Coffee, tea and caffeine intake and the risk of non-melanoma skin cancer: a review of the literature and meta-analysis

Purpose Laboratory studies suggested that caffeine and other nutrients contained in coffee and tea may protect against non-melanoma skin cancer (NMSC). However, epidemiological studies conducted so far have produced conflicting results. Methods We performed a literature review and meta-analysis of o...

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Veröffentlicht in:European journal of nutrition 2017-02, Vol.56 (1), p.1-12
Hauptverfasser: Caini, Saverio, Cattaruzza, Sofia, Bendinelli, Benedetta, Tosti, Giulio, Masala, Giovanna, Gnagnarella, Patrizia, Assedi, Melania, Stanganelli, Ignazio, Palli, Domenico, Gandini, Sara
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container_issue 1
container_start_page 1
container_title European journal of nutrition
container_volume 56
creator Caini, Saverio
Cattaruzza, Sofia
Bendinelli, Benedetta
Tosti, Giulio
Masala, Giovanna
Gnagnarella, Patrizia
Assedi, Melania
Stanganelli, Ignazio
Palli, Domenico
Gandini, Sara
description Purpose Laboratory studies suggested that caffeine and other nutrients contained in coffee and tea may protect against non-melanoma skin cancer (NMSC). However, epidemiological studies conducted so far have produced conflicting results. Methods We performed a literature review and meta-analysis of observational studies published until February 2016 that investigated the association between coffee and tea intake and NMSC risk. We calculated summary relative risk (SRR) and corresponding 95 % confidence intervals (95 % CI) by using random effects with maximum likelihood estimation. Results Overall, 37,627 NMSC cases from 13 papers were available for analysis. Intake of caffeinated coffee was inversely associated with NMSC risk (SRR for those in the highest vs. lowest category of intake: 0.82, 95 % CI 0.75–0.89, I 2  = 48 %), as well as intake of caffeine (SRR 0.86, 95 % CI 0.80–0.91, I 2  = 48 %). In subgroup analysis, these associations were limited to the basal cell cancer (BCC) histotype. There was no association between intake of decaffeinated coffee (SRR 1.01, 95 % CI 0.85–1.21, I 2  = 0) and tea (0.88, 95 % CI 0.72–1.07, I 2  = 0 %) and NMSC risk. There was no evidence of publication bias affecting the results. The available evidence was not sufficient to draw conclusions on the association between green tea intake and NMSC risk. Conclusions Coffee intake appears to exert a moderate protective effect against BCC development, probably through the biological effect of caffeine. However, the observational nature of studies included, subject to bias and confounding, suggests taking with caution these results that should be verified in randomized clinical trials.
doi_str_mv 10.1007/s00394-016-1253-6
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However, epidemiological studies conducted so far have produced conflicting results. Methods We performed a literature review and meta-analysis of observational studies published until February 2016 that investigated the association between coffee and tea intake and NMSC risk. We calculated summary relative risk (SRR) and corresponding 95 % confidence intervals (95 % CI) by using random effects with maximum likelihood estimation. Results Overall, 37,627 NMSC cases from 13 papers were available for analysis. Intake of caffeinated coffee was inversely associated with NMSC risk (SRR for those in the highest vs. lowest category of intake: 0.82, 95 % CI 0.75–0.89, I 2  = 48 %), as well as intake of caffeine (SRR 0.86, 95 % CI 0.80–0.91, I 2  = 48 %). In subgroup analysis, these associations were limited to the basal cell cancer (BCC) histotype. There was no association between intake of decaffeinated coffee (SRR 1.01, 95 % CI 0.85–1.21, I 2  = 0) and tea (0.88, 95 % CI 0.72–1.07, I 2  = 0 %) and NMSC risk. There was no evidence of publication bias affecting the results. The available evidence was not sufficient to draw conclusions on the association between green tea intake and NMSC risk. Conclusions Coffee intake appears to exert a moderate protective effect against BCC development, probably through the biological effect of caffeine. However, the observational nature of studies included, subject to bias and confounding, suggests taking with caution these results that should be verified in randomized clinical trials.</description><identifier>ISSN: 1436-6207</identifier><identifier>EISSN: 1436-6215</identifier><identifier>EISSN: 1435-1293</identifier><identifier>DOI: 10.1007/s00394-016-1253-6</identifier><identifier>PMID: 27388462</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Caffeine - administration &amp; dosage ; Carcinoma, Basal Cell - epidemiology ; Chemistry ; Chemistry and Materials Science ; Coffee - chemistry ; Humans ; Nutrition ; Observational Studies as Topic ; Review ; Risk Factors ; Skin Neoplasms - epidemiology ; Tea - chemistry</subject><ispartof>European journal of nutrition, 2017-02, Vol.56 (1), p.1-12</ispartof><rights>Springer-Verlag Berlin Heidelberg 2016</rights><rights>European Journal of Nutrition is a copyright of Springer, 2017.