Abstract
Objectives
This study aimed to identify sex differences in the association between depression and the risk of developing cardiovascular disease (CVD).
Methods
A secondary analysis was conducted of data from the fifth to seventh waves (2010−2018) of the Korea National Health and Nutrition Examination Survey. The participants were adults aged 30−74 years who had no diagnosis of CVD. The CVD risk was calculated using the Framingham Risk Score algorithm. Multiple linear regression analysis was conducted to identify the association between depression and CVD risk using a complex sample design.
Results
The mean CVD risk was higher in males and females with current depression (14.72% vs. 6.35%, respectively) than in males without current depression (11.67% and 4.42%, respectively). Current depression showed a significant association with CVD risk after controlling for only health-related characteristics, but the significance disappeared in both males and females when demographic characteristics were additionally controlled.
Conclusion
The presence of depression was not associated with CVD risk regardless of sex after controlling for confounding factors. Further studies are recommended to investigate the relationship between depression and CVD risk in a larger sample of both males and females with depression.
Keywords: Cardiovascular diseases, Depression, Risk, Sex
Introduction
Cardiovascular disease (CVD) refers to a range of conditions such as ischemic heart disease, stroke, heart failure, atrial fibrillation, and rheumatic heart disease [1], and was the top cause of death worldwide in 2015 [2] and the second leading cause of death in South Korea, with 108.3 deaths per 100,000 people in 2017 [3]. The prevalence of CVD in Korea was 12.2% (16.0% in males, 17.4% in females); it was higher in males than in females below 50 years of age, but its prevalence significantly increased in females at ages over 50 [4]. Meanwhile, CVD risk in Korea is higher in males than in females [5]. Hypertension, dyslipidemia, diabetes, obesity, and poor health behaviors such as smoking, drinking, and lack of physical activity are major risk factors for CVD [1]. Social factors (e.g., marital status, education level, and social status) and psychological factors (e.g., stress, social support, and depression) are also considered to be important risk factors for CVD [6−8].
Depression is experienced by more than 300 million people globally [9]. In Korea, the lifetime prevalence of major depressive disorder in Korea was found to be 5.0% (3.0% for males and 6.9% for females), making it the second most common mental illness in 2016 after alcohol and nicotine abuse [10]. Depression may be linked to CVD through various factors, including lifestyle factors, autonomic nervous system disturbances, endocrine disruption, inflammatory diseases, platelet aggregation, and endothelial dysfunction [11,12]. More specifically, many patients with depression show poor lifestyle habits that increase the risk of CVD, including sleep deprivation, smoking, drinking, lack of physical activity, poor hygiene, and lack of adherence to medication [13].
Several studies have investigated the relationships between depression and CVD occurrence and/or risks [11−15], and some of them have shown significant associations between these variables [8,14,15]. However, studies of the relationships between these variables according to sex did not show consistent results [15−17]. In Korea, few studies have examined the relationship between depression and CVD risk factors [18−20]. Moreover, no study has directly identified the relationship between depression and CVD occurrence or CVD risk; in particular, no analytical study has explored these variables separately in males and females. In addition, in a meta-analysis of the relationship between depression and the onset of coronary atherosclerosis, most studies were conducted in Western countries [21]. Therefore, this study investigated the relationship between depression and CVD risk using data from the Korea National Health and Nutrition Survey (KNHANES), with the aim of filling the existing gap by examining that relationship by sex in an Asian population.
Materials and Methods
Participants
We conducted a secondary analysis of data collected from 5th to 7th waves (2010−2018) of the KNHANES, which is conducted by the Korea Centers for Disease Control and Prevention. The KNHANES is an ongoing national survey system conducted to assess the health and nutritional status of Koreans, monitor changes in health risk factors and the prevalence of major diseases, and provide evidence to develop health policies and programs in Korea [22,23]. It was initiated in 1998, and the seventh survey has been completed. It was a triannual survey up to the third KNHANES, after which it was conducted annually (from 2007 onwards). The sample of KNHANES VII was selected using 2-stage stratified cluster sampling for enumeration districts and households, and a health survey, health examination, and nutrition survey were conducted among appropriate household members.
