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Antioxidant intake among Brazilian adults - The Brazilian Osteoporosis Study (BRAZOS): a cross-sectional study



Antioxidant nutrient intake and the lesser formation of free radicals seem to contribute to chronic diseases. The aim of the present study was to evaluate the intake profile of the main dietary antioxidants in a representative sample of the adult Brazilian population and discuss the main consequences of a low intake of these micronutrients on overall health.


The sample comprised 2344 individuals aged 40 years or older from 150 cities and was based on a probabilistic sample from official data. The research was conducted through in-home interviews administered by a team trained for this purpose. Dietary intake information was obtained through 24-h recall. The Nutrition Data System for Research software program was used to analyze data on the intake of vitamins A, C and E, selenium and zinc, which was compared to Dietary Reference Intakes (DRIs). Differences in intake according to sex, anthropometrics, socioeconomic status and region were also evaluated. The SPSS statistical package (version 13) was used for the statistical analysis. P-values < 0.05 were considered significant.


Higher proportions of low intake in relation to recommended values were found for vitamin E (99.7%), vitamin A (92.4%) and vitamin C (85.1%) in both genders. Intake variations were found between different regions, which may reflect cultural habits.


These results should lead to the development of public health policies that encourage educational strategies for improving the intake of micronutrients, which are essential to overall health and prevention of non-communicable diseases.

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In the last 50 years, Brazil has gone through changes in eating habits, with a greater intake of processed foods, meat, oil and vegetable fat as well as a low consumption of fruit, vegetables and cereals [13]. These aspects, together with a sedentary lifestyle, have contributed toward a greater prevalence of obesity and other non-communicable chronic diseases [4] as well as higher disability and mortality rates [5], especially those related to cardiovascular disease [46].

Previous national data demonstrate that only 2 to 3% of total food intake corresponds to fruit, legumes and vegetables [2], which are important sources of nutrients with antioxidant functions. These percentages correspond to approximately one third of the internationally recommended intake for the prevention of non-communicable chronic diseases [7, 9, 11, 12].

Antioxidants are substances that, at low concentrations, retard or minimize the oxidation of oxidable substrates [13]. Among the non-enzymatic antioxidant systems responsible for lesser cellular and molecular oxidative stress, vitamins A, C and E, zinc, and selenium merit particular attention [14]. Oxidative stress is a disorder of the state of equilibrium of the prooxidant/antioxidant system in intact cells, with consequent harm to lipids, proteins, carbohydrates and nucleic acid, leading to cell death [15]. More recently, some authors believe that it is not only an imbalance or a single entity, since redox of plasma GSH/GSSG is not equilibrated with the larger plasma cysteine/cystine (Cys/CySS) pool. Thus, from a mechanistic standpoint, oxidative stress may be better defined as a disruption of redox signaling and control [16, 17].

A number of studies have demonstrated the association between antioxidant nutrient intake and the lesser formation of free radicals as well as aspects related to the pathogenesis and emergence of non-communicable chronic diseases [6, 14, 1820]. On the other hand, none of these studies demonstrated that the supplementation with antioxidants has succeeded in reducing the rate of chronic diseases.

The aim of the present study was to describe the dietary intake of the main antioxidants in a representative sample of the adult Brazilian population and discuss the main consequences of a low intake of these micronutrients on overall health.


A total of 2344 individuals over 40 years of age, residents of rural and urban areas of 150 cities in the country were evaluated in the present cross-sectional study. Individuals of all socioeconomic classes, degrees of schooling, skin colors and types of occupation were included in order to maintain the Brazilian population as representative [1, 21]. The probabilistic sample was selected in three phases, controlled for gender, age and type of occupation [21, 22].

The interviews were held at the residences of the interviewees and administered face to face. Interviewers carried out interviews seven days a week during the entire day and evening. The residences were selected randomly. Individuals with cognitive disabilities (neurological diseases and dementia) who could provide dubious information were excluded from the study. All of the other diseases, including hypertension and diabetes, as well as concomitant medications and lifestyle habits (smoking, physical activity and alcohol intake) were not considered as exclusion criteria. Since these conditions may modify the needs of antioxidants, several statistical adjustements were performed to correct the possible confounders. Moreover, patients taking calcium and vitamin D as well as multivitamin or other dietary supplements were excluded of this nutritional analysis.

Anthropometric evaluation involved the determination of weight (kg) and height (m) using a portable digital scale and metric tape, respectively. The body mass index (BMI) was calculated by body weight divided by height squared (kg/m2). The classification of nutritional state was determined based on the criteria proposed by the World Health Organization [23].

