different regions of the world and with different study designs, adding credence to our findings.
Limitations include possible recall and selection bias, as most participating studies had a case–control design. However, results were generally similar for the two cohort studies. In addition, though our study is the largest to date, case numbers were small in some strata of the stratified analyses, such as women, and we lacked ability to assess associations in non-Caucasian ethnic groups.
In conclusion, in contrast to results for OSCC, we observed little evidence for an association between higher alcohol consumption with either OA or OGJA risk. Moderate alcohol consumption was associated with reduced OA and OGJA cancer risk, though these findings need to be examined further in future prospective cohort studies.
We thank the participants and staff of each participating study.
Funding This work was supported in part by the Intramural Program of the National Institutes of Health. The Population Health Study was funded by the Intramural Program of the National Institutes of Health. The Larynx, Oesophagus, and Oral Cavity (LEO) Study was funded by grants R01-CA30022 and R37-CA41530 (both awarded to TLV, David Thomas, Scott Davis, Bonnie Worthington Roberts, Ruth Little, and Mary Rogers). The US Multi-Center Study was funded by grants U01-CA57949 (awarded to TLV), U01-CA57983 (awarded to MDG), and U01-CA57923 (awarded to HAR). The Swedish Esophageal Cancer Study was funded by grant number R01 CA57947–03 (awarded to ON and Hans-Olov Adami). The Los Angeles County Multi-ethnic Case-control Study was funded by grants 3RT-0122 (‘Smoking and Risk of Proximal vs Distal Gastric Cancer’, awarded to AHW) and 10RT-0251 (‘Smoking, microsatellite instability & gastric cancers’, awarded to AHW) from the California Tobacco Related Research Program and grant CA59636 (awarded to LB) from the National Cancer Institute. The Nebraska Health Study was funded by the Intramural Program of the National Institutes of Health. The Nova Scotia Barrett Oesophagus Study was supported by the Nova Scotia Health Research Foundation (‘Molecular mechanisms and lifestyle risk factor interactions in the pathogenesis of human esophageal adenocarcinoma’, N419, awarded to AGC). The Factors Influencing the Barrett's Adenocarcinoma Relationship (FINBAR) study was funded by an Ireland-Northern Ireland Co-operation Research Project Grant sponsored by the Northern Ireland Research & Development Office, and the Health Research Board, Ireland (All-Ireland case-control study of Oesophageal Adenocarcinoma and Barrett's Oesophagus, awarded to LJM and Harry Comber). The Australian Cancer Study was supported by the Queensland Cancer Fund and the National Health and Medical Research Council (NHMRC) of Australia (Program no. 199600, awarded to DCW, ACG, Nicholas K Hayward, Peter G Parsons, David M Purdie, and Penelope M Webb). NIH-AARP was funded by the Intramural Program of the National Institutes of Health. Reported analyses with the Kaiser-Permanente Multiphasic Health check-up Study were funded by NIH grant number R01 DK063616 (Epidemiology and Incidence of Barrett's Oesophagus, Kaiser Permanente, awarded to DAC) and NIH grant R21DKO77742 (Barrett's Oesophagus: Risk Factors in Women, awarded to DAC and Nicholas J Shaheen).
Competing interests None.
Ethics approval Data acquisition was approved by the Institutional Review Board or Research Ethics Committee of each participating institution providing data for the study; permission to participate in the BEACON consortium was also provided by these boards if required by a study's home institution.
Provenance and peer review Not commissioned; externally peer reviewed.