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Obesogenic neighborhood environment is associated with body fat and low-grade inflammation in Brazilian children: could the mother’s BMI be a mediating factor?

Published online by Cambridge University Press:  30 November 2023

Mariana De Santis Filgueiras*
Affiliation:
Department of Nutrition and Health, Universidade Federal de Viçosa, Av. P.H. Rolfs s/n, Centro de Ciências Biológicas II, Campus Universitário, Viçosa, Minas Gerais 36570-900, Brazil
Milene Cristine Pessoa
Affiliation:
Department of Nutrition, Nursing School, Universidade Federal de Minas Gerais, Av. Prof. Alfredo Balena 190, Santa Efigênia, Belo Horizonte, Minas Gerais 30130-100, Brazil
Josefina Bressan
Affiliation:
Department of Nutrition and Health, Universidade Federal de Viçosa, Av. P.H. Rolfs s/n, Centro de Ciências Biológicas II, Campus Universitário, Viçosa, Minas Gerais 36570-900, Brazil
Ariene Silva do Carmo
Affiliation:
Department of Nutrition, Nursing School, Universidade Federal de Minas Gerais, Av. Prof. Alfredo Balena 190, Santa Efigênia, Belo Horizonte, Minas Gerais 30130-100, Brazil
Aline Siqueira Fogal Vegi
Affiliation:
Nutrition School, Universidade Federal de Ouro Preto, Rua Dois, Campus Morro do Cruzeiro, Ouro Preto, Minas Gerais 35400-000, Brazil
Fernanda Martins de Albuquerque
Affiliation:
Nutrition Institute, Universidade do Estado do Rio de Janeiro, Rua São Francisco Xavier 524, 12th floor, Maracanã, Rio de Janeiro 20550-900, Brazil
Juliana Farias de Novaes
Affiliation:
Department of Nutrition and Health, Universidade Federal de Viçosa, Av. P.H. Rolfs s/n, Centro de Ciências Biológicas II, Campus Universitário, Viçosa, Minas Gerais 36570-900, Brazil
*
*Corresponding author: Email mdsfilgueiras@gmail.com
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Abstract

Objective:

To evaluate the direct and indirect associations of obesogenic and leptogenic neighborhood environments with body fat, and pro- and anti-inflammatory adipokines in Brazilian children.

Design:

Cross-sectional study. The body fat distribution was assessed using dual-energy X-ray absorptiometry (DXA). Concentrations of leptin and adiponectin were measured. Four hundred meters (0·25 miles) road network buffer was the neighborhood unit used to assess the environmental characteristics around households. Obesogenic and leptogenic environments were the latent variables obtained from the observed characteristics. The mother’s BMI, ultra-processed food consumption, and physical activity before and after school, were tested as mediating variables. A hybrid model of structural equations was used to test the direct and indirect associations of obesogenic and leptogenic environments with body fat, leptin and adiponectin concentrations.

Setting:

Urban area of Viçosa, Minas Gerais, Brazil.

Participants:

Children aged 8- and 9-years (n 367).

Results:

Obesogenic environment was directly associated with the mother’s BMI (β: 0·24, P = 0·02) and the child’s body fat (β: 0·19, P = 0·02). The mother’s BMI and body fat mediated the association of the obesogenic environment with leptin concentrations (β: 0·05, P = 0·02).

Conclusions:

Obesogenic neighborhood environment was directly associated with body fat and mother's BMI, and indirectly associated with leptin concentrations in Brazilian children, mediated by the mother’s BMI and body fat.

Type
Research Paper
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution and reproduction, provided the original article is properly cited.
Copyright
© The Author(s), 2023. Published by Cambridge University Press on behalf of The Nutrition Society

Overweight and pediatric obesity are considered public health problems, affecting over 340 million children and adolescents worldwide(1). Adipose tissue secretes several peptides, such as adipokines, which are involved in inflammatory and immune functions, cardiovascular homeostasis, among other biological and physiological functions(Reference Kershaw and Flier2,Reference Rodríguez, Ezquerro and Méndez-Giménez3) . Some studies have shown that children with overweight or obesity have higher concentrations of pro-inflammatory adipokines, such as leptin, and lower concentrations of anti-inflammatory adipokines, such as adiponectin(Reference Domingos, Machado-Coelho and Volp4Reference Zhang, Cheng and Zhao6).

The interaction of individual and environmental factors results in childhood obesity and adiposity-related inflammation(Reference Blüher7,Reference Davison and Birch8) . The child’s dietary pattern and practice of physical activity (PA) are considered proximal determinants of body fat(Reference Davison and Birch8). Jointly, the unhealthy lifestyle and the higher BMI of parents can influence a child’s behavior (for instance, unhealthy diet and physical inactivity) and excess of weight(Reference Davison and Birch8). However, several environmental characteristics may be directly or indirectly related to adiposity markers. An obesogenic environment, whose conditions favor choices for a lifestyle that promotes obesity, such as unhealthy eating and physical inactivity, may influence childhood obesity(Reference Davison and Birch8,Reference Swinburn, Egger and Raza9) . On the other hand, the presence of a leptogenic environment, that is, one that promotes choices for a healthy lifestyle, such as PA and healthy eating, can prevent and/or reduce body fat in children(Reference Davison and Birch8,Reference Swinburn, Egger and Raza9) .

In all age groups, the relationship of obesogenic and leptogenic environments with low-grade inflammatory markers is poorly investigated. In Brazilian children, the higher density of public PA facilities around schools was associated with lower leptin concentrations(Reference Filgueiras, Pessoa and Bressan10). In addition, obesogenic environmental factors, such as air pollution and exposure to ultra-processed foods (UPF), can promote endocrine dysfunction, impairing the differentiation and size of adipocytes and, consequently, stimulating the production of pro-inflammatory adipokines(Reference Heindel and Blumberg11). We highlighted that few studies with combined environmental characteristics used the structural equation modeling approach and verified their direct and indirect associations with individual characteristics, such as obesity(Reference Carmo, Mendes and Pessoa12,Reference Saelee, Gazmararian and Haardörfer13) and cardiometabolic risk(Reference Albuquerque, Pessoa and Filgueiras14).

