Next Article in Journal
Association between Depressive Symptoms and Adherence to the Mediterranean Diet in Nursing Students
Previous Article in Journal
Effect of Dietary Approaches on Glycemic Control in Patients with Type 2 Diabetes: A Systematic Review with Network Meta-Analysis of Randomized Trials
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Association between Consumption of Ultra-Processed Food and Body Composition of Adults in a Capital City of a Brazilian Region

by
Larisse Monteles Nascimento
1,
Layanne Cristina de Carvalho Lavôr
1,
Bruna Grazielle Mendes Rodrigues
2,
Felipe da Costa Campos
3,
Poliana Cristina de Almeida Fonseca Viola
1,
Massimo Lucarini
4,
Alessandra Durazzo
4,
Daniel Dias Rufino Arcanjo
5,
Maria do Carmo de Carvalho e Martins
5 and
Karoline de Macêdo Gonçalves Frota
1,*
1
Food and Nutrition Postgraduate Program, Department of Nutrition, Federal University of Piauí, Teresina 64049-550, PI, Brazil
2
Health Sciences Center, Health and Community Postgraduate Program, Federal University of Piauí, Teresina 64049-550, PI, Brazil
3
Department of Nutrition, Federal University of Piauí, Teresina 64049-550, PI, Brazil
4
CREA—Research Centre for Food and Nutrition, Via Ardeatina, 546, 00178 Rome, Italy
5
Department of Biophysics and Physiology, Federal University of Piauí, Teresina 64049-550, PI, Brazil
*
Author to whom correspondence should be addressed.
Nutrients 2023, 15(14), 3157; https://doi.org/10.3390/nu15143157
Submission received: 20 June 2023 / Revised: 7 July 2023 / Accepted: 12 July 2023 / Published: 15 July 2023
(This article belongs to the Section Nutrition and Public Health)

Abstract

:
The present study investigates the relationship between the consumption of ultra-processed foods (UPF) and anthropometric indices of body composition in adults and seniors living in Teresina, the state capital of an area in northeastern Brazil. The article seeks to address two questions: Is UPF consumption linked to worsening body composition in different age groups? Do anthropometric indicators of body composition change with the increasing consumption of UPF? The study is a cross-sectional, household, population study, carried out with 490 adults and seniors. The food consumption was obtained with a 24 h food recall, and the foods were classified using NOVA. Anthropometric indicators evaluated were waist-to-height ratio, triceps skinfold thickness, arm circumference, corrected arm muscle area, subscapular skinfold thickness, and calf circumference. The association between energy contribution of UPF with anthropometric indicators was verified with a simple and multiple linear regression analysis. Individuals aged 20 to 35 years showed a significant association between UPF consumption and skinfold thickness (ß: 0.04; CI: 0.03/0.09), demonstrating an increase in this subcutaneous body fat marker with higher UPF consumption. Moreover, in participants aged 36 to 59 years, an inverse correlation between UPF intake and muscle mass markers, arm circumference (ß: −0.02; confidence interval: −0.03/−0.01), and corrected arm muscle area (ß: −0.07; confidence interval: −0.12/−0.02) were observed. Such results suggest there is decreased muscle mass with increasing UPF consumption. This is the first study that verified an association between UPF consumption and low-cost body composition indicators in different age groups.

1. Introduction

Due to the link between body fat and the likelihood of developing chronic diseases, determining body composition is crucial for the clinical practice and nutritional assessment of populations [1,2,3]. Anthropometric indicators are considered simple, accessible and non-invasive methods that can be used in clinical practice and in the context of epidemiological studies to classify individuals/populations regarding the risk of diseases related to excess and redistribution of fat [4,5].
In older adults, abdominal obesity, which is unrelated to overall obesity, increases the risk of developing chronic diseases [6]. In this sense, studies typically concentrate on nutrients, foods, or dietary patterns to find dietary factors linked to an increased risk of overweight and obesity [7,8,9]. Since advancements in food processing and technology have led to a rise in the availability, accessibility, and marketing of highly processed foods, the world’s food systems have seen significant changes in recent decades [10].
In this regard, researchers have created systems to group foods into categories based on their level of processing, from minimal to highly processed [11,12]. The NOVA categorization of foods [13,14,15] introduced by Monteiro et al. [13], which categorizes foods according to the purpose and level of processing to which they are exposed, is one of the most popular systems in the literature. Specifically, this classification divides foods into four categories: unprocessed or minimally processed foods; processed culinary ingredients; processed foods; and ultra-processed foods (UPF). The NOVA classification has been applied in different studies [16,17,18] as well as argumentations/criticism on this issue are ongoing [19,20,21]. UPF is heavy in sugar, salt, and additives, and it is lacking in dietary fiber and vitamins; typical examples of these energy-packed foods are snacks, soft drinks, candies, ready meals, refined starchy foods, and reconstituted meat products [22]. Therefore, the increase in consumption of “ultra-processed” foods may draw attention, for example, to the increase in consumption of toxic advanced glycation end-products (AGEs) obtained from the Maillard reaction during food processing, as many UPFs contain high levels of sugars and fats, favoring the formation of AGEs [23,24].
Evidence shows that just as AGEs may be associated transversally with loss of muscle mass in individuals over 45 years of age [25], UPF is also associated with changes in body composition measures, highlighting the increase in fat mass in the long term as well as the decrease in lean mass [26].
High UPF intake has been linked in several prospective cohorts and clinical trials to an increased risk of obesity [27], weight gain [28,29], and total and visceral fat accumulation [30]. Particularly, a recent meta-analysis of adults found that consuming UPF was linked to a markedly higher risk of 36% and 51% for overweight and obesity, respectively [31].
Techniques with high accuracy for estimating body fat, such as dual-energy X-ray absorptiometry (DXA), air displacement plethysmography, computed tomography, and magnetic resonance imaging, are expensive and difficult to implement at a population level. Accordingly, in clinical practice, other approaches such as anthropometric markers that distinguish body fat with low operational costs are required [32]. Anthropometric measurements are also part of the methods available to estimate body composition, where one can estimate the percentage of body fat and lean mass from information derived from skinfold measurements as well as using algorithms that account for gender, age, body mass, and height [33].
Therefore, it becomes essential to confirm the relationship between UPF intake and anthropometric markers, since there are still no studies showing this association.

2. Materials and Methods

2.1. Study Design and Population

This cross-sectional study was carried out in the state of Piauí’s cities of Teresina and Picos between the months of August 2018 and December 2019. This study is a component of the main project titled “Population-based Health Survey” (Inquérito de Saúde de Base Populacional, ISAD-PI).
Participants in this study ranged in age from 20 to 59 years old and 60 years or older from the city of Teresina, Piauí. Individuals living in private homes were eligible, except for those living in collective homes, pregnant women, and those with some disability or incapacity that made it impossible to carry out the survey.

