General characteristics of participants (n = 2047).
Abstract
This cross-sectional study examined the independent and joint association of fatness and leg power (LP) with resting blood pressure (BP) in adolescents (12 to 15 years) in Benue state of Nigeria. The present study comprised 2047 adolescents, including 1087 girls. Participants were assessed for body mass index (BMI), LP, and resting BP. Multivariate regression models assessing the associations of the independent variables with BP were conducted. Fatness and LP were independent predictors of resting BP among participants and the relationship of LP with BP was more robust in girls than boys. Combined fatness and LP in predicting BP was modest (R2 = 10.4–14.3%) after controlling for maturity status. Low LP was associated with systolic blood pressure (SBP) in both girls (R2 = 9.0%, β = 0.260, p = 0.001) and boys (R2 = 11.0%, β = 0.226, p = 0.001). In the model for diastolic blood pressure (DBP), only fatness was associated with BP in girls (p = 0.001). The odd of hypertension (HTN) risk among overweight girls was 2.6 times that compared to their healthy-weight peers. Girls with low LP were 0.40 times more likely to develop HTN risk compared to their counterparts with high LP. This study has demonstrated that lower body muscle power is more important than fatness in predicting HTN in adolescent boys and girls.
Keywords
- adolescents
- adiposity
- hypertension
- leg muscle power
- ROC curves
1. Introduction
Hypertension (HTN) is a global health problem because of its high prevalence with concomitant risk of cardiovascular disease (CVD), kidney disease, and other co-morbidities [1]. Although HTN like many other CVD risk factors was previously considered an adult health problem, recent evidence has shown that it is increasingly becoming a pediatric health problem with its prevalence tracking into adulthood [2, 3]. Therefore, if youth at risk of this disorder are identified early, proactive steps can be initiated to enhance better health prospects in later life.
Previous studies in the pediatric population have identified HTN as a potent antecedent of CVD and its rising prevalence is noticeable not only in industrialized countries but more so in developing countries including those in Africa [3, 4, 5]. It has been documented that elevated blood pressure (BP) in adolescence can be associated with target organ damage, renal failure, and adverse changes in sympathetic nervous system, all of which can negatively impact cardiac output with resultant imbalance in cardiovascular homeostasis [2]. Although the specific etiology of HTN remains nebulous, high levels of body fat and low physical activity (PA) or fitness level have been found to be major predisposing factors [6]. Several studies in youth have demonstrated positive relationships between body fat and resting blood pressure [4, 7]. For instance, a cross-sectional study [7] found fatness as well as fitness to be independent predictors of resting blood pressure. There is increasing evidence linking muscle fitness including muscle power to cardiovascular health in youth [8, 9]. A population-based study of American adolescents [10] documented an independent association between lower body muscle strength and cardiometabolic risk including blood pressure.
Despite the emerging evidence linking muscle fitness to health outcomes in youth, studies examining the independent association of lower body muscle power (here-in referred to as LP or vertical jump power-VJP) and fatness with BP are exiguous. Further, the interactive effect of fatness and LP on BP needs to be explored. The present study aimed to examine the independent and combined associations of BMI and VJP with resting BP among in-school adolescents in Benue State, North central Nigeria. Specifically, the study determined the independent and joint associations of BMI and VJP with resting BP among adolescent girls and boys. The study further examined the relationships among BMI, VJP, and BP to determine population-specific thresholds for BMI and VJP for predicting risk of HTN among participants. The study also examined variations in fatness categories by VJP levels. A better understanding of these relationships will help inform more effective intervention programs that could lead to improved LP with a concomitant reduction in disease risk among youth including the overweight. Thus, it was hypothesized that LP would reduce BP values regardless of fatness levels.