Environmental characteristics were greatly influenced by the rapid urbanization that occurred in middle-income countries, such as Brazil(Reference Sallis, Bowles and Bauman15). Thus, knowing the role of these combined characteristics can help in the development of strategies to prevent and treat adiposity-related comorbidities. Given this, we aimed to evaluate the direct and indirect associations of obesogenic and leptogenic neighborhood environments with body fat, and pro- and anti-inflammatory adipokines in Brazilian children. Our hypothesis is that obesogenic and leptogenic environments are, directly and indirectly, associated with body fat and adipokine concentrations (leptin and adiponectin).

Methods

Study design, setting, and sample

This cross-sectional study was conducted in 2015 among children aged 8- and 9-years residents in the urban area of Viçosa, a medium-sized city in Minas Gerais, Brazil. The city has an area of 299 km2, 72 244 inhabitants, of which 93·2 % live in urban areas, and the Gross Domestic Product (GDP) per capita is US$ 4682·22 (R$ 19 869·94)(16). Viçosa is in the middle of a mountainous valley with predominantly rugged terrain. It presents a university city profile and has a more urban than agricultural economy, highlighting the role of the tertiary sector (commerce and services) as the main economic activity(Reference Pereira17).

This study came from two surveys:

1. Schoolchildren Health Assessment Survey (Pesquisa de Avaliação da Saúde do Escolar, PASE, in Portuguese), an investigation conducted in 2015 that aimed to assess the cardiovascular health of children aged 8 and 9 years enrolled in all schools in the urban area of Viçosa. The sample size calculation, sampling process, and non-inclusion criteria were described previously(Reference Milagres, Rocha and Filgueiras18). Briefly, 378 children were selected at school by stratified random sampling. We did not include children with health problems that altered their nutritional status or body composition; chronic use of medicine that affected the glucose and/or lipid metabolism; and when the parents/guardians could not be contacted after three attempts. For this study, we only analyzed data from children who lived in the urban area of Viçosa (n 367).

2. Data collection of the built environment of the urban area of Viçosa (MG), which has information on food environment, built environment, PA facilities, and neighborhood socioeconomic profile of the urban area.

Both surveys were carried out following the guidelines established in the Declaration of Helsinki and approved by the Human Research Ethics Committee of the Universidade Federal de Viçosa (UFV) (reference numbers 663·171/2014 and 1·821·618/2016). The Municipal Secretary of Education, the Regional Superintendent of Education and school principals approved the research. In addition, all parents/guardians signed an informed consent form.

Body fat

The body fat percentage (%) was determined by a specialized technician using the DXA method (Lunar Prodigy Advance, GE Medical Systems Lunar, Milwaukee, WI, USA) in the diagnostic imaging sector of the UFV Health Center. At the time of exam, the children were wearing light clothing and without metal, lying in supine position on a stretcher until the equipment completed the scanning.

Adipokines

The blood samples were collected in a 12-h fast in the clinical analysis sector of the UFV Health Center by venipuncture in the antecubital region. The serum and plasma were separated and stored in 1·5 ml Eppendorf tubes at -80ºC to measure leptin and adiponectin concentrations.

Leptin serum was analyzed by an enzyme immunoassay method (CV intra-assay <13·3 % and inter-assay <12·7 %) (KAP2281, DIAsource®, Louvain-la-Neuve, Belgium; standardized protocols from Diagnósticos do Brasil). Plasma adiponectin was determined by commercials ELISA sandwich kits, (coefficients of variation intra-assay <10 % and inter-assay <12 %) (human adiponectin: SEA605Hu, Cloud Clone Corp.®, Houston, TX, USA; standardized protocols from Laboratório Especializado em Análises Científicas – LEAC).

Obesogenic and leptogenic environmental characteristics

The assessment of environmental characteristics has been previously described(Reference Filgueiras, Pessoa and Bressan10). Briefly, an objective assessment of the food stores and the public PA facilities in the city was performed. Trained researchers, with the aid of urban census tracts maps, walked every street and, when identifying a food store and a PA facility (squares, places for walking, among others), a specific questionnaire was filled out. Four types of questionnaires, adapted from a tool developed in Brazil, were used for the objective assessment of food stores for: (a) household consumption; (b) immediate consumption; (c) mobile food vendors; and (d) farmer’s markets(Reference Duran19). Food stores were classified according to the Technical Study ‘Mapping Food Deserts in Brazil’ by Câmara Interministerial de Segurança Alimentar e Nutricional (CAISAN), which considers the degree of food processing sold by store according to the NOVA classification system(Reference Monteiro, Levy and Claro20). Stores whose UPF represents more than 50 % of the total products available for sale were classified as predominantly UPF stores(21). To assess the public PA facilities, we used the adapted Physical Activity Resource Assessment (PARA) instrument(Reference Lee, Booth and Reese-Smith22).

Each food store, PA facility, and household’s geographic coordinates (latitude and longitude) were obtained from addresses using the Google Maps online search service (https://www.google.com/maps?hl=en). Data on traffic accidents and crime was provided by the Secretaria de Segurança Pública do Estado de Minas Gerais, and its geographical coordinates (latitude and longitude). All characteristics presented in geographical coordinates were reprojected from the WGS 84 Geographic Coordinate System to the Projected Coordinate System, Universal Transverse Mercator System (UTM), 23S spindle, SIRGAS 2000 datum, using ArcGIS Pro (ESRI, Redlands, CA, USA).

The green spaces and neighborhood income were obtained from the georeferenced database at the Instituto Brasileiro de Geografia e Estatística (23). The presence of green spaces was identified if, on the face of the block at observation or its facing face or the median strip, there was a tree along the sidewalk and/or on a median strip that separates opposing lanes of traffic on divided roadways, even if only in part. The presence of green space was also considered when existing in areas without paving and/or without sidewalks(23). The percentage of green spaces in the census tract was determined by dividing the total number of households that had the characteristic by the total number of households in the tract and multiplying by 100(23). The neighborhood income was obtained by the mean household income of the census tracts from the 2010 Census (https://censo2010.ibge.gov.br/) inserted within buffer around household.

