Abstract
Background
In adults, heart rate recovery is a predictor of mortality, while in adolescents it is associated with cardio-metabolic risk factors. The aim of this study was to examine the relationship between body composition measures and heart rate recovery (HRR) after step test in Malaysian secondary school students.
Methods
In the Malaysian Health and Adolescents Longitudinal Research Team (MyHEART) study, 1071 healthy secondary school students, aged 13 years old, participated in the step test. Parameters for body composition measures were body mass index z-score, body fat percentage, waist circumference, and waist height ratio. The step test was conducted by using a modified Harvard step test. Heart rate recovery of 1 minute (HRR1min) and heart rate recovery of 2 minutes (HRR2min) were calculated by the difference between the peak pulse rate during exercise and the resting pulse rate at 1 and 2 minutes, respectively. Analysis was done separately based on gender. Pearson correlation analysis was used to determine the association between the HRR parameters with body composition measures, while multiple regression analysis was used to determine which body composition measures was the strongest predictor for HRR.
Results
For both gender groups, all body composition measures were inversely correlated with HRR1min. In girls, all body composition measures were inversely correlated with HRR2min, while in boys all body composition measures, except BMI z-score, were associated with HRR2min. In multiple regression, only waist circumference was inversely associated with HRR2min (p=0.024) in boys, while in girls it was body fat percentage for HRR2min (p=0.008).
Conclusion
There was an inverse association between body composition measurements and HRR among apparently healthy adolescents. Therefore, it is important to identify cardio-metabolic risk factors in adolescent as an early prevention of consequent adulthood morbidity. This reiterates the importance of healthy living which should start from young.
Introduction
Heart rate recovery (HRR) is the rate where the heart beat declines to resting levels after an exercise is performed [1]. HRR is mediated by the autonomic nervous system (ANS), with the rate in the early phase being controlled by the parasympathetic reactivation and later by the withdrawal of sympathetic activity [2-5]. HRR is considered a predictor of cardiovascular related mortality and all-cause mortality in all healthy adult patients. A decreased parasympathetic activity is identified to increase the risk [6-8]. In healthy children, HRR is associated with cardio-metabolic risk factors [9-11]. HRR manifests faster in children than in adults [12], with the rate declining faster in boys than in girls [13]. It becomes slower as children progress in age. However, regular physical activities and exercises can blunt the age effect [14].
The prevalence and health consequences of obesity are a growing pandemic in the world, including Malaysia [15-18]. Childhood obesity, in particular, has been shown to be associated with a compromised ANS control of the heart [19,20]. In children, the measurement of obesity includes looking at body mass index (BMI), waist circumference (WC), waist to height ratio (WHtR), body fat percentage and the sum of skinfold thickness. However, the relationship and predictive value of these body composition parameters to various cardio-metabolic risk factors is still unclear [21,22]. Several studies on paediatric population showed that BMI is the best predictor for cardio-metabolic risk factors [23-27]. However, BMI does not differentiate fat mass from fat free mass in thinner children, but in relatively fat children BMI is a validated index of adiposity[28]. Thus, it is suggested that WC and WHtR are better predictors [29]. WC is an indicator for intra-abdominal obesity in children and adolescent [30] and it is strongly associated with cardio-metabolic risk factors [31-33]. WHtR is also considered as an indicator of intra-abdominal obesity [34,35]. Compared to WC, WHtR is not influenced by age and gender in children [36], and it is also a good predictor of cardio-metabolic risks [37-39]. Body fat percentage recorded from non-invasive bioelectrical impedance analyser (BIA) is also associated with increased risk [40,41]. Some studies suggested that BIA is an accurate predictor of body composition in both adolescent and adults [42-44]. Interestingly there are also studies that indicated BMI and WC as equal predictors of cardio-metabolic risk factors [21,25].
Previous studies have investigated the association of HRR with a cluster of cardio-metabolic risk factors in children and adolescents [9-11]. One study showed that age, gender, pulse rate, and BMI accounted for 39% of the variance to HRR [9]. Another study indicated that WC was the only predictor that was associated with HRR in boys, whereas for girls the predictors include systolic blood pressure, serum glucose and serum C reactive protein. A more current study showed that diastolic blood pressure was inversely associated in girls but in boys it was systolic blood pressure, homeostasis model assessment, WC and skinfold thickness [11]. Looking at these results, body composition parameters appear to be consistently associated with HRR.
Thus far, there are no studies investigating other types of body composition such as WHtR and body fat percentage, or even tests to determine which body composition parameters has the strongest predictive value for HRR in adolescents. This gap is of interest since obesity in adolescents is associated with a compromised ANS control of the heart [19,20]. Moreover, obesity frequently continues into adulthood, and consequently, can lead to health complications such as cardiovascular and metabolic diseases [45] in adults. In this regard, locating a suitable body composition parameter which has the strongest predictive value for HRR is of clinical interest for mass screening purposes and subsequent medical management.
Previous studies involved with exercise testing were conducted in laboratory settings, using either the treadmill or cycle ergometer protocol [9-14]. The limitations of laboratory based studies include the procurement of specialised equipment and technicians, and longer time period to complete the study. Laboratory settings also make it difficult to extrapolate the results to population-based studies.
The aim of this study is twofold: 1) to determine the association of HRR with BMI, WC, WHtR , and body fat percentage; and 2) to identify which body composition parameter in the mass screening of Malaysian adolescents, can be considered as the strongest predictor of HRR after step test.
Materials and Methods
Ethics Statement
Ethical approval which complied with the International Conference on Harmonization - Guidelines for Good Clinical Practice (ICH-GCP) and the Declaration of Helsinki, was obtained from the Medical Ethics Committee of the University of Malaya Medical Centre, Malaysia (IRB number 896.34).