2. Methods
2.1 Participants
This cross-sectional study included volunteer participants from selected secondary schools in Benue State, North Central Nigeria. Participants were eligible to participate in the study if they had no musculoskeletal problems, history of CVD, other reported health problems and sickness or had not participated in organized exercise programs at least 6 months before data collection. The study purpose and test procedures were fully explained to participants after permission was duly obtained from the heads of participating schools. The study protocol was approved by the health research ethics committee of Benue State University (Ref. No. BSUTHMKD/HREC/2013/017). Written informed consent of parents/guardians and assent of participants were sought before data collection. All tests were conducted in accordance with the ethical guidelines of the Helsinki declaration.
2.2 Study setting
The present study was conducted among adolescents aged 12–16 years in the three senatorial districts of Benue State, Nigeria (Benue North, Benue Central, and Benue South). Benue state with its capital at Makurdi is located in the North central geopolitical zone of Nigeria. The predominant tribes are Tivs, Idomas, Igedes and Etulos. The study covered 11 secondary schools comprising 2100 adolescent girls and boys. Like any typical state in Nigeria, secondary schools in Benue State are in two main categories: public and private. The public schools are owned by the government while private schools are owned by private individuals and Christian missionaries. The schools start lessons by 8:00 am and close by 2:00 pm with a 45 minutes break at 10 am.
2.3 Physical characteristics measurement
Participants’ physical characteristic measurements were in accordance with the protocol of the International Society for the Advancement of Kinanthropometry (ISAK) [11]. Specifically, bare-foot body mass and stature were measured in light clothing without shoes and socks with the aid of a calibrated digital weighing scale (Model Sec-880, Seca Birmingham, UK) and wall-mounted stadiometer (Model Sec-206; Seca, Birmingham, UK) to the nearest 0.1 kg and 0.1 cm, respectively. BMI was computed by dividing body mass in kilograms by stature in meter-square (kg.m−2). BMI was used to estimate body fatness. Body fat was estimated from triceps and medial calf skinfolds with the aid of Harpenden skinfold calipers (Creative Health Products, Ann Arbor, MI, USA). Measurements were taken three times on the right side of a participant’s body and the median was recorded. The revised regression equations for black children were used to estimate percent body fat [12]. On the basis of their BMI values, participants were categorized into healthy weight (HW) and overweight (OW) according to FitnessGram revised data [12].
Waist circumference (WC) which estimates abdominal fat [13] was measured with a Lufkin non-extensible flexible anthropometric tape (W606PM Rosscraft, Canada) to the nearest 0.1 cm. Details of the measurement procedure have been previously described [7]. All physical characteristics measurements were conducted by an accredited ISAK-Certified level 2 Anthropometrist (Lead author).
2.4 Pilot test
Before data collection, a pilot test was conducted to refine test administration procedures and determine precision of the instruments for data collection. Forty adolescent girls and boys ranging in age from 12–15 years that did not form part of the sample were recruited for the pilot test. All measurements were made according to standard procedures and the Cronbach’s Alpha coefficients were calculated to determine test reliability. In all cases, the alpha coefficients ranged from 0.820 to 0.896, indicating good internal consistency [14].
2.5 Leg power testing
Leg muscle power, a component of muscle fitness was assessed using a vertical jump (VJ) field test. The test was conducted indoors on a flat floor with a smooth wall using the countermovement jump (CMJ) protocol. Participants were instructed to rub chalk on the fingertips of the dominant hand and had a couple of practice sessions and then took their turns for the test. In the CMJ protocol, a participant stood with the dominant shoulder about 15 cm from the wall with both feet flat on the floor, reached as high as possible with the dominant hand, and made a chalk mark on the wall. He/she lowered the dominant hand, performed a countermovement by flexing the knees and hips, moving the trunk forward and downward and swinging the arms backward, and jumped with a swiping motion as high as possible making a second mark on the wall. The score was the vertical distance between the two chalk marks. Participants’ scores were converted into VJP values using a regression equation [15]. Each participant was given two trials and the best recorded to the nearest centimeter. Detailed description of the protocol is available elsewhere [16]. Participants were categorized into high and low groups using their sex-specific VJP receiver operating characteristic (ROC) cut-off values.
