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Abstract
Trends in biliary tract cancer incidence rates have increased in Shanghai, China. These trends have coincided with economic and developmental growth, as well as a shift in dietary patterns to a more Westernized diet. To examine the effect of dietary changes on incident disease, we evaluated associations between diet and biliary tract cancers amongst men and women from a population-based case-control study in Shanghai, China. Biliary tract cancer cases were recruited from 42 collaborating hospitals in urban Shanghai, and population-based controls were randomly selected from the Shanghai Household Registry. Food frequency questionnaire data were available for 225 gallbladder, 190 extrahepatic bile duct, and 68 ampulla of Vater cancer cases. A total of 39 food groups were created and examined for associations with biliary tract cancer. Interestingly, only four food groups demonstrated a suggested association with gallbladder, extrahepatic bile duct, or ampulla of Vater cancers. The allium food group, consisting of onions, garlic, and shallots showed an inverse association with gallbladder cancer (OR: 0.81, 95% CI: 0.68–0.97). Similar trends were seen in the food group containing seaweed and kelp (OR: 0.79, 95% CI: 0.67–0.96). In contrast, both preserved vegetables and salted meats food groups showed positive associations with gallbladder cancer (OR:1.27, 95% CI: 1.06–1.52; OR: 1.18, 95% CI: 1.02–1.37, respectively). Each of these four food groups showed similar trends for extrahepatic bile duct and ampulla of Vater cancers. The results of our analysis suggest intake of foods with greater anti-inflammatory properties may play a role in decreasing the risk of biliary tract cancers. Future studies should be done to better understand effects of cultural changes on diet, and to further examine the impact diet and inflammation have on biliary tract cancer incidence.
Citation: Nelson SM, Gao Y-T, Nogueira LM, Shen M-C, Wang B, Rashid A, et al. (2017) Diet and biliary tract cancer risk in Shanghai, China. PLoS ONE 12(3): e0173935. https://doi.org/10.1371/journal.pone.0173935
Editor: Heather Francis, Digestive Disease Research Center, Scott & White Healthcare, UNITED STATES
Received: December 7, 2016; Accepted: February 28, 2017; Published: March 13, 2017
This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication.
Data Availability: All relevant data are within the paper and its Supporting Information files.
Funding: This work was supported by general funds from the Intramural Research Program of the National Institutes of Health, National Cancer Institute, Division of Cancer Epidemiology and Genetics (DCEG). The funders had no role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Introduction
A relatively rare disease, biliary tract cancer is divided into three anatomic types: gallbladder, extrahepatic bile duct, and ampulla of Vater [1, 2]. Regional variations in biliary tract cancer incidence have been well documented, with higher rates in Central and South America, and parts of Asia, including India and Shanghai, China [3, 4, 5]. Biliary tract cancer incidence rates in Shanghai increased from 1977–2010, in both men and women [6]. Women, however, have seen greater increases in incidence and number.
Diet has likely affected general disease incidence, as China has seen major economic and developmental growth, accompanied with an emerging obesity epidemic [7, 8]. Studies have shown that following a westernized dietary pattern high in red and processed meats, fats, simple carbohydrates and sugars shows positive associations with inflammatory markers [9, 10, 11, 12]. Today, Shanghai has significantly increased animal based diets, where pork is consumed at higher rates than processed and grilled meats [13]. Conversely, foods such as fruits, vegetables, fish, nuts, and whole grains, and dietary patterns such as the Mediterranean diet, are inversely associated with inflammation and inflammatory markers like C-reactive protein (CRP) and IL-6 [9, 14, 15, 16, 17]. Moreover, a recent study in Nepal demonstrated high intake of fruits to be a protective factor for gallbladder cancer [18]. These pro- and anti-inflammatory foods may be associated with cancer risk.
Diet has been associated with many cancers in China. For example, consumption of salted fish, a staple in many Chinese homes, has been linked to increased inflammation and incidence of nasopharyngeal carcinoma [19], while consumption of red meat, fish, and eggs have been associated with increased incidence of colon cancer [20]. The link between diet and biliary tract cancer is less clear, however. Although epidemiological case-control studies, and a recent meta-analysis, have shown associations between diet, obesity, and biliary tract cancer [21, 22, 23, 24], the World Cancer Research Fund and the American Institute of Cancer Research (WCRF/AICR) have determined associations between diet, supplement intake and biliary tract cancer are “limited-no conclusion” [25], indicating that more research is needed. In this report, we evaluated the role of diet and its associations with biliary tract cancers amongst men and women from a population-based case-control study in Shanghai, China.
