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1. Introduction
Haskell et al. confirmed that moderate physical exercise can help with weight loss and the reduction of the risk of cardiovascular diseases (CVD) [1]. Physical exercise is now viewed as one of the treatment options for diabetes mellitus (DM) and CVD. The World Health Organization (WHO) recommends that individuals perform at least 150 minutes of moderate-intensity exercise or 75 minutes of high-intensity exercise, weekly, to maintain physical function and health [2]. However, there are still not enough studies involved in the relationship between physical activity and chronic disease based on a Chinese population, especially people in different health conditions.
Kidney disease, as one of the main causes of death, can lead to an increased incidence of CVD [3]. It is reported that in developing countries, chronic kidney disease is associated with high morbidity. The estimated number of people with chronic kidney disease, in China, has reached 119.5 million in 2011 [4, 5]. However, the majority of people with renal dysfunction are unaware of it and still do more exercise to keep fit. Hence, it is significant to identify the risk factors for renal dysfunction, for prevention as well as early treatment.
There are some studies that showed moderate-intensity exercise could be beneficial to reduce the risk of CVD in patients with chronic kidney disease [6]. However, O’Keefe et al. found that participants in long-term high-intensity physical activity increased the risk of atrial fibrosis and atherosclerosis [7]. Additionally, Hiraki et al. found that moderate-intensity exercise did not improve the renal function of patients with chronic kidney disease [8]. A decreased estimated glomerular filtration rate (eGFR) and increased urinary protein-to-creatinine ratio were observed after high-intensity exercise in athletes and healthy individuals [9, 10]. But there is still a lack of evidence on the relationship between metabolic equivalent of energy (MET) (MET hours per week), a measure of physical activity, and eGFR. Therefore, the aim of the cross-sectional study is to investigate the relationships between MET hours per week and eGFR as well as the relationships in different subgroups, based on a large Chinese population.
2. Materials and Methods
2.1. Participants
This cross-sectional study was part of the REACTION Study, an ongoing longitudinal study, designed to investigate the association between diabetes and the risk of cancer among the Chinese population, reported previously [11]. Participants aged 40 years and older were recruited between May 2011 and December 2011. This study used a cluster random sampling method and was conducted in the Gansu, Guangxi, Guangdong, Henan, Hubei, Liaoning, Shanghai, and Sichuan provinces, in China. Initially, a total of 45,130 participants were recruited. Participants with missing information and a history of kidney cancer and related diseases and without eGFR data were excluded as shown in Figure 1. Finally, a total number of 43767 individuals were included in the cross-sectional study.
[figure omitted; refer to PDF]2.2. Data Collection
Data were collected by the same trained staff, according to standardized operational procedures. All the participants completed a standard questionnaire with the assistance of the trained staff. The questionnaire included education level, lifestyle, physical activity, smoking status, drinking status, medical history, and family history of tumors and DM. Regular smokers were defined as those who smoked at least one cigarette per day. Occasional smokers were participants who smoked less than one cigarette per day or less than 7 cigarettes per week. Regular drinkers were defined as participants who had consumed alcohol at least once a week for over six months. Occasional drinkers were defined as participants who drank less than once a week. Height and weight were clinically measured (when participants were wearing light clothing), and body mass index (BMI) was calculated using the formula
After a resting period of five minutes, participants’ blood pressure and pulse were measured three times with intervals of one minute in a seated position. The pulse rate was measured while the blood pressure was recorded. After at least 12 hours of fasting overnight, the first fasting blood samples of all the participants were obtained. Patients without a history of DM underwent a 75 g oral glucose tolerance test; they were required to drink 300 mL of a glucose solution containing 75 g of glucose within 5 minutes, and after 2 hours, the second venous blood sampling was performed. All blood samples were centrifuged for 30 minutes and stored at -80°C by the professional staff. Blood glucose, blood lipids, triglycerides (TGs), high-density lipoprotein (HDL), low-density lipoprotein (LDL), and serum creatinine were detected by the automatic enzyme method. This cross-sectional study is part of the REACTION study, using the baseline data, and the design and methodology of the REACTION study have previously been described in detail [11, 12].
2.3. Definition of Variables
The variables were defined as follows: hypertension (any self-reported history of hypertension or systolic blood pressure
Based on the Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) showed as Table 1, the eGFRs were calculated [13].
Table 1
Sex | Age (years) | Formula (mL/min/1.732) |
Female | ≤62 | |
>62 | ||
Male | ≤62 | |
>62 |
According to the minimum recommendations provided by the American College of Sports Medicine and American Heart Association, we classified the participants into 3 groups based on MET hours per week as follows: <7.5 MET hours per week that equals <150 minutes per week of moderate-intensity physical activity, ≥7.5 MET hours per week <21, and ≥21 MET hours per week that equals ≥420 minutes per week of moderate-intensity physical activity on the basis of the Institute of Medicine recommendation [14, 15].
The primary outcome was the loss of renal function, which was defined as
2.4. Statistical Analysis
All statistical analyses were performed using Empower(R) (www.empowerstats.com, X & Y Solutions Inc., Boston, MA) and R (http://www.R-project.org). A
Data are expressed as median (25th percentile-75th percentile) for continuous variables of nonnormal distribution. Category variables are expressed as percentage (%). The continuous variables of nonnormal distribution were analyzed using the Kruskal-Wallis test. The category variables were tested using the chi-square test. Linear regression analysis was conducted to detect the relationship between different MET hours per week and eGFR as a continuous variable. A logistic regression model was built to investigate the correlation between different MET hours per week and renal dysfunction which was defined as
3. Results
3.1. Demographic Data and Hematologic Parameters
A total of 43767 participants were included in our study. The average age was 56.84 (51.16-63.00) years. A total of 30.84% of the participants were male and 69.16% were female. DM, hypertension, and cardiovascular events were observed in 14.66%, 31.54%, and of 4.21% of the participants, respectively. A total of 8945 (20.44%) individuals had the decreased eGFR defined as an
Table 2
Characteristics of the participants in different groups of MET hours per week.
