Next Article in Journal
Demographic, Social, and Behavioral Determinants of Lung Cancer Perceived Risk and Worries in a National Sample of American Adults; Does Lung Cancer Risk Matter?
Next Article in Special Issue
Physical Activity Level Using Doubly-Labeled Water in Relation to Body Composition and Physical Fitness in Preschoolers
Previous Article in Journal
A Systematic Review and Meta-Analysis Evaluating Antibiotic Prophylaxis in Dental Implants and Extraction Procedures
Previous Article in Special Issue
Association between Sleep Quality and Body Composition in Sedentary Middle-Aged Adults
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Association between Cluster of Lifestyle Behaviors and HOMA-IR among Adolescents: ABCD Growth Study

by
André Oliveira Werneck
*,
Ricardo Ribeiro Agostinete
,
Suziane Ungari Cayres
,
Jacqueline Bexiga Urban
,
Andréa Wigna
,
Lucas Gabriel de Moraes Chagas
,
Wesley Torres
and
Rômulo Araújo Fernandes
Laboratory of InVestigation in Exercise—LIVE, Department of Physical Education, Sao Paulo State University (UNESP), Presidente Prudente, Sao Paulo 19060-900, Brazil
*
Author to whom correspondence should be addressed.
Submission received: 25 October 2018 / Revised: 25 November 2018 / Accepted: 29 November 2018 / Published: 1 December 2018

Abstract

:
Objective: To analyze the association of potential risk factors to health with body fatness and insulin resistance. Baseline measures of the ongoing longitudinal Analysis of Behaviors of Children During (ABCD) Growth Study. Materials and Methods: The sample was composed of 280 adolescents of both sexes (198 boys and 82 girls) aged from 10 to 18 years. Four risk factors were considered, as follows: no sports practice, skipping breakfast, poor sleep quality, and TV viewing. The outcomes considered were insulin resistance (HOMA-IR) and body fatness (densitometer scanner). Age, sex, maturity offset, and ethnicity were treated as covariates. Results: No sports practice and skipping breakfast were associated with higher body fatness (Sports practice: Wald: 8.786; p = 0.003. Breakfast: Wald: 9.364; p = 0.002). Poor sleep quality was related to a greater HOMA-IR index (Wald: 6.013; p = 0.014). Adolescents with ≥3 risk factors presented a higher risk of high HOMA-IR (OR = 4.89 (95%CI: 1.61 to 14.84)) than their counterparts with no risk factors. Conclusion: Lifestyle risk factors seem relevant to affect obesity and insulin resistance, while the aggregation of these risk factors affects insulin resistance, independent of adiposity.

1. Introduction

Homeostatic Model Assessment of Insulin Resistance (HOMA-IR), derived from an equation with fasting glucose and insulin, is an important technique for the diagnosis and surveillance of insulin resistance, being a marker of type 2 diabetes mellitus [1,2]. Type 2 diabetes mellitus is an important public health problem, affecting 422 million people in 2014, and increases the risk of developing cardiovascular diseases such as hypertension and dyslipidemia [3,4]. Since early life (childhood and adolescence), IR has been related to different health outcomes, such as higher triglycerides, higher total cholesterol, lower high-density lipoprotein (HDL), and changes in blood pressure [5].
Insulin resistance is strongly affected by body fatness [6]. It is known that adipose tissue is a metabolically active tissue responsible for the secretion of protein and non-protein factors [7,8,9]. Although all mechanisms underlying the link between obesity and IR are not entirely clear, it is known that hormones and cytokines such as resistin, tumor necrosis factor (TNF-α), and interleukin-6 (IL-6) secreted by adipocytes unbalance the action of insulin [7,8,9]. Obesity is an outcome of multifactorial origin [10] being affected by lifestyle factors that also affect IR [11,12] and, thus the role of obesity in the relationship between insulin resistance and these lifestyle behaviors remains unclear.
Moreover, the current literature seeks to understand the effects of different lifestyle behaviors on obesity, and metabolic and cardiovascular health, such as alcohol consumption, tobacco, practice of physical exercise, and dietary patterns [13,14,15] as a study developed by Garoufi et al. (2017) [14], who related overweight/obesity with behavioral habits (smoking, physical activity, screen time and dietary habits) and its association with blood pressure and lipid profile and concluded that behavioral habits affect obesity and cardiovascular risk during adolescence. Other recent study developed by Silva et al. (2017) [15] found that adolescents who were active during childhood until adolescence had better cardiorespiratory fitness, as well as a lower risk of developing hypertension and high metabolic risk. However, there are other not so commonly investigated lifestyle behaviors (e.g., sports participation, skipping breakfast, poor sleep quality, and television viewing (TV viewing)), which can affect health outcomes even during adolescence, including obesity and insulin resistance.
For instance, sport participation, which is a domain of physical activity, is the most relevant manifestation of physical exercise mainly among adolescents, but little is known about its impact on health [15,16], as when physical activity is assessed among adolescents the burden of sports participation is seldom considered. Skipping breakfast and TV viewing (one domain of sedentary behavior) are common behaviors among adolescents, which are linked to body weight gain, and lipid and glucose abnormalities [17,18]. Moreover, sleep quality is a fundamental aspect of human health in all periods of life [19], but the investigation of poor sleep quality and its impacts on adolescent health seems to be a neglected aspect in the literature.
Thus, the aim of this study is to analyze the association between lifestyle behaviors on insulin resistance, as well as to identify whether adiposity affects this association. Based in previous findings, we hypotheses is that cluster of lifestyle behaviors are associated with insulin resistance and adiposity can affect this association.

