Cardiovascular Outcomes of Obesity According to Menopausal Status: A Nationwide Population-Based Study.

BACKGROUND: We estimated the effect of obesity on the incidence of cardiovascular disease (CVD) and mortality in women according to menopausal status.
METHODS: Women aged 40 to 69 years under routine health check-ups provided by the National Health Insurance Service in 2009 were followed up till 2018 (n=2,208,559).
RESULTS: In premenopausal women, a significant increment of mortality rate was found in underweight and obesity class II (hazard ratio [HR], 1.48; 95% confidence interval [CI], 1.31 to 1.67; and HR, 1.25; 95% CI, 1.12 to 1.39) compared to normal body mass index (BMI); overweight and obesity class I did not affect mortality rate. In postmenopausal women, obesity as well as overweight status reduced the risk of mortality compared to normal BMI (HR, 0.86; 95% CI, 0.83 to 0.88; and HR, 0.84; 95% CI, 0.82 to 0.86). By contrast, there was a linear association between CVD and BMI above the normal range irrespective of menopausal status, which was attenuated in diabetic women.
CONCLUSION: The current study replicated the J-shaped relationship between BMI and mortality, being more prominent in the postmenopausal group. The risk of CVD was linearly increased as BMI was increased above the normal range irrespective of menopausal status.

INTRODUCTION

The phenomenon of obesity paradox has gained attention in recent decades based on the finding that overweight individuals had the lowest risk for total mortality and cardiovascular mortality compared with those with a normal body mass index (BMI) [1]. However, several prospective studies showed that smoking status [2,3] and age [3,4] might be confounders in the association between BMI and mortality. In subjects aged <65 years, all-cause mortality was higher in overweight individuals (BMI 25.0 to 26.4 kg/m2) than those with normal BMI irrespective of sex; this was not the case for those aged 65 years or more [3]. There was no difference in the mortality rate among individuals aged ≥65 years with normal BMI and those who were overweight [3], and these results were replicated in a healthy participant group from the National Cancer Institute Cohort [4]. Coexistence of co-morbidities such as diabetes mellitus (DM), chronic obstructive pulmonary disease (COPD), chronic kidney disease (CKD), or cancer also affect both of mortality and BMI [2,5,6].

The relationship between mortality and BMI has been reported to be varied according to sex in the Korean population [2] as well as in Caucasians [3]. In women, menopause is an independent risk factor for cardiovascular disease (CVD) [7,8] and CVD-related mortality [9] even in the same age group, menopausal status as well as age should be considered when investigating the effect of bodyweight on CVD or mortality in women; however, the impact of menopausal status on the relationship between BMI and CVD and/or mortality has been rarely reported.

In the current study, the effect of BMI on the incidence of CVD and mortality in Korean women was investigated using the National Health Insurance Service (NHIS) database with stratification according to menopausal status. To elucidate the independent effect on BMI on the outcomes, smoking status, DM, coexistence of co-morbidities, and age as well as menopausal status were also incorporated in the analysis.

The NHIS in Korea covers the claims of 97.0% of the population in Korea. Accordingly, the NHIS database contains information on almost the entirety of demographic and socioeconomic data and the insurance claims, including prescribed medications and procedures, for the Korean population of approximately 50 million [10]. The present study was performed to estimate the incidence of CVD and mortality in women, according to not only BMI but also waist circumference (WC), using the NHIS data from 2002 to 2018.

METHODS

Data collection

We used NHIS database between January 1, 2002 and December 31, 2018. The NHIS offers national health examination programs biennially, and the entire population of women aged 40 to 69 years who underwent routine health check-ups provided by the NHIS during 2009 were selected for the analysis (n=3,109,506). After exclusion of individuals with insufficient data for BMI or menopausal status, with a previous history of hysterectomy, or with a previous diagnosis of myocardial infarction (MI) or stroke during the wash-out period (2002 to 2008), 2,208,559 subjects were finally included (Fig. 1).

Fig. 1

Consort diagram for study population. MI, myocardial infarction.

Their claims data were followed up till 2018. As previously described [11], the NHIS provided the data after de-identification, and the following data were included: age, sex, diagnosis, date of hospital visits, drug prescribed during inpatient and outpatient visits, the date and the duration of hospital admissions, medical procedures undertaken, and emergency department visits. Diagnoses were coded according to the International Classification of Disease (10th revision; ICD-10) codes.

The date of death of the participants undergoing the routine health check-ups provided by the NHIS, was retrieved from the National Death Registry maintained by the Korea National Statistical Office.

This study was approved by the Boramae Medical Center Institutional Review Board (07-2019-26). Informed consent was waived by the board.

Definition of obesity and chronic diseases

BMI was classified based on the World Health Organization (WHO) Asia-Pacific criteria and the Korean Society for the Study of Obesity criteria as follows: BMI 18.5 to 22.9 kg/m2 indicates normal; BMI 23.0 to 24.9 kg/m2 is overweight; BMI 25.0 to 29.9 kg/m2 is obesity class I, and BMI ≥30.0 kg/m2 is obesity class II [12,13]. BMI 27.5 kg/m2 was also selected for the analysis considering WHO additionally suggested it as a potential public health action point [14]. WC was measured to the nearest 0.1 cm from the narrowest point between the lower borders of the rib cage and the iliac crest at the end of normal expiration; abdominal obesity was defined as WC ≥85 cm [13,15].

DM was defined as the use of anti-diabetic medication, including insulin, under ICD-10 E11–14 at the point of the survey, or an 8-hour fasting plasma glucose level ≥126 mg/dL. Dyslipidemia was defined as total cholesterol ≥240 mg/dL or the use of cholesterol-lowering agents under ICD-10 E78. CKD was diagnosed using the estimated glomerular filtration rate (eGFR), which was calculated via the following Modification of Diet in Renal Disease (MDRD) equation: eGFR (mL/min/1.73 m2)= 175×(sCr)−1.154×(age in years)−0.203×(0.742 if female), and eGFR <30 mL/min/1.73 m2 was defined as CKD [16,17]. COPD was defined as at least one claim under ICD-10 J41, J42, J43, or J44. Presence of comorbidity was defined as the presence of any of cancer, CKD, and COPD, or if the participant is a current smoker.

