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. 2020 Jul 30;15(7):e0236665. doi: 10.1371/journal.pone.0236665

Association between disability and cardiovascular event and mortality: A nationwide representative longitudinal study in Korea

Ki Young Son 1, Seung Hee Kim 1, Sung Sunwoo 1, Ji-Yun Lee 1, Seongmi Lim 2, Young Sik Kim 1,*
Editor: Xianwu Cheng3
PMCID: PMC7392251  PMID: 32730313

Abstract

This study aimed to examine the association between disability and cardiovascular (CV) disease incidence and mortality in Korea longitudinally, using a national representative sample. We used the National Health Insurance Service-National Health Screening Cohort (NHIS-HEALS) database, which includes information on the disability of the National Screening Program participants such as severity and type of disability, which were obtained from the Korean National Disability Registry. Cox proportional hazard models were used to evaluate the association between disability and CV disease incidence and mortality. We constructed four models with different levels of adjustment, in which Model 3 was a fully adjusted model. This study included 514,679 participants, and 7,317 CV deaths were reported within a mean follow up of 10.8 ± 3.9 years (maximum, 13.9 years). For 5,572,130 person-year (PY) follow-up, the CV mortality rate was 1.313 per 1,000 PY. In Models 1 and 2, CV disease incidence was significantly higher in participants with disability than in those without disability. In Model 3, the incidence was higher only among participants aged 50–64 years and severe disabled participants aged <50 years. CV mortality was significantly higher in participants with disability than in those without disability in all Models, and the mortality increased in both sexes in Models 1 and 2 but only increased in men in Model 3. Similar results were observed in the subgroup analysis of health behavior and chronic diseases. People with disability showed higher CV disease incidence and mortality than those without disability, regardless of the type of disability or risk factors for CV disease.

Introduction

Disability is defined by the International Classification of Functioning, Disability and Health as the state of having limitations in body functions, structures, activities, and participation [1]. According to the National Disability Registry (NDR) of Korea, over 2.4 million individuals were registered as people with disability, which accounted for 5% of the Korean population [2].

Despite the importance of health in people with disabilities, they have received little attention within the health care system [3, 4]. A previous study in Korea showed that people with disability were more likely to be physically inactive, have higher incidence of osteoporosis, to be underweight, have suicidal thoughts, and have impaired quality of life [5]. Several studies in western countries also showed that people with disability often have adverse health behaviors (i.e., cigarette smoking, at-risk alcohol drinking, physical inactivity, and unhealthy diet) [611], receive fewer preventive health care services (i.e., cancer screening and vaccination) [1216], and have chronic diseases [6, 1720]. Furthermore, total and cardiovascular (CV) mortality increased in people with disability [2125], and a study on elderly people aged >80 years showed that disability exerts an important influence on mortality regardless of age and multimorbidity [26]. For this reason, we hypothesized that people with disability would show higher CV disease incidence and mortality owing to higher CV risk factors.

However, most previous studies that investigated the association between disability and mortality were small studies limited to a specific population or were focused only on a specific measure of disability such as physical capability measured by handgrip strength or gait speed. To our knowledge, there is no large longitudinal general population study evaluating the association between disability and CV disease incidence and mortality, especially in Asian countries.

This study aimed to examine the association between disability and CV disease incidence and mortality in Korea longitudinally, using a national representative sample.

Materials and methods

Study setting

The Korean National Health Insurance Service (KNHIS) is a public health insurance that provides universal health coverage to almost all Koreans, except Medicaid beneficiaries who account for <3% of the Korean population. The KNHIS provides a National Screening Program (NSP), a biennial health screening program for all people aged >40 years and all employees regardless of age. KNHIS created the National Health Information Database (NHID), which includes data on healthcare utilization, health screening results in NSP, sociodemographic variables, and mortality for over 50 million individuals in Korea [27]. The NHID has been widely used in various epidemiological and health policy studies, and details of the database profile are described elsewhere [27, 28].

Data sources and study population

We used the National Health Insurance Service-National Health Screening Cohort (NHIS-HEALS) database of NHID, in which 515,867 participants were included. This represents 10% of a randomly selected people from the total Korean participants aged 40–79 years who participated in the NSP at least once in 2002–2003. After excluding participants with missing data or who were misclassified, 514,679 were included in the present study.

The database included participants’ demographic data (i.e., age, sex, residential area, and income status); disability information; survey data regarding past medical history and health behaviors; and screening results including height, weight, abdominal circumference, and laboratory tests. We also obtained data on medical facility utilization and the number of deaths.

The Asan Medical Center Institutional Review Board approved this study (IRB number: 2019–0563), and the requirement for informed consent was waived because the KNHIS database was constructed after anonymization according to strict confidentiality guidelines.

Variables

Independent variable

In this study, we used severity and type of disability as the independent variable, which is baseline characteristic at the time of NSP and time-invariant in our analysis model. The NHIS-HEALS dataset includes information on disability of NSP participants such as severity and type of disabilities, which were obtained from the Korean National Disability Registry. The severity of disability was divided into six grades, from 1 to 6. Grade 1 indicates extremely severe disability, while grade 6 indicates the least severe disability. In NHIS-HEALS dataset, grades 1 and 2 are categorized as “severe disability,” while grades 3–6 as “mild disability.” If participants have no disability grade, they are categorized as “normal,” which indicates that they are persons without disability. The types of disability were divided into eight categories: physical impairment, brain impairment, visual impairment, hearing impairment, linguistic impairment, mental impairment, and others (i.e., developmental disability, renal function impairment, heart function impairment, respiratory function impairment, liver function impairment, facial deformity, intestinal and urinary tract function impairment, and epilepsy). The definition of type of disability as following: physical impairment is disability related to amputation, motor disturbance, joint disability, deformity of limbs, or spinal cord injury. Brain impairment is related to brain disability caused by stroke, brain damage, or cerebral palsy. Visual impairment is related to visual loss or visual field defect, and hearing impairment is related to hearing disability or disability in sense of equilibrium. Linguistic impairment is related to mogilalia or dysphonia. Mental impairment is mental illness with limitation of daily life such as depression or schizophrenia, which is different from mental retardation that means intelligence quotient < 70. Because there were only small number of participants except physical impairment, we aggregated type of disability as following: physical, sensory (visual impairment + hearing impairment), neuropsychological (brain impairment + linguistic impairment + mental impairment + mental retardation), and others.