The walkability was evaluated by an index that considers residential density, presence of sidewalk (%), commercial density, presence of public lighting (%), and the density of intersections between streets (connectivity), as previously described(Reference Vegi, Fernandes Filho and Pessoa24).

To assess the obesogenic and leptogenic environmental characteristics around households, we used 400 m (0·25 miles) road network buffer as the neighborhood unit, corresponding to a 5 min’ walk(Reference Day and Pearce25,Reference Smith, Cummins and Clark26) . Within each buffer, the absolute density was calculated. Then, the density per 1000 inhabitants was obtained for predominantly UPF food stores, PA facilities, traffic accidents, and crime. For green spaces, neighborhood income, walkability, the census tracts averages inserted within a buffer around households were obtained. Then, all environmental characteristics were categorized according to the 50th percentiles.

Mediating and adjusting variables

Through a semi-structured questionnaire, individual and family data, such as sex, per capita household income (US$), maternal education (years), receipt of government benefit (yes/no), and PA before and after school (yes/no), were collected. Per capita income was calculated by dividing the total household income by the number of dependent residents on that household income.

The mother’s weight and height were measured by an electronic digital scale with a capacity of 150 kg and a sensitivity of 50 g (Tanita®, model BC 553, Arlington Heights, IL, USA) and a vertical stadiometer, divided into centimeters and subdivided into millimeters (Alturexata®, Belo Horizonte, MG, Brazil), respectively. Then, the mother’s BMI was calculated.

UPF consumption was estimated using the average of three 24-h dietary recalls (24HR) obtained on non-consecutive days, including 1 weekend day. The data were collected from the parents/guardian and the child simultaneously. All 24HR were conducted by trained dietitians using the 5-step multiple-pass method(Reference Conway, Ingwersen and Moshfegh27). To improve portion size estimation and increase data reliability, during the interviews the participants had access to kitchen measuring utensils and food photographic records(Reference Vianna and Gil28). The software Diet Pro® 5i, version 5.8, was used to record food consumption information. To analyze the food composition, the Tabela Brasileira de Composição de Alimentos (TACO)(29) was used preferentially, following by the US Department of Agriculture’s of Food Composition Database(30). Measures utilizing kitchen utensils were converted into grams (g), milligrams (mg), or milliliters (ml) to estimate consumption of total energy (kcal) and UPF, defined according to the NOVA classification(Reference Monteiro, Levy and Claro20). The mean percentage of UPF energy contribution from the three 24HR was calculated.

Data analysis and structural equation modeling

Descriptive analysis was performed by calculating frequency distributions for categorical variables and median and interquartile range (IQR) for continuous variables using the statistical software Stata® version 14 (StataCorp., LP). The normality of numerical variables was assessed using the Shapiro-Wilk test. The Mann-Whitney test and Pearson’s chi-squared test compared numerical and categorical variables according to sex, respectively. The level of significance for all statistical tests was set at 0·05.

Structural equation modeling was conducted in the software Mplus version 8.2 (Muthén & Muthén). The initial theoretical hybrid model of structural equations was composed of obesogenic and leptogenic environments in a distal position, related to the UPF consumption, mother’s BMI, and PA before and after school. In the model, the obesogenic and leptogenic environments might directly associate with %BF and pro- and anti-inflammatory adipokines. Furthermore, the environments may be indirectly associated with body fat, being mediated by the UPF consumption, mother’s BMI, and PA before and after school. Therefore, body fat was also considered a mediating variable in the relationship between the obesogenic/leptogenic environments and adipokines. According to the literature review, the obesogenic environment was initially composed of the variables predominantly UPF stores, traffic accidents, and crime. In contrast, the leptogenic environment would consist of walkability, PA facilities, green spaces, and neighborhood income (Fig. 1).

Fig. 1 Initial theoretical model of structural equations hypothesized for the associations of obesogenic and leptogenic environments with % body fat and adipokine concentrations in children. Viçosa, Minas Gerais, Brazil, 2015. Abbreviations: %BF: %body fat; BMI: body mass index; PA: physical activity; q1: predominantly ultra-processed food stores; q2: traffic accidents; q3: crime; q4: walkability; q5: physical activity facilities; q6: green spaces; q7: neighborhood income; UPF: ultra-processed food. The observed variables were presented in rectangular shapes and the latent variables in circular shapes. Models with % body fat, adipokines, ultra-processed food consumption, and physical activity before and after school as outcome were adjusted for child’s sex and socioeconomic status. Models with mother’s BMI as outcome were adjusted for socioeconomic status

Latent variables were validated, with exploratory and confirmatory analyses. The exploratory evaluation was performed through principal component analysis (PCA), obtaining the Kaiser-Meyer-Olkin (KMO) index with values between 0·5 and 1·0 considered acceptable(Reference Hair, Black and Babin31). For the construction of latent variables, a factor loading greater than 0·4 and a P < 0·05 were considered to indicate that the correlation between the observed variable and the latent variable had a moderately high magnitude(Reference Kline32). After confirmatory analyses, latent variables for the obesogenic and leptogenic environments were obtained from observed environmental variables and categorized according to the 50th percentile of the sample:

• Obesogenic environment: predominantly UPF stores, traffic accidents, crime, and walkability.

• Leptogenic environment: public PA facilities, green spaces, and neighborhood income.

Estimates were obtained using the Weighted Least Squares Mean and Variance Adjusted (WLSMV), which is applied to categorical variables, robust in the absence of normality and imputes missing data using Full Information Maximum Likelihood (FIML) estimation(Reference Kline32). Theta parameterization was used to control for differences in residual variances(Reference Muthén and Muthén33).

