Literature DB >> 33007979

The Relationship between Leisure-Time Sedentary Behaviors and Metabolic Risks in Middle-Aged Chinese Women.

Jing Fan1, Caicui Ding1, Weiyan Gong1, Fan Yuan1, Yanning Ma1, Ganyu Feng1, Chao Song1, Ailing Liu1.   

Abstract

The prevalence of metabolic diseases has increased over the past few decades, and epidemiological studies suggest that metabolic diseases may be associated with lifestyle. The purpose of the present study was to investigate the relationship between leisure-time sedentary behaviors (LTSBs) and metabolic risks in middle-aged women in China. Data came from the China National Nutrition and Health Surveillance (CNNHS) in 2010-2012. A total of 2643 women aged 46 to 53 years were involved. Multiple linear regression was used to examine the association of leisure-time sedentary duration (LTSD) with total cholesterol (TC), triglyceride (TG), waist circumference (WC), and body mass index (BMI). Restrictive cubic splines (RCS) were used to plot the curves between LTSD and the risk of metabolic diseases. Region, education, income, alcohol consumption, exercise, daily energy intake, and fat energy ratio were adjusted for all models. After adjusting for potential influencing factors, the results of multiple linear regression showed that for each additional hour increase in LTSD, TC and TG increased by 0.03 mmol/L and 0.04 mmol/L, respectively. The results of RCS curves showed that the risks of MetS (p for trend = 0.0276), obesity (p for trend = 0.0369), hypertension (p for trend = 0.0062), and hypercholesteremia (p for trend = 0.0033) increased with the increase in LTSD. LTSB was associated with the risks of MetS, obesity, hypertension, and hypercholesteremia in middle-aged women. Reducing LTSD may be an effective way of preventing metabolic diseases in middle-aged women.

Entities:  

Keywords:  metabolic diseases; sedentary behaviors; women’s health

Mesh:

Year:  2020        PMID: 33007979      PMCID: PMC7594022          DOI: 10.3390/ijerph17197171

Source DB:  PubMed          Journal:  Int J Environ Res Public Health        ISSN: 1660-4601            Impact factor:   3.390


1. Introduction

Globally, metabolic diseases are gradually increasing in prevalence all around the world. The number of adults with diabetes has increased by about three times since 1980, from 108 million in 1980 to 422 million in 2014 [1]. Each year, diabetes leads to 1.5 million deaths worldwide. The World Health Organization (WHO) estimates that dyslipidemia contributes to one-third of global ischemic heart disease and one-fifth of global cerebrovascular disease, which is equivalent to nearly 2.6 million deaths worldwide each year [2]. From 1990 to 2015, the rate of hypertension increased from 17,307 to 20,526 per 10,000 persons, and the estimated rate of annual deaths related to hypertension increased from 97.9 to 106.3 per 10,000 persons [3]. Meanwhile, hypertension led to a loss of disability-adjusted life years (DALYs) from 95.9 million to 143.0 million around the world [3]. Over the past three decades, the prevalence of metabolic syndrome (MetS) has increased in many countries. It is estimated that about one billion people worldwide are suffering from MetS [4]. The Consortium of Global Burden of Disease Obesity analyzed data on adults in 195 countries between 1980 and 2015, showing that the global prevalence of overweight and obesity continued to increase during those 35 years and about four million deaths were directly related to high body mass index (BMI) [5]. The prevalence of metabolic diseases is also on the rise in China. From 2002 to 2012, the prevalence of overweight and obesity increased from 22.8% and 7.1% to 30.1% and 11.9%, respectively, and the prevalence of diabetes and hypertension rose from 4.2% and 18.8% to 9.7% and 22.8%, respectively [6]. During that decade, the number of patients with MetS increased by about 50 million, and the prevalence of dyslipidemia increased from 18.6% to 40.4% [6]. Between 6% and 30% of chronic diseases in China can be attributed to overweight and obesity, with the direct economic burden as high as CNY 90.768 billion [7]. The DALYs caused by hypertension in the Chinese population has reached 37.94 million years [8]. Diabetes is a major cause of blindness, kidney failure, cardiovascular and cerebrovascular accidents, and amputation in China, and the burden of disease is heavy [9]. It is predicted that elevated total cholesterol (TC) levels will lead to an increase of 9.2 million cardiovascular events in China between 2010 and 2030 [10]. The increasing prevalence of metabolic diseases may be due to changes in lifestyle, including dietary habits, physical activities, and sedentary behavior (SB), where the role of SB for metabolic risks is gradually being recognized. Leisure-time sedentary behaviors (LTSBs) which are a component of SB, refer to sedentary activities in leisure time including reading, watching television, using a computer or smart phone, and other screen-based pastimes [11]. The association of LTSB with metabolic diseases such as type 2 diabetes [12,13], obesity [14,15], dyslipidemia, elevated blood pressure (BP) [16,17], and MetS [18,19] was investigated in previous studies. Independent of physical activity, LTSBs, especially TV viewing, were strongly associated with increased risk of type 2 diabetes and obesity [12]. Hormonal changes in middle-aged women may adversely affect metabolic and cardiovascular processes, such as reduced energy consumption, elevated fasting insulin levels, and elevated high-density lipoprotein cholesterol (HDL-C) levels, making them more susceptible to many metabolic disorders [20,21]. In addition, women at that age are less physically active than men, which is related to the roles they play and workloads they undertake in society and at home [22]. Cardiovascular diseases account for half of all deaths among women over 50 in developing countries, and more than 70 million women worldwide are affected by diabetes [22]. Thus, our study focused on estimating the relationship between leisure-time sedentary duration (LTSD) and a variety of metabolic diseases in middle-aged women. At present, large sample studies or relatively comprehensive studies on the relationship between SB and metabolic diseases were mainly conducted abroad, while these kinds of studies were seldom conducted in China. Therefore, data from the China National Nutrition and Health Surveillance (CNNHS) in 2010–2012 were utilized to explore the relationship between SB and metabolic risks in middle-aged women.

