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Dietary glycemic index and glycemic load and breast cancer risk in the European Prospective Investigation into Cancer and Nutrition (EPIC)123
Background: The glycemic potential of a diet is associated with chronically elevated insulin concentrations, which may augment breast cancer (BC) risk by stimulating insulin receptor or by affecting insulin-like growth factor I (IGF-I)–mediated mitogenesis. It is unclear whether this effect differs...
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Published in: | The American journal of clinical nutrition 2012-08, Vol.96 (2), p.345-355 |
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creator | Romieu, Isabelle Ferrari, Pietro Rinaldi, Sabina Slimani, Nadia Jenab, Mazda Olsen, Anja Tjonneland, Anne Overvad, Kim Boutron-Ruault, Marie-Christine Lajous, Martin Kaaks, Rudolf Teucher, Birgit Boeing, Heiner Trichopoulou, Antonia Naska, Androniki Vasilopoulo, Effie Sacerdote, Carlotta Tumino, Rosario Masala, Giovanna Sieri, Sabina Panico, Salvatore Bueno-de-Mesquita, H Bas Van-der-A, Daphne van Gils, Carla H Peeters, Petra HM Lund, Eiliv Skeie, Guri Asli, Lene Angell Rodriguez, Laudina Navarro, Carmen Amiano, Pilar Sanchez, Maria-José Barricarte, Aurelio Buckland, Genevieve Sonestedt, Emily Wirfält, Elisabet Hallmans, Göran Johansson, Ingegerd Key, Timothy J Allen, Naomi E Khaw, Kay-Tee Wareham, Nicholas J Norat, Teresa Riboli, Elio Clavel-Chapelon, Françoise |
description | Background: The glycemic potential of a diet is associated with chronically elevated insulin concentrations, which may augment breast cancer (BC) risk by stimulating insulin receptor or by affecting insulin-like growth factor I (IGF-I)–mediated mitogenesis. It is unclear whether this effect differs by BC phenotype.
Objective: The objective was to investigate the relation between glycemic index (GI), glycemic load (GL), and total carbohydrate intake with BC by using data from the European Prospective Investigation into Cancer and Nutrition (EPIC).
Design: We identified 11,576 women with invasive BC among 334,849 EPIC women aged 34–66 y (5th to 95th percentiles) at baseline over a median follow-up of 11.5 y. Dietary GI and GL were calculated from country-specific dietary questionnaires. We used multivariable Cox proportional hazards models to quantify the association between GI, GL, and carbohydrate intake and BC risk. BC tumors were classified by receptor status.
Results: Overall GI, GL, and carbohydrates were not related to BC. Among postmenopausal women, GL and carbohydate intake were significantly associated with an increased risk of estrogen receptor–negative (ER−) BC when extreme quintiles (Q) were compared [multivariable HRQ5–Q1 (95% CI) = 1.36 (1.02, 1.82; P-trend = 0.010) and HRQ5–Q1 = 1.41 (1.05, 1.89; P-trend = 0.009), respectively]. Further stratification by progesterone receptor (PR) status showed slightly stronger associations with ER−/PR− BC [HRQ5–Q1 (95% CI) = 1.48 (1.07, 2.05; P-trend = 0.010) for GL and HRQ5–Q1 = 1.62 (1.15, 2.30; P-trend = 0.005) for carbohydrates]. No significant association with ER-positive BC was observed.
Conclusion: Our results indicate that a diet with a high GL and carbohydrate intake is positively associated with an increased risk of developing ER− and ER−/PR− BC among postmenopausal women. |
doi_str_mv | 10.3945/ajcn.111.026724 |
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Objective: The objective was to investigate the relation between glycemic index (GI), glycemic load (GL), and total carbohydrate intake with BC by using data from the European Prospective Investigation into Cancer and Nutrition (EPIC).
Design: We identified 11,576 women with invasive BC among 334,849 EPIC women aged 34–66 y (5th to 95th percentiles) at baseline over a median follow-up of 11.5 y. Dietary GI and GL were calculated from country-specific dietary questionnaires. We used multivariable Cox proportional hazards models to quantify the association between GI, GL, and carbohydrate intake and BC risk. BC tumors were classified by receptor status.