Models with body fat, adipokines, UPF consumption, and PA before and after school as outcomes were adjusted for the child’s sex and socioeconomic status (latent variable composed of per capita income, maternal education, and government benefit). Models with the mother’s BMI as outcome were adjusted for socioeconomic status. The latent variable of socioeconomic status was also validated.

To assess the quality of fit of the hybrid structural equation model, the following criteria were considered: chi-squared test with P > 0·05; root-mean-square error of approximation (RMSEA) with values less than 0·08; values of the comparative fit index (CFI) and the Tucker Lewis index (TLI) approximately or greater than 0·95; standardized root mean square residual (SRMR) less than 1(Reference Wang and Wang34).

The modindices command was used to calculate the modification indices, to obtain suggestions for changes in the initial hypotheses. To carry out the changes, theoretical plausibility and modification index values equal to or greater than 10 were considered(Reference Kline32,Reference Wang and Wang34) . All direct and indirect associations of latent and observed variables were evaluated in the final model.

Sensitivity analysis was also performed to verify the robustness of the associations in all models, with the variables being tested in different ways: 1st: body fat was categorized according to tertiles; 2nd: body fat was replaced by % android fat, being tested continuously and categorized into tertiles; 3rd: adipokines were categorized according to quintiles; 4th: per capita income (in tertiles) and maternal education (<4 years, 5–8 years, 9–11 years and ≥ 12 years) were also categorically tested.

Results

Sample characterization

We evaluated 367 children and their respective mothers, with age mean 8·5 ± 0·5 years; 51·8 % were girls, 22·9 % were government program beneficiaries. The median of body fat and leptin and adiponectin concentrations were 22·7 %, 1·7 ng/ml, and 2·4 µg/dl, respectively. According to sex, female children had higher body fat, leptin concentration, and less PA before and after school (Table 1).

Table 1 Body fat, adipokine concentrations, socioeconomic, and health behaviors in children, according to sex. Viçosa, Minas Gerais, Brazil, 2015

Abbreviations: BMI: body mass index; PA: physical activity; UPF: ultra-processed food.

* Mann-Whitney test.

Pearson’s chi-squared test.

Bold values (P < 0·05).

Data presented as median (interquartile range) for numerical variables or n (%) for categorical variables.

Validation of latent variables

We performed an exploratory analysis of the available environmental variables and identified two principal components, presenting a satisfactory KMO (0·80). The first component contributed to 47·7 % of the variance and the second contributed to 25·5 %, totaling 73·2 % of the variance. The constructs were satisfactory in convergent and discriminatory validities, in which each construct had different measurement, and the correlation between them was significant, but less than 0·90 (0·62, P < 0·001). In general, the first component was composed of variables that characterize an obesogenic environment, while the second component was composed of variables that characterize a leptogenic environment (Fig. 2(a)).

Fig. 2 Validation of latent variables (a) obesogenic and leptogenic environments, and (b) socioeconomic status. Abbreviations: SES: socioeconomic status. Data presented as factor loading (SE). The observed variables were presented in rectangular shapes and the latent variables in circular shapes. For environmental variables, Kaiser-Meyer-Olkin (KMO) index = 0·80, % variance of 1st component (obesogenic environment): 47·7 %, % variance of 2nd component (leptogenic environment): 25·5 %, % variance total = 73·2 %. For socioeconomic status, Kaiser-Meyer-Olkin (KMO) index = 0·59, and % variance total = 58·1 %. *P < 0·001

From the socioeconomic variables, we obtained only one principal component, which presented a satisfactory KMO (0·59) and convergent validity, and explained 58·1 % of the total variance (Fig. 2(b)).

Structural equation models

The obesogenic environment was directly associated with the mother’s BMI (β: 0·24, P = 0·02) and the child’s body fat (β: 0·19, P = 0·02). We identified an indirect association of the obesogenic environment with the child’s body fat (β: 0·08, P = 0·04), being mediated by the mother’s BMI (β: 0·09, P = 0·02). We also observed an indirect association of the obesogenic environment with leptin concentrations (β: 0·17, P = 0·001), being mediated by child’s body fat (β: 0·10, P = 0·03), as well by mother’s BMI and child’s body fat (β: 0·05, P = 0·02) (Table 2; Fig. 3).

Table 2 Standardized coefficients (β) of the direct and indirect associations of obesogenic neighborhood environment with body fat and adipokine concentrations in children. Viçosa, Minas Gerais, Brazil, 2015

Abbreviations: % BF: % body fat; BMI: body mass index; PA: physical activity; se: standard error; UPF: ultra-processed food; β: standard coefficient.

Structural equation modeling. Model fit information: X 2 = 206·88, P < 0·001; Root Mean Square of Approximation: 0.06, 90 % CI (0 05, 0·07); Comparative Fit Index = 0·99; Tucker Lewis Index = 0·99; Standardized Root Mean Square Residual: 0·06.

Models with % body fat, adipokines, ultra-processed food consumption, and physical activity before and after school as outcomes were adjusted for child’s sex and socioeconomic status. Models with mother’s BMI as outcome were adjusted for socioeconomic status.

Bold values (P < 0·05).

Fig. 3 Direct and indirect associations of the obesogenic neighborhood environment with body fat and adipokine concentrations in Brazilian children. Abbreviations: % BF: % body fat; BMI: body mass index. Solid lines represent direct associations and dotted lines represent indirect associations

The direct and indirect associations of the leptogenic environment with body fat and adipokine concentrations were not observed (Table 3).

Table 3 Standardized coefficients (β) of the direct and indirect associations of leptogenic neighborhood environment with body fat and adipokine concentrations in children. Viçosa, Minas Gerais, Brazil, 2015

Abbreviations: % BF: % body fat; BMI: body mass index; PA: physical activity; se: standard error; UPF: ultra-processed food; β: standard coefficient.

Structural equation modeling. Model fit information: X 2 = 206·88, P < 0·001; Root Mean Square of Approximation: 0·06, 90 % CI (0 05, 0·07); Comparative Fit Index = 0·99; Tucker Lewis Index = 0·99; Standardized Root Mean Square Residual: 0·06.

