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Magnesium intake in a Longitudinal Study of Adult Health: associated factors and the main food sources

Ingestão de magnésio no Estudo Longitudinal de Saúde do Adulto: fatores associados e os principais alimentos contribuintes

Abstract

This study aimed to identify the sociodemographic and lifestyle factors associated with magnesium intake and describe the main food sources in the Brazilian Longitudinal Study of Adult Health (ELSA-Brazil). This observational, cross-sectional study was conducted using the baseline data from the ELSA-Brazil (2008-2010). Associations between usual magnesium intake and sociodemographic and lifestyle factors were analyzed using multiple linear regression. Food sources were identified by calculating the percentage contribution of each FFQ item to the amount of magnesium provided by all foods. The analysis was performed using Stata® software (version 12), assuming a statistical significance level of 5%. The top food sources to magnesium intake were as follows: beans, oats, nuts, white rice, orange, French bread, cooked fish, boneless meat, whole milk, and whole wheat bread. There were positive associations between magnesium intake and female sex; age ≥60 years; self-reported black, indigenous, or brown skin colors; per capita income ≥3 minimum wages, and moderate or vigorous physical activity levels. Sociodemographic and lifestyle factors were associated with magnesium intake among the evaluated individuals.

Key words
Magnesium; Sociodemographic factors; Lifestyle; Food sources

Resumo

O estudo tem por objetivo identificar fatores sociodemográficos e de estilo de vida associados à ingestão de magnésio e descrever seus principais alimentos contribuintes no Estudo Longitudinal de Saúde do Adulto (ELSA-Brasil). Trata-se de um estudo observacional, transversal, desenvolvido com dados da linha de base do ELSA-Brasil (2008-2010). Associações entre a ingestão habitual de magnésio e fatores sociodemográficos e de estilo de vida foram testadas por regressão linear múltipla. Contribuintes alimentares foram identificados a partir do cálculo do porcentual de magnésio fornecido por cada item do QFA em relação quantidade total proveniente de todos os alimentos. Os principais alimentos contribuintes para a ingestão de magnésio foram: feijão, aveia, nozes, arroz branco, laranja, pão francês, peixe cozido, carne sem osso, leite integral e pão integral. Foram encontradas associações positivas entre consumo de magnésio e sexo feminino, faixa etária ≥ 60 anos, cor de pele autodeclarada como negra, indígena ou parda, renda “per capita” ≥ 3 salários mínimos e níveis de atividade física moderado ou vigoroso. Alimentos da dieta tradicional do brasileiro foram os maiores contribuintes para a ingestão de magnésio, que também foi influenciada por fatores sociodemográficos e de estilo de vida.

Palavras-chave
Magnésio; Fatores sociodemográficos; Estilo de vida; Alimentos contribuintes

Introduction

Magnesium is the second most abundant intracellular ion and is involved in many metabolic functions, being vital for the activity of more 300 enzymes11 Pickering G, Morel V, Simen E, Cardot JM, Moustafa F, Delage N, Picard P, Eschalier S, Boulliau S, Dubray C. Oral magnesium treatment in patients with neuropathic pain: A randomized clinical trial. Magnes Res 2011; 24(2):28-35.. It plays an important role in ATP synthesis and activates almost all glycolytic enzymes and those of citric acid cycle. It is related to cell membrane permeability and electrical activity, besides being important for bone mineralization, muscle relaxation, and neurotransmission22 Helena Monteiro T, Vannucchi H. Magnésio. In: Funções Plenamente Reconhecidas de Nutrientes. São Paulo: ILSI Brasil; 2010. [cited 2019 Jul 2]. Available from: http://ilsi.org/brasil/wp-content/uploads/sites/9/2016/05/16-Magnésio.pdf
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3 Bagis S, Karabiber M, AS I, Tamer L, Erdogan C, Atalay A. Is magnesium citrate treatment effective on pain, clinical parameters and functional status in patients with fibromyalgia? Rheumatol Int 2013; 33(1):167-172.
-44 Crosby V, Elin RJ, Twycross R, Mihalyo M, Wilcock A. Magnesium. J Pain Symptom Manage 2013; 45(1):137-144.. Deficiency of this ion can favor the development of various chronic noncommunicable diseases (NCDs), such as metabolic syndrome55 Ford ES, Li C, McGuire LC, Mokdad AH, Liu S. Intake of dietary magnesium and the prevalence of the metabolic syndrome among U.S. adults. Obesity (Silver Spring) 2007; 15(5):1139-1146.

