Relation between Active Transportation, Screen Time and Sleep Quality among Metabolically Healthy versus Unhealthy Congolese Obese

Abstract

Objective: This study aims to analyze the relationship between active transportation, screen time and sleep quality among metabolically health versus unhealthy Congolese schoolboys and girls obese. Method: A cross-sectional study was conducted among 58 obese aged 15.36 ± 1.22 years in Brazzaville (Republic of Congo). They were divided into metabolically healthy obese (MHO, n = 29) and metabolically unhealthy obese (MUHO, n = 29). Data collection consisted of anthropometric measurements, lipids profile parameters, Pittsburgh Sleep Quality Index and the screen time measurements. The relationship was analyzed by using the logistic regression for healthy and unhealthy schoolboys and obese girls. Results: Compared to MUH obese subjects, MUHO obese subjects were significantly less engaged in active transportation (p = 0.03), TV and smartphone times significantly increased (p = 0.000 and p = 0.003), sleep quality significantly poor (p = 0.001). They were 1.85 (95% CI: 0.85 - 3.88) lower odds to engage in active transportation, had 1.82 (95% CI: 1.11 - 3.10) and 2.04 (95% CI: 1.11 - 3.10) higher odds of TV time respectively, had 1.87 (95% CI: 1.24 - 2.84) and 2.04 (95% CI: 1.47 - 2.85) higher odds of smartphone time respectively and have 2.35 (95% CI: 1.62 - 3.41) higher odds of poor sleep. Conclusion: MUHO subjects underwent high screen time and poor sleep quality. Higher TV-viewing/smartphone time and poorer sleeping quality were found to be associated with less time spent in active transportation. This bad habit on screen and sleep negatively affects the cardiometabolic parameters.

Share and Cite:

Kounga, P. , Boussana, A. and Agbodjogbé, W. (2024) Relation between Active Transportation, Screen Time and Sleep Quality among Metabolically Healthy versus Unhealthy Congolese Obese. Open Journal of Endocrine and Metabolic Diseases, 14, 199-212. doi: 10.4236/ojemd.2024.1412021.

1. Introduction

By 2035, more than half of humans worldwide on track to be overweight or obese [1], because of the heterogeneity which extends obesity to metabolically healthy or metabolically unhealthy concepts [2] [3]. It is known that body mass index of 30 kg/m2 or higher as well as excess deposits of fat in the abdominal region are used to identify individuals with obesity. However, excess weight and abdominal obesity have been shown to be associated with patterns of unfavorable metabolic. According to International Diabetes Federation (IDF), metabolic syndrome (MS) is defined by the presence of: 1) high blood pressure, defined as blood pressure ≥ 130/85 mmHg or drug treatment; 2) high fasting blood glucose level, defined as glucose ≥ 100 mg/dL or drug treatment for type 2 diabetes; 3) high serum triglycerides, defined as triglycerides ≥ 150 mg/dL or drug treatment; 4) low high density lipoprotein cholesterol (HDL-C) level, defined as HDL-C < 40 mg/dL in men and < 50 mg/dL in women or drug treatment for dyslipidemia [4]. Due to the presence or absence of metabolic syndrome, obesity can be defined as having large quantities of fat mass or body weight but exhibit a healthy metabolic profile or exhibit unhealthy metabolic profile [5] [6]. The metabolically unhealthy obesity (MUHO) is considered when ≥3 of the above criteria were met [7].

The prevalence of MUHO varies between 10.6% - 20.1% when obesity is defined by BMI and from 22.7% - 49.0% when defined by waist circumference (WC) [8]. Due to its potential impact, MUHO constitutes a concern worldwide (150 to 160 million among children and adolescents aged 5 to 17 years) and could constitute a very particular situation in Africa by 2025 (around three quarters of the obese world population will be on its ground [9]. Without widespread awareness about the risk of a low level of physical activity, poor sleep and screen media exposure, the risk of overweight and obesity will continue to increase [5] [10]-[12]. Screen time, even with a very small dose of use at night [13] or use beyond 2 hours of use per day, is more destructive compared to other sedentary activities and leads to excess weight and obesity [14]. Accordingly, poor sleep by decreasing melatonin secretions [15]-[19], reduced plasma triglycerides absorption and increases fat deposition [20] [21].

In recent years, the lifestyle of Congolese adolescents has shifted toward a more sedentary lifestyle with increased use of smartphones and other screen-based media. Over the years, we have noticed that this population does not have the will to change its bad lifestyle habits which, in its extreme cases, involve immoral behavior (for example, alcohol consumption, and transport by car to work, to school and to majority of destination rather than transport on foot). At the level of government and those responsible for health, there is no strategy to counteract the evolution of these lifestyle habits despite the fact that many studies report the importance of active transportation. The latter, which includes walking to work, to school, to any neighborhood amenity, and to any destination, with durations ranging from zero to 10-minutes, to greater than five hours, has confirmed health‐promoting benefits in preventing and mitigating obesity and obesity‐related commodities [22]-[24].

