Prevalence of associations among sarcopenia, obesity, and metabolic syndrome in Brazilian older adults
Luiz Carlos Holanda Torres Pinheiro1 
Marcelo Rossi1* 
Carlos André Freitas dos Santos2,3 
Luis Vicente Franco Oliveira4 Sergio Vencio5 Rodolfo de Paula Vieira4,6,7 Yara Juliano1 
Jane Armond1 Carlos Hassel Mendes Silva4 
Adriano Luís Fonseca4 Carolina Nunes França1 
André Luís Lacerda Bachi1- 1Post-graduation Program in Health Science, Santo Amaro University (UNISA), São Paulo, Brazil
- 2Discipline of Geriatrics and Gerontology, Department of Medicine, Paulista School of Medicine, Federal University of São Paulo (UNIFESP), São Paulo, Brazil
- 3Postgraduate Program in Translational Medicine, Department of Medicine, Paulista School of Medicine, Federal University of São Paulo (UNIFESP), São Paulo, Brazil
- 4Human Movement and Rehabilitation Post Graduation Program, Evangelical University of Goiás (UniEVANGELICA), Anápolis, Brazil
- 5Institute of Pharmaceutical Sciences, Goiania, Brazil
- 6Brazilian Institute of Teaching and Research in Pulmonary and Exercise Immunology (IBEPIPE), São José dos Campos, Brazil
- 7Post-graduation Program in Science of Human and Rehabilitation, Federal University of São Paulo (UNIFESP), Santos, Brazil
Background: Although aging is a process associated with the development of obesity, metabolic syndrome (MetS), and sarcopenia, the prevalence of these conditions in older adults from São Paulo, Brazil, is unclear.
Methods: Therefore, the current study aimed to investigate the prevalence of obesity, sarcopenia, and MetS, both separately and together, in a community-based sample of older adults from São Paulo, Brazil. Data from the medical records of 418 older adults of both genders, aged 60 years or older (mean age 69.3 ± 6.5 years), who were not physically active, were used to conduct this retrospective cross-sectional study. Anthropometric variables were used to determine both body mass index (BMI) and Conicity index (C index). Sarcopenia and MetS were defined according to the criteria of the European Working Group on Sarcopenia in Older People and by the Brazilian Society of Endocrinology and Metabolism, respectively.
Results: Based on BMI, the group of older men (n = 91) showed a predominance of adequate weight (n = 49) and the group of older women (n = 327) showed a predominance of obesity (n = 181). In association with obesity, while only the group of older women presented with sarcopenia (n = 5), 52 older women and 9 older men presented with MetS, and two older women presented with sarcopenia + MetS [prevalence ratio = 0.0385, 95% CI (0.007;0.1924)]. Based on the C index, 58 older women and 11 older men presented with MetS, while the occurrence of sarcopenia or MetS + sarcopenia was found in 32 and 5 older women, respectively [prevalence ratio = 0.0910, 95% CI (0.037;0.2241)].
Discussion: Our results suggest that obesity, as measured by BMI or the C Index, was more closely associated with the occurrence of MetS than sarcopenia, regardless of gender, and also that sarcopenic obesity was only found in the group of older women. Additionally, the prevalence ratio of obesity, sarcopenia, and MetS evidenced using the C index was 2.3 times higher than the values found using the BMI classification.
1. Introduction
Population aging is one of the most impactful global changes in different societies. For instance, in 1991, the number of people aged 60 and over represented 7.3% of the total population, whereas in 2025, this group will represent 15%. According to global projections, the number of older adults could reach 2 billion individuals in 2050, representing 21.5% of the world’s population (1, 2).
Among several characteristics, it is widely accepted that aging or senescence is a natural, dynamic, progressive, and therefore inevitable phenomenon in which morphological, functional, biochemical, and psychological alterations can be observed, resulting from the interaction of a series of variables, such as genetics, lifestyle, and diseases (3). With regard to lifestyle, there is convincing evidence that physical inactivity can promote metabolic syndrome (MetS), which predisposes to increased risk factors for the development of chronic diseases and comorbidities associated with aging, such as metabolic syndrome (4).
According to the World Health Organization (WHO), MetS can be fundamentally defined by clinical and laboratory data, and its worldwide prevalence is approximately 25 to 35% (5, 6). The literature points out that one of the factors that may potentiate the occurrence of MetS in older adults is the development of obesity associated with aging (7). The excessive increase in body weight due to the accumulation of fat in adipose tissue, a fact that characterizes obesity, varies between 20 and 40% in the older adult population, depending on the evaluation model used. It has been emphasized that the increase in the manifestation of obesity in older adults is associated, among other factors, with a significant reduction in the level of daily physical activity, which can even lead individuals to become sedentary (8).