2.6 Blood pressure measurement
Blood pressure of participants was assessed in the morning while they occupied a sitting position after 10 minutes of rest with an oscillometric device. (HEM-705 CP, Omron Tokyo, Japan). The resting systolic blood pressure (SBP) and diastolic blood pressure (DBP) were monitored on each participant’s right arm using appropriate cuff sizes. Measurements were taken 3 times at 2-min intervals, and the average was recorded. Specific details of the BP protocol have been previously described [7]. The cut-off points for HTN (95th percentile for age and sex) in this study were based on the standards of the fourth report on the diagnosis, evaluation, and treatment of high blood pressure in children and adolescents 2004 [17].
2.7 Data analysis
Data were checked for normality before analyses with the Kolmogorov–Smirnov test. Complete data for all variables were available for 2047 out of 2100 adolescents, with a compliance rate of 97.5%. Descriptive statistics were presented as means ± SDs, frequencies, and percentage distributions. Student's t-test was used to compare the means of both genders on all study variables. Zero-order correlation coefficients were calculated to assess the relationships among BMI, VJP, and BP of participants. Multiple linear regression analyses were conducted to determine the independent and combined associations of BMI, VJP, and resting BP. All analyses were adjusted for biological maturation. Biological maturation was estimated from height and chronological age using the regression equation of Moore and Co-workers [18]. The equation estimates maturity offset (MO) directly. Then, age at peak height velocity (APHV) was estimated as the difference between chronological age and MO. The independent association of BMI and VJP with BP was further examined using binary logistics regression models. Separate analyses were conducted for girls and boys. Odd ratios (95%CI) of being hypertensive were calculated between BMI and VJP categories. The amount of variation in BP explained by the model was determined using the Cox and Snell R square and Nergelkerke R square [14]. Models were adjusted for MO as a potential confounding variable. The predictive capacities of the independent variables for the risk of BP were determined through the ROC analysis with 95% confidence intervals (95%CI). Threshold values for identifying risk of HTN were determined through area under curve (AUC) values, sensitivity, and specificity. A diagnostic test with AUC equal to 1 is perfectly accurate and another with a value of 0.5 has no discriminatory power. Tests with the AUC of 0.9–1.0 = highly accurate; 0.7–0.9 = moderate; and < 0.7 = less accurate [19]. All analyses were conducted using the statistical package for the social sciences (SPSS Version 20, IBM corporation, Armonk, NY, USA).
3. Results
3.1 Physical and performance characteristics
Participants’ general characteristics are summarized in Table 1. Girls were taller (
Variable | Combined (n = 2047) | Girls (n = 1087) | Boys (n = 960) | t-value | |
---|---|---|---|---|---|
Age (y) | 13.6 ± 1.3 | 13.6 ± 1.3 | 13.6 ± 1.3 | 0.786 | 0.432 |
APHV (y) | 13.4 ± 1.1 | 12.6 ± 0.7 | 14.2 ± 0.7 | 50.075 | <0.001 |
Stature (cm) | 150.3 ± 11.6 | 150.8 ± 11.0 | 149.7 ± 12.2 | 2.149 | 0.032 |
MO (y) | 0.2 ± 1.4 | 1.0 ± 1.0 | −0.6 ± 1.0 | 33.6 | <0.001 |
Body mass (kg) | 43.5 ± 9.0 | 44.2 ± 8.7 | 42.6 ± 9.3 | 3.931 | <0.001 |
BMI (kg.m−2) | 19.3 ± 3.8 | 19.5 ± 3.7 | 19.1 ± 3.9 | 2.319 | 0.021 |
Fat (%) | 16.0 ± 6.5 | 18.4 ± 5.6 | 13.4 ± 6.4 | 18.597 | <0.001 |
WC (cm) | 66.2 ± 8.4 | 67.1 ± 8.2. | 65.1 ± 8.5 | 5.460 | <0.001 |
LBM (kg) | 36.4 ± 7.4 | 35.9 ± 6.5 | 36.9 ± 8.3 | 2.935 | 0.003 |
VJH (cm) | 23.8 ± 7.6 | 22.7 ± 7.1 | 25.0 ± 7.9 | 6.774 | <0.001 |
VJP (w) | 1397.9 ± 507.9 | 1392.6 ± 481.7 | 1403.9 ± 536.2 | 0.501 | 0.617 |
SBP (mmHg) | 113.6 ± 17.4 | 115.5 ± 18.1 | 111.5 ± 16.4 | 5.174 | <0.001 |
DBP (mmHg) | 69.2 ± 13.7 | 68.8 ± 13.7 | 69.7 ± 13.7 | 1.465 | 0.143 |
r between BMI and VJP | 0.504 | 0.517 |
3.2 Predicators of BP
As shown in Table 2, VJP had the strongest correlation with the dependent variables, especially SBP. Because MO also had strong relationship with the dependent variables, models were adjusted for MO in both genders. Multiple regression was conducted to determine independent association of fatness and LP with resting BP (Table 3). LP was the only independent predictor (p < 0.001) of SBP and DBP in both genders, the association with the SBP being stronger. Fatness was not significantly associated (p > 0.005) with SBP and DBP in both genders.