Study Design
The Malaysian Health and Adolescents Longitudinal Research Team (MyHEART) is an on-going prospective longitudinal cohort study that involves three states in the northern and central zone of Malaysia – Perak, Selangor and Kuala Lumpur. The objective of the study is to identify the trends of prevalence of non-communicable diseases’ risk factors among adolescents in Peninsular Malaysia, and to determine how lifestyles in early adolescence influence the development of chronic non-communicable disease in early adulthood.
Participants of this study comprise students of both genders who are studying in government secondary schools and who read and understand the national language, Malay. Participants in boarding, religious, or vernacular schools were excluded as they are not representative of Malaysian schools where majority students attend. In Malaysia, secondary school starts from ages of 13 to 17 years old.
Using the formula n= (z 2 . p.q/r.e 2)x Design Effect, and the prevalence of smoking among 13 to 15 year olds in school based adolescents in Malaysia as 33% [46], the total sample size calculated for this study was at 1500.
The total number of secondary schools in the three states involved in this study was 595. The method of sampling and randomization was based on two stages of cluster sampling. The schools were primary sampling units and the students were secondary sampling units. Based on a feasibility study done in 2011 that had response rate of 50% (80-120 students per school), 15 schools were randomly selected as a cluster from a computer generated random number list. Eight schools were from the urban area, and seven schools from the rural area. All Form One (13 years old) adolescents in these schools were invited to participate in the study. All were presented with consent forms for their parents, agreement forms for themselves, and information sheets detailing the study. Participants were those who attended schools during the study and who had handed in both the agreed written consent forms of their parents and individual agreement forms. The MyHEART study lasted three months, from March to May 2012.
Baseline and Anthropometric Data
First the participant’s socio-demographic data such as date of birth, age, and gender were collected. Participants were then asked to fill in a standardised form under the supervision of trained enumerators. Once the forms were completed, their blood pressures and pulse rates were measured by medically trained persons who were either paediatricians, medical officers or staff nurses. The participants sit upright with his or her right upper arm positioned at the level of the heart with both feet flat on the floor. They were allowed to relax for 5 minutes before their blood pressure and pulse rate were taken. Both their systolic (SBP) and diastolic blood pressure (DBP) were obtained using a stethoscope and a mercurial sphygmomanometer (CK-101C, Spirit Medical Co., Taiwan). Three readings of blood pressure were taken with 2 minutes interval between each reading. The mean SBP and DBP were used in the analysis. Their pulse rate was taken using a finger pulse oximeter (Baseline 12-1926 Fingertip Pulse Oximeter, Fabrication Enterprises Inc., USA).
Height was taken without socks and shoes with a calibrated vertical stadiometer (Seca Portable 217, Seca, UK) and was recorded to the nearest 0.1cm. Focusing on light clothings, weight was measured with a digital electronic weighing scale (Seca 813, Seca, UK) and was recorded to the nearest 0.1 kilogram. BMI was calculated by using weight in kilograms divided by the square of height in meters. BMI z-score for age and gender was calculated using the World Health Organisation (WHO) Anthro Software version 3.2.2 for SPSS macro, based on WHO reference 2007 (WHO,Geneva, Switzerland). Body fat percentage was measured using a portable body composition analyzer (Tanita SC 240 MA Portable Body Composition Analyser, Tanita Europe B.V., The Netherlands). Particapants’ WC was then measured with a non-elastic measuring tape (Seca 201, Seca, UK) that is positioned mid-way between the lowest rib margin and the iliac crest. Measurement was calculated to the nearest millimetre. WHtR was calculated by considering WC in cm divided by height in cm.
Exercise Test
The exercise test was performed under the close supervision of a sports physician. All participants were first screened before the actual testing. Participants with known medical conditions, musculoskeletal injuries, or who were acutely ill were excluded. The modified Harvard Step Test protocol was chosen as a tool for exercise test because it is one of the step tests developed that objectively categorise the performance level of children. This tool has been successfully used by others among this age group where a 30 cm high step box was applied [47-49]. The 30cm high step box was a typical step box used in Malaysian schools for fitness assessment. The process began with the participants got onto the step box and off the step box at a pace of 30 cycles per minute with a metronome set at 120 beats per minute (bpm), for a total of 5 minutes. A finger pulse oximeter (Baseline 12-1926 Fingertip Pulse Oximeter, Fabrication Enterprises Inc., USA) was attached to one of the student’s fingers, and the pulse rate was then continuously monitored. The peak pulse rate of each student during each minute of the step box exercise was recorded. Those with a pulse rate of 200 bpm, and those who had difficulty in breathing, or were unable to finish, were stopped immediately.
Once the students completed the step test or were stopped due to the reasons mentioned above, they were told to sit down on the bench and rest. Their pulse rates at 1 and 2 minutes of the rest were then recorded simultaneously with the total duration of the exercise recorded in seconds.
Heart Rate Recovery in 1 minute (HRR1min) and Heart Rate Recovery in 2 minutes (HRR2min) were next calculated by taking the difference between the highest peak pulse rate during exercise and pulse rate at 1 and 2 minutes rest, respectively.
Statistical Analysis
Test for normality was performed for the sample. Analysis was conducted for boys and for girls separately. The participants’ baseline and exercise variables were calculated as mean ±SD and the independent t-test was used as it was appropriate for examining differences for continuous variables with normal distribution. The correlation between each HRR parameters (HRR1min and HRR2min) with body composition measures (BMI z-score, body fat percentage, WC and WHtR) was then determined by using Pearson correlation analysis. Multiple linear regressions were performed separately by sex to determine the strength of association between body composition measurements with each HRR1 min and HRR2 min. For respective boys and girls analysis, there is a separate multiple regression models for each HRR parameters. One consists of HRR1 min as the dependant variable and body composition measurements as independent variables, while the other model consists of HRR2 min as the dependant variable with body composition as independent variables. Age, pulse rate, blood pressure and smoking status were factors that were controlled. All statistical analyses were completed using SPSS version 20 and the level of significance is viewed at p<0.05.