In particular, the decline in physical activity observed in the older adult population is closely associated with the progressive loss of skeletal muscle mass, which can vary between 10 and 40%. Corroborating this information, studies have reported a 30 to 50% decrease in muscle mass in individuals between the ages of 40 and 80. This reduction is linked to a significant loss of functional capacity of approximately 3% per year after the age of 60. According to the literature, the reduction in skeletal muscle mass and loss of muscle strength (defined as dynapenia) associated with reduced physical mobility characterize the occurrence of the geriatric syndrome called sarcopenia. Sarcopenia is related to clinical outcomes such as loss of mobility, increased risk of falls, frailty syndrome, cardiovascular disease, neurodegenerative disease, and osteoporosis, and is also a predictor of mortality in older adults (9).
Recent epidemiologic studies have highlighted the possible coexistence of a sarcopenic condition in older adults with obesity, a situation called sarcopenic obesity (OS), which occurs mainly in individuals over 55 years of age (10).
Since obesity is a prominent factor in both MetS and sarcopenia in older adults, it is very important to correctly define its occurrence. According to the WHO, obesity can be defined as abnormal or excessive fat accumulation that poses a health risk. In addition to the BMI index, central obesity, which is common in older adults, can be estimated by the conicity index (C index), proposed by Valdez (11) in the early 1990s, as an indicator of adiposity and body fat distribution, especially in older adults (12).
Although it is possible to find reports on MetS and sarcopenia in the older adult population, studies aimed at comparing different models of obesity assessment and their association with the occurrence of MetS and sarcopenia in this population are still scarce in the literature. Therefore, the aim of the current study was, first, to evaluate the presence of obesity using two different models and, second, to correlate the presence of obesity with the manifestations of MetS and sarcopenia, either alone or together, in older adults.
2. Methods
2.1. Study population
This study has a retrospective cross-sectional design, based on the medical records of older adults attending the “Centro de Referência do Idoso – Casa do Idoso,” an institution belonging to the Municipal Social Assistance Office in São José dos Campos City, São Paulo, Brazil. The sample consisted of 418 individuals of both genders, aged 60 years and older at the time of data collection, without a diagnosis of chronic degenerative disease, type 1 diabetes, neoplasm, respiratory, renal, or liver disease, autoimmune, infectious, and/or neurological disease, and who were not engaged in any exercise training program.
It is paramount to mention that we obtained data from the population aged 60 years and older because, according to the Brazilian Ministry of Health, these individuals are considered older adults. Moreover, in the present study, we did not include older adults who reported regular engagement in any exercise training program, since it is widely known that the regular practice of exercise training is beneficial for everybody, particularly the older adult population, and can improve several physiological, metabolic, and physical characteristics. In addition, the older adults who were physically active reported regular engagement in a wide range of exercise training programs, which included types, intensities, and modalities that did not allow us to adequately separate them into one or even two or three groups.
The primary endpoint was the diagnosis of MetS, and the secondary endpoint was sarcopenia. To assess the associations between MetS and sarcopenia, the BMI was measured at baseline, and the prevalence of the association between MetS and sarcopenia was determined for ranges of BMI. Figure 1 shows the analysis process performed.
Figure 1. Flow diagram of the study design. BMI, Body Mass Index; C Index, Conicity Index; MetS, Metabolic Syndrome.
2.2. Anthropometric measurements
The older adult participants were clinically evaluated by the same geriatrician responsible for each “Centro de Referência do Idoso – Casa do Idoso.” Data on the age, gender, race, body weight (kg), height (cm), and waist circumference (cm) of each subject were recorded in the initial database. Body composition was assessed using body mass index (BMI), which represents a diagnostic criterion for obesity, and muscle mass, which was defined using Lee’s equation (13), as shown below.
2.3. Body mass index calculation
Older adults were categorized by BMI, according to the stratification developed by Adams et al. (14) as follows: underweight = BMI < 18.5 kg/m2; adequate weight = BMI between 18.5 and 24.9 kg/m2; overweight = BMI between 25 and 29.9 kg/m2; and obesity = BMI > 30 kg/m2.