2.2. Sample Size

The research sample was selected through a two-stage conglomerate sampling process: census sectors make up the main sampling units (PSU), while households make up the second stage, based on information from the IBGE census for the year 2010 [34].
The population size and the number of private houses in Teresina (767,557 people; 210,093 households) were taken into account while determining the sample size [34]. From these data, the average number of individuals for both genders per household was calculated in each of the following age groups: children under 2 years old; children aged 3 to 4 years; children aged 5 to 9 years; adolescents aged 10 to 14 years; adolescents aged 15 to 19 years; adults aged 20 to 59 and elderly over 6. A total of 578 households were then estimated to be enough. Using the formula n = n0/0.90 and assuming a response rate of 90%, the final sample size for this study was adjusted, yielding n = 642 households, approximately. Further details about the sample size and sampling plan were previously published by Rodrigues et al. [35]. Using the same sampling strategy, 50% of the households were chosen to form a subsample for the purpose of gathering information on food consumption using 24 h recalls.
Upon completion of the study, 497 Teresina households were included in the final sample, and the subsample consisted of 248 households. In the end, data were obtained from 490 individuals, with 154 participants aged 20 to 35 years, 207 aged 36 to 59 years, and 129 individuals aged 60 years or over (Figure 1). This study was approved by the Committee for Ethics in Research from the Federal University of Piauí, under decision n° 2.552.426.

2.3. Data Collection and Anthropometric Measurements

The National Health Survey, conducted in 2013 by the Brazilian Institute of Geography and Statistics [36], and other Brazilian studies, including “ISA 2008: Health Surveys in the city of São Paulo” [37], were both used as models for the structured questionnaires that trained researchers used to collect demographic, socioeconomic, anthropometric, lifestyle, and food consumption data. The data were collected using mobile devices and the Epicollect 5® application (Imperial College London; https://five.epicollect.net/project/isad, accessed on 3 April 2023).
Anthropometric measurements were estimated in accordance with recommendations by Cameron [38] as well as Jelliffe and Jelliffe [39]. The participants were weighed using a portable electronic scale (SECA®, model 803, Hamburg, Germany) with a precision of 100 g, and their heights were measured using a stadiometer (SECA®, model messband 206, Hamburg, Germany) with a precision of 0.1 cm. Adults’ Body Mass Index (BMI) was categorized in accordance with the World Health Organization’s guidelines [40]; for elderly individuals, the values established by Lipschitz et al. [41] were used.
According to WHO recommendations [42], waist circumference (WC) was measured using an inelastic measuring tape with a precision of 0.1 cm at the midpoint between the last rib and the iliac crest. The waist-to-height ratio (WHtR) was calculated by dividing WC in centimeters by height, also in centimeters [43].
According to Frisancho [44], the arm circumference (AC), or the distance between the acromion and the olecranon on the right arm, was measured in order to calculate the arm muscle circumference (AMC) and the arm muscle area (AMA).
AMC was calculated from the formula: AC-(π*TSF) in centimeters. In turn, AMA was calculated using the formula: AMA = (AMC2/4*π). The AMA correction (CAMA) was 10 for men and 6.5 for women.
The triceps (TSF) and subscapular skinfolds were measured using an adipometer (Lange®, Cambridge Scientific Industries, Inc., Cambridge, MA, USA) calibrated with an accuracy of 0.1 mm. The TSF measurement was taken on the posterior surface of the right arm, parallel to the longitudinal axis, at the midpoint between the acromion and the olecranon. The measurement of the subscapular skinfold (SSF) was estimated only in adults, on the right side of the individual, and two centimeters below the inferior angle of the scapula [45].
Calf circumference (CC) was measured only in elderly individuals with an inelastic measure tape with a precision of 1 mm positioned in the largest volume of the left calf, with the individual in a chair with the leg flexed at 90° [46]. Values below 31 cm were considered indicative of loss of muscle mass [42].

2.4. Dietary Assessment

The food consumption of the studied population was obtained by applying the 24 h food recall (R24h) based on the multiple pass method, which proposes five steps for collecting dietary data: 1st stage—quick listing of foods and schedules; 2nd stage—filling out the commonly forgotten foods; 3rd stage—setting the schedule and naming the meals; 4th stage—detailing and reviewing the meals, including the amount eaten, form of preparation, origin, commercial brand, portion size, including the addition of salt, sugar, butter, or margarine to foods and preparations; 5th stage—final review of the R24h. Should be reviewed the foods whose reporting was difficult, if R24h is complete and ask about the consumption of alcoholic beverages, snacks and at social events [47,48].
In order to correct intrapersonal variability, a second R24h was administered to 40% of the population after a two-month break, using the identical techniques from the first interview. Based on a study by Verly-Júnior et al. [49], it was determined that regardless of sample size, the application of a second R24h in 40% of the sample resulted in no decrease in precision for predicting food intake.
The Table for Measuring Household Food Consumption [50] was used to convert the household measures obtained from the interviews into grams (g) or milliliters (mL). The Brazilian Table of Food Composition [51], Table of Nutritional Composition of Foods Consumed in Brazil [52], and Table of Food Composition: Support for Nutritional Decision [53] were used to compute the energy intake.
Using the NOVA classification, the reported food items were divided into 4 groups based on the degree of processing they underwent [14]. Foods in groups 1, 2, and 4 were minimally or not at all processed, treated for use in cooking, and extremely processed. The first and fourth groups, however, were the only ones examined in this study.
Once removed from nature, unprocessed foods include edible parts of plants or animals, as well as mushrooms, algae, and water. These edible parts include those from plants (such as seeds, fruits, leaves, and roots) or animals (such as muscles, eggs, and milk). Fresh foods that have undergone minimal processing include those that have had undesirable or inedible parts removed, were dried, dehydrated, ground or milled, fractioned, roasted, pasteurized, cooled or frozen, vacuum-packed, gone through non-alcoholic fermentation, and/or gone through other processes without having salt, sugar, oils, or fats added. For example, wheat grains are converted into products like flour, couscous, and pasta [14].
UPF is in group 4, and its industrial formulations often contain five chemicals or more. These ingredients frequently include preservatives, stabilizers as well as other ingredients or additions used in the production of processed meals such as salt, sugar, oils, and fats. UPF is frequently found in products including soft drinks, rehydration supplements, “packaged snacks”, ice cream, and chocolate, among others [14]. The Total Energy Value (TEV) of the study participants’ diets was used to calculate the proportion of each food group’s consumption. All food consumption analyses were carried out using Stata software (version 13.0).