SBP | DBP | |||||
---|---|---|---|---|---|---|
Group | MO | BMI | VJP | MO | BMI | VJP |
Girls | 0.207** | 0.147** | 0.314** | 0.120** | 0.110** | 0.118** |
Boys | 0.298** | 0.172** | 0.334** | 0.076* | 0.072* | 0.094* |
Group | Dependent variable | Predictors | r2 | Β | |
---|---|---|---|---|---|
Girls | SBP | BMI | 0.099 | −0.016 | 0.662 |
VJP | 0.321 | <0.001 | |||
DBP | BMI | 0.017 | 0.068 | 0.051 | |
VJP | 0.084 | 0.016 | |||
Boys | SBP | BMI | 0.111 | −0.001 | 0.968 |
VJP | 0.335 | <0.001 | |||
DBP | BMI | 0.010 | 0.032 | 0.398 | |
VJP | 0.078 | 0.039 |
3.3 Multivariate models for predicting BP
Hierarchical multiple regression analyses were conducted to determine the joint associations of fatness and LP with BP controlling for MO in both genders (Table 4). For the girls’ SBP model, the covariate explained only 4.3% of the variance in step 1. The addition of BMI and VJP in step 2 increased the total variance to 10.4% indicating that both the independent variables explained an additional variance of 6.1%. LP (
Predictor | Model 1 | Model 2 | ||||||
---|---|---|---|---|---|---|---|---|
Group | variable | r2 | Β | r2 | Β | |||
Girls | SBP | MO | 0.043 | 0.207 | <0.001 | 0.104 | 0.087 | 0.014 |
BMI | — | — | — | — | 0.021 | 0.568 | ||
VJP | — | — | — | — | 0.263 | <0.001 | ||
Boys | MO | 0.089 | 0.298 | <0.001 | 0.143 | 0.231 | <0.001 | |
BMI | — | — | — | — | 0.111 | 0.005 | ||
VJP | — | — | — | — | 0.165 | <0.001 | ||
Girls | DBP | MO | 0.014 | 0.120 | <0.001 | 0.029 | 0.130 | <0.001 |
BMI | — | — | — | — | 0.121 | 0.001 | ||
VJP | — | — | — | — | −0.003 | 0.949 | ||
Boys | MO | 0.006 | 0.076 | 0.019 | 0.013 | 0.071 | 0.091 | |
BMI | — | — | — | — | 0.066 | 0.122 | ||
VJP | — | — | — | — | 0.026 | 0.592 |
Results of the logistic regression models (Table 5) indicated that in general only VJP and BMI made significant contributions, which were greater in girls. In the girls’ model, both fatness (OR = 2.6, 95% CI = 1.29–5.35;
SBP | DBP | |||||||||
---|---|---|---|---|---|---|---|---|---|---|
Group | Pred | β | OR | 95%CI | β | OR | 95%CI | |||
Girls | MO | 0.30 | 1.35 | 1.12–1.64 | 0.002 | 0.34 | 1.40 | 1.15–1.72 | 0.001 | |
BMI | ||||||||||
HW OW | 0.966 | 1 2.63 | 1.29–5.35 | 0.008 | 0.82 | 1 2.27 | 0.96–5.34 | 0.061 | ||
VJP | ||||||||||
High Low | −0.923 | 1 0.40 | 0.25–0.64 | <0.001 | 0.431 | 1 1.54 | .96–2.48 | 0.076 | ||
Boys | MO | 0.595 | 1.81 | 1.44–2.29 | <0.001 | 0.194 | 1.20 | 0.96–1.53 | 0.103 | |