Menopausal status was assessed was based on the responses to a self-report questionnaire; in the case of menopausal women, status of hormone replacement therapy (HRT) was additionally asked. Subjects who exercised regularly were classified into two groups: moderate-intensity exercise: ≥30 min/day and ≥5 times a week, and vigorous-intensity exercise: ≥30 min/day and ≥3 times a week. Subjects consuming alcohol were classified into three groups: non-drinker, mild drinker (daily alcohol intake, 0 to 29 g/day), and heavy drinker (daily alcohol intake, ≥30 g/day). Subjects with low income were defined as those on medical aid or with a standardized monthly family income in the lowest 20% of the entire population. Standardized monthly family income with equivalence scaling was calculated as follows: equivalent income=mean monthly family income/(family size)1/2.

Study outcomes

The primary outcome was incident MI, stroke, and all-cause mortality during the follow-up period, from 2009 to 2018. MI was diagnosed based on hospitalization with the primary diagnostic codes ICD-10 I21–22 [18], and stroke was defined according to ICD-10 I63–64 for diagnoses made during hospitalization and according to brain imaging such as computed tomography and magnetic resonance imaging. Previous history of MI or stroke was diagnosed as I21–22 or I63–64, with more than one diagnosis during admission or at outpatient clinics, respectively [18].

Statistical analysis

All data were analyzed using SAS version 9.3 (SAS Institute Inc., Cary, NC, USA). To compare the clinical characteristics according to menopausal status, independent t test for continuous variables and chi-square test for categorical variables were used. For variables not normally distributed, log-transformation was performed before analysis. The hazard ratio (HR) and 95% confidence interval (CI) for primary outcomes were calculated using multivariable Cox proportional hazards regression analysis. P values <0.05 were considered statistically significant.

RESULTS

Baseline characteristics

The mean age of premenopausal (n=1,019,160) and postmenopausal women (n=1,189,399) in the current study was 45±4 and 59±6 years, respectively (P<0.001). Postmenopausal women were more obese (mean BMI, 24.2±3.1 kg/m2 vs. 23.2±3.1 kg/m2, P<0.001) and had higher blood pressure (mean systolic blood pressure, 124.4±15.8 mm Hg vs. 117.3±14.4 mm Hg, P<0.001) and blood triglyceride (TG) levels (geometric mean TG level, 113.7 mg/dL vs. 89.0 mg/dL, P<0.001) compared to those in premenopausal women (Table 1).

Table 1

Baseline Characteristics According to Menopausal Status

Characteristic	Premenopausal women (n=1,019,160)	Postmenopausal women (n=1,189,399)	P value
Age, yr	45.1±4.1	58.5±5.8	<0.001
BMI, kg/m2	23.2±3.1	24.2±3.1	<0.001
Waist circumference, cm	75.3±8.1	79.6±8.5	<0.001
Systolic blood pressure, mm Hg	117.3±14.4	124.4±15.8	<0.001
Total cholesterol, mg/dL	192.8±39.1	208.8±43.4	<0.001
Triglyceride, mg/dLa	89.0 (88.9–89.1)	113.7 (113.6–113.8)	<0.001
HDL-C, mg/dL	60.5±36.0	58.2±35.7	<0.001
LDL-C, mg/dL	114.8±71.4	127.9±72.1	<0.001
Fasting plasma glucose, mg/dL	93.7±18.0	99.1±23.7	<0.001
Obesity	252,687 (24.8)	443,426 (37.3)	<0.001
Abdominal obesity	120,759 (11.9)	308,140 (25.9)	<0.001
DM	37,049 (3.6)	136,964 (11.5)	<0.001
Hypertension	139,603 (13.7)	452,014 (38.0)	<0.001
Dyslipidemia	117,683 (11.6)	399,747 (33.6)	<0.001
CKD
eGFR <60 mL/min/1.73 m2	43,443 (4.3)	108,725 (9.1)	<0.001
eGFR <30 mL/min/1.73 m2	12,071 (1.2)	15,414 (1.3)	<0.001
COPD	75,404 (7.4)	160,239 (13.5)	<0.001
Cancer	16,083 (1.6)	36,834 (3.1)	<0.001
Smoking history			<0.001
Non-smoker	967,597 (94.9)	1,145,113 (96.3)
Ex-smoker	16,504 (1.6)	12,615 (1.1)
Current smoker	35,059 (3.4)	31,671 (2.7)
Alcohol drinking history			<0.001
Never	731,937 (71.8)	1,024,875 (86.2)
Mild	275,376 (27.0)	157,546 (13.3)
Heavy	11,847 (1.2)	6,978 (0.6)
Regular exercise	176,210 (17.3)	236,304 (19.9)	<0.001
Low income	262,723 (25.8)	285,201 (24.0)	<0.001
WC, cm			<0.001
<65	59,226 (5.8)	25,533 (2.2)
65–74.9	454,705 (44.6)	299,575 (25.2)
75–84.9	374,470 (37.7)	556,151 (46.8)
85–94.9	102,779 (10.1)	258,444 (21.7)
≥95	17,980 (1.8)	49696 (4.2)
BMI, kg/m2			<0.001
<18.5	28,456 (2.8)	20,351 (1.7)
18.5–22.9	499,611 (49.0)	406,277 (34.2)
23.0–24.9	238,406 (23.4)	319,345 (26.9)
25.0–29.9	220,949 (21.7)	391,509 (32.9)
≥30.0	31,738 (3.1)	51,917 (4.4)

Values are expressed as mean±standard deviation, geometric mean (95% confidence interval), or number (%).

