Literature DB >> 31027490

10-year ASCVD risk is positively correlated with depressive symptoms in a large general population.

Guo-Zhe Sun1, Ning Ye1, Shao-Jun Wu1, Ying Zhou1, Ying-Xian Sun2.   

Abstract

BACKGROUND: To explore the potential correlation between 10-year atherosclerotic cardiovascular disease (ASCVD) risk and depressive symptoms in a general population.
METHODS: A cross-sectional study involving 11,956 permanent residents of Liaoning Province in China ≥35 years of age was conducted. Depressive symptoms were assessed with the Patient Health Questionnaire-9 (PHQ-9) while 10-year ASCVD risk was calculated using the tool suitable for China.
RESULTS: Males had significantly higher 10-year ASCVD risk than females (14.2 ± 10.7% vs. 9.3 ± 9.1%; P <  0.001) but lower PHQ-9 score (2.34 ± 3.13 vs. 3.63 ± 4.02; P <  0.001). The mean PHQ-9 score increased significantly with advancing 10-year ASCVD risk category in both males (from 2.03 to 2.61; P for trend < 0.001) and females (from 3.04 to 4.61; P for trend < 0.001), and the increasing trend was more apparent in females (P <  0.001). Pearson correlation analyses showed that 10-year ASCVD risk positively correlated with PHQ-9 score in both sexes (Ps <  0.001). In multivariate linear regression analyses adjusting for confounding risk factors, the independent associations of 10-year ASCVD risk with PHQ-9 score were all significant in the total (β = 2.61; P <  0.001), male (β = 1.64; P = 0.001), and female subjects (β = 3.71; P <  0.001). Further, the interaction analysis proved the impacts of 10-year ASCVD risk on PHQ-9 score were more apparent in females than males (Ps < 0.001).
CONCLUSIONS: The 10-year ASCVD risk was positively associated with depressive symptoms in both males and females, which was more apparent in the latter. These findings provided some novel data about the value of 10-year ASCVD risk in estimating depressive symptoms.

Entities:  

Keywords:  10-year ASCVD risk; Depressive symptoms; Patient health Questionnaire-9

Mesh:

Year:  2019        PMID: 31027490      PMCID: PMC6486683          DOI: 10.1186/s12888-019-2114-7

Source DB:  PubMed          Journal:  BMC Psychiatry        ISSN: 1471-244X            Impact factor:   3.630


Background

Nowadays, cardiovascular disease (CVD) has become the leading cause of death and disease burden in China and world-wide [1, 2]. Great efforts have focused on the prevention and treatment of CVD. The Framingham Risk Score has long been proved a strong predictor of developing coronary heart disease (CHD) and cardiovascular events [3, 4]. And it’s used as a simple tool to evaluate the 10-year risk of CHD to inform the initiating of primary prevention. In China, Gu et al. developed and validated the Chinese atherosclerotic cardiovascular disease (ASCVD) risk equation based on the China-PAR project (Prediction for ASCVD Risk in China) in multiple contemporary Chinese cohorts [5]. This equation was suitable for China and popular-used for the prediction of ASCVD risk. Depression has become a worldwide public health problem, especially in women [6, 7], which contributes to an increased risk of disability [8] and mortality [9]. The prevalence of depression is significantly higher in patients with CVD and its presence increases the risk of adverse cardiovascular events [10]. Furthermore, depression has been proved recently to be an independent risk factor for the incidence of CHD [11] or even ischemic heart disease [12]. Therefore, it’s quite an important issue to define those with high possibility of depression so that we could make some strategies to control depressive symptoms and prevent its increased risk of ASCVD. However, whether the 10-year ASCVD risk is also associated with depressive symptoms or not has never been reported, even though the prevalence of depression was proved to be apparently higher in patients with CVD [13]. Therefore, the current study was designed to explore the potential correlation between 10-year ASCVD risk and depressive symptoms in a large general Chinese population.

Methods

A multi-stage, random, stratified, cluster-sampling scheme was performed in this study. The details about research design, data collection and measurements have been described previously [14, 15]. This study was approved by the Ethics Committee of China Medical University, and written consent was obtained from each participant or the proper proxy.

Study population

A total of 14,016 eligible permanent residents ≥35 years of age were invited to participate in the study, and 11,956 agreed and completed the study with a response rate of 85.3%. The exclusion criteria included pregnancy, malignant tumor and severe mental disorders (for example psychosis).

