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Featured researches published by Petra H. Peeters.


Nature Genetics | 2010

A genome-wide association study identifies pancreatic cancer susceptibility loci on chromosomes 13q22.1, 1q32.1 and 5p15.33

Gloria M. Petersen; Laufey Amundadottir; Charles S. Fuchs; Peter Kraft; Rachael Z. Stolzenberg-Solomon; Kevin B. Jacobs; Alan A. Arslan; H. Bas Bueno-de-Mesquita; Steven Gallinger; Myron D. Gross; Kathy J. Helzlsouer; Elizabeth A. Holly; Eric J. Jacobs; Alison P. Klein; Andrea Z. LaCroix; Donghui Li; Margaret T. Mandelson; Sara H. Olson; Harvey A. Risch; Wei Zheng; Demetrius Albanes; William R. Bamlet; Christine D. Berg; Marie-Christine Boutron-Ruault; Julie E. Buring; Paige M. Bracci; Federico Canzian; Sandra Clipp; Michelle Cotterchio; Mariza de Andrade

We conducted a genome-wide association study of pancreatic cancer in 3,851 affected individuals (cases) and 3,934 unaffected controls drawn from 12 prospective cohort studies and 8 case-control studies. Based on a logistic regression model for genotype trend effect that was adjusted for study, age, sex, self-described ancestry and five principal components, we identified eight SNPs that map to three loci on chromosomes 13q22.1, 1q32.1 and 5p15.33. Two correlated SNPs, rs9543325 (P = 3.27 × 10−11, per-allele odds ratio (OR) 1.26, 95% CI 1.18–1.35) and rs9564966 (P = 5.86 × 10−8, per-allele OR 1.21, 95% CI 1.13–1.30), map to a nongenic region on chromosome 13q22.1. Five SNPs on 1q32.1 map to NR5A2, and the strongest signal was at rs3790844 (P = 2.45 × 10−10, per-allele OR 0.77, 95% CI 0.71–0.84). A single SNP, rs401681 (P = 3.66 × 10−7, per-allele OR 1.19, 95% CI 1.11–1.27), maps to the CLPTM1L-TERT locus on 5p15.33, which is associated with multiple cancers. Our study has identified common susceptibility loci for pancreatic cancer that warrant follow-up studies.


BMJ | 2010

Association between Pre-Diagnostic Circulating Vitamin D Concentration and Risk of Colorectal Cancer in European Populations: a Nested Case-Control Study

Mazda Jenab; H. Bas Bueno-de-Mesquita; Pietro Ferrari; Fränzel J.B. Van Duijnhoven; Teresa Norat; Tobias Pischon; Eugene Jansen; Nadia Slimani; Graham Byrnes; Sabina Rinaldi; Anne Tjønneland; Anja Olsen; Kim Overvad; Marie Christine Boutron-Ruault; Françoise Clavel-Chapelon; Sophie Morois; Rudolf Kaaks; Jakob Linseisen; Heiner Boeing; M. Bergmann; Antonia Trichopoulou; Gesthimani Misirli; Dimitrios Trichopoulos; Franco Berrino; Paolo Vineis; Salvatore Panico; Domenico Palli; Rosario Tumino; Martine M. Ros; Carla H. van Gils

