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Annals of Oncology Advance Access originally published online on October 25, 2005
Annals of Oncology 2006 17(2):341-345; doi:10.1093/annonc/mdj051
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© 2005 European Society for Medical Oncology

Consumption of sweet foods and breast cancer risk in Italy

A. Tavani1,*, L. Giordano1, S. Gallus1, R. Talamini2, S. Franceschi3, A. Giacosa4, M. Montella5 and C. La Vecchia1,6

1 Istituto di Ricerche Farmacologiche ‘Mario Negri’, Milan, Italy; 2 Centro di Riferimento Oncologico, Aviano (Pordenone), Italy; 3 International Agency for Research on Cancer, Lyon, France; 4 Istituto Nazionale per la Ricerca sul Cancro, Genoa, Italy; 5 Istituto Tumori ‘Fondazione Pascale’, Naples, Italy; 6 Istituto di Statistica Medica e Biometria, Università degli Studi di Milano, Milan, Italy

* Correspondence to: Dr A. Tavani, Istituto di Ricerche Farmacologiche ‘Mario Negri’, Via Eritrea 62, 20157 Milan, Italy. Tel: +39-02-39014-460; Fax: +39-02-39001-916; E-mail: tavani{at}marionegri.it


    Abstract
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 Abstract
 introduction
 patients and methods
 results
 discussion
 References
 
Background: The relation between the intake of sugar and sweets and the risk of breast cancer has been considered in ecological, prospective and case–control studies, but the results are unclear. We analyzed such a relation in a case–control study conducted between 1991 and 1994 in Italy.

Patients and methods: Cases were 2569 women with histologically confirmed incident breast cancer and controls were 2588 women admitted to hospital for acute, non-neoplastic, non-hormone-related conditions. Information on diet was based on an interviewer-administered questionnaire tested for reproducibility and validity. The odds ratios (OR) and 95% confidence intervals (CI) were computed by multiple logistic regression equations.

Results: Compared with women with the lowest tertile of intake, women in the highest tertile of intake of desserts (including biscuits, brioches, cakes, puffs and ice-cream) and sugars (including sugar, honey, jam, marmalade and chocolate) had multivariate ORs of 1.19 (95% CI 1.02–1.39) and 1.19 (95% CI 1.02–1.38), respectively. The results were similar in strata of age, body mass index, total energy intake and other covariates.

Conclusions: We found a direct association between breast cancer risk and consumption of sweet foods with high glycemic index and load, which increase insulin and insulin growth factors.

Key words: breast cancer, case–control study, risk factors, sweets, sugar


    introduction
 Top
 Abstract
 introduction
 patients and methods
 results
 discussion
 References
 
The influence of sugar and sweets on the risk of breast cancer has been considered in several ecological, prospective and case–control studies, but the results are unclear. Among 20 ecological studies, 10 found a positive correlation between sugar or sweet intakes and incidence or mortality from breast cancer. The correlations were more consistent in international studies than in within-country analyses [1Go].

An increased breast cancer risk with cake intake was found in a prospective study from Norway [2Go], whereas no relation with sweets was found in another cohort study conducted among Japanese women living in Hawaii [3Go]. Some case–control studies found elevated risks with sweetened beverages [4Go], or with intake of sweet foods [5Go–8Go], although the excess risk was generally small. In two case–control studies, one Canadian [5Go] and one Spanish [7Go], elevated risks were found for the highest intake of sweets (odds ratio, OR, 1.5 and 2.3, respectively). In a French case–control study, desserts and chocolate were directly associated with breast cancer risk [6Go]. A population-based case–control study on American women younger than 45 years found a significant increase of breast cancer risk with sweet items (OR 1.3 for the highest intake), in the absence of a relation with several other foods, calories, macronutrients or types of fats [9Go]. However, other studies found no consistent relation between breast cancer risk and intake of sugar [4Go, 10Go–14Go], mono or disaccarides [15Go, 16Go], or sweet foods [4Go, 10Go, 17Go–20Go].

