Next Article in Journal
Antihistamines Increase Body Mass Index Percentiles and Z-Scores in Hispanic Children
Next Article in Special Issue
Waist Circumference Is Not Associated with Impaired Fasting Blood Glucose in a Sample of Mexican Children and Teenagers: Results from a State Screening Program
Previous Article in Journal
The Use of a Kinetic Therapy Rotational Bed in Pediatric Acute Respiratory Distress Syndrome: A Case Series
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

An Approach to Early Detection of Metabolic Syndrome through Non-Invasive Methods in Obese Children

by
Rafael Molina-Luque
1,2,
Natalia Ulloa
3,*,
Andrea Gleisner
4,
Martin Zilic
5,
Manuel Romero-Saldaña
1,2 and
Guillermo Molina-Recio
1,2
1
Grupo Asociado de Investigación Estilos de Vida, Innovación y Salud, Instituto Maimónides de Investigación Biomédica de Córdoba (IMIBIC), 14004 Córdoba, Spain
2
Departamento de Enfermería, Farmacología y Fisioterapia, Facultad de Medicina y Enfermería, Universidad de Córdoba, 14004 Córdoba, Spain
3
Centro de Vida Saludable y Departamento de Bioquímica Clínica e Inmunología, Facultad de Farmacia, Universidad de Concepción, Concepción 4070386, Chile
4
Departamento de Pediatría, Facultad de Medicina, Universidad de Concepción, Concepción 4070386, Chile
5
Facultad de Medicina, Universidad de Concepción, Concepción 4070386, Chile
*
Author to whom correspondence should be addressed.
Submission received: 26 October 2020 / Revised: 6 December 2020 / Accepted: 15 December 2020 / Published: 17 December 2020

Abstract

:
Background: Metabolic Syndrome (MetS) has a high prevalence in children, and its presence increases in those with a high BMI. This fact confirms the need for early detection to avoid the development of other comorbidities. Non-invasive variables are presented as a cost-effective and easy to apply alternative in any clinical setting. Aim: To propose a non-invasive method for the early diagnosis of MetS in overweight and obese Chilean children. Methods: We conducted a cross-sectional study on 221 children aged 6 to 11 years. We carried out multivariate logistic regressions, receiver operating characteristic curves, and discriminant analysis to determine the predictive capacity of non-invasive variables. The proposed new method for early detection of MetS is based on clinical decision trees. Results: The prevalence of MetS was 26.7%. The area under the curve for the BMI and waist circumference was 0.827 and 0.808, respectively. Two decision trees were calculated: the first included blood pressure (≥104.5/69 mmHg), BMI (≥23.5 Kg/m2) and WHtR (≥0.55); the second used BMI (≥23.5 Kg/m2) and WHtR (≥0.55), with validity index of 74.7% and 80.5%, respectively. Conclusions: Early detection of MetS is possible through non-invasive methods in overweight and obese children. Two models (Clinical decision trees) based on anthropometric (non-invasive) variables with acceptable validity indexes have been presented. Clinical decision trees can be applied in different clinical and non-clinical settings, adapting to the tools available, being an economical and easy to measurement option. These methods reduce the use of blood tests to those patients who require confirmation.

Graphical Abstract

1. Introduction

Metabolic Syndrome (MetS) is defined as a group of cardiometabolic disorders that increase the risk of suffering from cardiovascular diseases and type 2 diabetes, pathologies that are among the leading causes of death worldwide [1,2]. Abdominal obesity, low levels of high-density lipoprotein cholesterol (Chol-HDL), and elevated blood pressure, triglycerides, and fasting blood glucose are essential alterations [3].
MetS prevalence has increased in the last years and has become a public health problem due to the increase in morbi-mortality [4,5,6]. Although it has generally been considered a typical affectation of the adult population, it increasingly appears in a higher proportion in the younger population groups [7]. This fact has been related to the exponential increase in the prevalence of overweight and obesity. These conditions are linked to insulin resistance, one of the physiopathological mechanisms of MetS [8,9]. Prevalence among children ranges from 3.3 to 29.2%, with higher values among children with higher BMI [10]. The Chilean population is not an exception to this problem. The latest national health survey revealed that the prevalence of MetS is around 40.1% in the adult population [11]. Several studies show oscillations between 20% and 40% in the child population, depending on the selected diagnostic criteria, regions where the study was carried out, and overweight and obesity prevalence in those areas [12,13].
This high proportion of MetS has led to looking for methods to detect it early, limiting the development of associated comorbidities. Among the tools proposed for early diagnosis, those that do not require invasive techniques stand out. These guarantee their use in diverse clinical settings, especially in places with scarce healthcare resources, and offer a high cost-efficiency, as they do not require blood tests [14,15]. In this sense, several works have shown that the waist to height ratio (WHtR) has a high predictive capacity in the adult population. Besides, they have provided methods with high validity indexes together with other parameters such as blood pressure [16]. On this point, several authors have denoted that the anthropometric variables are the most appropriate for early detection of MetS in children. Neck circumference, waist circumference, or BMI are associated with MetS at pediatric ages [17,18]. However, although the variables are linked separately with MetS, no work has proposed a non-invasive algorithm to improve children’s screening at high risk for this syndrome.
Therefore, this study aims to propose a method that uses non-invasive variables for the early detection of MetS in overweight and obese Chilean children.