2.5. Statistical Analysis

The Stata software, version 13.0, was used to analyze the data. In order to compensate for the complex sampling of this research, all analyses were carried out in survey mode. Standard deviation and average were used to express continuous variables, whereas absolute and relative values were used to convey categorical variables. Using the Shapiro–Wilk test, the distributions of continuous variables were examined. In turn, in order to make comparisons among averages related to the Student’s t-test and ANOVA, a variance analysis was used, followed by Tukey’s post-hoc test. The association between the energy contribution of UPF consumption and anthropometric indicators was verified using simple and multiple linear regression analyses that were corrected for potential confounding variables. The independent variables included in the modified model were selected by creating the Directed Acyclic Graph (DAG) in the software Daggity, version 3.0, in order to control for confounding questions (Figure S1). In accordance with the backdoor criterion [54], it was identified that there was a need for minimal adjustment for gender, education, family income, marital status, alcohol consumption, smoking, practice of physical activity, BMI, and WC. A 5% level of significance and 95% confidence intervals were used.

3. Results

A total of 490 people took part in the study, with the majority (76.3%) earning less than or equal to two minimum wages, being between the ages of 36 and 59 as well as 42.2% of them being female. In addition, when it came to lifestyle choices, 80.4% of people were active, 78% did not smoke, and 60% did not consume alcoholic beverages. There was a greater participation of fresh or minimally processed foods in relation to the average percentage of contribution in the Total Energy Value (TEV) for the NOVA classification food groups (67.9% of the TEV 18.9); however, the UPF group obtained an expressive contribution in terms of TEV (19.7% of the TEV 17.9) (Table 1).
The average percentage of the contribution in terms of the TEV of UPF consumption and fresh or minimally processed foods according to age group is displayed in Figure 2; it is noted (Figure 2) that UPF consumption was significantly higher for the group of individuals aged 20 to 35 years (25.2%) when compared to the participants aged 36 to 59 years (17.9%) and over 60 years (16.1%). With regard to the consumption of fresh or minimally processed foods, the younger group (20 to 35 years old) again maintained a less healthy profile with an intake of 63.1%, compared to 68.9% and 72.0%, consumed by adult individuals aged 36 to 59 years and elderly individuals, respectively (Figure 2).
Table 2 shows the distribution of anthropometric indicators according to age group. The waist-to-height ratio increased significantly with age; however, TSF decreased when comparing the group aged 36 to 59 years (25.1 ± 10.4) and the elderly population (21.1 ± 8.7) (Table 2). Furthermore, for the AC measurement, a significant increase in individuals aged 20 to 35 years (31.2 ± 4.8) with respect to the group aged between 36 to 59 years (32.2 ± 4.7) was observed, whereas a reduction in this measurement with increasing age (30.3 ± 4.6) in the elderly population was observed. As reported in Table 2, subscapular skinfold thickness (SST) increased with advancing age when comparing the groups aged 20 to 35 years (21.4 ± 9.0) and individuals aged 36 to 59 years (23.7 ± 9.5).
The analyses of the association between UPF consumption and anthropometric indicators according to age group are reported in Table 3. In the group of individuals aged 20 to 35 years, there was a significant association between UPF consumption and TSF (ß: 0.04; CI: 0.03/0.09; p = 0.04), thus demonstrating an increase in this subcutaneous fat marker with a higher UPF consumption. Furthermore, for participants aged 36 to 59 years, there was an inverse and significant association between UPF consumption and the muscle mass markers AC (ß: −0.02; CI: −0.03/−0.01; p = 0.03) and CAMA (ß: −0.07; CI: −0.12/−0.02; p = 0.01) were, respectively, observed. Such results suggest a decrease in muscle mass indirectly measured with the AC and CAMA parameters with the increase in UPF consumption.

4. Discussion

This study explored the relationship between UPF intake and anthropometric measurements of body composition. These methodologies are used in population studies and in clinical practice for estimating fat and lean body mass at low cost. The greater contribution of UPF to the diet was associated with increased markers of subcutaneous fat and decreased markers of lean body mass, for adults aged 20 to 35 years and for those aged 36 to 59 years, respectively. These findings demonstrate that a higher UPF consumption entails a negative impact on the body composition of adults in different age groups, thus contributing to an increase in subcutaneous fat as a risk factor for the emergence of CNCD.
The contribution of UPF consumption in this research was greater for younger adults, and it was also observed that the consumption of this food group decreased with increasing age. Such results corroborate those by Costa et al. [55], who showed that, in the population of 27 Brazilian capitals, the frequency of UPF consumption decreased linearly with age. This evidence may be due to the greater concern of older and long-living adults with health, in addition to the possibility that most of them have more consistent eating patterns and conventional culinary techniques. Furthermore, along with having less stable dietary habits and being more willing to test out these items, these population groups might also be less susceptible to marketing strategies that appeal to the younger generation [56].
The increase in body fat among the participants of this research was observed through waist-to-height ratio (WHtR) and subscapular skinfold thickness (SST) measurements with advancing age. On the other hand, among the elderly individuals, a loss of fat mass was observed, based on the TSF levels’ observations, as well as a loss of lean mass through CAMA levels. In old age, the body composition changes as fat mass increases and redistributes. Fat-free mass consisting mainly of skeletal muscle decreases by 40% between the ages of 20 and 70 years, and after age 70, both fat mass and lean mass decrease together. Accordingly, with the redistribution of fat mass, an increase in visceral and muscular fat deposits takes place [57,58].
A growing body of research indicates that consuming UPF increases the risk of obesity [59]. UPF consumption is strongly correlated with obesogenic dietary nutritional profiles, according to analyses of nationally representative dietary surveys carried out in numerous nations, including the United Kingdom [60]. Recent population-based cross-sectional studies in Brazil [61], the United States [62], and Canada [63] have shown a positive correlation between eating ultra-processed foods and obesity. Additionally, a two-week randomized controlled crossover study of 20 adults in weight stability found that eating more ultra-processed food resulted in higher energy intake, a significant increase in body weight, and a rise in fat mass [28].
This is the first research with the aim of investigating the influence of UPF consumption on body composition, assessed using anthropometric indicators. The association presented in this study highlighted that higher UPF consumption may reflect an increase in fat mass through the increase in terms of TSF in adults aged 20 to 35 years. Similar results were verified by Liu et al. [64], who—despite using a more sensitive method, such as dual-energy X-ray absorptiometry (DXA), in order to measure the body composition of adults aged between 20 and 59 years—also observed that higher UPF consumption was associated with increased body fat in a population sample assessed in the United States.
Furthermore, the reduction in lean body mass was observed in adults aged 36 to 59 years in this study when highlighting an inverse association between UPF consumption and AC and CAMA measurements. The study by Viola et al. [65] with Brazilian adolescents also demonstrated the association between the decrease in muscle mass measured using a DXA and the increase in the participation of UPF consumption in the diet. The unbalanced nutritional composition of foods and beverages favors increased energy intake, a reduction in protein intake, and an increase in nutrients/ingredients of low nutritional quality, such as refined sugars. The AGEs present in UPF are one mechanism that, according to scientific evidence, promotes changes in body composition [13,24,25,66]. The presence of food additives and contaminants created during processing alters the profile and composition of the intestinal microbiota [67], and changes in the food matrix induced by food processing seem to influence the kinetics of nutrient absorption and changes in the gut–brain signaling of satiety, among other unclear mechanisms that are interrelated, and promote inflammation, oxidative stress, and ensuing weight gain [26,28,62].
Accordingly, considering the results of this study that show an association between UPF consumption and increased body fat and decreased lean mass, the importance of further research investigating the association between this food group and body composition is reiterated and assessed using accessible anthropometric indicators that can be easily used in clinical practice. In addition, it is important to raise awareness about reducing UPF consumption, which is the second most consumed food group by the Brazilian population, as they are convenient formulations, often sold in large portions, aggressively marketed, and extremely tasty [68].
Some limitations of this study are important to be highlighted, such as its cross-sectional design, which limits the relationships between cause and effect. Moreover, when using the 24 h dietary recall, some inconsistencies can be identified, partially due to stated consumption errors (over or underreporting), in part. However, two recalls were employed: the first applied to the complete population, and the second applied to 40% of this population, with the purpose of correcting intrapersonal variability in order to minimize these inaccuracies [49]. Among the strengths of this research, originality stands out since it is the first study to show an association between the consumption of ultra-processed foods and anthropometric indicators in adult and elderly people.