2. Materials and Methods

2.1. Sampling

The present study is part of the ongoing longitudinal study “Analysis of Behaviors of Children During Growth” (ABCD Growth Study), which is designed to identify the impact of sport participation and other lifestyle behaviors on different health aspects of adolescents. Since 2017, the ABCD Growth Study has been ongoing in the city of Presidente Prudente in the state of São Paulo, Brazil. The Laboratory of InVestigation in Exercise (LIVE) linked to the Department of Physical Education of the São Paulo State University (UNESP) through its researchers is responsible for the ABCD Growth Study. The ethics committee of São Paulo State University (UNESP) approved the study (process number 1.677.938/2016) and parents/legal guardians and the adolescents themselves signed a written consent form before taking part in any assessment.
Researchers contacted adolescents aged 11–18 years at schools (public and private) and sports clubs of the metropolitan region of the city, after previous authorization from principals and coaches, respectively. Adolescents were contacted to explain all the objectives and inclusion criteria of the study, as well as which ethical forms were delivered to request parental/guardian authorization. Inclusion criteria were adopted as follow: (1) 11–18 years of age; (2) parents’ consent form signed; (3) if athletes, at least one year of training experience; if schoolchildren, at least one year without practicing any organized sport. Adolescents who agreed to participate and brought back the ethical forms properly signed by their parents were included in the baseline measures of the ABCD Growth Study.
After the fieldwork, 285 adolescents registered in 11 schools/sports clubs were involved in the baseline measures of the ABCD Growth Study. The baseline measurements were developed in two steps: (1) Questionnaires and analysis of body composition in university laboratories and (2) Blood samples collected in a private laboratory collaborating in the study. However, 27 adolescents, even providing the informing consent, had missing data in some variables (n = 5 in body composition (fat mass) and n = 22 in blood sample (HOMA-IR)) and were excluded from this study, leading to a final sample size of 280 adolescents for fat mass variable and 263 for HOMA-IR of both sexes.

2.2. HOMA-IR

Blood samples were collected after 10 h fasting by a trained nurse in a private laboratory (glucose and insulin were assessed). Insulin levels were analyzed by the chemiluminescence method using a microparticle immunoassay kit (brand ABBOTT), processed in a biochemical Autohumalyzer (brand ARCHITECT, model i2000) obtained from the ABBOTT Diagnostics company, Green Oaks, Illinois, USA. The HOMA-IR (Homeostatic Model Assessment-Insulin resistance) was calculated using (fasting insulin (mcUI/mL) × fasting glucose (mg/dL))/405 [20]. HOMA-IR ≥ 2.0 was classified as high HOMA-IR [20,21,22].

2.3. Body Fatness

Fat mass (in percentage values (%)) was assessed using dual-energy X-ray absorptiometry (Lunar DPX-NT scanner; General Electric Healthcare, Little Chalfont, Buckinghamshire, UK) with GE Medical System Lunar software (version 4.7). This software (Lunar DPX) provide accurate and precise results of bone and tissue composition (lean soft tissue and fat mass) and the measurements are fast and non-invasive. The scanner quality was tested by a trained researcher before each day of measurement, following the manufacturer’s recommendations, and all scans were carried out at the university laboratory in a temperature-controlled room by the same researcher and following the International Society of Clinical Densitometry guidelines [23]. The participants wore light clothing, without shoes and remained in the supine position on the machine (approximately 15 min). The precision of the machine in terms of coefficient of variation was 0.66% (n = 30 subjects not involved in this study).

2.4. Cluster of Lifestyle Behaviors

Lifestyle behaviors were assessed through a face-to-face interview, as follows: (1) No sport participation: the absence of sport participation was performed considering the sample selection, in which, were selected adolescents from sports clubs (considered as the group with sports practice) and adolescents from elementary and high schools, which did not practice sports (considered as the no sports participation group). (2) Skipping breakfast: the adolescent reported, considering a normal week, the number of days that they consumed breakfast (ranging from zero to seven days). Adolescents who reported their breakfast intake <7 days/week were characterized as having the habit of “skipping breakfast”. (3) Sleep quality: Quality of sleep was assessed using the Mini-Sleep Questionnaire (MSQ), translated to Brazilian Portuguese [24]. The questionnaire is composed of 10 questions with 7 possible answers (ranging from 0 to 7; never = 1, very rarely = 2, rarely = 3, sometimes = 4, often = 5, very often = 6, and always = 7) and the sum of the answers generates a numerical score. Adolescents who presented a score ≥25 points were characterized as “poor sleep quality” [24]. (4) TV viewing: Time spent in front of a TV was assessed by one question in the leisure-time section of the Baecke questionnaire [25]: “During leisure time I watch television” (possible responses: never, seldom, sometimes, often, and very often). Adolescents that responded “very often” in the Likert scale were characterized in “High TV viewing”.
Lifestyle behaviors were treated in two ways, separately and clustered together (variables ranging from zero (no lifestyle behavior) to four (simultaneous presence of skipping breakfast, poor sleep quality, no sport participation, and high TV viewing)). In terms of frequency, the cluster variable was divided as follow: None (n = 35, 12.3%), one lifestyle behavior (n = 98, 34.4%), two lifestyle behaviors (n = 102, 35.8%), three lifestyle behaviors (n = 46, 16.1%), and four lifestyle behaviors (n = 4, 1.4%). For statistical purposes, categories three and four of lifestyle behaviors were merged into one category (n = 50, 17.5%).