2. Materials and Methods

2.1. Design, Population, Sample

A cross-sectional study was carried out on boys and girls between the ages of 6 and 11 in the urban area of the city of Hualpén in the Biobío Region, Chile in 2010. The minimum sample size was 188 for an expected prevalence of 22.7% [12] in a population of 1,550,248 [19], 6% precision and a 95% confidence interval (CI). The final sample consisted of 221 boys and girls.
We included children whose parents signed informed consent. We excluded those suffering from some chronic pathology.

2.2. Study Variables and Measurements

The diagnosis of Metabolic Syndrome was determined following the criteria established by Cook [20], defined by the presence of three or more of the following alteration: waist circumference (WC) ≥ 90th percentile, systolic blood pressure (SBP) or diastolic (DBP) ≥ 90th percentile, HDL ≥ 40 mg/dL, triglycerides ≥ 110 mg/dL, and fasting glycemia levels ≥100 mg/dL, as established by the American Diabetes Association (ADA) [21].
The independent variables included were sex (boy, girl), age (years), and those grouped into:
  • Anthropometric variables: weight (Kg), height (cm), BMI (Kg/m2), waist circumference (WC, cm), WHtR, fat-free mass (Kg), fat mass (Kg), fat mass percentage, SBP (mmHg) and DBP (mmHg).
  • Analytical variables: glucose (mg/dL), Chol-HDL (mg/dL), Chol-LDL (mg/dL), triglycerides (mg/dL) and total cholesterol (mg/dL)
The anthropometric measurements were measured following the recommendations in the reference manual for anthropometric standardization [22]. Height was measured with a SECA 209 stadiometer with a precision of 0.1 cm. Weight and body composition (percentage of fat, fat mass, and fat-free mass) were measured with a bioimpedance meter (TANITA TBF-300, TANITA, Tokyo, Japan) with a precision of 0.1 kg. WC was measured halfway between the lower costal border and the iliac crest at the end of a normal aspiration, using a non-elastic flexible tape. The established recommendations were followed for measuring blood pressure (BP) [23], employing a calibrated digital sphygmomanometer (OMRON M3, OMRON, Kyoto, Japan). Analysis of circulating metabolites was performed from a fasting venous blood sample taken between 8.00 and 10.00 a.m. Measurements of lipid and glycidic indicators were performed using commercial kits (Cobas C11Roche, Indianapolis, IN, USA). Experienced technicians performed all the measurements to minimize the coefficient of variation. Each measure was made three times, and the average value was calculated.
The classification of nutritional status was performed following the criteria established by the World Health Organization for the BMI Z-Score [24]:
  • Normal weight: Z-Score BMI > −2SD (standard deviation) and < +1SD;
  • Overweight: Z-Score BMI > +1SD and < +2SD;
  • Obesity: Z-Score BMI > +2SD.
To determine the presence of abdominal obesity (waist circumference > 90th percentile) and high blood pressure (HBP; SBP or DPB > 90th percentile), the reference tables were used according to age and sex, and height in the case of arterial pressure [25,26].

2.3. Ethical and Legal Aspects

The study was carried out in compliance with the fundamental principles laid down in the Declaration of Helsinki (1964), the Council of Europe Convention on Human Rights and Biomedicine (1997), the UNESCO Universal Declaration on the Human Genome and Human Rights (1997), as well as with the requirements laid down in Chilean legislation for biomedical research, the protection of personal data and bioethics. The Bioethics Committee of the Vice-Rectory of Research of the University of Concepción approved the study protocol (352-2019).

2.4. Statistical Analysis

The quantitative variables are presented with mean and standard deviation, and the qualitative values are shown with frequencies and percentages.
To assess the goodness of fit to a normal distribution of data from quantitative variables, the Kolmogorov-Smirnov test with the Lilliefors correction was used. To bivariate hypothesis contrast, the Student t-test for two means and the Mann–Whitney U was performed (using the Levene test for the contrast of homoscedasticity).
The multivariate analysis was performed through two statistical approaches:
  • Binary logistic regression models adjusted by diverse qualitative and quantitative predictive variables. The Odds Ratio (OR) adjusted with its 95% confidence interval was determined. The goodness of fit tests (–2 log-likelihood, goodness of fit statistic, Cox and Snell R2, Nagelkerke R2 y Hosmer–Lemeshow tests) were calculated to evaluate the overall fit of the model.
  • Discriminant Analysis models adjusted only by quantitative predictive variables. The coefficients for each of Fisher’s linear discriminant functions (MetS negative and MetS positive) were obtained. The Box M test was used to contrast the equalness of the matrixes for the two groups (MetS negative and MetS positive), and the Wilks Lambda test for contrasting the discriminant capacity compared with the predictive variables.
We also performed Receiver Operating Characteristic (ROC) curves and area under the curve (AUC) to determine each variable’s diagnostic accuracy to establish which best predicted the Metabolic Syndrome. Sensitivity, specificity, Youden, and validity indices were analyzed to determine its best cut off value for higher diagnostic accuracy.
The new MetS early detection model was obtained from a clinical decision tree (classification) using the chi-squared automatic interaction detection (CHAID) technique as a growth method. The statistical significance level for splitting nodes and merging categories was p < 0.05, significance values were corrected by the Bonferroni method, and the maximum number of iterations was 100. Various decision trees were produced with different modifications in the growth criteria, with a final minimum number of subjects of 50 and 30 in parent and child nodes, respectively.
The probability of an α error of below 5% (p < 0.05) was considered statistically significant for all the statistical analyses. The confidence interval was calculated at 95%. For the statistical analysis, IBM SPSS Statistics 22.0 software (IBM, Chicago, IL, USA) and Epidat 4.2. (Department of Sanidade, Xunta de Galicia, Galicia, Spain) were used.

