Nina Føns Johnsen
University of Copenhagen
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Featured researches published by Nina Føns Johnsen.
Cancer Epidemiology, Biomarkers & Prevention | 2006
Christine Friedenreich; Teresa Norat; Karen Steindorf; Marie-Christine Boutron-Ruault; Tobias Pischon; Mathieu Mazuir; Françoise Clavel-Chapelon; Jakob Linseisen; Heiner Boeing; Manuela M. Bergman; Nina Føns Johnsen; Anne Tjønneland; Kim Overvad; Michelle A. Mendez; J. Ramón Quirós; Carmen Martinez; Miren Dorronsoro; Carmen Navarro; Aurelio Barricarte Gurrea; Sheila Bingham; Kay-Tee Khaw; Naomi E. Allen; Timothy J. Key; Antonia Trichopoulou; Dimitrios Trichopoulos; Natassa Orfanou; Vittorio Krogh; Domenico Palli; Rosario Tumino; Salvatore Panico
We investigated several aspects of the role of physical activity in colon and rectal cancer etiology that remain unclear in the European Prospective Investigation into Nutrition and Cancer. This cohort of 413,044 men and women had 1,094 cases of colon and 599 cases of rectal cancer diagnosed during an average of 6.4 years of follow-up. We analyzed baseline data on occupational, household, and recreational activity to examine associations by type of activity, tumor subsite, body mass index (BMI), and energy intake. The multivariate hazard ratio for colon cancer was 0.78 [95% confidence interval (95% CI), 0.59-1.03] among the most active participants when compared with the inactive, with evidence of a dose-response effect (Ptrend = 0.04). For right-sided colon tumors, the risk was 0.65 (95% CI, 0.43-1.00) in the highest quartile of activity with evidence of a linear trend (Ptrend = 0.004). Active participants with a BMI under 25 had a risk of 0.63 (95% CI, 0.39-1.01) for colon cancer compared with the inactive. Finally, an interaction between BMI and activity (Pinteraction = 0.03) was observed for right-sided colon cancers; among moderately active and active participants with a BMI under 25, a risk of 0.38 (95% CI, 0.21-0.68) was found as compared with inactive participants with BMI >30. No comparable decreased risks were observed for rectal cancer for any type of physical activity for any subgroup analyses or interactions considered. We found that physical activity reduced colon cancer risk, specifically for right-sided tumors and for lean participants, but not rectal cancer. (Cancer Epidemiol Biomarkers Prev 2006;15(12):2398–407)
British Journal of Cancer | 2008
Naomi E. Allen; Timothy J. Key; Paul N. Appleby; Ruth C. Travis; Andrew W. Roddam; Anne Tjønneland; Nina Føns Johnsen; Kim Overvad; J. Linseisen; Sabine Rohrmann; Heiner Boeing; Tobias Pischon; H. B. Bueno-de-Mesquita; Lambertus A. Kiemeney; Giovanna Tagliabue; Domenico Palli; Paolo Vineis; R. Tumino; Antonia Trichopoulou; Christina Kassapa; D. Trichopoulos; E. Ardanaz; Nerea Larrañaga; M. J. Tormo; Clementina González; J. R. Quiros; M. J. Sánchez; S. Bingham; Kay-Tee Khaw; Jonas Manjer
We examined consumption of animal foods, protein and calcium in relation to risk of prostate cancer among 142 251 men in the European Prospective Investigation into Cancer and Nutrition. Associations were examined using Cox regression, stratified by recruitment centre and adjusted for height, weight, education, marital status and energy intake. After an average of 8.7 years of follow-up, there were 2727 incident cases of prostate cancer, of which 1131 were known to be localised and 541 advanced-stage disease. A high intake of dairy protein was associated with an increased risk, with a hazard ratio for the top versus the bottom fifth of intake of 1.22 (95% confidence interval (CI): 1.07–1.41, Ptrend=0.02). After calibration to allow for measurement error, we estimated that a 35-g day−1 increase in consumption of dairy protein was associated with an increase in the risk of prostate cancer of 32% (95% CI: 1–72%, Ptrend=0.04). Calcium from dairy products was also positively associated with risk, but not calcium from other foods. The results support the hypothesis that a high intake of protein or calcium from dairy products may increase the risk for prostate cancer.