Models with % body fat, adipokines, ultra-processed food consumption, and physical activity before and after school as outcomes were adjusted for child’s sex and socioeconomic status. Models with mother’s BMI as outcome were adjusted for socioeconomic status.

In general, the models showed good quality of fit, satisfying most of the criteria: chi-squared test: 206·88, P < 0·001; RMSEA: 0·06, 90 % CI: 0·05, 0·07, P = 0·05; CFI: 0·99; TLI: 0·99; SRMR: 0·06.

When the sensitivity analysis was performed, considering different categorization forms of variables and the replacement of body fat by android fat, the same results were observed (data not shown).

Discussion

Our findings supported the hypothesis that the obesogenic neighborhood environment has a direct and indirect association with children’s body fat, with the mother’s BMI as the main mediator. Furthermore, the obesogenic environment was indirectly associated with leptin concentrations, with the mother’s BMI and child´s body fat as mediators.

The relationship between the obesogenic environment and child health has been investigated, however the studies were conducted in high-income countries and evaluated the isolated environmental characteristics(Reference Ghenadenik, Kakinami and Van Hulst35,Reference Zhou, Buck and Maier36) . In this study, we have two innovations. First, it is known that middle-income countries, such as Brazil, have a different development and urbanization profile compared to high-income countries(Reference Gascon, Vrijheid and Nieuwenhuijsen37). Second, when we used the latent variables of obesogenic and leptogenic environments, we considered jointly the association of all variables that composed them with outcomes.

The obesogenic environment had a direct association with the child’s body fat. Although some evidence did not confirm this relationship(Reference Carmo, Mendes and Pessoa12,Reference Nesbit, Kolobe and Sisson38) , other studies showed similar results(Reference Saelee, Gazmararian and Haardörfer13,Reference Carmo, Rodrigues and Nogueira39) . Among Portuguese schoolchildren, there was a direct association of an unsafety environment (excessive traffic and intersections, high crime rates) with the increase in the BMI Z score(Reference Carmo, Rodrigues and Nogueira39). In addition, the neighborhood socioeconomic status (lower education, poverty level, unemployment rates, lower per capita income, and vacant housing) and social disorganization (single-parent households and the proportion of those divorce or separated for both males and females) had a direct association with obesity among American adolescents(Reference Saelee, Gazmararian and Haardörfer13). In adolescents from the United States, the access to PA facilities (recreation center, sidewalks/walking paths, and parks/playgrounds) was directly associated for reducing obesity(Reference Carmo, Rodrigues and Nogueira39).

Additionally, our results showed that the mother’s BMI was the main mediator in the association of the obesogenic environment with body fat and leptin concentrations. A study conducted among children from Seattle and San Diego, United States, showed a direct association between the obesogenic environment, obesity, and parental obesity(Reference Saelens, Sallis and Frank40). In Brazilian children, the mother’s BMI can be a proxy for the child’s body adiposity due to genetic and unhealthy behavioral factors, considering eating habits and PA(Reference Warkentin, Mais and Latorre41,Reference Ribeiro, Taddei and Colugnatti42) , and it was also a mediator in the relationship between the obesogenic environment and a higher cardiometabolic risk(Reference Albuquerque, Pessoa and Filgueiras14). These findings suggest that strategies to reduce the obesogenic environment around households may impact the child’s body fat as well as their parents, who are mainly responsible for the acquisition of food and encourage the practice of physical and leisure activities by children. However, we did not find studies investigating these relationships with leptin concentrations in childhood.

The obesogenic and leptogenic environments were not directly associated with UPF consumption and PA before and after school. Furthermore, these behavioral characteristics were not mediators of the association with body fat and adipokines. Similarly, among Portuguese, there was a lack of mediation of characteristics related to PA between favorable/unsafety environments and a child’s BMI(Reference Carmo, Rodrigues and Nogueira39). It is important to consider that other factors can be related with these behavioral characteristics beyond the community environment, such as shopping preferences, the modes of transportation, and home environment(Reference Mei, Huang and Xia43).

This is the first investigation that evaluated the association of the obesogenic and leptogenic environments with adiposity-related inflammation markers. There is no evidence of mediating role of mother’s BMI on a child’s inflammatory markers; however, it is known that obesity is the main mediator between food consumption and low-grade inflammation(Reference Park, Zhang and Steck44). From the knowledge about the association between adipokines and cardiometabolic outcomes, such as insulin resistance markers and blood pressure(Reference Filgueiras, Pessoa and Bressan45), it is necessary to assess the relationship between the environment and markers beyond the traditional body adiposity measures. Evidence has shown associations of the obesogenic environment with the child’s BMI(Reference Mei, Huang and Xia43), an easy-to-use and low-cost measure. Nevertheless, phenotyping of obesity has been proposed considering other measures/markers, such as those obtained by reference methods (DXA) and pro- and anti-inflammatory adipokines(Reference Blundell, Dulloo and Salvador46).

We emphasize that walkability was part of the latent variable obesogenic environment, with a direct factor loading, even initially being part of the leptogenic environment in the theoretical model. Walkability quantifies the safety and desirability of the walking routes(Reference Smith47), being a measure of urban design in connecting places and facilitating PA(Reference Yang, Chen and Wang48). However, in urban areas, greater walkability was associated with a higher BMI among children(Reference Stowe, Hughey and Hallum49). We used a walkability index proposed to the city studied that considers important characteristics that favor walking (residential and commercial densities, intersections between roads, the presence of sidewalks and public lighting)(Reference Smith, Cummins and Clark26). The city is more walkable in the downtown; however, this region also has a higher density of UPF stores, traffic accidents, and crime. In this sense, further studies are needed to understand the role of walkability on health outcomes, considering different aspects of urbanization.