Materials and methods
Study population
In a population-based study conducted in Shanghai, China, incident biliary tract cancers were identified between June 1997 and May 2001. Cases, ages 35–74, were identified using a rapid reporting system established across 42 collaborating hospitals in urban Shanghai [3, 26]. Collectively, these hospitals captured over 95% of the eligible biliary tract cancer cases in Shanghai during the study period. We enrolled a total of 627 cases, including 368 gallbladder, 191 extrahepatic bile duct, and 68 ampulla of Vater cancer patients (ICD9 156). To assess and identify unique and shared risk factors associated with biliary tract cancers, 1,037 biliary stone cases without a history of cancer (774 with gallstones and 263 with bile duct stones) were selected from the same hospital as the cancer cases and frequency-matched on age (5-year groups) and sex. Moreover, a total of 959 permanent residents of Shanghai, with no history of cancer, were randomly selected from the Shanghai Household Registry as population controls and frequency-matched to cases based on age (5-year groups) and sex. Written informed consent was provided by all study subjects. The Institutional Review Boards of the National Cancer Institute and Shanghai Cancer Institute approved the study protocol.
Clinical and pathology review
Surgical and pathology reports from local hospitals were used to diagnose all biliary tract cancer cases. Each was confirmed as previously described [3] by a panel of clinicians. Histological confirmation for each cancer was completed by expert review [3, 27]. Only 70% of the cancer cases had available materials to use for confirmation due to the late-stage diagnosis of most biliary tract cancers. For cases without pathology material, image data, medical records, and surgical reports were reviewed. Biliary stone cases were confirmed clinically, through review of abdominal ultrasound data or ERCP films [22].
Interviews
In-person interviews were conducted for all study subjects as previously described [3]. Briefly, subjects were interviewed using a structured questionnaire, collecting information on demographics, diet, and life-style factors. Information on history of gallstones was also collected. Each interview was taped, reviewed, and verified to ensure study protocol adherence. The interview response rate for cases was > 95% and 82% for population controls. To check interview reproducibility, 5% of controls were randomly selected and re-interviewed 3 months after the original. Concordance was over 95%.
Creation of food groups
We used a food frequency questionnaire with portion size to assess dietary intake. Portion size was capture by the liang (with one liang equivalent to 50 grams). The questionnaire included 115 dietary food items, posing questions such as: ‘Five years ago, how many times per day/week/month did you eat the following foods, and how many liang of each food did you eat?’. Each food items in the FFQ is treated as a continuous variable, representing amount consumed in a day. Using the median as the cut-off, each food item was divided into high and low intake. Foods identified in the questionnaire were categorized into 39 food groups using information gathered from previous studies and AICR, WCRF, and International Agency for Research on Cancer (IARC) reports including food likeness, association with inflammatory markers and cancer, and food type [19, 25, 28]. Vegetables, fish, red meat, poultry, beans, fats, and proteins were categorized into representative groups. For example, bacon, pork chops, spare ribs, pig feet, pork, and fried pork were categorized together (S1 Table).
Statistical analysis
To determine associations between biliary tract cancers and diet, we performed unconditional logistic regression to calculate odds ratios (ORs) and 95% confidence intervals (CIs). Biliary tract cancer cases were compared to controls within each food group category (low intake = reference group). Population-based controls without a history of cholecystectomy (n = 884) were compared to gallbladder cases. Extrahepatic bile duct and ampulla of Vater cancer cases were compared with all population controls (n = 947). Gallstone controls (n = 774) were also compared with all population controls. Forward selection was used to create the final regression model, where age, sex, education, gallstones and body mass index (BMI; weight (kg)/height (m2)) accounted for at least a 10% change in the association between diet and each cancer. Additionally, hepatitis, coronary heart disease (CHD), liver cirrhosis, and liver cancer were evaluated. However, each variable showed no change in the ORs of any food group by 10% or more, and therefore were not included in the final model. Total energy intake was adjusted for using the residuals method [29]. Within each food group, high and low food intake were compared, with low intake as the referent group. Differences between cases and controls were detected using Fisher’s exact test. Stratification by sex was used to investigate effect modification of the associations between biliary tract cancers and diet by sex for gallbladder cancer and extrahepatic bile duct cancer. Numbers were too limited to evaluate ampulla of Vater cancer. The Wald test was used to statistically test for interaction on the multiplicative scale. To test for multiple comparisons, we applied a Bonferroni correction based on 39 food groups (adjusted p-value = 0.001).