Cancer Epidemiology, Biomarkers & Prevention | 2008
Tobias Pischon; Heiner Boeing; Steffen Weikert; Naomi E. Allen; Timothy J. Key; Nina Føns Johnsen; Anne Tjønneland; Marianne Tang Severinsen; Kim Overvad; Sabine Rohrmann; Rudolf Kaaks; Antonia Trichopoulou; Gitaki Zoi; Dimitrios Trichopoulos; Valeria Pala; Domenico Palli; Rosario Tumino; Carlotta Sacerdote; H. Bas Bueno-de-Mesquita; Anne May; Jonas Manjer; Peter Wallström; Pär Stattin; Göran Hallmans; Genevieve Buckland; Nerea Larrañaga; Maria Dolores Chirlaque; Carmen Martinez; María L. Redondo Cornejo; Eva Ardanaz
Background: Body size has been hypothesized to influence the risk of prostate cancer; however, most epidemiologic studies have relied on body mass index (BMI) to assess adiposity, whereas only a few studies have examined whether body fat distribution predicts prostate cancer. Methods: We examined the association of height, BMI, waist and hip circumference, and waist-hip ratio with prostate cancer risk among 129,502 men without cancer at baseline from 8 countries of the European Prospective Investigation into Cancer and Nutrition (EPIC), using Cox regression, with age as time metric, stratifying by study center and age at recruitment, and adjusting for education, smoking status, alcohol consumption, and physical activity. Results: During a mean follow-up of 8.5 years, 2,446 men developed prostate cancer. Waist circumference and waist-hip ratio were positively associated with risk of advanced disease. The relative risk of advanced prostate cancer was 1.06 (95% confidence interval, 1.01-1.1) per 5-cm-higher waist circumference and 1.21 (95% confidence interval, 1.04-1.39) per 0.1-unit-higher waist-hip ratio. When stratified by BMI, waist circumference and waist-hip ratio were positively related to risk of total, advanced, and high-grade prostate cancer among men with lower but not among those with higher BMI (Pinteraction for waist with BMI, 0.25, 0.02, and 0.05, respectively; Pinteraction for waist-hip ratio with BMI, 0.27, 0.22, and 0.14; respectively). Conclusions: These data suggest that abdominal adiposity may be associated with an increased risk of advanced prostate cancer. This association may be stronger among individuals with lower BMI; however, this finding needs confirmation in future studies. (Cancer Epidemiol Biomarkers Prev 2008;17(11):3252–61)
Cancer Epidemiology, Biomarkers & Prevention | 2007
Naomi E. Allen; Timothy J. Key; Paul N. Appleby; Ruth C. Travis; Andrew W. Roddam; S. Rinaldi; Lars Egevad; Sabine Rohrmann; J. Linseisen; Tobias Pischon; Heiner Boeing; Nina Føns Johnsen; Anne Tjønneland; Henning Grønbæk; Kim Overvad; Lambertus A. Kiemeney; H. B. Bueno-de-Mesquita; Sheila Bingham; Kay-Tee Khaw; R. Tumino; Franco Berrino; Amalia Mattiello; C. Sacerdote; Domenico Palli; J. R. Quiros; E. Ardanaz; C. Navarro; Nerea Larrañaga; Clementina González; M. J. Sánchez