BMI | ||||||||||
HW OW | 0.920 | 1 2.51 | 0.96–6.56 | 0.060 | −1.426 | 1 0.24 | .032–1.80 | 0.165 | ||
VJP | ||||||||||
High Low | −0.289 | 1 0.75 | 0.46–1.23 | 0.252 | −0.312 | 1 0.73 | 0.45–1.19 | 0.208 |
3.4 Threshold of independent variables for detecting HTN
The ROC curve analyses are presented in Table 6. In both genders, the AUCs were significantly greater than 0.5 for both VJP and BMI (p < 0.05). The optimal threshold in girls for VJP and BMI were 1501.5 W and 18.9 kg.m−2, respectively. Corresponding values for boys were 1340.7 W and 18.9 kg.m−2, respectively. Details of the results are shown in Table 5. The gender-specific ROC curves are presented in Figures 2 and 3.
Group | Variable | AUC | 95%CI | Cut-point | Se | Sp | |
---|---|---|---|---|---|---|---|
Girls | BMI | 0.573 | .518–.627 | 18.9 | 0.575 | 0.516 | 0.014 |
VJP | 0.696 | .649–.743 | 1501.5 | 0.698 | 0.373 | <0.001 | |
Boys | BMI | 0.607 | .547–.667 | 18.9 | 0.606 | 0.413 | 0.001 |
VJP | 0.667 | .605–.729 | 1340.7 | 0.670 | 0.484 | <0.001 |
In order to further evaluate the influence of fatness and LP on BP, participants were divided into four fat/power groups and the results are presented in Table 7. The proportion of girls within these categories was 42.1%, 53.0%, 3.6%, and 1.3% for low fat/high power, low fat/low power, high fat/high power, and high fat/low power, respectively. Corresponding values for boys were 42.2%, 53.3%, 3.0%, and 1.3%. There were significant group differences in SBP for both girls (F(3,1083) = 7.50,
Girls (n = 1087) | Boys (n = 960) | |||||
---|---|---|---|---|---|---|
Group | n | SBP | DBP | n | SBP | DBP |
Low fat/High power | 458 | 108.6 ± 21.3 | 70.0 ± 13.5 | 407 | 106.2 ± 18.9 | 70.7 ± 13.7 |
Low fat/Low power | 576 | 111.0 ± 16.3 | 67.6 ± 13.8 | 512 | 107.6 ± 15.2 | 68.8 ± 13.7 |
Fat/High power | 39 | 108.3 ± 17.6 | 69.9 ± 12.3 | 29 | 102.8 ± 15.9 | 72.0 ± 13.1 |
Fat/Low power | 14 | 128.0 ± 17.6 | 74.8 ± 19.6 | 12 | 123.4 ± 24.6 | 69.8 ± 12.2 |
4. Discussion
Recent evidence from both observational and prospective studies in high-and middle-income societies has shown overweight youth with low leg muscle power exhibit unfavorable cardiometabolic disease risk, including high BP [20, 21]. Although HTN, like in the developed world is becoming a health problem in sub-Saharan Africa, the significance of fatness and leg muscle power in the development of HTN remains to be fully investigated among Nigerian youth.