2.5. Covariates

Sex, chronological age, ethnicity, and somatic maturation were treated as covariates. Body weight (kg) was measured using a digital scale (Filizzola PL 150; Filizzola Ltd., São Paulo, Brazil) and height (cm) using a stadiometer with a precision of 0.1 cm. Both measures were collected using standard protocols and used to calculate the Body Mass Index (BMI). In addition, measurements of the sitting height and length of the legs were performed to calculate the maturity deviation, which denotes the time (years) from/to the peak of height velocity (PHV) proposed by Mirwald (2002) [26], an important maturational event.

2.6. Statistical Analyses

The descriptive analyses were composed of mean and standard deviation. General estimating equations (GEE), including the analysis of Wald test, were used to analyze the association between lifestyle behaviors, body fatness, and HOMA-IR (isolated and cluster) adjusted by sex, chronological age, maturity offset, ethnicity, and body fatness (for HOMA analysis). The logistic regression analyzed the association between the lifestyle behaviors cluster (no sport participation, high TV viewing, skipping breakfast, and poor sleep quality) and HOMA-IR in different models. All analyzes were performed in software SPSS (version 24.0) and the significance value was previously set at p-value < 0.05.

3. Results

General characteristics of the sample, stratified according to sex, are presented in Table 1. Girls presented greater maturity offset and body fatness (p-value < 0.001), while all lifestyle behaviors, even presenting a considerable prevalence of ≥3 lifestyles behavior risk in both sexes (boys: 18.2% vs. Girls: 17.1%), were similar between boys and girls even when considered as a cluster variable (p-value = 0.351).
Table 2 presents GEE of the association between isolated lifestyle behaviors and outcomes (body fatness and HOMA-IR), in which results were adjusted by sex, chronological age, maturity offset, ethnicity, and BMI (for HOMA-IR analysis). Adolescents who were not engaged in sport participation as well as frequently skipping breakfast presented higher body fatness (Sport participation: Wald: 8.786; p-value = 0.003; Breakfast: Wald: 9.364; p-value = 0.002). Moreover, poor sleep quality was associated with a higher HOMA-IR index (Wald: 6.013; p-value = 0.014).
After the first set of analyses, we created a cluster indicator of lifestyle behaviors, with four categories (no lifestyle behavior, 1 lifestyle behavior, 2 lifestyle behaviors, ≥3 lifestyle behaviors). Therefore, GEE of the association between cluster of lifestyle behaviors, body fatness, and HOMA-IR are presented in Figure 1. Adolescents with no lifestyle behavior presented lower body fatness than their counterparts with 2 lifestyle behaviors (p-value = 0.031) and ≥3 lifestyle behaviors (p-value = 0.014), while the group with 1 lifestyle behavior presented lower body fatness than the group with ≥3 lifestyle behaviors (p-value = 0.045). Similarly, adolescents with no lifestyle behaviors presented a lower HOMA-IR index than their peers with 2 lifestyle behaviors (p-value = 0.003) and ≥3 lifestyle behaviors (p-value = 0.006).
Regarding categorical HOMA-IR, the prevalence of an elevated HOMA-IR index was higher among subjects with no lifestyle behaviors: 17.6% (CI 95%: 7.8% to 35.1%) vs. 1 lifestyle behavior: 29.2% (CI 95%: 20.8% to 39.2%), 2 lifestyle behaviors: 38.0% (CI 95%: 28.9% to 48.0%), and ≥3 lifestyle behaviors: 52.0% (CI 95%: 37.9% to 65.8%) (p-trend: 0.005). Logistic regression analyses of the association between lifestyle behavior cluster and an elevated HOMA-IR index are presented in Table 3. After the adjustment by sex, age, maturity offset, and ethnicity (model 2), clusters of two (p-value = 0.020) and three (p-value = 0.001) lifestyle behaviors were more likely to present elevated HOMA-IR when compared to subjects with no lifestyle behaviors. However, after the adjustment by body fatness (Model 3), only presenting 3 or more lifestyle behaviors was considered a risk factor for elevated HOMA-IR (389% more likely; p-value = 0.005).