The inconsistent results of epidemiological studies may depend on chance or bias or different approaches to data analysis and interpretation, but they may also reflect heterogeneity in components of sweet foods (i.e. cereals, sugars and fats), or recipes in various populations, or different correlates of sweet food intake.

Using data from an Italian case–control study on diet and breast cancer [21Go], we found that sweet foods were directly associated with breast cancer risk. In order to elucidate better the issue of the relationship between sweet foods and breast cancer risk, we analyzed in detail the potential role of various types of sweets and of selected covariates in a uniquely large dataset.


    patients and methods
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 Abstract
 introduction
 patients and methods
 results
 discussion
 References
 
Data were derived from a case–control study of breast cancer conducted between June 1991 and April 1994 in six Italian areas: greater Milan; the province of Pordenone; the urban area of Genoa; the province of Forlì, in northern Italy; the province of Latina in central Italy; and the urban area of Naples in southern Italy [21Go]. Cases were 2569 women with incident, histologically confirmed breast cancer (median age 55 years, range 23–74 years) and controls were 2588 women (median age 56 years, range 20–74 years) with no history of cancer admitted to the same hospitals for acute, non-neoplastic, non-gynaecological conditions, unrelated to hormonal or digestive tract diseases or to long-term modification of diet. Among controls 22% had traumas, 33% other orthopaedic diseases, 15% acute surgical condition, 18% eye diseases and 12% other miscellaneous diseases. On average, less than 4% of cases and controls who were approached for interview refused to participate.

Centrally trained interviewers conducted interviews in hospital for both cases and controls using a structured questionnaire, including information on socio-demographic factors, anthropometric variables, smoking, alcohol and other lifestyle habits, physical activity, a problem-oriented medical history and history of breast cancer in first-degree relatives. Information on diet referred to the previous 2 years and was based on a food frequency questionnaire, including 78 foods or food groups or complex recipes, plus questions aimed at assessing fat intake and general dietary habits. The questionnaire was tested for validity [22Go] and reproducibility [23Go]. Subjects were asked to indicate their average weekly consumption of single food items or recipes; intakes lower than once a week, but at least once per month were coded as 0.5 per week. Sweet items were grouped into two food groups: desserts and sugars. ‘Desserts’ was created using six food items of the questionnaire and included biscuits, brioches, croissants, puffs, cream cakes, cream puffs, sponge cakes, panettone, fruit or jam tarts, ice cream and cooked fruit (half portion). ‘Sugars’ was created using three food items of the questionnaire and included sugar, honey, jam, marmalade and chocolate. Desserts and sugars were categorized into approximate tertiles based on the distribution of controls. To compute energy intake, Italian food composition databases were used, appropriately checked and supplemented with other published data and information from the manufacturers [24Go].

ORs and 95% confidence intervals (CI) were estimated by multiple logistic regression models fitted by the method of maximum likelihood [25Go]. Regression equations included terms for quinquennia of age, study center, year of interview, education, body mass index (BMI), total energy intake, parity, menopausal status and family history of breast cancer in first-degree relatives.


    results
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 Abstract
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 patients and methods
 results
 discussion
 References
 
The distribution of 2569 cases of breast cancer and 2588 controls according to frequency of sweet food consumption is shown in Table 1. Among food items, compared with the lowest level of intake, a direct association was found for the highest level of consumption of biscuits (OR 1.19), sugar (OR 1.23) and chocolate (OR 1.19). No association was found for the other sweet food items considered. Sweet items were grouped into two groups: desserts and sugars. For dessert intake the ORs of breast cancer were 1.11 for the second and 1.19 for the third tertile, compared with the lowest tertile. For sugars, the corresponding ORs were 1.22 and 1.19. Trends in risk were significant for both desserts and sugars.


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Table 1. Distribution of 2569 breast cancer cases and 2588 controls, and odds ratios (OR) with 95% confidence intervals (CI) according to selected sweet foods and food groups (Italy 1991–1994)

 
Table 2 considers the intake of desserts and sugars across strata of age at diagnosis, body mass index (BMI), total energy, total alcohol intake, physical activity at work, parity and family history of breast cancer. No heterogeneity across any strata was found either for desserts or for sugars, all ORs being above unity in the highest level of intake.


