Skip to main content
Heliyon logoLink to Heliyon
. 2024 Mar 29;10(7):e28845. doi: 10.1016/j.heliyon.2024.e28845

The association between physical activities combined with dietary habits and cardiovascular risk factors

Weiwei Wang a, Hairong Zhou a, Shengxiang Qi a, Huafeng Yang a,b, Xin Hong a,b,
PMCID: PMC11002288  PMID: 38596005

Abstract

Objectives

The aim of this study was to investigate the association between physical activities combined with dietary habits and cardiovascular risk factors in adults from Nanjing, China.

Methods

The cross-sectional survey conducted in 2017 involved a sample of 60 283 individuals aged ≥18 years in Nanjing municipality, China. The sampling method used was multistage stratified cluster sampling. The primary outcomes from multivariate logistic regression analysis with adjusted potential confounders were the relationships between physical activities combined with dietary habits and cardiovascular risk variables. Relative excess risk due to interaction (RERI), attributable proportion due to interaction (AP), and synergy index (S) were used to assess an additive interaction between dietary habits and physical activities.

Results

After adjusting potential confounders, cardiovascular risk factors were significantly associated with the association of physical inactivity and unhealthy diet, with the highest odds ratios (ORs) for low density lipoprotein-cholesterol (HLDL-c) (1.64, 95% CI [1.47, 1.84]) and hypertension (1.55, 95% CI [1.46, 1.64]). Additive interactions between physical inactivity and unhealthy diet were found in on cardiovascular risk factors of higher low-density lipoprotein-cholesterol (HLDL-c) (S, 2.57; 95% CI [1.27, 5.21]), type 2 diabetes (T2D) (S, 1.96; 95% CI [1.23, 3.13]), dyslipidemia (S, 1.69; 95% CI [1.08, 2.66]) and hypertension (S, 1.46; 95% CI [1.12, 1.89]). Their RERI was 0.39 (95% CI [0.18, 0.60]), 0.22 (95% CI [0.09, 0.35]), 0.11 (95% CI [0.03, 0.19]) and 0.17 (95% CI [0.06, 0.28]), respectively. OR of being HLDL-c, T2D, hypertension and dyslipidemia in participants of physical inactivity and unhealthy diet was 24%, 15%, 11% and 8.3%, respectively. Multiplicative interaction was detected in obesity, hypertension, T2D and HLDL-c.

Conclusion

An unhealthy diet and physical inactivity were strongly linked to cardiovascular risk factors. This study also showed that an unhealthy diet and physical inactivity combined to produce an additive effect on T2D, hypertension, HLDL-c, and dyslipidemia, suggesting a higher risk than the total of these factors, especially HLDL-c. Preventive strategies aimed at reducing cardiometabolic risks such as hypertension, T2D, HLDL-c, and dyslipidemia are necessary for targeting physical inactivity and unhealthy diet.

Keywords: Physical activities, Dietary habits, Cardiovascular diseases, Risk factors, Additive interaction

1. Introduction

The majority of deaths in China are caused by non-communicable diseases (NCDs). In 2019, they were responsible for 90.1% (9.60 million) of the 10.65 million deaths and 85.1% (0.325 billion) of the 0.382 billion disability-adjusted life years (DALYs) that occurred in Chinese people [1]. In China, the leading cause of deaths from cardiovascular diseases (CVDs) and disability-adjusted life years (DALYs) are caused by stroke and ischemic heart disease (IHD). In 2019, these conditions caused 4.58 million deaths (43.03% of all deaths) and 91.9 million DALYs (24.05% of all DALYs) [1]. China aims to cut the number of premature deaths from NCDs by one-third by 2030. In that case, there is an urgent need to concentrate on adopting current cost-effective therapies and health policies [2]. Various dietary-related dangers combined with a decline in physical activities have likely contributed to the sharp rise in incidence of NCDs [3,4]. There is mounting evidence linking unhealthy diet and physical inactivity to NCDs, especially CVDs [5] and metabolic syndromes (MetS) [6]. US cohort studies suggest that a healthy lifestyle with regular exercise and a balanced diet could reduce about 33% of cardiovascular deaths [7]. Cardiometabolic health is favorable with moderate to vigorous physical activities [8]. Additionally, numerous studies have demonstrated that exercise lowers non-traditional cardiovascular risk factors in adolescents, including inflammatory markers and irregular heart rate [[9], [10], [11]].

According to the 2008 Physical Activity Guidelines for Americans, an individual should engage in moderate-intensity aerobic activity for at least 150 min or vigorous-intensity aerobic activity for 75 min per week [12]. However, 43.3% of Americans are physically sedentary, an exceedingly common condition worldwide [13]. Similar figures are found in Shenzhen, China, where the percentage of people who are not physically active is 63.1% [14], and in Shanghai, where the percentage is only 18.4% of participants engaged in physical activities [15]. In 1990, there were 0.95 million (95% UI: 0.46 to 1.93 million) DALYs in China because of low physical inactivity; by 2019, that figure has risen to 2.51 million (95% UI: 1.20 to 4.84 million) [1].

With the economic boom, the dietary pattern of Chinese people has already changed [16]. The daily intake of vegetables and fruits is lower than the recommended level, but meat and salt are consumed in excess [17]. Long-term prospective observational studies have shown a potential causal relationship between certain dietary components (including fruits, vegetables, trans fat, and salt) and non-communicable diseases like diabetes, colon cancer, and cardiovascular diseases [18,19]. In 2019, the second leading modifiable risk factor for attributable CVDs burden was dietary risks. In China, dietary risks were responsible for 1.76 million (95% UI: 1.30 to 2.30 million) annual mortality and 39.05 million (95% UI: 29.19 to 49.71 million) annual DALYs [20]. Consuming a high intake of grains, beans, and veggies can reduce the risk of getting cardiometabolic disease [17]. In the current investigation, we examined 5 dietary components based on previously identified risky dietary factors for CVDs [21] and related studies in Nanjing, China [22,23].

Most prior studies focused on the single relationship between dietary habits and metabolic syndromes such as obesity, high blood pressure, dyslipidemia, and hyperglycemia or between physical activities and metabolic syndromes [[24], [25], [26]]. Metabolic syndromes have been identified as risk factors for several chronic diseases, including diabetes, renal disease, and cardiovascular diseases. The analysis of the literature reveals that the association between physical activities combined with dietary habits and cardiometabolic indicators are scant. Thus, the current study aims to investigate their relationship and interaction with cardiometabolic risk factors in Chinese individuals from Nanjing.