3. Results

3.1. Prevalence of MetS and Anthropometric Predictor Variables

Of 221 children, 51.2% (95% CI 43.4–57%) were girls. The overall mean age was 9.1 ± 1.3 years (95% CI 8.9–9.3 years), with no significant differences between girls and boys (p > 0.05). Following the Z-Score BMI criteria, 67% (95% CI 60.3–73.1%) were overweight or obese, reaching the prevalence of 68.5% (95% CI 59–77%) and 65.5% (95% CI 55.8–74.3%) in girls and boys (p > 0.05), respectively. The prevalence of MetS observed in the sample was 26.7% (95% CI 21–33%), with a significantly higher proportion in girls than boys (OR = 2.2; p <0.05).
Table 1 shows the characteristics of the sample, the results of the independent variables for the groups with and without MetS and the analysis of raw and adjusted logistic regression. Of the variables studied, being overweight or obese (OR = 22.236; 95% CI 5.249–94.206; p < 0.001) and showing WHtR higher than or equal to 0.55 (OR = 16.763; 95% CI 5.801–48.441; p < 0.001), produced the greatest increase in the prevalence of MetS. We only took into account variables that did not require invasive procedures for the adjusted model. After adjusting for school children’s age and sex, only BMI and systolic blood pressure showed an association.
Figure 1 shows the ROC curves, cut-off points, sensitivity, specificity, and Youden’s index of the variables that presented a significant MetS discrimination capacity. Chol-HDL showed an AUC of 84% and, for a cut-off point of 41.3 mg/dL, sensitivity and specificity of 93.2% and 67.8%, respectively. BMI obtained an AUC of 82.7% and, with a cut-off point of 23.5 kg/m2, 86.4% sensitivity, and 72.2% specificity.

3.2. Designing the Decision Tree to Detect MetS Based on Anthropometric Variables (Non-Invasive Method)

Two predictive models are proposed and compared based on the non-invasive variables that were statistically significant in the raw and adjusted logistic regression analysis.
-
Model 1: based on sex (male and female) and dichotomization (according to whether the value is higher or lower than the cut-off point shown in Figure 1) of the WHtR (0.55), blood pressure (104.5/69 mmHg) and BMI (23.5 Kg/m2).
-
Model 2: including sex (male and female), WC, HBP according to age, sex and height, and BMI (≥23.5 Kg/m2).
Table 2 shows the indicators’ results (sensitivity, specificity, and validity index) of each model. Model 1 and 2 have shown a sensitivity of 45.8% and 66.1%, and a specificity of 95.1% and 90.7%, respectively. As a complement to the models obtained by binary logistic regression, another was calculated through discriminant analysis. This model reached a sensitivity of 81.4%, a specificity of 75.3%, and a validity index of 76.9%. Table 3 shows these results and the coefficients for discriminant function variables.
Finally, to offer a tool that is easy to understand and apply in clinical settings, several clinical decision trees were designed for the early detection of MetS. For this purpose, we used the variables shown to be significant in models 1 and 2. Figure 2 presents the decision trees (classification algorithm) with the best predictive capacity. The decision tree, shown in Figure 2a, reached a sensitivity of 86.4%, a specificity of 70.4%, and a validity index of 74.7%, being the BMI the variable with the highest association with the MetS ( χ2 = 56.446). The decision tree represented in Figure 2b performed a sensitivity, specificity, and validity index of 76.3%, 82.1%, and 80.5%, respectively.