Objective To examine the association between pre-diagnostic circulating vitamin D concentration, dietary intake of vitamin D and calcium, and the risk of colorectal cancer in European populations. Design Nested case-control study. Setting The study was conducted within the EPIC study, a cohort of more than 520u2009000 participants from 10 western European countries. Participants 1248 cases of incident colorectal cancer, which developed after enrolment into the cohort, were matched to 1248 controls Main outcome measures Circulating vitamin D concentration (25-hydroxy-vitamin-D, 25-(OH)D) was measured by enzyme immunoassay. Dietary and lifestyle data were obtained from questionnaires. Incidence rate ratios and 95% confidence intervals for the risk of colorectal cancer by 25-(OH)D concentration and levels of dietary calcium and vitamin D intake were estimated from multivariate conditional logistic regression models, with adjustment for potential dietary and other confounders. Results 25-(OH)D concentration showed a strong inverse linear dose-response association with risk of colorectal cancer (P for trend <0.001). Compared with a pre-defined mid-level concentration of 25-(OH)D (50.0-75.0 nmol/l), lower levels were associated with higher colorectal cancer risk (<25.0 nmol/l: incidence rate ratio 1.32 (95% confidence interval 0.87 to 2.01); 25.0-49.9 nmol/l: 1.28 (1.05 to 1.56), and higher concentrations associated with lower risk (75.0-99.9 nmol/l: 0.88 (0.68 to 1.13); ≥100.0 nmol/l: 0.77 (0.56 to 1.06)). In analyses by quintile of 25-(OH)D concentration, patients in the highest quintile had a 40% lower risk of colorectal cancer than did those in the lowest quintile (P<0.001). Subgroup analyses showed a strong association for colon but not rectal cancer (P for heterogeneity=0.048). Greater dietary intake of calcium was associated with a lower colorectal cancer risk. Dietary vitamin D was not associated with disease risk. Findings did not vary by sex and were not altered by corrections for season or month of blood donation. Conclusions The results of this large observational study indicate a strong inverse association between levels of pre-diagnostic 25-(OH)D concentration and risk of colorectal cancer in western European populations. Further randomised trials are needed to assess whether increases in circulating 25-(OH)D concentration can effectively decrease the risk of colorectal cancer.


Cancer Epidemiology, Biomarkers & Prevention | 2012

Prediagnostic 25-Hydroxyvitamin D, VDR and CASR Polymorphisms, and Survival in Patients with Colorectal Cancer in Western European Populations

Veronika Fedirko; Elio Riboli; Anne Tjønneland; Pietro Ferrari; Anja Olsen; H. Bas Bueno-de-Mesquita; Fränzel J.B. Van Duijnhoven; Teresa Norat; Eugene Jansen; Christina C. Dahm; Kim Overvad; Marie Christine Boutron-Ruault; Françoise Clavel-Chapelon; Antoine Racine; Annekatrin Lukanova; Birgit Teucher; Heiner Boeing; Krasimira Aleksandrova; Antonia Trichopoulou; Vassiliki Benetou; Dimitrios Trichopoulos; Sara Grioni; Paolo Vineis; Salvatore Panico; Domenico Palli; Rosario Tumino; Peter D. Siersema; Petra H. Peeters; Guri Skeie; Magritt Brustad

Background: Individuals with higher blood 25-hydroxyvitamin D [25(OH)D] levels have a lower risk of developing colorectal cancer (CRC), but the influence of 25(OH)D on mortality after CRC diagnosis is unknown. Methods: The association between prediagnostic 25(OH)D levels and CRC-specific (N = 444) and overall mortality (N = 541) was prospectively examined among 1,202 participants diagnosed with CRC between 1992 and 2003 in the European Prospective Investigation into Cancer and Nutrition (EPIC) cohort. Multivariable Cox proportional hazards models were used to calculate HRs and corresponding 95% CIs according to 25(OH)D quintiles and genetic variation within the VDR and CASR genes. Potential dietary, lifestyle, and metabolic effect modifiers were also investigated. Results: There were 541 deaths, 444 (82%) due to CRC. Mean follow-up was 73 months. In multivariable analysis, higher 25(OH)D levels were associated with a statistically significant reduction in CRC-specific (Ptrend = 0.04) and overall mortality (Ptrend = 0.01). Participants with 25(OH)D levels in the highest quintile had an adjusted HR of 0.69 (95% CI: 0.50–0.93) for CRC-specific mortality and 0.67 (95% CI: 0.50–0.88) for overall mortality, compared with the lowest quintile. Except for a possible interaction by prediagnostic dietary calcium intake (Pinteraction = 0.01), no other potential modifying factors related to CRC survival were noted. The VDR (FokI and BsmI) and CASR (rs1801725) genotypes were not associated with survival. Conclusions: High prediagnostic 25(OH)D levels are associated with improved survival of patients with CRC. Impact: Our findings may stimulate further research directed at investigating the effects of blood vitamin D levels before, at, and after CRC diagnosis on outcomes in CRC patients. Cancer Epidemiol Biomarkers Prev; 21(4); 582–93. ©2012 AACR.


