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Journal of Urban Health : Bulletin of the New York Academy of Medicine logoLink to Journal of Urban Health : Bulletin of the New York Academy of Medicine
. 2011 Dec 28;89(2):329–338. doi: 10.1007/s11524-011-9636-8

Association of Suboptimal Health Status and Cardiovascular Risk Factors in Urban Chinese Workers

Yu X Yan 1, Jing Dong 2, You Q Liu 2, Xing H Yang 1, Man Li 1, Gilbert Shia 1, Wei Wang 1,3,
PMCID: PMC3324604  PMID: 22203493

Abstract

Suboptimal health status (SHS) has become a new public health challenge in urban China. Despite indications that SHS may be associated with progression or development of chronic diseases such as cardiovascular and metabolic diseases, there are few reports on SHS investigations. To explore the relationship between SHS and traditional cardiovascular risk factors, a cross-sectional study was conducted in a sample of 4,881 workers employed in 21 companies in urban Beijing. Blood pressure, glucose, lipid levels (total cholesterol, high-density lipoprotein [HDL] cholesterol, low-density lipoprotein [LDL] cholesterol and triglycerides), cortisol, and body mass index were measured. SHS score was derived from data collection in the SHS questionnaire (SHSQ-25). Univariate analysis and linear two-level model were used to analyze the association of SHS with the cardiovascular risk factors. Serum cortisol level was much higher among the SHS high-score group than that among the low SHS score group (204.31 versus 161.33 ng/ml, P < 0.001). In a linear two-level model, we found correlation between SHS and systolic blood pressure, diastolic blood pressure, plasma glucose, total cholesterol, and HDL cholesterol among men, and correlation between SHS and systolic blood pressure, diastolic blood pressure, total cholesterol, triglyceride, and HDL cholesterol among women after controlling for age, education background, occupation, smoking, and physical activity. SHS is associated with cardiovascular risk factors and contributes to the development of cardiovascular disease. SHS should be recognized in the health care system, especially in primary care.

Keywords: Suboptimal health status, Cardiovascular disease, Risk factors

Introduction

There has been an increase in the number of people who reported poor health in the absence of a diagnosable condition, which is known as suboptimal health status (SHS).1,2 SHS is characterized by ambiguous health complaints, general weakness, and lack of vitality. It is deemed that SHS may be associated with progression or development of chronic disease.

In the past 30 years, economic growth and associated sociodemographic changes in China have increased the prevalence of the major risk factors for chronic disease, which leads to an increased burden of cardiovascular disease and other chronic diseases.3 Preclinical status of diseases and its early detection have become major issues in the promotion of the basic health service in the reform of health care in China. Despite poor perceived health is a subjective construct lacking in precision, it has been found to hold considerable predictive validity in relation to functional disability, morbidity, and mortality.46 We have established a previously proposed instrument (suboptimal health status questionnaire-25, SHSQ-25) for investigating suboptimal health status.2 In our recent data analysis, work stress was among the most mentioned factors influencing general health. The multiple linear regression analyses revealed that competition, high job demands, poor relationship with colleagues, and lack of physical activities were the main factors associated with SHS (adjusted R2 = 0.573), independent of sex, age, education, smoking, and drinking.7 There is growing evidence that stress adversely affects cardiovascular health. Melamed et al.8 demonstrated that some of the pathways linking psychosocial factors (job stress) and cardiovascular disease incidence are (1) elevation of physiological/hematochemical variables (e.g., blood pressure and serum lipid lipoprotein levels);9,10 (2) direct and indirect effects of adverse risk behaviors such as smoking, lack of physical exercise, and poor diet and health care habits;11 and (3) heightened emotional states, such as anger, tension, and anxiety,12,13 implicated in cardiovascular disease development through neuroendocrine mediation.

China has experienced a cardiovascular disease epidemic in recent decades. During the next 20 years, cardiovascular disease morbidity and mortality are predicted to increase in China.14 Despite SHS may be associated with progression or development of chronic diseases such as cardiovascular and metabolic diseases, few evidences have been shown in any studies so far. The aim of this cross-sectional study is to verify the relationship between the main risk factors of cardiovascular disease and SHS.