The inclusion criteria for this study were as follows: no missing data for sampling weight, age between 30 and 74 years, the availability of depression data, no history of CVD (e.g., stroke, angina pectoris, or myocardial infarction), and no missing data on socio-demographics, health-related characteristics, depression, and CVD risk. Among 72,751 participants in the fifth to seventh survey, a total of 24,537 (10,183 males and 14,354 females) met those inclusion criteria (Figure 1).
Figure 1.
The selection process of study subjects.
Variables and Definitions
CVD risk, as the main outcome variable, was assessed using the Framingham Risk Score (FRS), which is a sex-specific algorithm used to estimate the 10-year CVD risk of an individual based on the Framingham Heart Study [24]. The formulas for males and females are presented separately so that the probability of developing CVD in the next 10 years can be predicted as a percentage according to sex (Table S1). There are 2 models for calculating the risk of CVD: the primary model (P model) and the simple office-based non-laboratory model (S model). Common variables in both models are sex, age, systolic blood pressure (SBP) (with/without treatment), current smoking, and diabetes. Additional variables are total cholesterol or high-density lipoprotein (HDL) cholesterol (mg/dL) for the P model, and body mass index for the S model [25]. We used the P model for the FRS, as the laboratory results were available. SBP was measured by taking the average of 3 readings. People without diagnosed hypertension were regarded as “not treated.”
Depression, as the major explanatory variable, was categorized as “never,” “past,” and “current” according to the responses to the survey question on the history of diagnosed depression (“I have been diagnosed [with depression] by a doctor” and “I am currently suffering [from depression]”). Confounding variables included socio-demographic factors (age, employment, and household income) and health-related characteristics (alcohol intake, current smoking, physical activity, perceived stress, and comorbidities) known to be associated with depression [26−31] or CVD risk [32,33]. The variables were categorized as follows: “30−39,” “40−49,” “50−59,” “60−69,” and “over 70 years old” for age; “no,” “yes, regular job,” and “yes, irregular job” for employment; quartiles 1−4 for household income; “less than once per month,” “1−4 times per month,” and “2 times and higher per week” for alcohol intake; “yes” and “no” for current smoking; “yes” or “no” for engagement in high- or moderate-intensity physical activity during work or leisure for physical activity; and “much” and “little” for perceived stress. Comorbidities consisted of hypertension, diabetes, and dyslipidemia, and each disease was classified as “yes” or “no” depending on whether it had been diagnosed by a physician or not.
Data Analysis
The data were analyzed with IBM SPSS ver. 25.0 (IBM Corp., Armonk, NY, USA) using a complex sample design considering strata, cluster, and the combined sampling weight of 2 years. A 2-tailed test was performed with a significance level (α) of 0.05. The variables in the study were calculated using non-weighted frequency, weighted percentage, or mean and standard error according to sex. The distribution of CVD risk according to characteristics of the participants was analyzed using the chi-square test. As the CVD risk data did not satisfy the assumption of normality, CVD risk was classified as “lower risk” and “higher risk” based on the top 25% (15% for males and 5% for females). Multiple logistic regression analyses were conducted to evaluate the association of depression and CVD risk after controlling for confounding factors. We considered 4 models according to confounding factors input in the models: age (continuous) only in model 1; age (continuous), income, and occupation in model 2; drinking, smoking, physical activity, stress, and comorbidities in model 3; and all factors in model 4. Multi-collinearity was assessed based on a correlation coefficient ≥0.85. Meanwhile, we performed a sensitivity analysis to check the robustness of the findings on the impact of depression on CVD risk using the S model, which is used to calculate the FRS using body mass index instead of laboratory tests with total and HDL cholesterol results [24].
Ethical Considerations
This study was conducted after receiving permission for the use of data from the website of the KNHANES, and approval of exemption from review (IRB No: 2019_141_HR) from the Pusan National University Institutional Review Board.