2. Materials and Methods

2.1. Study Participants

The data came from the China National Nutrition and Health Surveillance (CNNHS) in 2010–2012. The multi-stage stratification method and the population proportional cluster random sampling method was used. In the first stage, a total of 150 study sites were selected from the four categories of areas, including 34 large cities, 41 small and medium-sized cities, 45 ordinary rural areas, and 30 poor rural areas. In the second stage, six villages or communities were selected from each site by using the proportional method of population. In the third stage, 75 households were randomly selected from each selected village or community. All family members in each selected family were included as respondents after signing the informed consent form [23]. In the present study, a total of 2643 middle-aged (ages 46 to 53) women with complete blood glucose, blood lipid, blood pressure, height, weight, and dietary information were selected as participants. This study was approved by the ethics review committee of the National Institute for Nutrition and Health, Chinese Center for Disease Control and Prevention (No. 2013-018); all participants signed the informed consent.

2.2. Anthropometric Measurements

Height was measured in centimeters with an accuracy of 0.1 cm. Fasting weight was measured in kilograms with an accuracy of 0.1 kg. Waist circumference (WC) was measured twice, and the mean value was taken (the accuracy was 0.1 cm). A standard mercury sphygmomanometer (scale 0 to 300 mmHg) was applied to measure blood pressure (BP). Systolic and diastolic blood pressure (SBP and DBP) were determined by the onset (KrotkoFF phase I) and the disappearance (KrotkoFF phase V) of sound, respectively. BP was measured three times, and the average of the three readings was calculated for the final analysis. Blood samples harvested from veins was checked for fasting blood glucose (FBG), oral glucose tolerance (OGTT), and serum lipids [23].

2.3. Categories of LTSB

In the present study, LTSB included watching TV, using a computer, playing video games, reading, and doing homework in spare time, information on which was collected using an interview-administrated questionnaire. The participants were asked to recall the average total daily amount of LTSB over the past year. The values of LTSD at the 25th and 75th percentiles of a frequency distribution divided the data into three parts. LTSD < 2 h was classified as low-level LTSB, 2 h > LTSD < 3 h was classified as middle-level LTSB, and LTSD ≥ 3 h was classified as high-level LTSB.

2.4. Definitions of Outcome Variables

2.4.1. Diabetes

China’s national guidelines for the prevention and control of diabetes in primary care (2018) define diabetes as FBG ≥ 7.0 mmol/L or OGTT ≥ 11.1 mmol/L [9].

2.4.2. Dyslipidemia

Total cholesterol (TC) ≥ 6.2 mmol/L was defined as hypercholesterolemia. Triglyceride (TG) ≥ 2.3 mmol/L was defined as hypertriglyceridemia. High-density lipoprotein cholesterol (HDL-C) < 1.0 mmol/L was defined as low HDL-C [10].

2.4.3. Hypertension

According to the Chinese guideline for the prevention and treatment of hypertension, the diagnostic criteria for hypertension were SBP ≥ 140 mmHg and/or DBP ≥ 90 mmHg [24].

2.4.4. Overweight and Obesity

Chinese guidelines for the prevention and control of overweight and obesity for adults classify body mass index (BMI) < 18.5 kg/m2 as underweight, BMI between 18.5 kg/m2 and 23.9 kg/m2 as normal, BMI between 24.0 kg/m2 and 27.9 kg/m2 as overweight, and BMI ≥ 28 kg/m2 as obese. Central obesity was defined as waist circumference ≥80 cm for females [25].

2.4.5. Metabolic Syndrome

The diagnostic criteria for MetS were based on the National Cholesterol Education Program Expert Panel (NCEP) and Adult Treatment Panel III (ATP III), which were modified in 2004 and adapted for Asians. The definition of MetS consists of the clinical condition meeting at least three of the following risk factors: WC ≥ 80 cm, HDL-C < 1.0 mmol/L or under treatment, TG ≥ 1.7 mmol/L or under treatment, increased blood pressure >130/85 mmHg or under treatment, and FBG≥ 5.6 mmol/L or under treatment [26].

2.5. Statistical Analyses

Statistical analysis was performed using the Statistical Analysis System (SAS) 9.4 software (SAS Institute Inc., Cary, NC, USA). The continuous variables were described by means and standard deviation and analyzed by linear regression. The categorical variables were described by rate and analyzed by chi-square test. Simple linear regression and multiple linear regression were used to analyze the relationship between LTSD and TC content, TG content, HDL-C content, WC, and BMI. Educational level (primary school and below = 0, junior high school = 1, senior high school and above = 2), occupation (employer = 1, others = 2, farmer = 3), and economic level (per capita annual income CNY 40,000 was the high economic level), drinking (no drinking = 0, drinking = 1), leisure exercise level (no leisure exercise = 0, leisure exercise = 1), energy intake (kcal), and fat energy ratio (%) were included in the model as confounders. In previous studies, SB was usually incorporated into the logistic model as a categorical variable; however, when a continuous variable is converted into a categorical variable, some of the original information is often lost, especially in the study of biological clinical indicators [27]. When the variable is continuous, a nonlinear correlation method is strongly recommended, and restrictive cubic splines (RCS) is a good method. This approach was used in some studies to examine the association of certain continuous variables (such as shift years [28] and sleep duration [29]) with disease, as well as the relationship between sedentary behaviors and mortality in patients with type 2 diabetes [30]. Therefore, in the present study, we applied this method to investigate the relationship between LTSD as a continuous variable and the risk of diabetes, MetS, hypercholesteremia, hypertriglyceridemia, low HDL-C level, hyperglycemia, hypertension, central obesity, overweight, and obesity. In addition, a limitation of the RCS method is reflected by using a large number of knots, which may lead to “overfitting” the data [27]. Therefore, we only chose three knots in the analysis to avoid such a phenomenon.