4. Discussion

The study aimed to present a non-invasive method that allows early detection of MetS without the need for invasive techniques. In this sense, we have proposed two algorithms and a discriminant model based on non-invasive variables (BMI, WHtR, and BP).
The prevalence of MetS rose to 26.7%, with a higher proportion in the female population, something observed in other works [27,28]. Although this prevalence is different from that shown by other authors, it depends mainly on the diagnostic criteria used, and the characteristics of the population studied [28,29]. Eyzaguirre et al. found a prevalence of 22.7% in the study of obese Chilean children, similar to that observed in our results [12]. Bustos et al. observed a proportion of 44% in another population with similar characteristics [13]. As demonstrated by our results, the literature has shown that overweight and obesity are the most important characteristics that contribute to the increase in the presence of MetS in children [30]. Therefore, we consider that the high prevalence of overweight and obesity in our sample (67%) has influenced the high presence of MetS (OR = 22.236). This trend has been observed by other authors [27,28,30,31].
This study has also revealed a strong association of all non-invasive variables (anthropometric and blood pressure) with MetS. Of these, BMI (AUC = 0.827) and WC (AUC = 0.808) presented the highest predictive capacity. Our work obtained a sensitivity of 86.4% for BMI (cut-off point of 23.5 kg/m2) and 83.1% for WC (cut-off point of 77.9 cm). Radetti et al. evidenced that the BMI, despite its limitations, showed better validity indexes in the prediction of MetS than other adiposity markers, emphasizing the ease of calculating BMI [32]. Other authors have indicated that this parameter (following different criteria) is a good predictor of the MetS components [33,34]. In the same vein, several investigations have highlighted the role of waist circumference and its ratio to height in the prediction of MetS [35,36]. However, various meta-analyses have shown that the cut-off points of these variables vary according to the reference population, making it difficult to compare our results’ predictive capacity with those obtained in other research [37,38].
These results are reinforced by those found in the different multivariate models described. Concerning the logistic regression models, adjusting for the variables mentioned above (WC, quantitative; HBP; qualitative; BMI; qualitative), we reached 66.1%, 90.7%, and 84.2% of sensitivity, specificity, and validity index, respectively. Additionally, the importance of BMI and altered blood pressure is perceived in the discriminant analysis. These variables, in its quantitative version, were capable of correctly discriminating against 76.9% of children. The inclusion of blood pressure in non-invasive diagnostic models is crucial because, as other authors have pointed out, HBP values are frequent in obese children suffering from MetS [12,14,39].
Moreover, data show the critical role of BMI, WC, WHtR, and BP in the early non-invasive diagnosis of MetS. However, the application of multivariate models in some clinical settings (schools, fieldwork, etc.) could be complicated by the need for mathematical calculations.
For this reason, two algorithms were performed to facilitate the clinical decision in the diagnosis. The first one was based on three variables (BP, BMI, and WHtR). In contrast, two variables (BMI and WHtR) were used to perform the second one. Wicklow et al., in a prospective study, showed that these variables are related to the appearance over time of cardiometabolic risk factors, which would justify their use in children, as is currently done in the adult population [15,16,18]. This fact is essential in our study population, given that, from the age of 9, the public education system does not maintain health control within healthy children program. Although in other populations, WC and WHtR have been proposed as an alternative to BMI in MetS discrimination, our results have shown that their combined use can increase their discriminatory capacity [40,41].
Regarding its applicability, the first of them, with high sensitivity (86.4%), could facilitate the screening of children suffering from MetS, even in clinical settings where blood pressure monitors are not available. On the other hand, the second algorithm presented a higher validity index (80.5%), allowing the proper classification of a higher number of cases correctly. This tree is recommended in situations where blood pressure measures are available.
In summary, from our point of view, this work puts at the disposal of the scientific community the first tools and the development of a methodology that would help in the early detection of MetS in children, something demanded by several authors [42,43]. Specifically, Ahadi et al. and Bianchini et al. encourage the routine use of non-invasive variables to screen metabolic risk factors and MetS in childhood [44,45]. However, given the phenotypic variability between different geographical locations, adaptations should be made according to the reference populations (hence the importance of this methodological approach). The inclusion of other variables associated with cardio-metabolic risks, such as neck circumference, could be considered [46]. The importance of early screening lies in achieving a good state of health and avoiding the possible alterations that develop in the following stages of life [47]. As we commented previously, from 9 onwards, the girls and boys do not continue the health control. For this reason, this proposal could have a high impact since it is based on quick and simple techniques that could be applied in schools by nurses, nutritionists, or even adequately trained teachers.
The proposed screening methods could facilitate early detection in the school setting, referral to primary care, and early intervention.

Limitations

The sample presents a high prevalence of overweight and obesity, which raises the prevalence of MetS above that shown in the general child population. Besides, the study only included a population from South America. Given the heterogeneity of criteria for the diagnosis and the scarce consensus around them, the modified Cook’s criteria were used to facilitate comparison with other works carried out in similar populations. The CHAID methodology used to elaborate decision trees recommends large sample sizes to optimize statistical significance. In the sample used in this study (n = 221), the criteria for forming the parent and child nodes were low (50 and 30, respectively). Based on this, future work should consider larger samples with better representation of nutritional status and other ethnicities to contrast the proposed method more reliably. It is important to highlight as a strength that, to our knowledge, these models are the first tools for detecting MetS presented for Chilean children.

5. Conclusions

The prevalence of MetS is high in this child population, especially among those children who are overweight and obese. Two models have been found based on non-invasive variables that can be easily measured in any context (school, primary care, etc.). They present a good diagnostic precision and the potential to reduce the blood extractions involved (they would only be indicated for diagnostic confirmations). Therefore, they represent convenient and cost-efficient methods.