Outcome variables

CV event and mortality were outcome variables of this study. Data regarding the diagnosis of a CV event, the date of event, the cause of death, and date of death were obtained from the NHIS-HEALS database in 2002–2015. CV event or death was defined as event of or death caused by ischemic heart diseases (I20–25) or cerebrovascular disease (I60–69) during the follow-up period. If participants did not have the date of death, they were considered alive at the end of 2015. We assumed there is no right censoring other than death. Because all persons are supposed to be beneficiaries of the National Health Insurance in Korea, dropouts other than due to death are virtually impossible.

The follow-up time for CV disease was calculated as the time from the date of the NSP examination to the first diagnosis of CV disease, date of death, or the end of 2015, whichever comes first. And the follow-up time for CV mortality was calculated as the time from the date of the NSP examination to date of CV death, or the end of 2015, whichever comes first.

Potential confounders

Potential confounders included data on health behavior, chronic diseases, and Body mass index (BMI), which are baseline characteristics at the time of NSP and time-invariant in our analysis model.

Data on health behavior were collected using a self-administered questionnaire at the time of NSP examination. In terms of smoking status, we categorized the respondents as current smokers, ex-smokers, or nonsmokers. An at-risk alcohol drinker was defined as a man <65 years who drank more than 14 drinks per week or four drinks per occasion, or a man aged ≥65 years or a woman of any age who drank more than seven drinks per week or three drinks per occasion [29].

Data on chronic diseases such as hypertension, diabetes mellitus, and dyslipidemia were collected using the same questionnaire and laboratory results of NSP. If participants responded that they took medications for hypertension, diabetes mellitus, or dyslipidemia, they were considered to have the disease. If their systolic blood pressure was ≥140 mmHg or diastolic blood pressure was ≥ 90 mmHg, they were considered to have hypertension. If their serum fasting glucose level was ≥126 mg/dL, they were considered to have diabetes mellitus. If their serum total cholesterol level was ≥240 mg/dL, they were considered to have dyslipidemia.

BMI was calculated as weight divided by height in meters squared (kg/m2). We used Asian-specific criteria for BMI to define normal BMI. Normal BMI is defined as 18.5 and 23 kg/m2, underweight as <18.5 kg/m2, and obese as BMI ≥ 25 kg/m2.

Statistical analysis

Baseline characteristics are expressed as frequencies and percentages. We hypothesized that people with disability would show increased CV event and mortality owing to higher CV risk factors such as sex, age, health behavior, and chronic disease status compared with people without disability [2, 5]. To test this hypothesis, we conducted a survival analysis and subgroup analysis according to CV risk factors. Cox proportional hazard models were used to evaluate the association between type or severity of disability, and CV event, CV death, or all-cause death.

In the survival analyses, we built four different models. In addition to crude model, Model 1 was adjusted for sex and age. In Model 2, hypertension, diabetes mellitus, and dyslipidemia were added to Model 1. In Model 3, cigarette smoking, at-risk alcohol drinking, and BMI were added to Model 2. We calculated the hazard ratio and 95% confidence interval (CI) for each model.

We conducted subgroup analyses. First, we performed a survival analysis according to sex and age group and then according to behavioral factors such as cigarette smoking; alcohol drinking; and chronic diseases such as hypertension, diabetes mellitus, and dyslipidemia. Furthermore, we conducted a survival analysis according to aggregated type of disability. For subgroup analysis, we used the model without variable of stratification. For example, we used model 1 without sex in model 1 of subgroup analysis for sex (i.e. the model 1 in subgroup analysis for sex was adjusted only for age). Statistical analyses were performed using STATA software (version 16.1; STATA. Corp, College Station, Texas). A P-value of <0.05 was considered significant.

Results

Basal characteristics of participants

The mean follow-up duration was 10.8 ± 3.9 years (maximum, 13.9 years). At the end of 2015, 47,514 participants (9.2%) died. Of the deceased participants, 7,317 (1.4%) died of CV disease. In 5,572,130 person-year (PY) follow-up, the CV mortality rate was 1.313 per 1,000 PY.

Among the 514,679 participants included in the analysis, 445 (0.09%) had mild disability and 1,561 (0.30%) had severe disability. Approximately 45% of the participants were women, and the number of men with disability was higher than that of women. About 44% of total study participants were aged <50 years, while about 30% of them were aged ≥65 years. Participants with disabilities were older than those without disabilities. Over 60% of the participants had normal baseline body weight, while one-third were overweight. Two-thirds of the participants declared that they never smoked, while 23% of them answered that they smoked. The proportions of participants with disabilities who are current smokers were lesser than that of participants without disabilities. In addition, one-third of the participants revealed that they were at-risk drinkers. Half of the participants answered that they had hypertension, 12% had diabetes mellitus, and 16% had dyslipidemia (Table 1).

Table 1. Basic characteristics of participants.