5. Conclusions

This study provides significant research demonstrating links between UPF consumption, obesity, and measures of lean body mass, thus indicating the negative influence of these foods on body composition in the population. In addition, these findings indicate the need to take policy initiatives, especially with regard to the labeling of UPF with an emphasis on the obligation supported by legislation, in the sense of informing the consumer about the real harm to health that the replacement of natural or minimally processed foods with UPF can cause. Such information could be presented through a QR code present on UPF packaging, emphasizing that reduction in terms of UPF consumption should be considered, as the high consumption of this food group can be harmful to health.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/nu15143157/s1. Figure S1: Directed Acyclic Graph (DAG).

Author Contributions

Conceptualization, L.M.N., and K.d.M.G.F.; methodology, L.M.N., and K.d.M.G.F.; formal analysis, L.M.N., K.d.M.G.F., and L.C.d.C.L.; investigation, L.M.N., K.d.M.G.F., and L.C.d.C.L.; data curation, L.M.N., L.C.d.C.L., A.D., M.L., and K.d.M.G.F.; writing—original draft preparation, L.M.N.; writing—review and editing, M.L., A.D., D.D.R.A., M.d.C.d.C.e.M., and K.d.M.G.F.; visualization, B.G.M.R., F.d.C.C., and P.C.d.A.F.V.; supervision, K.d.M.G.F.; project administration, K.d.M.G.F.; funding acquisition, K.d.M.G.F. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

The study was conducted in accordance with the Declaration of Helsinki and was approved by the Ethics Committee of the Universidade Federal do Piauí (protocol code 2.552.426).

Informed Consent Statement

Informed consent was obtained from all subjects involved in the study.