The leptogenic environment was not associated with adiposity and related inflammation in children. This lack of association may be attributed to the urban environment of Viçosa, since leptogenic characteristics coexist with obesogenic ones in the downtown area(Reference Filgueiras, Pessoa and Bressan10). Additionally, these outcomes are derived from a multi-complex model, involving not only the environment, but also family and individual-child factors(Reference Davison and Birch8). In this sense, further studies are needed to investigate the environmental characteristics that promote healthy habits in childhood. This evidence may help health planners to develop strategies, jointly with other sectors of urban planning, to improve children’s quality of life and, consequently, preventing and/or reducing obesity and adiposity-related inflammation.

This work has several strengths. First, this study is a pioneer in evaluating the associations of obesogenic and leptogenic environments with children’s health in a middle-income country. Second, the structural equation modeling approach allowed us to assess the direct and indirect associations between the environment and unhealthy outcomes. Third, we conducted a sensitivity analysis, testing android fat and other forms of variable categorization, which confirmed these results. Also, this is the first study to evaluate the associations of obesogenic and leptogenic environments with pro- and anti-inflammatory adipokines and the use body fat obtained from a reference method (DXA). Finally, we highlight that, although some environmental characteristics were obtained from the 2010 Census database, the information has high quality and allows for the replication and comparison of results between different Brazilian cities.

As limitation, this investigation was carried out in a Brazilian medium-sized city, which is largely made up of a young population (university students), and justifies a greater concentration of activities and services in the downtown area and near to the university(Reference Filgueiras, Pessoa and Bressan10). Therefore, extrapolation of these results should be cautious, and studies in different geographic locations are necessary to better understand the relationship between environmental characteristics and adiposity-related inflammation in children. Furthermore, the cross-sectional design does not allow the establishment of a cause-effect relationship. As the urban environment is dynamic, longitudinal studies must be conducted to verify the long-term effect of environmental characteristics on child health.

We conclude that the obesogenic neighborhood environment was directly associated with body fat and the mother’s BMI, and indirectly with leptin concentrations (pro-inflammatory marker) in Brazilian children, mediated by the child’s body fat and mother’s BMI. Therefore, encouraging the development of urban environments that promote healthier food and lifestyle choices can be one of the steps to prevent and/or reduce these childhood comorbidities.

Acknowledgements

We are grateful to all the children who participated in this study and their guardians. We thank the Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) and the Fundação de Amparo à Pesquisa do Estado de Minas Gerais (FAPEMIG) for their financial support; and the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) and the FAPEMIG for the scholarships granted to MS Filgueiras and FM Albuquerque. We appreciate the Research Fellowship from CNPq for JF Novaes; and the BioClin® (Belo Horizonte, Minas Gerais, Brazil) for their support in the biochemical analyses. We thank Professor Dr Andréia Queiroz Ribeiro from the Department of Nutrition and Health at UFV for authorizing the use of health-related environmental data collected by an audit in the city of Viçosa; and Professor Dr Marcos Vinícius Sanches Abreu from the Department of Civil Engineering at UFV who provided us information on the length and width of streets in the city of Viçosa to obtain the network buffers. We appreciate the Minas Gerais State Secretariat of Justice and Public Security (Secretaria de Estado de Justiça e Segurança Pública – Sejusp-MG) for providing data on crime and traffic accidents.

Financial support

This work was supported by the Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq – grant numbers 407547/2012-6, 478910/2013-4, and 458523/2014-3); Fundação de Amparo à Pesquisa do Estado de Minas Gerais (FAPEMIG – grant numbers APQ-02052-14 and CDS-APQ-02979-16); and the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES – code 001). The CNPq, FAPEMIG, and CAPES had no role in the design, analysis or writing of this paper.

Conflicts of interest

There are no conflicts of interest.

Authorship

M.S.F. assisted the conception and design of this work, assisted data collection, analysis, and interpretation of the data, conducted the literature search, as well as wrote the manuscript. A.S.F.V. assisted data collection, analysis, interpretation of the data, revised, and approved the final version to be published. F.M.A. assisted data collection, revised, and approved the final version to be published. A.S.C. assisted data analysis, interpretation of data revised, and approved the final version. J.B. revised and approved the final version to be published. M.C.P. and J.F.N. designed the study, including the data collection, coordinated, supervised, and approved the final version.

Ethics of human subject participation

This study was conducted according to the guidelines laid down in the Declaration of Helsinki and all procedures involving research study participants were approved by the Human Research Ethics Committee of the Universidade Federal de Viçosa (UFV) (reference numbers 663·171/2014 and 1·821·618/2016). It was also approved by the Municipal Secretary of Education, the Regional Superintendent of Education and school principals. Written informed consent was obtained from all parents/guardians.