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Table 2. Relation between intake of desserts or sugars and the risk of breast cancer in strata of age and other selected covariates (Italy 1991–1994)

 

    discussion
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In this study, sweet consumption was directly associated to breast cancer risk. The risk was consistently elevated in strata of age (also an indicator of menopausal status), BMI, total calorie intake, alcohol, physical activity and family history of breast cancer.

Our results are in agreement with some epidemiological studies that have considered the issue of sweets, including studies from the USA [9Go], Canada [5Go] and Spain [7Go].

We also found that women in the highest decile of consumption of cakes and desserts and refined sugars had higher breast cancer risk [26Go], suggesting that sweet foods are among the features of a high-risk dietary pattern. In the Swedish Mammography Screening Cohort, based on a factor analysis, sweets were also included in the definition of unfavorable Western dietary pattern [27Go]. Moreover, sweet foods were rich in several nutrients potentially involved in the aetiology of breast cancer, such as refined carbohydrates and saturated fats [28Go–33Go]. It is difficult to completely allow for these in the analyses, because reciprocal allowance of various foods and nutrients is hampered by problems of collinearity [34Go]. Alternatively, consumption of sweet foods may reduce intake of foods with favourable influence on the risk of breast cancer, such as vegetables [21Go], fibers [35Go], olive oil [36Go, 37Go], or n-3 polyunsaturated fatty acids [38Go]. A frequent consumption of sugars or foods with a high glycemic index may lead to insulin resistance, and a direct association between glycemic index or glycemic load and breast cancer risk has been suggested [30Go, 39Go, 40Go]. This may cause an increase of insulin-related growth factors (IGF), which are promoters of breast carcinogenesis [41Go–44Go]. Insulin also stimulates ovarian steroid secretion, including estrogens and androgens, which have been related to excess breast cancer risk [45Go, 46Go]. Desserts are also rich in trans-fatty acids, which have been related to unfavourable health effects [47Go], as well as in saturated fatty acids, which have been associated with breast cancer risk in a pooled analysis of cohort studies [31Go, 48Go].

Furthermore, the association between sweets and breast cancer risk can be related to reduced diversity of diet for favourable foods [21Go], or greater meal frequency [49Go], which again may interfere with the insulin-related pathways of breast carcinogenesis [9Go]. Finally, it has been shown that calorie restriction has a favourable impact on breast cancer risk [50Go]. Consequently, although we allowed for energy intake in the analyses, some residual excess risk due to high calorie intake in women with frequent sweet consumption is possible.

Only patients admitted to hospital for acute, non hormone-related conditions were included in the control group, whereas patients with admission diagnosis related to major changes in diet and other lifestyle factors were excluded. Among the strengths of this study, are its large size, and the satisfactory reproducibility and validity of the questionnaire [22Go, 23Go]. Furthermore, interviews were conducted in the same setting for cases and controls, cases and controls were drawn from the same catchment areas and participation rate was almost complete.

In relative terms, the excess risk associated with highest sweet consumption is moderate, but most dietary correlates in breast cancer show similar modest associations [21Go, 28Go, 31Go, 51Go]. However, if real, the excess risk for frequent sweet consumption may account for 12% of breast cancer cases in this Italian population [52Go, 53Go] and, therefore, is far from negligible on a public health level [54Go].


    Acknowledgements
 
The study was supported by the Italian Association for Research on Cancer (AIRC), Milan, Italy, the Italian League against Cancer, and the Italian Ministry of Education (COFIN 2003).

Received for publication June 29, 2005. Revision received September 9, 2005. Accepted for publication September 21, 2005.