BMI, body mass index; HDL-C, high-density lipoprotein cholesterol; LDL-C, low-density lipoprotein cholesterol; DM, diabetes mellitus; CKD, chronic kidney disease; eGFR, estimated glomerular filtration rate; COPD, chronic obstructive pulmonary disease; WC, waist circumference.

Logarithmic transformation was proceeded for analysis on triglyceride level.

The median follow-up duration was 9.3 years: 9,495,469 person-year (PY) and 11,088,205 PY in premenopausal and postmenopausal women, respectively. Stroke, MI, and death were observed in 6,013, 6,598, and 7,826 women, respectively, in the premenopausal group, and in 21,302, 30,851, and 35,475 women, respectively, in the postmenopausal group (Supplemental Table S1).

The incidence of MI, stroke, and mortality according to BMI in the premenopausal women

In the premenopausal women, the event rates of stroke and MI (per 1,000 PY) in those with normal BMI were 0.52 and 0.54, respectively. In these women, there was an increasing trend of risk in MI and stroke as BMI increased from normal range (Table 2, Fig. 2A, B). Overweight individuals (BMI 23.5 to 24.9 kg/m2) showed a significantly higher risk of both stroke and MI compared to those with normal BMI after adjustment for age, smoking history, alcohol consumption, regular exercise, low income, hypertension, dyslipidemia, CKD, and DM (HR, 1.144; 95% CI, 1.071 to 1.221; and HR, 1.189; 95% CI, 1.117 to 1.266, respectively).

Table 2

Incidence of Cardiovascular Disease or Mortality According to BMI

	BMI, kg/m2	Event	FU duration, PY	Incidence,/1,000 PY	Model 1		Model 2		Model 3
					HR (95% CI)	P value	HR (95% CI)	P value	HR (95% CI)	P value
Premenopausal women
MI	<18.5	136	264,101	0.51	0.983 (0.827–1.169)	0.850	1.057 (0.889–1.257)	0.528	1.055 (0.888–1.254)	0.543
	18.5–22.9	2,438	4,647,249	0.52	1 (reference)		1 (reference)		1 (reference)
	23.0–24.9	1,457	2,217,425	0.66	1.252 (1.173–1.336)	<0.001	1.150 (1.078– 1.228)	<0.001	1.144 (1.071–1.221)	<0.001
	25.0–29.9	1,672	2,052,721	0.81	1.552 (1.458–1.652)	<0.001	1.333 (1.250–1.421)	<0.001	1.306 (1.225–1.393)	<0.001
	≥30.0	310	293,966	1.05	2.012 (1.787–2.264)	<0.001	1.616 (1.431–1.824)	<0.001	1.522 (1.347–1.717)	<0.001
Stroke	<18.5	127	264,019	0.48	0.889 (0.744–1.062)	0.196	0.991 (0.829–1.184)	0.917	0.990 (0.828–1.183)	0.912
	18.5–22.9	2,516	4,645,957	0.54	1 (reference)		1 (reference)		1 (reference)
	23.0–24.9	1,646	2,216,041	0.74	1.371 (1.289–1.459)	<0.001	1.199 (1.126–1.276)	<0.001	1.189 (1.117–1.266)	<0.001
	25.0–29.9	1,936	2,050,768	0.94	1.743 (1.643–1.849)	<0.001	1.348 (1.268–1.433)	<0.001	1.312 (1.234–1.396)	<0.001
	≥30.0	373	293,647	1.27	2.347 (2.105–2.616)	<0.001	1.575 (1.408–1.762)	<0.001	1.456 (1.304–1.633)	<0.001
Mortality	<18.5	285	264,490	1.08	1.416 (1.255–1.598)	<0.001	1.511 (1.339–1.706)	<0.001	1.477 (1.309–1.667)	<0.001
	18.5–22.9	3,544	4,655,073	0.76	1 (reference)		1 (reference)		1 (reference)
	23.0–24.9	1,769	2,222,361	0.80	1.045 (0.987–1.107)	0.128	0.964 (0.910–1.021)	0.211	0.959 (0.906–1.016)	0.155
	25.0–29.9	1,851	2,058,436	0.90	1.181 (1.116–1.249)	<0.001	1.017 (0.96–1.078)	0.568	0.999 (0.942–1.058)	0.966
	≥30.0	377	295,109	1.28	1.678 (1.509–1.866)	<0.001	1.345 (1.206–1.499)	<0.001	1.247 (1.118–1.392)	<0.001
Postmenopausal women
MI	<18.5	344	186,154	1.85	1.206 (1.082–1.345)	0.001	1.185 (1.063–1.322)	0.002	1.195 (1.072–1.332)	0.001
	18.5–22.9	5,790	3,765,114	1.54	1 (reference)		1 (reference)		1 (reference)
	23.0–24.9	5,365	2,962,639	1.81	1.176 (1.133–1.221)	<0.001	1.060 (1.021–1.100)	0.002	1.054 (1.015–1.094)	0.006
	25.0–29.9	8,384	3,622,904	2.31	1.502 (1.452–1.553)	<0.001	1.219 (1.178–1.262)	<0.001	1.196 (1.156–1.238)	<0.001
	≥30.0	1,419	477,508	2.97	1.931 (1.822–2.046)	<0.001	1.442 (1.359–1.53)	<0.001	1.353 (1.275–1.436)	<0.001
Stroke	<18.5	496	185,376	2.68	1.169 (1.068–1.28)	0.001	1.149 (1.05–1.258)	0.003	1.165 (1.064–1.275)	0.001
	18.5–22.9	8,600	3,752,445	2.29	1 (reference)		1 (reference)		1 (reference)
	23.0–24.9	7,948	2,950,158	2.69	1.175 (1.14–1.212)	<0.001	1.022 (0.991–1.054)	0.166	1.015 (0.984–1.046)	0.357
	25.0–29.9	11,816	3,606,588	3.28	1.430 (1.391–1.47)	<0.001	1.080 (1.049–1.111)	<0.001	1.055 (1.026–1.086)	<0.001
	≥30.0	1,991	474,810	4.19	1.832 (1.744–1.923)	<0.001	1.239 (1.179–1.302)	<0.001	1.152 (1.096–1.211)	<0.001
Mortality	<18.5	1,150	187,083	6.15	2.018 (1.899–2.144)	<0.001	1.872 (1.761–1.989)	<0.001	1.835 (1.727–1.950)	<0.001
	18.5–22.9	11,568	3,784,473	3.06	1 (reference)		1 (reference)		1 (reference)
	23.0–24.9	8,504	2,981,041	2.85	0.932 (0.907–0.959)	<0.001	0.837 (0.814–0.861)	<0.001	0.839 (0.816–0.863)	<0.001
	25.0–29.9	12,075	3,653,037	3.31	1.080 (1.052–1.107)	<0.001	0.864 (0.842–0.887)	<0.001	0.856 (0.834–0.879)	<0.001
	≥30.0	2,178	482,572	4.51	1.475 (1.409–1.544)	<0.001	1.094 (1.045–1.147)	<0.001	1.029 (0.982–1.079)	0.226