All statistical tests were two-sided, and p-values < 0.05 were considered statistically significant. Analyses were performed using SAS software, version 9.3.
Results
Most biliary tract cancer patients in this case-control study were married with a normal BMI (18.5–25 kg/m2), did not report diabetes, and were never smokers (Table 1). Population controls were more likely to be never drinkers, while gallbladder, extrahepatic bile duct, and ampulla of Vater cases were more likely to be drinkers. Moreover, gallbladder cancer cases were more likely to be women, while extrahepatic bile duct and ampulla of Vater cases were both more likely to be men.
For most of the 39 food groups created, we did not see consistent associations within the cancer sites, nor across the cancer sites (S1 Table). Four food groups, however, showed interesting patterns. The allium vegetable group, including onions, shallots, and garlic, showed an inverse association with gallbladder (OR: 0.81, 95% CI: 0.68–0.97), extrahepatic bile duct (OR: 0.77, 95% CI: 0.64–0.92), and ampulla of Vater cancers (OR: 0.74, 95% CI: 0.49–1.14), compared to the appropriate population-based controls (Table 2). Similar trends were seen in the food group that consisted of seaweed and kelp. Both of these food groups showed a 20% or greater reduction in biliary tract cancer risk. In contrast, preserved vegetables were positively associated across the three cancer sites; the strongest association was with extrahepatic bile duct cancer (OR: 1.37, 95% CI: 1.14–1.65). Salted meats and salted fish were also positively associated across all three cancer sites and showed the strongest association with ampulla of Vater cancer; ampulla of Vater cancer cases were 74% more likely to have consumed salted meats and fish than population-based controls (OR: 1.74, 95% CI: 1.16–2.61). However, none of the associations for the four food groups were significant at the Bonferroni-corrected level.
Comparing gallbladder cancer to gallstone controls, associations with the four food groups were in the same direction as the associations for gallbladder cancer compared to population controls. However, only the association with the seaweed and kelp food group was statistically significant (OR: 0.82, 95% CI: 0.70–0.96, p-value = 0.03). Upon examining associations with gallstones, the food group containing onions, shallots, and garlic was inversely associated with gallstones compared to population controls (OR: 0.78, 95% CI: 0.64–0.96, p-value = 0.02) (S2 Table). Both the preserved vegetables food group and the salted meats and salted fish food group showed positive associations with gallstones compared to population-based controls (OR: 1.18, 95% CI: 0.94–1.49; OR: 1.21, 95% CI: 0.99–1.46, respectively).
In our stratified models, associations between gallbladder cancer and each food group showed some differences between men and women (Table 3). In women, gallbladder cancer was inversely associated with the onions, shallots, and garlic food group (OR: 0.69, 95% CI: 0.54–0.88), and the preserved vegetables and salted meats/fish food groups had positive associations (OR: 1.48, 95% CI: 1.19–1.84; OR: 1.12, 95% CI: 1.01–1.45, respectively). Conversely, in men only the seaweed and kelp food group showed an inverse association with gallbladder cancer (OR: 0.65, 95% CI: 0.47–0.91), while it was null in women (OR: 0.88, 95% CI: 0.70–1.09). However, there was no statistically significant modification by sex for gallbladder cancer across all four food groups on the multiplicative scale (P-interaction range = 0.07–0.25). Furthermore, stratification revealed no modification by sex of the associations between extrahepatic bile duct cancer and any of the four food groups (P-interaction range: 0.46–0.52) (Table 3).
Discussion
In this population-based study, we evaluated 39 food groups and their association with gallbladder, extrahepatic bile duct, and ampulla of Vater cancer. In general, the associations between most dietary factors, food items and food groups, and biliary tract cancer were null. However, four food groups produced interesting results. Risk at all three biliary tract cancer sites was reduced with higher consumption of onions, shallots, and garlic and of seaweed and kelp. Conversely, consumption of preserved vegetables and salted and preserved meats and fish were associated with increased the risk of biliary tract cancer.