Results
Characteristics and CVD Risk of the Participants
Table 1 shows participants’ socio-demographic and health-related characteristics according to sex. Most of the 10,183 males were under 50 years old (61.2%), currently employed (80.8%), and in the third and fourth quartile income groups (65.3%); 43.2% were current smokers; and 1.1% had current depression. The majority of the 14,354 females were under 50 years old (60.6%), currently unemployed (53.8%), and in the third and fourth quartile income groups (61.0%); only 6.4% were current smokers; and 3.2% had current depression. All characteristics of the participants were significantly different according to sex. The distribution of CVD risk and its components is presented in Table 2. The mean CVD risk was 11.70% among males and 4.48% among females, reflecting a significant difference.
Table 1.
Characteristics of the study participants according to sex
| Characteristic | Male (n=10,183) | Female (n=14,354) | p |
|---|---|---|---|
| Age group (y) | 0.005 | ||
| 30−39 | 2,725 (32.8) | 4,055 (31.0) | |
| 40−49 | 2,484 (28.4) | 3,717 (29.6) | |
| 50−59 | 2,112 (21.6) | 3,254 (22.8) | |
| ≥60 | 2,862 (17.1) | 3,328 (16.6) | |
| Employment | <0.001 | ||
| No | 2,491 (19.2) | 8,003 (53.8) | |
| Yes, irregular | 1,281 (12.8) | 2,124 (15.4) | |
| Yes, regular | 6,411 (68.0) | 4,227 (30.8) | |
| Household income (quartile) | <0.001 | ||
| 1st | 1,286 (10.3) | 2,031 (12.5) | |
| 2nd | 2,516 (24.4) | 3,724 (26.5) | |
| 3rd | 3,151 (32.8) | 4,328 (31.0) | |
| 4th | 3,230 (32.5) | 4,271 (30.0) | |
| Alcohol intake | <0.001 | ||
| <1 time/mo | 2,317 (21.9) | 7,636 (50.9) | |
| 1−4 times/mo | 3,905 (39.2) | 5,063 (36.9) | |
| ≥2 times/wk | 3,961 (38.9) | 1,655 (12.2) | |
| Smoking | <0.001 | ||
| Never | 1,843 (18.8) | 12,723 (87.5) | |
| Past | 4,256 (37.8) | 826 (6.1) | |
| Current | 4,084 (43.3) | 802 (6.4) | |
| Physical activity | 3,415 (35.7) | 3,586 (26.1) | <0.001 |
| Perceived stress | 0.005 | ||
| Much | 2,429 (25.3) | 3,777 (27.2) | |
| Little | 7,754 (74.7) | 10,577 (72.8) | |
| Comorbidities | |||
| Hypertension | 2,194 (17.2) | 2,374 (13.6) | <0.001 |
| Diabetes | 891 (6.7) | 794 (4.6) | <0.001 |
| Dyslipidemia | 1,261 (11.1) | 2,139 (12.8) | <0.001 |
| Depression diagnosed | <0.001 | ||
| Never | 9,983 (98.0) | 13,454 (93.9) | |
| Past | 85 (0.9) | 409 (2.9) | |
| Current | 115 (1.1) | 491 (3.2) |
Data are unweighted number and weighted proportions.
Table 2.
Distribution of cardiovascular disease risk and its components according to sex
| Characteristic | Male (n=10,183) | Female (n=14,354) | p |
|---|---|---|---|
| Age (y) | 47.00±0.15 | 47.19±0.13 | 0.210 |
| Total cholesterol (mg/dL) | 194.24±0.42 | 193.37±0.36 | 0.104 |
| HDL cholesterol (mg/dL) | 47.07±0.13 | 54.51±0.13 | <0.001 |
| SBP (mmHg) | 120.13±0.18 | 113.84±0.18 | <0.001 |
| Hypertension treatment | 1,935 (14.8) | 2,185 (12.4) | <0.001 |
| Diabetes | 891 (6.7) | 794 (4.6) | <0.001 |
| Current smoking | 4,069 (43.2) | 773 (6.2) | <0.001 |
| CVD risk (%) | <0.001 | ||
| <5 | 2,820 (33.4) | 9,462 (71.6) | |
| 5−9 | 2,294 (25.5) | 2,744 (17.1) | |
| 10−19 | 2,600 (24.1) | 1,674 (9.1) | |
| ≥20 | 2,468 (17.0) | 473 (2.2) | |
| Mean±SE | 11.70±0.13 | 4.48±0.05 | <0.001 |
Data are presented as mean±SE or n (%). Data are unweighted number and weighted proportions.