The patient health Questionnaire-9 score

In this study, we adopted the Patient Health Questionnaire-9 (PHQ-9) to evaluate depressive disorder, which was widely used in primary health settings as a screening instrument with good reliability and validity [16-18]. Based on the PHQ-9 tool, the total score would range from 0 to 27, and the severity of depressive disorder was then estimated by the level of PHQ-9 score [19]. And in this study, we conducted the analyses using PHQ-9 score as continuous scale.

10-year ASCVD risk

The 10-year predicted risk of ASCVD was calculated using the equations suitable for China developed by Gu et al. [5]. In the equations, besides the major risk factors including age, treated or untreated systolic blood pressure (SBP), total cholesterol (TC), high density lipid cholesterol (HDL-C), current smoking, and diabetes mellitus, 4 additional variables including waist circumference, geographic region, urbanization, and family history of ASCVD were added to the equation.

Definitions

In this study, educational level was divided into three types: primary school or less, middle school, high school or more. Family income was divided into three levels (China Yuan/year): low (≤ 5000), middle (5000–20,000) and high (> 20,000). As recommended by the Working Group on Obesity in China, obesity was defined as a body mass index (BMI) of 28.0 kg/m2 or higher [20]. In accordance with the JNC 7 Guidelines [21], hypertension was defined as a SBP ≥ 140 mmHg and/or a diastolic blood pressure (DBP) ≥ 90 mmHg and/or the use of antihypertensive medications. Diabetes mellitus was defined as a fasting blood glucose (FBG) ≥ 7.0 mmol/L, and/or being on treatment by the World Health Organization criteria [22]. The National Cholesterol Education Program-Third Adult Treatment Panel criteria was followed for defining dyslipidemia (one of the following elements: TC ≥ 6.21 mmol/L, HDL-C < 1.03 mmol/L, low density lipid cholesterol (LDL-C) ≥ 4.16 mmol/L and triglycerides (TG) ≥ 2.26 mmol/L) [23].

Statistical analysis

Data were expressed as mean ± standard deviation, percentage, correlation coefficient and β. Differences between groups were compared using two-tailed Student’s t-test, variance analysis or χ2 test as appropriate. The mean levels of PHQ-9 score among different 10-year ASCVD risk categories by sex were calculated and presented. Univariate general lineal model was used to test the interaction of sex and 10-year ASCVD risk category for PHQ-9 score. Pearson correlation analysis was performed to investigate the correlations between 10-year ASCVD risk and PHQ-9 score by sex and different medical conditions. Univariate and multivariate linear regression analyses were both conducted to identify the crude and adjusted linear associations of sex and 10-year ASCVD risk with PHQ-9 score. Further, the potential interaction of sex and 10-year ASCVD risk on PHQ-9 score was tested. All statistical analyses were performed using SPSS 17.0 software (SPSS Inc., Chicago, IL, USA), and a P <  0.05 was considered as statistically significant.

Results

Characteristics of the study population

Of the 11,956 participants, 896 had incomplete data and were excluded from the analysis, leaving a total of 11,060 participants (5080 males and 5980 females) with a mean age of 53.9 years. Table 1 presented the sex-specific baseline characteristics of the study population. Differences between males and females were compared using two-tailed Student’s t-test or χ2 test as appropriate. As a result, the male subjects were significantly older than females (54.4 ± 10.8 vs. 53.4 ± 10.3; P <  0.001). They had significantly higher levels of SBP, DBP, FBG and education, lower levels of BMI, TC, LDL-C and income, and higher percentage of smoking and drinking (all Ps <  0.05), whereas, there were no significant differences in TG and HDL-C between two groups. It’s worth nothing that males had significantly higher 10-year ASCVD risk than females (14.2 ± 10.7% vs. 9.3 ± 9.1%; P <  0.001) but lower level of PHQ-9 score (2.34 ± 3.13 vs. 3.63 ± 4.02; P <  0.001).
Table 1

Characteristics of the study sample

VariableMale (n = 5080)Female (n = 5980)P value
Age, years54.4 ± 10.853.4 ± 10.3<  0.001
BMI, kg/m224.7 ± 3.524.9 ± 3.80.038
SBP, mmHg143.5 ± 22.5140.0 ± 24.0<  0.001
DBP, mmHg83.7 ± 11.780.6 ± 11.5<  0.001
FBG, mmol/L5.95 ± 1.635.87 ± 1.610.011
TC, mmol/L5.17 ± 1.045.30 ± 1.12<  0.001
TG, mmol/L1.65 ± 1.621.62 ± 1.340.266
HDL-C, mmol/L1.41 ± 0.421.41 ± 0.340.683
LDL-C, mmol/L2.88 ± 0.792.97 ± 0.84<  0.001
Current smoker2906 (57.2)980 (16.4)<  0.001
Current drinker2303 (45.3)171 (2.9)<  0.001
Education<  0.001
 ≤ Primary school2134 (42.0)3405 (56.9)
 Middle school2381 (46.9)2110 (35.3)
 ≥ High school565 (11.1)465 (7.8)
Family income0.016
 Low683 (13.4)696 (11.6)
 Middle2733 (53.8)3292 (55.1)
 High1664 (32.8)1992 (33.3)
PHQ-9 score2.34 ± 3.133.63 ± 4.02<  0.001
10-year ASCVD risk, %14.2 ± 10.79.3 ± 9.1<  0.001

Abbreviations: BMI body mass index, ASCVD atherosclerotic cardiovascular disease, DBP diastolic blood pressure, FBG fasting blood glucose, HDL-C high density lipid cholesterol, LDL-C low density lipid cholesterol, PHQ-9 Patient Health Questionnaire-9, SBP systolic blood pressure, TC total cholesterol, TG triglycerides. Data are expressed as mean ± standard deviation or n (%)

Characteristics of the study sample Abbreviations: BMI body mass index, ASCVD atherosclerotic cardiovascular disease, DBP diastolic blood pressure, FBG fasting blood glucose, HDL-C high density lipid cholesterol, LDL-C low density lipid cholesterol, PHQ-9 Patient Health Questionnaire-9, SBP systolic blood pressure, TC total cholesterol, TG triglycerides. Data are expressed as mean ± standard deviation or n (%)

The sex-specific PHQ-9 score by 10-year ASCVD risk category

The mean levels of PHQ-9 score by sex and 10-year ASCVD risk category were presented in Fig. 1. Variance analysis was used to compare PHQ-9 score at different 10-year ASCVD risk categories. As a result, the mean PHQ-9 score increased significantly with advancing 10-year ASCVD risk category in both males (from the lowest of 2.03 to the highest of 2.61; P for trend < 0.001) and females (from the lowest of 3.04 to the highest of 4.61; P for trend < 0.001). Among each 10-year ASCVD risk category, the mean PHQ-9 score was significantly higher in females than males (all Ps <  0.001). Further, the univariate general lineal model was used to test the interaction of sex and 10-year ASCVD risk category for PHQ-9 score, showing significant difference (P <  0.001).
Fig. 1

The sex-specific PHQ-9 score by 10-year ASCVD risk category. Error bars represent standard deviation. ASCVD = atherosclerotic cardiovascular disease; PHQ-9 = Patient Health Questionnaire-9

The sex-specific PHQ-9 score by 10-year ASCVD risk category. Error bars represent standard deviation. ASCVD = atherosclerotic cardiovascular disease; PHQ-9 = Patient Health Questionnaire-9

Pearson correlations between 10-year ASCVD risk and PHQ-9 score

The sex-specific pearson correlation analyses for associations between 10-year ASCVD risk and PHQ-9 score were conducted and presented in Table 2. In both sexes, 10-year ASCVD risk showed significant and positive correlations with PHQ-9 score (Ps <  0.001). Further pearson correlation analyses presented various correlation coefficients according to different medical conditions (all Ps <  0.05).
Table 2

Pearson correlations between 10-year ASCVD risk and PHQ-9 score

MaleFemale
Correlation coefficientP valueCorrelation coefficientP value
All0.079<  0.0010.131<  0.001
Age, years
  < 600.0510.0030.087<  0.001
  ≥ 600.0620.0150.0640.009
Obesity
 Yes0.126<  0.0010.141<  0.001
 No0.074<  0.0010.136<  0.001
Hypertension
 Yes0.101<  0.0010.115<  0.001
 No0.0430.0360.100<  0.001
Diabetes
 Yes0.0950.0330.0820.036
 No0.064<  0.0010.120<  0.001
Dyslipidemia
 Yes0.116<  0.0010.133<  0.001
 No0.0450.0110.121<  0.001

Abbreviations: ASCVD atherosclerotic cardiovascular disease, PHQ-9 Patient Health Questionnaire-9

Pearson correlations between 10-year ASCVD risk and PHQ-9 score Abbreviations: ASCVD atherosclerotic cardiovascular disease, PHQ-9 Patient Health Questionnaire-9

Linear relationship between 10-year ASCVD risk and PHQ-9 score

The univariate and multivariate linear regression analyses for associations of sex and 10-year ASCVD risk with PHQ-9 score were performed and presented in Table 3. Significant correlations of sex and 10-year ASCVD risk with PHQ-9 score were observed in univariate linear regression (all Ps <  0.001). In the multivariate linear regression model, we included 10-year ASCVD risk, sex, and clinical covariates not in the 10-year ASCVD risk equation including BMI, DBP, TG, LDL-C, drinking, education and income. As a result, the independent association of 10-year ASCVD risk with PHQ-9 score remained in the total (β = 2.61; P <  0.001), male (β = 1.64; P = 0.001), and female subjects (β = 3.71; P <  0.001). The independent influence of sex on PHQ-9 score was also significant (P <  0.001). Finally, we tested the interaction of sex and 10-year ASCVD risk in both univariate and multivariate linear regression models, showing that sex had significant influence on the associations between 10-year ASCVD risk and PHQ-9 score with larger regression coefficients in females (Ps <  0.001).
Table 3

Sex-specific linear regression analyses for associations between 10-year ASCVD risk and PHQ-9 score

Model 1Model 2
βP valueβP value
All
 Sex*1.29<  0.0011.19<  0.001
 10-year ASCVD risk2.17<  0.0012.61<  0.001
Male
 10-year ASCVD risk2.31<  0.0011.640.001
Female
 10-year ASCVD risk5.81†<  0.0013.71†<  0.001

Abbreviations: ASCVD atherosclerotic cardiovascular disease, PHQ-9 Patient Health Questionnaire-9

Model 1: univariate linear regression model; Model 2: multivariate linear regression model including 10-year ASCVD risk, gender, body mass index, diastolic blood pressure, triglyceride, low density lipid cholesterol, drinking, education, and income

*: “0” for male and “1” for female in the analysis

†:P < 0.001 for gender difference

Sex-specific linear regression analyses for associations between 10-year ASCVD risk and PHQ-9 score Abbreviations: ASCVD atherosclerotic cardiovascular disease, PHQ-9 Patient Health Questionnaire-9 Model 1: univariate linear regression model; Model 2: multivariate linear regression model including 10-year ASCVD risk, gender, body mass index, diastolic blood pressure, triglyceride, low density lipid cholesterol, drinking, education, and income *: “0” for male and “1” for female in the analysis †:P < 0.001 for gender difference

Discussion

The results of this study indicated that the mean level of PHQ-9 score increased with advancing ASCVD risk category in both sexes, and the trend was more apparent in females than males. 10-year ASCVD risk positively correlated with PHQ-9 score with larger regression coefficients in females. Sex had significant effects not only on PHQ-9 score but also on the associations of 10-year ASCVD risk and PHQ-9 score. These findings firstly provide some data about associations between 10-year ASCVD risk and depressive symptoms in a general population. Recent studies demonstrated that depression was positively associated with both CVD incidence among healthy individuals [24] and adverse cardiovascular events among patients with established CVD [25, 26]. Therefore, great efforts were conducted to make clear of the epidemiological characteristics of depression and to make population-based prevention strategies. Accordingly, depression was reported to be quite common among patients with CVD [27]. Similarly, the prevalence of depression was significantly higher in patients with heart failure [28], hypertension [29], diabetes [30], stroke [31] than healthy population. Thus, high prevalence of depression was presented among patients with CVD. Now, our data firstly indicated that depressive symptoms was more common in subjects with higher 10-year predicted risk of ASCVD, suggesting that screening and controlling of the potential depressive symptoms were needed among subjects with high risk of ASCVD. The equation found by Gu et al. has been used widely as a tool suitable for China to assess the incidence risk of ASCVD, which was calculated based on age, treated or untreated SBP, TC, HDL-C, current smoking, diabetes mellitus, waist circumference, geographic region, urbanization and family history of ASCVD [5]. Previous studies have demonstrated that advancing age [7, 32], smoking [33], low HDL-C [34] and high SBP [28] were mostly correlated with depression although serum TC and depression might be inversely related [35]. Therefore, depression and ASCVD have some co-existing risk factors, which might partially explain the positive relationship between 10-year predicted risk and depressive symptoms in our current study. Further, health behaviors, inflammatory processes and heart rate variability might be the potential mechanisms that actually mediated the incidence of ASCVD and depression [36, 37]. However, some limitations are existing in our study. First, there was only PHQ-9 tool assessing depressive symptoms but no clinical diagnosis of depression by a psychiatrist. Second, the number of participants in some subgroups was relatively small so that an unintentional bias might be brought. Third, the current study was part of NCRCHS, and only rural Chinese subjects ≥35 years of age were included. In addition, covariates in the current study were relatively limited and some other possible covariates might give a bias.

Conclusions

10-year ASCVD risk was positively associated with depressive symptoms in both males and females. And more apparent impacts of 10-year ASCVD risk on PHQ-9 score were observed in females. These findings provided some novel insights into the value of 10-year ASCVD risk in estimating depressive symptoms. Much attention should be paid to depressive disorders among subjects with high 10-year ASCVD risk.
  36 in total

1.  Depression is a risk factor for incident coronary heart disease in women: An 18-year longitudinal study.

Authors:  Adrienne O'Neil; Aaron J Fisher; Katherine J Kibbey; Felice N Jacka; Mark A Kotowicz; Lana J Williams; Amanda L Stuart; Michael Berk; Paul A Lewandowski; Craig B Taylor; Julie A Pasco
Journal:  J Affect Disord       Date:  2016-02-16       Impact factor: 4.839

2.  Validation of the nine-item Patient Health Questionnaire to screen for major depression in a Chinese primary care population.

Authors:  Shulin Chen; Yu Fang; Helen Chiu; Hainan Fan; Tao Jin; Yeates Conwell
Journal:  Asia Pac Psychiatry       Date:  2013-03-27       Impact factor: 2.538

Review 3.  Prevalence of depression in survivors of acute myocardial infarction.

Authors:  Brett D Thombs; Eric B Bass; Daniel E Ford; Kerry J Stewart; Konstantinos K Tsilidis; Udita Patel; James A Fauerbach; David E Bush; Roy C Ziegelstein
Journal:  J Gen Intern Med       Date:  2006-01       Impact factor: 5.128

4.  Depression as a risk factor for mortality in patients with coronary heart disease: a meta-analysis.

Authors:  Jürgen Barth; Martina Schumacher; Christoph Herrmann-Lingen
Journal:  Psychosom Med       Date:  2004 Nov-Dec       Impact factor: 4.312

5.  Are cholesterol and depression inversely related? A meta-analysis of the association between two cardiac risk factors.

Authors:  Ju Young Shin; Jerry Suls; René Martin
Journal:  Ann Behav Med       Date:  2008-09-12

Review 6.  Depression as a risk factor for coronary artery disease: evidence, mechanisms, and treatment.

Authors:  Heather S Lett; James A Blumenthal; Michael A Babyak; Andrew Sherwood; Timothy Strauman; Clive Robins; Mark F Newman
Journal:  Psychosom Med       Date:  2004 May-Jun       Impact factor: 4.312

7.  Predicting the 10-Year Risks of Atherosclerotic Cardiovascular Disease in Chinese Population: The China-PAR Project (Prediction for ASCVD Risk in China).

Authors:  Xueli Yang; Jianxin Li; Dongsheng Hu; Jichun Chen; Ying Li; Jianfeng Huang; Xiaoqing Liu; Fangchao Liu; Jie Cao; Chong Shen; Ling Yu; Fanghong Lu; Xianping Wu; Liancheng Zhao; Xigui Wu; Dongfeng Gu
Journal:  Circulation       Date:  2016-09-28       Impact factor: 29.690

8.  Risks of all-cause and suicide mortality in mental disorders: a meta-review.

Authors:  Edward Chesney; Guy M Goodwin; Seena Fazel
Journal:  World Psychiatry       Date:  2014-06       Impact factor: 49.548

9.  Depression and cardiac disease: epidemiology, mechanisms, and diagnosis.

Authors:  Jeff C Huffman; Christopher M Celano; Scott R Beach; Shweta R Motiwala; James L Januzzi
Journal:  Cardiovasc Psychiatry Neurol       Date:  2013-04-07

Review 10.  Prevalence of Depression in Patients With Hypertension: A Systematic Review and Meta-Analysis.

Authors:  Zhanzhan Li; Yanyan Li; Lizhang Chen; Peng Chen; Yingyun Hu
Journal:  Medicine (Baltimore)       Date:  2015-08       Impact factor: 1.889

View more
  3 in total

1.  Association of Depression With 10-Year and Lifetime Cardiovascular Disease Risk Among US Adults, National Health and Nutrition Examination Survey, 2005-2018.

Authors:  Steven D Barger; Gabrielle C Struve
Journal:  Prev Chronic Dis       Date:  2022-05-26       Impact factor: 4.354

2.  Chronic Stress A Potential Suspect Zero of Atherosclerosis: A Systematic Review.

Authors:  Ling-Bing Meng; Yuan-Meng Zhang; Yue Luo; Tao Gong; De-Ping Liu
Journal:  Front Cardiovasc Med       Date:  2021-12-20

3.  Biological and clinical correlates of the patient health questionnaire-9: exploratory cross-sectional analyses of the baseline health study.

Authors:  Robert M Califf; Celeste Wong; P Murali Doraiswamy; David S Hong; David P Miller; Jessica L Mega
Journal:  BMJ Open       Date:  2022-01-04       Impact factor: 2.692

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.