Food intake was evaluated based on 24-h recall. The interviewers were trained by a nutritionist specialized in the application of eating habit surveys. The questionnaires of individuals with a calorie intake below 400 Kcal or above 5500 Kcal were excluded. The data were analyzed with the aid of the Nutrition Data System for Research software program [24], which uses the food composition table of the US Department of Agriculture (USDA) as its database. Dietary energy and micronutrient intake was then evaluated in relation to antioxidant function, such as vitamins A, C and E, selenium, and zinc. Food supplement intake was considered and used in the final evaluation. Data on macronutrients and micronutrients related to bone health have recently been published [22, 25].

For all analyses, adjustments for the energy of the diet were made based on the residual nutrient method proposed by Willett and Stampfer [26]. Dietary intake was analyzed considering the different characteristics of the population: gender, age, nutritional state, physical activity levels, region and socioeconomic status in order to correct possible confounders. Furthermore, all questionnaires were revised by an independent supervisor and underwent continuous process of criticism and consistency. Inconsistently filled questionnaires were returned for correction. About 25% of the questionnaires were verified in loco or post hoc by phone call. The Dietary Reference Intakes (DRIs) [810] were used as the reference values, considering age and gender.

All participants received an explanation of the goals and outcomes of this study and signed terms of informed consent. The study received approval from the Ethics Committee of the Universidade Federal de São Paulo/ Escola Paulista de Medicina, Brazil.

Statistical analyses were performed using the SPSS statistical package for Windows (version 13.0). The descriptive data were expressed as mean and standard deviation for numerical variables and percentage for qualitative variables. The Student's t-test was used for the comparison of numerical variables between groups. Analysis of variance (ANOVA) was used for multiple comparisons of numerical variables between three or more groups. When significant differences were found in the numerical variables between three or more groups, Tukey test was applied for each pair of variables separately in order to identify what levels differed between one another by calculating the adjusted p-value. The Kolmogorov-Smirnov test was used in all analyses to ensure the normal distribution of the nutrients. Either the chi-square test or Fisher's exact test was used to determine associations between categorical variables. For all analyses, p-values less than 0.05 were considered statistically significant.


The sample was made up of 2344 individuals, 693 (29.6%) of whom were men and 1651 (70.4%) of whom were women. Mean age was 58.4 ± 12.8 and 60.1 ± 13.7 years for males and females, respectively. The largest portion of the individuals was over 51 years of age and was therefore at greater risk of non-communicable chronic diseases, especially osteoporosis. Geographic and socioeconomic distributions simulated the official data of the Brazilian Institute of Geography and Statistics [1] and National Home Sampling Survey [21]. Based on nutritional state (determined by the BMI), there was a high frequency of individuals with overweight and obesity (57.5%), particularly in the male gender (Table 1). There were no significant differences in nutritional state in relation to socioeconomic class or region of the country.

Table 1 General characteristics of Brazilian adults

With the exception of vitamin C there were significant differences in intakes of all nutrients between genders. Men had a higher mean intake of vitamin E and zinc, while women had higher intakes of vitamin A and selenium (Table 2).

Table 2 Daily intake of antioxidants in Brazilian adults

A greater intake of selenium and vitamin A was found in the northern region. Vitamin C ingestion was significantly higher in the northeastern region. There was a greater intake of vitamin E in the central-western region, with a similar intake of these nutrients in the southeastern region. The southern and central-western regions had a greater intake of zinc (Table 3).

Table 3 Daily intake of antioxidants in Brazilian adults according to macro-region

The association between antioxidant intake and nutritional state was significant only for zinc, which was higher among individuals with a normal nutritional state than those with overweight or obesity (Table 4).

Table 4 Daily intake of antioxidants in Brazilian adults according to nutritional state

There was a high proportion of individuals with low intake of all antioxidant nutrients, with the exception of selenium. The highest proportion of individuals with low daily intake was for vitamin E, followed by vitamin A. A greater proportion of men had a low intake of zinc and selenium. Although we found a similar mean intake of vitamin C for men and women as shown in Table 2, the proportion of men with lower intake was significantly higher (Table 5).

Table 5 Proportion of Brazilian adults with low antioxidant intake based on DRI recommendations for gender

There was no statistically significant difference in the proportion of individuals with low dietary intake of vitamin A, vitamin E, and zinc in relation to region of the country. Although mean intake was below that recommended by the DRIs, there was a lower proportion of individuals with low vitamin C intake in the northeastern region. There is a lower proportion of individuals with low selenium intake in the entire country, especially in the southern region (p < 0.05) (Table 6).

Table 6 Proportion of Brazilian adults with low antioxidant intake according to geographic region

Based on the presence of fractures due to bone frailty, there was no significant association with the intake of any of antioxidants investigated (data not shown). The same was true regarding the intake of macronutrients and micronutrients related to bone health (calcium, phosphorus, magnesium, vitamins D, K and A) [22, 25].