3. Results

3.1. Baseline Characteristics of the Study Population

A total of 2643 participants were investigated. Overall, 17.5% had a low-level LTSB, 36.4% had a middle-level LTSB, and 46.1% had a high-level LTSB. The level of LTSB varied from urban to rural (p < 0.05), and in those with different levels of education (p < 0.05). With an increase in LTSB level, TC content, TG content, and the prevalence of hyperlipidemia increased (Table 1).
Table 1

Basic characteristics between middle-aged women with different leisure-time sedentary behavior (LTSB) levels.

VariablesLow-Level LTSB (<2.0 h/day)Middle-Level LTSB (2.0–3.0 h/day)High-Level LTSB (≥3.0 h/day) p
Total463 (17.5%)962 (36.4%)1218 (46.1%)
Residence (%)
Urban47.545.557.2<0.0001
Rural52.554.542.8
Education (%)
Primary school and low46.437.930.9<0.0001
Middle school33.736.537.7
High school and above19.925.631.4
Family income
Low income50.846.944.60.184
Middle income36.536.039.2
High income8.010.810.8
Unknown4.86.35.5
BMI (kg/m²)24.3 ± 13.324.6 ± 3.324.6 ± 3.60.097
WC (cm)81.3 ± 9.081.5 ± 8.981.3 ± 9.30.203
Leisure exercise (%)13.813.615.30.509
Drinking (%)19.217.317.20.583
Energy intake (kcal)1912.8 ± 737.61936.2 ± 743.21908.7 ± 818.80.485
Fat energy ratio (%)26.6 ± 13.327.2 ± 12.827.7 ± 12.80.000
TC (mmol/L)4.66 ± 0.934.72 ± 0.934.83 ± 0.960.007
TG (mmol/L)1.38 ± 0.911.43 ± 0.991.49 ± 1.070.031
HDL-C (mmol/L)1.21 ± 0.341.22 ± 0.321.22 ± 0.330.264
Hypercholesteremia (%)4.35.28.20.002
Hypertriglyceridemia (%)11.012.613.10.528
Low HDL-C level (%)29.225.025.90.230
Diabetes (%)5.26.85.90.477
Hypertension (%)20.725.925.90.068
BMI status <0.0001
Underweight2.22.42.4
Normal46.240.843.3
Overweight37.442.638.1
Obesity14.314.216.3
Central Obesity (%)55.355.955.70.975
Metabolic syndrome (%)25.727.428.20.601

Note: BMI: body mass index; WC: waist circumference; TC: total cholesterol; TG: triglyceride; HDL-C: high-density lipoprotein cholesterol.

3.2. The Relationship between LTSB and TC, TG, HDL-C, WC, and BMI

Table 2 shows the association of LTSD with TC and TG content, WC, BMI, and HDL-C. The results of simple linear regression showed that, for every hourly increase in LTSD, TC and TG increased by 0.04 mmol/L and 0.03 mmol/L respectively. After adjusting for potential influencing factors, multiple linear regression results showed that, for every hourly increase in LTSD, TC and TG increased by 0.03 mmol/L (p < 0.05) and 0.04 mmol/L (p < 0.05), respectively.
Table 2

Linear regression analysis of the relationship between leisure-time sedentary duration (LTSD) and TC, TG, HDL-C, WC, and BMI.

VariablesSimple Linear RegressionMultiple Linear Regression 1
β1 p 1 β2 p 2
TC0.040.0040.030.019
TG0.030.0300.040.015
HDL-C0.000.5340.000.336
WC0.150.2530.230.076
BMI0.080.1120.100.055

Note: β simple linear regression coefficient; : p value of simple linear regression; β multiple linear regression coefficient. : p value of multiple linear regression. 1 Region, education, income, alcohol consumption, exercise, daily energy intake, and fat energy ratio were adjusted for all multiple linear regression models.

3.3. RCS Curves for LTSD and Metabolic Diseases

Figure 1 shows the RCS curves for LTSD with respect to the risks of metabolic diseases, while the odds ratio (OR) and 95% confidence interval (CI) of statistically significant outcome variables are listed in Table 3, Table 4, Table 5 and Table 6. The risks of MetS (p for trend = 0.0276), obesity (p for trend = 0.0369), hypertension (p for trend = 0.0062), and hypercholesteremia (p for trend = 0.0033) gradually increased with each additional unit of increased LTSD.
Figure 1

Restrictive cubic spline (RCS) curves for sedentary duration and (A) diabetes, (B) central obesity, (C) overweight, (D) obesity, (E) hypercholesterolemia, (F) hypertriglyceridemia, (G) low HDL-C level, (H) hypertension, and (I) metabolic syndrome (MetS). Region, education, income, alcohol consumption, exercise, daily energy intake, and fat energy ratio were adjusted for all RCS curves.

Table 3

Odds ratio (OR) and 95% confidence interval (CI) for the restrictive cubic spline of MetS.

LTSDOR95% CIp for Trend
1.31.06(0.79–1.42)0.0276
2.31.12(0.72–1.75)
3.31.21(0.76–1.93)
4.31.32(0.85–2.06)
5.31.44(0.93–2.22)
6.31.56(1.00–2.44)
7.31.70(1.06–2.72)
8.31.85(1.10–3.10)
9.32.01(1.13–3.58)
10.32.19(1.15–4.16)
11.32.39(1.17–4.87)
Table 4

OR and 95% CI for the restrictive cubic spline of obesity.

LTSDOR95% CIp for Trend
1.01.10(0.83–1.47)0.0369
2.01.21(0.72–2.05)
3.01.33(0.73–2.42)
4.01.46(0.82–2.58)
5.01.59(0.91–2.76)
6.01.75(1.00–3.04)
7.01.90(1.07–3.39)
8.02.08(1.11–3.88)
9.02.27(1.15–4.51)
10.02.49(1.17–5.31)
11.02.72(1.17–6.31)
Table 5

OR and 95% CI for the restrictive cubic spline of hypertension.

LTSDOR95% CIp for Trend
2.01.54(1.00–2.38)0.0062
3.01.75(1.06–2.89)
4.01.85(1.14–2.99)
5.01.94(1.22–3.08)
6.02.03(1.27–3.24)
7.02.13(1.30–3.48)
8.02.23(1.31–3.80)
9.02.34(1.30–4.21)
10.02.45(1.28–4.71)
11.02.57(1.24–5.31)
Table 6

OR and 95% CI for the restrictive cubic spline of hypercholesteremia.

LTSDOR95% CIp for Trend
1.72.02(0.94–4.34)0.0033
2.72.64(1.00–6.96)
3.73.00(1.14–7.88)
4.73.31(1.31–8.32)
5.73.64(1.47–8.99)
6.74.01(1.62–9.97)
7.74.42(1.73–11.33)
8.74.87(1.80–13.17)
9.75.37(1.85–15.60)
10.75.92(1.87–18.77)

4. Discussion

In this cross-sectional study of middle-aged women, we found that an increase in TC and TG content was associated with the increase in LTSD. The odds ratios of MetS, obesity, hypertension, and hypercholesteremia were constantly on the rise with the increase in LTSD. LTSB is a kind of static behavior that, in addition to having a low energy expenditure, may also underlie a deleterious influence on other lifestyle and eating behaviors. For example, foods are more accessible while sitting at a table or desk than when engaging in other activities such as walking or doing housework, which may lead to an unconscious increase in food intake. At present, watching TV, using computers, and using mobile phones are becoming the main recreational activities for people in their leisure time, which makes people more susceptible to temptation from advertisements for energy-dense foods on their electronic equipment, leading to them being more likely to eat more calories or form unhealthy eating patterns [13,31]. In addition, the amount of time available for other physical activities is compressed for a prolonged sedentary duration, which can contribute to metabolic disease if excess energy cannot be consumed in time. Another reason for the detrimental effect of LTSB on metabolic diseases is that LTSBs cause metabolic dysfunction. SB inhibits lipoprotein lipase (LPL) activity, which is an enzyme that promotes the uptake of free fatty acids into skeletal muscle and adipose tissue [32] Low LPL levels can partially account for the elevated levels of circulating triglycerides, the reduced levels of HDL cholesterol, and the increased risk of cardiovascular disease [32]. Moreover, SB can also affect carbohydrate metabolism by changing muscle glucose transporter (GLUT) protein content, which is essential to glucose uptake [32]. With prolonged sedentary duration, reduced skeletal muscle contraction may lead to decreased lipoprotein lipase activity, decreased triglyceride clearance, decreased oral glucose load clearance, and decreased glucose-stimulated insulin secretion [33,34,35]. The relationship between SB and metabolic diseases was discussed in previous studies; however, the components of SB vary. Most researchers paid more attention to the relationship between watching TV and metabolic diseases [19,36], but other SBs should not be ignored. It seems more suitable to include all SBs rather than particular kinds of SBs when estimating the association of LTSB with metabolic diseases. Especially in this rapidly developing society, smart phones and computers have largely replaced televisions as new forms of entertainment, such that using TV time as a proxy for total LTSD paints only a partial picture. In this study, SB referred to total LTSD. Moreover, we considered LTSD as a continuous variable by using RCS regression to explore its relationship with metabolic risks rather than as a categorical variable by using logistic regression (as done in most previous research), allowing us to preserve the original characteristics of the data. We also adjusted for demographic characteristics, alcohol consumption, exercise, and dietary factors, thereby improving the reliability of the results. Our study also had some limitations. First, this was a cross-sectional study and, as such, the causal relationship between LTSB and metabolic diseases could not be determined. Second, LTSD was obtained through questionnaires, with limited accuracy. Third, active physical activity might have a positive effect on metabolic diseases. However, we only adjusted for whether the participants exercised regularly in their spare time or not. The quantity and the intensity of physical activity were not determined. Overall, the present study still provides important clues and supplementary evidence for future prospective studies and randomized clinical trials on the relationship between SB and metabolic diseases. It is of great significance for preserving and enhancing the health of middle-aged women.

5. Conclusions

The results of the present study suggest that higher LTSB is associated with the presence of MetS, obesity, hypertension, and hypercholesteremia in middle-aged women. Considering that middle-aged women are susceptible to metabolic diseases, this study has important implications for addressing prolonged LTSD as a new public health issue in women at that age.
  30 in total

1.  Sedentary behaviors and the risk of incident hypertension: the SUN Cohort.

Authors:  Juan José Beunza; Miguel Angel Martínez-González; Shah Ebrahim; Maira Bes-Rastrollo; Jorge Núñez; José Alfredo Martínez; Alvaro Alonso
Journal:  Am J Hypertens       Date:  2007-11       Impact factor: 2.689

2.  Longitudinal association of leisure time physical activity and sedentary behaviors with body weight among Chinese adults from China Health and Nutrition Survey 2004-2011.

Authors:  C Su; X F Jia; Z H Wang; H J Wang; Y F Ouyang; B Zhang
Journal:  Eur J Clin Nutr       Date:  2017-01-11       Impact factor: 4.016

3.  [Scheme of the 2010-2012 Chinese nutrition and health surveillance].

Authors:  Liyun Zhao; Guansheng Ma; Jianhua Piao; Jian Zhang; Dongmei Yu; Yuna He; Junsheng Huo; Xiaoqi Hu; Zhenyu Yang; Xiaoguang Yang
Journal:  Zhonghua Yu Fang Yi Xue Za Zhi       Date:  2016-03

4.  Cubic splines to model relationships between continuous variables and outcomes: a guide for clinicians.

Authors:  J Gauthier; Q V Wu; T A Gooley
Journal:  Bone Marrow Transplant       Date:  2019-10-01       Impact factor: 5.483

5.  Physical activity and television viewing in relation to risk of undiagnosed abnormal glucose metabolism in adults.

Authors:  David W Dunstan; Jo Salmon; Neville Owen; Timothy Armstrong; Paul Z Zimmet; Timothy A Welborn; Adrian J Cameron; Terence Dwyer; Damien Jolley; Jonathan E Shaw
Journal:  Diabetes Care       Date:  2004-11       Impact factor: 19.112

6.  [Prevalence of metabolic syndrome in Chinese adults in 2010-2012].

Authors:  Y N He; W H Zhao; L Y Zhao; D M Yu; J Zhang; X G Yang; G G Ding
Journal:  Zhonghua Liu Xing Bing Xue Za Zhi       Date:  2017-02-10

7.  2016 Chinese guidelines for the management of dyslipidemia in adults.

Authors: 
Journal:  J Geriatr Cardiol       Date:  2018-01       Impact factor: 3.327

8.  Global, regional, and national comparative risk assessment of 79 behavioural, environmental and occupational, and metabolic risks or clusters of risks in 188 countries, 1990-2013: a systematic analysis for the Global Burden of Disease Study 2013.