Results
A total of 1361 students agreed to participate in the MyHEART study but 285 refused to participate in the exercise test. Two who were acutely ill, two with medical conditions and one with musculoskeletal injuries were excluded. Thus, a total of 1071 students participated in the step test. Their mean age was 12.9 ± 0.3 years (range 12-14) and the average response rate for the study was 51%. The socio-demographic characteristics between respondents and non-respondents in terms of gender and locality were then compared and there was no significant difference shown.
The characteristics of the participants are shown in Table 1. Boys had a significantly higher WC and WHtR (p<0.001), while for girls it was body fat percentage (p<0.001). There was no significant difference for BMI and BMI z-score in both genders. As for HRR parameters, boys have significantly faster HRR 1 min and HRR 2 min (p<0.001).
Table 1. Baseline characteristics and exercise parameters of the participants.
Boys | Girls | p | |
---|---|---|---|
n | 405 | 666 | - |
Smokers (%) | 13.3 | 2.4 | - |
Age (years) | 12.8±0.3 | 12.9±0.3 | 0.028 |
SBP (mmHg) | 110.9 ±10.5 | 108.6 ±11.9 | 0.001 |
DBP (mmHg) | 68.9 ±10.6 | 66.6 ±10.4 | 0.001 |
Pulse rate (beats/min) | 85.6 ± 14.1 | 90.0 ±13.2 | <0.001 |
Height (cm) | 150.6 ±9.2 | 150.9 ±6.2 | 0.455 |
Weight (kg) | 45.7±14.5 | 45.1±11.5 | 0.488 |
BMI (kg/m2) | 19.9 ±5.4 | 19.7 ± 4.3 | 0.353 |
BMI z-score | 0.2 ± 1.6 | 0.02 ± 1.4 | 0.060 |
Body fat (%) | 18.9 ± 14.6 | 25.6 ±10.1 | <0.001 |
WC(cm) | 70.6 ± 12.9 | 67.5 ± 9.8 | <0.001 |
WHtR | 0.47 ±0.08 | 0.45 ±0.06 | <0.001 |
Peak heart rate (beats/min) | 177.6 ± 14.5 | 185.8 ± 11.9 | <0.001 |
Heart rate at 1 min rest (beats/min) | 126.8 ± 19.6 | 144.7 ± 15.5 | <0.001 |
Heart Rate at 2 min rest (beats/min) | 115.1 ± 17.8 | 131.3 ± 14.6 | <0.001 |
HRR 1 min | 50.8 ± 13.6 | 41.0 ± 11.9 | <0.001 |
HRR 2 min | 62.6 ± 12.8 | 54.5 ± 11.9 | <0.001 |
Data are mean ± SD. % = percentage SBP = Systolic blood pressure, DBP = Diastolic blood pressure, HRR = Heart rate recovery, BMI = Body mass index, WC = waist circumference, WHtR = Waist height ratio
The correlation analysis (Table 2) showed that parameters such as BMI z-score, body fat percentage, WC and WHtR were all negatively correlated to HRR 1 min (r = -0.157, -0.189, -0.218, and -0.198 respectively for boys; r = -0.201, -0.214, -0.164, -0.164 respectively for girls). HRR2 min were negatively correlated with all body composition measures in girls (r = -0.107, -0.134, -0.078, and -0.067 respectively), while for boys, only body fat percentage, WC and WHtR (r = -0.101, -0.133, and -0.110 respectively) were negatively correlated with HRR 2 min.
Table 2. Correlation coefficient (r) between HRR parameters and body composition measures using Pearson correlation analysis.
Body Composition |
Boys
|
Girls
|
||||||
---|---|---|---|---|---|---|---|---|
HRR 1 min
|
HRR 2 min
|
HRR 1 min
|
HRR 2 min
|
|||||
r | p | r | p | r | p | r | p | |
BMI z-score | -0.157 | 0.001 | -0.077 | 0.061 | -0.201 | <0.001 | -0.107 | 0.003 |
Body Fat (%) | -0.189 | <0.001 | -0.101 | 0.022 | -0.214 | <0.001 | -0.134 | <0.001 |
WC ( cm) | -0.218 | <0.001 | -0.133 | 0.004 | -0.164 | <0.001 | -0.078 | 0.022 |
WHtR | -0.198 | <0.001 | -0.110 | 0.014 | -0.164 | <0.001 | -0.067 | 0.043 |
BMI = Body mass index, HRR = Heart rate recovery, WC = Waist circumference, WHtR = Waist height ratio
The multiple regression analysis (Table 3) showed that only WC was negatively associated with HRR 2 min (p= 0.024) in boys whereas body fat percentage was negatively associated with HRR 2 min (p=0.008) in girls.
Table 3. Standardised coefficients (β) between HRR and body composition measures using multiple linear regression after controlling for age, pulse rate, blood pressure and smoking status.
Body Composition |
Boys
|
Girls
|
||||||
---|---|---|---|---|---|---|---|---|
HRR 1 min
|
HRR 2 min
|
HRR 1 min
|
HRR 2 min
|
|||||
β | p | Β | p | β | p | β | p | |
BMI z-score | 0.153 | NS | 0.132 | NS | -0.108 | NS | -0.008 | NS |
Body Fat (%) | -0.102 | NS | -0.029 | NS | -0.233 | NS | -0.325 | 0.008 |
WC ( cm) | -0.367 | NS | -0.418 | 0.024 | 0.192 | NS | 0.078 | NS |
WHtR | 0.166 | NS | 0.260 | NS | -0.061 | NS | 0.130 | NS |
NS = Not significant, BMI = Body mass index, HRR = Heart rate recovery, WC = Waist circumference, WHtR = Waist height ratio
Discussion
This study showed that there is inverse association of body composition measures with HRR in both boys and girls. For HRR 2 min, WC served as the strongest predictor in boys, while in girls it was body fat percentage.