European Journal of Epidemiology | 2007

Modified Mediterranean diet and survival after myocardial infarction: the EPIC-Elderly study

Antonia Trichopoulou; Christina Bamia; Teresa Norat; Kim Overvad; Erik Berg Schmidt; Anne Tjønneland; Jytte Halkjær; F. Clavel-Chapelon; M. N. Vercambre; M. C. Boutron-Ruault; J. Linseisen; Sabine Rohrmann; Heiner Boeing; Cornelia Weikert; Vassiliki Benetou; Theodora Psaltopoulou; Philippos Orfanos; Paolo Boffetta; Giovanna Masala; Valeria Pala; Salvatore Panico; R. Tumino; Carlotta Sacerdote; H. B. Bueno-de-Mesquita; Marga C. Ocké; Petra H. Peeters; Y. T. van der Schouw; Clementina González; M. J. Sánchez; M. D. Chirlaque

Mediterranean diet is associated with lower incidence of coronary heart disease, and two randomised trials indicated that it improves prognosis of coronary patients. These trials, however, relied on a total of 100 deaths and evaluated designer diets in the clinical context. We have evaluated the association of adherence to the modified Mediterranean diet, in which unsaturates were substituted for monounsaturates, with survival among elderly with previous myocardial infarction within the European Prospective Investigation into Cancer and nutrition (EPIC) study. As of December 2003, after a median follow-up of 6.7xa0years, 2671 EPIC participants from nine countries were 60xa0years or older and had prevalent myocardial infarction but no stroke or cancer at enrolment, complete information on dietary intakes and important covariates and known survival status. Adherence to the modified Mediterranean diet was assessed through a 10-unit-scale. Mortality ratio in relation to modified Mediterranean diet was estimated through Cox regression controlling for possible confounding. Increased adherence to modified Mediterranean diet by two units was associated with 18% lower overall mortality rate (95% confidence interval 7–27%, fixed effects model). There was no significant heterogeneity by sex, age at enrolment, or country, although the association tended to be less evident among northern Europeans. Associations between food groups contributing to the modified Mediterranean diet and mortality were generally weak. A diet inspired by the Mediterranean pattern that can be easily adopted by Western populations is associated with substantial reduction of total mortality of coronary patients in the community.


American Journal of Epidemiology | 2013

Hormonal, Metabolic, and Inflammatory Profiles and Endometrial Cancer Risk Within the EPIC Cohort—A Factor Analysis

Laure Dossus; Annekatrin Lukanova; Sabina Rinaldi; Naomi E. Allen; Anne E. Cust; Susen Becker; Anne Tjønneland; Louise Hansen; Kim Overvad; Nathalie Chabbert-Buffet; Sylvie Mesrine; Françoise Clavel-Chapelon; Birgit Teucher; Jenny Chang-Claude; Heiner Boeing; Dagmar Drogan; Antonia Trichopoulou; Vasiliki Benetou; Christina Bamia; Domenico Palli; Claudia Agnoli; Rocco Galasso; Rosario Tumino; C. Sacerdote; H. Bas Bueno-de-Mesquita; Fränzel J.B. Van Duijnhoven; Petra H. Peeters; N. Charlotte Onland-Moret; Maria Luisa Redondo; Noémie Travier

A Western lifestyle characterized by physical inactivity and excess weight is associated with a number of metabolic and hormonal dysregulations, including increased circulating estrogen levels, hyperinsulinemia, hyperglycemia, and chronic inflammation. The same hormonal and metabolic axes might mediate the association between this lifestyle and the development of endometrial cancer. Using data collected within the European Prospective Investigation into Cancer and Nutrition (EPIC), a prospective cohort study carried out in 10 European countries during 1992-2000, we conducted a factor analysis to delineate important components that summarize the variation explained by a set of biomarkers and to examine their association with endometrial cancer risk. Prediagnostic levels of testosterone, androstenedione, dehydroepiandrosterone sulfate, sex hormone-binding globulin, estrone, estradiol, C-peptide, insulin-like growth factor-binding proteins 1 and 2, adiponectin, high- and low-density lipoprotein cholesterol, glucose, triglycerides, tumor necrosis factor (TNF) α, soluble TNF receptors 1 and 2, C-reactive protein, interleukin-6, and interleukin-1 receptor antagonist were measured in 233 incident endometrial cancer cases and 446 matched controls. Factor analysis identified 3 components associated with postmenopausal endometrial cancer risk that could be labeled insulin resistance/metabolic syndrome, steroids, and inflammation factors. A fourth component, lipids, was not significantly associated with endometrial cancer. In conclusion, besides the well-known associations of risk with sex hormones and insulin-regulated physiological axes, our data further support the hypothesis that inflammation factors play a role in endometrial carcinogenesis.