Model 1: without adjustment; Model 2: with adjustment for age, smoking, drinking history, low income, regular exercise, hormone replacement therapy (in the case of postmenopausal women), hypertension, dyslipidemia, and estimated glomerular filtration rate <60 mL/min/1.73 m2; Model 3: with adjustment for diabetes mellitus in addition to Model 2.

BMI, body mass index; FU, follow-up; PY, person-year; HR, hazard ratio; CI, confidence interval; MI, myocardial infarction.

Fig. 2

The risk of myocardial infarction, stroke, and mortality during the follow-up period according to body mass index and waist circumference. Hazard ratios for myocardial infarction (A), stroke (B) and mortality (C) according to body mass index and waist circumference (D, E, F, respectively) after adjustment for age, smoking history, alcohol consumption, regular exercise, low income, hypertension, dyslipidemia, chronic kidney disease, and diabetes mellitus in premenopausal (circle) and postmenopausal women (square). CI, confidence interval.

In contrast, there was a J-shaped association between BMI and mortality in the premenopausal women (Fig. 2C). The nadir of mortality in premenopausal women was found in those who were overweight (HR, 0.959; 95% CI, 0.906 to 1.016) (Table 2), but this was not statistically different from those with normal BMI (Table 2). The mortality rate of women in obesity class I (BMI 25.0 to 29.9 kg/m2) did not differ from that of women with normal BMI (HR, 0.999; 95% CI, 0.942 to 1.058). Women with BMI <18.5 kg/m2 and those with BMI ≥30 kg/m2 (obesity class II) had a significantly higher mortality rate compared to those with normal weight (HR, 1.477; 95% CI, 1.309 to 1.667; and HR, 1.247; 95% CI, 1.118 to 1.392, respectively) (Table 2). Subsequent classification of the group with BMI 25.0–29.9 kg/m2 into 25.0–27.5 and 27.6–29.9 kg/m2 confirmed that the nadir of mortality in premenopausal women was in those who were overweight (HR in BMI 25.0–27.5 kg/m2, 0.968; 95% CI, 0.907 to 1.034; and HR in BMI 27.6–29.9 kg/m2, 1.076; 95% CI, 0.984 to 1.177) (Supplemental Fig. S1).

After excluding subjects with histories of malignancy, a similar trend was found (Supplemental Fig. S2A). The nadir of mortality was found in overweight women (HR, 0.952; 95% CI, 0.896 to 1.012), which was not statistically different from that of women with normal BMI (Supplemental Table S2). Additional exclusion of subjects with CKD or COPD and current smokers also confirmed the lowest mortality rate to be in those who were overweight (HR, 0.951; 95% CI, 0.890 to 1.016) (Table 3, Supplemental Fig. S2A). In premenopausal women with comorbidities, the nadir of mortality was found in those with BMI 25.0 to 29.9 kg/m2 (HR, 0.972; 95% CI, 0.864 to 1.093), which was not statistically different from that in normal BMI. Furthermore, in premenopausal women with comorbidities, the mortality rate of women with BMI ≥30 kg/m2 was not statistically different from that of women with normal BMI (HR, 1.154; 95% CI, 0.933 to 1.428).

Table 3

Incidence of Cardiovascular Disease or Mortality According to BMI/WC in Women with and without Comorbidities Including Cancer, CKD (eGFR <30 mL/min/1.73 m2), COPD, and Current Smoker

