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      Spicy food consumption and risk of gastrointestinal-tract cancers: findings from the China Kadoorie Biobank

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          Abstract

          Background

          Previous case–control studies have reported positive associations of spicy food consumption with risks of certain gastrointestinal-tract (GI) cancers. However, there is no prospective evidence on such associations, particularly from China, where there are high incidence rates of GI cancers and spicy food is widely consumed.

          Methods

          The prospective China Kadoorie Biobank study recruited >512 000 adults aged 30–79 years from 10 areas in China during 2004–2008; 2350 oesophageal, 3350 stomach and 3061 colorectal incident cancer cases were recorded by 1 January 2017, after a median of 10.1 years of follow-up. Cox regression yielded adjusted hazard ratios (HRs) for each cancer associated with spicy food intake.

          Results

          Overall, 30% of participants reported daily spicy food consumption at baseline. Spicy food consumption was inversely associated with oesophageal cancer risk, with adjusted HRs of 1.00, 0.88, 0.76, 0.84 and 0.81 for those who never/rarely consumed (reference) and consumed monthly, 1–2 days/week, 3–5 days/week and 6–7 days/week, respectively ( p trend < 0.002). The association remained similar after excluding the first 3 years of follow-up but appeared stronger in participants who did not smoke or drink alcohol regularly ( p trend < 0.0001). The corresponding HRs for stomach cancer were 1.00, 0.97, 0.95, 0.92 and 0.89 ( p trend  = 0.04), with the association disappearing after excluding the first 3 years of follow-up. For colorectal cancer, the HRs were 1.00, 1.00, 0.95, 0.87 and 0.90, respectively ( p trend = 0.04) and the inverse association appeared to be restricted to rectal rather than colon cancer ( p heterogeneity = 0.004). The types and strength of spice used showed little additional effects on these associations.

          Conclusion

          In Chinese adults, higher spicy food consumption was associated with lower risks of certain GI cancers, particularly among individuals who never smoked or drank alcohol regularly.

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          Most cited references41

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          Alcohol consumption and site-specific cancer risk: a comprehensive dose–response meta-analysis

          Background: Alcohol is a risk factor for cancer of the oral cavity, pharynx, oesophagus, colorectum, liver, larynx and female breast, whereas its impact on other cancers remains controversial. Methods: We investigated the effect of alcohol on 23 cancer types through a meta-analytic approach. We used dose–response meta-regression models and investigated potential sources of heterogeneity. Results: A total of 572 studies, including 486 538 cancer cases, were identified. Relative risks (RRs) for heavy drinkers compared with nondrinkers and occasional drinkers were 5.13 for oral and pharyngeal cancer, 4.95 for oesophageal squamous cell carcinoma, 1.44 for colorectal, 2.65 for laryngeal and 1.61 for breast cancer; for those neoplasms there was a clear dose–risk relationship. Heavy drinkers also had a significantly higher risk of cancer of the stomach (RR 1.21), liver (2.07), gallbladder (2.64), pancreas (1.19) and lung (1.15). There was indication of a positive association between alcohol consumption and risk of melanoma and prostate cancer. Alcohol consumption and risk of Hodgkin's and Non-Hodgkin's lymphomas were inversely associated. Conclusions: Alcohol increases risk of cancer of oral cavity and pharynx, oesophagus, colorectum, liver, larynx and female breast. There is accumulating evidence that alcohol drinking is associated with some other cancers such as pancreas and prostate cancer and melanoma.
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            China Kadoorie Biobank of 0.5 million people: survey methods, baseline characteristics and long-term follow-up.

            Large blood-based prospective studies can provide reliable assessment of the complex interplay of lifestyle, environmental and genetic factors as determinants of chronic disease. The baseline survey of the China Kadoorie Biobank took place during 2004-08 in 10 geographically defined regions, with collection of questionnaire data, physical measurements and blood samples. Subsequently, a re-survey of 25,000 randomly selected participants was done (80% responded) using the same methods as in the baseline. All participants are being followed for cause-specific mortality and morbidity, and for any hospital admission through linkages with registries and health insurance (HI) databases. Overall, 512,891 adults aged 30-79 years were recruited, including 41% men, 56% from rural areas and mean age was 52 years. The prevalence of ever-regular smoking was 74% in men and 3% in women. The mean blood pressure was 132/79 mmHg in men and 130/77 mmHg in women. The mean body mass index (BMI) was 23.4 kg/m(2) in men and 23.8 kg/m(2) in women, with only 4% being obese (>30 kg/m(2)), and 3.2% being diabetic. Blood collection was successful in 99.98% and the mean delay from sample collection to processing was 10.6 h. For each of the main baseline variables, there is good reproducibility but large heterogeneity by age, sex and study area. By 1 January 2011, over 10,000 deaths had been recorded, with 91% of surviving participants already linked to HI databases. This established large biobank will be a rich and powerful resource for investigating genetic and non-genetic causes of many common chronic diseases in the Chinese population.
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              Pathogenesis of Helicobacter pylori infection.