6 He K, Liu K, Daviglus ML, Morris SJ, Loria CM, Van Horn L, Jacobs Junior DR, Savage PJ. Magnesium intake and incidence of metabolic syndrome among young adults. Circulation 2006; 113(13):1675-1682.
-77 McKeown NM, Jacques PF, Zhang XL, Juan W, Sahyoun NR. Dietary magnesium intake is related to metabolic syndrome in older Americans. Eur J Nutr 2008; 47(4):210-216., type 2 diabetes mellitus88 Song Y, Manson JE, Buring JE, Liu S. Dietary Magnesium Intake in Relation to Plasma Insulin Levels and Risk of Type 2 Diabetes in Women. Diabetes Care. 2004; 27(1):59-65.,99 Lopez-Ridaura R, Willett WC, Rimm EB, Liu S, Stampfer MJ, Manson JE, Hu FB. Magnesium Intake and Risk of Type 2 Diabetes in Men and Women. Diabetes Care 2004; 27(1):134-140., fibromyalgia1010 King JL, Miller RJ, Blue JP, O'Brien WD, Erdman JW. Inadequate dietary magnesium intake increases atherosclerotic plaque development in rabbits. Nutr Res 2009; 29(5):343-349., hypertension88 Song Y, Manson JE, Buring JE, Liu S. Dietary Magnesium Intake in Relation to Plasma Insulin Levels and Risk of Type 2 Diabetes in Women. Diabetes Care. 2004; 27(1):59-65.,1111 Touyz RM. Transient receptor potential melastatin 6 and 7 channels, magnesium transport, and vascular biology: implications in hypertension. AJP Hear Circ Physiol 2007; 294(3):H1103-H1118.,1212 Sontia B, Touyz RM. Role of magnesium in hypertension. Arch Biochem Biophys 2007; 458(1):33-39., osteoporosis1313 Rude RK, Singer FR, Gruber HE. Skeletal and hormonal effects of magnesium deficiency. J Am Coll Nutr 2009; 28(2):131-141., and cardiovascular diseases1414 Rosanoff A, Weaver CM, Rude RK. Suboptimal magnesium status in the United States: Are the health consequences underestimated? Nutr Rev 2012; 70(3):153-164..

The Estimated Average Requirement (EAR)1515 Food and Nutriton Board, IOM. Dietary Reference Intakes (DRIs): Estimated Average Requirements. Nutrition Reviews 2004; 62(10):400-401. of magnesium is between 255 mg and 265 mg for women and between 330 mg/day and 350 mg/day for adult and elderly men. Magnesium is present in dark green vegetables, legumes, oilseeds, milk and dairy products, and whole grains. Fish, meat, and some fruits are the poorest sources of this mineral22 Helena Monteiro T, Vannucchi H. Magnésio. In: Funções Plenamente Reconhecidas de Nutrientes. São Paulo: ILSI Brasil; 2010. [cited 2019 Jul 2]. Available from: http://ilsi.org/brasil/wp-content/uploads/sites/9/2016/05/16-Magnésio.pdf
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. In the United States, 60% of the adult population have insufficient magnesium intake to attend the EAR1616 Agarwal S, Reider C, Brooks JR, Fulgoni VL. Comparison of Prevalence of Inadequate Nutrient Intake Based on Body Weight Status of Adults in the United States: An Analysis of NHANES 2001-2008. J Am Coll Nutr 2015; 34(2):126-134.. This scenario was observed in more than 70% of the Brazilian adult population, according to the 2008-2010 National Food Survey (INA)1717 Instituto Brasileiro de Geografia e Estatística (IBGE). Pesquisa de Orçamentos Familiares: 2008-2009. Análise Do Consumo Alimentar Pessoal No Brasil. Rio de Janeiro: IBGE; 2011..

Food consumption of an individual or a population is strongly influenced by age, sex, income, and schooling1818 Jaime PC, Stopa SR, Oliveira TP, Vieira ML, Szwarcwald CLMD. Prevalence and sociodemographic distribution of healthy eating markers, National Health Survey, Brazil 2013. Epidemiol e Serviços Saúde 2015; 24(2):267-276.