We compared our study with previous published studies [9-11]. The Children’s Hospital study in Boston revealed BMI for age was associated with HRR 1 min for both genders [9], while The National Health and Nutrition Examination Survey 1999-2002 study showed that WC was the only body composition measures associated with HRR parameters (HRR 1 min, HRR 2 min and HRR 3 min for boys, and HRR 2 min and HRR 3 min for girls)[10]. The European Youth Heart Study, which measured HRR 1 min, HRR 3 min and HRR 5 min, showed that WC was associated with HRR 3 min in boys, but there was no association between body composition measures with HRR parameters in girls[11] . The researchers investigated association between HRR with several cardio-metabolic risk factors which included body composition measures [9-11]. These factors, and the different HRR parameters used, would have led to outcomes that differ from ours. Our study investigated HRR 1 min and HRR 2 min. Both HRR parameters have been validated as an ideal and prognostic measurement for HRR [50].
Another possible reason is the difference in exercise protocols. This study utilised mass screening step test and passive resting recovery while other studies were conducted in controlled laboratory settings, used active resting period for treadmills [9,10] or cycle ergometers [11]. Different exercise protocols have shown to influence HRR outcome [51,52].
The difference in results between the genders could be due to variances with fitness level, haematological parameters, and ventricular chamber size [13]. In girls, fat accumulate as total body fat and subcutaneous fat deposits [53]. It is different in boys, as fat accumulation occurs more in the intra-abdominal area, especially visceral adipose tissue [53]. WC has shown to be strongly correlated with boys [25]. These are probable reasons why our result showed that WC was the strongest predictor for HRR in boys and body fat percentage in girls.
It has been shown that childhood obesity is associated with ANS dysfunction. It has been postulated that obesity is linked to reduced parasympathetic drive [19], but a recent study has revealed that obesity affects both parasympathetic and sympathetic pathways in children [20]. This disparity suggests that more studies are needed in this field.
Since the effect of obesity on ANS control of HRR can occur at an early age, lifestyle changes are important for the well-being of the children. In relation to this, inducing weight loss and introducing lifestyle programmes for overweight and obese children has been shown to improve their HRR [54,55] with the greatest improvement occurring in HRR 1 min [54]. This finding reiterates the importance of introducing a healthy lifestyle to the participants from a young age as it carries many positive effects of exercise and weight control on body composition measures as well as ANS of the heart.
During exercising, the heart rate (HR) increase is due to withdrawal of parasympathetic activity, while further increments in HR are mediated by the sympathetic drive [1,56-58]. During recovery, HRR 1 min is due to vagal reactivation, while HRR 2 min and beyond is due to a combination of vagal drive, reduction in sympathetic pathway, and clearance of metabolites [2,11,12,59]. The increased interest of HRR in adults is its relationship with mortality and it has been shown that decreased vagal activity is a predictor of all-cause mortality in both healthy adults and post myocardial infarction (MI)patients [6-8,60,61]. A study has shown that among MI patients, there is a reduction of parasympathetic drive with dominance of sympathetic pathway [62]. HRR 1 min of less than 12 bpm during active rest [6] or 18 bpm during passive rest [63]indicates higher risk of cardiovascular mortality while HRR 2 min of less than 43 bpm is likewise, also considered unfavourably [7].
In children, other than HRR’s association with cardio-metabolic risks, several studies have shown that HRR may be considered as a marker for CVS health [13,64], and for the assessment of parasympathetic tone in post congenital cardiac surgery [65,66].
The strength of this study lies in the large sample of participants. The modified Harvard Step Test which was used as a tool in the study population suggests that it could be considered as an alternative tool for fitness assessment. The step test is relatively safe, simple, cheap, and portable[67]. In this study, five students could perform the exercise simultaneously since it can be conducted within a small space, and it requires minimal equipment. Moreover, not much specialized training is required and since it is not a laboratory setting, the atmosphere is more relaxed. The time taken for conducting each test was usually less than 10 minutes and this short duration is ideal for on field mass testing. Within a period of three months, the study was able to cover 15 schools within the three zones in Malaysia. Further studies are warranted to compare the modified Harvard Step Test with other established fitness assessment protocols.
As is present in all studies, there are limitations. Since the sample is of the same age group, the results reflected in this study may not exhibit the abilities of the rest of the paediatric population. Moreover, the cross sectional design used in this study does not establish causality. A longitudinal study on young adults has indicated that obesity and cardio-metabolic risks develop first prior to any effects on HRR[68], and since MyHEART is an on-going longitudinal study, it is our plan to investigate this matter on the current group of adolescents.
Conclusion
This study has shown that body composition measures are inversely associated with HRR in healthy Malaysian adolescent with waist circumference as the strongest predictor for boys and body fat percentage for girls respectively. MyHEART is a continuing longitudinal study, with future plans for follow-up at 15 years old (MyHEART II, 2014) and 17 years old (MyHEART III, 2016). This would enable us to determine how lifestyle factors operating in early adolescence affect cardio-metabolic health in early adulthood, and to assist the design and development of effective prevention program in Malaysia. It is also our aim to investigate the longitudinal association between HRR with body composition measures.
Acknowledgments
We would like to thank all the enumerators who helped us throughout data collection. We are also grateful for the support and guidance provided by the Centre of Population Health, University of Malaya and the Centre of Public Health, Queen’s University Belfast.
