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Comparative Study
. 2007 Dec 1;100(11):1654-8.
doi: 10.1016/j.amjcard.2007.06.073.

Comparison of usefulness of body mass index versus metabolic risk factors in predicting 10-year risk of cardiovascular events in women

Affiliations
Comparative Study

Comparison of usefulness of body mass index versus metabolic risk factors in predicting 10-year risk of cardiovascular events in women

Yiqing Song et al. Am J Cardiol. .

Abstract

The objective of this study was to prospectively examine the comparative importance of body mass index (BMI) and metabolic syndrome (MS) related risk factors in predicting future risk of cardiovascular disease (CVD) in women. Of 25,626 women aged>or=45 years and free of CVD, cancer, and diabetes at baseline in the Women's Health Study, all women were classified into 6 groups according to 3 BMI categories (<25, 25 to 29.9, and >or=30 kg/m2) and the presence or absence of MS, defined using modified criteria of the National Cholesterol Education Program Adult Treatment Program III. During a median 10-year follow-up, 724 incident CVD events were documented. Compared with lean women without MS, multivariate relative risks of CVD, adjusting for age, physical activity, and other covariates, were 2.40 (95% confidence interval [CI] 1.71 to 3.37) for lean women who had MS, 1.08 (95% CI 0.87 to 1.33) for overweight women who had no MS, 3.01 (95% CI 2.30 to 3.94) for overweight women with MS, 1.58 (95% CI 1.21 to 2.08) for obese women without MS, and 2.89 (95% CI 2.19 to 3.80) for obese women with MS. Similar associations were evident for total coronary heart disease, but were not significant for total stroke. Overall, although C-reactive protein added additional prognostic information beyond BMI and MS, it did not fully account for the observed high risk of CVD associated with MS. In conclusion, MS may largely account for the increased risk of CVD associated with BMI in apparently healthy women.

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Figures

Figure 1
Figure 1
Multivariate-adjusted relative risks of CVD during 10 years of follow-up according to BMI (<25, 25–29.9, ≥30), the presence of MS (yes vs no), and plasma CRP concentrations (≤3 mg/L and >3 mg/L) at baseline. RRs were adjusted for age, randomized treatment assignment (aspirin and vitamin E), smoking status, exercise, alcohol intake, total calorie intake, postmenopausal hormone use, multivitamin use, and parental history of myocardial infarction before 60 years.
Figure 2
Figure 2
Multivariate-adjusted relative risks of CVD according to BMI (<25, 25–29.9, ≥30) and the presence of individual metabolic factors (yes vs no) including baseline hypertension, dyslipidemia (defined as low high density lipoprotein cholesterol and/or high triglycerols), and incident diabetes, or at least 1 or at least 2 factors. Analyses were adjusted for age, randomized treatment assignment, smoking, exercise, total calories, alcohol use, multivitamin use, postmenopausal hormone use, and parental history of myocardial infarction before 60 y. Adjustment for dyslipidemia and incident diabetes were further made in the models for joint associations with hypertension, baseline hypertension and dyslipidemia were controlled for joint associations with incident diabetes, and hypertension and incident diabetes were adjusted in the models for joint associations with dyslipidemia.

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