Methods

Study Participants

A cross-sectional study was conducted among workers in urban Beijing. A random third of all the 64 companies whose workers took annual physical examination for at least two consecutive years at the physical examination center of Beijing Xuanwu Hospital, Capital Medical University were selected for cluster sampling. Participants had to meet the following inclusion criteria: (1) no history of somatic or psychiatric abnormalities, as confirmed by their medical records, (2) age from 20 through 60 years; and (3) no history of medication consumption in the previous 2 weeks. All participants attended a standardized examination protocol in Beijing Xuanwu Hospital, including medical history, physical examination, blood hematology and biochemistry analysis, rest electrocardiography, and abdominal ultrasonography. We excluded individuals who met the diagnostic criteria of specific disease concerning cardiovascular system, respiratory system, genitourinary system, digestive system, hematic system, and diabetes. Of the 4,881 workers from 21 companies, 1,476 were excluded from the study. Finally, a total of 3,405 people were investigated in this study. A self-reported questionnaire was used to assess the respondents’ sociodemographics and SHS. Median was used as a cut point in grouping into high versus low of two dimensions of SHS. To assure comparability of the findings, all participants were examined by the physicians who were specially trained for the study. Both the hospital and university research ethical committees approved the study, and written informed consents were obtained from all participants.

Data Collection

Suboptimal Health Status

SHS was measured by the suboptimal health questionnaire (SHSQ-25) including 25 items.2 Each subject was asked to rate a specific statement on a five-point Likert-type scale, based on how often they suffered various specific complaints in the preceding 3 months: (1) never or almost never, (2) occasionally, (3) often, (4) very often, and (5) always. The raw scores of 1 to 5 on the questionnaire were recoded as 0 to 4. SHS scores were calculated for each respondent by summing the ratings for the 25 items. A high score represents a high level of SHS (poor health). The Cronbach’s α coefficient of the SHSQ-25 was 0.91, indicating good internal consistency.

Cardiovascular Risk Factors

We included classical risk factors, i.e., blood pressure, glucose, lipid levels, cortisol, and body mass index (BMI) in our analyses. Blood pressure was measured three times consecutively after 5 minutes rest, with each participant seated and using a standard mercury sphygmomanometer. The average of the second and third measurements was used to estimate the systolic and diastolic blood pressures. Overnight fasting blood specimens were obtained for the measurement of plasma glucose, serum lipids, and cortisol. Plasma glucose was measured using a modified hexokinase enzymatic method (Hitachi automatic clinical analyzer, model 7060, Japan). Concentrations of total cholesterol, high-density lipoprotein (HDL) cholesterol, and triglycerides (TG) were assessed enzymatically with commercially available reagents. Lipid measurements were standardized according to the criteria of the Centers for Disease Control and Prevention-National Heart, Lung, and Blood Institute Lipid Standardization Program.15 Low-density lipoprotein (LDL) cholesterol was computed by the Friedewald formula using the equation (LDL = total cholesterol − [HDL + TG/5]).16 Fasting cortisol was analyzed by γ radioimmunoassay counter (GC-911) in the Endocrinology Institute. The intra-assay and inter-assay coefficient of variations of this assay were <5.5% and <7.5%, respectively. The reference value was 50–280 ng/ml. Strict quality controls were applied throughout all these assays.

Body weight and height were measured twice during the interview. Weight was measured in light indoor clothing without shoes on electronic scales placed on a firm, level surface to the nearest 0.1 kg. Height was measured without shoes with a wall-mounted stadiometer to the nearest 0.1 cm. BMI was calculated as body weight (in kilograms) divided by height (in meters) squared.

Sociodemographic Information and Health-Related Behaviors

Data on sociodemographic information and health-related behaviors were collected during interviews. These variables were used as confounders to control for potential confounding. Demographic variables included age, education, occupation, average monthly income, and marital status. The health-related behaviors include current smoking, alcohol use, and physical activity. Smoking status was dichotomized as current smoker (≥1 filter per day) and nonsmoker. Physical activity was assessed by asking to list the average hours of physical activity for each day of the week prior to the questionnaire.

Statistical Analyses

Data were reported as mean ± SD for continuous variables and frequencies for categorical variables. Univariate and multivariate analyses were performed to estimate the relations of SHS to risk factors for cardiovascular disease. A two-level model was used in multivariate analysis to account for the nested nature of the data,17 with “sampling company” and “study participant” as the first and second levels, respectively.