Total Normal Mild disabled Severe disabled
N (%) N (%) N (%) N (%)
Sex (women) (%) 235,715 (45.8) 233,710 (45.9) 445 (31.3) 1,560 (36.1)
Age (years)
 <50 225,584 (43.8) 225,153 (44.2) 215 (15.1) 216 (5.0)
 50–64 122,759 (23.9) 122,007 (24.0) 319 (22.5) 433 (10.0)
 ≥ 65 166,336 (32.3) 161,773 (31.8) 887 (62.4) 3,676 (85.0)
BMI (kg/m2)
 Underweight (<18.5) 12,489 (2.4) 12,267 (2.4) 75 (5.3) 147 (3.4)
 Normal weight (18.5–25) 323,147 (62.8) 319,642 (62.9) 936 (66.1) 2,569 (59.4)
 Overweight (≥25) 178,651 (34.7) 176,639 (34.7) 406 (28.9) 1,606 (37.2)
Cigarette smoking
 Never 329,827 (66.4) 326,137 (68.3) 944 (68.3) 2,746 (64.5)
 Ex–smoker 54,006 (10.9) 53,023 (10.8) 199 (14.4) 784 (18.4)
 Current smoker 112,900 (22.7) 111,930 (22.8) 240 (17.4) 730 (17.1)
At–risk alcohol drinking 71,686 (33.4) 71,221 (33.4) 140 (38.3) 325 (42.8)
Hypertension 287,211 (55.8) 283,234 (55.7) 971 (68.4) 3,016 (69.7)
Diabetes mellitus 64,008 (12.4) 62,743 (12.3) 346 (24.4) 919 (21.3)
Dyslipidemia 81,303 (15.8) 80,253 (15.8) 231 (16.3) 819 (19.0)
Cardiovascular event 3,778 (0.7) 3654 (0.7) 38 (2.7) 86 (2.0)
Cardiovascular death 7,317 (1.4) 7066 (1.4) 110 (7.7) 141 (3.3)
All-cause death 47,514 (9.2) 46,345 (9.1) 489 (34.4) 680 (15.7)

*Mild disabled: disability grades 3–6

**Severe disability: disability grades 1–2

Cardiovascular incidence, mortality, all-cause mortality rate according to type of disability

A quarter of mild disabled and a half of severe disabled participants were physically impaired. Physical impairment was the most common type of disability in both mild and severe disabled groups in both sexes, except in women with mild disability, followed by visual and hearing impairments (Table 2).

Table 2. Proportion of participants by types of disability.

Type of disability Mild disabled (N = 1,421) Severe disabled (N = 4,325)
Men (N = 976) Women (N = 445) Men (N = 2,765) Women (N = 1,560)
Physical impairment 249 (25.5%) 93 (20.9%) 1,365 (46.4%) 885 (56.7%)
Brain impairment 137 (14.0%) 57 (12.8%) 235 (8.5%) 105 (6.7%)
Visual impairment 103 (10.6%) 93 (21.1%) 389 (14.1%) 222 (14.2%)
Hearing impairment 159 (16.3%) 74 (16.6%) 376 (13.6%) 188 (12.1%)
Linguistic impairment 66 (6.8%) 18 (4.0%) 155 (5.6%) 50 (3.2%)
Mental retardation 69 (7.1%) 39 (8.8%) 62 (2.2%) 21 (1.4%)
Mental impairment 50 (5.1%) 26 (5.8%) 27 (1.0%) 21 (1.4%)
Others 143 (14.7%) 45 (10.1%) 156 (5.6%) 68 (4.4%)

Among the type of disability, physically impaired participants showed the highest CV disease incidence and mortality rate in both mild and severe disabled groups (incidence rate: 10.7 per 1,000 PY for mild disabled group and 14.5 per 1,000 PY for severe disabled group; mortality rate: 26.2 per 1,000 PY for mild disabled group and 10.8 per severe disabled group). CV disease incidence and mortality were lower in patients with other types of disabilities. CV disease incidence ranged from 0 to 3.6 per 1,000 PY, while CV mortality ranged from 2.5 to 8.2 per 1,000 PY (Fig 1).

Fig 1.

Fig 1

Cardiovascular disease incidence and mortality rate according to types of disability: A) Cardiovascular disease incidence. B) Cardiovascular mortality.

For aggregated types of disability, CV mortality, and all-cause mortality increased regardless of type of disability. The CV incidence and mortality were highest in neuropsychological disability, which contains person with previous stroke history. (Table 3).

Table 3. Cardiovascular disease and all-cause mortality according to type of disability.

Disability Number Event Duration (PY) Incidence rate aHR (95% CI)
Cardiovascular event All 514,679 3,778 5,572,226 0.679
Normal 508,933 3,654 5,538,403 0.660 Ref
Disabled 5,746 124 33,823 3.784 2.890 (2.412–3.463)
Physical 2,592 24 10,895 2.203 1.418 (0.948–2.122)
Sensory 1,604 21 10,905 1.926 1.322 (0.860–2.033)
Neuropsychological 1,156 59 9,308 6.389 6.854 (5.270–8.913)
Others 412 20 2,582 7.746 8.183 (5.207–12.857)
Cardiovascular death All 514,679 7,317 5,572,341 1.313
Normal 508,933 7,066 5,538,518 1.275 Ref
Disabled 5,746 251 33,823 7.421 2.030 (1.784–2.309)
Physical 2,592 80 10,895 7.343 1.704 (1.362–2.132)
Sensory 1,604 62 10,905 5.686 1.313 (1.020–1.691)
Neuropsychological 1,156 90 9,308 9.669 4.020 (3.252–4.670)
Others 412 19 2,582 7.359 2.846 (1.791–4.521)
All–cause death All 514,679 47,514 5,572,341 8.527
Normal 508,933 46,345 5,538,518 8.368 Ref
Disabled 5,746 1,169 33,823 34.651 1.513 (1.426–1.607)
Physical 2,592 371 10,895 34.052 1.275 (1.149–1.414)
Sensory 1,604 340 10,905 31.179 1.161 (1.041–1.295)
Neuropsychological 1,156 301 9,308 32.339 2.065 (1.839–2.318)
Others 412 157 2,582 60.805 3.608 (3.073–4.236)