Authors:  Mohammad H Forouzanfar; Lily Alexander; H Ross Anderson; Victoria F Bachman; Stan Biryukov; Michael Brauer; Richard Burnett; Daniel Casey; Matthew M Coates; Aaron Cohen; Kristen Delwiche; Kara Estep; Joseph J Frostad; K C Astha; Hmwe H Kyu; Maziar Moradi-Lakeh; Marie Ng; Erica Leigh Slepak; Bernadette A Thomas; Joseph Wagner; Gunn Marit Aasvang; Cristiana Abbafati; Ayse Abbasoglu Ozgoren; Foad Abd-Allah; Semaw F Abera; Victor Aboyans; Biju Abraham; Jerry Puthenpurakal Abraham; Ibrahim Abubakar; Niveen M E Abu-Rmeileh; Tania C Aburto; Tom Achoki; Ademola Adelekan; Koranteng Adofo; Arsène K Adou; José C Adsuar; Ashkan Afshin; Emilie E Agardh; Mazin J Al Khabouri; Faris H Al Lami; Sayed Saidul Alam; Deena Alasfoor; Mohammed I Albittar; Miguel A Alegretti; Alicia V Aleman; Zewdie A Alemu; Rafael Alfonso-Cristancho; Samia Alhabib; Raghib Ali; Mohammed K Ali; François Alla; Peter Allebeck; Peter J Allen; Ubai Alsharif; Elena Alvarez; Nelson Alvis-Guzman; Adansi A Amankwaa; Azmeraw T Amare; Emmanuel A Ameh; Omid Ameli; Heresh Amini; Walid Ammar; Benjamin O Anderson; Carl Abelardo T Antonio; Palwasha Anwari; Solveig Argeseanu Cunningham; Johan Arnlöv; Valentina S Arsic Arsenijevic; Al Artaman; Rana J Asghar; Reza Assadi; Lydia S Atkins; Charles Atkinson; Marco A Avila; Baffour Awuah; Alaa Badawi; Maria C Bahit; Talal Bakfalouni; Kalpana Balakrishnan; Shivanthi Balalla; Ravi Kumar Balu; Amitava Banerjee; Ryan M Barber; Suzanne L Barker-Collo; Simon Barquera; Lars Barregard; Lope H Barrero; Tonatiuh Barrientos-Gutierrez; Ana C Basto-Abreu; Arindam Basu; Sanjay Basu; Mohammed O Basulaiman; Carolina Batis Ruvalcaba; Justin Beardsley; Neeraj Bedi; Tolesa Bekele; Michelle L Bell; Corina Benjet; Derrick A Bennett; Habib Benzian; Eduardo Bernabé; Tariku J Beyene; Neeraj Bhala; Ashish Bhalla; Zulfiqar A Bhutta; Boris Bikbov; Aref A Bin Abdulhak; Jed D Blore; Fiona M Blyth; Megan A Bohensky; Berrak Bora Başara; Guilherme Borges; Natan M Bornstein; Dipan Bose; Soufiane Boufous; Rupert R Bourne; Michael Brainin; Alexandra Brazinova; Nicholas J Breitborde; Hermann Brenner; Adam D M Briggs; David M Broday; Peter M Brooks; Nigel G Bruce; Traolach S Brugha; Bert Brunekreef; Rachelle Buchbinder; Linh N Bui; Gene Bukhman; Andrew G Bulloch; Michael Burch; Peter G J Burney; Ismael R Campos-Nonato; Julio C Campuzano; Alejandra J Cantoral; Jack Caravanos; Rosario Cárdenas; Elisabeth Cardis; David O Carpenter; Valeria Caso; Carlos A Castañeda-Orjuela; Ruben E Castro; Ferrán Catalá-López; Fiorella Cavalleri; Alanur Çavlin; Vineet K Chadha; Jung-Chen Chang; Fiona J Charlson; Honglei Chen; Wanqing Chen; Zhengming Chen; Peggy P Chiang; Odgerel Chimed-Ochir; Rajiv Chowdhury; Costas A Christophi; Ting-Wu Chuang; Sumeet S Chugh; Massimo Cirillo; Thomas K D Claßen; Valentina Colistro; Mercedes Colomar; Samantha M Colquhoun; Alejandra G Contreras; Cyrus Cooper; Kimberly Cooperrider; Leslie T Cooper; Josef Coresh; Karen J Courville; Michael H Criqui; Lucia Cuevas-Nasu; James Damsere-Derry; Hadi Danawi; Lalit Dandona; Rakhi Dandona; Paul I Dargan; Adrian Davis; Dragos V Davitoiu; Anand Dayama; E Filipa de Castro; Vanessa De la Cruz-Góngora; Diego De Leo; Graça de Lima; Louisa Degenhardt; Borja del Pozo-Cruz; Robert P Dellavalle; Kebede Deribe; Sarah Derrett; Don C Des Jarlais; Muluken Dessalegn; Gabrielle A deVeber; Karen M Devries; Samath D Dharmaratne; Mukesh K Dherani; Daniel Dicker; Eric L Ding; Klara Dokova; E Ray Dorsey; Tim R Driscoll; Leilei Duan; Adnan M Durrani; Beth E Ebel; Richard G Ellenbogen; Yousef M Elshrek; Matthias Endres; Sergey P Ermakov; Holly E Erskine; Babak Eshrati; Alireza Esteghamati; Saman Fahimi; Emerito Jose A Faraon; Farshad Farzadfar; Derek F J Fay; Valery L Feigin; Andrea B Feigl; Seyed-Mohammad Fereshtehnejad; Alize J Ferrari; Cleusa P Ferri; Abraham D Flaxman; Thomas D Fleming; Nataliya Foigt; Kyle J Foreman; Urbano Fra Paleo; Richard C Franklin; Belinda Gabbe; Lynne Gaffikin; Emmanuela Gakidou; Amiran Gamkrelidze; Fortuné G Gankpé; Ron T Gansevoort; Francisco A García-Guerra; Evariste Gasana; Johanna M Geleijnse; Bradford D Gessner; Pete Gething; Katherine B Gibney; Richard F Gillum; Ibrahim A M Ginawi; Maurice Giroud; Giorgia Giussani; Shifalika Goenka; Ketevan Goginashvili; Hector Gomez Dantes; Philimon Gona; Teresita Gonzalez de Cosio; Dinorah González-Castell; Carolyn C Gotay; Atsushi Goto; Hebe N Gouda; Richard L Guerrant; Harish C Gugnani; Francis Guillemin; David Gunnell; Rahul Gupta; Rajeev Gupta; Reyna A