Animal studies have shown dietary garlic and onions reduce diet-induced cholesterol gallstones [30], a well-established risk factor for gallbladder cancer [3, 31, 32, 33]. Evidence from our study supports this finding, as consumption of both garlic and onions was associated with a moderately decreased risk of gallbladder cancer. In addition, seaweed, kelp, garlic, and onions may have anti-inflammatory properties [34, 35, 36]. To date, many of the findings from the Shanghai Study have been related to inflammation [27, 37]. Recent publications have shown increasing levels of CRP are associated with increased risk of gallbladder cancer [38] and other bile duct cancers [39]. Given these trends, if foods such as seaweed, kelp, garlic, and onions can reduce CRP and other inflammatory marker levels, as shown in previous studies [40, 41], they may also help reduce the risk of biliary tract cancers. Furthermore, results from a study from the EPIC cohort show increasing amounts of fiber decrease the risk of biliary tract cancer [42]. High amounts of fiber are contained in many foods, including seaweed and kelp, which were associated with decreased biliary tract cancer risk in our study.
In contrast, foods such as preserved vegetables and salted and preserved meats have been shown to have pro-inflammatory properties [19, 28]. The process of preserving vegetables consists of pickling with salt and brine. Evidence from epidemiological studies shows a strong association between esophageal cancer and consumption of preserved and pickled vegetables [43]. A recent meta-analysis showed a 52% increase in gastric cancer risk from consumption of pickled vegetables [44]; an 86% increase in gastric cancer risk was seen in those from mainland China [30]. In a study of Japanese men and women, high intake of salted foods including salted fish, increased the risk of gastric cancer in men (RR Q5vs.Q1: 2.23, p-value = 0.001); however, similar trends were not seen in women (RRQ5vs.Q1:1.32, p-value = 0.48) [45]. Very few studies have examined consumption of preserved vegetables and salted food in relation to biliary tract cancer risk, but in one study, the relative risk of gallstones decreased by 81% among those who consumed salted fish (RR: 0.19, 95% CI: 0.05–0.68) [46]. These findings are inconsistent with our study, since a decreased risk of gallstones would presumably be associated with a decreased risk of gallbladder cancer, while we found that increased salted fish was associated with an increased risk of gallbladder cancer. These differences may be due to environmental or genetic factors involved in the development of gallstones, and progression to gallbladder cancer. Differences in the kind and quantity of salted foods could also be related. For example, higher quantities of salted fish are consumed in the south of China than in Shanghai [19], while allium vegetables are more frequently consumed in Shanghai than other populations [47]. The positive association between preserved vegetables and salted meats is also supported by studies implicating nitrates and nitrites in carcinogenesis [48], and a cross-sectional study in India showed that nitrate concentrations in bile were significantly higher in gallbladder cancer cases compared to gallstone patients (mean nitrate concentration in gallbladder cancer cases = 79.33 mg/L vs. choleslithiasis cases = 3.37 mg/L) [49]. This potential biological plausibility provides compelling support for future investigations of these food components and biliary tract cancer risk to improve our understanding of the biologic mechanisms involved and potential cancer prevention strategies.
Although we did not see statistically significant effect modification by sex on a multiplicative scale with respect to gallbladder and extrahepatic bile duct cancer, there was some evidence of differences in associations with specific food groups for gallbladder cancer. Given the small number of cases in our study, additional studies are necessary to determine whether sex may modify the effect of dietary components on biliary tract cancer risk.
Our study has a number of strengths. It is a population-based study with high participation rates (> 80%). Although not terribly large, the study has sufficient numbers for us to examine associations between diet and the three biliary anatomic subsites separately, allowing us to evaluate patterns within and across these subsites. Moreover, we established food groups with known biological relevance supported by evidence from AICR and the WCRF. This study was also able to evaluate foods that are more commonly consumed in Shanghai than in other parts of the world. For example, seaweed, kelp, and salted fish are staples in Chinese kitchens, with less consumption in Western populations. This specificity has limited other studies from examining these foods in the context of biliary tract cancer risk, highlighting the novelty of our findings.
Limitations of the study include the case-control design, which may have influenced the observed associations through the introduction of recall bias (or reverse causation). Respondents were asked to report food consumption five years prior to the study in order to assess exposure prior to development of cancer. However, we cannot rule out potential associations due to chance. The small sample size also limited our ability to examine possible effect modification by sex, especially for ampulla of Vater cancer cases.
In conclusion, while most food groups were not associated with biliary tract cancers, we found modest to moderate associations between vegetables with anti-oxidant properties and decreased risk of biliary tract cancer. Conversely, consumption of meats and vegetables that have been salted or preserved, were associated with increased risk of biliary tract cancer. These results suggest that future studies of diet and inflammation may be warranted to better understand the impact of diet on biliary tract cancers.