Adjusted for sex, age, hypertension, diabetes mellitus, dyslipidemia, BMI, cigarette smoking, at-risk drinking

Physical: physical impairment, Sensory: visual impairment + hearing impairment, Neuropsychological: brain impairment + linguistic impairment + mental impairment + mental retardation

N/A: not applicable due to high missing rate

Cardiovascular disease incidence and mortality according to severity of disability

CV disease incidence was significantly higher in participants with disability than in those without disability in Models 1 and 2 for both mild and severe disabled groups. However, in Model 3, CV disease incidence was three to five times higher only among participants aged 50–64 years and severe disabled participants aged <50 years. No significant difference was observed in participants aged ≥65 years. Furthermore, CV disease incidence increased in both sexes in Models 1 and 2 but not in Model 3.

Similarly, CV mortality was significantly higher in participants with disability than in those without disability in all Models. Compared with CV disease incidence, CV mortality was one and a half to six times higher in participants with disability in all age groups, except for those with severe disability aged <50 years. Moreover, CV mortality increased in both sexes in Models 1 and 2 but in only men in Model 3 (Tables 4 and 5).

Table 4. Association between severity of disability and cardiovascular event.

Disability Number Event Duration (PY) Incidence rate Crude Model 1 Model 2 Model 3
HR (95% CI) aHR (95% CI) aHR (95% CI) aHR (95% CI)
Total All 514,679 3,778 5,572,015 0.678
Normal 508,933 3,654 5,538,329 0.660 Ref Ref Ref Ref
Mild 1,421 38 11,821 3.214 6.297(4.574–8.670) 2.748(1.994–3.788) 2.758(2.001–3.800) 1.394(0.578–3.360)
Severe 4,325 86 21,864 3.933 7.945(6.413–9.843) 2.822(2.273–3.502) 2.868(2.311–3.560) 1.548(0.927–2.585)
Sex
Men All 278,694 2,496 3,023,064 0.826
Normal 275,223 2,407 3,000,020 0.802 Ref Ref Ref Ref
Mild 976 29 8,052 3.602 5.908 (4.095–8.523) 2.507 (1.736–3.620) 2.505 (1.734–3.617) 1.469 (0.609–3.542)
Severe 2,765 60 14,992 4.002 6.700 (5.183–8.661) 2.412 (1.862–3.124) 2.431 (1.876–3.148) 1.456 (0.840–2.524)
Women All 235,715 1,282 2,548,951 0.503
Normal 233,710 1,247 2,538,309 0.491 Ref Ref Ref Ref
Mild 445 9 3,770 2.388 6.226 (3.231–11.996) 3.629 (1.882–6.995) 3.620 (1.878–6.979) N/A
Severe 1,560 26 6,873 3.783 10.466 (7.093–15.442) 4.279 (2.894–6.326) 4.408 (2.981–6.516) 2.359 (0.577–9.637)
Age
<50 All 225,584 731 2,891,196 0.253
Normal 225,153 726 2,885,839 0.252 Ref Ref Ref Ref
Mild 215 2 2,638 0.758 3.826(0.955–15.329) 3.327(0.830–13.333) 3.267(0.815–13.097) 5.481(0.769–39.085)
Severe 216 3 2,718 1.104 4.359(1.402–13.547) 3.655(1.176–11.364) 3.567(1.147–11.091) 5.570(1.386–22.376)
50–64 All 122,759 1,149 1,490,664 0.771
Normal 122,007 1,117 1,482,506 0.753 Ref Ref Ref Ref
Mild 319 14 3,310 4.229 7.822(4.616–13.254) 6.033(3.557–10.232) 5.787(3.410–9.822) 4.590(1.469–14.343)
Severe 433 18 4,848 3.713 5.978(3.752–9.525) 4.498(2.819–7.176) 4.541(2.846–7.245) 3.349(1.248–8.991)
≥ 65 All 166,336 1,898 1,190,155 1.595
Normal 161,773 1,811 1,169,984 1.548 Ref Ref Ref Ref
Mild 887 22 5,873 3.745 2.496(1.639–3.800) 2.232(1.465–3.401) 2.232(1.465–3.401) 0.411(0.058–2.926)
Severe 3,676 65 14,298 4.546 3.198(2.496–4.096) 2.916(2.273–3.741) 2.921(2.277–3.748) 1.396(0.720–2.705)
Health behavior
Current smoker All 112,900 810 1,287,568 0.628
Normal 111,930 785 1,280,710 0.613 Ref Ref Ref Ref
Mild 240 4 2,209 1.811 4.122(1.542–11.015) 1.904(0.712–5.094) 1.905(0.712–5.098) 1.776(0.442–7.139)
Severe 730 20 4,648 4.303 9.818(6.293–15.317) 3.236(2.063–5.077) 3.281(2.091–5.148) 2.675(1.372–5.213)
At-risk drinking All 71,686 483 792,504 0.609
Normal 71,221 473 788,162 0.600 Ref Ref Ref Ref
Mild 140 4 1,367 2.927 6.207(2.319–16.615) 2.893(1.079–7.760) 2.867(1.069–7.688) 2.956(1.102–7.927)
Severe 325 6 2,976 2.016 4.250(1.899–9.514) 1.284(0.571–2.888) 1.312(0.583–2.952) 1.384(0.615–3.115)
Chronic disease
Hypertension All 287,221 2,631 2,953,790 0.891
Normal 283,234 2,541 2,931,174 0.867 Ref Ref Ref Ref
Mild 971 27 7,730 3.493 5.107(3.495–7.464) 2.711(1.853–3.965) 2.682(1.833–3.923) 0.749(0.187–3.001)
Severe 3,016 63 14,886 4.232 6.352(4.945–8.159) 2.762(2.146–3.555) 2.786(2.165–3.586) 1.313(0.701–2.457)
Diabetes mellitus All 64,008 658 581,099 1.132
Normal 62,743 628 574,878 1.092 Ref Ref Ref Ref
Mild 346 12 2,485 4.828 5.103(2.882–9.037) 3.586(2.023–6.355) 3.592(2.207–6.366) 1.226(0.172–8.751)
Severe 919 18 3,736 4.818 5.688(3.556–9.098) 2.907(1.812–4.665) 2.936(1.829–4.712) 1.760(0.559–5.539)
Dyslipidemia All 81,303 643 806,647 0.797
Normal 80,253 623 801,370 0.777 Ref Ref Ref Ref
Mild 231 8 1,851 4.322 7.118(3.542–14.306) 3.652(1.812–7.358) 3.589(1.781–7.232) 2.072(0.289–14.849)
Severe 819 12 3,427 3.502 5.825(3.286–10.323) 2.765(1.556–4.914) 2.827(1.591–5.026) 0.852(0.119–6.124)

Model 1: sex and age

Model 2: Model 1 + hypertension, diabetes mellitus, and dyslipidemia

Model 3: Model 2 + body mass index, cigarette smoking, and at-risk alcohol drinking

For subgroup analysis, we used the model without variable of stratification. For example, we used model 1 without sex in model 1 of subgroup analysis for sex

N/A: not applicable due to high missing rate, CI: confidence interval, PY: person-year, HR: hazard ratio

Table 5. Association between severity of disability and cardiovascular death.

Age Disability Number Death Duration (PY) Mortality rate Crude Model 1 Model 2 Model 3
HR (95% CI) aHR (95% CI) aHR (95% CI) aHR (95% CI)
Total All 514,679 7,317 5,572,130 1.313
Normal 508,984 7,066 5,538,444 1.275 Ref Ref Ref Ref
Mild 1,421 110 11,821 9.305 7.543 (6.248–9.106) 2.908 (2.407–3.513) 2.905 (2.403–3.512) 3.182 (2.217–4.567)
Severe 4,325 141 21,864 6.449 5.426 (4.592–6.411) 1.586 (1.341–1.876) 1.613 (1.364–1.907) 1.729 (1.285–2.327)
Sex
Men All 278,962 4,401 3,023,155 1.456
Normal 275,223 4,213 3,000,112 1.404 Ref Ref Ref Ref
Mild 976 84 8,052 10.432 7.618 (6.138–9.456) 3.011 (2.424–3.740) 3.032 (2.441–3.765) 3.402 (2.369–4.885)
Severe 2,765 106 14,992 7.071 5.316 (4.386–6.447) 1.688 (1.390–2.049) 1.717 (1.414–2.084) 1.718 (1.258–2.345)
Women All 235,715 2,914 2,548,975 1.143
Normal 233,710 2,853 2,538,332 1.124 Ref Ref Ref Ref
Mild 445 26 3,770 6.897 6.384 (4.339–9.393) 2.927 (1.989–4.307) 2.810 (1.895–4.167) N/A
Severe 1,560 35 6,873 5.092 4.987 (3.572–6.961) 1.444 (1.034–2.017) 1.451 (1.039–2.027) 1.790 (0.661–4.849)
Age
<50 All 225,584 604 2,891,255 0.208
Normal 225,153 597 2,885,899 0.206 Ref Ref Ref Ref
Mild 215 6 2,638 1.022 11.092 (4.963–24.788) 9.064 (4.053–20.269) 8.166 (3.648–18.278) 6.250 (1.553–25.152)
Severe 216 1 2,718 0.368 1.788 (0.251–12.715) 1.470 (0.207–10.458) 1.404 (0.197–9.988) 2.539 (0.356–18.090)
50–64 All 122,759 2,022 1,490,703 1.356
Normal 122,007 1,977 1,482,544 1.334 Ref Ref Ref Ref
Mild 319 22 3,310 6.646 5.089 (3.343–7.747) 3.407 (2.237–5.190) 2.946 (1.915–4.534) 3.459 (1.641–7.289)
Severe 433 23 4,848 4.744 3.594 (2.383–5.422) 2.269 (1.503–3.426) 2.263 (1.499–3.416) 2.550 (1.320–4.925)
≥65 All 166,336 4,691 1,190,170 3.941
Normal 161,773 4,492 1,169,999 1.839 Ref Ref Ref Ref
Mild 887 82 5,873 13.962 3.670 (2.950–4.566) 2.688 (2.159–3.346) 2.720 (2.185–3.386) 2.709 (1.756–4.178)
Severe 3,676 117 14,298 6.827 2.277 (1.895–2.735) 1.489 (1.238–1.791) 1.497 (1.245–1.801) 1.483 (1.057–2.081)
Health behavior
Current smoker All 112,900 1,997 1,287,632 1.549
Normal 111,930 1,947 1,280,774 1.519 Ref Ref Ref Ref
Mild 240 23 2,209 10.411 6.935 (4.597–10.462) 2.931 (1.941–4.425) 3.017 (1.998–4.556) 2.985 (1.687–5.281)
Severe 730 27 4,648 5.809 3.965 (2.711–5.797) 1.121 (0.765–1.642) 1.162 (0.793–1.702) 1.270 (0.761–2.120)
At-risk drinking All 71,686 1,162 792,527 1.466
Normal 71,221 1,128 788,186 1.431 Ref Ref Ref Ref
Mild 140 11 1,367 8.049 5.719 (3.158–10.257) 2.430 (1.340–4.405) 2.473 (1.364–4.484) 2.610 (1.439–4.732)
Severe 325 23 2,976 7.730 5.546 (3.670–8.381) 1.592 (1.050–2.413) 1.653 (1.091–2.506) 1.526 (0.988–2.358)
Chronic disease
Hypertension All 287,221 5,668 2,953,874 1.919
Normal 283,234 5,476 2,931,258 1.868 Ref Ref Ref Ref
Mild 971 83 7,730 10.737 5.974 (4.810–7.421) 2.858 (2.300–3.553) 2.825 (2.274–3.516) 3.169 (2.098–4.787)
Severe 3,016 109 14,886 7.322 4.216 (3.487–5.096) 1.593 (1.317–1.928) 1.601 (1.323–1.938) 1.779 (1.282–2.469)
Diabetes mellitus All 64,008 1,565 581,109 2.693
Normal 62,743 1,504 574,888 2.616 Ref Ref Ref Ref
Mild 346 30 2,485 12.070 4.812 (3.352–6.908) 3.390 (2.361–4.868) 3.280 (2.271–4.739) 2.951 (1.319–6.602)
Severe 919 31 3,736 8.298 3.071 (2.878–3.277) 1.725 (1.206–2.466) 1.697 (1.187–2.427) 2.450 (1.375–4.366)
Dyslipidemia All 81,303 1,262 806,647 1.565
Normal 80,253 1,228 801,370 1.532 Ref Ref Ref Ref
Mild 231 16 1,851 8.644 5.819 (3.553–9.529) 2.640 (1.610–4.329) 2.631 (1.604–4.314) 3.146 (1.171–8.448)
Severe 819 18 3,427 5.253 3.745 (2.351–5.966) 1.541 (0.966–2.458) 1.583 (0.992–2.526) 0.984 (0.314–3.081)