The main findings of this study include: First, the prevalence of HTN is comparable with prevalent rates documented in both industrialized and developing countries [22, 23] and it is higher in girls. Second, the relationships among the independent and dependent variables are generally weak to moderate. Third, Fatness and LP are independent predictors of BP, but LP demonstrated a greater explanatory capacity than fatness in girls. Fourth, the joint contribution of fatness and LP in predicting blood pressure is modest (10.4–14.3%). Finally, SBP and DBP values varied by fat-power groups, with the low fat-high power group indicating the most favorable BP profile compared to the fat-low power group with the most adverse profile.
For the total sample documented in this study, the systolic and diastolic HTN prevalence of 9.8% and 8.9, respectively, is higher than the rates of 4.9 and 6.5% reported for South African adolescents [22]. Similarly, the Global prevalence rate of 6.9% for African children [23] is also lower than the rates documented in the present study. This result implies that HTN in Nigerian youth is increasing at a disturbing rate.
In this study, both fatness and LP are weakly related to BP in both genders, though the relationship between leg power and BP is stronger. However, the relationship between fatness and LP can be said to be moderate. These results are in agreement with previous research [21, 24]. A probable reason for these weak correlations may be the low prevalence of overweight among study participants. This has been previously observed [25]. Despite the modest relationship between the independent variables and BP, the link is still important in health terms.
Results of this study clearly show that LP but not fatness was the independent predictor of SBP and DBP in both girls and boys. Our results are consistent with some previous reports [20, 25]. These results indicate that leg muscle power is a problem among the study participants. As indicated, large proportions of both girls (54.4%) and boys (54.8%) had low LP. This result highlights the need to focus on this aspect of fitness among this cohort of adolescents. Muscle power is now considered an important component of health-related physical fitness, which is associated with a positive health prognosis and a lower risk of developing CVD risk in the pediatric population [8].
The present study shows the joint contribution of fatness and LP in predicting resting SBP was moderate (Girls = 10.4%; Boys = 14.3%). But the major determinant of SBP in girls was LP while in boys, maturity status. The association of LP with SBP was stronger in girls than boys. A plausible reason for the result in girls may be early maturation (Table 1), they also often participate in less vigorous physical activities than boys, hence the higher BP levels. Our results are in agreement with those of several investigators [20, 21, 26]. But surprisingly, the relationship between LP and BP was positive, indicating that participants with greater leg power also had higher SBP. It has been observed that confounding variables such as excessive intake of salt, alcohol, and cigarette could lead to these results [20]. We are in agreement with these speculations as they appear plausible. Fatness was significantly associated with only SBP in boys and DBP in girls.
Findings from the present study clearly indicate that resting BP levels varied by cut-points of fatness and LP. The poorest BP profile was documented in adolescents who are overweight with low leg muscle power. Specifically, high levels of LP resulted in lower resting BP irrespective of fatness status. This result is supported by previous research in Norwegian adolescents [21]. This finding is of public health significance.
Based on our results and those of others, it may be realistic to believe that fatness and LP are important variables that contribute to the development of HTN in adolescents. Worthy of note is the importance of lower body muscle power in cardiovascular and musculoskeletal health. For instance, there is increasing evidence linking muscle fitness, including muscle power to cardiovascular and general health in youth [9, 26, 27]. Indeed, current physical activity guidelines for youth emphasize muscle-strengthening activities on a regular basis for improvement in muscle fitness [28, 29]. Based on empirical evidence, several authorities have emphasized the development of muscle fitness due to its overall health benefits [30, 31, 32]. Therefore, evidence from the present study and others should serve to stimulate effective public health strategies to minimize HTN in adolescents by improving leg muscle power and reducing fatness.
Findings from this study should be interpreted in the light of some limitations. The cross-sectional design precludes confirmation of cause-and-effect relationship. A major strength of this study was the use of valid field tests of health-related physical fitness. These tests use standards that discriminate well between children with more favorable cardiovascular health profiles from those with less favorable profiles. For instance, results from the logistic regression models showed a very high percentage accuracy classification (PAC) in both genders (Girls = 90.2%; Boys = 90.2%).