Data Availability Statement

The authors declare that the data supporting the findings of this study are available within the article. All other data are available on reasonable request from the corresponding authors.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Azevedo, E.C.; Diniz Ada, S.; Monteiro, J.S.; Cabral, P.C. Dietary risk patterns for non-communicable chronic diseases and their association with body fat—A systematic review. Cien Saude Colet. 2014, 19, 1447–1458. [Google Scholar] [CrossRef] [PubMed]
  2. Goossens, G.H. The Metabolic Phenotype in Obesity: Fat Mass, Body Fat Distribution, and Adipose Tissue Function. Obes. Facts 2017, 10, 207–215. [Google Scholar] [CrossRef] [PubMed]
  3. Nimptsch, K.; Konigorski, S.; Pischon, T. Diagnosis of obesity and use of obesity biomarkers in science and clinical medicine. Metabolism 2019, 92, 61–70. [Google Scholar] [CrossRef] [PubMed]
  4. Beraldo, R.A.; Meliscki, G.C.; Silva, B.R.; Navarro, A.M.; Bollela, V.R.; Schmidt, A.; Foss-Freitas, M.C. Comparing the Ability of Anthropometric Indicators in Identifying Metabolic Syndrome in HIV Patients. PLoS ONE 2016, 11, e0149905. [Google Scholar] [CrossRef]
  5. Piqueras, P.; Ballester, A.; Durá-Gil, J.V.; Martinez-Hervas, S.; Redón, J.; Real, J.T. Anthropometric Indicators as a Tool for Diagnosis of Obesity and Other Health Risk Factors: A Literature Review. Front. Psychol. 2021, 12, 631179. [Google Scholar] [CrossRef]
  6. Hirani, V. Generalised and abdominal adiposity are important risk factors for chronic disease in older people: Results from a nationally representative survey. J. Nutr. Health Aging 2011, 15, 469–478. [Google Scholar] [CrossRef] [Green Version]
  7. Tapsell, L.C.; Neale, E.P.; Satija, A.; Hu, F.B. Foods, Nutrients, and Dietary Patterns: Interconnections and Implications for Dietary Guidelines. Adv. Nutr. 2016, 7, 445–454. [Google Scholar] [CrossRef] [Green Version]
  8. Chao, A.M.; Quigley, K.M.; Wadden, T.A. Dietary interventions for obesity: Clinical and mechanistic findings. J. Clin. Investig. 2021, 131, e140065. [Google Scholar] [CrossRef]
  9. Aaseth, J.; Ellefsen, S.; Alehagen, U.; Sundfør, T.M.; Alexander, J. Diets and drugs for weight loss and health in obesity—An update. Biomed. Pharmacother. 2021, 140, 111789. [Google Scholar] [CrossRef]
  10. Poti, J.M.; Braga, B.; Qin, B. Ultra-processed Food Intake and Obesity: What Really Matters for Health—Processing or Nutrient Content? Curr. Obes. Rep. 2017, 6, 420–431. [Google Scholar] [CrossRef]
  11. Moubarac, J.C.; Parra, D.; Cannon, G.; Monteiro, C.A. Food classification systems based on food processing: Significance and implications for policies and actions. A systematic literature review and assessment. Curr. Obes. Rep. 2014, 3, 256–272. [Google Scholar] [CrossRef] [PubMed]
  12. Fardet, A.; Lakhssassi, S.; Briffaz, A. Beyond nutrient-based food indices: A data mining approach to search for a quantitative holistic index reflecting the degree of food processing and including physicochemical properties. Food Funct. 2018, 9, 561–572. [Google Scholar] [CrossRef] [PubMed]
  13. Monteiro, C.A.; Levy, R.B.; Claro, R.M.; Castro, I.R.; Cannon, G. A new classification of foods based on the extent and purpose of their processing. Cad. Saude Publica 2010, 26, 2039–2049. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  14. Monteiro, C.A.; Cannon, G.; Levy, R.B.; Moubarac, J.C.; Jaime, P.; Martins, A.P.; Canella, D.; Louzada, M.; Parra, D.; Ricardo, C.; et al. NOVA. The star shines bright [Food classification. Public health]. World Nutr. 2016, 7, 28–38. [Google Scholar]
  15. Monteiro, C.A.; Cannon, G.; Levy, R.B.; Moubarac, J.C.; Louzada, M.L.; Rauber, F.; Khandpur, N.; Cediel, G.; Neri, D.; Martinez-Steele, E.; et al. Ultra-processed foods: What they are and how to identify them. Public Health Nutr. 2019, 22, 936–941. [Google Scholar] [CrossRef]
  16. Batal, M.; Johnson-Down, L.; Moubarac, J.C.; Ing, A.; Fediuk, K.; Sadik, K.; Tikhonov, C.; Chan, L.; Willows, N. Quantifying associations of the dietary share of ultra-processed foods with overall diet quality in First Nations peoples in the Canadian provinces of British Columbia, Alberta, Manitoba and Ontario. Public Health Nutr. 2018, 21, 103–113. [Google Scholar] [CrossRef] [Green Version]
  17. Marrón-Ponce, J.A.; Sánchez-Pimienta, T.G.; Louzada, M.L.D.C.; Batis, C. Energy contribution of NOVA food groups and sociodemographic determinants of ultra-processed food consumption in the Mexican population. Public Health Nutr. 2018, 21, 87–93. [Google Scholar] [CrossRef] [Green Version]
  18. Phillips, N.E.; Mareschal, J.; Schwab, N.; Manoogian, E.N.C.; Borloz, S.; Ostinelli, G.; Gauthier-Jaques, A.; Umwali, S.; Gonzalez Rodriguez, E.; Aeberli, D.; et al. The Effects of Time-Restricted Eating versus Standard Dietary Advice on Weight, Metabolic Health and the Consumption of Processed Food: A Pragmatic Randomised Controlled Trial in Community-Based Adults. Nutrients 2021, 13, 1042. [Google Scholar] [CrossRef]
  19. Gibney, M.J.; Forde, C.G.; Mullally, D.; Gibney, E.R. Ultra-processed foods in human health: A critical appraisal. Am. J. Clin. Nutr. 2017, 106, 717–724, Erratum in: Am. J. Clin. Nutr. 2018, 107, 482–483. [Google Scholar] [CrossRef] [Green Version]
  20. Sadler, C.R.; Grassby, T.; Hart, K.; Raats, M.; Sokolovi´c, M.; Timotijevic, L. Processed food classification: Conceptualisation and challenges. Trends Food Sci. Technol. 2021, 112, 149–162. [Google Scholar] [CrossRef]
  21. Braesco, V.; Souchon, I.; Sauvant, P.; Haurogné, T.; Maillot, M.; Féart, C.; Darmon, N. Ultra-processed foods: How functional is the NOVA system? Eur. J. Clin. Nutr. 2022, 76, 1245–1253. [Google Scholar] [CrossRef] [PubMed]