Variables | Total | Physical activity (MET hours per week) | |||
<7.5 | ≥21 | ||||
43767 | 8258 | 5874 | 29635 | ||
Age (y) | 56.84 (51.16-63.00) | 56.61 (50.52-62.97) | 57.49 (51.92-64.09) | 56.80 (51.12-62.83) | <0.001 |
Male (%) | 13497 (30.84%) | 2392 (28.97%) | 1697 (28.89%) | 9408 (31.75%) | <0.001 |
BMI (kg/m2) | 24.13 (21.98-26.42) | 24.05 (21.83-26.49) | 24.16 (22.04-26.46) | 24.13 (22.02-26.39) | 0.881 |
SBP (mmHg) | 128.00 (116.00-143.00) | 128.00 (116.00-143.00) | 129.00 (116.00-144.00) | 128.00 (115.00-142.00) | <0.001 |
DBP (mmHg) | 76.00 (70.00-84.00) | 76.00 (70.00-84.00) | 77.00 (70.00-84.00) | 76.00 (70.00-84.00) | 0.237 |
Pulse (bpm) | 78.00 (71.00-86.00) | 78.00 (72.00-86.00) | 78.00 (71.00-86.00) | 78.00 (71.00-86.00) | <0.001 |
HDL (mmol/L) | 1.29 (1.08-1.53) | 1.30 (1.08-1.55) | 1.29 (1.08-1.51) | 1.29 (1.08-1.53) | <0.001 |
LDL (mmol/L) | 2.90 (2.31-3.53) | 2.90 (2.29-3.52) | 2.90 (2.29-3.54) | 2.95 (2.37-3.56) | <0.001 |
TG (mmol/L) | 1.30 (0.93-1.88) | 1.30 (0.93-1.88) | 1.35 (0.95-1.93) | 1.30 (0.93-1.87) | 0.048 |
GGT (mmol/L) | 20.00 (14.00-30.00) | 20.00 (14.00-31.00) | 20.00 (14.00-31.00) | 20.00 (14.00-30.00) | 0.131 |
FBG (mmol/L) | 5.46 (5.09-5.93) | 5.46 (5.10-5.92) | 5.45 (5.08-5.92) | 5.46 (5.09-5.94) | 0.005 |
PBG (mmol/L) | 7.08 (5.86-8.81) | 7.09 (5.91-8.86) | 7.10 (5.83-8.80) | 7.07 (5.85-8.80) | 0.015 |
HbA1c (%) | 5.80 (5.50-6.10) | 5.80 (5.50-6.10) | 5.80 (5.50-6.10) | 5.80 (5.50-6.10) | 0.614 |
eGFR (mL/min/1.732) | 100.10 (92.43-106.43) | 101.00 (93.56-107.24) | 99.81 (91.92-105.90) | 99.90 (92.25-106.27) | <0.001 |
>90 | 34822 (79.56%) | 6699 (81.12%) | 4605 (78.40%) | 23518 (79.36%) | |
≤90 | 8945 (20.44%) | 1559 (18.88%) | 1269 (21.60%) | 6117 (20.64%) | |
Region (%) | <0.001 | ||||
Northern | 19484 (44.52%) | 3227 (39.08%) | 2721 (46.32%) | 13536 (45.68%) | |
Southern | 24283 (55.48%) | 5031 (60.92%) | 3153 (53.68%) | 16099 (54.32%) | |
Education (%) | <0.001 | ||||
Illiteracy | 1911 (4.37%) | 557 (6.74%) | 204 (3.47%) | 1150 (3.88%) | |
Primary school | 5187 (11.85%) | 1150 (3.88%) | 1150 (3.88%) | 1150 (3.88%) | |
Junior high school | 14985 (34.24%) | 2876 (34.83%) | 1803 (30.69%) | 10306 (34.78%) | |
Senior high school | 15780 (36.05%) | 2643 (32.01%) | 2176 (37.04%) | 10961 (36.99%) | |
College | 5904 (13.49%) | 1053 (12.75%) | 1105 (18.81%) | 3746 (12.64%) | |
Smoking status (%) | <0.001 | ||||
No | 37641 (86.00%) | 7156 (86.66%) | 5110 (86.99%) | 25375 (85.63%) | |
Occasional smokers | 1047 (2.39%) | 156 (1.89%) | 122 (2.08%) | 769 (2.59%) | |
Regular smokers | 5079 (11.60%) | 946 (11.46%) | 642 (10.93%) | 3491 (11.78%) | |
Drinking status (%) | <0.001 | ||||
No | 32375 (73.97%) | 6280 (76.05%) | 4374 (74.46%) | 21721 (73.30%) | |
Occasional drinkers | 8348 (19.07%) | 1428 (17.29%) | 1092 (18.59%) | 5828 (19.67%) | |
Regular drinkers | 3044 (6.96%) | 550 (6.66%) | 408 (6.95%) | 2086 (7.04%) | |
Prevalence of diseases (%) | |||||
Diabetes mellitus | 6418 (14.66%) | 1294 (15.67%) | 798 (13.59%) | 4326 (14.60%) | <0.001 |
Hypertension | 13804 (31.54%) | 2614 (31.65%) | 1990 (33.88%) | 9200 (31.04%) | <0.001 |
Cardiovascular events | 1842 (4.21%) | 312 (3.78%) | 296 (5.04%) | 1234 (4.16%) | <0.001 |
Medication (%) | |||||
Antihypertensive drugs | 5955 (13.61%) | 905 (10.96%) | 990 (16.85%) | 4060 (13.70%) | <0.001 |
Hypoglycemic drugs | 55 (0.13%) | 17 (0.21%) | 2 (0.03%) | 36 (0.12%) | <0.001 |
Lipid-lowering drugs | 399 (0.91%) | 64 (0.78%) | 74 (1.26%) | 261 (0.88%) | 0.007 |
Family history of disease (%) | |||||
Family history of diabetes | 6593 (15.06%) | 1018 (12.33%) | 1040 (17.71%) | 4535 (15.30%) | <0.001 |
Family history of tumor | 6109 (13.96%) | 994 (12.04%) | 975 (16.60%) | 4140 (13.97%) | <0.001 |
Data of characteristics expressed as median (25th percentile-75th percentile) for continuous variables of nonnormal distribution and percentage (%) for categorical variables. BMI: body mass index; SBP: systolic blood pressure; DBP: diastolic blood pressure; eGFR: estimated glomerular filtration rate; TG: triglyceride; LDL: low-density lipoprotein cholesterol; HDL: high-density lipoprotein cholesterol; GGT: gamma-glutamyltranspeptidase; FBG: 0-hour fasting blood glucose; PBG: 2-hour postprandial blood glucose. An expenditure of 7.5 MET hours per week is equivalent to 150 minutes per week of moderate-intensity physical activity, the minimum recommended by the federal government; 21 MET hours per week is equivalent to 60 minutes per day (420 min/week) of moderate-intensity physical activity, recommended by the Institute of Medicine.
