Prevalence and prognostic impact of subclinical cardiovascular disease in individuals with the metabolic syndrome and diabetes

被引:83
作者
Ingelsson, Erik
Sullivan, Lisa M.
Murabito, Joanne M.
Fox, Caroline S.
Benjamin, Emelia J.
Polak, Joseph F.
Meigs, James B.
Keyes, Michelle J.
O'Donnell, Christopher J.
Wang, Thomas J.
D'Agostino, Ralph B., Sr.
Wolf, Philip A.
Vasan, Ramachandran S.
机构
[1] Natl Heart Lund & Blood Inst Framingham Study, Framingham, MA USA
[2] Boston Univ, Dept Biostat, Boston, MA 02215 USA
[3] Boston Univ, Sch Med, Gen Internal Med Sect, Boston, MA 02215 USA
[4] Harvard Univ, Sch Med, Brigham & Womens Hosp, Div Endocrinol Diabet & Hypertens, Boston, MA USA
[5] Boston Univ, Sch Med, Dept Prevent Med, Boston, MA USA
[6] Boston Univ, Sch Med, Cardiol Sect, Boston, MA USA
[7] Tufts Univ, New England Med Ctr, Boston, MA 02111 USA
[8] Massachusetts Gen Hosp, Dept Med, Div Gen Med, Boston, MA 02114 USA
[9] Boston Univ, Dept Math & Stat, Boston, MA 02215 USA
[10] Massachusetts Gen Hosp, Div Cardiol, Boston, MA 02114 USA
[11] NHLBI, Ctr Populat Studies, Bethesda, MD 20892 USA
[12] Boston Univ, Sch Med, Dept Neurol, Boston, MA 02215 USA
[13] Boston Univ, Sch Med, Dept Prevent Med, Boston, MA 02215 USA
[14] Boston Univ, Sch Med, Dept Epidemiol, Boston, MA 02215 USA
关键词
D O I
10.2337/db07-0078
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Data are limited regarding prevalence and prognostic significance of subclinical cardiovascular disease (CVD) in individuals with metabolic syndrome (MetS). We investigated prevalence of subclinical CVD in 1,945 Framingham Offspring Study participants (mean age 58 years; 59% women) using electrocardiography, echocardiography, carotid ultrasound, ankle-brachial blood pressure, and uriary albumin excretion. We prospectively evaluated the incidence of CVD associated with MetS and diabetes according to presence versus absence of subclinical disease. Cross-sectionally, 51% of 581 participants with MetS had subclinical disease in at least one test, a frequency higher than individuals without MetS (multivariable-adjusted odds ratio 2.06 [95% CI 1.67-2.55]; P < 0.0001). On follow-up (mean 7.2 years), 139 individuals developed overt CVD, including 59 with MetS (10.2%). Overall, MetS was associated with increased CVD risk (multivariable-adjusted hazards ratio [HR] 1.61 [95% CI 1.12-2.33]). Participants with MetS and subclinical. disease experienced increased risk of overt CVD (2.67 [1.62-4.41] compared with those without MetS, diabetes, or subclinical diseease), whereas the association of MetS with CVD risk was tenuated in absence of subclinical disease (HR 1.59 [95% CI 0.87-2.90]). A similar attenuation of CVD risk in absence of subclinical disease was observed also for diabetes. Subclinical disease was a significant predictor of overt CVD in participants without MetS or diabetes (1.93 [1.15-3.24]). In our community-based sample, individuals with MetS have a high prevalence of subclinical atherosclerosis that likely contributes to the increased risk of overt CVD associated with the condition.
引用
收藏
页码:1718 / 1726
页数:9
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