In general, a greater proportion of individuals with overweight or obesity had low vitamin A intake (Table 7). There were no significant differences regarding the intake of the other antioxidants.

Table 7 Proportion of Brazilian adults with low antioxidant intake according to nutritional state


The results of the present study demonstrate that, while there was a difference in dietary antioxidant intake between Brazilian men and women, mean vitamin A and vitamin E intake was below the reference values, regardless of gender, age, skin color, economic status, social class, nutritional state and region of the country.

Brazil has been following the worldwide tendency of an extended life expectancy and ageing of the population [27, 28]. The low intake of antioxidants, especially among individuals over 60 years of age, can have serious public health consequences. In elderly individuals, besides the reduction in the capacity to prevent and remove oxidation products, there is also a greater possibility of generating reactive oxygen species and a lesser dietary antioxidant intake related to a series of factors inherent to ageing, such as a reduction in ingestion and the absorption capacity of the digestive tract [27, 29]. Thus, the low intake identified in the BRAZOS study may be an indicator that antioxidant intake should be improved.

In the present study, Brazilian people had significantly lower intakes of antioxidants. This may be consequence of consumption underreporting. However, other factors can particularly affect the intake. The simple fact of living longer is associated with less functional abilities, and other conditions, i.e. being widowed and with children living geographically apart can reduce motivation for cooking. Financial issues, such as living on a fixed/low income, increased dependence on social security or pension may also contribute to a greater nutrient inadequacy [30].

Currently, obesity is considered the second greatest cause of avoidable death in modern society. According to data from the 2002-2003 Brazilian Family Budget Survey [2], 40.6% of the population is overweight, with greater prevalence among individuals between 50 and 70 years of age. The BRAZOS study reveals a similar frequency of overweight and obesity (57.7%) among men and women over 40 years of age [22, 23]. Obesity and the consequent non-communicable chronic diseases stemming from it do not only affect the mortality rate, but are also associated to concomitant diseases that represent a huge economic burden on the healthcare system and society alike. Costs with care and medication are significantly higher for patients with excess weight, increasing with each unit of body mass index in the shape of a "J" curve [31].

In western societies, the increase in obesity and associated chronic disease has been related to an increase in calorie intake stemming from the choice of unbalanced diets, the intake of foods with a high energy density rich in fats and carbohydrates [32] as well as a progressive increase in the portions of food [6, 3234]. It should be stressed that the greater total food and calorie intake by obese individuals is not necessarily associated to the consumption of foods that are a source of micronutrients, as evidenced in the present study. In general, there is an insufficient intake of sources of vitamins and minerals, which, in the long run, could increase the risk of the development or aggravation of metabolic disorders.

Conversely, the relation between anthropometric nutritional state and food intake data or the concentrations of vitamins and minerals is controversial. A number of studies have found lower serum levels of carotenoids in obese individuals in comparison to individuals within the ideal weight range, with no significant difference regarding food intake [31, 3538]. Thus, greater serum inadequacy of these antioxidants is believed to be associated with a greater metabolic demand rather than oxidative stress in obese individuals [39].

Traditionally, vitamin A deficiency is related to alterations in visual acuity and the immune system. Its role as a modulator of fat tissue, causing greater adipogenesis, has recently been demonstrated [40]. Moreover, individuals with a lower plasma concentration of this vitamin may be at greater risk for cardiovascular mortality [41], as vitamin A participates in the prevention and slowing of the atherogenesis process through the inhibition of the oxidation of LDL-cholesterol and a reduction in the formation of foam cells [20, 42]. The data from the present study corroborate previous studies carried out in Bambuí (Minas Gerais, Brazil) [43] and Ponta Porã (Mato Grosso do Sul, Brazil) [44] regarding the high proportion of individuals with low vitamin A intake (92.4%, 99.8% and 87.5%, respectively). The most likely explanation for this finding, even in regions with a large amount of food sources of this vitamin, such as the northern and northeastern regions, is more related to cultural and eating habits than economic factors [45, 46]. According to the National Demographic Children's and Women's Health Survey [47], The greatest prevalence of vitamin A deficiency was found in the southeastern region and the lowest was found in the northern region.