Descriptive statistics and univariate analysis were carried out using SAS version 8.2. For multilevel analysis, we used MLwin software (version 2.02, 2005). P values for the fixed part of the model were obtained by calculating the chi-square statistics for joint contrasts provided by the MLwin software package. P < 0.05 was considered statistically significant.

Results

Our analysis was restricted to 3,019 individuals who had completed the questionnaire and laboratory results. Their mean age was 40.6 years (SD 13.4) and 48.6% were women. The participants were divided into two groups by the median SHS score of 44: high SHS score group (SHS score ≥44) and low SHS score group (SHS score <44). The mean SHS score among the SHS group was 55.73 ± 9.58 and 35.02 ± 6.51 among the control group, respectively. Table 1 presents the participants’ characteristics according to the SHS score. The proportion of white-collar workers and those with university/college degree among the high-score group was significantly higher than that among the low-score group (P < 0.001). Gender and age distribution were also different between the two groups (P < 0.001). Since over half of the individuals aged over 50 years were excluded because of the results of their general medical examination, the number of this age group was significantly lower than the younger age groups. SHS was correlated with current smoking and physical inactivity (P < 0.001), whereas monthly income, marital status, and alcohol use were not different between groups.

Table 1.

Characteristics of study sample

Variables SHS sore ≥44 n (%) SHS sore <44 n (%) χ2 P
Gender
 Female 806 (52.10) 660 (44.84) 15.933 <0.001
 Male 741 (47.90) 812 (55.16)
Age (years)
 20–30 167 (10.80) 376 (25.54) 128.978 <0.001
 31–40 606 (39.17) 575 (39.06)
 41–50 559 (36.13) 380 (25.82)
 51–60 215 (13.90) 141 (9.58)
Highest education level
 Compulsory school (through grade 9) 72 (4.65) 171 (11.62) 185.420 <0.001
 High school graduate 213 (13.77) 432 (29.35)
 University/college degree 1262 (81.58) 869 (59.04)
Occupation
 White-collar worker 1431 (92.50) 986 (66.98) 307.665 <0.001
 Blue-collar worker 116 (7.50) 486 (33.02)
Monthly income (RMB)
 <2,000 324 (20.94) 316 (21.47) 3.852 0.146
 2,001–5,000 1012 (65.42) 990 (67.26)
 ≥5,000 211 (13.64) 166 (11.28)
Marital status
 Single or divorced 196 (12.67) 168 (11.41) 1.123 0.289
 Married 1351 (87.33) 1304 (88.59)
Current smoking
 Yes 476 (30.77) 187 (12.70) 143.638 <0.001
 No 1071 (69.23) 1285 (87.30)
Alcohol use
 Every day 72 (4.65) 54 (3.67) 2.309 0.511
 3–4 × a week 351 (22.69) 348 (23.64)
 1–2 × a week 988 (63.87) 948 (64.40)
 Never 136 (8.79) 122 (8.29)
Physical activity (h)
 ≥5 44 (2.84) 47 (3.19) 31.772 <0.001
 3–4 341 (22.04) 437 (29.69)
 1–2 641 (41.44) 486 (33.02)
 <1 521 (33.68) 502 (34.10)

SHS suboptimal health status

Table 2 presents the mean values and standard deviation of cardiovascular risk factors of the study groups. Overall, the participants who gave higher SHS score also had a higher risk of cardiovascular disease than those with lower scores. Compared to the low-score group, systolic and diastolic blood pressure, plasma glucose, total cholesterol, triglyceride levels, and BMI were significantly higher among the high-score group (P < 0.001). Meanwhile HDL cholesterol levels were higher in low-score group than in high-score group (P > 0.05). Serum cortisol level was much higher among the high-score group than that among the low-score group (204.31 versus 161.33 ng/ml, P < 0.001). The ranges of cortisol in high-score and low-score group were 122.64–324.17 and 107.12–221.59 ng/ml, respectively. A significant linear correlation between SHS sore and serum cortisol was evident (r = 0.381, P < 0.001).

Table 2.