Results: Overall GI, GL, and carbohydrates were not related to BC. Among postmenopausal women, GL and carbohydate intake were significantly associated with an increased risk of estrogen receptor–negative (ER−) BC when extreme quintiles (Q) were compared [multivariable HRQ5–Q1 (95% CI) = 1.36 (1.02, 1.82; P-trend = 0.010) and HRQ5–Q1 = 1.41 (1.05, 1.89; P-trend = 0.009), respectively]. Further stratification by progesterone receptor (PR) status showed slightly stronger associations with ER−/PR− BC [HRQ5–Q1 (95% CI) = 1.48 (1.07, 2.05; P-trend = 0.010) for GL and HRQ5–Q1 = 1.62 (1.15, 2.30; P-trend = 0.005) for carbohydrates]. No significant association with ER-positive BC was observed.
Conclusion: Our results indicate that a diet with a high GL and carbohydrate intake is positively associated with an increased risk of developing ER− and ER−/PR− BC among postmenopausal women.</description><identifier>ISSN: 0002-9165</identifier><identifier>EISSN: 1938-3207</identifier><identifier>DOI: 10.3945/ajcn.111.026724</identifier><language>eng</language><publisher>Elsevier Inc</publisher><ispartof>The American journal of clinical nutrition, 2012-08, Vol.96 (2), p.345-355</ispartof><rights>2012 American Society for Nutrition.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S000291652302885X$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,3549,27924,27925,45780</link.rule.ids></links><search><creatorcontrib>Romieu, Isabelle</creatorcontrib><creatorcontrib>Ferrari, Pietro</creatorcontrib><creatorcontrib>Rinaldi, Sabina</creatorcontrib><creatorcontrib>Slimani, Nadia</creatorcontrib><creatorcontrib>Jenab, Mazda</creatorcontrib><creatorcontrib>Olsen, Anja</creatorcontrib><creatorcontrib>Tjonneland, Anne</creatorcontrib><creatorcontrib>Overvad, Kim</creatorcontrib><creatorcontrib>Boutron-Ruault, Marie-Christine</creatorcontrib><creatorcontrib>Lajous, Martin</creatorcontrib><creatorcontrib>Kaaks, Rudolf</creatorcontrib><creatorcontrib>Teucher, Birgit</creatorcontrib><creatorcontrib>Boeing, Heiner</creatorcontrib><creatorcontrib>Trichopoulou, Antonia</creatorcontrib><creatorcontrib>Naska, Androniki</creatorcontrib><creatorcontrib>Vasilopoulo, Effie</creatorcontrib><creatorcontrib>Sacerdote, Carlotta</creatorcontrib><creatorcontrib>Tumino, Rosario</creatorcontrib><creatorcontrib>Masala, Giovanna</creatorcontrib><creatorcontrib>Sieri, Sabina</creatorcontrib><creatorcontrib>Panico, Salvatore</creatorcontrib><creatorcontrib>Bueno-de-Mesquita, H Bas</creatorcontrib><creatorcontrib>Van-der-A, Daphne</creatorcontrib><creatorcontrib>van Gils, Carla H</creatorcontrib><creatorcontrib>Peeters, Petra HM</creatorcontrib><creatorcontrib>Lund, Eiliv</creatorcontrib><creatorcontrib>Skeie, Guri</creatorcontrib><creatorcontrib>Asli, Lene Angell</creatorcontrib><creatorcontrib>Rodriguez, Laudina</creatorcontrib><creatorcontrib>Navarro, Carmen</creatorcontrib><creatorcontrib>Amiano, Pilar</creatorcontrib><creatorcontrib>Sanchez, Maria-José</creatorcontrib><creatorcontrib>Barricarte, Aurelio</creatorcontrib><creatorcontrib>Buckland, Genevieve</creatorcontrib><creatorcontrib>Sonestedt, Emily</creatorcontrib><creatorcontrib>Wirfält, Elisabet</creatorcontrib><creatorcontrib>Hallmans, Göran</creatorcontrib><creatorcontrib>Johansson, Ingegerd</creatorcontrib><creatorcontrib>Key, Timothy J</creatorcontrib><creatorcontrib>Allen, Naomi E</creatorcontrib><creatorcontrib>Khaw, Kay-Tee</creatorcontrib><creatorcontrib>Wareham, Nicholas J</creatorcontrib><creatorcontrib>Norat, Teresa</creatorcontrib><creatorcontrib>Riboli, Elio</creatorcontrib><creatorcontrib>Clavel-Chapelon, Françoise</creatorcontrib><title>Dietary glycemic index and glycemic load and breast cancer risk in the European Prospective Investigation into Cancer and Nutrition (EPIC)123</title><title>The American journal of clinical nutrition</title><description>Background: The glycemic potential of a diet is associated with chronically elevated insulin concentrations, which may augment breast cancer (BC) risk by stimulating insulin receptor or by affecting insulin-like growth factor I (IGF-I)–mediated mitogenesis. It is unclear whether this effect differs by BC phenotype.