According to Millett et al. [25], it is a key strategy to increase physical activity and reduce the growing burden of non-communicable diseases. But less time spent in active transportation, combined with higher TV-viewing, smartphone time and poorer sleep quality clustered together produces higher odds with cardiometabolic disease [26]-[28]. Although not referring to MUHO directly, previous studies regarding higher screen time and poorer sleep quality with leisure physical activity, have reported the strongest associations [29]-[31]. But whether screen media exposure and sleep quality helps explain the relationship with active transportation among Congolese MHO and MUHO has not been previously investigated. Therefore, we hypothesize that less time spent in active transportation is associated to higher screen media exposure and poorer sleep among MUHO group.

2. Material and Methods

2.1. Subjects

The modified sampling method reported by Prasomsri et al. [32] was used for sample size calculation. Briefly, the sample size was calculated using Gpower 3.1 software, considering an alpha of 0.05, an effect size of 0.91 and a power of 0.95. The total number of participants required for the study is 58. Twenty-nine obese subjects were needed per group, in the MUHO group and MHO group, according to the sample size calculation. We conducted this cross-sectional study in one Brazzaville’s private school selected for convenience. This school has the particularity of having a large space for children to be sufficiently active and of receiving students from the districts in the center and Brazzaville. Before this study, there is no information about metabolically unhealthy and healthy obese students. We used a cross-sectional design to collect the multiple data required from the selected study population at a single time point. Subjects were randomly selected based on overweight or obese status. Thereafter, they participated in an interview, physical examination, and a laboratory exam. All participants provided written informed consent, and a parent/guardian also provided informed consent for any participant less than 18 years. Procedures for data collection were approved by the National laboratory Board, and this work was accepted by the ethics committee of MARIEN NGOUABI University. Only subjects who appear for a blood sample, with a body mass index > 25 kg/m2, a biochemical profile and WC values were included. All participants who did not appear for a blood sample as well as those without a body mass index > 25 kg/m2, without a biochemical profile and WC values were excluded.

2.2. Anthropometric Measurements

Anthropometric measurements were carried out in a specially prepared room taking into account the recommended procedure in indoor clothing, without shoes. Weight was measured to the nearest 0.1 kg using a bioelectric impedance meter (Tanita BC 545N, Japan). Height was measured using a wooden measuring rod with an accuracy of 0.1 cm. Waist circumference (WC) was measured midway between the iliac crest and the lowest rib to the nearest 0.1 cm, as reported by Swainson et al. [33]. Body mass index (BMI) was calculated by dividing weight (kg) by the square of height (m2). Obesity was defined based on age- and gender-specific BMI percentiles [34]. Cardiometabolic risk prediction was determined by calculating the waist circumference/height ratio [35]. To determine cardiac output, systolic blood pressure (PAS) and diastolic blood pressure (PAD) were measured with a cuff blood pressure monitor (HEM7121, OMRON Healthcare, China).

2.3. Fasting Blood Glucose (FBG) and Blood Lipid Biomarkers

All laboratory tests were conducted in the National Laboratory (Republic of Congo) using standard procedures. Clinical measurements and venous blood from the median cubital vein were taken in the morning after fasting. Total blood glucose was analyzed immediately after collection using a Hemocue Glucose 201 analyzer (Hemocue, Danmark). Blood glucose levels were defined as follows: 1): slightly increased: FBG ≤ 1.10 g/L 2); moderately increased: FBG 1.10 - 1.26 g/L and 3) severely increased: FBG > 1.26 g/L [36]. For lipid biomarkers, blood samples were collected and serum was extracted and frozen at −80˚C until analysis. Blood lipid biomarkers, total cholesterol (TC), high-density lipoprotein cholesterol (HDL-C), high triglycerides (TG) were measured in a certified laboratory using appropriate biochemical assays as previously described [37] [38].

2.4. Active Transportation

Information on mode of travel to and from home to school was gathered from respondents by asking, “How do they usually travel to school?” [25] [39]. There were four potential responses: public transport (bus or minibus), parent’s vehicle, taxi, walking. We categorized these responses into two categories of passive transportation (bus or minibus), parent’s vehicle, taxi) and active transportation (walking). We categorized respondents according to whether they were sufficient level (walking more than 30 min) or they were low level (walking less than 30 min).

2.5. Screen Time

Screen time measurement was based on the frequent use and duration of different screen devices, such as television and smartphone. They were asked to report the types of devices they use most often. Additionally, they reported their screen time between 1 to 11 AM, 12 to 5 PM, and 6 to 11 PM for seven days. The time spent on mainly television and smartphone media was summed. A total weighted mean recreational screen use was calculated as reported by Nagata et al. [40]: ([weekday average × 5] + [weekend average × 2])/7. Screen time was calculated as a continuous variable and categorized into four-hour increments. Excessive screen viewing time was defined as screen viewing for >2 h/day [41].

2.6. Sleep Quality Assessment

The sleep quality was assessed using Pittsburgh Sleep Quality Index (PSQI) [42]. PSQI includes 19 items summarized into seven components: 1) subjective sleep quality, 2) sleep latency, 3) sleep duration, 4) habitual sleep efficiency, 5) sleep disturbances, 6) sleeping medications, and 7) daytime dysfunction. The score of each component ranges from 0 to 3 and the total PSQI score is calculated by summation of the scores of the seven components. This total PSQI score ranges from 0 to 21 and a score of more than five was considered to identify the subjects with poor sleep quality [43].