2. Methods

2.1. Study design and participants

The Chronic Diseases and Risk Factors Survey in Nanjing, which took place between January 2017 and June 2018, was a population-based, cross-sectional study conducted in Nanjing, in the eastern Chinese province of Jiangsu. The multistage stratified random cluster sampling method was adopted to obtain a representative sample of individuals in the general population over the age of 18 [27]. Firstly, five districts were random, taking into consideration the districts' geographic location and level of economic and cultural development. Secondly, four rural townships or urban streets from each chosen district were randomly chosen by probability proportion to size (PPS). Thirdly, three administrative villages or neighborhood communities from each township/street were selected based on PPS. Fourthly, one residential group with at least 50 households was randomly drawn by a simple random sampling from each chosen administrative village/neighborhood community. Finally, one eligible individual was randomly selected by a Kish grid from each chosen household. Inclusion criteria: (i) aged 18 years and older; (ii) lived in local villages/communities for at least 6 months; (iii) agreed to participate in all procedures and signed the informed consent. Exclusion criteria: (i) communal residences (e.g., university dormitory, military unit, nursing home); (ii) patients with severe diseases or cognitive, language, or mental disorders who could not participate in the interview; (iii) pregnancy. This study was approved by the Academic and Ethical Committee of Nanjing Municipal Center for Disease Control and Prevention (Nanjing CDC).

2.2. Sample size

The sample size of this study was roughly 58 250, based on the 10.4% prevalence of diabetes among Chinese individuals over the age of 18 [27], α of 0.05, the relative error of sampling of 5%, a design effect of 4 and a non-response rate of 10%. A total of 61 098 adult residents were invited to participate in the study, and finally, 60 283 eligible individuals were recruited.

2.3. Questionnaire data collection

Anthropometric measurements, laboratory testing, and face-to-face interviews were conducted at the local community health service center in the participants’ residential area to collect the date. Before collecting data via questionnaires, all investigators underwent standardized training to ensure data quality. A structured questionnaire was created that asked questions about age, gender, marital status, socioeconomic characteristics (education, occupation, and yearly household income) and lifestyle risk factors (drugs, alcohol, smoking, physical activities during leisure time, and dietary habits), as well as medical history.

Education level was divided into three categories: elementary (years of schooling <7 years), secondary (7–12 years), and beyond secondary (>12 years). The yearly household income per capita calculation entails dividing the aggregate household income by the entire count of family members, which is categorized into three groups: lower, middle, and higher. The physical activity level (PAL) was determined by the International Physical Activity Questionnaire (IPAQ) [12,28]. The four PAL domains—physical activity at work, at home, transportation, and leisure—were assessed and assigned a metabolic equivalent of task (MET). 4 and 8 METs, respectively, were used to represent moderate and vigorous activities. Based on a weekly average of 600 MET minutes, PAL was categorized as either physical inactivity (defined as <600 MET minutes) or physical activity (defined as ≥ 600 MET minutes). The amount of food and beverages consumed over the preceding year, as well as the frequency of consumption (daily, weekly, monthly, yearly, or never), were measured using a validated semi-quantitative food frequency questionnaire (FFQ) [29]. Examples of serving sizes were given to the participants, and they were asked to report how many serves they typically consumed of food and drink per time. Individuals were classified as having unhealthy dietary habits if they met three or more of the following criteria [30,31]: less than 400 g of fruits and vegetables per day, less than 300 g of dairy products per day, less than 25 g of bean products (e.g., tofu, dry beans, bean sprouts, soy chicken, and bean curd sheets), more than 100 g of red meat (like pork, beef, and mutton) per day, and more than 5 g of salt per day [32].

Participants were further divided into four groups: physical activities and healthy diet, physical activities and unhealthy diet, physical inactivity and healthy diet, and physical inactivity and unhealthy diet, with the first group as the reference.

2.4. Physical examinations

Each participant was instructed to wear light clothing and maintain an erect stance while barefoot in to measure their height and weight. The mid-point in a horizontal plane between the inferior margin of the last rib and the iliac crest was used to calculate the waist circumference (WC). The maximum protrusion level of the buttocks was used to measure the hip circumference (HC). The body weight (kg) divided by the square of the height (m) yields the body mass index (BMI). After 10 min of rest, three blood pressure (BP) readings were taken by skilled professionals using an electronic sphygmomanometer (OMRON HBP-1300, Japan). The mean value of the last two BP measurements was recorded.

2.5. Blood sample collection and biochemical analyses

Participants were collected venous blood samples after fasting overnight for at least 10 h. The glucose oxidase method was used to measure fasting blood glucose (FBG). Low-density lipoprotein cholesterol (LDL-c), high-density lipoprotein cholesterol (HDL-c), triglyceride (TG), and total cholesterol (TC) were measured utilizing an immunoassay analyzer (Abbott Laboratories, Illinois, USA).

2.6. Definition of cardiovascular risk factors

Participants were categorized into underweight (BMI<18.5 kg/m2), normal (18.5 kg/m2≤BMI<24.0 kg/m2), overweight (24.0 kg/m2≤BMI<28.0 kg/m2), and obesity (BMI≥28.0 kg/m2) according to the Chinese-specific cut-off point of BMI [33]. For men, center obesity was defined as WC ≥ 95 cm, and for women, WC ≥ 90 cm [33]. Diabetes was defined as FPG ≥7.0 mmol/L, and/or self-reported current treatment with anti-diabetes medication (insulin or oral hypoglycemic agents) [34]. Hypertension was defined as an average mean systolic BP (SBP) ≥140 mmHg and/or an average diastolic BP (DBP) ≥90 mmHg, and/or self-reported current treatment with antihypertensive medication in the past two weeks [35]. Dyslipidemia was defined as having at least one of the following in the field survey: LDL-C ≥4.1 mmol/L, HDL-C <1.0 mmol/L, TG ≥ 2.3 mmol/L, TC ≥ 6.2 mmol/L, and/or self-reported history of dyslipidemia and/or the use of antilipemic medication [36].

2.7. Statistical analysis

Numbers and proportions were expressed for categorical data, while mean ± standard deviation (SD) was utilized for continuous variables. The Chi-square test and variance analysis methods were applied to examine differences in categorical and continuous data, respectively. The weighted means or prevalence rates were determined by the weight coefficients to represent the total Nanjing adults aged 18 years and older. Weight coefficients included the sampling weight for differential selection probabilities, as well as the post-stratification weights, which harmonized the standard population of the 2009 Nanjing Sixth National Population Census in terms of age and gender composition [37].

Taking into consideration potential confounding variables, multivariate linear regression analyses were performed to identify the relationship between physical activities combined with dietary habits and continuous outcomes. Standardized beta coefficients with corresponding 95% confidence intervals (95% CIs) were calculated. Multivariate logistic regression analyses were used to identify the association between physical activities combined with dietary habits and binary outcomes. The results were presented as Odds ratio (OR) with the corresponding 95% CI. All models were adjusted for age, gender, education, occupation, income, smoking and drinking. Statistical analyses were conducted by SPSS software (version 20; IBM, Armonk, NY, USA). Statistical power analyses were performed using the ‘pwr’ R package [38]. 80% statistical power is the commonly accepted level [39]. All P-values had a two-tailed significance level of <0.05.

A multiplicative interaction was assessed through the term of physical activities dietary habits interaction in the multivariate logistic regression models. The additive interaction was analyzed using Excel 2019 software developed by Andersson et al. [40]. Relative risk due to interaction (RERI), attributable proportion (AP), synergy index (S) were calculated using the regression coefficients and covariance matrix obtained from the multi-variate logistic regression analyses.