3.2. Different MET Hours per Week and the Risk of Decreased eGFR
As shown in Table 3, higher MET hours per week was associated with the risk of the decreased eGFR (7.5 to <21:
Table 3
Correlation analysis between physical activity (MET hours per week) and the risk of decreased eGFR.
Variable | Nonadjusted | Model I | Model II | |||
eGFR category | ||||||
Physical activity (MET hours per week) | 0.0047 | <0.0001 | <0.0001 | |||
<7.5 | 1.0 | 1.0 | 1.0 | |||
7.5 to <21 | 1.18 (1.09, 1.29) | 1.12 (1.01, 1.23) | 1.14 (1.01, 1.29) | |||
≥21 | 1.12 (1.05, 1.19) | 1.27 (1.18, 1.37) | 1.24 (1.14, 1.36) | |||
Continuous eGFR (mL/min/1.73 m2) | ||||||
Physical activity (MET hours per week) | 0.0009 | <0.0001 | <0.0001 | |||
<7.5 | 0 | 0 | 0 | |||
7.5 to <21 | -1.38 (-1.90, -0.86) | -0.58 (-1.04, -0.12) | -0.45 (-0.85, -0.04) | |||
≥21 | -0.82 (-1.20, -0.44) | -0.93 (-1.26, -0.60) | -0.64 (-0.94, -0.34) |
Nonadjusted model. Model I adjusted for age and BMI; model II adjusted for age, sex, BMI, region, education level, SBP, DBP, pulse, LDL, HDL, TG, FBG, PBG, HbA1c, GGT, smoking status, drinking status, history of hypertension, cardiovascular history, diabetes history, medication history, and family history of diabetes and tumors.
3.3. Different MET Hours per Week and the Risk of eGFR in Subgroups
As shown in Table 4 and Figure 2, there was a clear association between different MET hours per week and the risk of decreased eGFR in different subgroups. Compared to men expending less than 7.5 MET hours per week, those expending 7.5 to <21 MET hours per week had an OR of 1.05 (95% CI [0.89, 1.25]) and those expending ≥21 MET hours per week had a higher OR of 1.18 (95% CI [1.05, 1.34]) in model II (
Table 4
Correlation analysis between physical activity (MET hours per week) and the risk of decreased eGFR in subgroups.
Variable | Nonadjusted | Model I | Model II | ||||
Male | eGFR category | ||||||
Physical activity (MET hours per week) | 0.2692 | 0.0310 | 0.0035 | ||||
<7.5 | 1.0 | 1.0 | 1.0 | ||||
7.5 to <21 | 1.27 (1.12, 1.44) | 1.05 (0.90, 1.23) | 1.05 (0.89, 1.25) | ||||
≥21 | 1.10 (1.00, 1.20) | 1.13 (1.01, 1.26) | 1.18 (1.05, 1.34) | ||||
Continuous eGFR (mL/min/1.73 m2) | |||||||
Physical activity (MET hours per week) | 0.1464 | 0.8981 | 0.1057 | ||||
<7.5 | 0 | 0 | 0 | ||||
7.5 to <21 | -1.95 (-2.95, -0.96) | -0.18 (-0.94, 0.59) | -0.16 (-0.92, 0.60) | ||||
≥21 | 0.08 (-0.63, 0.80) | -0.00 (-0.56, 0.55) | -0.43 (-0.98, 0.13) | ||||
Female | eGFR category | ||||||
Physical activity (MET hours per week) | 0.5679 | <0.0001 | 0.0001 | ||||
<7.5 | 1.0 | 1.0 | 1.0 | ||||
7.5 to <21 | 1.19 (1.04, 1.37) | 1.25 (1.05, 1.48) | 1.25 (1.04, 1.49) | ||||
≥21 | 1.01 (0.91, 1.12) | 1.34 (1.17, 1.52) | 1.33 (1.15, 1.52) | ||||
Continuous eGFR (mL/min/1.73 m2) | |||||||
Physical activity (MET hours per week) | 0.0143 | 0.0001 | <0.0001 | ||||
<7.5 | 0 | 0 | 0 | ||||
7.5 to <21 | -1.16 (-1.68, -0.64) | -0.74 (-1.21, -0.26) | -0.53 (-1.00, -0.07) | ||||
≥21 | -0.63 (-1.01, -0.25) | -0.74 (-1.08, -0.39) | -0.75 (-1.09, -0.41) | ||||
eGFR category | |||||||
Physical activity (MET hours per week) | 0.0351 | 0.0549 | 0.2080 | ||||
<7.5 | 1.0 | 1.0 | 1.0 | ||||
7.5 to <21 | 1.19 (0.89, 1.60) | 1.11 (0.82, 1.50) | 1.16 (0.82, 1.64) | ||||
≥21 | 1.26 (1.02, 1.57) | 1.23 (0.99, 1.53) | 1.20 (0.93, 1.55) | ||||
Continuous eGFR (mL/min/1.73 m2) | |||||||
Physical activity (MET hours per week) | 0.0172 | 0.1714 | 0.0031 | ||||
<7.5 | 0 | 0 | 0 | ||||
7.5 to <21 | -0.94 (-1.39, -0.49) | -0.37 (-0.77, 0.03) | -0.53 (-0.84, -0.22) | ||||
≥21 | -0.50 (-0.82, -0.19) | -0.24 (-0.52, 0.04) | -0.30 (-0.52, -0.08) | ||||
Age 55-64 years | eGFR category | ||||||
Physical activity (MET hours per week) | <0.0001 | <0.0001 | <0.0001 | ||||
<7.5 | 1.0 | 1.0 | 1.0 | ||||
7.5 to <21 | 1.05 (0.92, 1.21) | 1.04 (0.90, 1.20) | 1.09 (0.91, 1.31) | ||||
≥21 | 1.22 (1.11, 1.35) | 1.24 (1.12, 1.38) | 1.26 (1.10, 1.45) | ||||
Continuous eGFR (mL/min/1.73 m2) | |||||||
Physical activity (MET hours per week) | <0.0001 | <0.0001 | <0.0001 | ||||
<7.5 | 0 | 0 | 0 | ||||
7.5 to <21 | -0.69 (-1.35, -0.02) | -0.71 (-1.36, -0.06) | -0.70 (-1.28, -0.12) | ||||
≥21 | -1.22 (-1.71, -0.73) | -1.22 (-1.71, -0.74) | -1.06 (-1.49, -0.63) | ||||
eGFR category | |||||||
Physical activity (MET hours per week) | 0.7888 | 0.2445 | 0.7046 | ||||
<7.5 | 1.0 | 1.0 | 1.0 | ||||
7.5 to <21 | 1.11 (0.96, 1.28) | 1.18 (1.01, 1.37) | 1.15 (0.95, 1.38) | ||||
≥21 | 1.05 (0.94, 1.17) | 1.23 (1.10, 1.38) | 1.15 (1.00, 1.32) | ||||
Continuous eGFR (mL/min/1.73 m2) | |||||||
Physical activity (MET hours per week) | 0.6376 | 0.7733 | 0.9339 | ||||
<7.5 | 0 | 0 | 0 | ||||
7.5 to <21 | -0.52 (-2.24, 1.20) | -1.15 (-2.80, 0.50) | -0.31 (-1.73, 1.11) | ||||
≥21 | -0.51 (-1.81, 0.78) | -2.43 (-3.69, -1.17) | -1.22 (-2.32, -0.13) | ||||
Nondiabetes | eGFR category | ||||||
Physical activity (MET hours per week) | 0.0001 | <0.0001 | <0.0001 | ||||
<7.5 | 1.0 | 1.0 | 1.0 | ||||
7.5 to <21 | 1.23 (1.09, 1.39) | 1.13 (0.98, 1.30) | 1.18 (0.99, 1.41) | ||||
≥21 | 1.21 (1.11, 1.32) | 1.39 (1.25, 1.55) | 1.42 (1.24, 1.62) | ||||
Continuous eGFR (mL/min/1.73 m2) | |||||||
Physical activity (MET hours per week) | 0.0001 | <0.0001 | <0.0001 | ||||
<7.5 | 0 | 0 | 0 | ||||
7.5 to <21 | -1.48 (-2.11, -0.85) | -0.51 (-1.04, 0.02) | -0.38 (-0.85, 0.09) | ||||
≥21 | -1.06 (-1.52, -0.60) | -1.07 (-1.46, -0.68) | -0.78 (-1.12, -0.44) | ||||
Prediabetes | eGFR category | ||||||
Physical activity (MET hours per week) | 0.8518 | 0.0113 | 0.9813 | ||||
<7.5 | 1.0 | 1.0 | 1.0 | ||||
7.5 to <21 | 1.21 (1.05, 1.39) | 1.17 (0.99, 1.38) | 1.22 (0.71, 2.08) | ||||
≥21 | 1.05 (0.94, 1.17) | 1.19 (1.05, 1.35) | 1.07 (0.71, 1.62) | ||||
Continuous eGFR (mL/min/1.73 m2) | |||||||
Physical activity (MET hours per week) | 0.0720 | 0.0025 | 0.2905 | ||||
<7.5 | 0 | 0 | 0 | ||||
7.5 to <21 | -1.69 (-2.70, -0.68) | -0.97 (-1.89, -0.05) | -1.70 (-3.46, 0.06) | ||||
≥21 | -0.94 (-1.69, -0.19) | -1.11 (-1.79, -0.43) | -0.80 (-2.12, 0.51) | ||||
Diabetes | eGFR category | ||||||
Physical activity (MET hours per week) | 0.7555 | 0.1762 | 0.7344 | ||||
<7.5 | 1.0 | 1.0 | 1.0 | ||||
7.5 to <21 | 1.05 (0.86, 1.30) | 1.03 (0.92, 1.16) | 1.21 (0.94, 1.56) | ||||
≥21 | 1.03 (0.89, 1.19) | 1.07 (0.96, 1.19) | 1.22 (1.00, 1.48) | ||||
Continuous eGFR (mL/min/1.73 m2) | |||||||
Physical activity (MET hours per week) | 0.5247 | 0.8804 | 0.4650 | ||||
<7.5 | 0 | 0 | 0 | ||||
7.5 to <21 | -0.53 (-2.21, 1.15) | -0.14 (-1.69, 1.41) | 0.12 (-1.26, 1.50) | ||||
≥21 | 0.26 (-0.93, 1.44) | 0.05 (-1.05, 1.15) | 0.33 (-0.65, 1.31) |
Nonadjusted model for none. Model I adjusted for age and BMI. Model II adjusted for age, sex, BMI, region, education level, SBP, DBP, pulse, LDL, HDL, TG, FBG, PBG, HbA1c, GGT, smoking status, drinking status, history of hypertension, cardiovascular history, diabetes history, medication history, and family history of diabetes and tumor.
[figure omitted; refer to PDF]As shown in Table 4 and Figure 2, MET hours per week was significantly associated with the risk of decreased eGFR in participants aged from 55 to less than 65 years, but not in participants younger than 55 or older than 65 years. After further adjustment for confounding factors, the multivariable adjusted OR for MET hours per week from 7.5 to less than 21 and more than 21 was 1.09 (95% CI [0.91, 1.31]) and 1.26 (95% CI [1.10, 1.45]), respectively (
Table 4 and Figure 2 show that there was a positive relationship of MET hours per week with the risk of decreased eGFR among participants without diabetes and prediabetes, but not among participants with diabetes or prediabetes. After further adjustment for the multiple variables, the relationship was strengthened and remained significant among participants without diabetes and prediabetes (7.5 to <21:
Table 5
Correlation analysis between physical activity (MET hours per week) and the risk of decreased eGFR in IFG, IGT, and IFG+IGT groups.
Variable | Nonadjusted | Model I | Model II | ||||
IFG | eGFR category | ||||||
Physical activity (MET hours per week) | 0.5640 | 0.6828 | 0.5091 | ||||
<7.5 | 1.0 | 1.0 | 1.0 | ||||
7.5 to <21 | 1.14 (0.80, 1.63) | 0.88 (0.58, 1.34) | 1.22 (0.71, 2.08) | ||||
≥21 | 0.96 (0.74, 1.25) | 0.90 (0.66, 1.23) | 1.07 (0.71, 1.62) | ||||
Continuous eGFR (mL/min/1.73 m2) | |||||||
Physical activity (MET hours per week) | 0.9681 | 0.7192 | 0.4421 | ||||
<7.5 | 0 | 0 | 0 | ||||
7.5 to <21 | -2.11 (-4.37, 0.16) | -0.60 (-2.61, 1.41) | -1.70 (-3.46, 0.06) | ||||
≥21 | -0.38 (-2.05, 1.29) | -0.23 (-1.71, 1.25) | -0.80 (-2.12, 0.51) | ||||
IGT | eGFR category | ||||||
Physical activity (MET hours per week) | 0.5841 | 0.0030 | 0.0685 | ||||
<7.5 | 1.0 | 1.0 | 1.0 | ||||
7.5 to <21 | 1.19 (1.00, 1.43) | 1.21 (0.98, 1.49) | 1.21 (0.94, 1.56) | ||||
≥21 | 1.07 (0.94, 1.22) | 1.28 (1.09, 1.49) | 1.22 (1.00, 1.48) | ||||
Continuous eGFR (mL/min/1.73 m2) | |||||||
Physical activity (MET hours per week) | 0.0575 | 0.0031 | 0.0344 | ||||
<7.5 | 0 | 0 | 0 | ||||
7.5 to <21 | -1.55 (-2.83, -0.27) | -0.99 (-2.15, 0.17) | -0.76 (-1.78, 0.27) | ||||
≥21 | -1.11 (-2.05, -0.16) | -1.38 (-2.24, -0.52) | -0.87 (-1.64, -0.11) | ||||
IFG+IGT | eGFR category | ||||||
Physical activity (MET hours per week) | 0.4556 | 0.6495 | 0.9494 | ||||
<7.5 | 1.0 | 1.0 | 1.0 | ||||
7.5 to <21 | 1.30 (0.93, 1.81) | 1.21 (0.82, 1.78) | 1.37 (0.85, 2.21) | ||||
≥21 | 1.04 (0.80, 1.34) | 1.09 (0.81, 1.46) | 1.06 (0.74, 1.53) | ||||
Continuous eGFR (mL/min/1.73 m2) | |||||||
Physical activity (MET hours per week) | 0.7212 | 0.3478 | 0.3827 | ||||
<7.5 | 0 | 0 | 0 | ||||
7.5 to <21 | -1.79 (-4.18, 0.60) | -1.10 (-3.27, 1.06) | -0.78 (-2.69, 1.14) | ||||
≥21 | -0.66 (-2.44, 1.11) | -0.87 (-2.48, 0.74) | -0.72 (-2.15, 0.71) |
The combination of the propensity score and multivariable model was used to analyze the association between MET and eGFR, including total population and subgroups. In order to further adjust for confounding factors, a logistic regression model adjusted for the propensity score was also used and the results are consistent with our previous results, which are presented in Supplementary Materials (available here).
The above results showed that the association between MET hours per week and the risk of decreased eGFR can be modified by age and diabetes status, and we found significant interactions with age and diabetes states as shown in Figure 2.
4. Discussion
This cross-sectional study shows that higher MET hours per week is significantly associated with the risk of decreased eGFR. After further investigation, the study indicates that the results vary in different subgroups of age and diabetic states. Compared to participants engaged in less than 7.5 MET hours per week (equivalent to less than 150 minutes per week of moderate-intensity exercise), those taking part in more than 7.5 MET hours per day (equivalent to more than 150 to less than 420 minutes or more than 420 minutes per week of moderate-intensity exercise) are more likely to have a decreased eGFR, suggesting renal dysfunction probably, especially in participants aged from 55 to less than 65 years or those without diabetes and prediabetes.