Cancer Causes & Control | 2007

Fruit and vegetable consumption and lymphoma risk in the European Prospective Investigation into Cancer and Nutrition (EPIC)

Sabine Rohrmann; Nikolaus Becker; Jakob Linseisen; Alexandra Nieters; Thomas Rüdiger; Ole Raaschou-Nielsen; Anne Tjønneland; Hans Erik Johnsen; Kim Overvad; Rudolf Kaaks; Manuela M. Bergmann; Heiner Boeing; Vasiliki Benetou; Theodora Psaltopoulou; Antonia Trichopoulou; Giovanna Masala; Amalia Mattiello; Vittorio Krogh; Rosario Tumino; Carla H. van Gils; Petra H. Peeters; H. Bas Bueno-de-Mesquita; Martine M. Ros; Eiliv Lund; Eva Ardanaz; Maria Dolores Chirlaque; Paula Jakszyn; Nerea Larrañaga; Adamina Losada; Carmen Martinez-Garcia

IntroductionLymphomas are a heterogeneous group of malignant diseases of cells of the immune system. The best-established risk factors are related to dys-regulation of immune function, and evidence suggests that factors such as dietary or lifestyle habits may be involved in the etiology.Material and methodsIn the European Prospective Investigation into Cancer and Nutrition (EPIC), 849 lymphoma cases were identified in a median follow-up period of 6.4 years. Fruit and vegetable consumption was estimated from validated dietary questionnaires. Cox proportional hazard models were used to examine the association between fruit and vegetable intake with the risk of lymphomas overall and subentities.ResultsThere was no overall association between total fruit and vegetable consumption and risk of lymphoma [hazard ratio (HR) = 0.95, 95% confidence interval (CI) 0.78–1.15 comparing highest with lowest quartile]. However, the risk of diffuse large B-cell lymphomas (DLBCL) tended to be lower in participants with a high intake of total vegetables (HR = 0.49, 95% CI 0.23–1.02).ConclusionIn this large prospective study, an inverse associations between fruit and vegetable consumption and risk of lymphomas overall could not be confirmed. Associations with lymphoma subentities such as DLBCL warrant further investigation.


Journal of Clinical Oncology | 2015

Human Papillomavirus Antibodies and Future Risk of Anogenital Cancer: A Nested Case-Control Study in the European Prospective Investigation Into Cancer and Nutrition Study

Aimée R. Kreimer; Paul Brennan; Krystle A. Lang Kuhs; Tim Waterboer; Gary M. Clifford; Silvia Franceschi; Angelika Michel; Martina Willhauck-Fleckenstein; Elio Riboli; Xavier Castellsagué; Allan Hildesheim; Renée T. Fortner; Rudolf Kaaks; Domenico Palli; Salvatore Panico; Franc¸oise Clavel-Chapelon; Marie Christine Boutron-Ruault; Sylvie Mesrine; Antonia Trichopoulou; Pagona Lagiou; Dimitrios Trichopoulos; Petra H. Peeters; Amanda J. Cross; H. Bas Bueno-de-Mesquita; Paolo Vineis; Nerea Larrañaga; Valeria Pala; María José Roca Sánchez; Carmen Navarro; Aurelio Barricarte