RERI=OR11OR10OR01+1 (1)
S=(OR111)/[(OR011)+(OR101)] (2)
AP=RERI/OR11 (3)

where OR11 is the ratio in the group with exposures a and b (1 = exposed, 0 = unexposed) compared with the doubly unexposed group. If an additive interaction between the two risk factors is absent, the 95% CI of RERI and AP should contain 0, and the 95% CI of S should contain 1.

3. Results

3.1. Social-demographic and anthropometric characteristics of participants

The present study included 60 283 eligible individuals, 29 848 (49.5%) males and 30 435 (50.5%) females. The participants had an average age of 43.7 ± 16.4 years. Irrespective of dietary habits, individuals categorized as physically active demonstrated an increased probability of having a higher income, being male, exhibiting a lower WC and BMI, and consequently, a reduced prevalence of obesity in comparison to those who were physically inactive. The metabolic indicators generally improved as well, except DBP and TG. Individuals who were categorized as having unhealthy diets, regardless of their PAL status, were more likely to have higher levels of education and HC than those who adhered to a healthy diet. The highest annual household income per capita, HDL-c, and lowest BMI, HC and SBP were detected in participants of the physical activities and healthy diet group (Table 1).

Table 1.

Social-demographic and anthropometric characteristics of participants classified by physical activities and dietary habits.

Characteristics Physical activities
Physical inactivity
P value
Healthy diet Unhealthy diet Healthy diet Unhealthy diet
Social-demographic characteristics
Age (n, %) <0.001
 18–34 years 2023 (30.2) 6046 (39.6) 3717 (35.8) 11376 (40.7)
 35–59 years 2992 (44.8) 6402 (41.8) 4595 (44.3) 11543 (41.3)
 >60 years 1669 (25.0) 2836 (18.6) 2066 (19.9) 5018 (18.0)
Sex (n, %) <0.001
 Male 3520 (52.7) 8299 (54.3) 4815 (46.4) 13214 (47.3)
 Female 3164 (47.3) 6985 (45.7) 5563 (53.6) 14723 (52.7)
Marriage (n, %) <0.001
 Single 1310 (17.3) 3157 (21.9) 1624 (13.9) 4465 (16.7)
 Married/living with a partner 5981 (79.1) 10807 (75.0) 9582 (82.3) 21166 (79.4)
 Separated/divorced/widowed 270 (3.6) 443 (3.1) 444 (3.8) 1034 (3.9)
Socioeconomic characteristics
Annual household income per capita (thousand yuan) 40.1 (37.6) 39.4 (31.2) 38.0 (35.1) 35.2 (33.6) <0.001
Education level (n, %) <0.001
 <7 years 654 (9.8) 1034 (6.8) 1136 (10.9) 2634 (9.4)
 7–12 years 3291 (49.2) 6493 (42.5) 5149 (49.6) 12087 (43.3)
 >12 years 2739 (41.0) 7757 (50.7) 4093 (39.5) 13216 (47.3)
Occupation (n, %) <0.001
 Blue collar 2016 (30.2) 4472 (29.3) 3876 (37.3) 10162 (36.4)
 White collar 1983 (29.7) 5278 (34.5) 3056 (29.4) 9089 (32.5)
 Unemployed/retired/student 2685 (40.1) 5534 (36.2) 3446 (33.3) 8686 (31.1)
Obesity-related variables
BMI (kg/m2) 23.54 (3.32) 23.81 (3.40) 23.56 (3.22) 23.98 (3.24) <0.001
BMI classification (n, %) <0.001
 <18.5 kg/m2 220 (3.3) 617 (4.0) 424 (4.1) 1290 (4.6)
 18.5–23.9 kg/m2 3314 (49.6) 8313 (54.4) 5293 (51.0) 14935 (53.5)
 24.0–27.9 kg/m2 2427 (36.3) 5018 (32.8) 3519 (33.9) 9148 (32.7)
 ≥28.0 kg/m2 723 (10.8) 1336 (8.7) 1142 (11.0) 2564 (9.2)
WC (cm) 81.15 (9.72) 81.63 (9.79) 81.29 (9.42) 82.30 (9.41) <0.001
HC (cm) 93.46 (9.63) 94.24 (9.10) 94.06 (9.07) 94.85 (8.84) <0.001
Metabolism-related variables
SBP (mmHg) 122.89 (19.47) 124.04 (21.25) 123.40 (16.95) 125.13 (16.81) <0.001
DBP (mmHg) 77.01 (15.05) 77.92 (14.96) 77.06 (10.79) 78.09 (14.04) <0.001
FBG (mmol/L) 5.25 (1.47) 5.26 (1.61) 5.27 (1.47) 5.36 (1.52) <0.001
TC (mmol/L) 4.56 (1.10) 4.67 (1.07) 4.55 (1.11) 4.70 (1.17) <0.001
TG (mmol/L) 1.49 (1.09) 1.50 (1.19) 1.47 (1.13) 1.51 (1.14) 0.623
HDL-c (mmol/L) 1.49 (0.54) 1.45 (0.50) 1.46 (0.51) 1.43 (0.50) <0.001
LDL-c (mmol/L) 2.59 (0.85) 2.66 (0.86) 2.61 (0.87) 2.71 (0.88) <0.001

The weighted means or prevalence rates were calculated using the weight coefficients.

Physical activities and healthy diet group was considered as the reference.

Except for the age, sex, education level, occupation and BMI classification, other data were expressed as mean (standard deviation).

Blue collar referred as farmers, factory workers, forestry workers, fishers, salespersons, houseworkers and vehicle drivers; White collar referred as office workers, professional and technical personnel and government official staffs; BMI, body mass index; WC, waist circumference; HC, hip circumference; SBP, systolic blood pressure; DBP, diastolic blood pressure; FBG, fasting blood glucose; TC, total cholesterol; TG, triglycerides; HDL-c, high density lipoprotein-cholesterol; LDL-c, low density lipoprotein-cholesterol.

3.2. The association between physical activities combined with dietary habits and cardiovascular risk factors

The results of the linear regression analysis indicated a significant association between physical inactivity, an unhealthy diet, or a combination of physical inactivity and an unhealthy diet, and obesity as well as metabolic indicators. The group that engaged in physical activities and had an unhealthy diet (standardized β, 0.43; 95% CI [0.22, 0.64]), the group that engaged in physical inactivity and had a healthy diet (standardized β, 0.59; 95% CI [0.39, 0.79]), and the group that engaged in physical inactivity and had an unhealthy diet (standardized β, 1.18; 95% CI [0.93, 1.43]) exhibited a significant correlation with hip circumference (HC). Except for TG, diet and physical inactivity were positively correlated with markers linked to metabolism(Table 2).

Table 2.

The association between physical activities combined with healthy habits and cardiovascular risk factors.