Supporting information
S1 Table. A complete list of the 39 food groups, depicting associations between diet food groups three biliary tract cancer types.
https://doi.org/10.1371/journal.pone.0173935.s001
(PDF)
S2 Table. Adjusted ORs (95% CIs) for associations between diet food groups (Fg) and gallstones.
Models adjusted for: age, gender, education, kcal and body mass index.
https://doi.org/10.1371/journal.pone.0173935.s002
(PDF)
S1 File. Shanghai Cancer Institute Health Study questionnaire.
https://doi.org/10.1371/journal.pone.0173935.s003
(PDF)
S2 File. The Nutrition and Health Study in Shanghai Enrollment interview guide.
https://doi.org/10.1371/journal.pone.0173935.s004
(PDF)
Author Contributions
- Conceptualization: SMN JK LMN.
- Data curation: SMN JK LMN.
- Formal analysis: SMN JK LMN.
- Funding acquisition: JK.
- Investigation: JK YG BW MS.
- Methodology: JK LN AWH AR.
- Project administration: JK YG MS BW.
- Resources: JK YG MS BW.
- Software: JK LMN SMN.
- Supervision: JK.
- Validation: JK.
- Visualization: SMN JK LMN YG AR AWH YG.
- Writing – original draft: JK LMN SMN.
- Writing – review & editing: SMN JK LMN YG AR AWH MS BW.
References
- 1. de Groen PC, Gores GJ, LaRusso NF, Gunderson LL, Nagorney DM. Biliary tract cancers. N Engl J Med. 1999;341(18):1368–78. pmid:10536130
- 2. Wistuba II, Gazdar AF. Gallbladder cancer: lessons from a rare tumour. Nat Rev Cancer. 2004;4(9):695–706. pmid:15343276
- 3. Hsing AW, Gao YT, Han TQ, Rashid A, Sakoda LC, Wang BS, et al. Gallstones and the risk of biliary tract cancer: a population-based study in China. Br J Cancer. 2007;97(11):1577–82. pmid:18000509
- 4. Wernberg JA, Lucarelli DD. Gallbladder cancer. Surg Clin North Am. 2014;94(2):343–60. pmid:24679425
- 5. Randi G, Franceschi S, La Vecchia C. Gallbladder cancer worldwide: geographical distribution and risk factors. Int J Cancer. 2006;118(7):1591–602. pmid:16397865
- 6. Bao PP, Zheng Y, Wu CX, Huang ZZ, Gao YT, Jin F, et al. Cancer incidence in urban Shanghai, 1973–2010: an updated trend and age-period-cohort effects. BMC Cancer. 2016;16:284. pmid:27102013
- 7. Qin Y, Melse-Boonstra A, Pan X, Zhao J, Yuan B, Dai Y, et al. Association of dietary pattern and body weight with blood pressure in Jiangsu Province, China. BMC Public Health. 2014;14:948. pmid:25216777
- 8. Shen J, Goyal A, Sperling L. The emerging epidemic of obesity, diabetes, and the metabolic syndrome in china. Cardiol Res Pract. 2012;2012:178675. pmid:21961074
- 9. Giugliano D, Ceriello A, Esposito K. The effects of diet on inflammation: emphasis on the metabolic syndrome. J Am Coll Cardiol. 2006;48(4):677–85. pmid:16904534
- 10. Esmaillzadeh A, Kimiagar M, Mehrabi Y, Azadbakht L, Hu FB, Willett WC. Dietary patterns and markers of systemic inflammation among Iranian women. J Nutr. 2007;137(4):992–8. pmid:17374666
- 11. Lopez-Garcia E, Schulze MB, Fung TT, Meigs JB, Rifai N, Manson JE, et al. Major dietary patterns are related to plasma concentrations of markers of inflammation and endothelial dysfunction. Am J Clin Nutr. 2004;80(4):1029–35. pmid:15447916
- 12. Barbaresko J, Koch M, Schulze MB, Nothlings U. Dietary pattern analysis and biomarkers of low-grade inflammation: a systematic literature review. Nutr Rev. 2013;71(8):511–27. pmid:23865797