2.4. Conicity index calculation
The Conicity index (C index) was used to assess the visceral fat adipose mass as a measure of central adiposity obesity. This index was chosen because of the ease of interpretation of the values obtained. For instance, a C index of 1.25 indicates that the individual has a waist circumference 25% greater than the circumference of a cylinder with the same height, weight, waist circumference, and human body density. This index also offers the highest level of discrimination between MetS and sarcopenia.
The cut-off points were C Index values >1.25 for men and C Index >1.18 for women (15).
2.5. Assessment of metabolic syndrome
To determine the manifestation of metabolic syndrome (MetS), the criteria proposed by the Brazilian Society of Endocrinology and Metabolism were adopted (16), as also discussed in Freitas et al. (4).
2.6. Assessment of sarcopenia
The assessment of the occurrence of sarcopenia followed the criteria recently presented by the European Working Group on Sarcopenia in Older People (EWGSOP) (9). Muscle strength was determined using the handgrip test, with values < 29 kg for men and < 17 kg for women indicating low muscle strength. Muscle mass was estimated using appendicular skeletal muscle mass (aSMM) according to Lee’s equation (13), as described below:
where body weight was measured in kilograms and height in meters; regarding gender, a value of 0 was used for women and 1 for men; regarding race, 0 was used for white people or Hispanics, 1.4 for African-Americans, and − 1.2 for Asian people. After applying the equation, the values obtained were divided by the square of the height (m2) of each subject to calculate the muscle mass index for each participant. The characterization of the presence of low muscle mass was defined when the values reached < 7 kg/m2 for men and < 5.5 kg/m2 for women.
2.7. Statistical analysis
Continuous variables were expressed as mean and standard deviation (X ± SD), and the number of subjects with MetS and sarcopenia was used to express prevalence data.
A McNemar’s test with continuity correction was used to test the hypothesis of an association between MetS and sarcopenia in the older adult population based on the BMI classification and C Index. In addition, both the BMI and C Index were used to compute the prevalence ratios (PR) for each group of participants (older women and older men), separated by their BMI and C Index values, showing an association with MetS and sarcopenia in comparison to those who did not show an association.
The statistical analysis was carried out using GraphPad Prism version 10.0 at a significance level of alpha = 5.0% (p < 0.05).
3. Results
Table 1 shows the anthropometric, physical, and clinical characteristics of the older adult participants in the present study, both pooled (total) and separated by gender.
Table 1. Anthropometric, body composition, and clinical characteristics data of the older adult participants in this study.
Table 2 shows the number of participants with or without MetS and sarcopenia, both pooled (total) and separated by gender, in addition to their prevalence ratio. It was demonstrated that most of the subjects did not present with MetS and/or sarcopenia. It is worth mentioning that the absolute number of older women with MetS was higher than the value found in the group of older men, and the proportional occurrence of this syndrome in the group of older women was almost 1:4 (19.3%), whereas in the group of older men it was 1:6 (13.3%). In addition, because none of the older men presented with sarcopenia, the concomitant occurrence of MetS and sarcopenia was observed only in the group of older women, with a percentage of 1.8%. Interestingly, a McNemar’s test performed on the pooled subjects (total group) showed a significant value of p, which suggests an association between the occurrence of sarcopenia and MetS.
Table 2. The absolute number (n) and the percentage (%), total and categorized by gender, of subjects with metabolic syndrome (MetS), sarcopenia, or both (MetS + sarcopenia).
Table 3 presents the classification of the participants according to their BMI values, both pooled (total) and separated by gender. According to the values found, it is possible to demonstrate that the majority of older men were classified as having adequate weight, while older women were classified as obese. The table also shows the prevalence of MetS and sarcopenia in the older adult subjects categorized as underweight, adequate weight, or obese according to their BMI values. Regarding the group of older men, it was found that the participants with adequate weight or obesity had MetS, and the number of older adults with obesity with MetS was almost two times higher than those with adequate weight. As previously noted, none of these subjects presented with sarcopenia. However, in relation to the older women group, the occurrence of MetS was verified in all groups when separated by their nutritional status. It is important to point out that the number of older women with MetS increased concomitantly with the increase in BMI values; thus, the obese subgroup showed the highest number of individuals with MetS. Specifically, regarding the occurrence of sarcopenia, the adequate weight subgroup had the highest incidence of this clinical condition, followed by the underweight group and the obese group. Interestingly, the number of older women with MetS and sarcopenia was similar between the subgroups. Finally, in addition to the significant p-values shown in McNemar’s analysis, except in the group of older men with adequate weight, the prevalence ratios observed in the group of older women with obesity were 17- and 6-fold lower than those found in the underweight and adequate weight groups, respectively.