  22. De Amicis, R.; Mambrini, S.P.; Pellizzari, M.; Foppiani, A.; Bertoli, S.; Battezzati, A.; Leone, A. Ultra-processed foods and obesity and adiposity parameters among children and adolescents: A systematic review. Eur. J. Nutr. 2022, 61, 2297–2311. [Google Scholar] [CrossRef]
  23. Harsha, P.S.C.; Lavelli, V. Use of Grape Pomace Phenolics to Counteract Endogenous and Exogenous Formation of Advanced Glycation End-Products. Nutrients 2019, 11, 1917. [Google Scholar] [CrossRef] [Green Version]
  24. Velayoudom-Cephise, F.L.; Cano-Sanchez, M.; Bercion, S.; Tessier, F.; Yu, Y.; Boulanger, E.; Neviere, R. Receptor for advanced glycation end products modulates oxidative stress and mitochondrial function in the soleus muscle of mice fed a high-fat diet. Appl. Physiol. Nutr. Metab. 2020, 45, 1107–1117. [Google Scholar] [CrossRef]
  25. Wagas, K.; Chen, J.; Lu, T.; van der Eerden, B.C.J.; Rivadeneira, F.; Uitterlinden, A.G.; Voortman, T.; Zillikens, M.C. Dietary advanced glycation end-products (dAGEs) intake and its relation to sarcopenia and frailty—The Rotterdam Study. Bone 2022, 165, 116564. [Google Scholar] [CrossRef] [PubMed]
  26. Rudakoff, L.C.S.; Magalhães, E.I.S.; Viola, P.C.A.F.; Oliveira, B.R.; Coelho, C.C.N.S.; Bragança, M.L.B.M.; Arruda, S.P.M.; Cardoso, V.C.; Bettiol, H.; Barbieri, M.A. Ultra-processed food consumption is associated with increase in fat mass and decrease in lean mass in Brazilian women: A cohort study. Front. Nutr. 2022, 9, 1006018. [Google Scholar] [CrossRef] [PubMed]
  27. Canhada, S.L.; Luft, V.C.; Giatti, L.; Duncan, B.B.; Chor, D.; Fonseca, M.; Matos, S.M.A.; Molina, M.; Barreto, S.M.; Levy, R.B.; et al. Ultra-processed foods, incident overweight and obesity, and longitudinal changes in weight and waist circumference: The Brazilian Longitudinal Study of Adult Health (ELSA-Brasil). Public. Health Nutr. 2020, 23, 1076–1086. [Google Scholar] [CrossRef] [Green Version]
  28. Hall, K.D.; Ayuketah, A.; Brychta, R.; Cai, H.; Cassimatis, T.; Chen, K.Y.; Chung, S.T.; Costa, E.; Courville, A.; Darcey, V.; et al. Ultra-processed diets cause excess calorie intake and weight gain: An inpatient randomized controlled trial of ad libitum food intake. Cell Metab. 2019, 30, 67–77.e63. [Google Scholar] [CrossRef] [Green Version]
  29. Nascimento, L.M.; Monteiro, N.V.N.; Vilar, T.M.; Ibiapina, C.R.L.S.; Frota, K.M.G. The influence of ultra-processed food consumption in anthropometric and atherogenic indices of adolescents. Rev. Nutr. 2021, 34, e200036. [Google Scholar] [CrossRef]
  30. Konieczna, J.; Morey, M.; Abete, I.; Bes-Rastrollo, M.; Ruiz-Canela, M.; Vioque, J.; Gonzalez-Palacios, S.; Daimiel, L.; Salas-Salvado, J.; Fiol, M.; et al. Contribution of ultra-processed foods in visceral fat deposition and other adiposity indicators: Prospective analysis nested in the PREDIMED-Plus trial. Clin. Nutr. 2021, 40, 4290–4300. [Google Scholar] [CrossRef]
  31. Lane, M.M.; Davis, J.A.; Beattie, S.; Gomez-Donoso, C.; Loughman, A.; O’Neil, A.; Jacka, F.; Berk, M.; Page, R.; Marx, W.; et al. Ultraprocessed food and chronic noncommunicable diseases: A systematic review and meta-analysis of 43 observational studies. Obes. Rev. 2021, 22, e13146. [Google Scholar] [CrossRef] [PubMed]
  32. Alves Junior, C.A.S.; Mocellin, M.C.; Gonçalves, E.C.A.; Silva, D.A.S.; Trindade, E.B.S.M. Anthropometric Indicators as Body Fat Discriminators in Children and Adolescents: A Systematic Review and Meta-Analysis. Adv. Nutr. 2017, 8, 718–727. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  33. Lewandowski, Z.; Dychała, E.; Pisula-Lewandowska, A.; Danel, D.P. Comparison of Skinfold Thickness Measured by Caliper and Ultrasound Scanner in Normative Weight Women. Int. J. Environ. Res. Public Health 2022, 19, 16230. [Google Scholar] [CrossRef]
  34. Instituto Brasileiro de Geografia e Estatística. Censo Demográfico 2010: Características Gerais da População e dos Domicílios, Resultados do Universo. Rio de Janeiro: Instituto. 2010. Available online: https://censo2010.ibge.gov.br/resultados.html (accessed on 12 August 2021).
  35. Rodrigues, L.A.R.L.; Costa e Silva, D.M.; Oliveira, E.A.R.; Lavôr, L.C.C.; Sousa, R.R.; Carvalho, R.B.N.; Farias Junior, G.; Formiga, L.M.F.; Sousa, A.F.; Cardoso, M.R.A.; et al. Sampling plan and methodological aspects: A household healthcare survey in Piauí. Rev. Saude Publica 2021, 55, 118. [Google Scholar] [CrossRef]
  36. Instituto Brasileiro de Geografia e Estatística. Pesquisa Nacional de Saúde: Percepção do Estado de Saúde, Estilos de Vida e Doenças Crônicas: 2013; IBGE: Rio de Janeiro, Brazil, 2014. [Google Scholar]
  37. Fisberg, R.M.; Marchioni, D.M.L. Manual de Avaliação do Consumo Alimentar em Estudos Populacionais: A Experiência do Inquérito de Saúde em São Paulo (ISA); Faculdade de Saúde Pública da Universidade de São Paulo: São Paulo, Brazil, 2012; 197p. [Google Scholar]
  38. Cameron, N. Anthropometric Measurements. In The Measurement of Human Growth; Cameron, N., Ed.; Croom Helm: London, UK, 1984; pp. 56–99. [Google Scholar]
  39. Jelliffe, D.B.; Jelliffe, E.F.P. Anthropometry: Major measurements. In Community Nutritional Assessment with Special Reference to Less Technically Developed Countries, 2nd ed.; Jelliffe, D.B., Jelliffe, E.F.P., Eds.; Oxford University Press: London, UK, 1989; pp. 68–105. [Google Scholar]
  40. World Health Organization. Obesity: Preventing and Managing the Global Epidemic; Technical Report Series 894, 9; WHO: Geneva, Switzerland, 2000. [Google Scholar]
  41. Lipschitz, D.A. Screening for nutritional status in the elderly. Prim. Care 1994, 21, 55–67. [Google Scholar] [CrossRef] [PubMed]
  42. World Health Organization. Physical Status: The Use and Interpretation of Anthropometry; WHO Technical Report Series n. 854; WHO: Geneva, Switzerland, 1995. [Google Scholar]