References

World Health Organization (2020) Fact Sheets: Obesity and Overweight. https://www.who.int/news-room/fact-sheets/detail/obesity-and-overweight (accessed November 2021).Google Scholar
Kershaw, EE & Flier, JS (2004) Adipose tissue as an endocrine organ. J Clin Endocrinol Metab 89, 25482556.CrossRefGoogle ScholarPubMed
Rodríguez, A, Ezquerro, S, Méndez-Giménez, L et al. (2015) Revisiting the adipocyte: a model for integration of cytokine signaling in the regulation of energy metabolism. Am J Physiol Endocrinol Metab 309, E691E714.CrossRefGoogle Scholar
Domingos, ALG, Machado-Coelho, GLL, Volp, ACP et al. (2014) Association between nutritional status, C-reactive protein, adiponectin and HOMA-AD in Brazilian children. Nutr Hosp 30, 6674.Google Scholar
Frithioff-Bøjsøe, C, Lund, MAV, Lausten-Thomsen, U et al. (2020) Leptin, adiponectin, and their ratio as markers of insulin resistance and cardiometabolic risk in childhood obesity. Pediatr Diabetes 21, 194202.CrossRefGoogle ScholarPubMed
Zhang, M, Cheng, H, Zhao, X et al. (2017) Leptin and leptin-to-adiponectin ratio predict adiposity gain in nonobese children over a 6-year period. Child Obes 13, 213221.CrossRefGoogle Scholar
Blüher, M (2019) Obesity: global epidemiology and pathogenesis. Nat Rev Endocrinol 15, 288298.CrossRefGoogle ScholarPubMed
Davison, KK & Birch, LL (2001) Childhood overweight: a contextual model and recommendations for future research. Obes Rev 2, 159171.CrossRefGoogle ScholarPubMed
Swinburn, B, Egger, G & Raza, F (1999) Dissecting obesogenic environments: the development and application of a framework for identifying and prioritizing environmental interventions for obesity. Prev Med 29, 563570.CrossRefGoogle ScholarPubMed
Filgueiras, MS, Pessoa, MC, Bressan, et al. (2023) Characteristics of the obesogenic environment around schools are associated with body fat and low-grade inflammation in Brazilian children. Public Health Nutr 26, 24072417.CrossRefGoogle ScholarPubMed
Heindel, JJ & Blumberg, B (2019) Environmental obesogens: mechanisms and controversies. Annu Rev Pharmacol Toxicol 59, 89106.CrossRefGoogle ScholarPubMed
Carmo, AS, Mendes, LL, Pessoa, MC et al. (2021) Family characteristics, perceived environment for physical activity, and childhood obesity: an approach with structural equation models. Am J Hum Biol 33, e23560.CrossRefGoogle ScholarPubMed
Saelee, R, Gazmararian, JA, Haardörfer, R et al. (2020) Associations between the neighborhood social environment and obesity among adolescents: do physical activity, screen time, and sleep play a role? Health Place 64, 102380.CrossRefGoogle ScholarPubMed
Albuquerque, FM, Pessoa, MC, Filgueiras, MS et al. (2023) Neighborhood obesogenic environment and cardiometabolic risk in Brazilian children: the mediation role of the mother’s body mass index. Am J Hum Biol 35, e23835.CrossRefGoogle ScholarPubMed
Sallis, JF, Bowles, HR, Bauman, A et al. (2009) Neighborhood environments and physical activity among adults in 11 countries. Am J Prev Med 36, 484490.CrossRefGoogle ScholarPubMed
Instituto Brasileiro de Geografia e Estatística (2010) Cidades@-Minas Gerais: Viçosa. Brasil: IBGE; available at http://cod.ibge.gov.br/690 (accessed November 2021).Google Scholar
Pereira, MFV (2005) Contradictions of a “scientific city”: urbanization process and urban specialization in Viçosa (MG). Caminhos Geografia 18, 197206.CrossRefGoogle Scholar
Milagres, LC, Rocha, NP, Filgueiras, MS et al. (2017) Vitamin D insufficiency/deficiency is associated with insulin resistance in Brazilian children, regardless of body fat distribution. Public Health Nutr 20, 28782886.CrossRefGoogle ScholarPubMed
Duran, ACFL (2013) Urban food environment in São Paulo, Brazil: assessment, inequalities and association with food consumption. Thesis, Universidade de São Paulo.Google Scholar
Monteiro, CA, Levy, RB, Claro, RM et al. (2010) A new classification of foods based on the extent and purpose of their processing. Cad Saude Publica 26, 20392049.CrossRefGoogle ScholarPubMed
Interministerial Chamber of Food Security and Nutrition & Ministry of Social Development (2018) Technical study: Mapping food deserts in Brazil. Brasília: MDSA, CAISAN.Google Scholar
Lee, RE, Booth, KM, Reese-Smith, JY et al. (2005) The physical activity resource assessment (PARA) instrument: evaluating features, amenities and incivilities of physical activity resources in urban neighborhoods. Int J Behav Nutr Phys Act 2, 19.CrossRefGoogle ScholarPubMed
Brazilian Institute of Geography and Statistics (2010) Demographic Census 2010. https://censo2010.ibge.gov.br/ (accessed November 2021).Google Scholar
Vegi, ASF, Fernandes Filho, EI, Pessoa, MC et al. (2020) Walkability and healthy aging: an analytical proposal for small and medium-sized Brazilian cities. Cad Saude Publica 36, e00215218.CrossRefGoogle ScholarPubMed
Day, PL & Pearce, J (2011) Obesity-promoting food environments and the spatial clustering of food outlets around schools. Am J Prev Med 40, 113121.CrossRefGoogle ScholarPubMed
Smith, D, Cummins, S, Clark, C et al. (2013) Does the local food environment around schools affect diet? Longitudinal associations in adolescents attending secondary schools in East London. BMC Public Health 13, 70.CrossRefGoogle ScholarPubMed
Conway, JM, Ingwersen, LA & Moshfegh, AJ (2004) Accuracy of dietary recall using the USDA five-step multiple-pass method in men: an observational validation study. J Am Diet Assoc 104, 595603.CrossRefGoogle ScholarPubMed
, CB, Vianna, RPT & Gil, MF (1996) Photographic Record to Dietetic Inquiries: Appliances and Portions. Goiânia: Nepa – Unicamp; available at https://www.fcm.unicamp.br/fcm/sites/default/files/2016/page/manual_fotografico.pdf (accessed November 2020).Google Scholar
Center for Food Studies and Research & Universidade Estadual de Campinas (2011) Brazilian Food Composition Table – TACO, 4th ed. rev. e Ampl. Campinas: Nepa – Unicamp; available at http://www.nepa.unicamp.br/taco/contar/taco_4_edicao_ampliada_e_revisada.pdf?arquivo=taco_4_versao_ampliada_e_revisada.pdf (accessed November 2020).Google Scholar
US Department of Agriculture & Agricultural Research Service (2016) National Nutrient Database for Standard Reference (Release 28). http://www.fnic.nal.usda.gov/food-composition/USDA-nutrient-data-laboratory (accessed July 2017).Google Scholar
Hair, JF, Black, WC, Babin, BJ et al. (2009) Multivariate Data Analysis, 5th ed. Porto Alegre: Bookman.Google Scholar
Kline, RB (2016) Principles and Practice of Structural Equation Modeling. New York: The Guilford Press.Google Scholar
Muthén, LK & Muthén, BO (2010) Mplus: Statistical Analysis with Latent Variables. User’s Guide (1998–2010), 6th ed. Los Angeles, CA: Muthén & Muthén.Google Scholar
Wang, J & Wang, X (2012) Structural Equation Modeling: Applications Using Mplus. West Sussex: John Wiley & Sons.CrossRefGoogle Scholar
Ghenadenik, AE, Kakinami, L, Van Hulst, A et al. (2018) Neighbourhoods and obesity: a prospective study of characteristics of the built environment and their association with adiposity outcomes in children in Montreal, Canada. Prev Med 111, 3540.CrossRefGoogle ScholarPubMed
Zhou, Y, Buck, C, Maier, W et al. (2020) Built Environment and childhood weight status: a multi-level study using population-based data in the city of Hannover, Germany. Int J Environ Res Public Health 17, 2694.CrossRefGoogle ScholarPubMed
Gascon, M, Vrijheid, M & Nieuwenhuijsen, MJ (2016) The built environment and child health: an overview of current evidence. Curr Environ Health Rep 3, 250257.CrossRefGoogle ScholarPubMed
Nesbit, KC, Kolobe, TH, Sisson, SB et al. (2015) A structural equation model of environmental correlates of adolescent obesity for age and gender groups. Pediatr Obes 10, 288295.CrossRefGoogle ScholarPubMed
Carmo, AS, Rodrigues, D, Nogueira, H et al. (2020) Influence of parental perceived environment on physical activity, TV viewing, active play and body mass index among Portuguese children: a mediation analysis. Am J Hum Biol 32, e23400.CrossRefGoogle ScholarPubMed
Saelens, BE, Sallis, JF, Frank, LD et al. (2012) Obesogenic neighborhood environments, child and parent obesity: the neighborhood impact on kids study. Am J Prev Med 42, e57e64.CrossRefGoogle ScholarPubMed
Warkentin, S, Mais, LA, Latorre, MDRDO et al. (2018) Parents matter: associations of parental BMI and feeding behaviors with child BMI in Brazilian preschool and school-aged children. Front Nutr 5, 69.CrossRefGoogle ScholarPubMed
Ribeiro, IC, Taddei, JA & Colugnatti, F (2003) Obesity among children attending elementary public schools in São Paulo, Brazil: a case--control study. Public Health Nutr 6, 659663.CrossRefGoogle Scholar
Mei, K, Huang, H, Xia, F et al. (2021) State-of-the-art of measures of the obesogenic environment for children. Obes Rev 22, e13093.CrossRefGoogle ScholarPubMed
Park, YM, Zhang, J, Steck, SE et al. (2017) Obesity mediates the association between Mediterranean diet consumption and insulin resistance and inflammation in US adults. J Nutr 147, 563571.CrossRefGoogle ScholarPubMed
Filgueiras, MS, Pessoa, MC, Bressan, J et al. (2021) Pro- and anti-inflammatory adipokines are associated with cardiometabolic risk markers in Brazilian schoolchildren. Eur J Pediatr 180, 29312941.CrossRefGoogle ScholarPubMed
Blundell, JE, Dulloo, AG, Salvador, J et al. (2014) Beyond BMI--phenotyping the obesities. Obes Facts 7, 322328.CrossRefGoogle ScholarPubMed
Smith, L (2015) Walkability audit tool. Workplace Health Saf 63, 420.CrossRefGoogle ScholarPubMed
Yang, S, Chen, X, Wang, L et al. (2021) Walkability indices and childhood obesity: a review of epidemiologic evidence. Obes Rev 22, e13096.CrossRefGoogle ScholarPubMed
Stowe, EW, Hughey, SM, Hallum, SH et al. (2019) Associations between walkability and youth obesity: differences by urbanicity. Child Obes 15, 555559.CrossRefGoogle ScholarPubMed
Figure 0