2.7. Statistical Analysis

All statistical data were processed using SPSS version 25 software (SPSS Inc., Chicago, IL, United States). The Shapiro-Wilk test was used to determine the normality distribution. Because data showed non parametric characteristics, Mann-Whitney U test and chi-square test were used. The association of active transportation (dependent variable) with the screen time and sleep quality levels of adolescents was analyzed by logistic regression. Statistical significance was determined using a p-value < 0.05.

3. Results

Table 1. Demographic and cardiometabolic characteristics of metabolically healthy (MHO) and metabolically unhealthy obese (MUHO) phenotypes obese subjects.

Groups

p-value

MHO

(n = 29, mean rank)

MUHO

(n = 29, mean rank)

Age (year)

31.31

27.69

0.393

Body mass (kg)

28.53

30.47

0.662

Height (m)

24.76

34.24

0.032

Body mass index (kg/m2)

28.55

30.45

0.668

Body fat (%)

23.79

35.21

0.010

Waist circumference (cm)

28.36

30.64

0.607

Hip circumference (cm)

27.28

31.72

0.313

Heart Rate rest (bpm)

24.31

34.69

0.016

Systolic blood pressure (mmHg)

18.21

40.79

0.000

Diastolic blood pressure (mmHg)

15.72

43.28

0.000

Fasting blood glucose (mg/dL)

31.22

27.78

0.429

Triglyceride (mg/dL)

27.74

31.26

0.420

HDL cholesterol levels (mg/dL)

40.71

18.29

0.000

Note: MHO: metabolically healthy obese; MUHO: metabolically unhealthy obese; HDL: high density lipoprotein.

Table 1 shows that adolescents with MHO were older and had lower mean BMI, Body fat, Waist circumference and hip circumference than those with MUHO. Significant differences were identified with respect to SBP, DBP and HDL cholesterol levels. By definition, individuals with a MHO phenotype had lower fasting blood glucose, triglycerides, systolic blood pressure, diastolic blood pressure and higher HDL-C. Those who were classified as MUHO were likely to be younger and had significant lower HDL-C and significant higher proportion of systolic and diastolic blood pressure.

Table 2. Comparison of active transportation, screen time and sleep quality among MHO and MUHO phenotypes adolescents.

Groups

p-value

MHO

(n = 29, n (%))

MUHO

(n = 29, n (%))

Active transportation n (%)

Yes

13 (68.4)

6 (31.6)

0.051

No

16 (41.0)

23 (59.0)

Most used medias

TV (heures/day)

≤1 h/day

4 (100.0)

0 (0.0)

0.000

2 - 3 h/day

9 (100.0)

0 (0.0)

4+ h/day

16 (37.2)

27 (62.8)

Smartphone (heures/day)

≤1 h/day

4 (100.0)

0 (0.0)

0.003

2 - 3 h/day

5 (100.0)

0 (0.0)

4+ h/day

12 (35.3)

22 (64.7)

Meeting recommendations n (%)

4 (100.0)

0 (0.0)

0.013

Sleep quality based on PSQI

Good sleep n (%)

13 (86.7)

2 (13.3)

0.001

Poor sleep n (%)

16 (37.2)

27 (62.8)

PSQI

18.05

40.95

0.000

*n (%). **≤1 hrs screen time per day as recommended for children and adolescents [41].

As shown in Table 2, there were some differences in the MHO and MUHO phenotypes adolescents. Compared to MUHO, those with the MHO phenotype significantly spent time in active transportation. They have significantly lower TV and smartphone time respectively (p = 0.000 and p = 0.003). They have met recommendations for screen time (p = 0.013) and have significant proportion of good sleep (p = 0.000).

In logistic regression analyses, as shown in Table 3, less active transportation significantly increased TV, smartphone times and worsen sleep quality. These variables were significantly associated with less active transportation in the MUHO phenotype.

Table 3. Associations between active transportation with screen time and sleep quality among MUHO phenotypes.

Usually walking, yes

Usually walking, no

OR (95 %CI)

p-value

OR (95 %CI)

p-value

Screen time

Television

≤1 h/day

Ref.

Ref.

2 - 3 h/day

1.38 (0.96 - 2.00)

0.087

1.82 (0.85 - 3.88)

0.05

4+ h/day

1.42 (0.98 - 2.08)

0.069

2.04 (0.65 - 6.43)

0.001

Smartphone

≤1 h/day

Ref.

Ref.

2 - 3 h/day

1.41 (0.98 - 2.06)

0.069

1.87 (1.24 - 2.84)

0.003

4+ h/day

1.19 (0.62 - 2.28)

0.583

2.04 (1.47 - 2.85)

0.001

Sleep quality

Good sleep n (%)

Ref.

Ref.