19 Olinto MT, Willett WC, Gigante DP, Victora CG. Sociodemographic and lifestyle characteristics in relation to dietary patterns among young Brazilian adults. Public Health Nutr 2011; 14(1):150-159.
-2020 Estima CCP, Philipp ST, Alvarenga MS. Fatores determinantes de consumo alimentar: por que os indivíduos comem o que comem? Rev Bras Nutr Clin 2009; 24(4):263-268.. In Brazil, family income is positively associated with the consumption of milk, meat, fruits, vegetables, and legumes; however, the consumption of vegetables and legumes is moderate even in the richest stratum of the population1717 Instituto Brasileiro de Geografia e Estatística (IBGE). Pesquisa de Orçamentos Familiares: 2008-2009. Análise Do Consumo Alimentar Pessoal No Brasil. Rio de Janeiro: IBGE; 2011.. Furthermore, some studies reported that families in less favored socioeconomic strata and mothers with lower educational level consume more sweets and products rich in fat2020 Estima CCP, Philipp ST, Alvarenga MS. Fatores determinantes de consumo alimentar: por que os indivíduos comem o que comem? Rev Bras Nutr Clin 2009; 24(4):263-268..

Knowledge about food components of a population diet and the identification of the determinants of nutrient consumption can serve as subsidies for the formulation of public policies for the promotion of healthy eating and of combating NCDs. This study aimed to identify the sociodemographic and lifestyle factors associated with magnesium intake and describe the main foods that contribute to this nutrient among participants of the Longitudinal Study of Adult Health (ELSA-Brazil), the largest multicenter cohort ever recruited for research incidence and risk factors of NCD in the Brazilian population2121 Aquino EML, Barreto SM, Bensenor IM, Carvalho MS, Chor D, Duncan BB, Lotufo PA, Mill JG, Molina Mdel C, Mota EL, Passos VM, Schmidt MI, Szklo M. Brazilian Longitudinal Study of Adult Health (ELSA-Brasil): Objectives and Design. Am J Epidemiol 2012; 175(4):315-324..

Methods

Study population

This observational, cross-sectional study was developed using the baseline data from the ELSA-Brazil. ELSA-Brazil participants were recruited between August 2008 and December 2010. ELSA-Brazil is a cohort of 15,105 participants of both genders, aged 35-74 years, and are active and retired workers from six different states of Brazil: Espírito Santo, Minas Gerais, Bahia, São Paulo, Rio de Janeiro, and Rio Grande do Sul. Data were collected by trained and certified personnel under strict quality control2121 Aquino EML, Barreto SM, Bensenor IM, Carvalho MS, Chor D, Duncan BB, Lotufo PA, Mill JG, Molina Mdel C, Mota EL, Passos VM, Schmidt MI, Szklo M. Brazilian Longitudinal Study of Adult Health (ELSA-Brasil): Objectives and Design. Am J Epidemiol 2012; 175(4):315-324.

22 Schmidt MI, Duncan BB, Mill JG, Lotufo PA, Chor D, Barreto SM, Aquino EM, Passos VM, Matos SM, Molina Mdel C, Carvalho MS, Bensenor IM. Cohort Profile: Longitudinal Study of Adult Health (ELSA-Brasil). Int J Epidemiol 2015; 44(1):68-75.
-2323 Bensenor IM, Griep RH, Pinto KA, Faria CP, Felisbino-Mendes M, Caetano EI, Albuquerque LS, Schmidt MI. Routines of organization of clinical tests and interviews in the ELSA-Brasil investigation center. Rev Saude Publica 2013; 47(Supl. 2):37-47.. Those without food consumption information (n = 24) were excluded from this study, totaling 15,081 participants. Individuals below the 1st percentile and above the 99th percentile of the total energy intake estimates (n = 362) were also disregarded in order to exclude possibly invalid food intake data. Thus, the final study sample consisted of 14,719 individuals.

The ELSA-Brazil was approved by the research ethics committees of all its research centers. All individuals voluntarily participated in this study and signed an informed consent form.

Food consumption assessment

The food frequency questionnaire (FFQ) developed and validated for ELSA-Brazil was used to evaluate the habitual food consumption of participants in the last 12 months2424 Molina MDCB, Benseñor IM, Cardoso LO, Velasquez-Melendez G, Drehmer M, Pereira TS, Faria CP, Melere C, Manato L, Gomes AL, Fonseca MJ, Sichieri R. Reproducibility and relative validity of the Food Frequency Questionnaire used in the ELSA-Brasil. Cad Saude Publica 2013; 29(2):379-389.. This semiquantitative FFQ has 114 food items and is answered by interview. The questions are structured into 3 sections: (1) food/preparations, (2) consumption portion measures, and (3) consumption frequencies, with 8 response options: “more than 3 times/day,” “2-3 times/day, “”once a day,””5-6 times a week,””2-4 times a week, “”once a week,””1-3 times a month,” and “never/almost never.” At the end of the FFQ, participants were asked if they changed their dietary intake or if they did a restrictive diet over the past six months, being the participants able to answer yes or no to this question.