Vitamin E is a lipophilic antioxidant in cell membranes and has considerable importance to the neutralization of peroxynitrites and protection from oxidative stress, particularly the sweeping away of free radicals [10]. This is the first study to evaluate the dietary intake of vitamin E among the Brazilian population. Two surveys in the United States found intakes of vitamin E superior to the values found in our study. The Third National Health and Nutrition Examination Survey (NHANES III 1988-94) reported a median intake for men and women (31 to 50 years old) of 11.7 mg and 9.1 mg, respectively, while the Continuing Survey of Food Intakes by Individuals (CSFII 1994-96) described lower median intake in this same age (9.3 mg for men and 6.8 mg for women) [9, 48]. A British cohort study that evaluated vitamin intake at 4 and 43 years of age identified that those with the lower intake had higher risk for hypertension and higher waist circumference. In this study, the highest intake of vitamin E, both in childhood and adulthood, was found in women (57%) [49]. These findings are different from our results, which indicate similar intake in both genders. In another study, Morris et al found that higher intake of vitamin E, from both food and supplements, was associated with lesser change in cognitive score/year in elderly [50]. In our study, the mean intake was similar to the values reported for median intakes in the lower quintile.

In order to achieve the current recommendation for vitamin E intake proposed by the DRIs, it is necessary to consume large quantities of food sources of this vitamin, such as oils, oil-rich foods and whole-grain cereals [51, 52], which are also a source of unsaturated fatty acids. Thus, a diet rich in fruit and vegetables, but with a low intake of these food sources, likely contains less than 15 mg of α-tocopherol. Some of these foods, such as nuts, are generally not part of Brazilian cultural habits. Soybean oil and margarine are the main sources of fats in Brazil [2], and vitamin E requirements increase as polyunsaturated fats intake increases. Furthermore, a diet rich in fats/ oils may not be of advantage due to their high-energy or caloric value [9]. The supplementation or fortification of foods with vitamin E may be an interesting strategy for improving dietary adequacy [53, 54]. However, it also should be taken into consideration that vitamin E is a difficult element for assessing. Low intakes may be due to underreporting of energy and consequently of fat intake, its primary source, or difficulty in estimating amounts of oils and fats added to food preparation and actual amount absorbed into the cooked product [9].

Selenium is an essential component for the formation of glutathione peroxydase, which is an enzyme involved in the detoxification of hydrogen peroxide and lipid hydroperoxidation as well as an important co-enzyme for the synthesis of proteins related to the immune and neurophysiological systems [55]. In the BRAZOS study, we found a small proportion of individuals (13.4%) with a low intake of this micronutrient, even lower than that reported by Fernandes et al. (21.1%) in adults with metabolic syndrome [33]. However, caution should be exercised when analyzing this finding, as the amount of selenium in foods is related to its presence in the soil and the amount found in a given food source differs depending on its region of origin [56]. For instance, in the case of the Brazil nut, which is an excellent source of this mineral, Freitas et al. [57] identified contents ranging from 0.003 mg to 5.12 mg in 100 g (range of 1:17000). Moreover, studies have found that the states of São Paulo and Mato Grosso have lower concentrations of this nutrient in the soil [58]. In the present study, selenium intake was highest in the northern region, probably due to the greater consumption of fish and cashews.

More than half of the sample, especially those over 60 years of age (data not shown) had an insufficient zinc intake, which corroborates the findings described by Cozzolino [58]. Rats with zinc deficiency have a reduced tolerance to glucose with no alteration in insulin production in response to glucose injection [59]. Likewise, individuals with type II diabetes may have a lower serum level of zinc [60]. More recently, Marreiro et al. [61] found low plasma concentrations of zinc in obese individuals and demonstrated that the supplementation of this mineral reduces insulin resistance.

Vitamin C (ascorbic acid) is one of the most important hydrosoluble antioxidants. It is capable of inhibiting the formation of hydroxyl free radicals and protecting from the peroxidation of lipids and LDL by sequestering peroxyl radicals [62] in joint action with vitamin E [15]. It should be stressed that the proportion of individuals with low vitamin C and E intake may be underestimated, as the percentage of regular smokers was 25% [25], which is a condition that increases the need for these vitamins [63].

The present study has limitations that should be considered. Incomplete information about micronutrients in software's database should always be accounted for since the American nutritional reference database used does not include the regional peculiarities of some typical Brazilian foods. However, the researchers took care to adjust the nutritional aspects by means of a laboratory analysis of foods reported by the population, such as regional fruit, dishes, spices, delicacies, etc. Another important aspect is there was no extrapolation to other age groups and/or stages of life, as only individuals over 40 years of age were included. Although an adequate data collection method for the estimation of mean dietary intake [64], the evaluation of intake based on a single 24-hour recall does not reflect habitual or long-term intake and does not allow an analysis of intake intra-variability. Moreover, although mean nutrient intake is adequate for the description of intake among groups, it does not allow comparisons with reference values (EAR) for the identification of the prevalence of deficiencies. Other substances not evaluated in this study should be considered in further analyzes due to their role in modulating oxidative stress, such as copper, manganese, as well as that bioactive. Finally, plasma concentrations of the antioxidants were not determined, which does not allow ensuring the clinical outcome.


The BRAZOS study revealed low dietary antioxidant intake in the adult Brazilian population, regardless of social class, economic status, region of the country or skin color. These data suggest that cultural habits and food choices seem to be the most determinant factors of the inadequate intake of micronutrients that are essential to overall health. The best medium and long-term public health strategy for improving the low dietary intake of nutrients is an adequate nutrition education policy in Brazil. Measures for fortifying foods and supplementation, in special cases, as well as the stimulus to guarantee on the availability of antioxidant-rich food, such as fruits and vegetables, could also have a substantial impact on minimizing inadequate nutrient intake. However, prospective studies are needed to demonstrate the association of these findings with a greater risk of non-communicable chronic diseases, especially obesity and osteoporosis.

Authors' information

Marcelo M Pinheiro: Assistant-Doctor, Rheumatology Sector, Federal University of Sao Paulo/ Paulista School of Medicine (Unifesp/ EPM), Brazil Rozana M Ciconelli: Assistant-Doctor, Paulista Center for Health Economics, Unifesp/ EPM, Brazil

Gabriela Villaça Chaves: Master in Internal Medicine, Doctoral student in Internal Medicine, Researcher at the Micronutrient Research Center, Josué de Castro Nutrition Institute, Federal University of Rio de Janeiro, Brazil

Luana Aquino: Master in Human Nutrition, Researcher at the Micronutrient Research Center, Josué de Castro Nutrition Institute, Federal University of Rio de Janeiro, Brazil

Claudia R Juzwiak: Doctor of Science, Adjunct Professor, Department of Health, Education and Society, Nutrition Course, Unifesp/Baixada Santista Campus, Brazil

Patrícia Souza Genaro: Doctor in Public Health, Post-Doc student, Rheumatology Division, Federal University of Sao Paulo, Unifesp/ EPM, Brazil

Marcos Bosi Ferraz: Adjunct Professor and Coordinator of the Paulista Center for Health Economics, Unifesp/ EPM, Brazil


  1. Instituto Brasileiro de Geografia e Estatística. 2000, []

  2. Instituto Brasileiro de Geografia e Estatística: Pesquisa de orçamentos familiares 2002-2003: Análise da disponibilidade domiciliar de alimentos e do estado nutricional no Brasil. 2004, Rio de Janeiro: Ministério do Planejamento e Orçamento/IBGE

    Google Scholar 

  3. Shetty P, Shimidhuber J: Introductory lecture the epidemiology and determinants of obesity in developed and developing countries. Int J Vitam Nutr Res. 2006, 4: 157-62.

    Article  Google Scholar 

  4. [WHO]. World Health Organization: The world report 2002: reducing risks, promoting healthy life. 2002, Geneve: World Health Organization

    Google Scholar 

  5. [WHO] World Health Organization: Prevention of cardiovascular disease: pocket guidelines for assessment and management of cardiovascular risk. 2007, Geneve

    Google Scholar 

  6. Riccioni G, Bucciarelli T, Mancini B, Corradi F, Di Ilio C, Mattei PA, D'Orazio N: Antioxidant vitamin supplementation in cardiovascular diseases. Ann Clin Lab Sci. 2007, 37: 89-95.

    CAS  PubMed  Google Scholar 

  7. Department of Health and Human Services: National Center for Health Statistics. Healthy people 2000: national health promotion and disease prevention objectives. 1991, Washington

    Google Scholar 

  8. [IOM] Institute of Medicine: Dietary Reference Intakes for thiamin, riboflavin, niacin, vitamin B6, folate, vitamin B12, panthotenic acid. 1998, Washington, D.C.: National Academy Press

    Google Scholar 

  9. [IOM] Institute of Medicine: Dietary reference intakes. Vitamin C, Vitamin E, Selenium, and Carotenoids. 2000, Washington, D.C.: National Academy Press

    Google Scholar 

  10. [IOM] Institute of Medicine: Dietary reference intakes. Vitamin A, Vitamin K, Arsenic, Boron, Chromium, Copper, Iodine, Iron, Manganese, Molybdenum, Nickel, Silicon, Vanadium, and Zinc. 2001, Washington, D.C.: National Academy Press

    Google Scholar 

  11. Després JP, Pascot A, Lemieux I: Risk factors associated with obesity: a metabolic perspective. Ann Endocrinol. 2000, 61 (Suppl 6): 31-38.

    Google Scholar 

  12. Schaefer EJ: Lipoproteins, nutrition, and heart disease. Am J Clin Nutr. 2002, 75: 191-212.

    CAS  PubMed  Google Scholar 

  13. Halliwell B, Aeschbach R, Löliger J, Aruoma OI: The characterization of antioxidants. Food Chem Toxicol. 1995, 33: 601-17. 10.1016/0278-6915(95)00024-V.

    Article  CAS  PubMed  Google Scholar 

  14. Berger MM: Can oxidative damage be treated nutritionally?. Clin Nutr. 2005, 24: 172-83. 10.1016/j.clnu.2004.10.003.

    Article  CAS  PubMed  Google Scholar 

  15. Clark SF: The biochemistry of antioxidants revisited. Nutr Clin Pract. 2002, 17: 5-17. 10.1177/011542650201700105.

    Article  PubMed  Google Scholar 

  16. Jones DP: Redefining oxidative stress. Antioxid Redox Signal. 2006, 8 (9-10): 1865-79. 10.1089/ars.2006.8.1865.

    Article  CAS  PubMed  Google Scholar 

  17. Sies H: Biological redox systems and oxidative stress. Cell Mol Life Sci. 2007, 64 (17): 2181-8. 10.1007/s00018-007-7230-8.

    Article  CAS  PubMed  Google Scholar 

  18. Czernichow S, Hercberg S: Interventional studies concerning the role of antioxidants vitamins in cardiovascular diseases; a review. J Nutrition Health & Aging. 2001, 5: 188-195.

    CAS  Google Scholar 

  19. Rissamen TH, Voutilainem S, Nyyssonen K, Salonen R, Kaplan GA, Salonen JT: Serun lycone concentrations and carotid atherosclerosis: the Kuopio ischaemic heart disease risk factor study. Am J Clin Nutr. 2003, 77: 133-38.

    Google Scholar 

  20. Sesso HD, Buring JE, Norkus EP, Gaziano JM: Plasma lycopene, other carotenoids, and retinol and the risk of cardiovascular disease in women. Am J Clin Nutr. 2004, 79: 47-53.

    CAS  PubMed  Google Scholar 

  21. National Home Sampling Survey (PNAD). 2003, []

  22. Pinheiro MM, Scuch NJ, Genaro PS, Ciconelli RM, Ferraz MB, Martini LA: Nutrient intakes related to osteoporotic fractures in men and women - The Brazilian Osteoporosis Study (BRAZOS). Nutr J. 2009, 8: 6-10.1186/1475-2891-8-6.

    Article  PubMed  PubMed Central  Google Scholar 

  23. [WHO] World Health Organization: Obesity: preventing and managing the global epidemic. Report of WHO consultation on obesity. 1998, World health organization, Geneva

    Google Scholar 

  24. Nutrition Coordinating Center (NCC), University of Minnesota: Nutrition Data System for Research-NDS-R [programa de computador]. 2005, University of Minnesota: Minneapolis

    Google Scholar 

  25. Pinheiro MM, Ciconelli RM, Martini LA, Ferraz MB: Clinical risk factors for osteoporotic fractures in Brazilian women and men: The Brazilian Osteoporosis Study (BRAZOS). Osteoporos Int. 2009, 20: 399-408. 10.1007/s00198-008-0680-5.

    Article  CAS  PubMed  Google Scholar 

  26. Willett W, Stampfer M: Implications of total energy intake for epidemiological analyses. Nutritional epidemiology. Edited by: Willett W. 1998, New York: Oxford University Press, 273-301. 2

    Chapter  Google Scholar 

  27. Campos MTFS, Monteiro JBR, Ornelas APRC: Fatores que afetam o consumo alimentar e a Nutrição do idoso. Rev Nutr Campinas. 2000, 13: 157-165.

    Google Scholar 

  28. Lebrão ML, Laurenti R: Saúde, bem-estar e envelhecimento: o estudo SABE no municipio de São Paulo. Rev Bras Epidemiol. 2005, 8: 127-41.

    Article  Google Scholar 

  29. Beckman KB, Ames BN: The free radical theory of aging matures. Physiol Rev. 1998, 78: 547-81.

    CAS  PubMed  Google Scholar 

  30. Chernoff R: Micronutrients requirements in older women. Am J Clin Nutr. 2005, 81 (suppl): 1240S-5S.

    CAS  PubMed  Google Scholar 

  31. Ancona-Lopez F, Juzwiak CR: Social impact of modern diet and tendencies. Food, diet, health: past, present and future tendencies. Edited by: Guiné RP. 2010, Hanppange, New York: Nova Science Publishers

    Google Scholar 

  32. Young LR, Nestle M: The contribution of expanding portion sizes to the US obesity epidemic. Am J Public Health. 2002, 92: 246-9. 10.2105/AJPH.92.2.246.

    Article  PubMed  PubMed Central  Google Scholar 

  33. Fernandes M, Paes C, Nogueira C, Souza G, Aquino L, Borges F, Ramalho A: Perfil de consumo de nutrientes antioxidantes em pacientes com síndrome metabólica. Rev Ciênc Méd. 2007, 16: 209-19.

    Google Scholar 

  34. Neumann AI, Martins IS, Marcopito LF, Araujo EA: Dietary patterns associated with risk factors for cardiovascular disease in a Brazilian city. Rev Panam Salud Publica. 2007, 22: 329-39. 10.1590/S1020-49892007001000006.

    Article  PubMed  Google Scholar 

  35. Neuhouser ML, Rock CL, Eldridge AL, et al: Serum concentrations of retinol, alfa-tocoferol and carotenoids are influenced by diet, race and obesity in a sample of health adolescents. J Nutr. 2001, 131: 2184-219.

    CAS  PubMed  Google Scholar 

  36. Sarni RS, Kochi C, et al: Vitamin A: blood level and dietetics intake in stunted children and adolescents without hormonal disease. Rev Assoc Med Bras. 2002, 48: 48-53. 10.1590/S0104-42302002000100032.

    Article  PubMed  Google Scholar 

  37. Sarni RS, Kochi C, et al: Impact of vitamin A megadose supplementation on the anthropometry of children and adolescents with non-hormonal statural deficit: a double-blind and randomized clinical study. Int J Vitam Nutr Res. 2003, 73: 303-11. 10.1024/0300-9831.73.4.303.

    Article  CAS  PubMed  Google Scholar 

  38. Silva LSVL, Veiga GVV, Ramalho RA: Association of serum concentrations of retinol and carotenoids with overweight in children and adolescents. Nutrition. 2007, 23: 392-97. 10.1016/j.nut.2007.02.009.

    Article  Google Scholar 

  39. Matsuoka H: Endothelial dysfunction associated with oxidative stress in human. Diab Res Clin Pract. 2001, 54: 65-72.

    Article  Google Scholar 

  40. Jeyakumar SM, Vajerswaria A, Giridharan NV: Chronic dietary vitamin A supplementation regulates obesity: in obese mutant rat model of WNIN/Ob strain. Obesity research. J Mol Endocrinol. 2006, 35: 391-98.

    Article  Google Scholar 

  41. Ochoa JJ, Vilchez MJ, Mataix J, Ibáñez-Quiles S, Palacios MA, Muñoz-Hoyos A: Oxidative stress in patients undergoing cardiac surgery: comparative study of revascularization and valve replacement procedures. J Surg Res. 2003, 111: 248-54. 10.1016/S0022-4804(03)00106-9.

    Article  CAS  PubMed  Google Scholar 

  42. Delport R: Antioxidants and coronary artery disease risk in South African males. Clinical Chimical Acta. 1998, 278: 55-60. 10.1016/S0009-8981(98)00131-4.

    Article  CAS  Google Scholar 

  43. Lopes ACS, Caiaffa WT, Sichieri R, Mingoti SA, Lima-Costa MF: Consumo de nutrientes em adultos e idosos em estudo de base populacional: Projeto Bambuí. Cad Saúde Pública. 2005, 21: 1201-09.

    Article  PubMed  Google Scholar 

  44. Fietz VR: Estado nutricional, consumo de alimentos e condições socioeconômicas das famílias de assentamento rural em Mato Grosso do Sul. PhD thesis. 2007, Faculdade de Engenharia de Alimentos. Universidade de Campinas

    Google Scholar 

  45. Ramalho RA, Flores H, Accioly E, Saunders C: Vitamin A Deficiency in Brasil. Revista da Sociedad Iberoamericana de Información Científica. 2005, 1: 1-9.

    Google Scholar 

  46. Ramalho RA: Diversificação Alimentar como parte de um Programa de Combate à Deficiência de Vitamina A. Nutrição em Pauta. 2008, 88: 5-9.

    Google Scholar 

  47. Ministério da Saúde: Pesquisa Nacional de Demografia da Saúde da Crianças e da Mulher. []

  48. Dixon LB, Winkleby MA, Radimer KL: Dietary intakes and serum nutrients differ between adults from food-insufficient and food-sufficient families: Third National Health and Nutrition Examination Survey, 1988-1994. J Nutr. 2001, 131 (4): 1232-46.

    CAS  PubMed  Google Scholar 

  49. Mishra GD, Malik NS, Paul AA, Wadsworth MEJ, Bolton-Smith C: Childhood and adult dietary vitamin E intake and cardiovascular risk factor in mid life in the 1946 British Birth Cohort. Eur J Clin Nutr. 2003, 57: 1418-25. 10.1038/sj.ejcn.1601706.

    Article  CAS  PubMed  Google Scholar 

  50. Morris MC, Evans DA, Bienias JL, Tangney CC, Wilson RS: Vitamin E and cognitive decline in older persons. Arch Neurol. 2002, 59: 1125-32. 10.1001/archneur.59.7.1125.