Poor sleep n (%)

1.75 (1.01 - 2.12)

0.009

2.35 (1.62 - 3.41)

0.000

4. Discussion

The present study was conducted to analyze the relationship between active transportation with media exposure and sleep quality among Congolese MHO and MUHO phenotypes. Our findings show that: i) MHO phenotype spent more time per day in active transportation, spent less time per day in screen media (TV viewing and smartphone use) and presented a better quality of sleep compared with MUHO phenotype; ii) higher TV viewing, smartphone use and worsen sleep quality were associated with low level of active transportation in MUHO phenotype.

To our knowledge, no universal consensus has been reached regarding the classification of obese subjects according to cardiometabolic risk factors. While some studies have defined the MHO and MUHO phenotypes based on zero cardiometabolic risk factors, the present study and others have defined them using up to ≥3 cardiometabolic risk factors [7] [44] [45]. Otherwise, by observing the link between obesity and metabolic diseases, it is well documented that Obesity is an important risk factor for decreased HDL-C, which predisposes to cardiovascular diseases [46]. In the present study, we observed that apart from obese MUHO, cardiometabolic risks are lower in obese MHO phenotype. Indeed, MHO obese subjects had significantly greater level of HDL-C. Along with this significantly higher HDL-C level, they spent more time per day in active transportation. Therefore, it could be argued that active transportation to and from school to home during school time have a significant impact on high-density lipoproteins and triglycerides among MHO phenotype [47]. It seems that when the active transport carried out is sufficiently long and intense, cardiometabolic health improves best. Moreover, substituting 10 to 30 mins/day of sedentary time with equal amounts of active transportation improved in overall physical and cardiometabolic health [22] [48]. It undoubtedly acts by significantly reducing waist circumference and systolic and diastolic blood pressure [49].

In this study, self-report questionnaires were used for the assessment of both screen media exposure time and sleep quality. Data suggests that MUHO group spends more time in TV-viewing and smartphone use and had poor sleep quality compared to MHO group. Our findings are consistent with those of previous research that suggests prolonged TV-viewing, smartphone use exposure, poor sleep quality, low level physical activity and their components at later stages of life, may thus contribute to the development of Metabolic syndrome [13] [18] [29] [30] [50] [51]. To achieve such results, it seems that the MUHO group not meeting some health guidelines recommendations of 60 min of moderate to vigorous physical activity (MVPA) per day, no more than 2 h of screen time per day, and age-specific sleep duration for children and adolescents [52]. Secondly, it may be explained by a media-rich bedroom culture in which children and adolescents have their own smartphone, Internet, game console and computer to which they are exposed to the contents of these devices before sleeping.

Based on these research results, there is association between no meeting the screen media exposure and sleep quality guideline with active transportation among MUHO group. However, this conclusion appears to be controversial, given that a study by Camhi et al. [48] put forward different arguments. These authors provide some evidence that physical activity, but not sedentary behavior, is associated with cardiometabolic phenotypes among adults. Unlike this study, our findings are consistent with those of previous research in obese people in general that suggests there is an association between shorter sleep duration and overweight and longer screen time and overweight [29] [31].

Overall, it can be stated that any watching television and/or using smartphones as well as poor sleep quality that MUHO group spends in a day, whether they spent less time in active transportation, increases their risk of having a cardiometabolic risk profile. Consistent with previous studies, all these three predictors of metabolic syndrome are interdependent. For example, Cassidy et al. [53] observed that all their respondents suffering from cardiometabolic diseases reported less physical activity, more television viewing and poorer sleep habits. Kolovos et al. also observed that participants with comorbid type 2 diabetes and cardiovascular disease reported poor sleep duration, high TV time, and low physical activity clustered together [54]. Given the interdependent and complex links between all these three parameters, we can deduce that apart from the fact that each influences the metabolic syndrome [26]-[28], the clustering of high TV or smartphone time, poor sleep quality and spent less time in active transportation produces higher odds with cardiometabolic disease. Börnhorst et al. [26] states that having a media device in child’s bedroom increased the odds for abdominal obesity and metabolic syndrome. Likewise, Barstad et al. [27] revealed that having higher screen-time increased the systolic BP and triglycerides, while lower HDL-c levels. Okubo et al. [28] showed that poor sleep quality (difficulties in initiating and maintaining sleep) by activating Hypothalamic-pituitary-adrenal axis (HPA), enhanced stress hormone secretion such as cortisol and catecholamine. Finally, these excess secretions lead to increased risk of metabolic syndrome.

Our results show that in the MUHO group in which participants spent less time in active transport, the odds ratio of TV-viewing, smartphone use and poor sleep quality were high. In line with our findings Cassidy et al. [53] have reported that even in cases where the clustering of negative lifestyle factors is not significant prevalent, metabolic syndrome disruption does occur in some individuals, for whom the risk for various health conditions may be increased. The current study provides a robust assessment of association of active transportation with TV-viewing, smartphone and sleep quality. It makes a unique contribution to the current literature in Republic of the Congo context, and provides practical implications, especially when metabolic syndrome with higher TV-viewing and smartphone use as well as poor sleeps quality increasing exponentially. The relationships between low level of active transportation and TV-viewing/smartphone use as well as sleep quality found in the current study implies that Congolese MUHO adolescents should regulate their amount of TV-viewing, smartphone usage and sleep quality in efforts to increasing active transportation and maintaining metabolic health.