4. Discussion

Although the association between “traditional” lifestyle behaviors (e.g., dietary patterns and physical activity) and HOMA-IR is widely explored in the literature [27,28,29], we tried to analyze the association between not so conventional lifestyle behaviors and HOMA-IR. Our main findings identified that these lifestyle behaviors can affect adiposity levels among adolescents, added to which, when they are considered as cluster variables, they are able to affect the insulin resistance score among adolescents.
In this study, no sport participation and skipping breakfast were associated with higher body fatness. Firstly, it was expected that adolescents engaged in sports would present lower body fatness as sports participation usually requires performance of physical exercises at higher intensity, leading to the athlete adolescents presenting lower body adiposity than their peers [30]. Similarly, skipping breakfast was associated with higher body fatness in our study, which is also consistent with previous findings in adolescents [31,32], possibly occurring through appetite regulation mechanisms [33]. Another recent study that corroborates these findings about breakfast, was developed by Cayres et al. [34]. The authors analyzed the longitudinal relationship between breakfast intake and obesity and the mediating effect of physical activity and observed that adolescents who ate breakfast regularly, presented lower body fat independently of physical activity.
Moreover, poor sleep quality was the only lifestyle behavior associated with HOMA-IR. These findings are somewhat in agreement with previous studies that found an association between poor sleep quality/sleep deprivation and insulin resistance, especially among obese adolescents [35,36,37]. A possible mechanism underlying this association is related to an imbalance in autonomic modulation, given the fact that poor sleep quality may affect autonomic function through a decrease in parasympathetic modulation [38,39], and is also associated with impaired tissue response via insulin resistance [40]. Moreover, a poorer sleep quality is also associated with an elevation of stress levels as well as the regulation of hypothalamic-pituitary-adrenal, which can cause a neuroendocrine disorder, which in turn can cause a deregulation in the glucose-insulin metabolism [41,42].
Apparently, the main contribution of our study was to identify that aggregation of these lifestyle behaviors was related to worse body composition and metabolic health. Moreover, even after the adjustment by body fatness, adolescents that presented ≥2 lifestyle behaviors showed higher HOMA-IR levels. Taking into account qualitative analyses, adolescents who presented three or more lifestyle behaviors were more likely to present elevated HOMA-IR than adolescents with no lifestyle behavior, emphasizing the importance of the presence of none of these unhealthy lifestyle behaviors.
The non-adiposity dependent association observed between these lifestyle behaviors and HOMA-IR seems interesting due to the central role exerted by adiposity in the development of insulin resistance. Body fatness could be a possible mediator (but only partially) of sport participation and skipping breakfast in the association with HOMA-IR, given the fact that the association of both with body fatness is closely related to HOMA-IR [43]. The associations between body fatness and HOMA-IR have been justified in the scientific literature by the fact that adipose tissue is an endocrine organ and secretes hormones as well as proinflammatory cytokines such as resistin, TNF-α, and IL-6, among others [44]. Resistin is an adipocytokine that, although controversial, has been considered as the main variable explaining the relationship between obesity and IR [7,44]. The release of resistin is positively related to proinflammatory cytokines, which in specific target cells affect different tissues such as IL-6 and TNF, among others. Specifically regarding IL-6 and TNF-α [45], both are responsible for stimulation of the IκB kinase-β (IKK-β)/nuclear factor-κB (NF-κB) and the c-Jun aminoterminal kinase (JNK) through specific receptors, elevating inflammation, impairing insulin signaling [46], besides the downregulation of glucose transporters (GLUT-4) causing insulin resistance in the long run [47].
None of these four lifestyle behaviors were significantly associated with each other (data not shown), denoting an interesting independence among them, mainly because the cluster of these lifestyle behaviors seems harmful to adolescent health. As a result, parents should focus effort on combating these four lifestyle behaviors separately, which means, for example, trying to decrease the time spent watching TV not expecting an improvement in sport participation engagement as a response. In this sense, our results lead to clear practical implications, given that the avoid of health risk behaviors should be a protection for the development of body adiposity and insulin resistance. Interventions should have broader spectrums aiming to reduce several health risk behaviors.
The present study has some limitations. In terms of design, the sampling process was not randomized, and the cross-sectional design does not offer support to causality statements. Moreover, our sample size did not allow more robust statistical procedures such as modeling possible mediators or even splitting the analyses by sex. Self-report of sleep quality and TV-viewing is prone to bias, firstly because TV-viewing represent just one domain of sedentary behavior and due the access through a Likert scale. Finally, the reasons related to “skipping breakfast” or which physiological aspects of sleep presented difficulties would better explain these metabolic alterations.

5. Conclusions

In conclusion, we found that the clustering of lifestyle behaviors (risk) was associated with higher HOMA-IR, independent of adiposity. In this sense, the cluster of two risk behaviors (among no sports participation, high TV-viewing, skipping breakfast and poor sleep quality) is a threshold for the increase of insulin resistance. Future studies should focus on longitudinal associations between non-traditional lifestyle behaviors and insulin resistance among adolescents.

Author Contributions

A.O.W. and R.R.A. was the main responsible for collection, analysis, and interpretation of data, and drafting the manuscript; S.U.C., J.B.U., A.W., L.G.d.M.C., W.T., R.A.F. had been involved in revising the manuscript critically for important intellectual content.

Funding

The authors would like to thank the Sao Paulo Research Foundation-FAPESP (Process: 2015/19710-3). The following authors were awarded grants by the São Paulo Research Foundation-FAPESP: AOW (2017/27234-2, RRA (2017/09182-5) and SUC (2015/04961-0).

Acknowledgments

The Sao Paulo Research Foundation (FAPESP) and the effort of the participants and their parents and coaches.

Conflicts of Interest

The authors declare that they have no conflict of interest.

References

  1. Martin, B.C.; Warram, J.H.; Krolewski, A.S.; Soeldner, J.S.; Kahn, C.R.; Bergman, R.N. Role of glucose and insulin resistance in development of type 2 diabetes mellitus: Results of a 25-year follow-up study. Lancet (London, England) 1992, 340, 925–929. [Google Scholar] [CrossRef]
  2. Bunt, J.C.; Krakoff, J.; Ortega, E.; Knowler, W.C.; Bogardus, C. Acute insulin response is an independent predictor of type 2 diabetes mellitus in individuals with both normal fasting and 2-h plasma glucose concentrations. Diabetes Metab. Res. Rev. 2007, 23, 304–310. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  3. Kannel, W.B.; McGee, D.L. Diabetes and cardiovascular disease. The Framingham study. JAMA 1979, 241, 2035–2038. [Google Scholar] [CrossRef]
  4. Ginsberg, H.N. Insulin resistance and cardiovascular disease. J. Clin. Investig. 2000, 106, 453–458. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  5. Williams, D.E.; Cadwell, B.L.; Cheng, Y.J.; Cowie, C.C.; Gregg, E.W.; Geiss, L.S.; Engelgau, M.M.; Narayan, K.M.V.; Imperatore, G. Prevalence of impaired fasting glucose and its relationship with cardiovascular disease risk factors in US adolescents, 1999–2000. Pediatrics 2005, 116, 1122–1126. [Google Scholar] [CrossRef] [PubMed]
  6. Jiménez-Pavón, D.; Castillo, M.J.; Moreno, L.A.; Kafatos, A.; Manios, Y.; Kondaki, K.; Béghin, L.; Zaccaria, M.; Henauw, S.; Widhalm, K.; et al. Fitness and fatness are independently associated with markers of insulin resistance in European adolescents; The HELENA Study. Int. J. Pediatr. Obes. 2011, 6, 253–260. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  7. Steppan, C.M.; Bailey, S.T.; Bhat, S.; Brown, E.J.; Benerjee, R.R.; Wright, C.M.; Patel, H.R.; Ahima, R.S.; Lazar, M.A. The hormone resistin links obesity to diabetes. Nature 2001, 409, 307–312. [Google Scholar] [CrossRef]
  8. Hotamisligil, G. Mechanisms of TNF-α-induced insulin resistance. Exp. Clin. Endocrinol. Diabetes 2009, 107, 119–125. [Google Scholar] [CrossRef]
  9. Hunter, C.A.; Jones, S.A. IL-6 as a keystone cytokine in health and disease. Nat. Immunol. 2015, 16, 448–457. [Google Scholar] [CrossRef] [PubMed]
  10. Grundy, S.M. Multifactorial causation of obesity: Implications for prevention. Am. J. Clin. Nutr. 1998, 67, 563S–572S. [Google Scholar] [CrossRef]
  11. Jensen, M.K.; Chiuve, S.E.; Rimm, E.B.; Dethlefsen, C.; Tjønneland, A.; Joensen, A.M.; Overvad, K. Obesity, Behavioral Lifestyle Factors, and Risk of Acute Coronary Events. Circulation 2008, 117, 3062–3069. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  12. Jiménez-Pavón, D.; Sesé, M.; Huybrechts, I.; Cuenca-Garcia, M.; Palacios, G.; Ruiz, J.R.; Breidenassel, C.; Leclercq, C.; Beghin, L.; Plada, M.; et al. Dietary and lifestyle quality indices with/without physical activity and markers of insulin resistance in European adolescents: The HELENA study. Br. J. Nutr. 2013, 110, 1919–1925. [Google Scholar] [CrossRef] [PubMed]
  13. Masana, L.; Ros, E.; Sudano, I.; Angoulvant, D. The lifestyle expert working group. Is there a role for lifestyle changes in cardiovascular prevention? What, when and how? Atheroscler. Suppl. 2017, 26, 2–15. [Google Scholar] [CrossRef]
  14. Garoufi, A.; Grammatikos, E.E.; Kollias, A.; Grammatikos, E.; Stergiou, G.S.; Soldatou, A. Associations between obesity, adverse behavioral patterns and cardiovascular risk factors among adolescent inhabitants of a Greek island. J. Pediatr. Endocrinol. Metab. 2017, 30, 445–454. [Google Scholar] [CrossRef] [PubMed]
  15. Silva, D.R.; Werneck, A.O.; Collings, P.J.; Fernandes, R.A.; Barbosa, D.S.; Ronque, E.R.V.; Sardinha, L.B.; Cyrino, E.S. Physical activity maintenance and metabolic risk in adolescents. J. Public Health (Bangkok) 2018, 40, 493–500. [Google Scholar] [CrossRef] [PubMed]
  16. Agostinete, R.R.; Duarte, J.P.; Valente-Dos-Santos, J.; Coellho-e-Silva, M.J.; Tavares, O.M.; Conde, J.M.; Fontes-Ribeiro, C.A.; Condello, G.; Capraninca, L.; Cayres, S.U.; et al. Bone tissue, blood lipids and inflammatory profiles in adolescent male athletes from sports contrasting in mechanical load. PLoS ONE 2017, 12, e0180357. [Google Scholar] [CrossRef]
  17. Duncan, S.; Duncan, E.K.; Fernandes, R.A.; Buonani, C.; Bastos, K.D.N.; Segatto, A.F.M.; Codogno, J.S.; Gomes, I.C.; Freitas-Junior, I.F. Modifiable risk factors for overweight and obesity in children and adolescents from São Paulo, Brazil. BMC Public Health 2011, 11, 585. [Google Scholar] [CrossRef]
  18. Freitas Júnior, I.F.; Christofaro, D.G.D.; Codogno, J.S.; Monteiro, P.A.; Silveira, L.S.; Fernandes, R.A. The association between skipping breakfast and biochemical variables in sedentary obese children and adolescents. J. Pediatr. 2012, 161, 871–874. [Google Scholar] [CrossRef]
  19. Hirshkowitz, M.; Whiton, K.; Albert, S.M.; Alessi, C.; Bruni, O.; DonCarlos, L.; Hazen, N.; Herman, J.; Hillard, P.J.A.; Katz, E.S.; et al. National Sleep Foundation’s updated sleep duration recommendations: Final report. Sleep Health 2015, 1, 233–243. [Google Scholar] [CrossRef]
  20. Turner, R.C.; Holman, R.R.; Matthews, D.; Hockaday, T.D.R.; Peto, J. Insulin deficiency and insulin resistance interaction in diabetes: Estimation of their relative contribution by feedback analysis from basal plasma insulin and glucose concentrations. Metabolism 1979, 28, 1086–1096. [Google Scholar] [CrossRef]
  21. Matthews, D.R.; Hosker, J.P.; Rudenski, A.S.; Naylor, B.A.; Treacher, D.F.; Turner, R.C. Homeostasis model assessment: Insulin resistance and beta-cell function from fasting plasma glucose and insulin concentrations in man. Diabetologia 1985, 28, 412–419. [Google Scholar] [CrossRef] [PubMed]
  22. Hills, S.A.; Balkau, B.; Coppack, S.W.; Dekker, J.M.; Mari, A.; Natali, A.; Walker, M.; Ferrannin, E. The EGIR-RISC STUDY (The European group for the study of insulin resistance: Relationship between insulin sensitivity and cardiovascular disease risk): I. Methodology and objectives. Diabetologia 2004, 47, 566–570. [Google Scholar] [CrossRef] [PubMed]
  23. Crabtree, N.J.; Arabi, A.; Bachrach, L.K.; Fewtrell, M.; El-Hajj Fuleihan, G.; Kecskemethy, H.H.; Jaworski, M.; Gordon, C.M.; International Society for Clinical Densitometry. Dual-energy X-ray absorptiometry interpretation and reporting in children and adolescents: The revised 2013 ISCD Pediatric Official Positions. J. Clin. Densitom. 2014, 17, 225–242. [Google Scholar] [CrossRef] [PubMed]
  24. Falavigna, A.; de Souza Bezerra, M.L.; Teles, A.R.; Kleber, F.D.; Velho, M.C.; Silva, R.C.; Mazzochin, T.; Santin, J.T.; Mosena, G.; Braga, G.L.; et al. Consistency and reliability of the Brazilian Portuguese version of the Mini-Sleep Questionnaire in undergraduate students. Sleep Breath 2011, 15, 351–355. [Google Scholar] [CrossRef] [PubMed]
  25. Baecke, J.; Burema, J.; Frijters, J. A short questionanaire for the measuremnet of habitual physical activity in epidemiological studies. Am. J. Clin. Nutr. 1982, 36, 936–942. [Google Scholar] [CrossRef] [PubMed]
  26. Mirwald, R.L.; Baxter-Jones, A.D.; Bailey, D.A.; Beunen, G.P. An assessment of maturity from anthropometric measurements. Med Sci Sports Exerc. 2002, 34, 689–694. [Google Scholar] [PubMed]
  27. Jago, R.; Wedderkopp, N.; Kristensen, P.L.; Møller, N.C.; Andersen, L.B.; Cooper, A.R.; Froberg, K. Six-year change in youth physical activity and effect on fasting insulin and HOMA-IR. Am. J. Prev. Med. 2008, 35, 554–560. [Google Scholar] [CrossRef]
  28. Forbes, L.E.; Fraser, S.N.; Downs, S.M.; Storey, K.E.; Plotnikoff, R.C.; Raine, K.D.; Spence, J.C.; Hanning, R.M.; McCargar, L.J. Changes in dietary and physical activity risk factors for type 2 diabetes in Alberta youth between 2005 and 2008. Can. J. Public Health 2013, 104, e490–e495. [Google Scholar] [CrossRef]
  29. Ruiz, J.R.; Rizzo, N.S.; Ortega, F.B.; Loit, H.M.; Veidebaum, T.; Sjostrom, M. Markers of insulin resistance are associated with fatness and fitness in school-aged children: The European Youth Heart Study. Diabetologia 2007, 50, 1401–1408. [Google Scholar] [CrossRef]
  30. Faustino-da-Silva, Y.D.S.V.; Agostinete, R.R.; Werneck, A.O.; Maillane-Vanegas, S.; Lynch, K.R.; Exuperio, I.N.; Ito, I.H.; Fernandes, R.A. Track and Field Practice and Bone Outcomes among Adolescents: A Pilot Study (ABCD-Growth Study). J. Bone Metab. 2018, 25, 35–42. [Google Scholar] [CrossRef] [Green Version]
  31. Marlatt, K.L.; Farbakhsh, K.; Dengel, D.R.; Lytle, L.A. Breakfast and fast food consumption are associated with selected biomarkers in adolescents. Prev. Med. Rep. 2016, 3, 49–52. [Google Scholar] [CrossRef] [PubMed]
  32. Hallström, L.; Labayen, I.; Ruiz, J.R.; Patterson, E.; Vereecken, C.A.; Breidenassel, C.; Gottrand, F.; Huybrechts, I.; Manios, Y.; Mistura, L.; et al. Breakfast consumption and CVD risk factors in European adolescents: The HELENA (Healthy Lifestyle in Europe by Nutrition in Adolescence) Study. Public Health Nutr. 2013, 16, 1296–1305. [Google Scholar] [CrossRef] [PubMed]
  33. Timlin, M.T.; Pereira, M.A. Breakfast frequency and quality in the etiology of adult obesity and chronic diseases. Nutr. Rev. 2007, 65, 268–281. [Google Scholar] [CrossRef] [PubMed]
  34. Cayres, S.U.; Urban, J.B.; Fernandes, R.A. Physical Activity and Skipping Breakfast Have Independent Effects on Body Fatness Among Adolescents. J. Pediatr. Gastroenterol. Nutr. 2018, 67, 666–670. [Google Scholar] [CrossRef] [PubMed]
  35. Liu, A.; Kushida, C.A.; Reaven, G.M. Habitual shortened sleep and insulin resistance: An independent relationship in obese individuals. Metabolism 2013, 62, 1553–1556. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  36. Sayin, F.K.; Buyukinan, M. Sleep Duration and Media Time Have a Major Impact on Insulin Resistance and Metabolic Risk Factors in Obese Children and Adolescents. Child. Obes. 2016, 12, 272–278. [Google Scholar] [CrossRef]
  37. Klingenberg, L.; Chaput, J.P.; Holmbäck, U.; Visby, T.; Jennum, P.; Nikolic, M.; Astrup, A.; Sjodin, A. Acute Sleep Restriction Reduces Insulin Sensitivity in Adolescent Boys. Sleep 2013, 36, 1085–1090. [Google Scholar] [CrossRef] [Green Version]
  38. Burgess, H.J.; Penev, P.D.; Schneider, R.; Van-Cauter, E. Estimating cardiac autonomic activity during sleep: Impedance cardiography, spectral analysis, and Poincaré plots. Clin. Neurophysiol. 2004, 115, 19–28. [Google Scholar] [CrossRef]
  39. Spiegel, K.; Knutson, K.; Leproult, R.; Tasali, E.; Van-Cauter, E. Sleep loss: A novel risk factor for insulin resistance and Type 2 diabetes. J. Appl. Physiol. 2008, 99, 2008–2019. [Google Scholar] [CrossRef]
  40. Redón, P.; Grassi, G.; Redon, J.; Álvarez-Pitti, J.; Lurbe, E. Sympathetic neural activity, metabolic parameters and cardiorespiratory fitness in obese youths. J. Hypertens. 2017, 35, 571–577. [Google Scholar] [CrossRef] [Green Version]
  41. Hirotsu, C.; Tufik, S.; Andersen, M.L. Interactions between sleep, stress, and metabolism: From physiological to pathological conditions. Sleep Sci. 2015, 8, 143–152. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  42. Conklin, A.I.; Guo, S.X.; Tam, A.C.; Richardson, C.G. Gender, stressful life events and interactions with sleep: A systematic review of determinants of adiposity in young people. BMJ Open 2018, 8, e019982. [Google Scholar] [CrossRef] [PubMed]