Background: Some studies suggest that elevated serum insulin-like growth factor (IGF)-I concentrations are associated with an increased risk of prostate cancer and, in particular, with an increased risk of advanced-stage prostate cancer. Methods: We analyzed the association between prediagnostic serum concentrations of IGF-I and IGF-binding protein-3 (IGFBP-3) and prostate cancer risk in a case-control study nested in the European Prospective Investigation into Cancer and Nutrition. This study includes 630 incident prostate cancer cases and 630 matched control subjects. Odds ratios and their 95% confidence intervals (95% CI) were calculated for prostate cancer risk associated with increasing IGF-I and IGFBP-3 concentrations using conditional logistic regression. Results: The risk of total prostate cancer in the highest versus the lowest third of serum peptide concentration was 1.35 (95% CI, 0.99-1.82; Ptrend = 0.08) for IGF-I, 1.39 (95% CI, 1.02-1.89; Ptrend = 0.12) for the IGF-I residuals after adjusting for IGFBP-3, 1.22 (95% CI, 0.92-1.64; Ptrend = 0.38) for IGFBP-3, and 1.01 (95% CI, 0.74-1.37; Ptrend = 0.75) for the IGFBP-3 residuals after adjusting for IGF-I. There was no significant difference in the association of peptide hormones and prostate cancer by stage of disease, although the association of serum IGF-I concentration with risk was slightly stronger for advanced-stage disease; the odds ratio for the highest versus the lowest third was 1.65 (95% CI, 0.88-3.08; Ptrend = 0.21) for IGF-I and 1.76 (95% CI, 0.92-3.40; Ptrend = 0.11) for IGF-I adjusted for IGFBP-3. Conclusions: In this large nested case-control study, serum IGF-I concentration is not strongly associated with prostate cancer risk, although the results are compatible with a small increase in risk, particularly for advanced-stage disease; no association for IGFBP-3 was observed. (Cancer Epidemiol Biomarkers Prev 2007;16(6):1121–7)
British Journal of Cancer | 2009
Ruth C. Travis; Elizabeth A. Spencer; Naomi E. Allen; Paul N. Appleby; Andrew W. Roddam; Kim Overvad; Nina Føns Johnsen; A. Olsen; R. Kaaks; J. Linseisen; Heiner Boeing; Ute Nöthlings; H. B. Bueno-de-Mesquita; Martine M. Ros; C. Sacerdote; Domenico Palli; R. Tumino; Franco Berrino; Antonia Trichopoulou; Vardis Dilis; Dimitrios Trichopoulos; M. D. Chirlaque; E. Ardanaz; Nerea Larrañaga; Clementina González; Laudina Rodríguez Suárez; M. J. Sánchez; S. Bingham; Kay-Tee Khaw; G. Hallmans
We examined plasma concentrations of phyto-oestrogens in relation to risk for subsequent prostate cancer in a case–control study nested in the European Prospective Investigation into Cancer and Nutrition. Concentrations of isoflavones genistein, daidzein and equol, and that of lignans enterolactone and enterodiol, were measured in plasma samples for 950 prostate cancer cases and 1042 matched control participants. Relative risks (RRs) for prostate cancer in relation to plasma concentrations of these phyto-oestrogens were estimated by conditional logistic regression. Higher plasma concentrations of genistein were associated with lower risk of prostate cancer: RR among men in the highest vs the lowest fifth, 0.71 (95% confidence interval (CI) 0.53–0.96, P trend=0.03). After adjustment for potential confounders this RR was 0.74 (95% CI 0.54–1.00, P trend=0.05). No statistically significant associations were observed for circulating concentrations of daidzein, equol, enterolactone or enterodiol in relation to overall risk for prostate cancer. There was no evidence of heterogeneity in these results by age at blood collection or country of recruitment, nor by cancer stage or grade. These results suggest that higher concentrations of circulating genistein may reduce the risk of prostate cancer but do not support an association with plasma lignans.