Table 3. The absolute number (n) and the percentage (%) of subjects with or without metabolic syndrome (MetS), sarcopenia, or both (MetS + sarcopenia), separated by gender and categorized by the BMI classification into underweight (< 18.5 kg/m2), adequate weight (between 18.5 and 24.9 kg/m2), and obese (> 30 kg/m2).
Table 4 shows the prevalence of MetS and sarcopenia in both groups classified as obese according to the C Index cut-off of 1.25 for men and 1.18 for women. It can be observed that only 11 older men presented with MetS, whereas 59 older women had been diagnosed with this syndrome. In addition, while 32 older women had sarcopenia, only five presented with both MetS and sarcopenia. Finally, the McNemar analysis showed significant associations between the outcomes in the two groups of subjects separated by the respective C Index cut-offs for men and women, and the prevalence ratio found in the group with older women was approximately 0.09.
Table 4. The absolute number (n) and percentage (%) of subjects, separated by gender, with C index values above the cut-offs of 1.25 for the older men group and above 1.18 for the older women group, and who also had or did not have metabolic syndrome (MetS), sarcopenia, or both (MetS + sarcopenia).
Figure 2 summarizes the main data found in the study.
Figure 2. Summarized representation of the main results in this study. BMI, Body Mass Index; C Index, Conicity Index; MetS, Metabolic Syndrome.
4. Discussion
In the present study, we demonstrated that when MetS was the primary outcome, among a total of 76 older adults who presented with this syndrome (Table 2), 63 older women and 13 older men also presented with obesity based on their BMI classification (Table 3). In addition, when sarcopenia was the primary outcome, it was found that, among the total of 47 older adults who had this clinical condition (Table 2), only five also had obesity based on BMI classification (Table 3), and they were found exclusively in the group of older women. Finally, it was demonstrated that the concomitant occurrence of MetS and sarcopenia was only observed in six older women, of whom two were underweight, two were of adequate weight, and two were obese (Table 3). Beyond these results, we also showed that, among the total subjects with obesity (n = 347), according to the C index (Table 4), the majority of individuals who also presented with MetS were in the group of older women (n = 59) compared to that of older men (n = 11). Moreover, in the same population that presented with obesity, the occurrence of sarcopenia was detected in 32 older women, while the concomitant occurrence of MetS and sarcopenia was detected in five older women. It is worth highlighting that the values of the prevalence ratio (PR) found in the group of older women classified as obese by the C index, who also had concomitant MetS and sarcopenia were 2.3 times higher than the values found in the group of older women classified as obese by the BMI values who also had concomitant MetS and sarcopenia. In addition, the significant results obtained in the McNemar test suggest the existence of a remarkable association between the occurrence of MetS and sarcopenia in the older adult population of participants in this study.
According to the WHO, obesity is a disease in which the accumulation of excess fat in the body can significantly affect human health. In fact, the prevalence of obesity worldwide is so high that the WHO considers it to be the global epidemic of the 21st century. Whether or not urgent action is taken to prevent and treat obesity, it is predicted that more than 50% of the world’s population will be obese in 2025. In this respect, the WHO reports that the occurrence of obesity can be defined through the BMI, and this index can also be used to estimate the prevalence of obesity in a population (17). However, it should be noted that although there is a good correlation between BMI and body fat mass, this index does not consider the variation in body fat distribution and may not correspond to the same degree of obesity or associated risks in different individuals and populations. Therefore, the WHO itself advises that BMI values should be interpreted with caution (18, 19).
Particularly in the context of clinical practice aimed at older adults, the evaluation of abdominal obesity by measuring waist circumference may be putatively considered a more important anthropometric measure than BMI to assess the risk of mortality. In agreement with the literature, the presence of visceral obesity is closely associated with the occurrence of dyslipidemia, arterial hypertension, endothelial dysfunction, polycystic ovary syndrome, coronary heart disease, and cerebral vascular disease. In addition, visceral obesity is also directly related to the development of insulin resistance and leads to the development of metabolic syndrome and death (20). In this sense, the use of the C index, as elaborated by Valdez et al. (11), is configured as an effective assessment of visceral obesity since it considers the distribution of central fat. It is paramount to point out that the C index evaluation not only takes into account weight, height, and waist circumference but is also based on the proposition that the accumulation of fat around the waist similar to “cone figure” in the human body (11, 21).