	Category	Premenopausal women				Postmenopausal women
		No comorbidities		Comorbidities (+)		No comorbidities		Comorbidities (+)
		HR (95% CI)	P value	HR (95% CI)	P value	HR (95% CI)	P value	HR (95% CI)	P value
BMI, kg/m2
MI	<18.5	0.932 (0.757–1.148)	0.510	1.471 (1.076–2.013)	0.016	1.053 (0.915–1.212)	0.469	1.456 (1.224–1.732)	<0.001
	18.5–22.9	1 (reference)		1 (reference)		1 (reference)		1 (reference)
	23.0–24.9	1.132 (1.053–1.218)	0.001	1.185 (1.021–1.375)	0.025	1.071 (1.026–1.119)	0.002	1.003 (0.932–1.079)	0.939
	25.0–29.9	1.322 (1.230–1.419)	<0.001	1.228 (1.059–1.424)	0.007	1.213 (1.166–1.263)	<0.001	1.134 (1.061–1.212)	<0.001
	≥30.0	1.449 (1.258–1.67)	<0.001	1.696 (1.329–2.164)	<0.001	1.402 (1.307–1.503)	<0.001	1.198 (1.070–1.342)	0.002
Stroke	<18.5	0.869 (0.703–1.074)	0.194	1.464 (1.049–2.042)	0.025	1.143 (1.025–1.275)	0.017	1.193 (1.013–1.404)	0.034
	18.5–22.9	1 (reference)		1 (reference)		1 (reference)		1 (reference)
	23.0–24.9	1.179 (1.101–1.263)	<0.001	1.233 (1.058–1.435)	0.007	1.023 (0.987–1.059)	0.210	0.988 (0.928–1.052)	0.703
	25.0–29.9	1.316 (1.230–1.408)	<0.001	1.282 (1.105–1.489)	0.001	1.073 (1.038–1.108)	<0.001	0.995 (0.939–1.054)	0.866
	≥30.0	1.536 (1.358–1.739)	<0.001	1.128 (0.856–1.487)	0.393	1.165 (1.099–1.234)	<0.001	1.096 (0.995–1.207)	0.063
Mortality	<18.5	1.394 (1.202–1.617)	<0.001	1.662 (1.348–2.049)	<0.001	1.775 (1.638–1.923)	<0.001	1.888 (1.719–2.074)	<0.001
	18.5–22.9	1 (reference)		1 (reference)		1 (reference)		1 (reference)
	23.0–24.9	0.951 (0.890–1.016)	0.134	0.985 (0.877–1.106)	0.798	0.858 (0.829–0.888)	<0.001	0.800 (0.761–0.841)	<0.001
	25.0–29.9	1.005 (0.940–1.075)	0.876	0.972 (0.864–1.093)	0.634	0.877 (0.850–0.905)	<0.001	0.808 (0.772–0.846)	<0.001
	≥30.0	1.278 (1.124–1.453)	<0.001	1.154 (0.933–1.428)	0.187	1.054 (0.995–1.116)	0.073	0.964 (0.890–1.045)	0.372
WC, cm
MI	<65.0	0.774 (0.667–0.896)	0.001	1.009 (0.766–1.328)	0.951	0.839 (0.729–0.965)	0.014	0.981 (0.792–1.216)	0.861
	65.0–74.9	0.867 (0.812–0.924)	<0.001	0.860 (0.752–0.984)	0.028	0.867 (0.829–0.906)	<0.001	0.927 (0.860–1.000)	0.049
	75.0–84.9	1 (reference)		1 (reference)		1 (reference)		1 (reference)
	85.0–94.9	1.172 (1.073–1.280)	<0.001	1.220 (1.031–1.442)	0.020	1.203 (1.159,1.249)	<0.001	1.127 (1.058–1.200)	<0.001
	≥95.0	1.379 (1.165–1.634)	<0.001	1.356 (1.009–1.821)	0.043	1.339 (1.254–1.430)	<0.001	1.257 (1.135–1.391)	<0.001
Stroke	<65.0	0.748 (0.647–0.865)	<0.001	0.970 (0.724–1.299)	0.837	0.999 (0.896–1.114)	0.988	1.134 (0.945–1.360)	0.177
	65.0–74.9	0.835 (0.785–0.888)	<0.001	0.837 (0.729–0.961)	0.012	0.892 (0.860–0.926)	<0.001	0.968 (0.906–1.034)	0.335
	75.0–84.9	1 (reference)		1 (reference)		1 (reference)		1 (reference)
	85.0–94.9	1.188 (1.097–1.286)	<0.001	1.156 (0.978–1.366)	0.089	1.088 (1.055,1.122)	<0.001	1.075(1.018,1.135)	0.009
	≥95.0	1.382 (1.193–1.601)	<0.001	0.933 (0.674–1.290)	0.673	1.192 (1.130,1.258)	<0.001	1.247(1.144,1.359)	<0.001
Mortality	<65.0	1.072 (0.951–1.209)	0.254	1.477 (1.232–1.770)	<0.001	1.427 (1.304–1.561)	<0.001	1.665 (1.487–1.865)	<0.001
	65.0–74.9	0.984 (0.928–1.044)	0.598	0.978 (0.883–1.084)	0.673	1.068 (1.032–1.105)	<0.001	1.126 (1.072–1.183)	<0.001
	75.0–84.9	1 (reference)		1 (reference)		1 (reference)		1 (reference)
	85.0–94.9	1.185 (1.091–1.287)	<0.001	0.987 (0.853–1.142)	0.860	1.034 (1.002–1.067)	0.038	1.001 (0.956–1.049)	0.952
	≥95.0	1.649 (1.424–1.909)	<0.001	1.363 (1.073–1.731)	0.011	1.287 (1.221–1.357)	<0.001	1.284 (1.194–1.381)	<0.001

CKD was defined as estimated glomerular filtration rate <30 mL/min/1.73 m2. HR with adjustment for age, smoking, drinking history, low income, regular exercise, hormone replacement therapy (in the case of postmenopausal women), hypertension, dyslipidemia, diabetes mellitus, and eGFR <60 mL/min/1.73 m2.

BMI, body mass index; WC, waist circumference; CKD, chronic kidney disease; eGFR, estimated glomerular filtration rate; COPD, chronic obstructive pulmonary disease; HR, hazard ratio; CI, confidence interval; MI, myocardial infarction.

The incidence of MI, stroke, and mortality according to BMI in postmenopausal women

In postmenopausal women, the trend of the risk of MI, stroke, and mortality according to BMI was similar to that in premenopausal women. There was an increasing risk of MI and stroke in overweight and obese women compared to that in women with normal weight (Table 2, Fig. 2A, B). Even individuals who were overweight (BMI 23.5 to 24.9 kg/m2) showed a significantly higher risk of MI compared to those with normal BMI, after adjustment for age, smoking history, alcohol consumption, regular exercise, low income, hypertension, dyslipidemia, CKD, and DM (HR, 1.054; 95% CI, 1.015 to 1.094). The risk of stroke significantly increased past the obesity range of BMI (≥25 kg/m2) (Table 2). However, age-stratification showed that in women aged 60 to 69 years, the risks of MI and stroke in the overweight group were not different compared to those for women with normal weight (HR, 1.011; 95% CI, 0.964 to 1.060; and HR, 0.976; 95% CI, 0.941 to 1.013, respectively) (Supplemental Table S3).