Funding Statement
1) University of Malaya Research Grant : RG299-11HTM; 2) Vice Chancellor Research Grant:UMQUB3D-2011. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript
References
- 1. Dimkpa U (2009) Post-exercise heart rate recovery: an index of cardiovascular fitness. J Exerc Physiol Online 12: 19-22. Available: http://www.asep.org/asep/asep/JEPonlineFebruary2009.html. Accessed 20 November 2011 [Google Scholar]
- 2. Imai K, Sato H, Hori M, Kusuoka H, Ozaki H et al. (1994) Vagally mediated heart rate recovery after exercise is accelerated in athletes but blunted in patients with chronic heart failure. J Am Coll Cardiol 24: 1529-1535. doi: 10.1016/0735-1097(94)90150-3. PubMed: 7930286. [DOI] [PubMed] [Google Scholar]
- 3. Sears CE, Choate JK, Paterson DJ (1998) Inhibition of nitric oxide synthase slows heart rate recovery from cholinergic activation. J Appl Physiol (1985) 84: 1596-1603. PubMed: 9572804. [DOI] [PubMed] [Google Scholar]
- 4. Arai Y, Saul JP, Albrecht P, Hartley LH, Lilly LS et al. (1989) Modulation of cardiac autonomic activity during and immediately after exercise. Am J Physiol 256: H132-H141. PubMed: 2643348. [DOI] [PubMed] [Google Scholar]
- 5. Perini R, Orizio C, Comandè A, Castellano M, Beschi M et al. (1989) Plasma norepinephrine and heart rate dynamics during recovery from submaximal exercise in man. Eur J Appl Physiol Occup Physiol 58: 879-883. doi: 10.1007/BF02332222. PubMed: 2767070. [DOI] [PubMed] [Google Scholar]
- 6. Cole CR, Blackstone EH, Pashkow FJ, Snader CE, Lauer MS (1999) Heart-rate recovery immediately after exercise as a predictor of mortality. N Engl J Med 341: 1351-1357. doi: 10.1056/NEJM199910283411804. PubMed: 10536127. [DOI] [PubMed] [Google Scholar]
- 7. Cole CR, Foody JM, Blackstone EH, Lauer MS (2000) Heart rate recovery after submaximal exercise testing as a predictor of mortality in a cardiovascularly healthy cohort. Ann Intern Med 132: 552-555. doi: 10.7326/0003-4819-132-7-200004040-00007. PubMed: 10744592. [DOI] [PubMed] [Google Scholar]
- 8. Cheng YJ, Lauer MS, Earnest CP, Church TS, Kampart JB, et al. (2003) Heart recovery following maximal exercise testing as a predictor of cardiovascular disease and all-cause mortality in men with diabetes. Diabetes Care 26: 2052-2057. doi: 10.2337/diacare.26.7.2052. PubMed: 12832312. [DOI] [PubMed] [Google Scholar]
- 9. Singh TP, Rhodes J, Gauvreau K (2008) Determinants of heart rate recovery following exercise in children. Med Sci Sports Exerc 40: 601-605. doi: 10.1249/MSS.0b013e3181621ec4. PubMed: 18317389. [DOI] [PubMed] [Google Scholar]
- 10. Lin LY, Kuo HK, Lai LP, Lin JL, Tseng CD et al. (2008) Inverse correlation between heart rate recovery and metabolic risks in healthy children and adolescents: insight from the National Health and Nutrition Examination Survey 1999-2002. Diabetes Care 31: 1015-1020. doi: 10.2337/dc07-2299. PubMed: 18268066. [DOI] [PubMed] [Google Scholar]
- 11. Laguna M, Aznar S, Lara MT, Lucía A, Ruiz JR (2013) Heart rate recovery is associated with obesity traits and related cardiometabolic risk factors in children and adolescents. Nutr Metab Cardiovasc Dis 23: 995-1001. doi: 10.1016/j.numecd.2012.10.002. PubMed: 23211756. [DOI] [PubMed] [Google Scholar]
- 12. Ohuchi H, Suzuki H, Yasuda K, Arakaki Y, Echigo S et al. (2000) Heart rate recovery after exercise and cardiac autonomic nervous activity in children. Pediatr Res 47: 329-335. doi: 10.1203/00006450-200003000-00008. PubMed: 10709731. [DOI] [PubMed] [Google Scholar]
- 13. Mahon AD, Anderson CS, Hipp MJ, Hunt KA (2003) Heart rate recovery from submaximal exercise in boys and girls. Med Sci Sports Exerc 35: 2093-2097. doi: 10.1249/01.MSS.0000099180.80952.83. PubMed: 14652507. [DOI] [PubMed] [Google Scholar]
- 14. Carnethon MR, Jacobs DR Jr., Sidney S, Sternfeld B, Gidding SS et al. (2005) A longitudinal study of physical activity and heart rate recovery: CARDIA, 1987-1993. Med Sci Sports Exerc 37: 606-612. doi: 10.1249/01.MSS.0000158190.56061.32. PubMed: 15809559. [DOI] [PubMed] [Google Scholar]
- 15. Kasmini K, Idris MN, Fatimah A, Hanafiah S, Iran H et al. (1997) Prevalence of overweight and obese school children aged between 7 to 16 years amongst the major 3 ethnic groups in Kuala Lumpur, Malaysia. Asia Pac J Clin Nutr 6: 172-174. [PubMed] [Google Scholar]
- 16. Zalilah MS, Mirnalini K, Khor GL, Merlin A, Bahaman AS et al. (2006) Estimates and distribution of body mass index in a sample of Malaysian adolescents. Med J Malaysia 61: 48-58. PubMed: 16708734. [PubMed] [Google Scholar]
- 17. Rampal L, Rampal S, Khor GL, Zain AM, Ooyub SB et al. (2007) A national study on the prevalence of obesity among 16,127 Malaysians. Asia Pac J Clin Nutr 16: 561-566. PubMed: 17704038. [PubMed] [Google Scholar]