- 13. Takata Y, Shu XO, Gao YT, Li H, Zhang X, Gao J, et al. Red meat and poultry intakes and risk of total and cause-specific mortality: results from cohort studies of Chinese adults in Shanghai. PLoS One. 2013;8(2):e56963. pmid:23451121
- 14. Nettleton JA, Steffen LM, Mayer-Davis EJ, Jenny NS, Jiang R, Herrington DM, et al. Dietary patterns are associated with biochemical markers of inflammation and endothelial activation in the Multi-Ethnic Study of Atherosclerosis (MESA). Am J Clin Nutr. 2006;83(6):1369–79. pmid:16762949
- 15. Nanri A, Moore MA, Kono S. Impact of C-reactive protein on disease risk and its relation to dietary factors. Asian Pac J Cancer Prev. 2007;8(2):167–77. pmid:17696726
- 16. Chrysohoou C, Panagiotakos DB, Pitsavos C, Das UN, Stefanadis C. Adherence to the Mediterranean diet attenuates inflammation and coagulation process in healthy adults: The ATTICA Study. J Am Coll Cardiol. 2004;44(1):152–8. pmid:15234425
- 17. Galland L. Diet and inflammation. Nutr Clin Pract. 2010;25(6):634–40. pmid:21139128
- 18. Tamrakar D, Paudel I, Adhikary S, Rauniyar B, Pokharel P. Risk Factors for Gallbladder Cancer in Nepal a Case Control Study. Asian Pac J Cancer Prev. 2016;17(7):3447–53. pmid:27509990
- 19. (2012) Chinese-style salted fish I.. IARC Monogr Eval Carcinog Risks Hum 100E:1–538.
- 20. Chiu BC, Ji BT, Dai Q, Gridley G, McLaughlin JK, Gao YT, et al. Dietary factors and risk of colon cancer in Shanghai, China. Cancer Epidemiol Biomarkers Prev. 2003;12(3):201–8. pmid:12646508
- 21. Park M, Song da Y, Je Y, Lee JE. Body mass index and biliary tract disease: a systematic review and meta-analysis of prospective studies. Prev Med. 2014;65:13–22. pmid:24721739
- 22. Zhang XH, Andreotti G, Gao YT, Deng J, Liu E, Rashid A, et al. Tea drinking and the risk of biliary tract cancers and biliary stones: a population-based case-control study in Shanghai, China. Int J Cancer. 2006;118(12):3089–94. pmid:16395699
- 23. Kato K, Akai S, Tominaga S, Kato I. A case-control study of biliary tract cancer in Niigata Prefecture, Japan. Jpn J Cancer Res. 1989;80(10):932–8. pmid:2515177
- 24. Moerman CJ, Bueno de Mesquita HB, Runia S. Dietary sugar intake in the aetiology of biliary tract cancer. Int J Epidemiol. 1993;22(2):207–14. pmid:8505175
- 25.
Research WCRFAIfC. Food, Nutrition, Physical Activity, and the Prevention of Cancer: a Global Perspective. Washington DC. 2007;AICR.
- 26. Hsing AW, Sakoda LC, Rashid A, Chen J, Shen MC, Han TQ, et al. Body size and the risk of biliary tract cancer: a population-based study in China. Br J Cancer. 2008;99(5):811–5. pmid:18728671
- 27. Liu E, Sakoda LC, Gao YT, Rashid A, Shen MC, Wang BS, et al. Aspirin use and risk of biliary tract cancer: a population-based study in Shanghai, China. Cancer Epidemiol Biomarkers Prev. 2005;14(5):1315–8. pmid:15894693
- 28. (1993) I. Pickled Vegetables. IARC MONOGRAPHS ON THE EVALUATION OF CARCINOGENIC RISKS TO HUMANS.56:83–113. pmid:8411630
- 29. Willett WC, Howe GR, Kushi LH. Adjustment for total energy intake in epidemiologic studies. Am J Clin Nutr. 1997;65(4 Suppl):1220S–8S; discussion 9S-31S.