Fig. 1 Initial theoretical model of structural equations hypothesized for the associations of obesogenic and leptogenic environments with % body fat and adipokine concentrations in children. Viçosa, Minas Gerais, Brazil, 2015. Abbreviations: %BF: %body fat; BMI: body mass index; PA: physical activity; q1: predominantly ultra-processed food stores; q2: traffic accidents; q3: crime; q4: walkability; q5: physical activity facilities; q6: green spaces; q7: neighborhood income; UPF: ultra-processed food. The observed variables were presented in rectangular shapes and the latent variables in circular shapes. Models with % body fat, adipokines, ultra-processed food consumption, and physical activity before and after school as outcome were adjusted for child’s sex and socioeconomic status. Models with mother’s BMI as outcome were adjusted for socioeconomic status

Figure 1

Table 1 Body fat, adipokine concentrations, socioeconomic, and health behaviors in children, according to sex. Viçosa, Minas Gerais, Brazil, 2015

Figure 2

Fig. 2 Validation of latent variables (a) obesogenic and leptogenic environments, and (b) socioeconomic status. Abbreviations: SES: socioeconomic status. Data presented as factor loading (SE). The observed variables were presented in rectangular shapes and the latent variables in circular shapes. For environmental variables, Kaiser-Meyer-Olkin (KMO) index = 0·80, % variance of 1st component (obesogenic environment): 47·7 %, % variance of 2nd component (leptogenic environment): 25·5 %, % variance total = 73·2 %. For socioeconomic status, Kaiser-Meyer-Olkin (KMO) index = 0·59, and % variance total = 58·1 %. *P < 0·001

Figure 3

Table 2 Standardized coefficients (β) of the direct and indirect associations of obesogenic neighborhood environment with body fat and adipokine concentrations in children. Viçosa, Minas Gerais, Brazil, 2015

Figure 4

Fig. 3 Direct and indirect associations of the obesogenic neighborhood environment with body fat and adipokine concentrations in Brazilian children. Abbreviations: % BF: % body fat; BMI: body mass index. Solid lines represent direct associations and dotted lines represent indirect associations

Figure 5

Table 3 Standardized coefficients (β) of the direct and indirect associations of leptogenic neighborhood environment with body fat and adipokine concentrations in children. Viçosa, Minas Gerais, Brazil, 2015