Cardiovascular risk factors Physical activities
Physical inactivity
Statistical power %
Healthy diet Unhealthy diet
Healthy diet
Unhealthy diet
ꞵ (95% CI) P ꞵ (95% CI) P ꞵ (95% CI) P
BMI Reference −0.04 (−0.04, 0.11) 0.334 0.10 (−0.03, 0.18) <0.001 0.21 (0.13, 0.30) <0.001 91.70
WC Reference −0.07 (−0.29, 0.15) 0.554 0.34 (0.13, 0.55) 0.001 0.64 (0.38, 0.90) <0.001 83.10
HC Reference 0.43 (0.22, 0.64) <0.001 0.59 (0.39, 0.79) <0.001 1.18 (0.93, 1.43) <0.001 88.27
SBP Reference −0.17 (−0.59, 0.25) 0.433 1.20 (0.80, 1.61) <0.001 1.18 (0.68, 1.68) <0.001 80.63
DBP Reference 0.30 (−0.03, 0.63) 0.077 0.40 (0.09, 0.72) 0.013 0.67 (0.28, 1.06) 0.001 89.06
FPG Reference 0.05 (0.01, 0.08) 0.010 0.06 (0.02, 0.10) 0.006 0.06 (0.03, 0.09) <0.001 86.49
TC Reference 0.03 (0.01, 0.06) 0.010 0.06 (0.03, 0.08) <0.001 0.11 (0.08, 0.14) <0.001 81.04
TG Reference −0.00 (−0.03, 0.03) 0.925 0.01 (−0.02, 0.03) 0.480 0.01 (−0.02, 0.04) 0.543 84.94
HDL-c Reference −0.02 (−0.04, −0.01) <0.001 −0.02 (−0.03, −0.01) <0.001 −0.06 (−0.07, −0.04) <0.001 93.26
LDL-c Reference 0.03 (0.01, 0.05) <0.001 0.05 (0.03, 0.07) <0.001 0.10 (0.0, 0.12) <0.001 87.82

Models were adjusted for age, gender, education, occupation, income, smoking and drinking.

BMI, body mass index; WC, waist circumference; HC, hip circumference; SBP, systolic blood pressure; DBP, diastolic blood pressure; FBG, fasting blood glucose; TC, total cholesterol; TG, triglycerides; HDL-c, high density lipoprotein-cholesterol; LDL-c, low density lipoprotein-cholesterol; CI, confidence interval.

80% statistical power is the commonly accepted level.

3.3. The influences of physical activities and dietary habits on cardiovascular risk factors

According to our findings, individuals in the physical inactivity and unhealthy diet groups had higher rates of dyslipidemia, HLDL-c, hypertension, T2D, and HTG than those in the physical activities and healthy diet groups. Moreover, a notable difference was observed in the metabolic indicators between the group in terms of risk and the reference group for high-density lipoprotein cholesterol (HLDL-c) (odds ratio [OR], 1.64; 95% confidence interval [CI], [1.47–1.84]). Specifically, the low diet and inactive lifestyle group exhibited a greater risk for HLDL-c (Table 3).

Table 3.

The odds ratio for cardiovascular risk factors determined by physical activities and dietary habits.

Cardiovascular risk factors Physical activities
Physical inactivity
Statistical power %
Healthy diet Unhealthy diet
Healthy diet
Unhealthy diet
OR (95% CI) P OR (95% CI) P OR (95% CI) P
Obesity Reference 1.00 (0.96, 1.05) 0.840 1.01 (0.97, 1.06) 0.539 1.13 (1.07, 1.19) <0.001 81.53
Central obesity Reference 1.05 (1.00, 1.11) 0.049 1.05 (0.99, 1.10) 0.054 1.09 (1.03, 1.16) 0.006 85.69
Hypertension Reference 1.14 (1.08, 1.21) <0.001 1.23 (1.17, 1.30) <0.001 1.55 (1.46, 1.64) <0.001 80.50
T2D Reference 1.02 (1.00, 1.13) 0.021 1.21 (1.12, 1.31) <0.001 1.45 (1.32, 1.59) <0.001 88.79
HTC Reference 1.05 (0.96, 1.15) 0.303 1.03 (0.94, 1.12) 0.584 1.16 (1.04, 1.29) 0.006 95.65
HTG Reference 1.07 (1.03, 1.17) 0.027 1.02 (1.00, 1.14) 0.039 1.11 (1.02, 1.21) 0.014 82.31
LHDL-c Reference 1.03 (0.94, 1.12) 0.547 1.01 (0.93, 1.09) 0.910 1.18 (1.07, 1.30) 0.001 85.22
HLDL-c Reference 1.13 (1.01, 1.25) <0.001 1.13 (1.02, 1.25) <0.001 1.64 (1.47, 1.84) <0.001 90.79
Dyslipidemia Reference 1.05 (1.02, 1.08) 0.010 1.07 (1.02, 1.12) 0.007 1.26 (1.19, 1.33) <0.001 94.84

Models were adjusted for age, gender, education, occupation, income, smoking and drinking.

T2D, Type 2 diabetes; HTC, higher total cholesterol; HTG, higher triglycerides; LHDL-c, lower high-density lipoprotein-cholesterol; HLDL-c, higher low-density lipoprotein-cholesterol; OR, odds ratio; CI, confidence interval.

80% statistical power is the commonly accepted level.

3.4. The interactions between physical activities and dietary habit on cardiovascular risk factors

Additive interactions between physical inactivity and unhealthy diet were found on cardiovascular risk factors of hypertension (S, 1.46; 95% CI [1.12, 1.89]), T2D (S, 1.96; 95% CI [1.23, 3.13]), HLDL-c (S, 2.57; 95% CI [1.27, 5.21]) and dyslipidemia (S, 1.69; 95% CI [1.08, 2.66]), suggesting that the risk of hypertension, T2D, HLDL-c and dyslipidemia in participants with physical inactivity combined with unhealthy diet was 1.46, 1.96, 2.57 and 1.69 times higher than those with the single exposure to a risk factor. RERI of hypertension, T2D, HLDL-c and dyslipidemia were 0.17 (95% CI [0.06, 0.28]), 0.22 (95% CI [0.09, 0.35]), 0.39 (95% CI [0.18, 0.60]) and 0.11 (95% CI [0.03, 0.19]), respectively, suggesting that there would be 0.17, 0.22, 0.39 and 0.11 relative excess risk due to the additive interaction between physical inactivity and unhealthy diet on them. OR of hypertension, T2D, HLDL-c and dyslipidemia in participants of physical inactivity and unhealthy diet was 11%, 15%, 24% and 8.3%, respectively. Multiplicative interaction was detected in obesity, hypertension T2D and HLDL-c (Table 4).

Table 4.

The multiplicative interaction and additive interaction between physical activities and dietary habits on cardiovascular risk factors.