Author Contributions

Conceptualization, R.M.-L. and M.R.-S.; Data curation, R.M.-L.; Formal analysis, R.M.-L. and G.M.-R.; Funding acquisition, N.U., A.G. and M.Z.; Investigation, N.U., A.G. and M.Z.; Methodology, R.M.-L. and M.R.-S.; Resources, N.U., A.G. and M.Z.; Writing–original draft, R.M.-L.; Writing—review and editing, N.U., M.R.-S. and G.M.-R. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by INNOVA CORFO, grant number 07CN131SM-19.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Kassi, E.; Pervanidou, P.; Kaltsas, G.; Chrousos, G.P. Metabolic syndrome: Definitions and controversies. BMC Med. 2011, 9, 48. [Google Scholar] [CrossRef] [Green Version]
  2. World Health Organization. Noncommunicable Diaseases. Available online: https://www.who.int/news-room/fact-sheets/detail/noncommunicable-diseases (accessed on 26 October 2020).
  3. Alberti, K.; Eckel, R.H.; Grundy, S.M.; Zimmet, P.Z.; Cleeman, J.I.; Donato, K.A.; Fruchart, J.-C.; James, W.P.T.; Loria, C.M.; Smith, S.C. Harmonizing the Metabolic Syndrome. Circulation 2009, 120, 1640–1645. [Google Scholar] [CrossRef] [Green Version]
  4. Lee, S.E.; Han, K.; Kang, Y.M.; Kim, S.-O.; Cho, Y.K.; Ko, K.S.; Park, J.-Y.; Lee, K.-U.; Koh, E.H. Trends in the prevalence of metabolic syndrome and its components in South Korea: Findings from the Korean National Health Insurance Service Database (2009–2013). PLoS ONE 2018, 13, e0194490. [Google Scholar] [CrossRef] [Green Version]
  5. Shin, D.; Kongpakpaisarn, K.; Bohra, C. Trends in the prevalence of metabolic syndrome and its components in the United States 2007–2014. Int. J. Cardiol. 2018, 259, 216–219. [Google Scholar] [CrossRef] [PubMed]
  6. Younis, A.; Younis, A.; Tzur, B.; Peled, Y.; Shlomo, N.; Goldenberg, I.; Fisman, E.Z.; Tenenbaum, A.; Klempfner, R. Metabolic syndrome is independently associated with increased 20-year mortality in patients with stable coronary artery disease. Cardiovasc. Diabetol. 2016, 15, 149. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  7. Ogden, C.L.; Carroll, M.D.; Lawman, H.G.; Fryar, C.D.; Kruszon-Moran, D.; Kit, B.K.; Flegal, K.M. Trends in Obesity Prevalence among Children and Adolescents in the United States, 1988-1994 through 2013–2014. JAMA 2016, 315, 2292–2299. [Google Scholar] [CrossRef]
  8. Al-Hamad, D.; Raman, V. Metabolic syndrome in children and adolescents. Transl. Pediatr. 2017, 6, 397–407. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  9. Cho, J.; Hong, H.; Park, S.; Kim, S.; Kang, H. Insulin Resistance and Its Association with Metabolic Syndrome in Korean Children. BioMed Res. Int. 2017, 2017, 8728017. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  10. Friend, A.; Craig, L.; Turner, S. The Prevalence of Metabolic Syndrome in Children: A Systematic Review of the Literature. Metab. Syndr. Relat. Disord. 2013, 11, 71–80. [Google Scholar] [CrossRef]
  11. Ministerio de Salud de Chile. Encuesta Nacional de Salud 2016–2017. Available online: https://www.minsal.cl/wp-content/uploads/2018/01/2-Resultados-ENS_MINSAL_31_01_2018.pdf (accessed on 26 October 2020).
  12. Eyzaguirre, F.; Silva, R.; Román, R.; Palacio, A.; Cosentino, M.; Vega, V.; García, H. Prevalencia de síndrome metabólico en niños y adolescentes que consultan por obesidad. Rev. Med. Chile 2011, 139, 732–738. [Google Scholar] [CrossRef] [Green Version]
  13. Bustos, P.; Orias, J.; Sáez, K.; Maldonado, M.; Cuadra, L.; Asenjo, S. Impacto del Programa de manejo de la obesidad Bright Bodies aplicado a niños y adolescentes chilenos. Rev. Med. Chile 2015, 143, 1136–1143. [Google Scholar] [CrossRef] [Green Version]
  14. Mastroeni, S.S.D.B.S.; Mastroeni, M.F.; Ekwaru, J.P.; Setayeshgar, S.; Veugelers, P.J.; Gonçalves, M.D.C.; Rondó, P.H.D.C. Anthropometric measurements as a potential non-invasive alternative for the diagnosis of metabolic syndrome in adolescents. Arch. Endocrinol. Metab. 2019, 63, 30–39. [Google Scholar] [CrossRef]
  15. Romero-Saldaña, M.; Tauler, P.; Vaquero-Abellán, M.; López-González, A.-A.; Fuentes-Jiménez, F.-J.; Aguiló, A.; Álvarez-Fernández, C.; Molina-Recio, G.; Bennasar-Veny, M. Validation of a non-invasive method for the early detection of metabolic syndrome: A diagnostic accuracy test in a working population. BMJ Open 2018, 8, e020476. [Google Scholar] [CrossRef] [Green Version]