Objective: The objective was to investigate the relation between glycemic index (GI), glycemic load (GL), and total carbohydrate intake with BC by using data from the European Prospective Investigation into Cancer and Nutrition (EPIC).
Design: We identified 11,576 women with invasive BC among 334,849 EPIC women aged 34–66 y (5th to 95th percentiles) at baseline over a median follow-up of 11.5 y. Dietary GI and GL were calculated from country-specific dietary questionnaires. We used multivariable Cox proportional hazards models to quantify the association between GI, GL, and carbohydrate intake and BC risk. BC tumors were classified by receptor status.
Results: Overall GI, GL, and carbohydrates were not related to BC. Among postmenopausal women, GL and carbohydate intake were significantly associated with an increased risk of estrogen receptor–negative (ER−) BC when extreme quintiles (Q) were compared [multivariable HRQ5–Q1 (95% CI) = 1.36 (1.02, 1.82; P-trend = 0.010) and HRQ5–Q1 = 1.41 (1.05, 1.89; P-trend = 0.009), respectively]. Further stratification by progesterone receptor (PR) status showed slightly stronger associations with ER−/PR− BC [HRQ5–Q1 (95% CI) = 1.48 (1.07, 2.05; P-trend = 0.010) for GL and HRQ5–Q1 = 1.62 (1.15, 2.30; P-trend = 0.005) for carbohydrates]. No significant association with ER-positive BC was observed.
Conclusion: Our results indicate that a diet with a high GL and carbohydrate intake is positively associated with an increased risk of developing ER− and ER−/PR− BC among postmenopausal women.</description><issn>0002-9165</issn><issn>1938-3207</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNqlj81OwzAQhC0EEuHnzNVHOCT4J02bcwiiF9QDd8vYS9kS7Mp2I_oQvDNOi8QDcFrt7MysPkJuOKtkW8_u9ca4inNeMdHMRX1CCt7KRSkFm5-SgjEmypY3s3NyEeOGMS7qRVOQ7weEpMOeroe9gU80FJ2FL6qd_ZMGr-1BeQ2gY6JGOwOBBowf2U7TO9B-F_wWtKOr4OMWTMIR6NKNEBOudULvsjN52h2jU9nzLgU8XG771bK740JekbM3PUS4_p2XpH3sX7qnEvIyIgQVDUJusBjyD2U9Ks7UxK8mfpX51ZFf_if7A-Zrafk</recordid><startdate>201208</startdate><enddate>201208</enddate><creator>Romieu, Isabelle</creator><creator>Ferrari, Pietro</creator><creator>Rinaldi, Sabina</creator><creator>Slimani, Nadia</creator><creator>Jenab, Mazda</creator><creator>Olsen, Anja</creator><creator>Tjonneland, 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Teresa</creatorcontrib><creatorcontrib>Riboli, Elio</creatorcontrib><creatorcontrib>Clavel-Chapelon, Françoise</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><jtitle>The American journal of clinical nutrition</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Romieu, Isabelle</au><au>Ferrari, Pietro</au><au>Rinaldi, Sabina</au><au>Slimani, Nadia</au><au>Jenab, Mazda</au><au>Olsen, Anja</au><au>Tjonneland, Anne</au><au>Overvad, Kim</au><au>Boutron-Ruault, Marie-Christine</au><au>Lajous, Martin</au><au>Kaaks, Rudolf</au><au>Teucher, Birgit</au><au>Boeing, Heiner</au><au>Trichopoulou, Antonia</au><au>Naska, Androniki</au><au>Vasilopoulo, Effie</au><au>Sacerdote, Carlotta</au><au>Tumino, Rosario</au><au>Masala, Giovanna</au><au>Sieri, Sabina</au><au>Panico, Salvatore</au><au>Bueno-de-Mesquita, H Bas</au><au>Van-der-A, Daphne</au><au>van Gils, Carla H</au><au>Peeters, Petra HM</au><au>Lund, Eiliv</au><au>Skeie, Guri</au><au>Asli, Lene Angell</au><au>Rodriguez, Laudina</au><au>Navarro, Carmen</au><au>Amiano, Pilar</au><au>Sanchez, Maria-José</au><au>Barricarte, Aurelio</au><au>Buckland, Genevieve</au><au>Sonestedt, Emily</au><au>Wirfält, Elisabet</au><au>Hallmans, Göran</au><au>Johansson, Ingegerd</au><au>Key, Timothy J</au><au>Allen, Naomi