Cardiovascular risk factors Multiplicative interaction
Additive interaction
OR (95% CI) RERI (95% CI) AP (95% CI) S (95% CI)
Obesity 1.11 (1.03, 1.19) 0.11 (−0.03, 0.19) 0.10 (−0.03, 0.16) 7.01 (0.15, 36.07)
Central obesity 1.09 (0.998, 1.18) −0.01 (−0.11, 0.08) −0.01 (−0.10, 0.07) 0.86 (0.35, 2.16)
Hypertension 1.10 (1.02, 1.19) 0.17 (0.06, 0.28) 0.11 (0.04, 0.18) 1.46 (1.12, 1.89)
T2D 1.18 (1.04, 1.33) 0.22 (0.09, 0.35) 0.15 (0.07, 0.24) 1.96 (1.23, 3.13)
HTC 1.08 (0.93, 1.25) 0.09 (−0.08, 0.25) 0.07 (−0.06, 0.21) 2.12 (0.31, 14.47)
HTG 1.02 (0.93, 1.18) 0.02 (−0.06, 0.10) 0.02 (−0.06, 0.09) 1.20 (0.55, 2.59)
LHDL-c 1.14 (0.99, 1.32) 0.15 (−0.01, 0.29) 0.13 (−0.01, 0.24) 5.81 (0.09, 40.00)
HLDL-c 1.29 (1.11, 1.50) 0.39 (0.18, 0.60) 0.24 (0.12, 0.36) 2.57 (1.27, 5.21)
Dyslipidemia 1.09 (0.99, 1.19) 0.11 (0.03, 0.19) 0.08 (0.02, 0.15) 1.69 (1.08, 2.66)

Models were adjusted for age, gender, education, occupation, income, smoking and drinking.

T2D, Type 2 diabetes; HTC, higher total cholesterol; HTG, higher triglycerides; LHDL-c, lower high-density lipoprotein-cholesterol; HLDL-c, higher low-density lipoprotein-cholesterol; OR, odds ratio; CI, confidence interval; RERI, relative excess risk due to interaction; AP, attributable proportion due to interaction; S, synergy index.

4. Discussion

An additive model was utilized in this study to study the relationship between physical activities combined with dietary habits and cardiovascular risk factors in the adult population of Nanjing, China. Prior validation of these interactions has not been done on an additive scale. Based on our studies, individuals who engage in sedentary behavior or adhere to unhealthy dietary habits may exhibit heightened vulnerability to cardiovascular risk factors. Physical activities and dietary habits had an additive interaction with dyslipidemia, T2D, hypertension, and HLDL-c. In other words, individuals with dyslipidemia, diabetes, and hypertension may benefit more from maintaining physical activities combined with a healthy diet.

One of the key main preventions in the management program for cardiovascular diseases has been confirmed to be leading an active lifestyle and a balanced healthy diet [[41], [42], [43], [44], [45], [46]]. However, the proportion of participants with insufficient physical activities, unhealthy diet, and both is as high as 63.6%, 68.1% and 44.2%, respectively, which was consistent with our findings in the representative population [23]. Female participants who had a higher education level or lower income were more likely to have an unhealthy lifestyle, which may be explained by the reason that people had a lower income were more likely to consume unhealthy foods, do insufficient physical activities and be obese [47,48]. Higher-educated adults were more likely to work long hours at sedentary employment, which could lead to high levels of stress and less opportunity for physical activities [49].

Physical activities were associated with the adiposity markers, which are known to reflect the cardiometabolic health [11]. More specifically, participants who had insufficient physical activities and a healthy diet were at greater risks for adiposity markers than those who had sufficient physical activities and an unhealthy diet, with the reference of physical activities and healthy diet group. The results also showed that metabolic markers were more affected by physical activities than dietary habits, because decreased physical activities contributed to enhance most of metabolic markers compared with the reference group. Except for TG, participants in the physical activities and healthy diet group presented increased risk factors. Previous studies have shown that moderate and vigorous physical activities are inversely associated with SBP, and high-intensity physical activities elicited a greater reduction in SBP than that of low-intensity [50,51]. In a longitudinal path analysis, residential environmental features supporting physical activities are found to be more important in influencing cardiometabolic outcomes than dietary intakes [52].

It is generally accepted that the two major modifiable risk factors for cardiometabolic diseases are unhealthy diet and physical inactivity. However, many studies employ odds ratios (ORs) to highlight risk differences because logistic regression is used for covariate adjustments. Consequently, interactions are frequently omitted from reporting on the additive scale, which is considered more reflective of biological interaction [40]. The epidemiological community has recognized that the most appropriate way to evaluate the relevance of public health is to measure interaction on an additive scale. If resources are few, therapies can be tailored to specific subgroups using the additive scale, which shows whether the influence of a risk factor will be larger in one subpopulation than in another [53]. Estimating an excess risk resulting from both exposures is made possible by measuring the interaction between physical inactivity and an unhealthy diet on an additive scale. Our study revealed that both exposures to physical inactivity and unhealthy diet had an additive effect on the OR of hypertension, T2D, HLDL-c and dyslipidemia, indicating an excess risk than the sum of them, especially HLDL-c (OR, 1.64; 95% CI [1.47, 1.84]). A significant additive interaction was identified between physical inactivity and unhealthy diet on HLDL-c, with the RERI, AP, and S and their corresponding 95% CIs of 0.39 (0.18, 0.60), 0.24 (0.12, 0.36), and 2.56 (1.27, 5.21), respectively.

Further study is required to determine how an unhealthy diet and physical inactivity raise the risk of metabolic diseases. On the other hand, physical inactivity has been found to raise the risk of numerous inflammatory physiological alterations, such as insulin resistance, dyslipidemia, endothelial dysfunction, and hypertension [54]. In persistently sedentary individuals, these alterations have been associated with an elevated risk for several ailments, such as T2D, CVDs, and various kinds of cancer [54,55]. A diet rich in processed foods that are highly desired and high in fat, salt, sugar, and flavor enhancers, along with low levels of physical activities, can aggravate systemic chronic inflammation (SCI), which can then lead to several chronic non-communicable diseases [56].

Conversely, improved TC, LDL, and SBP readings are linked to a number of dietary groups, particularly dairy, fruits, vegetables, nuts, seeds, and legumes [57]. One possible explanation is that the food mentioned above has more fiber and less energy overall, which can help reduce the total energy of daily dietary intake [58] and the antioxidant content of food, which helps to lessen systemic oxidative stress and fight free radicals. A further advantage of glucose could be its lower glycemic index [59]. The positive effects of exercise on body composition, such as increased skeletal muscle insulin sensitivity and decreased insulin resistance, may help explain the influences of physical activities [60].

Overall, the potential interaction between physical inactivity and unhealthy diet exerted an additive effect on increasing the risk of hypertension, T2D, HLDL-c and dyslipidemia than the single exposure. More attention should be paid to the population with both exposures. To encourage adult physical activities, many countries have devised practical and efficient public health interventions. One of the most important interventions to lower the quantity of insufficient physical activities is promoting physical activities by the media. Furthermore, dietary concerns related to sodium are a significant factor in determining hypertension blood pressure levels and total cardiovascular risk [61]. Strategies for reducing salt intake are a “best buy"—that is, the most cost-effective and feasible for implementation—for preventing NCDs [62].

Several highlights of this study should be considered. Firstly, our study is the first to evaluate, on an additive basis, the interactions between dietary habits and physical activities on cardiovascular risk variables in a community sample from Nanjing. Additive interactions possess a higher degree of direct relevance in disease prevention and risk prediction. We were able to estimate the additive interaction effect accurately due to the large and representative sample size. To confirm that the sample was representative of the area, a multistage random sampling procedure was adopted. Secondly, we employed standardized tools and procedures together with a structured questionnaire in accordance with the guidelines set forth by the Chinese Center for Disease Control and Prevention. Before, during, and after the study, the Nanjing Centers for Disease Control and Prevention put in place a stringent quality control process to guarantee the reliability and authenticity of the data. Thirdly, our analysis improved the reliability by considering known possible confounders. But there are also a lot of restrictions to take into account.

Limitations of this study should also be considered. First, determining causality was impossible due to the cross-sectional design. Second, selection bias may have occurred because participants altered their lifestyles after learning that their levels of metabolic risk variables were elevated. Third, even after adjusting for a few confounding factors, there may still be additional unaccounted confounders, including a family history of chronic disease. The prevalence of cardiovascular risk factors, health profiles, and dietary and physical exercise habits may vary throughout the survey year, which could lead to a misclassification bias; however, as our primary goal is to assess the interaction effect of dietary habits and physical activities on cardiovascular risk factors—rather than the prevalence of these factors—the conclusion of this study may not be greatly impacted. Therefore, the findings of this study provide valuable new information for addressing the issue of the additive interaction between dietary habits combined with physical activities and cardiovascular risk factors in various nations and locations, including China. To validate this additive interaction and clarify the underlying mechanism, more prospective cohort research is required, which will ultimately lead to better CVDs prevention measures.

5. Conclusions

In conclusion, the results of the cross-sectional study conducted among the people of Nanjing validated previous studies on the association of physical activities and dietary habits with cardiovascular risk factors. Moreover, this study also showed that an unhealthy diet and physical inactivity combined to provide an additive effect on T2D, hypertension, HLDL-c, and dyslipidemia, suggesting a higher risk than the total of these conditions, particularly HLDL-c. Preventive strategies aimed at reducing cardiometabolic risks such as hypertension, T2D, HLDL-c, and dyslipidemia are necessary for targeting physical inactivity and unhealthy diets.

Ethics statement

This study involves human participants and was approved by Ethics Committee: Nanjing Municipal Center for Disease Control and Prevention ID: PJ2017002. Participants gave informed consent to participate in the study before taking part.

Funding

This research work was funded by the Medical Science and Technology Development Foundation, Nanjing Municipality Health Bureau (grant no. 2017-YKK17199, no. 2018-ZKX18049). The funder had no role in the decision to collect data, data analysis, or reporting of the results.

Data availability statement

Data will be made available on request.

CRediT authorship contribution statement

Weiwei Wang: Writing – original draft, Visualization, Methodology, Investigation. Hairong Zhou: Visualization, Validation, Investigation, Data curation. Shengxiang Qi: Software, Investigation, Data curation. Huafeng Yang: Visualization, Methodology, Investigation. Xin Hong: Writing – review & editing, Validation, Supervision, Resources, Project administration, Conceptualization.

Declaration of competing interest

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Acknowledgements

We are grateful to all the dedicated fieldworkers who took part in the surveys and all participants who facilitated the survey implementation at each community.

Footnotes

Appendix A

Supplementary data to this article can be found online at https://doi.org/10.1016/j.heliyon.2024.e28845.

Appendix A. Supplementary data

The following is the Supplementary data to this article.

Multimedia component 1
mmc1.doc (56.5KB, doc)