International Journal of Cancer | 2007
Ruth C. Travis; Timothy J. Key; Naomi E. Allen; Paul N. Appleby; Andrew W. Roddam; Sabina Rinaldi; Lars Egevad; Peter H. Gann; Sabine Rohrmann; Jakob Linseisen; Tobias Pischon; Heiner Boeing; Nina Føns Johnsen; Anne Tjønneland; Kim Overvad; Lambertus A. Kiemeney; H. Bas Bueno-de-Mesquita; Sheila Bingham; Kay-Tee Khaw; Rosario Tumino; Sabina Sieri; Paolo Vineis; Domenico Palli; José Ramón Quirós; Eva Ardanaz; Maria Dolores Chirlaque; Nerea Larrañaga; Carlos A. González; Maria José Sánchez; Antonia Trichopoulou
We examined the hypothesis that serum concentrations of circulating androgens and sex hormone binding globulin (SHBG) are associated with risk for prostate cancer in a case‐control study nested in the European Prospective Investigation into Cancer and Nutrition (EPIC). Concentrations of androstenedione, testosterone, androstanediol glucuronide and SHBG were measured in serum samples for 643 prostate cancer cases and 643 matched control participants, and concentrations of free testosterone were calculated. Conditional logistic regression models were used to calculate odds ratios for risk of prostate cancer in relation to the serum concentration of each hormone. After adjustment for potential confounders, there was no significant association with overall risk for prostate cancer for serum total or free testosterone concentrations (highest versus the lowest thirds: OR, 1.02; 95% CI, 0.73–1.41 and OR, 1.07, 95% CI, 0.74–1.55, respectively) or for other androgens or SHBG. Subgroup analyses showed significant heterogeneity for androstenedione by cancer stage, with a significant inverse association of androstenedione concentration and risk for advanced prostate cancer. There were also weak positive associations between free testosterone concentration and risk for total prostate cancer among younger men and risk for high‐grade disease. In summary, in this large nested case‐control study, concentrations of circulating androgens or SHBG were not strongly associated with risk for total prostate cancer. However, our findings are compatible with a positive association of free testosterone with risk in younger men and possible heterogeneity in the association with androstenedione concentration by stage of disease; these findings warrant further investigation.
International Journal of Cancer | 2007
Christine Friedenreich; Anne E. Cust; Petra H. Lahmann; Karen Steindorf; Marie Christine Boutron-Ruault; Françoise Clavel-Chapelon; Sylvie Mesrine; Jakob Linseisen; Sabine Rohrmann; Tobias Pischon; Mandy Schulz; Anne Tjønneland; Nina Føns Johnsen; Kim Overvad; Michelle A. Mendez; Marcial Argüelles; Carmen Martinez Garcia; Nerea Larrañaga; Maria Dolores Chirlaque; Eva Ardanaz; Sheila Bingham; Kay-Tee Khaw; Naomi E. Allen; Timothy J. Key; Antonia Trichopoulou; Vardis Dilis; Dimitrios Trichopoulos; Valeria Pala; Domenico Palli; Rosario Tumino
The etiologic role of physical activity in endometrial cancer risk remains unclear given the few epidemiologic studies that have been conducted. To investigate this relation more fully, an analysis was undertaken in the European prospective investigation into cancer and nutrition (EPIC). During an average 6.6 years of follow‐up, 689 incident endometrial cancer cases were identified from an analytic cohort within EPIC of 253,023 women. Cox proportional hazards models were used to estimate the associations between type of activity (total, occupational, household, recreational) and endometrial cancer risk. For total activity, women in the highest compared with the lowest quartile of activity had a risk of 0.88 (95% confidence interval (95% CI = 0.61–1.27). No clear associations between each type of activity and endometrial cancer risk were found for the total study population combined. Associations were more evident in the stratified results, with premenopausal women who were active versus inactive experiencing a risk of 0.66 (95% CI = 0.38–1.14) overall. Among premenopausal women, for household and recreational activities the risk estimates in the highest as compared with the lowest quartiles were, respectively, 0.48 (95% CI = 0.23–0.99) and 0.78 (95% CI = 0.44–1.39). No effect modification by body mass index, hormone replacement therapy, oral contraceptive use or energy intake was found. This study provides no evidence of a protective effect of increased physical activity in endometrial cancer risk in all women but some support for a benefit among premenopausal women. The relative risk reductions are most apparent for household activities.