    References
 Top
 Abstract
 introduction
 patients and methods
 results
 discussion
 References
 
1. Burley VJ. Sugar consumption and human cancer in sites other than the digestive tract. Eur J Cancer Prev 1998; 7: 253–277.[CrossRef][Web of Science][Medline]

2. Gaard M, Tretli S, Loken EB. Dietary fat and the risk of breast cancer: a prospective study of 25,892 Norwegian women. Int J Cancer 1995; 63: 13–17.[Web of Science][Medline]

3. Nomura A, Henderson BE, Lee J. Breast cancer and diet among the Japanese in Hawaii. Am J Clin Nutr 1978; 31: 2020–2025.[Abstract/Free Full Text]

4. Witte JS, Ursin G, Siemiatycki J, Thompson WD, Paganini-Hill A, Haile RW. Diet and premenopausal bilateral breast cancer: a case–control study. Breast Cancer Res Treat 1997; 42: 243–251.[CrossRef][Web of Science][Medline]

5. Lubin JH, Burns PE, Blot WJ, Ziegler R, Lees AW, Fraumeni JF Jr. Dietary factors and breast cancer risk. Int J Cancer 1981; 28: 685–689.[Web of Science][Medline]

6. Richardson S, Gerber M, Cenee S. The role of fat, animal protein and some vitamin consumption in breast cancer: a case control study in southern France. Int J Cancer 1991; 48: 1–9.[Web of Science][Medline]

7. Landa MC, Frago N, Tres A. Diet and the risk of breast cancer in Spain. Eur J Cancer Prev 1994; 3: 313–320.[Medline]

8. Bala DV, Patel DD, Duffy SW et al. Role of dietary intake and biomarkers in risk of breast cancer: a case control study. Asian Pac Cancer Prev 2001; 2: 123–130.

9. Potischman N, Coates RJ, Swanson CA et al. Increased risk of early-stage breast cancer related to consumption of sweet foods among women less than age 45 in the United States. Cancer Causes Control 2002; 13: 937–946.[CrossRef][Web of Science][Medline]

10. Iscovich JM, Iscovich RB, Howe G, Shiboski S, Kaldor JM. A case–control study of diet and breast cancer in Argentina. Int J Cancer 1989; 44: 770–776.[Web of Science][Medline]

11. Toniolo P, Riboli E, Protta F, Charrel M, Cappa AP. Calorie-providing nutrients and risk of breast cancer. J Natl Cancer Inst 1989; 81: 278–286.[Abstract/Free Full Text]

12. Ewertz M, Gill C. Dietary factors and breast cancer risk in Denmark. Int J Cancer 1990; 46: 779–784.[Web of Science][Medline]

13. Ingram DM, Nottage E, Roberts T. The role of diet in the development of breast cancer: a case–control study of patients with breast cancer, benign epithelial hyperplasia and fibrocystic disease of the breast. Br J Cancer 1991; 64: 187–191.[Web of Science][Medline]

14. Mannisto S, Pietinen P, Virtanen M, Kataja V, Uusitupa M. Diet and the risk of breast cancer in a case–control study: does the threat of disease have an influence on recall bias? J Clin Epidemiol 1999; 52: 429–439.[CrossRef][Web of Science][Medline]

15. Rohan TE, McMichael AJ, Baghurst PA. A population-based case–control study of diet and breast cancer in Australia. Am J Epidemiol 1988; 128: 478–489.[Abstract/Free Full Text]

16. Zaridze D, Lifanova Y, Maximovitch D, Day NE, Duffy SW. Diet, alcohol consumption and reproductive factors in a case–control study of breast cancer in Moscow. Int J Cancer 1991; 48: 493–501.[Web of Science][Medline]

17. Simard A, Vobecky J, Vobecky JS. Nutrition and lifestyle factors in fibrocystic disease and cancer of the breast. Cancer Detect Prev 1990; 14: 567–572.[Web of Science][Medline]

18. Goodman MT, Nomura AM, Wilkens LR, Hankin J. The association of diet, obesity, and breast cancer in Hawaii. Cancer Epidemiol Biomarkers Prev 1992; 1: 269–275.[Abstract/Free Full Text]

19. Levi F, La Vecchia C, Gulie C, Negri E. Dietary factors and breast cancer risk in Vaud, Switzerland. Nutr Cancer 1993; 19: 327–335.[Web of Science][Medline]