Comparison of the cardiovascular risk factors between high and low SHS score group

SHS score high SHS score low t P valuea
Mean + Std. Mean + Std.
SBP (mmHg) 119.43 ± 13.27 115.31 ± 13.19 8.573 <0.001
DBP (mmHg) 77.57 ± 7.38 75.38 ± 7.89 7.880 <0.001
GLU (mmol/L) 5.23 ± 0.57 5.17 ± 0.55 2.941 <0.001
TCH (mmol/L) 4.48 ± 0.76 4.32 ± 0.78 5.708 <0.001
TG (mmol/L) 1.17 ± 0.58 1.08 ± 0.46 4.709 <0.001
HDLC (mmol/L) 1.32 ± 0.32 1.36 ± 0.36 −3.230 <0.001
LDLC (mmol/L) 2.82 ± 0.70 2.78 ± 0.71 1.558 0.119
COR (ng/ml) 204.31 ± 40.06 161.33 ± 27.83 34.076 <0.001
BMI (kg/m2) 23.24 ± 3.76 22.01 ± 3.52 9.268 <0.001

SHS suboptimal health status; SBP systolic blood pressure; DBP diastolic blood pressure; GLU plasma glucose; TCH total cholesterol; TG triglyceride; HDLC high-density lipoprotein cholesterol; LDLC low-density lipoprotein cholesterol; COR serum cortisol

We further used linear two-level model to analyze the association of SHS with the cardiovascular risk factors, with participants’ characteristics showing difference between the high and low SHS score groups (Table 1) as controlling variables and sex as a stratifying variable. In the models, SHS score was treated as a continuous variable.

Table 3 shows parameter estimates and standard errors from the two-level model among men. After adjusted for age, education background, occupation, smoking, and physical activity, the diastolic blood pressure, plasma glucose, total cholesterol, and serum cortisol were found to significantly predict SHS score (P < 0.05). HDL cholesterol level was negatively and significantly associated with SHS score (P < 0.05). In the fully adjusted multilevel analysis, no significant association was observed between triglyceride, LDL cholesterol, BMI, and SHS score (P > 0.05). As the major risk factors for most chronic diseases, smoking and lack of physical activity also significantly associated with SHS score among men (P < 0.05).

Table 3.

Multilevel estimates for SHS score in relation to cardiovascular risk factors among male participants

Estimate (b) SE P value
Systolic blood pressure 0.601 0.211 0.004
Diastolic blood pressure 0.486 0.230 0.035
Plasma glucose 0.636 0.302 0.035
Total cholesterol 1.003 0.333 0.003
Triglyceride 0.477 0.293 0.104
HDL cholesterol −0.986 0.400 0.014
LDL cholesterol 0.160 0.116 0.168
Serum cortisol 0.231 0.004 <0.001
Body mass index 0.180 0.214 0.400
Level 2 (person) intercept variance (SE) 6.903 (1.369)
Level 2 (company) intercept variance (SE) 3.418 (1.192)

HDL high-density lipoprotein cholesterol, LDL low-density lipoprotein cholesterol

Table 4 shows parameter estimates and standard errors from the two-level model among women. The results were similar to those among men, with the exception of plasma glucose and HDL cholesterol. After adjusted for age, education background, occupation, smoking, and physical activity, the diastolic blood pressure, total cholesterol, triglyceride, HDL cholesterol, and serum cortisol were found to significantly predict SHS score among woman (P < 0.05). No significant association was observed between plasma glucose, LDL cholesterol, BMI, and SHS score (P > 0.05). Smoking and lack of physical activity also significantly associated with SHS score among women (P < 0.05).

Table 4.

Multilevel estimates for SHS score in relation to cardiovascular risk factors among female participants

Estimate (b) SE P value
Systolic blood pressure 0.388 0.181 0.032
Diastolic blood pressure 0.751 0.280 0.007
Plasma glucose 0.151 0.116 0.193
Total cholesterol 1.353 0.423 0.001
Triglyceride 1.245 0.407 0.002
HDL cholesterol −1.516 0.669 0.024
LDL cholesterol 0.420 0.365 0.250
Serum cortisol 0.225 0.005 <0.001
Body mass index 0.250 0.197 0.205
Level 2 (person) intercept variance (SE) 4.152 (1.530)
Level 2 (company) intercept variance (SE) 2.414 (1.116)

HDL high-density lipoprotein cholesterol, LDL low-density lipoprotein cholesterol

Discussion

This large cross-sectional study addresses the relationship of self-rated ill health with classical cardiovascular risk factors in the primary prevention of cardiovascular disease. This study is conducted in a representative sample of workers in urban Beijing. The response rate was high (88.7%), which therefore limited the potential selection bias. We found correlation between SHS and systolic blood pressure, diastolic blood pressure, plasma glucose, total cholesterol, and HDL cholesterol among men and correlation between SHS and systolic blood pressure, diastolic blood pressure, total cholesterol, triglyceride, and HDL cholesterol among women.