Model 1: sex and age

Model 2: Model 1 + hypertension, diabetes mellitus, and dyslipidemia

Model 3: Model 2 + BMI, cigarette smoking, and at-risk alcohol drinking

For subgroup analysis, we used the model without variable of stratification. For example, we used model 1 without sex in model 1 of subgroup analysis for sex

N/A: not applicable due to high missing rate, CI: confidence interval, PY: person-year, HR: hazard ratio

Subgroup analysis

For current smokers, CV disease incidence was significantly increased in the severe disabled group in all Models, whereas CV mortality was increased only in the mild disabled group in all Models. At-risk drinkers with mild disability were more likely to have CV event in all Models. Similarly, at risk-drinkers with disability showed higher CV mortality, except for participants with severe disability, in Model 3.

Participants with hypertension or diabetes showed increased CV disease incidence when they had a disability in Models 1 and 2 but not in Model 3, while their mortality was significantly higher in all Models than that of participants without disability. Similarly, CV disease incidence was higher in participants with dyslipidemia in both mild and severe disability groups in Models 1 and 2, while only those with mild disability had higher CV incidence in Model 3. For CV mortality, participants with mild disability showed higher mortality in all Models when they had dyslipidemia.

Discussion

To our knowledge, this is the first large general population study to evaluate the association of CV disease incidence and mortality with disability in the Asian population, using a nationwide representative claim database. Overall, CV disease incidence, CV mortality, and all-cause mortality increased in participants with disability regardless of type or severity of disability after full adjustment of CV risk factors. This finding showed that CV mortality increase in people with disability is not fully explained by their higher CV risk factors. Although CV mortality increased in all age groups, the increase was more evident in young participants. Although CV disease incidence and mortality were not significantly different in the subgroup analysis of health behavior in the fully adjusted model, CV mortality increase was observed in the subgroup analysis of participants with chronic diseases.

Several previous studies showed that mortality increased in people with physical frailty or disability. A systematic review of 19 studies evaluating the association of handgrip strength and gait speed with CV mortality also showed that decreased physical performance was associated with increased CV mortality [23]. In the study, they found that the association was independent of anthropometric features (i.e., BMI and height) and traditional CV risk factors (i.e., smoking and dyslipidemia). However, the studies included in the review used a limited definition of physical disability measured by handgrip strength or gait speed, and no large-scale long-term study was conducted in the Asian population.

A previous study on older adults aged ≥80 years showed that disability was more predictive of all-cause mortality than multimorbidity [26]. In the study, people with disability had 2.36 times more risk of mortality than those without disability or comorbidity, while people with multimorbidity had 1.66 times more risk of mortality. This finding indicated that disability itself contributed to mortality in the study population regardless of comorbidities in people with disability. Similarly, we found that CV disease incidence and mortality increased after controlling chronic diseases (i.e., Model 2), and subgroup analyses of chronic diseases showed the same results. Based on these results, we assumed that disability is among the risk factors for CV regardless of chronic diseases, which are known traditional risk factors for CV.

The current study showed that CV mortality increased only in men in the fully adjusted model (i.e., Model 3). This finding suggests that there is discrepancy between sexes in terms of the effect of disability on CV mortality. A similar finding was reported in a Finnish study of 4,501 men and women aged ≥45 years, which showed that disability was predictive of mortality only in men not in women with coronary heart disease (CHD) [30]. In the study, the incidence of coronary heart disease-related death increased 1.3–1.5 times in men and women, except in women with a history of CHD, which indicates that risk factors for CV disease differ between men and women. This discrepancy is possibly explained by differences in sex hormone, which influences CV risk and physical performance in different ways in both sexes [3133].

We found that the effect of disability on CV disease incidence and mortality was not necessarily greater in older participants. CV mortality was six times higher in participants aged <50 years with mild disability, while it was less than four times in those aged ≥50 years. Although this study showed that disability was a risk factor for CV disease independent of conventional risk factors, our finding suggests that the effect of disability on CV disease is diluted when participants have more conventional CV risk factors, which are far more prevalent in older adults.