Gutiérrez; Nima Hafezi-Nejad; Holly Hagan; Maria Hagstromer; Yara A Halasa; Randah R Hamadeh; Mouhanad Hammami; Graeme J Hankey; Yuantao Hao; Hilda L Harb; Tilahun Nigatu Haregu; Josep Maria Haro; Rasmus Havmoeller; Simon I Hay; Mohammad T Hedayati; Ileana B Heredia-Pi; Lucia Hernandez; Kyle R Heuton; Pouria Heydarpour; Martha Hijar; Hans W Hoek; Howard J Hoffman; John C Hornberger; H Dean Hosgood; Damian G Hoy; Mohamed Hsairi; Guoqing Hu; Howard Hu; Cheng Huang; John J Huang; Bryan J Hubbell; Laetitia Huiart; Abdullatif Husseini; Marissa L Iannarone; Kim M Iburg; Bulat T Idrisov; Nayu Ikeda; Kaire Innos; Manami Inoue; Farhad Islami; Samaya Ismayilova; Kathryn H Jacobsen; Henrica A Jansen; Deborah L Jarvis; Simerjot K Jassal; Alejandra Jauregui; Sudha Jayaraman; Panniyammakal Jeemon; Paul N Jensen; Vivekanand Jha; Fan Jiang; Guohong Jiang; Ying Jiang; Jost B Jonas; Knud Juel; Haidong Kan; Sidibe S Kany Roseline; Nadim E Karam; André Karch; Corine K Karema; Ganesan Karthikeyan; Anil Kaul; Norito Kawakami; Dhruv S Kazi; Andrew H Kemp; Andre P Kengne; Andre Keren; Yousef S Khader; Shams Eldin Ali Hassan Khalifa; Ejaz A Khan; Young-Ho Khang; Shahab Khatibzadeh; Irma Khonelidze; Christian Kieling; Daniel Kim; Sungroul Kim; Yunjin Kim; Ruth W Kimokoti; Yohannes Kinfu; Jonas M Kinge; Brett M Kissela; Miia Kivipelto; Luke D Knibbs; Ann Kristin Knudsen; Yoshihiro Kokubo; M Rifat Kose; Soewarta Kosen; Alexander Kraemer; Michael Kravchenko; Sanjay Krishnaswami; Hans Kromhout; Tiffany Ku; Barthelemy Kuate Defo; Burcu Kucuk Bicer; Ernst J Kuipers; Chanda Kulkarni; Veena S Kulkarni; G Anil Kumar; Gene F Kwan; Taavi Lai; Arjun Lakshmana Balaji; Ratilal Lalloo; Tea Lallukka; Hilton Lam; Qing Lan; Van C Lansingh; Heidi J Larson; Anders Larsson; Dennis O Laryea; Pablo M Lavados; Alicia E Lawrynowicz; Janet L Leasher; Jong-Tae Lee; James Leigh; Ricky Leung; Miriam Levi; Yichong Li; Yongmei Li; Juan Liang; Xiaofeng Liang; Stephen S Lim; M Patrice Lindsay; Steven E Lipshultz; Shiwei Liu; Yang Liu; Belinda K Lloyd; Giancarlo Logroscino; Stephanie J London; Nancy Lopez; Joannie Lortet-Tieulent; Paulo A Lotufo; Rafael Lozano; Raimundas Lunevicius; Jixiang Ma; Stefan Ma; Vasco M P Machado; Michael F MacIntyre; Carlos Magis-Rodriguez; Abbas A Mahdi; Marek Majdan; Reza Malekzadeh; Srikanth Mangalam; Christopher C Mapoma; Marape Marape; Wagner Marcenes; David J Margolis; Christopher Margono; Guy B Marks; Randall V Martin; Melvin B Marzan; Mohammad T Mashal; Felix Masiye; Amanda J Mason-Jones; Kunihiro Matsushita; Richard Matzopoulos; Bongani M Mayosi; Tasara T Mazorodze; Abigail C McKay; Martin McKee; Abigail McLain; Peter A Meaney; Catalina Medina; Man Mohan Mehndiratta; Fabiola Mejia-Rodriguez; Wubegzier Mekonnen; Yohannes A Melaku; Michele Meltzer; Ziad A Memish; Walter Mendoza; George A Mensah; Atte Meretoja; Francis Apolinary Mhimbira; Renata Micha; Ted R Miller; Edward J Mills; Awoke Misganaw; Santosh Mishra; Norlinah Mohamed Ibrahim; Karzan A Mohammad; Ali H Mokdad; Glen L Mola; Lorenzo Monasta; Julio C Montañez Hernandez; Marcella Montico; Ami R Moore; Lidia Morawska; Rintaro Mori; Joanna Moschandreas; Wilkister N Moturi; Dariush Mozaffarian; Ulrich O Mueller; Mitsuru Mukaigawara; Erin C Mullany; Kinnari S Murthy; Mohsen Naghavi; Ziad Nahas; Aliya Naheed; Kovin S Naidoo; Luigi Naldi; Devina Nand; Vinay Nangia; K M Venkat Narayan; Denis Nash; Bruce Neal; Chakib Nejjari; Sudan P Neupane; Charles R Newton; Frida N Ngalesoni; Jean de Dieu Ngirabega; Grant Nguyen; Nhung T Nguyen; Mark J Nieuwenhuijsen; Muhammad I Nisar; José R Nogueira; Joan M Nolla; Sandra Nolte; Ole F Norheim; Rosana E Norman; Bo Norrving; Luke Nyakarahuka; In-Hwan Oh; Takayoshi Ohkubo; Bolajoko O Olusanya; Saad B Omer; John Nelson Opio; Ricardo Orozco; Rodolfo S Pagcatipunan; Amanda W Pain; Jeyaraj D Pandian; Carlo Irwin A Panelo; Christina Papachristou; Eun-Kee Park; Charles D Parry; Angel J Paternina Caicedo; Scott B Patten; Vinod K Paul; Boris I Pavlin; Neil Pearce; Lilia S Pedraza; Andrea Pedroza; Ljiljana Pejin Stokic; Ayfer Pekericli; David M Pereira; Rogelio Perez-Padilla; Fernando Perez-Ruiz; Norberto Perico; Samuel A L Perry; Aslam Pervaiz; Konrad Pesudovs; Carrie B Peterson; Max Petzold; Michael R Phillips; Hwee Pin Phua; Dietrich Plass; Dan Poenaru; Guilherme V Polanczyk; Suzanne Polinder; Constance D Pond; C Arden Pope; Daniel Pope; Svetlana Popova; Farshad Pourmalek; John Powles; Dorairaj Prabhakaran; Noela M Prasad; Dima M Qato; Amado D Quezada; D Alex A Quistberg; Lionel