HDL, high-density lipoprotein; SBP, systolic blood pressure; CVD, cardiovascular disease; SE, standard error.
The Association between Depression and CVD Risk
According to the bivariate analysis, as shown in Tables 3 and 4, current depression was associated with CVD risk in both males and females. The mean CVD risk was higher in males and females with current depression (14.72% vs. 6.35%, respectively) than in males without current depression (11.67% and 4.42%, respectively). The prevalence of current depression among those with higher CVD risk was 1.6% in males and 5.0% in females, which was significantly higher than the prevalence among those with lower CVD risk. According to multiple logistic regression analysis, current depression showed a significant association with CVD risk after controlling for health-related characteristics, but the significance disappeared in both males and females when demographic characteristics were additionally controlled (Table 5).
Table 3.
Relationship between the characteristics of the participants and cardiovascular disease risk among males (n=10,183)
| Characteristic | Mean±SE | Lower risk (n=6,624) | Higher risk (n=3,559) | pa) |
|---|---|---|---|---|
| Age group (y) | <0.001 | |||
| 30−39 | 3.70±0.05 | 2,715 (44.3) | 10 (0.4) | |
| 40−49 | 8.40±0.12 | 2,266 (35.0) | 218 (9.9) | |
| 50−59 | 15.90±0.23 | 1,187 (16.7) | 925 (35.4) | |
| ≥60 | 27.21±0.31 | 456 (4.0) | 2,406 (54.3) | |
| Employment | <0.001 | |||
| No | 20.35±0.36 | 769 (11.2) | 1,722 (41.9) | |
| Yes, irregular | 14.12±0.35 | 708 (11.3) | 473 (17.1) | |
| Yes, regular | 8.80±0.12 | 5,147 (77.5) | 1,264 (41.0) | |
| Household income (quartile) | <0.001 | |||
| 1st | 20.43±0.50 | 424 (6.4) | 862 (21.3) | |
| 2nd | 12.33±0.26 | 1,514 (23.7) | 1,002 (26.6) | |
| 3rd | 10.11±0.19 | 2,287 (35.2) | 864 (26.1) | |
| 4th | 10.05±0.17 | 2,399 (34.7) | 831 (26.0) | |
| Alcohol intake | <0.001 | |||
| <1 time/mo | 12.77±0.28 | 1,392 (21.1) | 925 (24.1) | |
| 1−4 times/mo | 9.97±0.18 | 2,803 (42.4) | 1,102 (30.3) | |
| ≥2 times/wk | 12.84±0.20 | 2,429 (36.5) | 1,532 (45.6) | |
| Current smoking | <0.001 | |||
| No | 10.04±0.14 | 4,152 (60.1) | 1,962 (47.7) | |
| Yes | 13.89±0.22 | 2,472 (39.9) | 1,597 (52.3) | |
| Physical activity | <0.001 | |||
| No | 12.71±0.17 | 4,154 (61.2) | 2,614 (72.8) | |
| Yes | 9.88±0.17 | 2,470 (38.8) | 945 (27.2) | |
| Perceived stress | <0.001 | |||
| Much | 9.64±0.21 | 1,852 (28.0) | 577 (17.7) | |
| Little | 12.40±0.15 | 4,772 (72.0) | 2,982 (82.3) | |
| Comorbidities | <0.001 | |||
| No | 8.48±0.10 | 5,645 (86.1) | 1,488 (43.7) | |
| Yes | 21.36±0.31 | 979 (13.9) | 2,071 (56.3) | |
| Current depression | 0.030 | |||
| No | 11.67±0.13 | 6,563 (99.0) | 3,505 (98.4) | |
| Yes | 14.72±1.17 | 61 (1.0) | 54 (1.6) |
Data are presented as mean±SE or n (%). Data are unweighted number and weighted proportions.
SE, standard error.
The value was obtained by the chi-square test.
Table 4.
Relationship between the characteristics of the participants and cardiovascular disease risk among females (n=14,354)
| Characteristic | Mean±SE | Lower risk (n=9,462) | Higher risk (n=4,892) | pa) |
|---|---|---|---|---|
| Age group (y) | <0.001 | |||
| 30−39 | 1.18±0.01 | 4,036 (43.1) | 19 (0.6) | |
| 40−49 | 2.67±0.03 | 3,416 (37.7) | 301 (9.1) | |
| 50−59 | 5.93±0.08 | 1,670 (16.6) | 1,584 (38.3) | |
| ≥60 | 11.90±0.15 | 340 (2.6) | 2,988 (52.0) | |
| Employment | <0.001 | |||
| No | 5.12±0.08 | 4,787 (50.3) | 3,216 (62.9) | |
| Yes, irregular | 4.83±0.12 | 1,297 (14.4) | 827 (17.9) | |
| Yes, regular | 3.19±0.06 | 3,378 (35.4) | 849 (19.2) | |
| Household income (quartile) | <0.001 | |||
| 1st | 8.66±0.20 | 656 (7.3) | 1,375 (25.5) | |
| 2nd | 4.74±0.10 | 2,266 (25.2) | 1,458 (29.8) | |
| 3rd | 3.60±0.07 | 3,235 (34.0) | 1,093 (23.6) | |
| 4th | 3.43±0.06 | 3,305 (33.5) | 966 (21.1) | |
| Alcohol intake | <0.001 | |||
| <1 time/mo | 5.11±0.07 | 4,588 (47.2) | 3,048 (59.9) | |
| 1−4 times/mo | 3.87±0.07 | 3,642 (39.4) | 1,421 (30.7) | |
| ≥2 times/wk | 3.74±0.12 | 1,232 (13.4) | 423 (9.4) | |
| Current smoking | <0.001 | |||
| No | 4.37±0.05 | 9,024 (94.7) | 4,557 (91.7) | |
| Yes | 6.17±0.26 | 438 (5.3) | 335 (8.3) | |
| Physical activity | <0.001 | |||
| No | 4.78±0.06 | 6,801 (71.3) | 3,967 (80.3) | |
| Yes | 3.65±0.07 | 2,661 (28.7) | 925 (19.7) | |
| Perceived stress | <0.001 | |||
| Much | 4.27±0.09 | 2,586 (28.1) | 1,191 (25.0) | |
| Little | 4.56±0.06 | 6,876 (71.9) | 3,701 (75.0) | |
| Comorbidities | <0.001 | |||
| No | 2.93±0.03 | 8,675 (92.1) | 2,023 (42.7) | |
| Yes | 10.02±0.14 | 787 (7.9) | 2,869 (57.3) | |
| Current depression | <0.001 | |||
| No | 4.42±0.05 | 9,231 (97.5) | 4,632 (95.0) | |
| Yes | 6.35±0.29 | 231 (2.5) | 260 (5.0) |
Data are presented as mean±SE or n (%). Data are unweighted number and weighted proportions.
The value was obtained by the chi-square test.
Table 5.
Multiple logistic regression results on the association between depression and cardiovascular disease risk by sex
| Modela) | Male (n=10,183) |
Female (n=14,354) |
||||
|---|---|---|---|---|---|---|
| OR (95% CI) | p | R2b) | OR (95% CI) | p | R2b) | |
| 0 | 1.62 (1.04−2.53) | 0.032 | 0.001 | 2.09 (1.69−2.60) | <0.001 | 0.004 |
| 1 | 1.26 (0.67−2.37) | 0.469 | 0.417 | 1.28 (0.88−1.87) | 0.203 | 0.457 |
| 2 | 1.06 (0.55−2.01 | 0.869 | 0.418 | 1.17 (0.79−1.71) | 0.433 | 0.459 |
| 3 | 1.81 (1.12−2.94) | 0.016 | 0.201 | 1.62 (1.24−2.13) | <0.001 | 0.253 |
| 4 | 1.07 (0.55−2.08) | 0.837 | 0.511 | 0.92 (0.64−1.33) | 0.671 | 0.494 |
OR, odds ratio; CI, confidence interval.