Some studies showed that physical activity is beneficial to reducing mortality [2]. However, other studies indicated that vigorous exercise has been found to be associated with an increased risk of CVD [18, 19]. Therefore, the association between different intensities of exercise and the risk of decreased eGFR is still not consistent. To the best of our knowledge, this is the first study to show that more than 7.5 MET hours per week of moderate-intensity exercise (equivalent to 150 minutes per week or more than 60 minutes per day) is associated with the risk of decreased eGFR, especially in different subgroups of age and diabetic states.
The relationship might be partially explained by the following mechanisms. Due to excessive physical activity causing oxidative stress [20, 21], there is an imbalance between the reactive oxygen species (ROS) and antioxidants produced by excessive physical activity [20, 22]. In 1978, Dillard et al. showed that physical activity led to an increase in lipid peroxidation [23]. Moreover, it could lead to an increased release of catecholamine; this, in turn, promotes the production of free radicals. In addition, a high level of physical activity is associated with temporary hypoxia in many organs, including the kidney [20]. During the course of physical activity, the blood of the visceral organs is diverted, to increase the blood supply to the active skeletal muscle and skin. After physical activity, reoxygenation occurs in hypoxic tissues. Reoxygenation and the production of ROS are related [24], and an increase in these can result in increased levels of oxidative stress and oxygen free radicals. The increased oxygen free radicals can damage lipid, protein, and DNA. ROS causes lipid peroxidation, resulting in cell membrane fluid loss and cell lysis. Also, it causes the loss of protein activity and attacks the nucleic acids which are related with DNA damage [25]. An imbalance in the production and scavenging of ROS can lead to cell dysfunction.
In some studies, excessive physical activity was associated with the low degree of inflammation. The elevated levels of neutrophils, monocytes, and leucocytes indicated a slightly greater degree of inflammation after high-intensity physical activity [20]. Long duration of physical activity may lead to greater metabolic demands and the increased release of stress hormones (catecholamines, growth hormones, and cortisol). The increased levels of stress hormones may affect the activation and mobilization of immune cells [26, 27]. Sahl et al. showed that among elderly adults, excessive physical activity increased plasma IL-6 concentrations and low-grade inflammation [28]. However, some studies found that physical activity reduced inflammation [29, 30]. An alternative explanation is that, during excessive physical activity, oxidative stress surpasses the antioxidant defense, resulting in a weakened anti-inflammatory effect, although, in the case of low-intensity physical activity, the antioxidant stress system defense may meet an increased production of ROS. Oxidative stress induces podocyte apoptosis, resulting in glomerular sclerosis and the activation of signal transduction, involved in renal tubular extracellular matrix secretion, to promote interstitial fibrosis [31]. Inflammation plays a key role in the loss of renal function.
In addition, renal tubular hypoxia is one of the important reasons of renal dysfunction. If physical activity is excessive, such as more than 60 minutes per day of moderate-intensity exercise, visceral hypoperfusion may occur. Kidney hypoperfusion is likely due to renal tubular hypoxia, and more than 21 MET hours per week might cause a decrease in renal blood flow leading to low perfusion of the kidneys, resulting in a decreased eGFR [32].
The above results of this cross-sectional study highlight 2 significant points for renal function protection. Firstly, long duration of exercise (more than 150 minutes per week of moderate-intensity or more than 60 minutes per day of moderate-intensity exercise) might not be appropriate for everyone. Individuals’ exercise plan should be considered based on individuals’ health conditions. Secondly, people aged from 55 to less than 65 years or without diabetes and prediabetes should maintain less than 150 minutes per week of moderate-intensity exercise to keep healthy. However, for those aged younger than 55 and older than 65 years or with prediabetes and diabetes, 60 minutes per day of moderate-intensity exercise may be a good recommendation to help them keep fit.
4.1. Perspective and Shortcomings
Our study is unique as the sample size was large. We conducted stratified analyses that fully explored not only the relationship between different MET hours per week and decreased eGFR but also the interaction. Though the confounding factors were adequately adjusted for as possible as we can, particularly in terms of sociological factors, region, and education level, it is possible that unmeasured variables are involved in that association between MET hours per week and the risk of decreased eGFR. Due to the study design, the changes occurring while carrying out the exercise were not monitored and the mechanism underlying the association between high MET hours per week and decreased eGFR was not explored.
5. Conclusion
In conclusion, more than 7.5 MET hours per week (equivalent to more than 150 minutes per week of moderate-intensity exercise) is associated with decreased eGFR. There is a clear association in participants aged ≥55 and <65 years and populations without diabetes and prediabetes, but not in populations aged <55 years or ≥65 years and those with prediabetes or diabetes. Duration of exercise may need to be individualized, to ensure optimal treatment in subgroups of different diabetic states. The positive effect of exercise may depend on the optimal duration of exercise based on individuals’ conditions. Should we just tell our patients to do some exercise to help them keep fit or provide individuals’ exercise plan in detail based on their condition?
Ethical Approval
The Chinese People’s Liberation Army General Hospital Ethics Committee approved the present study.
Consent
All participants signed informed consent forms.
Disclosure
This work is part of the REACTION study.
Conflicts of Interest
The authors report no conflicts of interest.
[1] W. L. Haskell, I. M. Lee, R. R. Pate, K. E. Powell, S. N. Blair, B. A. Franklin, C. A. Macera, G. W. Heath, P. D. Thompson, A. Bauman, American College of Sports Medicine, American Heart Association, "Physical activity and public health: updated recommendation for adults from the American College of Sports Medicine and the American Heart Association," Circulation, vol. 116 no. 9, pp. 1081-1093, DOI: 10.1161/CIRCULATIONAHA.107.185649, 2007.
[2] World Health Organization, "Global strategy on diet, physical activity and health: physical activity and adults," 2011. http://www.who.int/mediacentre/factsheets/fs385/en/
[3] A. S. Levey, R. Atkins, J. Coresh, E. P. Cohen, A. J. Collins, K. U. Eckardt, M. E. Nahas, B. L. Jaber, M. Jadoul, A. Levin, N. R. Powe, J. Rossert, D. C. Wheeler, N. Lameire, G. Eknoyan, "Chronic kidney disease as a global public health problem: approaches and initiatives - a position statement from Kidney Disease Improving Global Outcomes," Kidney International, vol. 72 no. 3, pp. 247-259, DOI: 10.1038/sj.ki.5002343, 2007.