There are several limitations in this study. There is a limitation in the database, which prevented the adjustment for well-known CV risk factors such as education and dietary intake. Moreover, the database did not include data on the severity of CV disease; therefore, the models cannot be adjusted for severity of the disease. Furthermore, we collected data on health behaviors using a questionnaire; thus, it is possible that there is recall bias in those data. We did not include physical activity as a covariate due to the large amount of missing information in the database, which is an important health behavior for CV disease prevention. Additionally, because NHID is a medical claims database, it is possible that the diagnoses of CV disease and cause of death were misclassified. However, all claims in this dataset were audited by the Korean Health Insurance Review and Assessment before payment, making the misclassification of diagnosis improbable.

In conclusion, people with disability showed higher CV disease incidence and mortality than those without disability, regardless of the type of disability or risk factors for CV disease.

Acknowledgments

This study used customized research database of the Korean National Health Insurance Service (NHIS-2019-2-213) made by KNHIS.

Data Availability

The dataset analyzed during the current study are available in National Health Insurance Sharing Service. The authors had no special access privileges, and have no right to share or provide the data. The information of how to request the database is available in https://nhiss.nhis.or.kr/bd/ab/bdaba021eng.do. The detail and cost of the database is described in https://nhiss.nhis.or.kr/bd/ab/bdaba022eng.do. To request the database, visit https://nhiss.nhis.or.kr/bd/ay/bdaya001iv.do.

Funding Statement

This study was supported by the Rehabilitation Research & Development Support Program (#NRC RSP-2019002), National Rehabilitation Center, Ministry of Health and Welfare, Korea. YSK received the grant. URL of funder is following: http://www.nrc.go.kr/eng/main.do The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