  43. Ashwell, M.; Hsieh, S.D. Six reasons why the waist-to-height ratio is a rapid and effective global indicator for health risks of obesity and how its use could simplify the international public health message on obesity. Int. J. Food Sci. Nutr. 2005, 56, 303–307. [Google Scholar] [CrossRef]
  44. Frisancho, A.R. Anthropometric Standards for the Assessment of Growth and Nutritional Status; University of Michigan Press: Ann Arbor, MI, USA, 1991. [Google Scholar]
  45. Lohman, T.G.; Roche, A.F.; Martorell, R. Anthropometric Standardization Reference Manual; Human Kinetics Books: Champaign, IL, USA, 1991. [Google Scholar]
  46. Martin, F.G.; Nebuloni, C.C.; Najas, M.S. Correlação entre estado nutricional e força de preensão palmar em idosos. Rev. Bras. Ger. Gerontol. 2012, 15, 493–504. [Google Scholar] [CrossRef] [Green Version]
  47. Moshfegh, A.J.; Rhodes, D.G.; Baer, D.J.; Murayi, T.; Clemens, J.C.; Rumpler, W.V.; Paul, D.R.; Sebastian, R.S.; Kuczynski, K.J.; Ingwersen, L.A.; et al. The US Department of Agriculture Automated Multiple-Pass Method reduces bias in the collection of energy intakes. Am. J. Clin. Nutr. 2008, 88, 324–332. [Google Scholar] [CrossRef] [Green Version]
  48. Raper, N.; Perloff, B.; Ingwersen, L.; Steinfeldt, L.; Anand, J. An overview of USDA’s Dietary Intake Data System. J. Food Compost. Anal. 2004, 17, 545–555. [Google Scholar] [CrossRef]
  49. Verly-Júnior, E.; Castro, M.A.; Fisberg, R.M.; Marchioni, D.M.L. Precision of Usual Food Intake Estimates According to the Percentage of Individuals with a Second Dietary Measurement. J. Acad. Nutr. Diet. 2012, 112, 1015–1020. [Google Scholar] [CrossRef]
  50. Pinheiro, A.B.V.; Lacerda, E.M.D.A.; Benzecry, E.H.; Gomes, M.C.D.S.; Costa, V.M.D. Tabela para Avaliação de Consumo Alimentar em Medidas Caseiras, 5th ed.; Atheneu: São Paulo, Brazil, 2005. [Google Scholar]
  51. TACO. Tabela Brasileira de Composição de Alimentos, 4th ed.; NEPA-UNICAMP: Campinas, Brazil, 2011; 161p. [Google Scholar]
  52. IBGE. Instituto Brasileiro de Geografia e Estatística. Pesquisa de Orçamentos Familiares (POF), 2008–2009: Tabela de Composição Nutricional dos Alimentos Consumidos No Brasil; Instituto Brasileiro de Geografia e Estatística: Rio de Janeiro, Brazil, 2011. [Google Scholar]
  53. Philippi, S.T. Tabela de Composição de Alimentos: Suporte para Decisão Nutricional, 6th ed.; Manole: São Paulo, Brazil, 2018; 160p. [Google Scholar]
  54. Textor, J.; Hardt, J.; Knuppel, S. DAGitty: A graphical tool for analyzing causal digrams. Epidemiology 2011, 22, 745. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  55. Costa, C.S.; Sattamini, I.F.; Martínez Steele, E.; Louzada, M.L.C.; Claro, R.M.; Monteiro, C.A. Consumption of ultra-processed foods and its association with sociodemographic factors in the adult population of the 27 Brazilian state capitals (2019). Rev. Saude Publica 2021, 55, 47. [Google Scholar] [CrossRef] [PubMed]
  56. Khandpur, N.; Cediel, G.; Obando, A.; Jaime, P.C.; Parra, D.C. Sociodemographic factors associated with the consumption of ultra-processed foods in Colombia. Rev. Saude Publica 2020, 54, 19. [Google Scholar] [CrossRef] [Green Version]
  57. Javed, A.A.; Aljied, R.; Allison, D.J.; Anderson, L.N.; Ma, J.; Raina, P. Body mass index and all-cause mortality in older adults: A scoping review of observational studies. Obes. Rev. 2020, 21, e13035. [Google Scholar] [CrossRef] [PubMed]
  58. Pimentel, E.L.A.; Oliveira, J.B.; Santana, A.A.; Maia, L.; Ramos, H.E. Prevalência de sobrepeso e obesidade em idosas frequentadoras da Universidade Aberta da Terceira Idade—UATI. Rev. Ciênc Méd Biol. 2020, 19, 543–546. [Google Scholar]
  59. Rauber, F.; da Costa Louzada, M.L.; Steele, E.M.; Millett, C.; Monteiro, C.A.; Levy, R.B. Ultra-processed food consumption and chronic non-communicable diseases-related dietary nutrient profle in the UK (2008–2014). Nutrients 2018, 10, 587. [Google Scholar] [CrossRef] [Green Version]
  60. Louzada, M.L.C.; Ricardo, C.Z.; Steele, E.M.; Levy, R.B.; Cannon, G.; Monteiro, C.A. The share of ultra-processed foods determines the overall nutritional quality of diets in Brazil. Public. Health Nutr. 2018, 21, 94–102. [Google Scholar] [CrossRef] [Green Version]
  61. Louzada, M.L.C.; Baraldi, L.G.; Steele, E.M.; Martins, A.P.; Canella, D.S.; Moubarac, J.C.; Levy, R.B.; Cannon, G.; Afshin, A.; Imamura, F.; et al. Consumption of ultraprocessed foods and obesity in Brazilian adolescents and adults. Prev. Med. 2015, 81, 9–15. [Google Scholar] [CrossRef] [Green Version]
  62. Juul, F.; Martinez-Steele, E.; Parekh, N.; Monteiro, C.A.; Chang, V.W. Ultra-processed food consumption and excess weight among US adults. Br. J. Nutr. 2018, 120, 90–100. [Google Scholar] [CrossRef] [Green Version]
  63. Nardocci, M.; Leclerc, B.S.; Louzada, M.L.; Monteiro, C.A.; Batal, M.; Moubarac, J.C. Consumption of ultra-processed foods and obesity in Canada. Can. J. Public Health 2019, 110, 4–14. [Google Scholar] [CrossRef]
  64. Liu, J.; Steele, E.M.; Li, Y.; Yi, S.S.; Monteiro, C.A.; Mozaffarian, D. Consumption of Ultraprocessed Foods and Body Fat Distribution Among U.S. Adults. Am. J. Prev. Medic. 2023, in press. [Google Scholar] [CrossRef] [PubMed]
  65. Viola, P.C.A.F.; Carvalho, C.A.; Bragança, M.L.B.M.; França, A.K.T.D.C.; Alves, M.T.S.S.B.E.; da Silva, A.A.M. High consumption of ultra-processed foods is associated with lower muscle mass in Brazilian adolescents in the RPS birth cohort. Nutrition. 2020, 79–80, 1–6. [Google Scholar] [CrossRef] [PubMed]
  66. Elizabeth, L.; Machado, P.; Zinöcker, M.; Baker, P.; Lawrence, M. Ultraprocessed foods and health outcomes: A narrative review. Nutrients 2020, 12, 1955. [Google Scholar] [CrossRef] [PubMed]