[4] A. S. Levey, J. Coresh, "Chronic kidney disease," Lancet, vol. 379 no. 9811, pp. 165-180, DOI: 10.1016/S0140-6736(11)60178-5, 2012.
[5] L. Zhang, F. Wang, L. Wang, W. Wang, B. Liu, J. Liu, M. Chen, Q. He, Y. Liao, X. Yu, N. Chen, J. E. Zhang, Z. Hu, F. Liu, D. Hong, L. Ma, H. Liu, X. Zhou, J. Chen, L. Pan, W. Chen, W. Wang, X. Li, H. Wang, "Prevalence of chronic kidney disease in China: a cross-sectional survey," Lancet, vol. 379 no. 9818, pp. 815-822, DOI: 10.1016/S0140-6736(12)60033-6, 2012.
[6] A. J. Rankin, A. C. Rankin, P. Macintyre, W. S. Hillis, "Walk or run? Is high-intensity exercise more effective than moderate-intensity exercise at reducing cardiovascular risk?," Scottish Medical Journal, vol. 57 no. 2, pp. 99-102, DOI: 10.1258/smj.2011.011284, 2012.
[7] J. H. O'Keefe, H. R. Patil, C. J. Lavie, A. Magalski, R. A. Vogel, P. A. McCullough, "Potential adverse cardiovascular effects from excessive endurance exercise," Mayo Clinic Proceedings, vol. 87 no. 6, pp. 587-595, DOI: 10.1016/j.mayocp.2012.04.005, 2012.
[8] K. Hiraki, A. Kamijo-Ikemori, T. Yasuda, C. Hotta, K. P. Izawa, S. Watanabe, T. Sugaya, K. Kimura, "Moderate-intensity single exercise session does not induce renal damage," Journal of Clinical Laboratory Analysis, vol. 27 no. 3, pp. 177-180, DOI: 10.1002/jcla.21579, 2013.
[9] M. Machado, E. N. Zini, S. D. Valadão, M. Z. Amorim, T. Z. Barroso, W. de Oliveira, "Relationship of glomerular filtration rate and serum CK activity after resistance exercise in women," International Urology and Nephrology, vol. 44 no. 2, pp. 515-521, DOI: 10.1007/s11255-011-9963-4, 2012.
[10] N. Shavandi, A. Samiei, R. Afshar, A. Saremi, R. Sheikhhoseini, "The effect of exercise on urinary gamma-glutamyltransferase and protein levels in elite female karate athletes," Asian Journal of Sports Medicine, vol. 3 no. 1, pp. 41-46, DOI: 10.5812/asjsm.34724, 2012.
[11] G. Ning, The REACTION Study Group, "Risk evaluation of cancers in Chinese diabetic individuals: a lONgitudinal (REACTION) study," Journal of Diabetes, vol. 4 no. 2, pp. 172-173, DOI: 10.1111/j.1753-0407.2012.00182.x, 2012.
[12] Y. Bi, J. Lu, W. Wang, Y. Mu, J. Zhao, C. Liu, L. Chen, L. Shi, Q. Li, Q. Wan, S. Wu, T. Yang, L. Yan, Y. Liu, G. Wang, Z. Luo, X. Tang, G. Chen, Y. Huo, Z. Gao, Q. Su, Z. Ye, Y. Wang, G. Qin, H. Deng, X. Yu, F. Shen, L. Chen, L. Zhao, J. Zhang, J. Sun, M. Dai, M. Xu, Y. Xu, Y. Chen, S. Lai, Z. T. Bloomgarden, D. Li, G. Ning, "Cohort profile: risk evaluation of cancers in Chinese diabetic individuals: a longitudinal (REACTION) study," Journal of Diabetes, vol. 6 no. 2, pp. 147-157, DOI: 10.1111/1753-0407.12108, 2014.
[13] A. S. Levey, L. A. Stevens, C. H. Schmid, Y. (. L.). Zhang, A. F. Castro, H. I. Feldman, J. W. Kusek, P. Eggers, F. van Lente, T. Greene, J. Coresh, for the CKD-EPI (Chronic Kidney Disease Epidemiology Collaboration), "A new equation to estimate glomerular filtration rate," Annals of Internal Medicine, vol. 150 no. 9, pp. 604-612, DOI: 10.7326/0003-4819-150-9-200905050-00006, 2009.
[14] Institute of Medicine, Dietary Reference Intakes for Energy, Carbohydrate, Fiber, Fat, Fatty Acids, Cholesterol, Protein, and Amino Acids (Macronutrients), 2002.
[15] I.-M. Lee, L. Djoussé, H. D. Sesso, L. Wang, J. E. Buring, "Physical activity and weight gain prevention," Journal of the American Medical Association, vol. 303 no. 12, pp. 1173-1179, DOI: 10.1001/jama.2010.312, 2010.
[16] C. C. Lin, C. I. Li, C. S. Liu, W. Y. Lin, C. H. Lin, M. M. Lai, Y. D. Lee, C. C. Chen, C. W. Yang, T. C. Li, "Risks of decreased renal function and increased albuminuria for glycemic status and metabolic syndrome components: Taichung Community Health Study," BioMed Research International, vol. 2014,DOI: 10.1155/2014/841497, 2014.
[17] K. U. Eckardt, J. Coresh, O. Devuyst, R. J. Johnson, A. Köttgen, A. S. Levey, A. Levin, "Evolving importance of kidney disease: from subspecialty to global health burden," The Lancet, vol. 382 no. 9887, pp. 158-169, DOI: 10.1016/S0140-6736(13)60439-0, 2013.