To evaluate energy and nutrient intakes, we used the United States Department of Agriculture (USDA) Food Composition Database, except when its values were outside of the range of 80% to 120% from those described in the Brazilian Table of Food Composition, which cases the latter database was used2424 Molina MDCB, Benseñor IM, Cardoso LO, Velasquez-Melendez G, Drehmer M, Pereira TS, Faria CP, Melere C, Manato L, Gomes AL, Fonseca MJ, Sichieri R. Reproducibility and relative validity of the Food Frequency Questionnaire used in the ELSA-Brasil. Cad Saude Publica 2013; 29(2):379-389.. To reduce the errors associated with dietary measurement, magnesium intake was adjusted by total energy intake using the residue method2525 Willett W. Nutritional epidemiology. Oxford Univ Press 1998; (January):768-772.. Energy-adjusted values were employed both in the stratification of quantiles and linear regression analysis.

Sociodemographic and lifestyle factors

The choice of sociodemographic and lifestyle factors that could influence the dietary pattern was based on previous studies that addressed the determinants of food intake in the Brazilian adult population1818 Jaime PC, Stopa SR, Oliveira TP, Vieira ML, Szwarcwald CLMD. Prevalence and sociodemographic distribution of healthy eating markers, National Health Survey, Brazil 2013. Epidemiol e Serviços Saúde 2015; 24(2):267-276.,1919 Olinto MT, Willett WC, Gigante DP, Victora CG. Sociodemographic and lifestyle characteristics in relation to dietary patterns among young Brazilian adults. Public Health Nutr 2011; 14(1):150-159.. Therefore, sex, age, schooling, income, self-reported skin color, smoking and alcohol habits, nutritional status, and physical activity level were selected for this study.

Participants were classified according to sex as male and female) and according to age as adults (34-59 years) and elderly (≥ 60 years). Schooling was categorized as “complete elementary school,” “complete high school,” and “higher education or postgraduate.” The family income per capita was initially calculated as equivalent to the average minimum wage in the period between 2008 and 2010 (R$ 463.33) and then stratified into < 3 or ≥ 3 minimum wages. The following categories of self-reported skin color proposed by the Brazilian Institute of Geography and Statistics in the demographic census were questioned: “white,” “black,” “brown or mixed,” “yellow,” and “indigenous”2626 Petruccelli JL, Saboia AL, organizadores. Pesquisa sobre as Características Étnico-raciais da População. Rio de Janeiro: IBGE; 2013.. Due the low frequency of yellow and indigenous reporters, these two categories were collapsed for analysis.

Smoking was evaluated using a semi-structured questionnaire about smoking habits at the time of the interview and in the past. Based on this questions, participants were categorized as “non-smokers,” “former smokers,” or “smokers.” Alcohol consumption data (grams of ethanol/day) were obtained from the FFQ. Participants were classified as alcohol “non-consumers” or “consumer” based on the reporting of consumption of any alcoholic beverages in the previous 12 months, irrespective of its frequency or amount.

To assess nutritional status, body mass index (BMI) was calculated and classified according to the World Health Organization criteria: low weight (< 18.5 kg/m2), eutrophia (18.5-24.9 kg/m2), overweight (25-29.9 kg/m2), and obesity (≥ 30 kg/m2)2727 World Health Organization (WHO). Global status report on noncommunicable diseases 2014. Geneva: WHO; 2014.. For the evaluation of physical activity level, we used the International Physical Activity Questionnaire (IPAQ)2828 International Physical Activity Questionniare Group. International physical activity questionnaire short last 7 days self-administered format for use with young and middle aged adults. Res Q Exerc Sport 2002; 71:3., which consist in predetermined questions on frequency and duration of walking as well as moderate and vigorous physical activities at work, commuting, home and leisure times2929 Matsudo S, Araújo T, Matsudo V, Andrade D, Andrade E, Oliveira LC, Braggion G. Questionário internacional de atividade física (IPAQ): estudo de validade e reprodutibilidade no Brasil. Rev Bras Atividade Física Saúde 2001; 6(2):5-18.. For the purposes of this study, we used only the domain of physical activity during leisure time, considering that these types of activities has been more consistently associated with socio-demographic factors, such as income, age, schooling and sex3030 Lindström M, Hanson BS, Ostergren PO. Socioeconomic differences in leisure-time physical activity: the role of social participation and social capital in shaping health related behaviour. Soc Sci Med 2001; 52(3):441-451.. Moreover, physical activity in leisure is most frequently studied in epidemiological surveys3131 Dias-da-Costa JS, Hallal PC, Wells JCK, Daltoé T, Fuchs SC, Menezes AM, Olinto MT. Epidemiology of leisure-time physical activity: a population-based study in southern Brazil. Cad Saude Publica 2005; 21(1):275-282.,3232 Monteiro CA, Conde WL, Matsudo SM, Matsudo VR, Bonseñor IM, Lotufo PA. A descriptive epidemiology of leisure-time physical activity in Brazil, 1996-1997. Rev Panam Salud Publica 2003; 14(4):246-254..

Statistical analysis

The consumption of energy-adjusted magnesium was stratified in quintiles in order to better represent the ranking of dietary magnesium, and sociodemographic and lifestyle factors were described according to the lowest (1st quintile) and highest (5th quintile) levels of its intake. Sociodemographic and lifestyle factors were presented as frequencies and percentages according to the sex of the participants. Pearson’s chi-squared test was used to evaluate the significant associations between variables.

The contribution of food to magnesium intake was calculated according to the methodology proposed by Block et al.3333 Block G, Dresser CM, Hartman AM, Carroll MD. Nutrient sources in the American diet: Quantitative data from the nhanes II survey: II. Macronutrients and fats. Am J Epidemiol 1985; 122(1):27-40.. Magnesium provided by each food item was divided by the total population magnesium intake to obtain the contribution of each food item. Then, the foods were listed according to the contribution ranking3434 Marchioni DML, Verly E, Steluti J, Cesar CLG, Fisberg RM. Folic acid intake before and after mandatory fortification: a population-based study in São Paulo, Brazil. Cad Saude Publica 2013; 29(10):2083-2092..

The associations between energy-adjusted magnesium intake (mg/day, dependent variable) and sociodemographic and lifestyle factors (predictors) were tested by multiple linear regression analysis using the stepwise backward method. The energy-adjusted magnesium consumption variable approaches normality, according to the Shapiro-Wilk test and the use of histogram and Q-Q plot graphs, thus meeting this assumption for multiple linear regression.The sociodemographic and lifestyle factors included in the model were sex (reference: male), age (reference: adults), income (reference: < 3 minimum salaries), skin color (reference: white), schooling (reference: complete primary school), smoking (reference: non-smoker), alcohol consumption (reference: non-consumer), assess nutritional status (reference: eutrophy) and physical activity (reference: light).

The multiple model was further adjusted by self-reported change in dietary habits over the past 6 months. All analyses were performed using the Stata® (version 12) software, assuming a level of statistical significance of 5%.

Results

The sample consisted of 14,719 participants, predominantly adults (78.5%), female sex (54.6%), non-smokers (57.1%), self-reported as white (52.6%), and with a higher education level or a post-graduate level (53.2%). As regards nutritional status, 40.3% of the population was classified as overweight and 22.8% were obese.

The distribution of sociodemographic and lifestyle characteristics according to the magnesium intake of men and women is presented in Table 1. Higher proportions of the elderly and individuals with a higher education or who achieved a postgraduate level, with income ≥ 3 minimum wages, who are former or non-smoker, with eutrophia, and with moderate or vigorous physical activity level had magnesium intake in the last quintile, compared with the first (Table 1).

Table 1
Socio-demographic and lifestyle data according to magnesium intake in ELSA-Brasil. Brazil, 2008-2010.

The top ten contributors to magnesium intake are described in Table 2. The highest contributors were beans (24.0%), oats (4.5%), nuts (3.6%), white rice (3.3%), orange (3.3%), French bread (3.2%), cooked fish (3.0%), boneless meat (2.6%), whole milk (2.3%), and whole-grain bread (2.1%) (Table 2).

Table 2
Main food sources of magnesium intake at ELSA-Brasil. Brazil, 2008-2010.

Except for schooling, all other sociodemographic and lifestyle variables investigated were independently associated with magnesium intake. As shown in Table 3, positive and significant correlations were found between intake of magnesium and female gender; age ≥60 years; skin color self-declared as black, brown, or indigenous; income ≥3 minimum wages; and moderate or vigorous physical activity levels. By contrast, smoking, alcohol consumption, and overweight or obesity were negatively associated with magnesium intake (Table 3).

Table 3
Multiple linear regression model between magnesium intake and socio-demographic and lifestyle factors in ELSA-Brasil, 2008-2010.

Discussion

In this study, variations in magnesium intake among ELSA-Brazil participants (2008-2010) were explained by sociodemographic characteristics that influence food sources, such as sex, age, race/ethnicity, and family income. In addition, smoking and consume alcohol were lifestyle habits that were negatively associated with mineral intake, as did obesity and overweight, while the opposite was evidenced in relation to the level of leisure physical activity, independently of other factors evaluated. Food sources that contributed to more than a half of total magnesium consumption included beans, cereals (oats, rice, and French bread), nuts, oranges, meats (fish and cattle), and milk, although dark green vegetables, almonds, nuts, and legumes had little expressive participation, suggesting a possible dietary inadequacy1717 Instituto Brasileiro de Geografia e Estatística (IBGE). Pesquisa de Orçamentos Familiares: 2008-2009. Análise Do Consumo Alimentar Pessoal No Brasil. Rio de Janeiro: IBGE; 2011.,3535 Sales CH, Fontanelli MDM, Vieira DiAS, Marchioni DiM, Fisberg RM. Inadequate dietary intake of minerals: Prevalence and association with socio-demographic and lifestyle factors. Br J Nutr 2017; 117(2):267-277.,3636 Sales CH, Nascimento DA, Medeiros ACQ, Lima KC, Pedrosa LFC, Colli C. There Is Chronic Latent Magnesium Deficiency in Apparently Healthy University Students. Nutr Hosp 2014; 30(1):200-204..

Consistent with our observations, in a population-based study, Sales et al.3535 Sales CH, Fontanelli MDM, Vieira DiAS, Marchioni DiM, Fisberg RM. Inadequate dietary intake of minerals: Prevalence and association with socio-demographic and lifestyle factors. Br J Nutr 2017; 117(2):267-277. reported that more than a quarter of the magnesium in the diet of São Paulo inhabitants came from beans, rice, and French bread, confirming the important contribution of typical Brazilian food standards. Moreover, age had a positive effect on the intake of magnesium and other minerals, such as calcium, phosphorus, and potassium, signaling better quality of diet among the elderly, in relation to adults and adolescents3535 Sales CH, Fontanelli MDM, Vieira DiAS, Marchioni DiM, Fisberg RM. Inadequate dietary intake of minerals: Prevalence and association with socio-demographic and lifestyle factors. Br J Nutr 2017; 117(2):267-277.. In our study, female gender, as well as age, was also associated with higher magnesium intake. In a previous analysis performed with the same ELSA-Brazil sample, Cardoso et al.3737 Cardoso LO, Carvalho MS, Cruz OG, Melere C, Luft VC, Molina MC, Faria CP, Benseñor IM, Matos SM, Fonseca MJ, Griep RH, Chor D. Eating patterns in the Brazilian Longitudinal Study of Adult Health (ELSA-Brasil): an exploratory analysis. Cad Saude Publica 2016; 32(5):e00066215. revealed that women and elderly had higher adherence to a “healthy” diet characterized by vegetables and fruits3838 Kaidar-Person O, Person B, Szomstein S, Rosenthal RJ. Nutritional deficiencies in morbidly obese patients: A new form of malnutrition? Part B: Minerals. Obes Surg 2008; 18(8):1028-1034., which could be related to the higher intake of magnesium among these individuals.

According to the data from POF 2008-2009, in the Brazilian population, schooling and income are indicators of socioeconomic status independently associated with the higher consumption of saturated fat, sodium, and lower consumption of fiber, indicating that purchasing power and educational level do not necessarily determine better food choices in our social context3333 Block G, Dresser CM, Hartman AM, Carroll MD. Nutrient sources in the American diet: Quantitative data from the nhanes II survey: II. Macronutrients and fats. Am J Epidemiol 1985; 122(1):27-40.. Furthermore, analyses showed that income, not schooling, was associated with higher magnesium intake, after adjusting for demographic and lifestyle characteristics. These findings may be due to factors related to access, availability, and prices of magnesium food sources (dairy products, fresh meats, and vegetables)1818 Jaime PC, Stopa SR, Oliveira TP, Vieira ML, Szwarcwald CLMD. Prevalence and sociodemographic distribution of healthy eating markers, National Health Survey, Brazil 2013. Epidemiol e Serviços Saúde 2015; 24(2):267-276.,3838 Kaidar-Person O, Person B, Szomstein S, Rosenthal RJ. Nutritional deficiencies in morbidly obese patients: A new form of malnutrition? Part B: Minerals. Obes Surg 2008; 18(8):1028-1034.. Notably, ELSA-Brazil participants, linked to teaching and research institutions, present a higher level of education than the general Brazilian population, which could make income a stronger determinant of food consumption. In fact, we notice a relatively higher contribution of oats, walnuts, cooked fish and whole grain bread, but lower of beans to the total magnesium intake among participants with an income per capita ≥ 3 minimum wages, suggesting a different pattern of this mineral food sources consumption among the richer participants (Supplementary Table 1), corroborating with literature3939 Bezerra IN, Souza AM, Pereira RA, Sichieri R. Contribution of foods consumed away from home to energy intake in Brazilian urban areas: The 2008-9 Nationwide Dietary Survey. Br J Nutr 2013; 109(7):1276-1283.,4040 Souza ADM, Pereira RA, Yokoo EM, Levy RB, Sichieri R. Alimentos mais consumidos no Brasil: Inquérito Nacional de Alimentação 2008-2009. Rev Saude Publica 2013; 47(Supl. 1):190-199..