  43. Kim, G.; Caprio, S. Diabetes and insulin resistance in pediatric obesity. Pediatr. Clin. N. Am. 2011, 58, 1355–1361. [Google Scholar] [CrossRef] [PubMed]
  44. Petersen, A.M.W.; Pedersen, B.K. The anti-inflammatory effect of exercise. J. Appl. Physiol. 2005, 98, 1154–1162. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  45. Codoñer-Franch, P.; Alonso-Iglesias, E. Resistin: Insulin resistance to malignancy. Clin. Chim. Acta 2015, 438, 46–54. [Google Scholar] [CrossRef] [PubMed]
  46. Kahn, S.E.; Hull, R.L.; Utzschneider, K.M. Mechanisms linking obesity to insulin resistance and type 2 diabetes. Nature 2006, 444, 840–846. [Google Scholar] [CrossRef]
  47. Hotamisligil, G.S.; Spiegelman, B.M. Tumor necrosis factor alpha: A key component of the obesity-diabetes link. Diabetes 1994, 43, 1271–1278. [Google Scholar] [CrossRef]
Figure 1. General estimating equations of the association between lifestyle behavior clusters (no sport participation, high TV-viewing, skipping breakfast, and poor sleep quality). Note. Values are presented as means and 95% standard deviations. Models are adjusted by sex, chronological age, maturity offset, ethnicity, and body fatness (for HOMA-IR analysis). a = significant difference vs. no lifestyle behavior group (p < 0.05). b = significant difference vs. 1 lifestyle behavior group (p < 0.05).
Figure 1. General estimating equations of the association between lifestyle behavior clusters (no sport participation, high TV-viewing, skipping breakfast, and poor sleep quality). Note. Values are presented as means and 95% standard deviations. Models are adjusted by sex, chronological age, maturity offset, ethnicity, and body fatness (for HOMA-IR analysis). a = significant difference vs. no lifestyle behavior group (p < 0.05). b = significant difference vs. 1 lifestyle behavior group (p < 0.05).
Medicina 54 00096 g001
Table 1. Characteristics of the sample stratified according to sex (n = 280).
Table 1. Characteristics of the sample stratified according to sex (n = 280).
Boys (n = 198)Girls (n = 82)
VariablesMean ± SDMean ± SDp-Value
Continuous variables
Chronological age (years)14.7 ± 2.014.9 ± 2.10.451
Maturity offset (years)0.94 ± 1.562.17 ± 1.34<0.001
BMI (kg/m2)21.3 ± 4.120.4 ± 3.40.070
Body fatness (%)19.4 ± 11.129.0 ± 9.4<0.001
HOMA-IR (score)1.97 ± 1.871.89 ± 1.150.547
Categorical variables
No sports practice (%)57.3 (50.3 to 64.1)53.7 (42.6 to 64.3)0.548
High TV viewing (%)14.7 (10.4 to 20.4)22.0 (14.2 to 32.4)0.142
Skipping breakfast (%)45.2 (38.3 to 52.2)35.4 (25.6 to 46.5)0.121
Poor sleep quality (%)44.2 (37.3 to 51.2)47.6 (36.8 to 58.5)0.580
Lifestyle behavior clusters 0.351
No lifestyle behavior (%)13.6 (9.5 to 19.2)8.5 (4.1 to 17.1)
1 lifestyle behavior (%)31.3 (25.2 to 38.2)41.5 (31.1 to 52.6)
2 lifestyle behaviors (%)36.9 (30.4 to 43.9)32.9 (23.5 to 44.0)
≥3 lifestyle behaviors (%)18.2 (13.4 to 24.2)17.1 (10.3 to 27.0)
BMI = body mass index; HOMA-IR = Homeostatic Model Assessment of Insulin Resistance. Note. Values are presented as means and standard deviations (SD) as well as frequencies and 95% confidence intervals.
Table 2. General estimating equations of the association between isolated lifestyle behaviors, body fatness, and the HOMA-IR index.
Table 2. General estimating equations of the association between isolated lifestyle behaviors, body fatness, and the HOMA-IR index.
Prevalence of Lifestyle Behavior
NoYes
Mean (95%CI)Mean (95%CI)Waldp-Value
Sport participation
Body fatness (%)24.33 (22.07 to 26.83)20.06 (18.63 to 21.61)8.7860.003
HOMA-IR (score)1.82 (1.47 to 2.24)1.93 (1.71 to 2.17)0.1890.663
High TV-viewing
Body fatness (%)21.83 (20.52 to 23.24)20.95 (18.02 to 24.36)0.2420.623
HOMA-IR (score)1.87 (1.67 to 2.11)1.90 (1.67 to 2.15)0.0240.877
Skipping breakfast
Body fatness (%)19.90 (18.51 to 21.39)23.93 (21.85 to 26.22)9.3640.002
HOMA-IR (score)1.82 (1.59 to 2.09)1.96 (1.70 to 2.27)0.6180.432
Poor sleep quality
Body fatness (%)21.58 (19.86 to 23.45)21.63 (20.03 to 23.37)0.0020.968
HOMA-IR (score)1.65 (1.54 to 1.78)2.16 (1.79 to 2.61)6.5770.010
HOMA-IR = Homeostatic Model Assessment of Insulin Resistance. Note. Adjusted by sex, chronological age, maturity offset, ethnicity, and body fatness (for HOMA-IR analysis).
Table 3. Logistic regression of the association between lifestyle behavior clusters (no sports practice, high TV-viewing, skipping breakfast and poor sleep quality) and elevated HOMA-IR.
Table 3. Logistic regression of the association between lifestyle behavior clusters (no sports practice, high TV-viewing, skipping breakfast and poor sleep quality) and elevated HOMA-IR.
BOR95%CIp-Value
Model 1
No lifestyle behavior--1.00--
1 lifestyle behavior0.681.970.73 to 5.300.181
2 lifestyle behaviors1.082.941.11 to 7.780.030
≥3 lifestyle behaviors1.655.201.83 to 14.80.002
Model 2
No lifestyle behavior-1.00--
1 lifestyle behavior0.782.190.79 to 6.030.131
2 lifestyle behaviors1.193.291.21 to 8.930.020
≥3 lifestyle behaviors1.816.122.07 to 18.110.001
Model 3
No lifestyle behavior-1.00--
1 lifestyle behavior0.702.020.71 to 5.700.185
2 lifestyle behaviors1.012.740.99 to 7.650.053
≥3 lifestyle behaviors1.594.891.61 to 14.840.005
Note. Model 1: adjusted by sex and chronological age. Model 2: Model 1 + maturity offset and ethnicity. Model 3: Model 2 + body fatness.