In the case of overall mortality, the nadir of mortality found in overweight women was more prominent in the postmenopausal group compared to that in the premenopausal group, and the mortality in overweight women was significantly lower than that in women with normal BMI (HR, 0.839; 95% CI, 0.816 to 0.863) (Fig. 2C). Furthermore, women with BMI 25.0 to 29.9 kg/m2 (obesity class I) also had a significantly lower mortality than women with normal BMI (HR, 0.856; 95% CI, 0.834 to 0.879); even in those with obesity class II (BMI ≥30.0 kg/m2), the risk of mortality was not different compared to that seen in those with normal BMI (HR, 1.029; 95% CI, 0.982 to 1.079) (Fig. 2C). The mortality rate of those with BMI <18.5 kg/m2 was 83.5% higher compared to that in those normal BMI (HR, 1.835; 95% CI, 1.727 to 1.950) (Table 2). Significantly lower mortality risk in overweight and obese women and significantly higher mortality in underweight women compared to women with normal BMI were found irrespective of the presence or the absence of comorbidities (Table 3, Supplemental Fig. S2B). The reduction of overall mortality in those with BMI 23.0–24.9 and 25.0–29.9 kg/m2 compared to the normal-weight population was more prominent with increasing age (Supplemental Table S3). In postmenopausal women aged 60 to 69 years, the HRs of mortality of women with BMI 23.0–24.9 and 25.0–29.9 kg/m2 were 0.829 (95% CI, 0.802 to 0.858) and 0.837 (95% CI, 0.811 to 0.863), respectively.

Differences in the effect of BMI on the outcomes according to DM

Subsequent stratified analysis according to DM showed that the risks of MI, stroke, and mortality according to BMI found in the entire population were also replicated in non-diabetic women irrespective of menopausal status (Table 4, Fig. 3). However, in diabetic women, there was no significant increment in the risk of MI or stroke in those with BMI above the normal range (Table 4, Fig. 3A, B). Furthermore, among diabetic postmenopausal women, the risks of MI and stroke were significantly lower in women with BMI 25.0 to 29.9 kg/m2 compared to those in women with normal BMI (Table 4).

Table 4

Incidence of Cardiovascular Disease or Mortality According to BMI/WC in Women with and without Diabetes Mellitus

	Category	Premenopausal women				Postmenopausal women
		No DM		DM		No DM		DM
		HR (95% CI)	P value	HR (95% CI)	P value	HR (95% CI)	P value	HR (95% CI)	P value
BMI, kg/m2
MI	<18.5	1.060 (0.889–1.265)	0.515	0.963 (0.393–2.356)	0.933	1.178 (1.046–1.327)	0.007	1.372 (1.046–1.799)	0.022
	18.5–22.9	1 (reference)		1 (reference)		1 (reference)		1 (reference)
	23.0–24.9	1.158 (1.083–1.239)	<0.001	0.878 (0.674–1.144)	0.336	1.092 (1.047–1.138)	<0.001	0.894 (0.822–0.972)	0.009
	25.0–29.9	1.336 (1.25–1.429)	<0.001	0.940 (0.746–1.185)	0.602	1.278 (1.230–1.329)	<0.001	0.917 (0.851–0.988)	0.023
	≥30.0	1.593 (1.393–1.823)	<0.001	1.042 (0.766–1.418)	0.794	1.503 (1.400–1.614)	<0.001	0.993 (0.891–1.107)	0.903
Stroke	<18.5	0.948 (0.786–1.144)	0.579	1.936 (1.075–3.485)	0.028	1.116 (1.009–1.233)	0.032	1.491 (1.206–1.844)	<0.001
	18.5–22.9	1 (reference)		1 (reference)		1 (reference)		1 (reference)
	23.0–24.9	1.205 (1.129–1.287)	<0.001	0.908 (0.723–1.14)	0.404	1.032 (0.997–1.068)	0.076	0.941 (0.880–1.006)	0.074
	25.0–29.9	1.361 (1.276–1.451)	<0.001	0.860 (0.702–1.053)	0.145	1.088 (1.054–1.124)	<0.001	0.939 (0.885–0.998)	0.042
	≥30.0	1.514 (1.333–1.720)	<0.001	1.015 (0.782–1.317)	0.911	1.213 (1.141–1.290)	<0.001	1.005 (0.921–1.096)	0.913
Mortality	<18.5	1.431 (1.263–1.622)	<0.001	2.553 (1.605–4.061)	<0.001	1.808 (1.692–1.931)	<0.001	2.044 (1.749–2.389)	<0.001
	18.5–22.9	1 (reference)		1 (reference)		1 (reference)		1 (reference)
	23.0–24.9	0.967 (0.911–1.026)	0.267	0.825 (0.661–1.03)	0.090	0.848 (0.822–0.875)	<0.001	0.795 (0.747–0.846)	<0.001
	25.0–29.9	1.035 (0.974–1.100)	0.265	0.689 (0.562–0.844)	<0.001	0.898 (0.872–0.925)	<0.001	0.722 (0.683–0.763)	<0.001
	≥30.0	1.307 (1.156–1.477)	<0.001	0.894 (0.688–1.161)	0.400	1.113 (1.052–1.179)	<0.001	0.846 (0.778–0.919)	<0.001
WC, cm
MI	<65.0	0.810 (0.710–0.924)	0.002	1.047 (0.464–2.363)	0.913	0.846 (0.747–0.958)	0.009	1.218 (0.858–1.727)	0.270
	65.0–74.9	0.862 (0.812–0.915)	<0.001	0.908 (0.703–1.175)	0.464	0.866 (0.831–0.903)	<0.001	0.985 (0.891–1.089)	0.772
	75.0–84.9	1 (reference)		1 (reference)		1 (reference)		1 (reference)
	85.0–94.9	1.180 (1.085–1.284)	<0.001	1.214 (0.979–1.507)	0.078	1.214 (1.170–1.260)	<0.001	1.108 (1.038–1.183)	0.002
	≥95.0	1.440 (1.218–1.702)	<0.001	1.235 (0.904–1.688)	0.184	1.373 (1.282–1.471)	<0.001	1.227 (1.118–1.348)	<0.001
Stroke	<65.0	0.810 (0.710–0.924)	0.002	1.047 (0.464–2.363)	0.913	1.024 (0.928–1.130)	0.636	1.129 (0.844–1.511)	0.414
	65.0–74.9	0.862 (0.812–0.915)	<0.001	0.908 (0.703–1.175)	0.464	0.902 (0.871–0.934)	<0.001	0.958 (0.883–1.040)	0.305
	75.0–84.9	1 (reference)		1 (reference)		1 (reference)		1 (reference)
	85.0–94.9	1.180 (1.085–1.284)	<0.001	1.214 (0.979–1.507)	0.078	1.092 (1.059–1.127)	<0.001	1.070 (1.016–1.128)	0.011
	≥95.0	1.440 (1.218–1.702)	<0.001	1.235 (0.904–1.688)	0.184	1.202 (1.134–1.274)	<0.001	1.225 (1.137–1.318)	<0.001
Mortality	<65.0	0.783 (0.686–0.894)	<0.001	0.996 (0.469–2.113)	0.991	1.473 (1.367–1.587)	<0.001	1.849 (1.497–2.282)	<0.001
	65.0–74.9	0.827 (0.78–0.877)	<0.001	1.045 (0.844–1.294)	0.684	1.069 (1.037–1.103)	<0.001	1.187 (1.105–1.274)	<0.001
	75.0–84.9	1 (reference)		1 (reference)		1 (reference)		1 (reference)
	85.0–94.9	1.213 (1.122–1.310)	<0.001	1.049 (0.868–1.267)	0.622	1.051 (1.020–1.084)	0.001	0.960 (0.912–1.011)	0.123
	≥95.0	1.351 (1.157–1.579)	<0.001	1.125 (0.862–1.467)	0.387	1.331 (1.261–1.405)	<0.001	1.219 (1.135–1.308)	<0.001