20. Katsouyanni K, Willett W, Trichopoulos D et al. Risk of breast cancer among Greek women in relation to nutrient intake. Cancer 1988; 61: 181–185.[CrossRef][Web of Science][Medline]

21. Franceschi S, Favero A, La Vecchia C et al. Influence of food groups and food diversity on breast cancer risk in Italy. Int J Cancer 1995; 63: 785–789.[Web of Science][Medline]

22. Decarli A, Franceschi S, Ferraroni M et al. Validation of a food-frequency questionnaire to assess dietary intakes in cancer studies in Italy. Results for specific nutrients. Ann Epidemiol 1996; 6: 110–118.[CrossRef][Web of Science][Medline]

23. Franceschi S, Negri E, Salvini S et al. Reproducibility of an Italian food fequency questionnaire for cancer studies: results for specific food items. Eur J Cancer 1993; 29A: 2298–2305.

24. Salvini S, Parpinel M, Gnagnarella P, Maisonneuve P, Turrini A. Banca Dati di Composizione degli Alimenti per Studi Epidemiologici in Italia. Milano, Italy: Istituto Europeo di Oncologia 1998.

25. Breslow NE, Day NE. Statistical Methods in Cancer Research, Vol I. The Analysis of Case–Control Studies, IARC Science Publication no. 32. Lyon: International Agency for Research on Cancer 1980.

26. Franceschi S, La Vecchia C, Russo A, Negri E, Favero A, Decarli A. Low-risk diet for breast cancer in Italy. Cancer Epidemiol Biomarkers Prev 1997; 6: 875–879.[Abstract]

27. Terry P, Suzuki R, Hu FB, Wolk A. A prospective study of major dietary patterns and the risk of breast cancer. Cancer Epidemiol Biomark Prev 2001; 10: 1281–1285.[Abstract/Free Full Text]

28. World Cancer Research Fund. Food, Nutrition, and the Prevention of Cancer: a Global Perspective. Washington DC: American Institute for Cancer Research 1997.

29. Franceschi S, Russo A, La Vecchia C. Carbohydrates, fat and cancer of the breast and colon-rectum. J Epidemiol Biostat 1998; 3: 217–218.

30. Augustin LSA, Dal Maso L, La Vecchia C et al. Dietary glycemic index and glycemic load, and breast cancer risk: a case–control study. Ann Oncol 2001; 12: 1533–1538.[Abstract/Free Full Text]

31. Smith-Warner S, Spiegelman D, Adami H-O et al. Types of dietary fat and breast cancer: a pooled analysis of cohort studies. Int J Cancer 2001; 92: 767–774.[CrossRef][Web of Science][Medline]

32. Boyd NF, Stone J, Vogt KN, Connelly BS, Martin LJ, Minkin S. Dietary fat and breast cancer risk revisited: a meta-analysis of the published literature. Br J Cancer 2003; 89: 1672–1685.[CrossRef][Web of Science][Medline]

33. Holmes MD, Liu S, Hankinson SE, Colditz GA, Hunter DJ, Willett WC. Dietary carbohydrates, fiber, and breast cancer risk. Am J Epidemiol 2004; 159: 732–739.[Abstract/Free Full Text]

34. Negri E, La Vecchia C, Franceschi S. Relations between vegetable, fruit and micronutrient intake. Implications for odds ratios in a case–control study. Eur J Clin Nutr 2002; 56: 166–170.[Web of Science][Medline]

35. La Vecchia C, Ferraroni M, Franceschi S, Mezzetti M, Decarli A, Negri E. Fibers and breast cancer risk. Nutr Cancer 1997; 28: 264–269.[Web of Science][Medline]

36. La Vecchia C, Negri E, Franceschi S, Decarli A, Giacosa A, Lipworth L. Olive oil, other dietary fats, and the risk of breast cancer (Italy). Cancer Causes Control 1995; 6: 545–550.[CrossRef][Web of Science][Medline]