Despite interesting findings, the current study has some limitations that must be highlighted. First, the cross-sectional design of this study limits our ability to make causal interpretations of the data with respect to being considered MUHO. Second, because of the design of the study, very few Congolese adolescents had this measure performed in the current study. Third, we did not collect information regarding the Objective tools for sleep assessment. Despite these limitations, our study is strengthened first by the use of many cardiometabolic risk factors to define MUHO, which allows us to capture a broader aspect of health.

3.2. Conclusion

Our results suggest that metabolically unhealthy obese group was more exposure to television, smartphone, poor sleep quality, and spent less time on active transportation than their metabolically healthy obese counterparts. Higher TV-viewing/smartphone time and poorer sleeping quality were found to be associated with less time spent in active transportation. However, these associations were not consistent across all metabolically obesity levels. Our findings add to the literature by showing that this association is stronger in metabolically unhealthy obese group compared with metabolically healthy obese group. Given the increasing screen media exposure, it is important to encourage active transportation in metabolically unhealthy obese, which may ameliorate some of the effects of extended screen time. Future research is needed to confirm the findings and to test interventions that encourage reduced screen time and increased active transportation among obese adolescents.

Acknowledgements

Authors acknowledge the immense help received from the scholars whose articles are cited and included in references of this manuscript. The authors are also grateful to authors/editors/publishers of all those articles, journals and books from where the literature for this article has been reviewed and discussed.

Ethical Approval and Informed Consent

The study designs were approved by Institutional Ethics Committee of High institute of physical education and sport, Marien Ngouabi University, Brazzaville, Republic of Congo. An informed assent form was obtained from all participants.

Conflicts of Interest

The authors declare no conflicts of interest regarding the publication of this paper.