HR with adjustment for age, smoking, drinking history, low income, regular exercise, hormone replacement therapy (in the case of postmenopausal women), hypertension, dyslipidemia, and estimated glomerular filtration rate <60 mL/min/1.73 m2.

BMI, body mass index; WC, waist circumference; DM, diabetes mellitus; HR, hazard ratio; CI, confidence interval; MI, myocardial infarction.

Fig. 3

The risk of myocardial infarction, stroke, and mortality during the follow-up period according to body mass index, diabetes mellitus (DM), and menopausal status. Hazard ratios for myocardial infarction (A), stroke (B), and mortality (C) according to body mass index after adjustment for age, smoking history, alcohol consumption, regular exercise, low income, hypertension, dyslipidemia, and chronic kidney disease in premenopausal (black) and postmenopausal (grey) women with (square) and without DM (circle). CI, confidence interval.

The nadir in mortality among the diabetic women was found in those with BMI 25.0 to 29.9 kg/m2, both in the premenopausal and the postmenopausal groups (HR, 0.689; 95% CI, 0.562 to 0.844; and HR, 0.722; 95% CI, 0.683 to 0.763, respectively) (Fig. 3C). Furthermore, among the postmenopausal women with DM, being in obesity class II (BMI ≥30 kg/m2) significantly decreased the risk of mortality compared to having normal weight (HR, 0.846; 95% CI, 0.778 to 0.919).

The risk of MI, stroke, and mortality according to WC

Subsequently, we compared the risk of MI and stroke according to WC and found that abdominal obesity significantly increased the risk of both stroke and MI, irrespective of menopausal status even after adjustment for age, smoking, drinking history, low income, regular exercise, HRT, hypertension, dyslipidemia, CKD, and DM (P for trend <0.001 in all) (Fig. 2D, E, Supplemental Table S4). Even for those within the normal range of WC (<85 cm), women with WC 65.0 to 74.9 cm had a lower risk of MI and stroke compared to those with WC 75.0 to 84.9 cm, in both the premenopausal and postmenopausal groups (Supplemental Table S4).

The nadir of mortality was found in those with WC 65.0–74.9 and 75.0–84.9 cm in premenopausal and postmenopausal women, respectively (Supplemental Table S4). A U-shaped relationship with mortality was also found for WC: the risk of mortality was significantly increased for those with WC ≥85.0 and ≥95.0 cm among premenopausal and postmenopausal women, respectively, as well as for those with WC <65.0 cm (Fig. 2F). Among subjects with comorbidity, the risk of mortality in those with WC <65.0 cm was more prominent both in the premenopausal and postmenopausal women compared to those in subjects without comorbidity (HR, 1.477; 95% CI, 1.232 to 1.770; and HR, 1.665; 95% CI, 1.487 to 1.865, in the premenopausal and the postmenopausal women, respectively) (Table 3, Supplemental Fig. S2C, D).

Stratified analysis according to DM status showed that in the case of premenopausal women without diabetes, a linear trend of HR according to WC was found (P for trend <0.001); women with WC <65.0 cm exhibited the lowest mortality (HR, 0.783; 95% CI, 0.686 to 0.894) (Table 4).