PURPOSEnHuman papillomavirus (HPV) type 16 (HPV16) causes cancer at several anatomic sites. In the European Prospective Investigation Into Cancer and Nutrition study, HPV16 E6 seropositivity was present more than 10 years before oropharyngeal cancer diagnosis and was nearly absent in controls. The current study sought to evaluate the extent to which HPV16 E6 antibodies are present before diagnosis of anogenital cancers within the same cohort.nnnMETHODSnFour hundred incident anogenital cancers (273 cervical, 24 anal, 67 vulvar, 12 vaginal, and 24 penile cancers) with prediagnostic blood samples (collected on average 3 and 8 years before diagnosis for cervix and noncervix cancers, respectively) and 718 matched controls were included. Plasma was analyzed for antibodies against HPV16 E6 and multiple other HPV proteins and genotypes and evaluated in relation to risk using unconditional logistic regression.nnnRESULTSnHPV16 E6 seropositivity was present in 29.2% of individuals (seven of 24 individuals) who later developed anal cancer compared with 0.6% of controls (four of 718 controls) who remained cancer free (odds ratio [OR], 75.9; 95% CI, 17.9 to 321). HPV16 E6 seropositivity was less common for cancers of the cervix (3.3%), vagina (8.3%), vulva (1.5%), and penis (8.3%). No associations were seen for non-type 16 HPV E6 antibodies, apart from anti-HPV58 E6 and anal cancer (OR, 6.8; 95% CI, 1.4 to 33.1). HPV16 E6 seropositivity tended to increase in blood samples drawn closer in time to cancer diagnosis.nnnCONCLUSIONnHPV16 E6 seropositivity is relatively common before diagnosis of anal cancer but rare for other HPV-related anogenital cancers.


Cancer Causes & Control | 2011

Exposure to environmental tobacco smoke in childhood and incidence of cancer in adulthood in never smokers in the European prospective investigation into cancer and nutrition.

Shu-Chun Chuang; Valentina Gallo; Dominique S. Michaud; Kim Overvad; Anne Tjønneland; Françoise Clavel-Chapelon; Isabelle Romieu; Kurt Straif; Domenico Palli; Valeria Pala; Rosario Tumino; Carlotta Sacerdote; Salvatore Panico; Petra H. Peeters; Eiliv Lund; Inger Torhild Gram; Jonas Manjer; Signe Borgquist; Elio Riboli; Paolo Vineis

The association between childhood environmental tobacco smoke (ETS) exposure and adult cancer risk is controversial; we examined this relationship in never smokers within the European Prospective Investigation into Cancer and Nutrition (EPIC) cohort. Over an average of 10xa0years, 8,372 cases of cancer were diagnosed in 112,430 never smokers in EPIC. Childhood ETS was self-reported by participants at baseline, along with other lifestyle factors. Hazard ratios (HR) for ETS exposure in childhood and their 95% confidence intervals (CI) were estimated by Cox proportional hazards models stratified by age, sex, and study center and adjusted for education, alcohol drinking, body mass index, physical activity, non-alcoholic energy intake, fruit and vegetable intake, and adulthood ETS exposure. Models were further adjusted for reproductive factors for female cancers, for meat intake for digestive system cancers, and for diabetes status for pancreatic cancer. No association was observed between childhood ETS exposure and overall cancer risks (HRxa0=xa00.97, 95% CIxa0=xa00.92–1.02), and for selected sites. The only exception was pancreatic cancer, as previously reported by Vrieling et al., among those who had been exposed daily in childhood (overall HRxa0=xa02.09, 95% CIxa0=xa01.14–3.84). In conclusion, childhood ETS exposure might not be a major risk factor for common cancers in adulthood.