References

[1] World Obesity Atlas Report (20240 Plus de la moitié des humains pourraient être en surpoids ou obèses d’ici 2035.
https://www.theguardian.com/society/2023/mar/02/more-than-half-of-humans-on-track-to-be-overweight-or-obese-by-2035-report
[2] Brandão, I., Martins, M.J. and Monteiro, R. (2020) Metabolically Healthy Obesity—Heterogeneity in Definitions and Unconventional Factors. Metabolites, 10, Article 48.
https://doi.org/10.3390/metabo10020048
[3] Sun, M., Fritz, J., Häggström, C., Bjørge, T., Nagel, G., Manjer, J., et al. (2023) Metabolically (un)healthy Obesity and Risk of Obesity-Related Cancers: A Pooled Study. Journal of the National Cancer Institute, 115, 456-467.
https://doi.org/10.1093/jnci/djad008
[4] Alberti, K.G.M.M., Eckel, R.H., Grundy, S.M., Zimmet, P.Z., Cleeman, J.I., Donato, K.A., et al. (2009) Harmonizing the Metabolic Syndrome. Circulation, 120, 1640-1645.
https://doi.org/10.1161/circulationaha.109.192644
[5] Phillips, C.M. (2013) Metabolically Healthy Obesity: Definitions, Determinants and Clinical Implications. Reviews in Endocrine and Metabolic Disorders, 14, 219-227.
https://doi.org/10.1007/s11154-013-9252-x
[6] Stefan, N. (2008) Identification and Characterization of Metabolically Benign Obesity in Humans. Archives of Internal Medicine, 168, 1609-1616.
https://doi.org/10.1001/archinte.168.15.1609
[7] Brant, L.C.C., Wang, N., Ojeda, F.M., LaValley, M., Barreto, S.M., Benjamin, E.J., et al. (2017) Relations of Metabolically Healthy and Unhealthy Obesity to Digital Vascular Function in Three Community-Based Cohorts: A Meta-Analysis. Journal of the American Heart Association, 6, e004199.
https://doi.org/10.1161/jaha.116.004199
[8] Beck, E., Paquot, N. and Scheen, A.J. (2008) Sujets «métaboliquement obèses» de poids normal. Première partie: Diagnostic, physiopathologie et prévalence. Obésité, 3, 184-193.
https://doi.org/10.1007/s11690-008-0137-1
[9] Beck, N. and Scheen, A. (2009) Sujets «métaboliquement obèses» sans excès de poids: Un phénotype interpellant. Revue Médicale de Liège, 64, 1422.
[10] Fang, K., Mu, M., Liu, K. and He, Y. (2019) Screen Time and Childhood Overweight/Obesity: A Systematic Review and Meta-Analysis. Child: Care, Health and Development, 45, 744-753.
https://doi.org/10.1111/cch.12701
[11] Bakour, C., Mansuri, F., Johns-Rejano, C., Crozier, M., Wilson, R. and Sappenfield, W. (2022) Association between Screen Time and Obesity in US Adolescents: A Cross-Sectional Analysis Using National Survey of Children’s Health 2016-2017. PLOS ONE, 17, e0278490.
https://doi.org/10.1371/journal.pone.0278490
[12] Kaul, A., Bansal, N., Sharma, P., Aneja, S. and Mahato, M. (2023) Association of Screen Time Usage and Physical Activity with Overweight and Obesity among School-Going Children in Uttar Pradesh. Cureus, 15, e47690.
[13] Diakiese, B.M., Zayoud, A., Gremy, I., Artely, S. and Parola, S.R. (2021) Association entre l’usage des écrans et les troubles de sommeil chez les collégiens et lycéens en Île-de-France. Médecine du Sommeil, 18, Article No. 25.
https://doi.org/10.1016/j.msom.2020.11.022
[14] Robinson, T.N., Banda, J.A., Hale, L., Lu, A.S., Fleming-Milici, F., Calvert, S.L., et al. (2017) Screen Media Exposure and Obesity in Children and Adolescents. Pediatrics, 140, S97-S101.
https://doi.org/10.1542/peds.2016-1758k
[15] Sahın, S., Ozdemir, K., Unsal, A. and Temiz, N. (2013) Evaluation of Mobile Phone Addiction Level and Sleep Quality in University Students. Pakistan Journal of Medical Sciences, 29, 913-918.
https://doi.org/10.12669/pjms.294.3686
[16] Hale, L. and Guan, S. (2015) Screen Time and Sleep among School-Aged Children and Adolescents: A Systematic Literature Review. Sleep Medicine Reviews, 21, 50-58.
https://doi.org/10.1016/j.smrv.2014.07.007
[17] Hysing, M., Harvey, A.G., Linton, S.J., Askeland, K.G. and Sivertsen, B. (2016) Sleep and Academic Performance in Later Adolescence: Results from a Large Population-Based Study. Journal of Sleep Research, 25, 318-324.
https://doi.org/10.1111/jsr.12373
[18] Qanash, S., Al-Husayni, F., Falata, H., Halawani, O., Jahra, E., Murshed, B., et al. (2021) Effect of Electronic Device Addiction on Sleep Quality and Academic Performance among Health Care Students: Cross-Sectional Study. JMIR Medical Education, 7, e25662.
https://doi.org/10.2196/25662
[19] Pivonello, C., Negri, M., Patalano, R., Amatrudo, F., Montò, T., Liccardi, A., et al. (2021) The Role of Melatonin in the Molecular Mechanisms Underlying Meta-Flammation and Infections in Obesity: A Narrative Review. Obesity Reviews, 23, e13390.
https://doi.org/10.1111/obr.13390
[20] Edwardson, C.L., Gorely, T., Davies, M.J., Gray, L.J., Khunti, K., Wilmot, E.G., et al. (2012) Association of Sedentary Behaviour with Metabolic Syndrome: A Meta-Analysis. PLOS ONE, 7, e34916.
https://doi.org/10.1371/journal.pone.0034916
[21] Haghjoo, P., Siri, G., Soleimani, E., Farhangi, M.A. and Alesaeidi, S. (2022) Screen Time Increases Overweight and Obesity Risk among Adolescents: A Systematic Review and Dose-Response Meta-Analysis. BMC Primary Care, 23, Article No. 161.
https://doi.org/10.1186/s12875-022-01761-4
[22] Lorenzo, E., Szeszulski, J., Shin, C., Todd, M. and Lee, R.E. (2020) Relationship between Walking for Active Transportation and Cardiometabolic Health among Adults: A Systematic Review. Journal of Transport & Health, 19, Article 100927.
https://doi.org/10.1016/j.jth.2020.100927
[23] Sadarangani, K.P., Von Oetinger, A., Cristi-Montero, C., Cortínez-O’Ryan, A., Aguilar-Farías, N. and Martínez-Gómez, D. (2018) Beneficial Association between Active Travel and Metabolic Syndrome in Latin-America: A Cross-Sectional Analysis from the Chilean National Health Survey 2009-2010. Preventive Medicine, 107, 8-13.
https://doi.org/10.1016/j.ypmed.2017.12.005
[24] Xu, F., Jin, L., Qin, Z., Chen, X., Xu, Z., He, J., et al. (2020) Access to Public Transport and Childhood Obesity: A Systematic Review. Obesity Reviews, 22, e12987.
https://doi.org/10.1111/obr.12987
[25] Millett, C., Agrawal, S., Sullivan, R., Vaz, M., Kurpad, A., Bharathi, A.V., et al. (2013) Associations between Active Travel to Work and Overweight, Hypertension, and Diabetes in India: A Cross-Sectional Study. PLOS Medicine, 10, e1001459.
https://doi.org/10.1371/journal.pmed.1001459
[26] Börnhorst, C., Russo, P., Veidebaum, T., Tornaritis, M., Molnár, D., Lissner, L., et al. (2020) The Role of Lifestyle and Non-Modifiable Risk Factors in the Development of Metabolic Disturbances from Childhood to Adolescence. International Journal of Obesity, 44, 2236-2245.
https://doi.org/10.1038/s41366-020-00671-8
[27] Barstad, L.H., Júlíusson, P.B., Johnson, L.K., Hertel, J.K., Lekhal, S. and Hjelmesæth, J. (2018) Gender-Related Differences in Cardiometabolic Risk Factors and Lifestyle Behaviors in Treatment-Seeking Adolescents with Severe Obesity. BMC Pediatrics, 18, Article No. 61.
https://doi.org/10.1186/s12887-018-1057-3
[28] Okubo, N., Matsuzaka, M., Takahashi, I., Sawada, K., Sato, S., Akimoto, N., et al. (2014) Relationship between Self-Reported Sleep Quality and Metabolic Syndrome in General Population. BMC Public Health, 14, Article No. 562.
https://doi.org/10.1186/1471-2458-14-562
[29] Guzmán, V., Lissner, L., Arvidsson, L., Hebestreit, A., Solea, A., Lauria, F., et al. (2021) Associations of Sleep Duration and Screen Time with Incidence of Overweight in European Children: The IDEFICS/I. Family Cohort. Obesity Facts, 15, 55-61.
https://doi.org/10.1159/000519418
[30] Sehn, A.P., Silveira, J.F.d.C., Brand, C., Lemes, V.B., Borfe, L., Tornquist, L., et al. (2024) Screen Time, Sleep Duration, Leisure Physical Activity, Obesity, and Cardiometabolic Risk in Children and Adolescents: A Cross-Lagged 2-Year Study. BMC Cardiovascular Disorders, 24, Article No. 525.
https://doi.org/10.1186/s12872-024-04089-2
[31] Li, L., Zhang, S., Huang, Y. and Chen, K. (2017) Sleep Duration and Obesity in Children: A Systematic Review and Meta-Analysis of Prospective Cohort Studies. Journal of Paediatrics and Child Health, 53, 378-385.
https://doi.org/10.1111/jpc.13434
[32] Prasomsri, J., Thueman, B., Yuenyong, P., Thongnoon, C., Khophongphaibun, N. and Ariyawatcharin, S. (2023) Effectiveness of Motor Imagery on Sports Performance in Football Players: A Randomized Control Trial. Hong Kong Physiotherapy Journal, 44, 29-37.
https://doi.org/10.1142/s1013702524500021
[33] Swainson, M.G., Batterham, A.M., Tsakirides, C., Rutherford, Z.H. and Hind, K. (2017) Prediction of Whole-Body Fat Percentage and Visceral Adipose Tissue Mass from Five Anthropometric Variables. PLOS ONE, 12, e0177175.
https://doi.org/10.1371/journal.pone.0177175
[34] Dietz, W.H. and Robinson, T.N. (1998) Use of the Body Mass Index (BMI) as a Measure of Overweight in Children and Adolescents. The Journal of Pediatrics, 132, 191-193.
[35] Nevill, A.M., Duncan, M.J., Lahart, I.M. and Sandercock, G.R. (2016) Scaling Waist Girth for Differences in Body Size Reveals a New Improved Index Associated with Cardiometabolic Risk. Scandinavian Journal of Medicine & Science in Sports, 27, 1470-1476.
https://doi.org/10.1111/sms.12780
[36] Wang, L., Yan, N., Zhang, M., Pan, R., Dang, Y. and Niu, Y. (2022) The Association between Blood Glucose Levels and Lipids or Lipid Ratios in Type 2 Diabetes Patients: A Cross-Sectional Study. Frontiers in Endocrinology, 13, Article 969080.
https://doi.org/10.3389/fendo.2022.969080
[37] Nomikos, T., Panagiotakos, D., Georgousopoulou, E., Metaxa, V., Chrysohoou, C., Skoumas, I., et al. (2015) Hierarchical Modelling of Blood Lipids’ Profile and 10-Year (2002-2012) All Cause Mortality and Incidence of Cardiovascular Disease: The ATTICA Study. Lipids in Health and Disease, 14, Article No. 108.
https://doi.org/10.1186/s12944-015-0101-7
[38] Georgoulis, M., Chrysohoou, C., Georgousopoulou, E., Damigou, E., Skoumas, I., Pitsavos, C., et al. (2022) Long-Term Prognostic Value of LDL-C, HDL-C, LP(a) and TG Levels on Cardiovascular Disease Incidence, by Body Weight Status, Dietary Habits and Lipid-Lowering Treatment: The ATTICA Epidemiological Cohort Study (2002-2012). Lipids in Health and Disease, 21, Article No. 141.