Each model was adjusted as follows: 0, no adjustment; 1, by age (continuous); 2, by age (continuous), income, and occupation; 3, by drinking, smoking, physical activity, stress, and comorbidities; 4, by all factors.
Cox & Sneel R2.
Sensitivity Analysis
In the sensitivity analysis of CVD risk calculated using the S model, the mean CVD risk was 13.11% for males and 4.93% for females (Table S2). In the bivariate analysis, CVD risk was higher in subjects with current depression than in subjects without current depression both for males (p=0.032) and for females (p<0.001). However, there was no significant association between depression and CVD risk after controlling for confounding factors, which showed similar trends to the results obtained by using the P model for CVD risk calculation (Table S3).
Discussion
This study aimed to investigate the relationship between depression and CVD risk by sex using data from a representative community-based health survey in Korea. The prevalence of current depression was 1.1% in males and 3.2% in females, and it increased to 2.0% in males and 6.1% in females when including past depression. This figure is slightly lower than the prevalence of 5.0% (3.0% in males, 6.9% in females) reported in a previous survey in 2016 [10], where depression was measured with the Korean version of Composite International Diagnostic Interview (CIDI). Since depression was identified by a self-reported physician’s diagnosis in this study, those who show depressive moods but have never been diagnosed by a physician were classified as “not depressed,” resulting in a potential underestimation of the prevalence of depression.
The CVD risk was measured with the FRS, which is a well-known measure of 10-year CVD risk, and its validity has been established in various populations including Koreans [34,35]. The CVD risk was higher in males than in females, which is consistent with a previous finding in a French cohort where CVD risk was measured by the FRS [36]. The CVD risk by sex also showed a similar trend in a sensitivity analysis with non-laboratory data, although CVD risk with non-laboratory data was consistently higher than CVD risk with laboratory data (Figure S1).
Without controlling for confounding factors, males and females with current depression showed 1.62 and 2.09 times higher CVD risk than those without depression, respectively, corresponding to a slightly higher effect size than that of 1.46 (95% confidence interval [CI], 1.37−1.55) reported in a meta-analysis [37]. However, depression was no longer associated with CVD risk after controlling for well-known confounding factors, including socio-demographic and health-related characteristics [26−33]. Nonetheless, an independent association between depression and CVD risk was found after controlling for only health-related characteristics for both males and females, with CVD risk calculated by the P model and S model. Health behaviors are important factors that explain the relationship between depression and CVD [11,12]. The prevalence of risk factors of CVD such as obesity, smoking, diabetes, and hypertension was found to be high in individuals with severe mental health disorders such as depression in a previous study [38]. According to our additional stratified analyses according to these categories, some health-related characteristics (e.g., alcohol intake, current smoking, and perceived stress) seem to act as effect modifiers, not as confounding factors, between the 2 variables (Table S4). For instance, males with depression who drank more than twice a week, smoked cigarettes, and experienced a high level of stress had higher CVD risk than their counterparts without depression. Unlike males, females with depression who drank fewer than 4 times a month and did not smoke had a higher CVD risk than those who did not have depression. This finding may be related to a lack of statistical power due to the small sample of heavy drinkers and smokers in females.
Meanwhile, the findings on the relationship between depression and CVD risk by sex are not consistent among studies [15−17]. In a cohort study of United States (US) middle-aged and older adults who had never been diagnosed with stroke or heart disease, CVD occurred 1.39 times (95% CI, 1.20−1.61) more often in males and 1.19 times (95% CI, 1.05−1.35) more often in females who had depressive symptoms than in those who did not have depression, showing a significant correlation in both sexes [15]. According to the study of Holt et al. [16] using cohort data in the United Kingdom, CVD incidence increased by 1.130 times (95% CI, 1.034−1.235; p=0.007) in males with high depression scores, but no significant relationship was found in females. However, the study of Kouvari et al. [17] using cohort data in healthy populations without chronic diseases showed that depression was only associated with the incidence and recurrence of CVD in females. The inconsistent findings of studies on the relationship between depression and CVD risk by sex underscore the importance of further replication studies.