- 18. Wee BS, Poh BK, Bulgiba A, Ismail MN, Ruzita AT, et al. (2011) Risk of metabolic syndrome among children living in metropolitan Kuala Lumpur: a case control study. BMC Public Health 11: 333 310.1186/1471-2458-1111-1333 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19. Yakinci C, Mungen B, Karabiber H, Tayfun M, Evereklioglu C (2000) Autonomic nervous system functions in obese children. Brain Dev 22: 151-153. doi: 10.1016/S0387-7604(00)00094-2. PubMed: 10814895. [DOI] [PubMed] [Google Scholar]
- 20. Baum P, Petroff D, Classen J, Kiess W, Blüher S (2013) Dysfunction of autonomic nervous system in childhood obesity: a cross-sectional study. PLOS ONE 8: e54546. doi: 10.1371/journal.pone.0054546. PubMed: 23358101. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 21. Bluher S, Molz E, Wiegand S, Otto KP, Sergeyev E et al. (2013) Body mass index, waist circumference, and waist-to-height ratio as predictors of cardiometabolic risk in childhood obesity depending on pubertal development. J Clin Endocrinol Metab 98: 3384-3393. doi: 10.1210/jc.2013-1389. PubMed: 23775352. [DOI] [PubMed] [Google Scholar]
- 22. Kuba VM, Leone C, Damiani D (2013) Is waist-to-height ratio a useful indicator of cardio-metabolic risk in 6-10-year-old children? BMC Pediatr 13: 91. doi: 10.1186/1471-2431-13-91. PubMed: 23758779. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 23. Kim C, Kim B, Joo N, Park Y, Lim H et al. (2010) Determination of the BMI threshold that predicts cardiovascular risk and insulin resistance in late childhood. Diabetes Res Clin Pract 88: 307-313. doi: 10.1016/j.diabres.2010.02.005. PubMed: 20223547. [DOI] [PubMed] [Google Scholar]
- 24. Aggoun Y, Farpour-Lambert NJ, Marchand LM, Golay E, Maggio AB et al. (2008) Impaired endothelial and smooth muscle functions and arterial stiffness appear before puberty in obese children and are associated with elevated ambulatory blood pressure. Eur Heart J 29: 792-799. doi: 10.1093/eurheartj/ehm633. PubMed: 18245115. [DOI] [PubMed] [Google Scholar]
- 25. Kelishadi R, Gheiratmand R, Ardalan G, Adeli K, Mehdi Gouya M et al. (2007) Association of anthropometric indices with cardiovascular disease risk factors among children and adolescents: CASPIAN Study. Int J Cardiol 117: 340-348. doi: 10.1016/j.ijcard.2006.06.012. PubMed: 16860411. [DOI] [PubMed] [Google Scholar]
- 26. Agirbasli M, Agaoglu NB, Ergonul O, Yagmur I, Aydogar H et al. (2011) Comparison of anthropometric indices in predicting metabolic syndrome components in children. Metab Syndr Relat Disord 9: 453-459. doi: 10.1089/met.2011.0018. PubMed: 21830913. [DOI] [PubMed] [Google Scholar]
- 27. Freedman DS, Khan LK, Dietz WH, Srinivasan SR, Berenson GS (2001) Relationship of childhood obesity to coronary heart disease risk factors in adulthood: the Bogalusa Heart Study. Pediatrics 108: 712-718. doi: 10.1542/peds.108.3.712. PubMed: 11533341. [DOI] [PubMed] [Google Scholar]
- 28. Freedman DS, Wang J, Maynard LM, Thornton JC, Mei Z et al. (2005) Relation of BMI to fat and fat-free mass among children and adolescents. Int J Obes (Lond) 29: 1-8. doi: 10.1038/sj.ijo.0802903. PubMed: 15278104. [DOI] [PubMed] [Google Scholar]
- 29. Hirschler V, Molinari C, Maccallini G, Aranda C, Oestreicher K (2011) Comparison of different anthropometric indices for identifying dyslipidemia in school children. Clin Biochem 44: 659-664. doi: 10.1016/j.clinbiochem.2011.02.004. PubMed: 21349259. [DOI] [PubMed] [Google Scholar]
- 30. Brambilla P, Bedogni G, Moreno LA, Goran MI, Gutin B et al. (2006) Crossvalidation of anthropometry against magnetic resonance imaging for the assessment of visceral and subcutaneous adipose tissue in children. Int J Obes (Lond) 30: 23-30. doi: 10.1038/sj.ijo.0803163. PubMed: 16344845. [DOI] [PubMed] [Google Scholar]
- 31. Johnson ST, Kuk JL, Mackenzie KA, Huang TT, Rosychuk RJ, et al. (2010) Metabolic risk varies according to waist circumference measurement site in overweight boys and girls. J Pediatr 156: 247-252 e1 [DOI] [PubMed] [Google Scholar]
- 32. Lee JM, Davis MM, Woolford SJ, Gurney JG (2009) Waist circumference percentile thresholds for identifying adolescents with insulin resistance in clinical practice. Pediatr Diabetes 10: 336-342. doi: 10.1111/j.1399-5448.2008.00474.x. PubMed: 19175894. [DOI] [PubMed] [Google Scholar]
- 33. Meng L, Luo N, Mi J (2011) Impacts of types and degree of obesity on non-alcoholic fatty liver disease and related dyslipidemia in Chinese school-age children? Biomed Environ Sci 24: 22-30. PubMed: 21440836. [DOI] [PubMed] [Google Scholar]
- 34. Haas GM, Liepold E, Schwandt P (2011) Percentile curves for fat patterning in German adolescents. World. J Pediatr 7: 16-23. [DOI] [PubMed] [Google Scholar]