  16. Romero-Saldaña, M.; Fuentes-Jiménez, F.J.; Vaquero-Abellán, M.; Álvarez-Fernández, C.; Molina-Recio, G.; López-Miranda, J. New non-invasive method for early detection of metabolic syndrome in the working population. Eur. J. Cardiovasc. Nurs. 2016, 15, 549–558. [Google Scholar] [CrossRef]
  17. Vasan, S.K.; Thomas, N.; Christopher, S.; Geethanjali, F.S.; Paul, T.V.; Sanjeevi, C.B. Anthropometric measurements for the prediction of the metabolic syndrome: A cross-sectional study on adolescents and young adults from southern india. Heart Asia 2011, 3, 2–7. [Google Scholar] [CrossRef] [Green Version]
  18. Wicklow, B.; Becker, A.; Chateau, D.; Palmer, K.; Kozyrskij, A.; Sellers, E.A.C. Comparison of anthropometric measurements in children to predict metabolic syndrome in adolescence: Analysis of prospective cohort data. Int. J. Obes. 2015, 39, 1070–1078. [Google Scholar] [CrossRef]
  19. Instituto Nacional de Estadística (Chile). Censo 2017. Available online: https://www.censo2017.cl (accessed on 26 October 2020).
  20. Cook, S.; Weitzman, M.; Auinger, P.; Nguyen, M.; Dietz, W.H. Prevalence of a metabolic syndrome phenotype in adolescents: Findings from the third National Health and Nutrition Examination Survey, 1988−1994. Arch. Pediatr. Adolesc. Med. 2003, 157, 821–827. [Google Scholar] [CrossRef] [Green Version]
  21. American Diabetes Association. Classification and Diagnosis of Diabetes: Standards of Medical Care in Diabetes—2019. Diabetes Care 2018, 42 (Suppl. 1), S13–S28. [Google Scholar] [CrossRef] [Green Version]
  22. Callaway, C.; Chumlea, W.; Bouchard, C.; Himes, J.; Lohman, T.; Martin, A.; Mitchell, C.D.; Mueller, W.H. Circumferences. In Anthropometric Standardization Reference Manual; Lohman, T.G., Roche, A., Martorell, R., Eds.; Human Kinetics Books: Champaign, IL, USA, 1991; pp. 44–45. [Google Scholar]
  23. Williams, B.; Mancia, G.; Spiering, W.; Rosei, E.A.; Azizi, M.; Burnier, M.; Clement, D.L.; Coca, A.; de Simone, G.; Dominiczak, A.F.; et al. 2018 ESC/ESH Guidelines for the management of arterial hypertension. Eur. Heart J. 2018, 39, 3021–3104. [Google Scholar] [CrossRef]
  24. Organización Mundial de la Salud. IMC Para Edad de Entre 5 y 19 Años. Available online: https://www.who.int/growthref/who2007_bmi_for_age/en/ (accessed on 26 October 2020).
  25. Ministerio de Salud. Orientaciones Técnicas Para el Control de Salud Integral de Adolescentes; Control Joven Sano 2014; Ministerio de Salud: Santiago, Chile, 2013. [Google Scholar]
  26. Fernández, J.R.; Redden, D.T.; Pietrobelli, A.; Allison, D.B. Waist circumference percentiles in nationally representative samples of African-American, European-American, and Mexican-American children and adolescents. J. Pediatr. 2004, 145, 439–444. [Google Scholar] [CrossRef]
  27. Mardones, F.; Araniz, P.; Barja, S.; Giadach, C.; Villarroel, L.; Domínguez, A. Estado nutricional, síndrome metabólico y resistencia a la insulina en niños de Santiago, Chile. Nutr. Hosp. 2013, 28, 1999–2005. [Google Scholar]
  28. Ahrens, W.; Moreno, L.; Mårild, S.; Molnár, D.; Siani, A.; de Henauw, S.; Böhmann, J.; Günther, K.; Hadjigeorgiou, C.; Iacoviello, L.; et al. Metabolic syndrome in young children: Definitions and results of the IDEFICS study. Int. J. Obes. 2014, 38 (Suppl. 2), S4–S14. [Google Scholar] [CrossRef] [Green Version]
  29. Pierlot, R.; Cuevas-Romero, E.; Rodríguez-Antolín, J.; Méndez-Hernández, P.; Martínez-Gómez, M. Prevalencia de síndrome metabólico en niños y adolescentes de américa. TIP 2017, 20, 40–49. [Google Scholar] [CrossRef]
  30. Gepstein, V.; Weiss, R. Obesity as the Main Risk Factor for Metabolic Syndrome in Children. Front. Endocrinol. 2019, 10, 568. [Google Scholar] [CrossRef]
  31. Sapunar, J.; Aguilar-Farías, N.; Navarro, J.; Araneda, G.; Chandia-Poblete, D.; Manríquez, V.; Brito, R.; Cerda, A. High prevalence of overweight, obesity, insulin resistance and metabolic syndrome in rural children and adolescents. Rev. Med. Chile 2018, 146, 978–986. [Google Scholar] [CrossRef] [Green Version]
  32. Radetti, G.; Fanolla, A.; Grugni, G.; Lupi, F.; Sartorio, A. Indexes of adiposity and body composition in the prediction of metabolic syndrome in obese children and adolescents: Which is the best? Nutr. Metab. Cardiovasc. Dis. 2019, 29, 1189–1196. [Google Scholar] [CrossRef]