In our study, a newly created instrument, SHSQ-25, was used for measurement of SHS.2 The SHSQ-25 is a self-rated questionnaire of perceived health complaints. SHS is more prevalent in women than in men and more in white-collar workers than in blue-collar workers. In addition, the prevalence of SHS increases with age. This trend is consistent with the prevalence of metabolic syndrome and cardiovascular disease in urban China.1820 The similarity could partially be accounted by sharing common risk factors.

Significant higher level of serum cortisol among high SHS score group compared to low-score group (t = 34.076, P < 0.001) and significant linear correlation between SHS score and serum cortisol (r = 0.381, P < 0.001) strengthen the evidence that stress is an important related factor for SHS. With the rapid economic progress across China, employees have been becoming more exposed to stressful situations such as excessive workload, competition, and perceived loneliness.21 Continuous psychosocial stress seems to be a part of the everyday life in Chinese, especially among white-collar workers.22 Endocrine measures of stress and self-rated health (SRH) were also proved in a longitudinal study: poorer SRH at each point in time was associated with higher levels of serum cortisol and prolactin.23 SRH may capture subclinical or undiagnosed disease.24 In addition, the measures of perceived health modified the effects of biomedical risk factors both in the prediction of myocardial infarction and stroke.25,26 A possible pathway for observed effects is that SRH reflects the presence or absence of psychosocial risk factors or resources.24 Psychological stress can affect health not only directly through neuroendocrine responses, but also indirectly through changes in health behaviors.11 Current smoking was significantly more common in individuals giving higher SHS score. They also reported significantly less physical activity.

A growing body of research has documented that jobs or organizational roles which are associated with overload, excessive demands, and many responsibilities lead to a high risk of adverse health outcomes, especially cardiovascular.2731 The largest INTERHEART study covering 11,119 cases and 13,648 controls from 52 different countries all over the world confirmed this association with regard to work, home, financial, and major life stress.29 A higher occupational stress index was directly associated with higher systolic and diastolic blood pressures and higher level of plasma triglyceride in Taiwan white-collar male workers.30 Smolin et al. reported that there was a significant elevation in plasma glucose and HDL cholesterol under academic stress.31 In this study, we also found high SHS score associated with increased risk of cardiovascular disease, including blood pressure, plasma glucose, lipid, and BMI. The results of linear two-level model showed that the correlation of SHS and plasma glucose and triglyceride are inconsistent among men and women. After confounding variables were adjusted, BMI was shown to be not associated with SHS.

In China, chronic noncommunicable diseases accounts for about 80% of deaths and 70% of disability-adjusted life-years.3 As a developing country with huge population, it is imperative that an economical and valid instrument is developed for screening major chronic diseases. The SHSQ-25 is short and easy to be completed, and therefore, suitable for use in general population and primary care service.2 In many developed counties, much attention has been paid on perceived poor health “somatization” and “medically unexplained symptoms” in community and primary care system.32,33 Somatic symptom is one of the main reasons for patients seeking health care.34,35 SHS cannot be fully understood from the conventional disease-oriented biomedical point of view. Instead, it requires a holistic biopsychosocial perspective in which complaints are viewed as the result of complex interactions of physiology, psychology, and social environment. Primary care providers must be able to detect and manage SHS. The SHSQ-25 is a valid instrument for such purpose. Effective intervention on SHS may be a cost-effective way for preventing cardiovascular disease.

It could be argued that our participants were not representative of the general urban Chinese workers because they were recruited at the physical examination center of Beijing Xuanwu Hospital, Capital Medical University. The sample had different demographic distributions compared with urban Chinese workers.36 This could affect the generalization of the results.

Acknowledgments

This study was funded by the National High Technology Research and Development Grant (863 Program; 2006AA02Z434), the National Science Foundation (81102208), the National Science and Technology Support Program (2012BAI37B03), the Beijing Municipal Project for Developing Advanced Human Resources (20081D0501800211), and the Capital Medical University Grant (10JL16).

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