https://doi.org/10.1186/s12944-022-01747-2
[39] Laverty, A.A., Hone, T., Goodman, A., Kelly, Y. and Millett, C. (2021) Associations of Active Travel with Adiposity among Children and Socioeconomic Differentials: A Longitudinal Study. BMJ Open, 11, e036041.
https://doi.org/10.1136/bmjopen-2019-036041
[40] Nagata, J.M., Weinstein, S., Alsamman, S., Lee, C.M., Dooley, E.E., Ganson, K.T., et al. (2024) Association of Physical Activity and Screen Time with Cardiovascular Disease Risk in the Adolescent Brain Cognitive Development Study. BMC Public Health, 24, Article No. 1346.
https://doi.org/10.1186/s12889-024-18790-6
[41] Jain, S., Shrivastava, S., Mathur, A., Pathak, D. and Pathak, A. (2023) Prevalence and Determinants of Excessive Screen Viewing Time in Children Aged 3-15 Years and Its Effects on Physical Activity, Sleep, Eye Symptoms and Headache. International Journal of Environmental Research and Public Health, 20, Article 3449.
https://doi.org/10.3390/ijerph20043449
[42] Shadzi, M.R., Rahmanian, M., Heydari, A. and Salehi, A. (2024) Structural Validity of the Pittsburgh Sleep Quality Index among Medical Students in Iran. Scientific Reports, 14, Article No. 1538.
https://doi.org/10.1038/s41598-024-51379-y
[43] Farrahi Moghaddam, J., Nakhaee, N., Sheibani, V., Garrusi, B. and Amirkafi, A. (2011) Reliability and Validity of the Persian Version of the Pittsburgh Sleep Quality Index (PSQI-P). Sleep and Breathing, 16, 79-82.
https://doi.org/10.1007/s11325-010-0478-5
[44] Sénéchal, M., Wicklow, B., Wittmeier, K., Hay, J., MacIntosh, A.C., Eskicioglu, P., et al. (2013) Cardiorespiratory Fitness and Adiposity in Metabolically Healthy Overweight and Obese Youth. Pediatrics, 132, e85-e92.
https://doi.org/10.1542/peds.2013-0296
[45] Lassale, C., Tzoulaki, I., Moons, K.G.M., Sweeting, M., Boer, J., Johnson, L., et al. (2017) Separate and Combined Associations of Obesity and Metabolic Health with Coronary Heart Disease: A Pan-European Case-Cohort Analysis. European Heart Journal, 39, 397-406.
https://doi.org/10.1093/eurheartj/ehx448
[46] Bora, K., Pathak, M.S., Borah, P. and Das, D. (2016) Association of Decreased High-Density Lipoprotein Cholesterol (HDL-C) with Obesity and Risk Estimates for Decreased HDL-C Attributable to Obesity. Journal of Primary Care & Community Health, 8, 26-30.
https://doi.org/10.1177/2150131916664706
[47] Pedersen, B.K. and Saltin, B. (2015) Exercise as Medicine—Evidence for Prescribing Exercise as Therapy in 26 Different Chronic Diseases. Scandinavian Journal of Medicine & Science in Sports, 25, 1-72.
https://doi.org/10.1111/sms.12581
[48] Camhi, S.M., Crouter, S.E., Hayman, L.L., Must, A. and Lichtenstein, A.H. (2015) Lifestyle Behaviors in Metabolically Healthy and Unhealthy Overweight and Obese Women: A Preliminary Study. PLOS ONE, 10, e0138548.
https://doi.org/10.1371/journal.pone.0138548
[49] Murtagh, E.M., Nichols, L., Mohammed, M.A., Holder, R., Nevill, A.M. and Murphy, M.H. (2015) The Effect of Walking on Risk Factors for Cardiovascular Disease: An Updated Systematic Review and Meta-Analysis of Randomized Control Trials. Preventive Medicine, 72, 34-43.
https://doi.org/10.1016/j.ypmed.2014.12.041
[50] Kanagasabai, T., Dhanoa, R., Kuk, J.L. and Ardern, C.I. (2017) Association between Sleep Habits and Metabolically Healthy Obesity in Adults: A Cross-Sectional Study. Journal of Obesity, 2017, 1-7.
https://doi.org/10.1155/2017/5272984
[51] Sina, E., Buck, C., Veidebaum, T., Siani, A., Reisch, L., Pohlabeln, H., et al. (2021) Media Use Trajectories and Risk of Metabolic Syndrome in European Children and Adolescents: The IDEFICS/I. Family Cohort. International Journal of Behavioral Nutrition and Physical Activity, 18, Article No. 134.
https://doi.org/10.1186/s12966-021-01186-9
[52] Chen, Z., Chi, G., Wang, L., Chen, S., Yan, J. and Li, S. (2022) The Combinations of Physical Activity, Screen Time, and Sleep, and Their Associations with Self-Reported Physical Fitness in Children and Adolescents. International Journal of Environmental Research and Public Health, 19, Article 5783.
https://doi.org/10.3390/ijerph19105783
[53] Cassidy, S., Chau, J.Y., Catt, M., Bauman, A. and Trenell, M.I. (2016) Cross-Sectional Study of Diet, Physical Activity, Television Viewing and Sleep Duration in 233 110 Adults from the UK Biobank; the Behavioural Phenotype of Cardiovascular Disease and Type 2 Diabetes. BMJ Open, 6, e010038.
https://doi.org/10.1136/bmjopen-2015-010038
[54] Kolovos, S., Jimenez-Moreno, A.C., Pinedo-Villanueva, R., Cassidy, S. and Zavala, G.A. (2019) Association of Sleep, Screen Time and Physical Activity with Overweight and Obesity in Mexico. Eating and Weight DisordersStudies on Anorexia, Bulimia and Obesity, 26, 169-179.
https://doi.org/10.1007/s40519-019-00841-2

Copyright © 2025 by authors and Scientific Research Publishing Inc.

Creative Commons License

This work and the related PDF file are licensed under a Creative Commons Attribution 4.0 International License.