Strengths and Limitations
To our knowledge, this is the first study to identify the relationship between depression and CVD risk by sex using nationwide community-based data. This study has many strengths. First, we identified the relationship between depression and CVD risk after controlling for socio-demographic and health-related characteristics that are known to affect the relationship. Second, we used a large, nationally representative dataset for the entire country during 9 years, which increases the generalizability of our findings.
However, the following limitations need to be taken into account when interpreting the results. First, this study did not control for the effects of variables such as potential biomarkers that affect CVD risk, since this was a secondary data analysis study and that information was not available. Second, as depression is defined by the subject’s reported diagnosis, the actual prevalence of depression may have been underestimated due to the possibility of undiagnosed depression. According to a nationwide survey of mental disorders in 2016, the use of mental health service over the past year was 9.6% [10], which was much lower than the rates of 14.2% in the US, 39.5% in Belgium, 35.5% in Spain, and 20% in Japan [39,40]. This underestimation leads to misclassification bias, as subjects with strong depressive symptoms who were undiagnosed by a physician were classified as not having depression, thereby weakening the strength of the association between the 2 variables. Third, CVD risk is a predicted value and may differ from the actual occurrence of CVD. In particular, CVD risk reflects the probability of CVD occurrence within 10 years. If the values used to calculate CVD risk change over time, CVD risk also changes, which may result in a difference in the actual incidence of CVD. Finally, study subjects with CVD, as well as those under 30 years old or over 75 years old, were excluded from the study, impeding the generalizability of the study results to these subjects.
Conclusion
According to our findings, the prevalence of depression was 3 times higher in females than in males, and CVD risk was more than 2.5 times as high in males as in females. The presence of depression was not associated with CVD risk in either males or females after controlling for confounding factors. This finding may be related to the small sample with depression and misclassification bias, as depression was defined according to a subject’s reported diagnosis. Therefore, we recommend that further research should investigate the relationship between depression and CVD risk in a larger sample of individuals with depression and take steps to minimize the underestimation of depression by using both subjects’ reported diagnoses and depressive symptoms in both males and females.
Footnotes
Ethics Approval
This study was conducted after receiving permission for the use of data from the website of the KNHANES, and approval of exemption from review (IRB No: 2019_141_HR) from the Pusan University Institutional Review Board.
Conflicts of Interest
The authors have no conflicts of interest to declare.
Funding
None.
Availability of Data
All the data supporting the results of this study are included in the article and the supplementary file.
Supplementary Material
Table S1. The cardiovascular risk functions; Table S2. The distribution of cardiovascular disease risk calculated by simple office-based non-laboratory model; Table S3. Multiple logistic regression results on the association between depression and cardiovascular disease risk by the simple office-based non-laboratory model; Table S4. Additional analysis results on the association between depression and cardiovascular disease risk after stratifying according to categories; Figure S1. Agreement of cardiovascular risk calculated by primary model and simple office-based non-laboratory model according to sex. Supplementary data is available at https://doi.org/10.24171/j.phrp.2021.12.2.08.
The cardiovascular risk functions
The distribution of cardiovascular disease risk calculated by simple office-based non-laboratory model
Multiple logistic regression results on the association between depression and cardiovascular disease risk by the simple office-based non-laboratory model
Additional analysis results on the association between depression and cardiovascular disease risk after stratifying according to categories
Agreement of cardiovascular risk calculated by primary model and simple office-based non-laboratory model according to sex
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Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Supplementary Materials
The cardiovascular risk functions
The distribution of cardiovascular disease risk calculated by simple office-based non-laboratory model
Multiple logistic regression results on the association between depression and cardiovascular disease risk by the simple office-based non-laboratory model
Additional analysis results on the association between depression and cardiovascular disease risk after stratifying according to categories
Agreement of cardiovascular risk calculated by primary model and simple office-based non-laboratory model according to sex