  67. Cuevas-Sierra, A.; Milagro, F.I.; Aranaz, P.; Martínez, J.A.; Riezu-Boj, J.I. Gut microbiota differences according to ultra-processed food consumption in a spanish population. Nutrients 2021, 13, 2710. [Google Scholar] [CrossRef] [PubMed]
  68. Brasil (2020). Pesquisa de Orçamentos Familiares 2017–2018: Análise do Consumo Alimentar Pessoal no Brasil/IBGE, Coordenação de Trabalho e Rendimento; IBGE: Rio de Janeiro, Brazil, 2020. [Google Scholar]
Figure 1. Study sample flowchart. Abbreviation: ISAD-PI, Population-Based Health Survey; R24h: 24 h food recall.
Figure 1. Study sample flowchart. Abbreviation: ISAD-PI, Population-Based Health Survey; R24h: 24 h food recall.
Nutrients 15 03157 g001
Figure 2. Mean percentage contribution to TEV from consumption of ultra-processed foods and fresh foods by age group. Equal letters do not differ statistically. Different letters indicate significant differences between means.
Figure 2. Mean percentage contribution to TEV from consumption of ultra-processed foods and fresh foods by age group. Equal letters do not differ statistically. Different letters indicate significant differences between means.
Nutrients 15 03157 g002
Table 1. Characterization of the study population.
Table 1. Characterization of the study population.
Age (Years)n (%)
20–35154 (31.4)
36–59207 (42.2)
≥60129 (26.3)
Gender
Masculine162 (33.1)
Feminine328 (66.9)
Marital status
Single286 (58.5)
Married203 (41.5)
Family income
(Brazilian minimum wage)
≤2374 (76.3)
>2116 (23.7)
Level of education
Not literate29 (5.9)
Primary education149 (30.4)
High school201 (41)
University education111 (22.7)
Alcohol consumption
No294 (60)
Yes196 (40)
Smoking
No382 (78)
Yes108 (22)
Physical activity
Insufficiently active96 (19.6)
Active394 (80.4)
Mean contribution percentage in the TEV of the food groups NOVA
Food groups NOVAMean ± SD
Unprocessed or minimally processed67.9 ± 18.9
Ultra-processed food19.7 ± 17.9
TEV: Total Energy Value.
Table 2. Distribution of anthropometric indicators according to age group.
Table 2. Distribution of anthropometric indicators according to age group.
Mean ± SD20–35 Years36–59 Years≥60 Years
WHtR0.56 ± 0.810.52 ± 0.07 a0.57 ± 0.07 b0.61 ± 0.07 c
TSF23.7 ± 10.123.9 ± 10.6 ab25.1 ± 10.4 a21.1 ± 8.7 b
AC31.4 ± 4.631.2 ± 4.8 a32.2 ± 4.7 b30.3 ± 4.6 a
AMC23.9 ± 3.623.7 ± 3.9 a24.3 ± 3.7 a23.7 ± 3.0 a
CAMA39.1 ± 13.738.3 ± 14.6 a40.6 ± 14.5 a37.8 ± 10.8 a
SSF22.7 ± 9.321.4 ± 9.0 a23. 7 ± 9.5 b-
CC34.1 ± 3.6---
SD: standard deviation; WHtR: waist-to-height ratio; TSF: triceps skinfold; AC: arm circumference; AMC: arm muscle circumference. AMC: AC(cm) − (3.14 × TSF); CAMA: arm muscular area corrected; SSF: subscapular skinfold; CC: calf circumference. Equal letters do not differ statistically. Different letters indicate a significant difference between means.
Table 3. Association between consumption of ultra-processed foods and anthropometric indicators according to age group (n = 490).
Table 3. Association between consumption of ultra-processed foods and anthropometric indicators according to age group (n = 490).
ß (CI95%)pß (CI95%)p *
20–35 years (n = 153)
WHtR−0.03 (−0.08/0.02)0.27−0.01 (−0.02/0.05)0.19
TSF0.03 (−0.07/0.12)0.540.04 (0.03/0.09)0.04
AC−0.00 (−0.05/0.04)0.82−0.01 (−0.01/0.02)0.38
AMC−0.01 (−0.04/0.01)0.21−0.01 (−0.02/0.01)0.49
CAMA−0.05 (−0.13/0.03)0.22−0.02 (−0.08/0.04)0.54
SSF−0.02 (−0.09/0.06)0.65−0.003 (−0.05/0.04)0.89
36–59 years (n = 207)
WHtR0.02 (−0.06/0.06)0.92−0.03 (−0.02/0.02)0.76
TSF0.04 (−0.05/0.13)0.36−0.00 (−0.05/0.04)0.92
AC−0.01 (−0.05/0.03)0.63−0.02 (−0.03/−0.01)0.03
AMC−0.02 (−0.04/−0.00)0.04−0.02 (−0.03/−0.00)0.01
CAMA−0.08 (−0.16/−0.006)0.04−0.07 (−0.12/−0.02)0.01
SSF0.03 (−0.03/0.10)0.320.01 (−0.04/0.06)0.65
≥60 years (n = 128)
WHtR0.00 (−0.01/0.01)0.89−0.03 (−0.04/0.02)0.80
TSF0.03 (−0.06/0.13)0.49−0.02 (−0.07/0.04)0.59
AC0.01 (−0.03/0.06)0.520.01 (−0.004/0.03)0.13
AMC0.00 (−0.03/0.03)0.770.02 (−0.002/0.04)0.08
CAMA0.03 (−0.08/0.13)0.610.06 (−0.01/0.13)0.10
CC−0.0005 (−0.04/0.04)0.980.006 (−0.02/0.03)0.61
CI: confidence interval; WHtR: waist-to-height ratio; TSF: triceps skinfold; AC: arm circumference; AMC: arm muscle circumference. AMC: AC(cm) − (3.14 × TSF); CAMA: arm muscular area corrected; SSF: subscapular skinfold; CC: calf circumference. * Adjusted for gender, schooling, family income, marital status, alcohol consumption, smoking, practice of physical activity, BMI, and WC.
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Monteles Nascimento, L.; de Carvalho Lavôr, L.C.; Mendes Rodrigues, B.G.; da Costa Campos, F.; de Almeida Fonseca Viola, P.C.; Lucarini, M.; Durazzo, A.; Arcanjo, D.D.R.; de Carvalho e Martins, M.d.C.; de Macêdo Gonçalves Frota, K. Association between Consumption of Ultra-Processed Food and Body Composition of Adults in a Capital City of a Brazilian Region. Nutrients 2023, 15, 3157. https://doi.org/10.3390/nu15143157

AMA Style

Monteles Nascimento L, de Carvalho Lavôr LC, Mendes Rodrigues BG, da Costa Campos F, de Almeida Fonseca Viola PC, Lucarini M, Durazzo A, Arcanjo DDR, de Carvalho e Martins MdC, de Macêdo Gonçalves Frota K. Association between Consumption of Ultra-Processed Food and Body Composition of Adults in a Capital City of a Brazilian Region. Nutrients. 2023; 15(14):3157. https://doi.org/10.3390/nu15143157

Chicago/Turabian Style

Monteles Nascimento, Larisse, Layanne Cristina de Carvalho Lavôr, Bruna Grazielle Mendes Rodrigues, Felipe da Costa Campos, Poliana Cristina de Almeida Fonseca Viola, Massimo Lucarini, Alessandra Durazzo, Daniel Dias Rufino Arcanjo, Maria do Carmo de Carvalho e Martins, and Karoline de Macêdo Gonçalves Frota. 2023. "Association between Consumption of Ultra-Processed Food and Body Composition of Adults in a Capital City of a Brazilian Region" Nutrients 15, no. 14: 3157. https://doi.org/10.3390/nu15143157

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop