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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
Main Authors: 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
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container_issue 2
container_start_page 345
container_title The American journal of clinical nutrition
container_volume 96
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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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><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. 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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. 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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
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