              Helicobacter pylori is the first formally recognized bacterial carcinogen and is one of the most successful human pathogens, as over half of the world's population is colonized with this gram-negative bacterium. Unless treated, colonization usually persists lifelong. H. pylori infection represents a key factor in the etiology of various gastrointestinal diseases, ranging from chronic active gastritis without clinical symptoms to peptic ulceration, gastric adenocarcinoma, and gastric mucosa-associated lymphoid tissue lymphoma. Disease outcome is the result of the complex interplay between the host and the bacterium. Host immune gene polymorphisms and gastric acid secretion largely determine the bacterium's ability to colonize a specific gastric niche. Bacterial virulence factors such as the cytotoxin-associated gene pathogenicity island-encoded protein CagA and the vacuolating cytotoxin VacA aid in this colonization of the gastric mucosa and subsequently seem to modulate the host's immune system. This review focuses on the microbiological, clinical, immunological, and biochemical aspects of the pathogenesis of H. pylori.
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                Author and article information

                Journal
                Int J Epidemiol
                Int J Epidemiol
                ije
                International Journal of Epidemiology
                Oxford University Press
                0300-5771
                1464-3685
                February 2021
                23 January 2021
                23 January 2021
                : 50
                : 1
                : 199-211
                Affiliations
                [1 ] Clinical Trial Service Unit and Epidemiological Studies Unit (CTSU), Nuffield Department of Population Health, University of Oxford , Oxford, UK
                [2 ] Medical Research Council Population Health Research Unit, Nuffield Department of Population Health, University of Oxford, Oxford, UK
                [3 ] Chinese Academy of Medical Sciences , Beijing, China
                [4 ] NCDs Prevention and Control Department, Huixian Center for Disease Control and Prevention , Henan, China
                [5 ] Department of Epidemiology and Biostatistics, School of Public Health, Peking University , Beijing, China
                Author notes

                Ling Yang and Zhengming Chen Joint senior authors

                Members of the China Kadoorie Biobank (CKB) Collaborative Group are listed at the end of the article.

                Corresponding author. Nuffield Department of Population Health, Big Data Institute, Old Road Campus, University of Oxford, Oxford, OX3 7FZ, UK. E-mail: ling.yang@ 123456ndph.ox.ac.uk
                Author information
                http://orcid.org/0000-0002-9814-0049
                http://orcid.org/0000-0001-5750-6588
                Article
                dyaa275
                10.1093/ije/dyaa275
                7938514
                33484129
                895ec830-08a4-4ad3-aa7e-5c459059be39
                © The Author(s) 2021. Published by Oxford University Press on behalf of the International Epidemiological Association.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 02 March 2020
                : 12 November 2020
                : 26 November 2020
                : 14 December 2020
                Page count
                Pages: 13
                Funding
                Funded by: Kadoorie Charitable Foundation in Hong Kong for the baseline and first resurvey;
                Funded by: UK Wellcome Trust;
                Award ID: 088158/Z/09/Z
                Award ID: 104085/Z/14/Z
                Funded by: Chinese Ministry of Science and Technology, DOI 10.13039/501100002855;
                Award ID: 2011BAI09B01
                Award ID: 2012–14
                Funded by: Chinese National Natural Science Foundation;
                Award ID: 81390540
                Award ID: 81390541
                Award ID: 81390544
                Funded by: National Key Research and Development Program of China, DOI 10.13039/501100012166;
                Award ID: 2016YFC0900500
                Award ID: 2016YFC0900501
                Award ID: 2016YFC0900504
                Award ID: 2016YFC1303904
                Funded by: The British Heart Foundation;
                Funded by: Medical Research Council and Cancer Research UK;
                Categories
                Effects of Diet
                AcademicSubjects/MED00860

                Public health
                spicy food,chilli peppers,gastrointestinal cancers,digestive cancers,prospective cohort studies

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