- 35. McCarthy HD, Ashwell M (2006) A study of central fatness using waist-to-height ratios in UK children and adolescents over two decades supports the simple message--'keep your waist circumference to less than half your height'. Int J Obes (Lond) 30: 988-992. doi: 10.1038/sj.ijo.0803226. [DOI] [PubMed] [Google Scholar]
- 36. Savva SC, Tornaritis M, Savva ME, Kourides Y, Panagi A et al. (2000) Waist circumference and waist-to-height ratio are better predictors of cardiovascular disease risk factors in children than body mass index. Int J Obes Relat Metab Disord 24: 1453-1458. doi: 10.1038/sj.ijo.0801401. PubMed: 11126342. [DOI] [PubMed] [Google Scholar]
- 37. Mokha JS, Srinivasan SR, Dasmahapatra P, Fernandez C, Chen W et al. (2010) Utility of waist-to-height ratio in assessing the status of central obesity and related cardiometabolic risk profile among normal weight and overweight/obese children: the Bogalusa Heart Study. BMC Pediatr 10: 73 PubMed: 20937123. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 38. Schwandt P, Bertsch T, Haas GM (2010) Anthropometric screening for silent cardiovascular risk factors in adolescents: The PEP Family Heart Study. Atherosclerosis 211: 667-671. doi: 10.1016/j.atherosclerosis.2010.03.032. PubMed: 20417933. [DOI] [PubMed] [Google Scholar]
- 39. Goulding A, Taylor RW, Grant AM, Parnell WR, Wilson NC et al. (2010) Waist-to-height ratios in relation to BMI z-scores in three ethnic groups from a representative sample of New Zealand children aged 5-14 years. Int J Obes (Lond) 34: 1188-1190. doi: 10.1038/ijo.2009.278. PubMed: 20065976. [DOI] [PubMed] [Google Scholar]
- 40. Faria FR, Faria ER, Cecon RS, Barbosa Junior DA, Franceschini Sdo C et al. (2013) Body fat equations and electrical bioimpedance values in prediction of cardiovascular risk factors in eutrophic and overweight adolescents. Int J Endocrinol 2013: 10 doi: 10.1155/2013/501638. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 41. Ramachandran A, Snehalatha C, Yamuna A, Murugesan N, Narayan KM (2007) Insulin resistance and clustering of cardiometabolic risk factors in urban teenagers in southern India. Diabetes Care 30: 1828-1833. doi: 10.2337/dc06-2097. PubMed: 17416794. [DOI] [PubMed] [Google Scholar]
- 42. Medici G, Mussi C, Fantuzzi AL, Malavolti M, Albertazzi A et al. (2005) Accuracy of eight-polar bioelectrical impedance analysis for the assessment of total and appendicular body composition in peritoneal dialysis patients. Eur J Clin Nutr 59: 932-937. doi: 10.1038/sj.ejcn.1602165. PubMed: 15928682. [DOI] [PubMed] [Google Scholar]
- 43. Malavolti M, Mussi C, Poli M, Fantuzzi AL, Salvioli G et al. (2003) Cross-calibration of eight-polar bioelectrical impedance analysis versus dual-energy X-ray absorptiometry for the assessment of total and appendicular body composition in healthy subjects aged 21-82 years. Ann Hum Biol 30: 380-391. doi: 10.1080/0301446031000095211. PubMed: 12881138. [DOI] [PubMed] [Google Scholar]
- 44. Kriemler S, Puder J, Zahner L, Roth R, Braun-Fahrländer C et al. (2009) Cross-validation of bioelectrical impedance analysis for the assessment of body composition in a representative sample of 6- to 13-year-old children. Eur J Clin Nutr 63: 619-626. doi: 10.1038/ejcn.2008.19. PubMed: 18285806. [DOI] [PubMed] [Google Scholar]
- 45. Velasquez-Mieyer P, Perez-Faustinelli S, Cowan PA (2005) Identifying Children at Risk for Obesity, Type 2 Diabetes, and Cardiovascular Disease. Diabetes Spectrum 18: 213-220. doi: 10.2337/diaspect.18.4.213. [DOI] [Google Scholar]
- 46. Institute of Public Health (2006) The National Heath and Morbidity Survey 2006. (NHMS III) 2006. Kuala Lumpur, Malaysia: Institute for Public Health; , National Institutes of Health, Ministry of Health Malaysia; . 188 p [Google Scholar]
- 47. Treviño RP, Marshall RM Jr., Hale DE, Rodriguez R, Baker G et al. (1999) Diabetes risk factors in low-income Mexican-American children. Diabetes Care 22: 202-207. doi: 10.2337/diacare.22.2.202. PubMed: 10333934. [DOI] [PubMed] [Google Scholar]
- 48. Treviño RP, Yin Z, Hernandez A, Hale DE, Garcia OA et al. (2004) Impact of the Bienestar school-based diabetes mellitus prevention program on fasting capillary glucose levels: a randomized controlled trial. Arch Pediatr Adolesc Med 158: 911-917. doi: 10.1001/archpedi.158.9.911. PubMed: 15351759. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 49. Hydrie MZI, Basit A, Badruddin N, Ahmedani MY (2004) Diabetes Risk Factors in Middle Income Pakistani School Children. Pak. J Nutr 3: 43-49. [Google Scholar]
- 50. Shetler K, Marcus R, Froelicher VF, Vora S, Kalisetti D et al. (2001) Heart rate recovery: validation and methodologic issues. J Am Coll Cardiol 38: 1980-1987. doi: 10.1016/S0735-1097(01)01652-7. PubMed: 11738304. [DOI] [PubMed] [Google Scholar]