[18] I. M. Lee, C. C. Hsieh, R. S. Paffenbarger, "Exercise intensity and longevity in men. The Harvard Alumni Health Study," JAMA, vol. 273 no. 15, pp. 1179-1184, DOI: 10.1001/jama.1995.03520390039030, 1995.
[19] T. J. Quinn, H. A. Sprague, W. D. van Huss, H. W. Olson, "Caloric expenditure, life status, and disease in former male athletes and non-athletes," Medicine & Science in Sports & Exercise, vol. 22 no. 6, pp. 742-750, DOI: 10.1249/00005768-199012000-00002, 1990.
[20] F. Seifi-Skishahr, M. Siahkohian, B. Nakhostin-Roohi, "Influence of aerobic exercise at high and moderate intensities on lipid peroxidation in untrained men," Journal of Sports Medicine and Physical Fitness, vol. 48 no. 4, pp. 515-521, 2008.
[21] W. L. Knez, J. S. Coombes, D. G. Jenkins, "Ultra-endurance exercise and oxidative damage: implications for cardiovascular health," Sports Medicine, vol. 36 no. 5, pp. 429-441, DOI: 10.2165/00007256-200636050-00005, 2006.
[22] C. E. Cooper, N. B. J. Vollaard, T. Choueiri, M. T. Wilson, "Exercise, free radicals and oxidative stress," Biochemical Society Transactions, vol. 30 no. 2, pp. 280-285, DOI: 10.1042/bst0300280, 2002.
[23] C. J. Dillard, R. E. Litov, W. M. Savin, E. E. Dumelin, A. L. Tappel, "Effects of exercise, vitamin E, and ozone on pulmonary function and lipid peroxidation," Journal of Applied Physiology, vol. 45 no. 6, pp. 927-932, DOI: 10.1152/jappl.1978.45.6.927, 1978.
[24] K. Koyama, M. Kaya, T. Ishigaki, J. Tsujita, S. Hori, T. Seino, A. Kasugai, "Role of xanthine oxidase in delayed lipid peroxidation in rat liver induced by acute exhausting exercise," European Journal of Applied Physiology and Occupational Physiology, vol. 80 no. 1, pp. 28-33, DOI: 10.1007/s004210050554, 1999.
[25] T. F. Slater, "Free-radical mechanisms in tissue injury," The Biochemical Journal, vol. 222 no. 1,DOI: 10.1042/bj2220001, 1984.
[26] K. Krüger, F. C. Mooren, "T cell homing and exercise," Exercise Immunology Review, vol. 13, pp. 37-54, 2007.
[27] D. A. McCarthy, I. Macdonald, M. Grant, M. Marbut, M. Watling, S. Nicholson, J. J. Deeks, A. J. Wade, J. D. Perry, "Studies on the immediate and delayed leucocytosis elicited by brief (30-min) strenuous exercise," European Journal of Applied Physiology and Occupational Physiology, vol. 64 no. 6, pp. 513-517, DOI: 10.1007/BF00843760, 1992.
[28] R. E. Sahl, P. R. Andersen, K. Gronbaek, T. H. Morville, M. Rosenkilde, H. K. Rasmusen, S. S. Poulsen, C. Prats, F. dela, J. W. Helge, "Repeated excessive exercise attenuates the anti-inflammatory effects of exercise in older men," Frontiers in Physiology, vol. 8,DOI: 10.3389/fphys.2017.00407, 2017.
[29] D. E. King, P. Carek, A. G. Mainous, W. S. Pearson, "Inflammatory markers and exercise: differences related to exercise type," Medicine & Science in Sports & Exercise, vol. 35 no. 4, pp. 575-581, DOI: 10.1249/01.MSS.0000058440.28108.CC, 2003.
[30] J. L. Abramson, V. Vaccarino, "Relationship between physical activity and inflammation among apparently healthy middle-aged and older US adults," Archives of Internal Medicine, vol. 162 no. 11, pp. 1286-1292, DOI: 10.1001/archinte.162.11.1286, 2002.
[31] S. Ogura, T. Shimosawa, "Oxidative stress and organ damages," Current Hypertension Reports, vol. 16 no. 8,DOI: 10.1007/s11906-014-0452-x, 2014.
[32] L. B. Rowell, "Human cardiovascular adjustments to exercise and thermal stress," Physiological Reviews, vol. 54 no. 1, pp. 75-159, DOI: 10.1152/physrev.1974.54.1.75, 1974.
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Abstract
Background. Physical activity is effective in preventing chronic diseases. However, the impact of different durations of exercise on human health is unknown, especially among people with diabetes or prediabetes. Objective. To explore the relationship between high MET hours per week and the change in glomerular filtration rate (eGFR) in the total population and different subgroups. Methods. A total of 43767 individuals from eight provinces, in China, were recruited. Logistic analysis was used to investigate the association. Participants were divided into 3 groups based on MET hours per week. The primary outcome was an
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Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer
Details







1 Department of Endocrinology, Chinese PLA General Hospital, Beijing, China; Medicine School of Nankai University, China
2 Department of Endocrinology, Chinese PLA General Hospital, Beijing, China
3 Shanghai National Research Centre for Endocrine and Metabolic Diseases, State Key Laboratory of Medical Genomics, Shanghai Institute for Endocrine and Metabolic Diseases, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China
4 Dalian Central Hospital, Dalian, Liaoning, China
5 First Hospital of Lanzhou University, Lanzhou, Gansu, China
6 Zhongshan University Sun Yat-sen Memorial Hospital, Guangzhou, Guangdong, China
7 Southwest Medical University Affiliated Hospital, Luzhou, Sichuan, China
8 First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, China
9 First Affiliated Hospital of Zhengzhou University, Zhenzhou, Henan, China
10 Wuhan Union Hospital, Huazhong University of Science and Technology, Wuhan, Hubei, China