  33. Lee, K. Comparison of Body Mass Index Percentiles to Detect Metabolic Syndrome Using the Korean, United States Centers for Disease Control and Prevention, and World Health Organization References in Korean Children Aged 10–16 Years. Metab. Syndr. Relat. Disord. 2019, 17, 210–216. [Google Scholar] [CrossRef]
  34. Jung, C.; Fischer, N.; Fritzenwanger, M.; Figulla, H.R. Anthropometric indices as predictors of the metabolic syndrome and its components in adolescents. Pediatr. Int. 2010, 52, 402–409. [Google Scholar] [CrossRef]
  35. De Oliveira, R.G.; Guedes, D.P. Performance of anthropometric indicators as predictors of metabolic syndrome in Brazilian adolescents. BMC Pediatr. 2018, 18, 33. [Google Scholar] [CrossRef] [Green Version]
  36. Nambiar, S.; Truby, H.; Davies, P.S.; Baxter, K. Use of the waist-height ratio to predict metabolic syndrome in obese children and adolescents. J. Paediatr. Child Health 2013, 49, E281–E287. [Google Scholar] [CrossRef]
  37. Sangrador, C.O.; Ochoa-Brezmes, J. Waist-to-height ratio as a risk marker for metabolic syndrome in childhood. A meta-analysis. Pediatr. Obes. 2018, 13, 421–432. [Google Scholar] [CrossRef] [PubMed]
  38. Lo, K.; Wong, M.; Khalechelvam, P.; Tam, W. Waist-to-height ratio, body mass index and waist circumference for screening paediatric cardio-metabolic risk factors: A meta-analysis. Obes. Rev. 2016, 17, 1258–1275. [Google Scholar] [CrossRef] [PubMed]
  39. Graf, C.; Ferrari, N. Metabolic Syndrome in Children and Adolescents. Visc. Med. 2016, 32, 357–362. [Google Scholar] [CrossRef] [Green Version]
  40. Aristizabal, J.C.; Estrada-Restrepo, A.; Barona, J. Waist-to-height ratio may be an alternative tool to the body mass index for identifying Colombian adolescents with cardiometabolic risk factors. Nutr. Hosp. 2019, 36, 96–102. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  41. Perona, J.; Schmidt, J.; Ramírez-Vélez, R.; Correa-Rodríguez, M.; Fernández-Aparicio, Á.; González-Jiménez, E. Waist circumference and abdominal volume index are the strongest anthropometric discriminators of metabolic syndrome in Spanish adolescents. Eur. J. Clin. Investig. 2018, 49, e13060. [Google Scholar] [CrossRef]
  42. Pacheco, L.S.; Blanco, E.; Burrows, R.; Reyes, M.; Lozoff, B.; Gahagan, S. Early Onset Obesity and Risk of Metabolic Syndrome Among Chilean Adolescents. Prev. Chronic Dis. 2017, 14, 170132. [Google Scholar] [CrossRef] [Green Version]
  43. Chiarelli, F.; Mohn, A. Early diagnosis of metabolic syndrome in children. Lancet Child Adolesc. Health 2017, 1, 86–88. [Google Scholar] [CrossRef]
  44. Ahadi, Z.; Bahreynian, M.; Qorbani, M.; Heshmat, R.; Motlagh, M.E.; Shafiee, G.; Gorabi, A.M.; Ziaodini, H.; Taheri, M.; Aminaei, T.; et al. Association of anthropometric measures and cardio-metabolic risk factors in normal-weight children and adolescents: The CASPIAN-V study. J. Pediatr. Endocrinol. Metab. 2018, 31, 847–854. [Google Scholar] [CrossRef]
  45. De Quadros, T.M.B.; Gordia, A.P.; Andaki, A.C.R.; Mendes, E.L.; Mota, J.; Silva, L.R. Utility of anthropometric indicators to screen for clustered cardiometabolic risk factors in children and adolescents. J. Pediatr. Endocrinol. Metab. 2019, 32, 49–55. [Google Scholar] [CrossRef]
  46. Ataie-Jafari, A.; Namazi, N.; Djalalinia, S.; Chaghamirzayi, P.; Abdar, M.E.; Zadehe, S.S.; Asayesh, H.; Zarei, M.; Gorabi, A.M.; Mansourian, M.; et al. Neck circumference and its association with cardiometabolic risk factors: A systematic review and meta-analysis. Diabetol. Metab. Syndr. 2018, 10, 72. [Google Scholar] [CrossRef]
  47. Koskinen, J.; Magnussen, C.G.; Sinaiko, A.; Woo, J.; Urbina, E.; Jacobs, D.R.; Steinberger, J.; Prineas, R.; Sabin, M.A.; Burns, T.; et al. Childhood Age and Associations Between Childhood Metabolic Syndrome and Adult Risk for Metabolic Syndrome, Type 2 Diabetes Mellitus and Carotid Intima Media Thickness: The International Childhood Cardiovascular Cohort Consortium. J. Am. Heart Assoc. 2017, 6, e005632. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Figure 1. Receiver Operating Characteristic curves for independent variables.
Figure 1. Receiver Operating Characteristic curves for independent variables.
Children 07 00304 g001
Figure 2. Clinical decision trees based on: (a) body mass index and weight to height ratio; (b) blood pressure, body mass index and weight to height ratio.
Figure 2. Clinical decision trees based on: (a) body mass index and weight to height ratio; (b) blood pressure, body mass index and weight to height ratio.