DISCUSSION

Using a nationwide health examination database and claims data covering 97.0% of the population in Korea, we found that the risk of MI during the 10-year follow-up period was significantly increased when BMI was ≥23 kg/m2 (overweight range) at baseline, irrespective of menopausal status. The risk of stroke during the same period significantly increased when BMI ≥23 and ≥25 kg/m2 in the premenopausal and postmenopausal women, respectively. However, the presence of DM, rather than other comorbidities such as cancer or COPD, attenuated the risk of MI and stroke associated with being overweight or obese; there was similar or significantly lower incidence of MI or stroke in those above the reference range of BMI compared to those in the normal range in women with DM.

The current study replicated the J-shaped relationship between BMI and mortality in postmenopausal women; in this group, those with BMI 23.0 to 24.9 kg/m2 (overweight) showed the lowest mortality. In postmenopausal women, those with BMI 25.0 to 29.9 kg/m2 (obesity) also had a significantly lower mortality compared to those with normal weight. In premenopausal women, the nadir of the risk of mortality was also found in those who were overweight; however, this was not statistically different from those with normal BMI. The mortality in the premenopausal women increased significantly from obesity class II, that is, BMI ≥30 kg/m2. Even for premenopausal women without comorbidity, the same trend in the association between BMI and mortality was replicated. However, age stratification demonstrated that the lower mortality found in overweight and obese women was attenuated by young age.

Age is an important determining factor in the association between BMI and overall mortality [3,4]. A prospective study of 14 years showed that mortality in overweight women was increased only in those aged <65 years; there was no difference in the mortality rate between women who are overweight and those who are normal weight in women aged ≥65 years [3]. Similarly, another study also confirmed that being overweight was an independent risk factor for the overall mortality only in those aged <60 years [4].

Contrasting overall mortality, obesity or overweight have been reported to increase the risk of CVD [19], and the current study results also support this. In the current study, obesity was an independent risk factor for MI or stroke, irrespectively of menopausal status. Among CVD, MI or heart failure was more highly associated with obesity compared to stroke [19]; this may explain the lack of increase of risk of stroke by obesity in several subgroups in the current study, such as postmenopausal women with comorbidities.

A pooled longitudinal cohort study reported that being overweight and obesity were independent risk factors for cumulative lifetime incident CVD events and CVD death [19]. By contrast, non-CVD death was lowered in overweight and obese people [19], which might explain the lower overall mortality in the obese and overweight population, despite their high CVD risk, compared to those in the normal-weight class in the current study. In addition, among patients with pre-existing CVD [1,20] or heart failure [21], being overweight lowered the CVD mortality as well as overall mortality during the follow-up period. In contrast, in individuals with good cardiorespiratory function, there was no benefit from being overweight or obese [22]. The current study also confirmed this through the stratification according to the presence of comorbidities; in addition, even being in obesity class II did not increase the risk of mortality in those with comorbidities, irrespective of menopausal status.

The current study showed the presence of DM, rather than other comorbidities such as cancer or COPD, attenuated the risk of MI and stroke associated with being overweight or obese. In previous prospective cohort studies, it was found that weight gain before the diagnosis of DM increased the risk of CVD; however, weight gain after the diagnosis of DM was not associated with risk of CVD [5,6], which might be due to the fact that after the development of DM, insulin resistance and the associated CVD risk is too high to be affected by any additional weight gain. In addition, hypertension or dyslipidemia, which frequently accompany DM as well as obesity, play more important roles in the development of CVD compared to obesity [23,24].

In the case of WC, a linear increasing trend with MI and stroke was found, irrespective of menopausal status, which corresponded to the results of a previous report in the European population [25]. WC can discriminate CVD outcomes better than BMI [25], and the effect of WC on clinical outcomes was maintained across diverse BMI categories [26,27]. In the current study, even in those within the normal range of WC (<85 cm), women with WC 75.0 to 84.9 cm had a higher risk of MI and stroke compared to those with WC 65.0 to 74.9 cm. Stratified analysis according to DM status also confirmed that abdominal obesity (WC ≥85 cm) increased the risk of MI in women. A J-shaped association with mortality was also found for WC; however, there was no significant increment of mortality in the normal range of WC (75.0 to 84.9 cm).

The current study has several limitations. First, the CVD events during the follow-up period were assessed using claims data. Claims data might underestimate the real incidence of CVD, especially in the case of ischemic stroke [28]. In addition, it provides limited information on disease severity. However, the definitions for CVD used in the current study were validated in a previous study in Korea; their sensitivity and positive predictive values for the claims data were reported to reach 90% [11]. Furthermore, the NHIS in Korea covers the claims of 97.0% of the population, thus proving invaluable in the estimation of the effect of obesity parameters on clinical outcomes in the entire Korean population; this also helps to build a cutoff value for the obesity parameter for public health in Korea. Second, we did not have cause-specific mortality data, which makes it more difficult to explain the different effect of overweight or obesity status on CVD events and overall mortality. Finally, the median duration of follow-up of the current study was 9.3 years, and follow-up duration affects the impact of BMI on mortality. The underweight group had been reported to have increased risk for CVD mortality and overall mortality [1], as is in the current study, but this was attenuated with longer-term follow-up [4]. In addition, the long-term benefit of obesity on CVD mortality in those with pre-existing CVD disappeared after 5 years of follow-up [20]. Further long-term studies should be performed, especially in the younger population, to estimate an optimal BMI or WC for long-term benefit.

In conclusion, for CVD prevention, the current reference range of BMI (18.5 to 22.9 kg/m2) may be optimal irrespective of menopausal status. However, in diabetic women or women aged ≥60 years, a less stringent cutoff for obesity can be applied. To estimate the risk of CVD events, WC might be more suitable than BMI in those with DM or comorbidities, especially in postmenopausal women. In postmenopausal women, being overweight and obese reduced the mortality rate significantly even in those without comorbidities, which suggests that consideration for menopausal status as well as age should be required for BMI cutoff for obesity management.