Racapé; Anwar Rafay; Kazem Rahimi; Vafa Rahimi-Movaghar; Sajjad Ur Rahman; Murugesan Raju; Ivo Rakovac; Saleem M Rana; Mayuree Rao; Homie Razavi; K Srinath Reddy; Amany H Refaat; Jürgen Rehm; Giuseppe Remuzzi; Antonio L Ribeiro; Patricia M Riccio; Lee Richardson; Anne Riederer; Margaret Robinson; Anna Roca; Alina Rodriguez; David Rojas-Rueda; Isabelle Romieu; Luca Ronfani; Robin Room; Nobhojit Roy; George M Ruhago; Lesley Rushton; Nsanzimana Sabin; Ralph L Sacco; Sukanta Saha; Ramesh Sahathevan; Mohammad Ali Sahraian; Joshua A Salomon; Deborah Salvo; Uchechukwu K Sampson; Juan R Sanabria; Luz Maria Sanchez; Tania G Sánchez-Pimienta; Lidia Sanchez-Riera; Logan Sandar; Itamar S Santos; Amir Sapkota; Maheswar Satpathy; James E Saunders; Monika Sawhney; Mete I Saylan; Peter Scarborough; Jürgen C Schmidt; Ione J C Schneider; Ben Schöttker; David C Schwebel; James G Scott; Soraya Seedat; Sadaf G Sepanlou; Berrin Serdar; Edson E Servan-Mori; Gavin Shaddick; Saeid Shahraz; Teresa Shamah Levy; Siyi Shangguan; Jun She; Sara Sheikhbahaei; Kenji Shibuya; Hwashin H Shin; Yukito Shinohara; Rahman Shiri; Kawkab Shishani; Ivy Shiue; Inga D Sigfusdottir; Donald H Silberberg; Edgar P Simard; Shireen Sindi; Abhishek Singh; Gitanjali M Singh; Jasvinder A Singh; Vegard Skirbekk; Karen Sliwa; Michael Soljak; Samir Soneji; Kjetil Søreide; Sergey Soshnikov; Luciano A Sposato; Chandrashekhar T Sreeramareddy; Nicolas J C Stapelberg; Vasiliki Stathopoulou; Nadine Steckling; Dan J Stein; Murray B Stein; Natalie Stephens; Heidi Stöckl; Kurt Straif; Konstantinos Stroumpoulis; Lela Sturua; Bruno F Sunguya; Soumya Swaminathan; Mamta Swaroop; Bryan L Sykes; Karen M Tabb; Ken Takahashi; Roberto T Talongwa; Nikhil Tandon; David Tanne; Marcel Tanner; Mohammad Tavakkoli; Braden J Te Ao; Carolina M Teixeira; Martha M Téllez Rojo; Abdullah S Terkawi; José Luis Texcalac-Sangrador; Sarah V Thackway; Blake Thomson; Andrew L Thorne-Lyman; Amanda G Thrift; George D Thurston; Taavi Tillmann; Myriam Tobollik; Marcello Tonelli; Fotis Topouzis; Jeffrey A Towbin; Hideaki Toyoshima; Jefferson Traebert; Bach X Tran; Leonardo Trasande; Matias Trillini; Ulises Trujillo; Zacharie Tsala Dimbuene; Miltiadis Tsilimbaris; Emin Murat Tuzcu; Uche S Uchendu; Kingsley N Ukwaja; Selen B Uzun; Steven van de Vijver; Rita Van Dingenen; Coen H van Gool; Jim van Os; Yuri Y Varakin; Tommi J Vasankari; Ana Maria N Vasconcelos; Monica S Vavilala; Lennert J Veerman; Gustavo Velasquez-Melendez; N Venketasubramanian; Lakshmi Vijayakumar; Salvador Villalpando; Francesco S Violante; Vasiliy Victorovich Vlassov; Stein Emil Vollset; Gregory R Wagner; Stephen G Waller; Mitchell T Wallin; Xia Wan; Haidong Wang; JianLi Wang; Linhong Wang; Wenzhi Wang; Yanping Wang; Tati S Warouw; Charlotte H Watts; Scott Weichenthal; Elisabete Weiderpass; Robert G Weintraub; Andrea Werdecker; K Ryan Wessells; Ronny Westerman; Harvey A Whiteford; James D Wilkinson; Hywel C Williams; Thomas N Williams; Solomon M Woldeyohannes; Charles D A Wolfe; John Q Wong; Anthony D Woolf; Jonathan L Wright; Brittany Wurtz; Gelin Xu; Lijing L Yan; Gonghuan Yang; Yuichiro Yano; Pengpeng Ye; Muluken Yenesew; Gökalp K Yentür; Paul Yip; Naohiro Yonemoto; Seok-Jun Yoon; Mustafa Z Younis; Zourkaleini Younoussi; Chuanhua Yu; Maysaa E Zaki; Yong Zhao; Yingfeng Zheng; Maigeng Zhou; Jun Zhu; Shankuan Zhu; Xiaonong Zou; Joseph R Zunt; Alan D Lopez; Theo Vos; Christopher J Murray
Journal:  Lancet       Date:  2015-09-11       Impact factor: 79.321

9.  Association of Sleep Duration and Overweight/Obesity among Children in China.

Authors:  Jing Fan; Caicui Ding; Weiyan Gong; Fan Yuan; Yan Zhang; Ganyu Feng; Chao Song; Ailing Liu
Journal:  Int J Environ Res Public Health       Date:  2020-03-17       Impact factor: 3.390

10.  Physical activity, sedentary leisure-time and risk of incident type 2 diabetes: a prospective study of 512 000 Chinese adults.

Authors:  Derrick A Bennett; Huaidong Du; Fiona Bragg; Yu Guo; Neil Wright; Ling Yang; Zheng Bian; Yiping Chen; Canqing Yu; Sisi Wang; Fanwen Meng; Jun Lv; Junshi Chen; Liming Li; Robert Clarke; Zhengming Chen
Journal:  BMJ Open Diabetes Res Care       Date:  2019-12-18
View more
  1 in total

1.  Authoritative Parents and Dominant Children as the Center of Communication for Sustainable Healthy Aging.

Authors:  Elizabeth Wianto; Elty Sarvia; Chien-Hsu Chen
Journal:  Int J Environ Res Public Health       Date:  2021-03-22       Impact factor: 3.390

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.