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c471t-29da76ac2837ff318cc0e002d94d8b357503cbcac1cd5688f33ebae4122990463</citedby><cites>FETCH-LOGICAL-c471t-29da76ac2837ff318cc0e002d94d8b357503cbcac1cd5688f33ebae4122990463</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00394-016-1253-6$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00394-016-1253-6$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>313,314,780,784,792,27922,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27388462$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Caini, Saverio</creatorcontrib><creatorcontrib>Cattaruzza, Sofia</creatorcontrib><creatorcontrib>Bendinelli, Benedetta</creatorcontrib><creatorcontrib>Tosti, Giulio</creatorcontrib><creatorcontrib>Masala, Giovanna</creatorcontrib><creatorcontrib>Gnagnarella, Patrizia</creatorcontrib><creatorcontrib>Assedi, Melania</creatorcontrib><creatorcontrib>Stanganelli, Ignazio</creatorcontrib><creatorcontrib>Palli, Domenico</creatorcontrib><creatorcontrib>Gandini, Sara</creatorcontrib><title>Coffee, tea and caffeine intake and the risk of non-melanoma skin cancer: a review of the literature and meta-analysis</title><title>European journal of nutrition</title><addtitle>Eur J Nutr</addtitle><addtitle>Eur J Nutr</addtitle><description>Purpose Laboratory studies suggested that caffeine and other nutrients contained in coffee and tea may protect against non-melanoma skin cancer (NMSC). However, epidemiological studies conducted so far have produced conflicting results. Methods We performed a literature review and meta-analysis of observational studies published until February 2016 that investigated the association between coffee and tea intake and NMSC risk. We calculated summary relative risk (SRR) and corresponding 95 % confidence intervals (95 % CI) by using random effects with maximum likelihood estimation. Results Overall, 37,627 NMSC cases from 13 papers were available for analysis. Intake of caffeinated coffee was inversely associated with NMSC risk (SRR for those in the highest vs. lowest category of intake: 0.82, 95 % CI 0.75–0.89, I 2  = 48 %), as well as intake of caffeine (SRR 0.86, 95 % CI 0.80–0.91, I 2  = 48 %). In subgroup analysis, these associations were limited to the basal cell cancer (BCC) histotype. There was no association between intake of decaffeinated coffee (SRR 1.01, 95 % CI 0.85–1.21, I 2  = 0) and tea (0.88, 95 % CI 0.72–1.07, I 2  = 0 %) and NMSC risk. There was no evidence of publication bias affecting the results. The available evidence was not sufficient to draw conclusions on the association between green tea intake and NMSC risk. Conclusions Coffee intake appears to exert a moderate protective effect against BCC development, probably through the biological effect of caffeine. 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However, epidemiological studies conducted so far have produced conflicting results. Methods We performed a literature review and meta-analysis of observational studies published until February 2016 that investigated the association between coffee and tea intake and NMSC risk. We calculated summary relative risk (SRR) and corresponding 95 % confidence intervals (95 % CI) by using random effects with maximum likelihood estimation. Results Overall, 37,627 NMSC cases from 13 papers were available for analysis. Intake of caffeinated coffee was inversely associated with NMSC risk (SRR for those in the highest vs. lowest category of intake: 0.82, 95 % CI 0.75–0.89, I 2  = 48 %), as well as intake of caffeine (SRR 0.86, 95 % CI 0.80–0.91, I 2  = 48 %). In subgroup analysis, these associations were limited to the basal cell cancer (BCC) histotype. There was no association between intake of decaffeinated coffee (SRR 1.01, 95 % CI 0.85–1.21, I 2  = 0) and tea (0.88, 95 % CI 0.72–1.07, I 2  = 0 %) and NMSC risk. There was no evidence of publication bias affecting the results. The available evidence was not sufficient to draw conclusions on the association between green tea intake and NMSC risk. Conclusions Coffee intake appears to exert a moderate protective effect against BCC development, probably through the biological effect of caffeine. However, the observational nature of studies included, subject to bias and confounding, suggests taking with caution these results that should be verified in randomized clinical trials.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>27388462</pmid><doi>10.1007/s00394-016-1253-6</doi><tpages>12</tpages></addata></record>
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subjects Caffeine - administration & dosage
Carcinoma, Basal Cell - epidemiology
Chemistry
Chemistry and Materials Science
Coffee - chemistry
Humans
Nutrition
Observational Studies as Topic
Review
Risk Factors
Skin Neoplasms - epidemiology
Tea - chemistry
title Coffee, tea and caffeine intake and the risk of non-melanoma skin cancer: a review of the literature and meta-analysis
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