References

  • 1.Institute for Health Metrics and Evaluation (IHME). GBD results tool. http://ghdx.healthdata.org/gbd-results-tool..
  • 2.Li Y., Zeng X., Liu J., et al. Can China achieve a one-third reduction in premature mortality from non-communicable diseases by 2030? BMC Med. 2017;15(1):132. doi: 10.1186/s12916-017-0894-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Du S.F., Wang H.J., Zhang B., Zhai F.Y., Popkin B.M. China in the period of transition from scarcity and extensive undernutrition to emerging nutrition-related non-communicable diseases, 1949–1992. Obes Rev Off J Int Assoc Study Obes. 2014;15(suppl 1):8–15. doi: 10.1111/obr.12122. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Yakoob M.Y., Micha R., Khatibzadeh S., et al. Impact of dietary and metabolic risk factors on cardiovascular and diabetes mortality in South Asia: analysis from the 2010 Global Burden of Disease Study. Am. J. Publ. Health. 2016;106:2113–2125. doi: 10.2105/AJPH.2016.303368. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Ambakederemo T.E., Chikezie E.U. Assessment of some traditional cardiovascular risk factors in medical doctors in southern Nigeria. Vasc. Health Risk Manag. 2018;14:299–309. doi: 10.2147/VHRM.S176361. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.El Bilbeisi A.H., Hosseini S., Djafarian K. The association between physical activity and the metabolic syndrome among type 2 diabetes patients in Gaza strip, Palestine. Ethiop J Health Sci. 2017;27:273–282. doi: 10.4314/ejhs.v27i3.9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Lanier J.B., Bury D.C., Richardson S.W. Diet and physical activity for cardiovascular disease prevention. Am. Fam. Physician. 2016;93(11):919. [PubMed] [Google Scholar]
  • 8.Franco O.H., de Laet C., Peeters A., et al. Effects of physical activity on life expectancy with cardiovascular disease. Arch. Intern. Med. 2005;165(20):2355–2360. doi: 10.1001/archinte.165.20.2355. [DOI] [PubMed] [Google Scholar]
  • 9.Mohammadi S., Jalaludin M.Y., Su T.T., et al. Dietary and physical activity patterns related to cardio-metabolic health among Malaysian adolescents: a systematic review. BMC Publ. Health. 2019;19(1) doi: 10.1186/s12889-019-6557-z. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Su T.T., Sim P.Y., Nahar A.M., et al. Association between self-reported physical activity and indicators of body composition in Malaysian adolescents. Prev. Med. 2014;67:100–105. doi: 10.1016/j.ypmed.2014.07.001. [DOI] [PubMed] [Google Scholar]
  • 11.Vella C.A., Allison M.A., Cushman M., et al. Physical activity and Adiposity-related inflammation: the MESA. Med. Sci. Sports Exerc. 2017;49:915–921. doi: 10.1249/MSS.0000000000001179. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.U.S. Department of Health and Human Services 2008 physical activity guidelines for Americans. Office of Disease Prevention and Health Promotion publication no. U0036. October 2008. http://health.gov/paguidelines/pdf/paguide.pdf
  • 13.Hallal P.C., Andersen L.B., Bull F.C., et al. Lancet physical activity series Working Group. Global physical activity levels: surveillance progress, pitfalls, and prospects. Lancet. 2012;380:247–257. doi: 10.1016/S0140-6736(12)60646-1. [DOI] [PubMed] [Google Scholar]
  • 14.Zhou Y., Wu J., Zhang S., et al. Prevalence and risk factors of physical inactivity among middle-aged and older Chinese in Shenzhen: a cross-sectional study. BMJ Open. 2018;8 doi: 10.1136/bmjopen-2017-019775. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Chen S.-T., Liu Y., Hong J.-T., et al. Co-Existence of physical activity and sedentary behavior among children and adolescents in Shanghai, China: do gender and age matter? BMC Publ. Health. 2018;18:1287. doi: 10.1186/s12889-018-6167-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Ezzati M., Riboli E. Behavioral and dietary risk factors for noncommunicable diseases. N. Engl. J. Med. 2013;369:954–964. doi: 10.1056/NEJMra1203528. [DOI] [PubMed] [Google Scholar]
  • 17.He Y., Li Y., Yang X., et al. The dietary transition and its association with cardiometabolic mortality among Chinese adults, 1982-2012: a cross-sectional population-based study. Lancet Diabetes Endocrinol. 2019;7(7):540–548. doi: 10.1016/S2213-8587(19)30152-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.World Cancer Research Fund/American Institute for Cancer Research Diet, nutrition, physical activity and cancer: a global perspective. Continuous Update Project Expert Report. 2018. https://www.wcrf.org/dietandcancer
  • 19.Micha R., Shulkin M.L., Peñalvo J.L., et al. Etiologic effects and optimal intakes of foods and nutrients for risk of cardiovascular diseases and diabetes: systematic reviews and meta-analyses from the Nutrition and Chronic Diseases Expert Group (NutriCoDE) PLoS One. 2017;12 doi: 10.1371/journal.pone.0175149. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Zhou M., Wang H., Zeng X., et al. Mortality, morbidity, and risk factors in China and its provinces, 1990-2017: a systematic analysis for the Global Burden of Disease Study 2017. Lancet. 2019;394(10204):1145–1158. doi: 10.1016/S0140-6736(19)30427-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.GBD 2017 Risk Factor Collaborators Global, regional, and national comparative risk assessment of 84 behavioral, environmental and occupational, and metabolic risks or clusters of risks for 195 countries and territories, 1990-2017: a systematic analysis for the Global Burden of Disease Study 2017. Lancet. 2018;392(10159):1923–1994. doi: 10.1016/S0140-6736(18)32225-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Ouyang X., Lou Q., Gu L., et al. Cardiovascular disease risk factors are highly prevalent in the office-working population of Nanjing in China. Int. J. Cardiol. 2012;155(2):212–216. doi: 10.1016/j.ijcard.2010.09.052. [DOI] [PubMed] [Google Scholar]
  • 23.Hong X., Ye Q., He J., et al. Prevalence and clustering of cardiovascular risk factors: a cross-sectional survey among Nanjing adults in China. BMJ Open. 2018;8(6) doi: 10.1136/bmjopen-2017-020530. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.He Y., Li Y., Lai J., et al. Dietary patterns as compared with physical activity in relation to metabolic syndrome among Chinese adults. Nutr. Metabol. Cardiovasc. Dis. 2013;23(10):920–928. doi: 10.1016/j.numecd.2012.09.001. [DOI] [PubMed] [Google Scholar]
  • 25.Kim Y.J., Hwang J.Y., Kim H., et al. Diet quality, physical activity, and their association with metabolic syndrome in Korean adults. Nutrition. 2019;59:138–144. doi: 10.1016/j.nut.2018.08.009. [DOI] [PubMed] [Google Scholar]
  • 26.Matta J., Hoertel N., Kesse-Guyot E., et al. Diet and physical activity in the association between depression and metabolic syndrome: constances study. J. Affect. Disord. 2018;244:25–32. doi: 10.1016/j.jad.2018.09.072. [DOI] [PubMed] [Google Scholar]
  • 27.Wang L., Gao P., Zhang M., et al. Prevalence and ethnic pattern of diabetes and prediabetes in China in 2013. JAMA. 2017;317(24):2515–2523. doi: 10.1001/jama.2017.7596. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Deng H.B., Macfarlane D.J., Thomas G.N., et al. Reliability and validity of the IPAQ-Chinese: the guangzhou biobank cohort study. Med. Sci. Sports Exerc. 2008;40:303–307. doi: 10.1249/mss.0b013e31815b0db5. [DOI] [PubMed] [Google Scholar]
  • 29.Hong X., Ye Q., Wang Z., et al. Reproducibility and validity of dietary patterns identified using factor analysis among Chinese populations. Br. J. Nutr. 2016;116(5):842–852. doi: 10.1017/S000711451600249X. [DOI] [PubMed] [Google Scholar]
  • 30.Neumann A.I., Martins I.S., Marcopito L.F., et al. Dietary patterns associated with risk factors for cardiovascular disease in a Brazilian city. Rev. Panam. Salud Públic. 2007;22(5):329–339. doi: 10.1590/s1020-49892007001000006. [DOI] [PubMed] [Google Scholar]
  • 31.Whitton C., Rebello S.A., Lee J., et al. A healthy asian A posteriori dietary pattern correlates with A priori dietary patterns and is associated with cardiovascular disease risk factors in a multiethnic asian population. J. Nutr. 2018;148(4):616–623. doi: 10.1093/jn/nxy016. [DOI] [PubMed] [Google Scholar]
  • 32.Chinese Nutrition Society . People’s Medical Publishing House; Beijing: 2022. The Chinese Dietary Guidelines. [Google Scholar]