International Journal of Cancer | 2009
Nina Føns Johnsen; Anne Tjønneland; Birthe L. Thomsen; Jane Christensen; Steffen Loft; Christine M. Friedenreich; Timothy J. Key; Naomi E. Allen; Petra H. Lahmann; Lotte Mejlvig; Kim Overvad; Rudolf Kaaks; Sabine Rohrmann; Heiner Boing; Gesthimani Misirli; Antonia Trichopoulou; Dimosthenis Zylis; Rosario Tumino; Valeria Pala; H. Bas Bueno-de-Mesquita; Lambertus A. Kiemeney; Laudina Rodríguez Suárez; Carlos A. González; María José Sánchez; José María Huerta; Aurelio Barricarte Gurrea; Jonas Manjer; Elisabet Wirfält; Kay-Tee Khaw; Nicholas J. Wareham
The evidence concerning the possible association between physical activity and the risk of prostate cancer is inconsistent and additional data are needed. We examined the association between risk of prostate cancer and physical activity at work and in leisure time in the European Prospective Investigation into Cancer and Nutrition (EPIC) cohort. In our study, including 127,923 men aged 20–97 years from 8 European countries, 2,458 cases of prostate cancer were identified during 8.5 years of followup. Using the Cox proportional hazards model, we investigated the associations between prostate cancer incidence rate and occupational activity and leisure time activity in terms of participation in sports, cycling, walking and gardening; a metabolic equivalent (MET) score based on weekly time spent on the 4 activities; and a physical activity index. MET hours per week of leisure time activity, higher score in the physical activity index, participation in any of the 4 leisure time activities, and the number of leisure time activities in which the participants were active were not associated with prostate cancer incidence. However, higher level of occupational physical activity was associated with lower risk of advanced stage prostate cancer (ptrend = 0.024). In conclusion, our data support the hypothesis of an inverse association between advanced prostate cancer risk and occupational physical activity, but we found no support for an association between prostate cancer risk and leisure time physical activity.
The American Journal of Clinical Nutrition | 2008
Naomi E. Allen; Paul N. Appleby; Andrew W. Roddam; Anne Tjønneland; Nina Føns Johnsen; Kim Overvad; Heiner Boeing; Steffen Weikert; Rudolf Kaaks; Jakob Linseisen; Antonia Trichopoulou; Gesthimani Misirli; Dimitrios Trichopoulos; Carlotta Sacerdote; Sara Grioni; Domenico Palli; Rosario Tumino; H. Bas Bueno-de-Mesquita; Lambertus A. Kiemeney; Aurelio Barricarte; Nerea Larrañaga; María José Sánchez; Antonio Agudo; María José Tormo; Laudina Rodríguez; Pär Stattin; Göran Hallmans; Sheila Bingham; Kay-Tee Khaw; Nadia Slimani
BACKGROUND Some evidence indicates that a low selenium intake may be associated with an increased risk of prostate cancer. OBJECTIVE The aim of this study was to investigate the association of plasma selenium concentration with subsequent prostate cancer risk and to examine this association by stage and grade of disease and other factors. DESIGN A nested case-control study was performed among men in the European Prospective Investigation into Cancer and Nutrition (EPIC). The association between plasma selenium concentration and prostate cancer risk was assessed in 959 men with incident prostate cancer and 1059 matched controls. RESULTS Overall, plasma selenium concentration was not associated with prostate cancer risk; the multivariate relative risk for men in the highest fifth of selenium concentration compared with the lowest fifth was 0.96 (95% CI: 0.70, 1.31; P for trend = 0.25). There were no significant differences in the association of plasma selenium with risk when analyzed by stage or grade of disease. Similarly, the association of selenium with risk did not differ by smoking status or by plasma alpha- or gamma-tocopherol concentration. CONCLUSION Plasma selenium concentration was not associated with prostate cancer risk in this large cohort of European men.