- 51. Buchheit M, Al Haddad H, Laursen PB, Ahmaidi S (2009) Effect of body posture on postexercise parasympathetic reactivation in men. Exp Physiol 94: 795-804. doi: 10.1113/expphysiol.2009.048041. PubMed: 19395660. [DOI] [PubMed] [Google Scholar]
- 52. Crisafulli A, Orrù V, Melis F, Tocco F, Concu A (2003) Hemodynamics during active and passive recovery from a single bout of supramaximal exercise. Eur J Appl Physiol 89: 209-216. doi: 10.1007/s00421-003-0796-4. PubMed: 12665987. [DOI] [PubMed] [Google Scholar]
- 53. Staiano AE, Katzmarzyk PT (2012) Ethnic and sex differences in body fat and visceral and subcutaneous adiposity in children and adolescents. Int J Obes (Lond) 36: 1261-1269. doi: 10.1038/ijo.2012.95. PubMed: 22710928. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 54. Wilks DC, Rank M, Christle J, Langhof H, Siegrist M et al. (2012) An inpatient lifestyle-change programme improves heart rate recovery in overweight and obese children and adolescents (LOGIC Trial). Eur J Prev Cardiol. doi: 10.1177/2047487312465691. [DOI] [PubMed] [Google Scholar]
- 55. Prado DM, Silva AG, Trombetta IC, Ribeiro MM, Guazzelli IC et al. (2010) Exercise training associated with diet improves heart rate recovery and cardiac autonomic nervous system activity in obese children. Int J Sports Med 31: 860-865. doi: 10.1055/s-0030-1267158. PubMed: 21072735. [DOI] [PubMed] [Google Scholar]
- 56. Drott C, Claes G, Göthberg G, Paszkowski P (1994) Cardiac effects of endoscopic electrocautery of the upper thoracic sympathetic chain. Eur J Surg Suppl: 65-70. PubMed: 7524789. [PubMed] [Google Scholar]
- 57. Hunt S (2001) Reinnervation of the transplanted heart--why is it important? N Engl J Med 345: 762-764. doi: 10.1056/NEJM200109063451011. PubMed: 11547748. [DOI] [PubMed] [Google Scholar]
- 58. Falcone C, Buzzi MP, Klersy C, Schwartz PJ (2005) Rapid heart rate increase at onset of exercise predicts adverse cardiac events in patients with coronary artery disease. Circulation 112: 1959-1964. doi: 10.1161/CIRCULATIONAHA.105.545111. PubMed: 16172270. [DOI] [PubMed] [Google Scholar]
- 59. Buchheit M, Papelier Y, Laursen PB, Ahmaidi S (2007) Noninvasive assessment of cardiac parasympathetic function: postexercise heart rate recovery or heart rate variability? Am J Physiol Heart Circ Physiol 293: H8-10. doi: 10.1152/ajpheart.00335.2007. PubMed: 17384128. [DOI] [PubMed] [Google Scholar]
- 60. Nishime EO, Cole CR, Blackstone EH, Pashkow FJ, Lauer MS (2000) Heart rate recovery and treadmill exercise score as predictors of mortality in patients referred for exercise ECG. JAMA 284: 1392-1398. doi: 10.1001/jama.284.11.1392. PubMed: 10989401. [DOI] [PubMed] [Google Scholar]
- 61. Schwartz PJ, La Rovere MT, Vanoli E (1992) Autonomic nervous system and sudden cardiac death. Experimental basis and clinical observations for post-myocardial infarction risk stratification. Circulation 85: I77-I91. PubMed: 1728509. [PubMed] [Google Scholar]
- 62. Rothschild M, Rothschild A, Pfeifer M (1988) Temporary decrease in cardiac parasympathetic tone after acute myocardial infarction. Am J Cardiol 62: 637-639. doi: 10.1016/0002-9149(88)90670-4. PubMed: 3414557. [DOI] [PubMed] [Google Scholar]
- 63. Watanabe J, Thamilarasan M, Blackstone EH, Thomas JD, Lauer MS (2001) Heart rate recovery immediately after treadmill exercise and left ventricular systolic dysfunction as predictors of mortality: the case of stress echocardiography. Circulation 104: 1911-1916. PubMed: 11602493. [PubMed] [Google Scholar]
- 64. Singh TP, Evans S (2010) Socioeconomic position and heart rate recovery after maximal exercise in children. Arch Pediatr Adolesc Med 164: 479-484. doi: 10.1001/archpediatrics.2010.57. PubMed: 20439800. [DOI] [PubMed] [Google Scholar]
- 65. Singh TP, Gauvreau K, Rhodes J, Blume ED (2007) Longitudinal changes in heart rate recovery after maximal exercise in pediatric heart transplant recipients: evidence of autonomic re-innervation? J Heart Lung Transplant 26: 1306-1312. doi: 10.1016/j.healun.2007.08.013. PubMed: 18096483. [DOI] [PubMed] [Google Scholar]
- 66. Singh TP, Curran TJ, Rhodes J (2007) Cardiac rehabilitation improves heart rate recovery following peak exercise in children with repaired congenital heart disease. Pediatr Cardiol 28: 276-279. doi: 10.1007/s00246-006-0114-0. PubMed: 17530324. [DOI] [PubMed] [Google Scholar]
- 67. Ohtake PJ (2005) Field Tests of Aerobic Capacity for Children and Older Adults. Cardiopulm Phys Ther J 16: 5-11 [Google Scholar]
- 68. Kizilbash MA, Carnethon MR, Chan C, Jacobs DR, Sidney S et al. (2006) The temporal relationship between heart rate recovery immediately after exercise and the metabolic syndrome: the CARDIA study. Eur Heart J 27: 1592-1596. doi: 10.1093/eurheartj/ehl043. PubMed: 16728422. [DOI] [PubMed] [Google Scholar]