Children 07 00304 g002
Table 1. Characteristics of the sample by MetS and (crude and adjusted) logistic regression.
Table 1. Characteristics of the sample by MetS and (crude and adjusted) logistic regression.
Raw Regression (No Adjusted)Adjusted Regression
VariablesTotal (n = 221)Presence (n = 59)Absence (n = 162)OR95% CIpOR95% CIp
Mean or n (SD or %)Mean or n (SD or %)Mean or n (SD or %)
Sex
Women111 (51.2)38 (64.4)73 (45.1)2.2061.191–4.086<0.053.4881.586–7.674<0.01
Men110 (49.8)21 (35.6)89 (54.9)1111
Age (years)9.1 (1.3)9.3 (1.2)9 (1.3)1.2170.949–1.559NS
Weight (Kg)41.2 (10.8)49.2 (9)38.3 (9.9)1.1241.081–1.168<0.001
Height (cm)135.2 (9)138.2 (8.6)134.1 (8.9)1.0571.019–1.097<0.01
WC (cm)74.6 (11.5)83.6 (10.8)71.3 (10.8)1.1311.086–1.177<0.001
WHtR > 0.55128 (57.9)55 (93.2)73 (45.1)16.7645.801–48.441<0.001
BMI (Kg/m2)22.2 (4.2)25.6 (3.1)21 (3.8)1.4351.276–1.613<0.0011.3801.219–1.563<0.001
Overweight/Obesity148 (67)57 (96.6)91 (56.2)22.2365.249–94.206<0.001
BF (%)30.1 (9.4)36.6 (6)27.7 (9.4)1.1391.087–1.193<0.001
FM (Kg)13.4 (6.7)18.3 (5.7)11.5 (6.2)1.1941.124–1.268<0.001
FFM (Kg)28.4 (5.1)31.1 (5.1)27.4 (4.7)1.1731.093–1.258<0.001
SBP (mmHg)101.5 (12)108.7 (12)98.9 (10.9)1.0861.051–1.121<0.0011.0591.022–1.098<0.001
DBP (mmHg)66 (10.8)71.1 (10.7)64.1 (10.2)1.0731.037–1.109<0.001
Glucose (mg/dL)88.2 (8.5)88.6 (10)88.1 (8)1.0060.972–1.042NS
CholT (mg/dL)181.7 (33.1)188.2 (36.4)179.3 (31.6)1.0080.999–1.017NS
Chol-HDL (mg/dL)50.5 (11.6)40.4 (10.2)54.2 (9.8)0.8590.821–0.899<0.001
Chol-LDL (mg/dL)108.2 (28.8)113.3 (32.9)106.3 (27.1)1.0080.998–1.019NS
Triglycerides (mg/dL)122.9 (73.8)186 (93.1)99.9 (48.1)1.0201.014–1.026<0.001
MetS: Metabolic Syndrome; SD: Standard Deviation; OR: Odds Ratio; WC: Waist circunference; WHtR: Waist to height ratio; BMI: Body Mass Index; BF: Body fat; FM: Fat Mass; FFM: Fat Free Mass; SBP/DBP: Systolic/Diastolic Blood Pressure; CholT: Total Cholesterol.
Table 2. Multivariate analysis and adjusted logistic regression for non-invasive categorical (dichotomous) variables.
Table 2. Multivariate analysis and adjusted logistic regression for non-invasive categorical (dichotomous) variables.
Model 1
VariableCoefficientOR95% CIp
Sex (Woman)1.1143.0471.392–6.669<0.01
WHtR ≥ 0.551.7145.5511.996–15.442<0.01
BP ≥ 104.5/691.4484.2531.743–10.375<0.01
BMI ≥ 23.51.4114.5441.120–14.999<0.05
Model 2
Sex1.2633.5351.511–8.273<0.01
WC0.0761.0791.020–1.142<0.01
HBP *1.9416.9643.012–16.104<0.001
BMI ≥ 23.51.2353.4431.070–11.081<0.05
Sensitivity, Specificity and Validity Index for the Predictive MetS Model
Model 1Model 2
Sensitivity45.8%66.1%
Specificity95.1%90.7%
Validity index81.9%84.2%
R2 Nagelkerke0.4550.511
R2 Cox-Snell0.3130.350
Hosmer-Lemeshow (p)0.7340.417
WHtR: Waist to height ratio; BP: Blood Pressure; BMI: Body Mass Index; WC: Waist circumference; BF: Body fat; Metabolic Syndrome; OR: Odds Ratio; CI: Confidence interval; * High Blood Pressure according to age, sex and height; Models adjusted by sex and age.
Table 3. Discriminant Analysis.
Table 3. Discriminant Analysis.
VariableMetS [No] CoefficientMetS [Yes] Coefficientp
BMI0.9601.251<0.001
SBP0.6740.721<0.001
Constant−44.106−55.778-
Sensitivity, Specificity and Validity Index for the Predictive MetS Model
Sensitivity81.4%
Specificity75.3%
Validity index76.9%
BMI: Body Mass Index; WC: Waist circumference; SBP: Systolic Blood Pressure; MetS: Metabolic Syndrome.
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Molina-Luque, R.; Ulloa, N.; Gleisner, A.; Zilic, M.; Romero-Saldaña, M.; Molina-Recio, G. An Approach to Early Detection of Metabolic Syndrome through Non-Invasive Methods in Obese Children. Children 2020, 7, 304. https://0-doi-org.brum.beds.ac.uk/10.3390/children7120304

AMA Style

Molina-Luque R, Ulloa N, Gleisner A, Zilic M, Romero-Saldaña M, Molina-Recio G. An Approach to Early Detection of Metabolic Syndrome through Non-Invasive Methods in Obese Children. Children. 2020; 7(12):304. https://0-doi-org.brum.beds.ac.uk/10.3390/children7120304

Chicago/Turabian Style

Molina-Luque, Rafael, Natalia Ulloa, Andrea Gleisner, Martin Zilic, Manuel Romero-Saldaña, and Guillermo Molina-Recio. 2020. "An Approach to Early Detection of Metabolic Syndrome through Non-Invasive Methods in Obese Children" Children 7, no. 12: 304. https://0-doi-org.brum.beds.ac.uk/10.3390/children7120304

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