  • 33.Wu Y., Huxley R., Li L., et al. Prevalence, awareness, treatment, and control of hypertension in China: data from the China National Nutrition and Health Survey 2002. Circulation. 2008;118(25):2679–2686. doi: 10.1161/CIRCULATIONAHA.108.788166. [DOI] [PubMed] [Google Scholar]
  • 34.Chinese Diabetes Society Chinese guidelines for type 2 diabetes 2017[J] Chin J Diabetes Mellitus. 2018;10(1):4–67. [Google Scholar]
  • 35.James P.A., Oparil S., Carter B.L., et al. 2014 evidence-based guideline for the management of high blood pressure in adults: report from the panel members appointed to the Eighth Joint National Committee (JNC8) JAMA. 2014;311(5):507–520. doi: 10.1001/jama.2013.284427. [DOI] [PubMed] [Google Scholar]
  • 36.Joint committee for developing Chinese guidelines on prevention and treatment of dyslipidemia in adults. Chinese guidelines on prevention and treatment of dyslipidemias in adults. Chinese Circulation Journal. 2016;31(10):937–950. [Google Scholar]
  • 37.Hu N., Jiang Y., Li Y.C. Weighting method of China chronic disease surveillance data in 2010. Chin J Health Stats. 2012;29:424–426. [Google Scholar]
  • 38.Champely S. 2016. https://CRAN.R-project.org/package=pwr (pwr: basic functions for power analysis). Retrieved from. [Google Scholar]
  • 39.Brydges C.R. Effect size guidelines, sample size calculations, and statistical power in gerontology. Innov Aging. 2019;3(4) doi: 10.1093/geroni/igz036. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40.Andersson T., Alfredsson L., Källberg H., et al. Calculating measures of biological interaction[J. Eur. J. Epidemiol. 2005;20(7):575–579. doi: 10.1007/s10654-005-7835-x. [DOI] [PubMed] [Google Scholar]
  • 41.Lichtenstein A.H., Appel L.J., Brands M., Carnethon M., Daniels S., Franch H.A., et al. Summary of American Heart Association diet and lifestyle recommendations revision 2006. Arterioscler. Thromb. Vasc. Biol. 2006;26:2186–2191. doi: 10.1161/01.ATV.0000238352.25222.5e. [DOI] [PubMed] [Google Scholar]
  • 42.LeFevre M.L. Behavioral counseling to promote a healthful diet and physical activity for cardiovascular disease prevention in adults with cardiovascular risk factors: U.S. Preventive Services Task Force recommendation statement. Ann. Intern. Med. 2014;161(8):587–593. doi: 10.7326/M14-1796. [DOI] [PubMed] [Google Scholar]
  • 43.Moyer V.A. Behavioral counseling interventions to promote a healthful diet and physical activity for cardiovascular disease prevention in adults: U.S. Preventive Services Task Force recommendation statement. Ann. Intern. Med. 2012;157(5):367–371. doi: 10.7326/0003-4819-157-5-201209040-00486. [DOI] [PubMed] [Google Scholar]
  • 44.US Preventive Services Task Force. Krist A.H., Davidson K.W. Behavioral counseling interventions to promote a healthy diet and physical activity for cardiovascular disease prevention in adults with cardiovascular risk factors: US preventive services task force recommendation statement. JAMA. 2020;324(20):2069–2075. doi: 10.1001/jama.2020.21749. [DOI] [PubMed] [Google Scholar]
  • 45.Salas-Salvadó J., Díaz-López A., Ruiz-Canela M., et al. Effect of a lifestyle intervention program with energy-restricted mediterranean diet and exercise on weight loss and cardiovascular risk factors: one-year results of the PREDIMED-plus trial. Diabetes Care. 2019;42(5):777–788. doi: 10.2337/dc18-0836. [DOI] [PubMed] [Google Scholar]
  • 46.Lanier J.B., Bury D.C., Richardson S.W. Diet and physical activity for cardiovascular disease prevention. Am. Fam. Physician. 2016;93(11):919–924. [PubMed] [Google Scholar]
  • 47.Thornton L.E., Crawford D.A., Ball K. Neighbourhood-socioeconomic variation in women's diet: the role of nutrition environments. Eur. J. Clin. Nutr. 2010;64(12):1423–1432. doi: 10.1038/ejcn.2010.174. [DOI] [PubMed] [Google Scholar]
  • 48.Lagström H., Halonen J.I., Kawachi I., Stenholm S., Pentti J., Suominen S., et al. Neighborhood socioeconomic status and adherence to dietary recommendations among Finnish adults: a retrospective follow-up study. Health Place. 2019;55:43–50. doi: 10.1016/j.healthplace.2018.10.007. [DOI] [PubMed] [Google Scholar]
  • 49.Du H., Bennett D., Li L., Whitlock G., Guo Y., Collins R., et al. Physical activity and sedentary leisure time and their associations with BMI, waist circumference, and percentage body fat in 0.5 million adults: the China Kadoorie Biobank study. Am. J. Clin. Nutr. 2013;97:487–496. doi: 10.3945/ajcn.112.046854. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 50.Clays E., De Bacquer D., Van Herck K., et al. Occupational and leisure time physical activity in contrasting relation to ambulatory blood pressure. BMC Publ. Health. 2012;12:1002. doi: 10.1186/1471-2458-12-1002. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 51.Eicher J.D., Maresh C.M., Tsongalis G.J., et al. The additive blood pressure lowering effects of physical activity intensity on post physical activity hypotension. Am. Heart J. 2010;160:513–520. doi: 10.1016/j.ahj.2010.06.005. [DOI] [PubMed] [Google Scholar]
  • 52.Carroll S.J., Dale M.J., Niyonsenga T., et al. Associations between area socioeconomic status, individual mental health, physical activity, diet and change in cardiometabolic risk amongst a cohort of Australian adults: a longitudinal path analysis. PLoS One. 2020;15(5) doi: 10.1371/journal.pone.0233793. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 53.Knol M.J., VanderWeele T.J. Recommendations for presenting analyses of effect modification and interaction. Int. J. Epidemiol. 2012;41(2):514–520. doi: 10.1093/ije/dyr218. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 54.Wahid A., Manek N., Nichols M., et al. Quantifying the association between physical activity and cardiovascular disease and diabetes: a systematic review and meta-analysis. J. Am. Heart Assoc. 2016;5(9) doi: 10.1161/JAHA.115.002495. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 55.Fiuza-Luces C., Santos-Lozano A., Joyner M., et al. Exercise benefits in cardiovascular disease: beyond attenuation of traditional risk factors. Nat. Rev. Cardiol. 2018;15(12):731–743. doi: 10.1038/s41569-018-0065-1. [DOI] [PubMed] [Google Scholar]
  • 56.Hall K.D. Did the food environment cause the obesity epidemic? Obesity. 2018;26(1):11–13. doi: 10.1002/oby.22073. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 57.Onvani S., Haghighatdoost F., Surkan P.J., Larijani B., Azadbakht L. Adherence to the Healthy Eating Index and Alternative Healthy Eating Index dietary patterns and mortality from all causes, cardiovascular disease and cancer: a meta-analysis of observational studies. J. Hum. Nutr. Diet. 2017;30(2):216–226. doi: 10.1111/jhn.12415. [DOI] [PubMed] [Google Scholar]
  • 58.Cooper A.J., Sharp S.J., Lentjes M.A., et al. A prospective study of the association between quantity and variety of fruit and vegetable intake and incident type 2 diabetes. Diabetes Care. 2012;35(6):1293–1300. doi: 10.2337/dc11-2388. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 59.Calton E.K., James A.P., Pannu P.K., Soares M.J. Certain dietary patterns are beneficial for the metabolic syndrome: reviewing the evidence. Nutr. Res. 2014;34(7):559–568. doi: 10.1016/j.nutres.2014.06.012. [DOI] [PubMed] [Google Scholar]
  • 60.Nguyen T.H., Tang H.K., Kelly P., van der Ploeg H.P., Dibley M.J. Association between physical activity and metabolic syndrome: a cross sectional survey in adolescents in Ho Chi Minh City, Vietnam. BMC Publ. Health. 2010;10:141. doi: 10.1186/1471-2458-10-141. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 61.Creating an Enabling Environment for Population-Based Salt Reduction Strategies: Report of a Joint Technical Meeting Held by WHO and the Food Standards Agency. World health Organization; United Kingdom. Geneva: 2010. [Google Scholar]
  • 62.Tackling NCDs: ‘best buys’ and other recommended interventions for the prevention and control of noncommunicable diseases. WHO. 2017:10–11. https://www.who.int/publications/i/item/WHO-NMH-NVI-17.9 [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Multimedia component 1
mmc1.doc (56.5KB, doc)

Data Availability Statement

Data will be made available on request.


Articles from Heliyon are provided here courtesy of Elsevier

RESOURCES