By contrast, individuals with self-declared skin color such as brown, black, or indigenous presented higher values of dietary magnesium. Due to ethnic miscegenation in Brazil, it is a fundamental element to understand the association of race/ethnicity with food consumption, given the recognized role of cultural heritage and historical value of food in the construction of traditional and healthy eating habits. In the National Health Survey (PNS, 2013), for example, black and brown skin colors were associated with a significantly higher frequency of regular bean consumption (≥ 5 times/week)1818 Jaime PC, Stopa SR, Oliveira TP, Vieira ML, Szwarcwald CLMD. Prevalence and sociodemographic distribution of healthy eating markers, National Health Survey, Brazil 2013. Epidemiol e Serviços Saúde 2015; 24(2):267-276.. As already commented, almost a quarter of the total intake of magnesium in ELSA-Brazil was attributed to this legume. Together with rice, beans make up the basis of traditional Brazilian lunch and dinner, and this combination has been shown to be a protective factor for obesity and other NCDs4141 Araujo MC, Verly Junior E, Junger WL, Sichieri R. Independent associations of income and education with nutrient intakes in Brazilian adults: 2008-2009 National Dietary Survey. Public Health Nutr. 2013; 17(12):2740-2752.

42 Sichieri R. Dietary patterns and their associations with obesity in the Brazilian City of Rio de Janeiro. Obes Res 2002; 10(1):42-48.
-4343 Belin RJ, He K. Magnesium physiology and pathogenic mechanisms that contribute to the development of the metabolic syndrome. Magnes Res 2007; 20(2):107-129..

Supplement Table 1
Main food sources of magnesium intake second income at ELSA-Brasil. Brazil, 2008-2010.

Changes in the gustatory ability of foods due to smoking and the recognized negative effect of excessive alcohol consumption on appetite and food consumption could explain the inverse correlation between these two lifestyle habits and the intake of magnesium. On the other hand, as already evidenced by another study3535 Sales CH, Fontanelli MDM, Vieira DiAS, Marchioni DiM, Fisberg RM. Inadequate dietary intake of minerals: Prevalence and association with socio-demographic and lifestyle factors. Br J Nutr 2017; 117(2):267-277., higher values of dietary magnesium were estimated among the participants classified in the levels of moderate and vigorous physical activity. As characteristics of the nutritional transition faced by the country, urbanization and the adoption of unhealthy lifestyle habits have accompanied the increase in the consumption of ultra-processed foods and of low nutritional value1818 Jaime PC, Stopa SR, Oliveira TP, Vieira ML, Szwarcwald CLMD. Prevalence and sociodemographic distribution of healthy eating markers, National Health Survey, Brazil 2013. Epidemiol e Serviços Saúde 2015; 24(2):267-276.,2222 Schmidt MI, Duncan BB, Mill JG, Lotufo PA, Chor D, Barreto SM, Aquino EM, Passos VM, Matos SM, Molina Mdel C, Carvalho MS, Bensenor IM. Cohort Profile: Longitudinal Study of Adult Health (ELSA-Brasil). Int J Epidemiol 2015; 44(1):68-75.. The findings indicate the importance of promoting diet quality, with a stimulus to the consumption of magnesium sources, especially among subgroups at risk for NCDs.

That way, there is an inverse association between magnesium intake and excessive body weight, that is, the worse the nutritional status the lower the consumption of magnesium, even after adjustment for energy consumption, physical activity level, and other sociodemographic and lifestyle characteristics evaluated. Some authors, based on evidence of a deleterious role of magnesium deficiency on insulin resistance, inflammation, and oxidative stress, support the hypothesis of a causal relationship between the inadequacy of the mineral and the aggravation of weight gain and expansion of body adiposity, a characteristic of obesity4444 Santos RO, Vieira DADS, Miranda AAM, Fisberg RM, Marchioni DM, Baltar VT. The traditional lunch pattern is inversely correlated with body mass index in a population-based study in Brazil. BMC Public Health 2017; 18(1):33.