Pereira et al. (22) demonstrated that the C index showed a better association with the presence of MetS in both older men and older women compared to the results obtained with the BMI (22).
As appealing as genetic predisposition may be in determining the higher accumulation of fat in the body in some individuals, it is well known that this accumulation can also occur regardless of the individual’s genetics, and, in these situations, a lifestyle with an evident excess of energy intake associated with reduced physical activity leads to fat accumulation, especially in the abdominal region (18).
Reduced levels of daily physical activity or physical inactivity not only increase the risk of obesity but also the risk of sarcopenia (8, 9). With regard to sarcopenia, epidemiologic studies conducted in Brazil showed a prevalence of 14 and 16% in older men and older women, respectively (23). Furthermore, sarcopenia is closely associated with several clinical outcomes, such as loss of mobility, an increased risk of falls, frailty syndrome, cardiovascular disease, neurodegenerative disease, and osteoporosis, and is also a relevant predictor of mortality (9).
Among the various biological processes that induce sarcopenia, we can highlight the decrease in protein synthesis and/or increase in protein degradation, loss of neuromuscular integrity, and increased intramuscular fat content. In fact, the remarkable reduction in muscle mass observed in sarcopenia can be attributed to some factors, such as reduced growth hormone release and physical inactivity, which can influence a lower expression of key proteins involved in protein synthesis and, consequently, an increase in protein degradation, leading to muscle atrophy (9, 24).
The data obtained regarding the presence of sarcopenia in the studied individuals, particularly when stratified by the BMI and C indexes, revealed interesting results. In this sense, it is important to note that: (1) the occurrence of sarcopenia was only detected in the group of older women; (2) most of the older women who presented with sarcopenia were classified in the group as having adequate weight compared to the obese group, according to the BMI; and (3) the number of older women with obesity, according to the C index, who presented with sarcopenia was higher than the amount of participants found in the group of older women with adequate weight and obesity, both classified according to their BMI. Furthermore, the prevalence ratio [PR = 0.0910 (95% CI 0.037, 0.2211)] observed in the group of older women with obesity, according to the C index, compared to the prevalence ratio [PR = 0.0385 (95% CI [0.0077, 0.1924)] observed in the group of older women with obesity classified based on BMI, allows us to putatively suggest that the C index was more effective in defining the presence of sarcopenia in the older adult population participating in the study.
Specifically in relation to the association between sarcopenia and obesity, the literature shows the occurrence of a phenotype known as sarcopenic obesity (SO), especially during aging (10).
It is widely accepted that the manifestation of SO is related to genetic, physiological, and environmental factors. However, studies have demonstrated that some molecular mechanisms associated with SO are dependent on a dynamic balance between positive and negative mediating substances for muscle growth and that this balance impacts the maintenance of mass and skeletal muscle functions (25). Thus, it has been proposed that the occurrence of an imbalance in the following factors may lead to sarcopenic obesity: (i) primary metabolic abnormalities leading to increased systemic and muscular oxidative stress, with increased inflammation and insulin resistance; (ii) a consequent decrease in the hormonal balance, which may putatively stimulate a cascade of negative events, such as an increase in muscle catabolic potential; (iii) ectopic lipid deposition, which compromises protein turnover; (iv) mitochondrial dysfunction, causing an increase in oxidative stress, a reduction in the production of ATP, low production of muscle strength, and resistance to the prolonged exercise; (v) functionally altered muscle stem cells that can differentiate from adipocytes with a concomitant increase in inflammation; and (vi) physical inactivity, which is directly related to the control of positive energy balance, muscle oxidation, and protein turnover (26, 27).
Since OS translates as a phenotype caused by an imbalance of several factors, it is worth noting that its occurrence has a deleterious effect on the life of the individual, as it favors both the increased incidence of non-communicable chronic diseases and the low quality of life in these individuals (28). Thus, our observation that the C index was more sensitive than BMI in detecting the occurrence of OS may guide further studies to better define its prevalence.
Based on this information, there is no doubt that the manifestation of sarcopenia and MetS has a negative impact on the quality of life of the older adult population. Therefore, the concomitant manifestation of MetS and sarcopenia in the older adult population with obesity leads to an increased risk of the occurrence of adverse health events when compared to individuals who do not have both of these conditions or even those who have only MetS or sarcopenia (29). In this sense, in the meta-analytic study by Zhang and collaborators (30), around 35% of the non-obese individuals who presented with sarcopenia also manifested MetS, whereas only approximately 22% of the population studied without sarcopenia presented with MetS. In addition, the same authors also reported the existence of a significantly positive odds ratio (OR) between MetS and sarcopenia in the population studied, particularly in those with adequate weight (30).