E</au><au>Khaw, Kay-Tee</au><au>Wareham, Nicholas J</au><au>Norat, Teresa</au><au>Riboli, Elio</au><au>Clavel-Chapelon, Françoise</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dietary glycemic index and glycemic load and breast cancer risk in the European Prospective Investigation into Cancer and Nutrition (EPIC)123</atitle><jtitle>The American journal of clinical nutrition</jtitle><date>2012-08</date><risdate>2012</risdate><volume>96</volume><issue>2</issue><spage>345</spage><epage>355</epage><pages>345-355</pages><issn>0002-9165</issn><eissn>1938-3207</eissn><abstract>Background: The glycemic potential of a diet is associated with chronically elevated insulin concentrations, which may augment breast cancer (BC) risk by stimulating insulin receptor or by affecting insulin-like growth factor I (IGF-I)–mediated mitogenesis. It is unclear whether this effect differs by BC phenotype.
Objective: The objective was to investigate the relation between glycemic index (GI), glycemic load (GL), and total carbohydrate intake with BC by using data from the European Prospective Investigation into Cancer and Nutrition (EPIC).
Design: We identified 11,576 women with invasive BC among 334,849 EPIC women aged 34–66 y (5th to 95th percentiles) at baseline over a median follow-up of 11.5 y. Dietary GI and GL were calculated from country-specific dietary questionnaires. We used multivariable Cox proportional hazards models to quantify the association between GI, GL, and carbohydrate intake and BC risk. BC tumors were classified by receptor status.
Results: Overall GI, GL, and carbohydrates were not related to BC. Among postmenopausal women, GL and carbohydate intake were significantly associated with an increased risk of estrogen receptor–negative (ER−) BC when extreme quintiles (Q) were compared [multivariable HRQ5–Q1 (95% CI) = 1.36 (1.02, 1.82; P-trend = 0.010) and HRQ5–Q1 = 1.41 (1.05, 1.89; P-trend = 0.009), respectively]. Further stratification by progesterone receptor (PR) status showed slightly stronger associations with ER−/PR− BC [HRQ5–Q1 (95% CI) = 1.48 (1.07, 2.05; P-trend = 0.010) for GL and HRQ5–Q1 = 1.62 (1.15, 2.30; P-trend = 0.005) for carbohydrates]. No significant association with ER-positive BC was observed.
Conclusion: Our results indicate that a diet with a high GL and carbohydrate intake is positively associated with an increased risk of developing ER− and ER−/PR− BC among postmenopausal women.</abstract><pub>Elsevier Inc</pub><doi>10.3945/ajcn.111.026724</doi><oa>free_for_read</oa></addata></record> |
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source | ScienceDirect |
title | Dietary glycemic index and glycemic load and breast cancer risk in the European Prospective Investigation into Cancer and Nutrition (EPIC)123 |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-27T16%3A57%3A20IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-elsevier&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Dietary%20glycemic%20index%20and%20glycemic%20load%20and%20breast%20cancer%20risk%20in%20the%20European%20Prospective%20Investigation%20into%20Cancer%20and%20Nutrition%20(EPIC)123&rft.jtitle=The%20American%20journal%20of%20clinical%20nutrition&rft.au=Romieu,%20Isabelle&rft.date=2012-08&rft.volume=96&rft.issue=2&rft.spage=345&rft.epage=355&rft.pages=345-355&rft.issn=0002-9165&rft.eissn=1938-3207&rft_id=info:doi/10.3945/ajcn.111.026724&rft_dat=%3Celsevier%3ES000291652302885X%3C/elsevier%3E%3Cgrp_id%3Ecdi_FETCH-elsevier_sciencedirect_doi_10_3945_ajcn_111_0267243%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true |