5. Conclusions
In conclusion, LP was independently associated with resting BP in Nigerian adolescents. The relationship of LP with BP was more robust in girls. Combination of fatness and LP in predicting BP was modest. Variation in BP for girls was best predicted by LP while that of boy was biological maturation. The combination of low LP and high fatness resulted in the most unfavorable BP profile. These results suggest that intervention targeting BP control in adolescents should focus more on leg muscle power with less emphasis on body composition, and this should be considered an important public health goal.
Acknowledgments
The authors gratefully acknowledge the cooperation of students, teachers, and head teachers of schools that participated in the project. The contribution of the research assistants who made data collection possible is gratefully acknowledged.
References
- 1.
World Health Organisation. The world health report. In: Reducing Risk, Promoting Healthy Lifestyle. Vol. 2002. Geneva, Switzerland: World Health Organisation; 2002. pp. 101-146 - 2.
Chiolero A, Bovet P, Paradis G. Screening for evaluated blood pressure in children and adolescents: A critical appraisal. JAMA Pediatrics. 2013; 167 :266-273 - 3.
Ejike CE. Prevalence of HTN in Nigerian children and adolescents: A systematic review and trend analysis of data from the past four decades. Journal of Tropical Pediatrics. 2017; 63 :229-241 - 4.
Musa DI, Lawal B, Fawa MS. Body fat and blood pressure levels in school boys in Kano city, Nigeria. The African Symposium: An on-line Educational Research Journal. 2002; 2 :1-7 - 5.
Noubiap JJ, Essoumam BJJ, Jingi AM, Aminde LN, Nansseu JR. Prevalence of elevated blood pressure in children and adolescents in Africa: A systematic review and meta-analysis. Lancet Public Health. 2017; 2 :C375-C386 - 6.
Crump C, Sundquist J, winkleby MA, Sundquist K. Interactive effects of physical fitness and body mass index on risk of hypertension. JAMA Internal Medicine. 2016; 176 (2):210-216 - 7.
Musa DI, Williams CA. Cardiorespiratory fitness, fatness, and blood pressure associations in Nigerian youth. Medicine and Science in Sports and Exercise. 2012; 44 (10):1978-1985 - 8.
Smith JJ, Eather N, Morgan PJ, Plotnikoff RC, Figerbaum AD, Lubans DR. The health benefits of muscular fitness for children and adolescents: A systematic review and meta-analysis. Sports Medicine. 2014; 44 :1209-1223 - 9.
Janz KF, Baptista F, Ren S, Zhu W, Laurson KR, Mahar MT, et al. Associations among musculoskeletal fitness assessments and health outcomes: The Lisbon study for the development and evaluation of musculoskeletal fitness standards in youth. Measurement in Physical Education and Exercise Science. 2021; 25 (Suppl.):1-9. DOI: 10.1080/1091367x.2021.2000414 - 10.
Peterson MD, Zang P, Saltarelli WA, Visich PS, Gordon PM. Low muscle strength thresholds for the detection of cardiometabolic risk in adolescents. American Journal of Preventive Medicine. 2015; 50 (5):593-599. DOI: 10.1016/j.amepre.2015.09.019 - 11.
Mafell-Jones MJ, Stewart AD, de Ridder JH. International Standards for Anthropometric Assessment. Wellington, New Zealand: International Society for the Advancement of Kinanthropometry; 2012. pp. 32-89 - 12.
The Cooper Institute. Fitness Gram Test Administration Manual. 5th ed. Champaign, IL, USA: Human Kinetics; 2017. pp. 39-64 - 13.
Maffies C. Aetiology of overweight in children and adolescents. European Journal of Pediatrics. 2000; 159 :S35-S44 - 14.
Pallant J. SPPS Survival Manual: A Step-by-step Guide to Data Analysis Using SPSS. 5th ed. Berkshire, England: Open University Press; 2017 - 15.
Mahar MT, Welk GJ, Janz KF, Laurson K, Zhu W, Baptista F. Estimation of lower body muscle power from vertical jump in youth. Measurement in Physical Education and Exercise Science. 2022; 26 (Suppl.):1-11. DOI: 10.1080/1091367x.2022.2041420 - 16.