- 30. Vidyashankar S, Sambaiah K, Srinivasan K. Dietary garlic and onion reduce the incidence of atherogenic diet-induced cholesterol gallstones in experimental mice. Br J Nutr. 2009;101(11):1621–9. pmid:18983715
- 31. Jain K, Sreenivas V, Velpandian T, Kapil U, Garg PK. Risk factors for gallbladder cancer: a case-control study. Int J Cancer. 2013;132(7):1660–6. pmid:22890893
- 32. Scott TE, Carroll M, Cogliano FD, Smith BF, Lamorte WW. A case-control assessment of risk factors for gallbladder carcinoma. Dig Dis Sci. 1999;44(8):1619–25. pmid:10492143
- 33. Tewari M. Contribution of silent gallstones in gallbladder cancer. J Surg Oncol. 2006;93(8):629–32. pmid:16724346
- 34. Duan X-JZ, Wei-Wei Li, Xiao-Ming Wang, Bin-Gui . Evaluation of antioxidant property of extract and fractions obtained from a red alga, Polysiphonia urceolata. Food Chemistry. 2006;95:37–43.
- 35. Lim SN, Cheung PC, Ooi VE, Ang PO. Evaluation of antioxidative activity of extracts from a brown seaweed, Sargassum siliquastrum. J Agric Food Chem. 2002;50(13):3862–6. pmid:12059172
- 36. Nicastro HL, Ross SA, Milner JA. Garlic and onions: their cancer prevention properties. Cancer Prev Res (Phila). 2015;8(3):181–9.
- 37. Hsing AW, Sakoda LC, Rashid A, Andreotti G, Chen J, Wang BS, et al. Variants in inflammation genes and the risk of biliary tract cancers and stones: a population-based study in China. Cancer Res. 2008;68(15):6442–52. pmid:18676870
- 38. Koshiol J, Castro F, Kemp TJ, Gao YT, Roa JC, Wang B, et al. Association of inflammatory and other immune markers with gallbladder cancer: Results from two independent case-control studies. Cytokine. 2016;83:217–25. pmid:27173614
- 39. Aleksandrova K, Boeing H, Nothlings U, Jenab M, Fedirko V, Kaaks R, et al. Inflammatory and metabolic biomarkers and risk of liver and biliary tract cancer. Hepatology. 2014;60(3):858–71. pmid:24443059
- 40. Kantor ED, Lampe JW, Vaughan TL, Peters U, Rehm CD, White E. Association between use of specialty dietary supplements and C-reactive protein concentrations. Am J Epidemiol. 2012;176(11):1002–13. pmid:23139249
- 41. Kumar R, Chhatwal S, Arora S, Sharma S, Singh J, Singh N, et al. Antihyperglycemic, antihyperlipidemic, anti-inflammatory and adenosine deaminase- lowering effects of garlic in patients with type 2 diabetes mellitus with obesity. Diabetes Metab Syndr Obes. 2013;6:49–56. pmid:23378779
- 42. Bradbury KE, Appleby PN, Key TJ. Fruit, vegetable, and fiber intake in relation to cancer risk: findings from the European Prospective Investigation into Cancer and Nutrition (EPIC). Am J Clin Nutr. 2014;100 Suppl 1:394S–8S.
- 43. Islami F, Ren JS, Taylor PR, Kamangar F. Pickled vegetables and the risk of oesophageal cancer: a meta-analysis. Br J Cancer. 2009;101(9):1641–7. pmid:19862003
- 44. Ren JS, Kamangar F, Forman D, Islami F. Pickled food and risk of gastric cancer—a systematic review and meta-analysis of English and Chinese literature. Cancer Epidemiol Biomarkers Prev. 2012;21(6):905–15. pmid:22499775
- 45. Tsugane S, Sasazuki S, Kobayashi M, Sasaki S. Salt and salted food intake and subsequent risk of gastric cancer among middle-aged Japanese men and women. Br J Cancer. 2004;90(1):128–34. pmid:14710219
- 46. Kato I, Kato K, Akai S, Tominaga S. A case-control study of gallstones: a major risk factor for biliary tract cancer. Jpn J Cancer Res. 1990;81(6–7):578–83. pmid:2119360
- 47. Hsing AW, Chokkalingam AP, Gao YT, Madigan MP, Deng J, Gridley G, et al. Allium vegetables and risk of prostate cancer: a population-based study. J Natl Cancer Inst. 2002;94(21):1648–51. pmid:12419792
- 48. Eichholzer M, Gutzwiller F. Dietary nitrates, nitrites, and N-nitroso compounds and cancer risk: a review of the epidemiologic evidence. Nutr Rev. 1998;56(4 Pt 1):95–105.
- 49. Shukla VK, Prakash A, Chauhan VS, Singh S, Puneet. Biliary nitrate and risk of carcinoma of the gallbladder. Eur J Cancer Prev. 2004;13(4):355–6. pmid:15554566