Annals of Oncology | 2013
Veronika Fedirko; A Lukanova; Christina Bamia; A. Trichopolou; Elisabeth Trepo; Ute Nöthlings; Sabrina Schlesinger; Krasimira Aleksandrova; Paolo Boffetta; Anne Tjønneland; Nina Føns Johnsen; Kim Overvad; Guy Fagherazzi; Antoine Racine; Marie-Christine Boutron-Ruault; Verena Grote; R. Kaaks; Heiner Boeing; A. Naska; George Adarakis; Elissavet Valanou; D. Palli; S. Sieri; R. Tumino; Paolo Vineis; Salvatore Panico; H. B. Bueno-De-Mesquita; Peter D. Siersema; Petra H. Peeters; Elisabete Weiderpass
BACKGROUND The type and quantity of dietary carbohydrate as quantified by glycemic index (GI) and glycemic load (GL), and dietary fiber may influence the risk of liver and biliary tract cancers, but convincing evidence is lacking. PATIENTS AND METHODS The association between dietary GI/GL and carbohydrate intake with hepatocellular carcinoma (HCC; N = 191), intrahepatic bile duct (IBD; N = 66), and biliary tract (N = 236) cancer risk was investigated in 477 206 participants of the European Prospective Investigation into Cancer and Nutrition cohort. Dietary intake was assessed by country-specific, validated dietary questionnaires. Hazard ratios and 95% confidence intervals were estimated from proportional hazard models. HBV/HCV status was measured in a nested case-control subset. RESULTS Higher dietary GI, GL, or increased intake of total carbohydrate was not associated with liver or biliary tract cancer risk. For HCC, divergent risk estimates were observed for total sugar = 1.43 (1.17-1.74) per 50 g/day, total starch = 0.70 (0.55-0.90) per 50 g/day, and total dietary fiber = 0.70 (0.52-0.93) per 10 g/day. The findings for dietary fiber were confirmed among HBV/HCV-free participants [0.48 (0.23-1.01)]. Similar associations were observed for IBD [dietary fiber = 0.59 (0.37-0.99) per 10 g/day], but not biliary tract cancer. CONCLUSIONS Findings suggest that higher consumption of dietary fiber and lower consumption of total sugars are associated with lower HCC risk. In addition, high dietary fiber intake could be associated with lower IBD cancer risk.BACKGROUND The type and quantity of dietary carbohydrate as quantified by glycemic index (GI) and glycemic load (GL), and dietary fiber may influence the risk of liver and biliary tract cancers, but convincing evidence is lacking. PATIENTS AND METHODS The association between dietary GI/GL and carbohydrate intake with hepatocellular carcinoma (HCC; N = 191), intrahepatic bile duct (IBD; N = 66), and biliary tract (N = 236) cancer risk was investigated in 477 206 participants of the European Prospective Investigation into Cancer and Nutrition cohort. Dietary intake was assessed by country-specific, validated dietary questionnaires. Hazard ratios and 95% confidence intervals were estimated from proportional hazard models. HBV/HCV status was measured in a nested case-control subset. RESULTS Higher dietary GI, GL, or increased intake of total carbohydrate was not associated with liver or biliary tract cancer risk. For HCC, divergent risk estimates were observed for total sugar = 1.43 (1.17-1.74) per 50 g/day, total starch = 0.70 (0.55-0.90) per 50 g/day, and total dietary fiber = 0.70 (0.52-0.93) per 10 g/day. The findings for dietary fiber were confirmed among HBV/HCV-free participants [0.48 (0.23-1.01)]. Similar associations were observed for IBD [dietary fiber = 0.59 (0.37-0.99) per 10 g/day], but not biliary tract cancer. CONCLUSIONS Findings suggest that higher consumption of dietary fiber and lower consumption of total sugars are associated with lower HCC risk. In addition, high dietary fiber intake could be associated with lower IBD cancer risk.