Mcguigan M. Administration, scoring and interpretation of selected tests. In: Halt GG, Triplet NT, editors. (CDS). Essentials of strength training and conditioning. 4th ed. Champaign, IL: Human Kinetics; 2015 - 17.
National High Blood Pressure Education Working Group on High Blood Pressure in Children and Adolescents. The fourth report on the diagnosis, evaluation and treatment of high blood pressure in children and adolescents. Pediatrics. 2004; 114 :555-576 - 18.
Moore SA, McKay HA, Macdonald H, Nettlefold L, Baxter-Jones AD, Cameron N, et al. Enhancing somatic maturity prediction model. Medicine & Science in Sports & Exercise. 2015; 47 (8):1755-1764 - 19.
Swets JA. Measuring the accuracy of diagnostic systems. Science. 1988; 240 (4857):1285-1293 - 20.
Nunes HEG, Alves CAS Jr, Goncalves ECA, Silva DAS. What physical fitness component is most closely associated with adolescents’ blood pressure? Perceptual and Motor Skills. 2017; 124 (6):1107-1120 - 21.
Steene-Johannessene J, Anderssen SA, Kolle E, Andesen LB. Low muscle fitness is associated with metabolic risk in youth. Medicine & Science in Sports & Exercise. 2009; 41 (7):1361-1367 - 22.
Awotidebe A, Monyeki MA, Moss SJ, Strydom GL, Amstrong M, Kemper HCG. Relationship of adiposity and cardiorespiratory fitness with resting blood pressure of South African adolescents: The PAHL study. Journal of Human Hypertension. 2015; 30 :245-251. DOI: 10.1038/jhh.2015.81 - 23.
Song P, Zhang Y, Yu J, Zha M, Zhu Y, Rahimi K, et al. Global prevalence of hypertension in children: A systematic review and meta-analysis. JAMA Pediatrics. 2019; 173 (12):1154-1163 - 24.
Buchan DS, Young JD, Boddy LM, Malina RM, Baker JS. Fitness and adiposity are independently associated with cardiometabolic risk in youth. BioMed Research International. 2013; 231 :1-6 - 25.
Eisenmann JC. Aerobic fitness, fatness and the metabolic syndrome in children and adolescents. Acta Pediatric. 2007; 96 :1723-1729 - 26.
Garcia-Artero E, Ortega FB, Ruiz R, et al. Lipid and metabolic profile in adolescents are affected more by physical fitness than physical activity (Avena Study). Revista Española de Cardiología. 2007; 60 (6):581-588 - 27.
Baptista F, Zymbal V, JanZ KF. Predictive validity of handgrip strength, vertical jump power and plank time in the identification of pediatric sarcopenia. Measurement in Physical Education and Exercise Science. 2021. DOI: 10.1080/1091307x.2021.1987242 - 28.
Welk G, Janz K, Laurson K, Mahar M, Zhu W, Paulovic A. Development of criterion- reference standards for musculoskeletal fitness in youth: Considerations and approaches by the fitnessgram scientific advisory board. Measurement in Physical Education and Exercise Science. 2022. DOI: 10.1080/1091367x.2021.2014331 - 29.
Weaver CM, Gordon CM, Janz KF, kalwarf HS, Lapped JM, Lewis R, et al. Peak bone mass development and lifestyle factors: A systematic review and implementation recommendations. Osteoporosis International. 2016; 27 (4):1281-1386 - 30.
US Department of Health and Human Services. Physical Activity Guidelines for Americans. 2nd ed. Washington, DC, USA: US Department of Health and Human Services; 2018 - 31.
Corbin C, Jan KF, Baptista F. Good health: The power of power. Journal of Physical Education, Recreation & Dance. 2017; 88 (9):28-35 - 32.
Pate RR, Daniels S. Institute of Medicine report on fitness measures and health outcomes in youth. JAMA Pediatrics. 2013; 167 (3):221-222