37. Lipworth L, Martinez ME, Angell J, Hsieh CC, Trichopoulous D. Olive oil and human cancer: an assessment of the evidence. Prev Med 1997; 26: 181–190.[CrossRef][Web of Science][Medline]

38. Tavani A, Pelucchi C, Parpinel MT et al. n-3 polyunsaturated fatty acid intake and cancer risk in Italy and Switzerland. Int J Cancer 2003; 105: 113–116.[CrossRef][Web of Science][Medline]

39. Augustin LS, Franceschi S, Jenkins DJA, Kendall CWC, La Vecchia C. Glycemic index in chronic disease: a review. Eur J Clin Nutr 2002; 56: 1049–1071.[CrossRef][Web of Science][Medline]

40. Lawlor DA, Smith GD, Ebrahim S. Hyperlinsulinaemia and increased risk of breast cancer: findings from the British women's heart and health study. Cancer Causes Control 2004; 15: 267–275.[CrossRef][Web of Science][Medline]

41. Kaaks R. Nutrition, hormones, and breast cancer: is insulin the missing link? Cancer Causes Control 1996; 7: 605–625.[CrossRef][Web of Science][Medline]

42. Yu H, Rohan T. Role of the insulin-like growth factor family in cancer development and progression. J Natl Cancer Inst 2000; 92: 1472–1489.[Abstract/Free Full Text]

43. Renehan AG, Zwahlen M, Minder C, O'Dwyer ST, Shalet SM, Egger M. Insulin-like growth factor (IGF)-I, IGF binding protein-3, and cancer risk: systematic review and meta-regression analysis. Lancet 2004; 363: 1346–1353.[CrossRef][Web of Science][Medline]

44. Shi R, Yu H, McLarty J, Glass J. IGF-I and breast cancer: A meta-analysis. Int J Cancer 2004; 111: 418–423.[CrossRef][Web of Science][Medline]

45. Endogenous Hormones and Breast Cancer Collaborative Group. Endogenous sex hormones and breast cancer in postmenopausal women: reanalysis of nine prospective studies. J Natl Cancer Inst 2002; 94: 606–616.[Abstract/Free Full Text]

46. Page JH, Colditz GA, Rifai N, Barbieri RL, Willett WC, Hankinson SE. Plasma adrenal androgens and risk of breast cancer in premenopausal women. Cancer Epidemiol Biomarkers Prev 2004; 13: 1032–1036.[Abstract/Free Full Text]

47. Ascherio A, Willett WC. Health effects of trans fatty acids. Am J Clin Nutr 1997; 66: 1006S-1010S.[Abstract/Free Full Text]

48. Willett WC. Specific fatty acids and risks of breast and prostate cancer: dietary intake. Am J Clin Nutr 1997; 66: 1557S–1563S.[Abstract/Free Full Text]

49. Favero A, Franceschi S, La Vecchia C, Negri E, Conti E, Montella M. Meal frequency and coffee intake in colon cancer. Nutr Cancer 1998; 30: 182–185.[Web of Science][Medline]

50. Michels KB, Ekbom A. Caloric restriction and incidence of breast cancer. JAMA 2004; 291: 1226–1230.[Abstract/Free Full Text]

51. Franceschi S, Favero A, Decarli A et al. Intake of macronutrients and the risk of breast cancer. Lancet 1996; 347: 1351–1356.[CrossRef][Web of Science][Medline]

52. Bruzzi P, Green SB, Byar DP, Brinton LA, Schairer C. Estimating the population attributable risk for multiple risk factors using case–control data. Am J Epidemiol 1985; 122: 904–914.[Abstract/Free Full Text]

53. Mezzetti M, Ferraroni M, Decarli A, La Vecchia C, Benichou J. Software for attributable risk and confidence interval estimation in case–control studies. Comput Biomed Res 1996; 29: 63–75.[CrossRef][Web of Science][Medline]

54. Boyle P, Ferlay J. Cancer incidence and mortality in Europe 2004. Ann Oncol 2005; 16: 481–488.[Abstract/Free Full Text]


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