45 Nielsen FH. Magnesium, inflammation, and obesity in chronic disease. Nutr Rev 2010; 68(6):333-340.
-4646 Rayssiguier Y, Libako P, Nowacki W, Rock E. Magnesium deficiency and metabolic syndrome: Stress and inflammation may reflect calcium activation. Magnes Res 2010; 23(2):73-80.. Although other population studies, such as ours, reported a lower intake of magnesium among obese individuals1616 Agarwal S, Reider C, Brooks JR, Fulgoni VL. Comparison of Prevalence of Inadequate Nutrient Intake Based on Body Weight Status of Adults in the United States: An Analysis of NHANES 2001-2008. J Am Coll Nutr 2015; 34(2):126-134.,4444 Santos RO, Vieira DADS, Miranda AAM, Fisberg RM, Marchioni DM, Baltar VT. The traditional lunch pattern is inversely correlated with body mass index in a population-based study in Brazil. BMC Public Health 2017; 18(1):33., it is still uncertain whether these findings reflect a poor overall quality of the diet or if the inadequacy of its consumption would be a risk factor for the disease4545 Nielsen FH. Magnesium, inflammation, and obesity in chronic disease. Nutr Rev 2010; 68(6):333-340.,4646 Rayssiguier Y, Libako P, Nowacki W, Rock E. Magnesium deficiency and metabolic syndrome: Stress and inflammation may reflect calcium activation. Magnes Res 2010; 23(2):73-80.. Due to the transversal design of the study, inferences of causality are not possible; however, they can be explored with a longitudinal follow up of these individuals.

Furthermore, we estimated magnesium intakes with a FFQ, which is a method widely used in large epidemiological studies to rank individual according to their levels of dietary intakes in the previous twelve months4545 Nielsen FH. Magnesium, inflammation, and obesity in chronic disease. Nutr Rev 2010; 68(6):333-340.. However, its use can be considered another study limitation since this method is not consider the most appropriate for the quantitative analysis of micronutrients, given its inherent inaccuracy, that preclude the evaluation of individual or population nutrients intake adequacy. However, ELSA-Brazil FFQ was previously validated and performed well in classifying individuals according to magnesium intake levels, allowing their use in our comparative analysis between groups2424 Molina MDCB, Benseñor IM, Cardoso LO, Velasquez-Melendez G, Drehmer M, Pereira TS, Faria CP, Melere C, Manato L, Gomes AL, Fonseca MJ, Sichieri R. Reproducibility and relative validity of the Food Frequency Questionnaire used in the ELSA-Brasil. Cad Saude Publica 2013; 29(2):379-389.,4747 Willett W. Nutritional Epidemiology. 3rd ed. New York: Oxford University Press; 2013..

To evaluate the energy and nutrient intake, the Food Composition Database of the United States Department of Agriculture (USDA) or the Brazilian Food Composition Table were used. In the Brazilian Table of Food Composition many foods are still presented only in their raw form; in addition, the table does not present many essential nutrients for analysis in studies on chronic diseases. The table used in the NDSR is representative for North American countries, therefore, the amounts of nutrients may vary in relation to food in Brazil. To overcome this issue, we used a systematic routine to correct contrasting nutrient values between databases, similarly to an approach employed by an American Latin multicentric study4848 Kovalskys I, Fisberg M, Gómez G, Rigotti A, Cortés LY, Yépez MC, Pareja RG, Herrera-Cuenca M, Zimberg IZ, Tucker KL, Koletzko B, Pratt M; ELANS Study Group. Standardization of the food composition database used in the latin american nutrition and health study (Elans). Nutrients 2015; 7(9):7914-7924 .

Conclusion

Foods from the traditional Brazilian diet were the largest contributors of dietary magnesium among the evaluated participants. In addition, not only sociodemographic but also lifestyle factors were associated with the ingestion of this mineral.

Acknowledgements

We thank ELSA-Brazil participants who agreed to collaborate in this study, with the support of the Ministry of Health, the Ministry of Science and Technology, National Research Council, and the Foundation for Research Support of the State of São Paulo.

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Publication Dates

  • Publication in this collection
    08 July 2020
  • Date of issue
    July 2020

History

  • Received
    08 Mar 2018
  • Accepted
    12 Nov 2018
  • Published
    14 Nov 2018
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