Even though the above information demonstrates that an association between MetS and sarcopenia can be found in different populations, which could provide important data for medical assistance, a recent study highlighted that heterogeneous aspects of individuals, related to social, biological, and clinical characteristics, in conjunction with other aspects, such as the location and conditions in which the evaluations are conducted, represent key points in the decisions regarding the variables to be used in epidemiological studies since they undoubtedly impact the results obtained in a real context, particularly in relation to clinical practice (31). For instance, in the epidemiological studies that have provided data on the risk factors associated with the occurrence of both sarcopenia and MetS, it is possible to observe a large number of different factors reported in association with a diversity of criteria used, which inevitably generates greater heterogeneity in the results, which in turn can preclude the attainment of consistent conclusions (31–33).
Considering the above, we can emphasize that this study has some strengths related to the sample size and the robust statistical analysis. However, some limitations should be pointed out, such as: (i) the lack of body composition assessment using Dual-energy X-ray Absorptiometry (DXA), which is considered the gold standard for this measure, or even bioelectrical impedance analysis (BIA), which is an alternative and low-cost method often used in a large population; (ii) the lack of comparison of the data obtained in this study with other older adult groups who regularly engage in physical exercise; (iii) the lack of a dietary assessment, which could provide us with relevant information regarding the dietary habits of the older adult participants in this study; and (iv) the cross-sectional nature of this study, which does not allow us to establish cause-and-effect relationships between the data evaluated.
5. Conclusion
Based on the results obtained in the present study, we were able to demonstrate that the occurrence of MetS is higher in older adults who present with obesity, regardless of their gender and the use of the BMI or C index, which agrees with the literature. In addition, we also showed interesting results regarding the presence of sarcopenia, not only because t it was found exclusively in the group of older women but also by the fact that the highest number of participants with this clinical condition belonged to the group with adequate weight and not to the group with obesity, specifically when BMI was used. Additionally, taking into account the data obtained in the analysis of the prevalence ratios, as far as we were able to establish, this is the first study to demonstrate that the C index was more effective than the BMI in identifying the prevalence estimates of the occurrence of obesity and the clinical conditions assessed here (MetS and sarcopenia), both individually and in combination, in an older adult population. Finally, further studies are needed, both to confirm the results presented here and to better understand the use of the C index in relation to the prevalence of obesity, MetS, and sarcopenia in the older adult population.
Data availability statement
The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.
Ethics statement
Ethical review and approval was not required for the study on human participants in accordance with the local legislation and institutional requirements. Written informed consent from the patients/ participants was not required to participate in this study in accordance with the national legislation and the institutional requirements.
Author contributions
AB conceived the study, analyzed the data, and wrote the first draft together with CS, SV, RP, and CF. LP, CS, AF, LO, and CF participated in the design and development of this study. LP, YJ, JA, and MR participated in the data analysis. All authors contributed to the article and approved the submitted version.
Acknowledgments
The authors would like to thank all participants in the study, in addition to the units of the “Centro de Referência do Idoso – Casa do Idoso” in the city of São José dos Campos.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher’s note
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Keywords: metabolic syndrome, sarcopenia, sarcopenic obesity, Conicity index, body mass index, obesity prevalence, aging
Citation: Pinheiro LCHT, Rossi M, dos Santos CAF, Oliveira LVF, Vencio S, de Paula Vieira R, Juliano Y, Armond J, Silva CHM, Fonseca AL, França CN and Bachi ALL (2023) Prevalence of associations among sarcopenia, obesity, and metabolic syndrome in Brazilian older adults. Front. Med. 10:1206545. doi: 10.3389/fmed.2023.1206545
Edited by:
Guilherme Eustaquio Furtado, Polytechnical Institute of Coimbra, PortugalReviewed by:
Roberta Zupo, University of Bari Aldo Moro, ItalyTábatta Brito, Federal University of Alfenas, Brazil
Copyright © 2023 Pinheiro, Rossi, dos Santos, Oliveira, Vencio, de Paula Vieira, Juliano, Armond, Silva, Fonseca, França and Bachi. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Marcelo Rossi, mrossi.biotec@gmail.com