    Article  PubMed  Google Scholar 

  51. Horwitt MK: Critique of the requirement for vitamin E. Am J Clin Nutr. 2001, 73: 1003-5.

    CAS  PubMed  Google Scholar 

  52. Traber MG: Vitamin E: too much or not enough?. Am J Clin Nutr. 2001, 73: 987-98.

    Google Scholar 

  53. Beitz R, Mensink GBM, Fischer B, Thamm M: Vitamins dietary intake and intake from dietary supplements in Germany. Eur J Clin Nutr. 2002, 56: 539-45. 10.1038/sj.ejcn.1601346.

    Article  CAS  PubMed  Google Scholar 

  54. Sichert-Hellert W, Kersting M, Manz F: Changes in time-trends of nutrient intake from fortified and non-fortified food in German children and adolescents: 15 year results of the DONALD Study. Eur J Nutr. 2001, 40: 49-55. 10.1007/PL00007385.

    Article  CAS  PubMed  Google Scholar 

  55. Navarro-Alarcon M, Cabrera-Vique C: Selenium in food and the human body: a review. Sci Total Environ. 2008, 400: 115-41. 10.1016/j.scitotenv.2008.06.024.

    Article  CAS  PubMed  Google Scholar 

  56. Gonzaga IB, Martens A, Cozzolino MF: Biodisponibilidade de nutrientes. 2005, São Paulo: Manole

    Google Scholar 

  57. Freitas SC, Gonçalves EB: Meta-análise do teor de selênio em castanha-do-brasil. Braz J Food Technol. 2008, 11: 54-62.

    Google Scholar 

  58. Cozzolino SMF: Deficiências de minerais. Estudos Avançados. 2007, 21: 119-26.

    Article  Google Scholar 

  59. Boquist L, Lernmark A: Effects on the endocrine pancreas in Chinese Hamsters fed zinc deficient diets. Acta Pathol Microbiol Scand. 1969, 6: 215-

    Google Scholar 

  60. Soinio M, Marniemi J, Laakso M, Pyörälä K, Lehto S, Rönnemaa T: Serum zinc level and coronary heart disease events in patients with type 2 diabetes. Diabetes Care. 2007, 30: 523-8. 10.2337/dc06-1682.

    Article  CAS  PubMed  Google Scholar 

  61. Marreiro DN, Fisberg M, Cozzolino SM: Zinc nutritional status and its relationships with hyperinsulinemia in obese children and adolescents. Biol Trace Elem Res. 2004, 100: 137-49. 10.1385/BTER:100:2:137.

    Article  PubMed  Google Scholar 

  62. Shills ME, Olson JA, Shike M, Ross AC: Modern Nutrition in Health and Disease. 1999, Dona Balado

    Google Scholar 

  63. Madruga de Oliveira A, Rondó PH, Barros SP: Concentrations of ascorbic acid in the plasma of pregnant smokers and non-smokers and their newborns. Int J Vitam Nutr Res. 2004, 74: 193-8. 10.1024/0300-9831.74.3.193.

    Article  CAS  PubMed  Google Scholar 

  64. Hoffmann K, Boeing H, Dufour A, Volatier JL, Telman J, Virtanen M, et al: Estimating the distribution of usual dietary intake by short-term measurements. Eur J Clin Nutr. 2002, 56: 53-62.

    Article  Google Scholar 

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We would like to thank Prof. Lígia A Martini by relevant scientific considerations and analysis of the nutritional data in this study (BRAZOS), as well as to Nutrition Department of Public Health School, São Paulo University (FSP/ USP).

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Correspondence to Marcelo Medeiros Pinheiro.

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Competing interests

This study was supported by a grant from Wyeth Consumer Healthcare.

Authors' contributions

MMP - has made substantial contributions to acquisition of data, analysis and interpretation of data also have been involved in drafting the manuscript. RMC - has made substantial contributions to acquisition of data, analysis and interpretation of data also have been involved in drafting the manuscript. GVC - has made substantial contributions to conception and design of data and also analysis and interpretation of data. LA - has been involved in drafting the manuscript or revising it critically for important intellectual content. CRJ - has been involved in drafting the manuscript, made substantial contributions to conception and design and revising it critically for important intellectual content. PSG - has been involved in training of interviewers on nutritional issues and revising final version of the manuscript. MBF - has made substantial contributions to conception and design, have been involved in drafting the manuscript and also revising it critically for important intellectual content and have given final approval of the version to be published. All authors read and approved the final manuscript.

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Pinheiro, M.M., Ciconelli, R.M., Chaves, G.V. et al. Antioxidant intake among Brazilian adults - The Brazilian Osteoporosis Study (BRAZOS): a cross-sectional study. Nutr J 10, 39 (2011).

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