American Journal of Epidemiology | 2013

Dietary Flavonoid Intake and Esophageal Cancer Risk in the European Prospective Investigation into Cancer and Nutrition Cohort

Esther Vermeulen; Raul Zamora-Ros; Eric J. Duell; Leila Lujan-Barroso; Heiner Boeing; Krasimira Aleksandrova; H. Bas Bueno-de-Mesquita; Augustin Scalbert; Isabelle Romieu; Veronika Fedirko; Marina Touillaud; Guy Fagherazzi; Florence Perquier; Esther Molina-Montes; Maria Dolores Chirlaque; Marcial Argüelles; Pilar Amiano; Aurelio Barricarte; Valeria Pala; Amalia Mattiello; Calogero Saieva; Rosario Tumino; Fulvio Ricceri; Antonia Trichopoulou; Effie Vasilopoulou; Gianna Ziara; Francesca L. Crowe; Kay Thee Khaw; Nicholas J. Wareham; Annekatrin Lukanova

We prospectively investigated dietary flavonoid intake and esophageal cancer risk in the European Prospective Investigation into Cancer and Nutrition (EPIC) cohort. The study included 477,312 adult subjects from 10 European countries. At baseline, country-specific validated dietary questionnaires were used. During a mean follow-up of 11 years (1992-2010), there were 341 incident esophageal cancer cases, of which 142 were esophageal adenocarcinoma (EAC), 176 were esophageal squamous cell carcinoma (ESCC), and 23 were other types of esophageal cancer. In crude models, a doubling in total dietary flavonoid intake was inversely associated with esophageal cancer risk (hazard ratio (HR) (log₂) = 0.87, 95% confidence interval (CI): 0.78, 0.98) but not in multivariable models (HR (log₂) = 0.97, 95% CI: 0.86, 1.10). After covariate adjustment, no statistically significant association was found between any flavonoid subclass and esophageal cancer, EAC, or ESCC. However, among current smokers, flavonols were statistically significantly associated with a reduced esophageal cancer risk (HR (log₂) = 0.72, 95% CI: 0.56, 0.94), whereas total flavonoids, flavanols, and flavan-3-ol monomers tended to be inversely associated with esophageal cancer risk. No associations were found in either never or former smokers. These findings suggest that dietary flavonoid intake was not associated with overall esophageal cancer, EAC, or ESCC risk, although total flavonoids and some flavonoid subclasses, particularly flavonols, may reduce the esophageal cancer risk among current smokers.


Breast Cancer Research and Treatment | 2008

Lifetime cumulative number of menstrual cycles and serum sex hormone levels in postmenopausal women

Mariana Chavez-MacGregor; Carla H. van Gils; Yvonne T van der Schouw; Evelyn M.|info:eu-repo Monninkhof; Paulus A. H. van Noord; Petra H. Peeters

ObjectiveLifetime cumulative number of menstrual cycles is related to breast cancer risk. The aim of this study is to investigate the relation between this index and serum sex hormone levels in postmenopausal women.MethodsCross-sectional study including 860 naturally postmenopausal Dutch participants of the European Prospective Investigation into Cancer and Nutrition. Lifetime cumulative number of menstrual cycles was computed using questionnaire data on ages at menarche and menopause, number of pregnancies, breastfeeding, oral contraceptive use (OC) and regularity pattern. Measurements of hormones included estrone (E1), estradiol (E2), andostrenedione, testosterone, sex-hormone binding globulin (SHBG) and dehydroepiandrostenedione sulfate (DHEAS). The relation between the lifetime cumulative number of menstrual cycles and hormone levels was assessed using analysis of covariance. Relations between reproductive characteristics and hormone levels were also studied. Adjustments for characteristics at blood collection included age, years since menopause, BMI, hormone replacement therapy use, OC use, smoking habits, alcohol intake and physical activity were done.ResultsLifetime cumulative number of cycles was related with SHBG; participants in the lowest category had higher SHBG levels. For the separate characteristics, DHEAS and androstenedione increased significantly with increasing age at menarche, while androstenedione and testosterone decreased with increasing age at menopause. For the parity characteristics, SHBG levels increased according to the number of live births.ConclusionsLifetime cumulative number menstrual cycles was related only to SHBG. Therefore, free levels of estrogens or androgens may be related to this number of menstrual cycles estimate, reflecting lifetime exposure to ovarian hormones.

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Rosario Tumino

International Agency for Research on Cancer

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Antonia Trichopoulou

National and Kapodistrian University of Athens

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Françoise Clavel-Chapelon

International Agency for Research on Cancer

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Valeria Pala

National Institutes of Health

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Salvatore Panico

International Agency for Research on Cancer

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Elio Riboli

Imperial College London

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