Share and Cite

MDPI and ACS Style

Werneck, A.O.; Agostinete, R.R.; Cayres, S.U.; Urban, J.B.; Wigna, A.; Chagas, L.G.d.M.; Torres, W.; Fernandes, R.A. Association between Cluster of Lifestyle Behaviors and HOMA-IR among Adolescents: ABCD Growth Study. Medicina 2018, 54, 96. https://0-doi-org.brum.beds.ac.uk/10.3390/medicina54060096

AMA Style

Werneck AO, Agostinete RR, Cayres SU, Urban JB, Wigna A, Chagas LGdM, Torres W, Fernandes RA. Association between Cluster of Lifestyle Behaviors and HOMA-IR among Adolescents: ABCD Growth Study. Medicina. 2018; 54(6):96. https://0-doi-org.brum.beds.ac.uk/10.3390/medicina54060096

Chicago/Turabian Style

Werneck, André Oliveira, Ricardo Ribeiro Agostinete, Suziane Ungari Cayres, Jacqueline Bexiga Urban, Andréa Wigna, Lucas Gabriel de Moraes Chagas, Wesley Torres, and Rômulo Araújo Fernandes. 2018. "Association between Cluster of Lifestyle Behaviors and HOMA-IR among Adolescents: ABCD Growth Study" Medicina 54, no. 6: 96. https://0-doi-org.brum.beds.ac.uk/10.3390/medicina54060096

Article Metrics

Back to TopTop