References

  • 1.World Health Organization. International classification of functioning, disability and health: ICF. World Health Organization; 2001. Report No.: 9241545429. [Google Scholar]
  • 2.National Rehabilitation Center. 2016 Statistics of Disability and Health. 2018.
  • 3.Drum CE, Krahn G, Culley C, Hammond L. Recognizing and responding to the health disparities of people with disabilities. Calif J Health Promot. 2005;3(3):29–42. [Google Scholar]
  • 4.Lawthers AG, Pransky GS, Peterson LE, Himmelstein J. Rethinking quality in the context of persons with disability. Int J Qual Health Care. 2003;15(4):287–99. 10.1093/intqhc/mzg048 [DOI] [PubMed] [Google Scholar]
  • 5.Ko KD, Lee KY, Cho B, Park MS, Son KY, Ha JH, et al. Disparities in health-risk behaviors, preventive health care utilizations, and chronic health conditions for people with disabilities: the Korean National Health and Nutrition Examination Survey. Arch Phys Med Rehabil. 2011;92(8):1230–7. 10.1016/j.apmr.2011.03.004 [DOI] [PubMed] [Google Scholar]
  • 6.Havercamp SM, Scandlin D, Roth M. Health disparities among adults with developmental disabilities, adults with other disabilities, and adults not reporting disability in North Carolina. Public Health Rep. 2004;119(4):418–26. 10.1016/j.phr.2004.05.006 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Rimmer JH, Rubin SS, Braddock D, Hedman G. Physical activity patterns of African-American women with physical disabilities. Med Sci Sports Exerc. 1999;31(4):613–8. 10.1097/00005768-199904000-00020 [DOI] [PubMed] [Google Scholar]
  • 8.Becker H, Brown A. Disparities in smoking behaviors among those with and without disabilities from 2001 to 2005. Public Health Nurs. 2008;25(6):526–35. 10.1111/j.1525-1446.2008.00739.x [DOI] [PubMed] [Google Scholar]
  • 9.Jones GC, Bell K. Adverse health behaviors and chronic conditions in working-age women with disabilities. Fam Community Health. 2004;27(1):22–36. 10.1097/00003727-200401000-00004 [DOI] [PubMed] [Google Scholar]
  • 10.Brawarsky P, Brooks D, Wilber N, Gertz R, Walker DK. Tobacco use among adults with disabilities in Massachusetts. Tob Control. 2002;11(suppl 2):ii29–ii33. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Bertoli S, Battezzati A, Merati G, Margonato V, Maggioni M, Testolin G, et al. Nutritional status and dietary patterns in disabled people. Nutr Metab Cardiovasc Dis. 2006;16(2):100–12. 10.1016/j.numecd.2005.05.007 [DOI] [PubMed] [Google Scholar]
  • 12.Iezzoni LI, McCarthy EP, Davis RB, Siebens H. Mobility impairments and use of screening and preventive services. Am J Public Health. 2000;90(6):955 10.2105/ajph.90.6.955 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Ramirez A, Farmer GC, Grant D, Papachristou T. Disability and preventive cancer screening: results from the 2001 California Health Interview Survey. Am J Public Health. 2005;95(11):2057–64. 10.2105/AJPH.2005.066118 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Diab ME, Johnston MV. Relationships between level of disability and receipt of preventive health services. Arch Phys Med Rehabil. 2004;85(5):749–57. 10.1016/j.apmr.2003.06.028 [DOI] [PubMed] [Google Scholar]
  • 15.Nosek MA, Howland CA. Breast and cervical cancer screening among women with physical disabilities. Arch Phys Med Rehabil. 1997;78(12):S39–S44. [DOI] [PubMed] [Google Scholar]
  • 16.Centers for Disease Control and Prevention (CDC). Use of cervical and breast cancer screening among women with and without functional limitations—United States, 1994–1995. MMWR Morb Mortal Wkly Rep. 1998;47(40):853 [PubMed] [Google Scholar]
  • 17.Jones GC, Sinclair LB. Multiple health disparities among minority adults with mobility limitations: An application of the ICF framework and codes. Disabil Rehabil. 2008;30(12–13):901–15. 10.1080/09638280701800392 [DOI] [PubMed] [Google Scholar]
  • 18.Smith ÉM, Comiskey CM, Carroll ÁM. A study of bone mineral density in adults with disability. Arch Phys Med Rehabil. 2009;90(7):1127–35. 10.1016/j.apmr.2008.09.578 [DOI] [PubMed] [Google Scholar]
  • 19.Månsson N-O, Eriksson KF, Israelsson B, Ranstam J, Melander A, Råstam L. Body mass index and disability pension in middle-aged men—non-linear relations. Int J Epidemiol. 1996;25(1):80–5. 10.1093/ije/25.1.80 [DOI] [PubMed] [Google Scholar]
  • 20.Ferraro KF, Su YP, Gretebeck RJ, Black DR, Badylak SF. Body mass index and disability in adulthood: a 20-year panel study. Am J Public Health. 2002;92(5):834–40. 10.2105/ajph.92.5.834 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Blaum CS, Volpato S, Cappola A, Chaves P, Xue QL, Guralnik J, et al. Diabetes, hyperglycaemia and mortality in disabled older women: The Women’s Health and Ageing Study I. Diabet Med. 2005;22(5):543–50. 10.1111/j.1464-5491.2005.01457.x [DOI] [PubMed] [Google Scholar]
  • 22.Ling CH, Taekema D, De Craen AJ, Gussekloo J, Westendorp RG, Maier AB. Handgrip strength and mortality in the oldest old population: the Leiden 85-plus study. CMAJ. 2010;182(5):429–35. 10.1503/cmaj.091278 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Chainani V, Shaharyar S, Dave K, Choksi V, Ravindranathan S, Hanno R, et al. Objective measures of the frailty syndrome (hand grip strength and gait speed) and cardiovascular mortality: A systematic review. Int J Cardiol. 2016;215:487–93. 10.1016/j.ijcard.2016.04.068 [DOI] [PubMed] [Google Scholar]
  • 24.Al Snih S, Markides KS, Ray L, Ostir GV, Goodwin JS. Handgrip strength and mortality in older Mexican Americans. J Am Geriatr Soc. 2002;50(7):1250–6. 10.1046/j.1532-5415.2002.50312.x [DOI] [PubMed] [Google Scholar]
  • 25.Rantanen T, Volpato S, Luigi Ferrucci M, Eino Heikkinen M, Fried LP, Guralnik JM. Handgrip strength and cause-specific and total mortality in older disabled women: exploring the mechanism. J Am Geriatr Soc. 2003;51(5):636–41. 10.1034/j.1600-0579.2003.00207.x [DOI] [PubMed] [Google Scholar]
  • 26.Landi F, Liperoti R, Russo A, Capoluongo E, Barillaro C, Pahor M, et al. Disability, more than multimorbidity, was predictive of mortality among older persons aged 80 years and older. J Clin Epidemiol. 2010;63(7):752–9. 10.1016/j.jclinepi.2009.09.007 [DOI] [PubMed] [Google Scholar]
  • 27.Cheol Seong S, Kim YY, Khang YH, Heon Park J, Kang HJ, Lee H, et al. Data resource profile: the national health information database of the National Health Insurance Service in South Korea. Int J Epidemiol. 2017;46(3):799–800. 10.1093/ije/dyw253 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Shin DW, Cho B, Guallar E. Korean national health insurance database. JAMA Intern Med. 2016;176(1):138-. [DOI] [PubMed] [Google Scholar]
  • 29.National Institute on Alcohol Abuse Alcoholism. Helping Patients who Drink Too Much: A Clinician’s Guide: Updated 2005 Edition. US Department of Health and Human Services, National Institutes of Health; 2007. [Google Scholar]
  • 30.Kattainen A, Reunanen A, Koskinen S, Martelin T, Knekt P, Aromaa A. Disability predicted mortality in men but not women with coronary heart disease. J Clin Epidemiol. 2004;57(5):513–21. 10.1016/j.jclinepi.2003.10.004 [DOI] [PubMed] [Google Scholar]
  • 31.Orwoll E, Lambert LC, Marshall LM, Blank J, Barrett-Connor E, Cauley J, et al. Endogenous testosterone levels, physical performance, and fall risk in older men. Arch Intern Med. 2006;166(19):2124–31. 10.1001/archinte.166.19.2124 [DOI] [PubMed] [Google Scholar]
  • 32.Ruige JB, Mahmoud AM, De Bacquer D, Kaufman JM. Endogenous testosterone and cardiovascular disease in healthy men: a meta-analysis. Heart. 2011;97(11):870–5. 10.1136/hrt.2010.210757 [DOI] [PubMed] [Google Scholar]
  • 33.Cooper R, Mishra G, Clennell S, Guralnik J, Kuh D. Menopausal status and physical performance in midlife: findings from a British birth cohort study. Menopause. 2008;15(6):1079 10.1097/gme.0b013e31816f63a3 [DOI] [PMC free article] [PubMed] [Google Scholar]

Associated Data

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

Data Availability Statement

The dataset analyzed during the current study are available in National Health Insurance Sharing Service. The authors had no special access privileges, and have no right to share or provide the data. The information of how to request the database is available in https://nhiss.nhis.or.kr/bd/ab/bdaba021eng.do. The detail and cost of the database is described in https://nhiss.nhis.or.kr/bd/ab/bdaba022eng.do. To request the database, visit https://nhiss.nhis.or.kr/bd/ay/bdaya001iv.do.


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