The association of microalbuminuria with clinical cardiovascular disease and subclinical atherosclerosis in the elderly: The Cardiovascular Health Study

被引:57
作者
Cao, Jie J.
Barzilay, Joshua I.
Peterson, Do
Manolio, Teri A.
Psaty, Bruce M.
Kuller, Lewis
Wexler, Jason
Bleyer, Anthony J.
Cushman, Mary
机构
[1] Univ Vermont, Coll Med, Dept Pathol & Med, Colchester, VT 05446 USA
[2] NHLBI, Nihon Univ, Bethesda, MD 20892 USA
[3] Emory Univ, Sch Med, Kaiser Permanente Georgia, Atlanta, GA USA
[4] Emory Univ, Sch Med, Div Endocrinol, Atlanta, GA USA
[5] Univ Washington, Dept Biostat, Seattle, WA 98195 USA
[6] Univ Washington, Dept Med, Seattle, WA 98195 USA
[7] Univ Washington, Dept Epidemiol, Seattle, WA 98195 USA
[8] Univ Washington, Dept Hlth Serv, Seattle, WA 98195 USA
[9] Univ Pittsburgh, Dept Epidemiol, Pittsburgh, PA 15261 USA
[10] Univ Calif Davis, Dept Med, Davis, CA 95616 USA
[11] Wake Forest Univ, Dept Med, Winston Salem, NC 27109 USA
关键词
microalbuminuria; cardiovascular disease; hypertension; diabetes mellitus;
D O I
10.1016/j.atherosclerosis.2005.09.015
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose: Microalbuminuria (MA) is a risk factor for cardiovascular disease (CVD). It is not known whether this association is due to the effect of MA on the development of subclinical atherosclerosis or whether MA destabilizes subclinical atherosclerosis, leading to clinical events. Methods: In a cross-sectional analysis we evaluated 3312 Cardiovascular Health Study participants, age >= 65 years, who had MA testing. Participants were divided into three groups: those without diabetes or hypertension (33%), those with hypertension (52%) and those with diabetes, with or without hypertension (15%). Clinical CVD was defined as presence of coronary heart disease (angina, MI, CABG, PTCA), cerebrovascular disease (stroke, TIA) and peripheral arterial disease (requiring intervention). Among those without clinical disease, subclinical atherosclerosis was defined as increased carotid artery intima-media thickness, decreased ankle arm index or increased left ventricular mass. Results: In each of the three groups of participants, the adjusted odds of prevalent clinical CVD in the presence of MA was 1.70-1.80-fold increased, independent of other risk factors. MA was not associated with risk of subclinical atherosclerosis in those without hypertension or diabetes (OR 1.14 [95% CI 0.59, 2.23]), whereas it was associated with subclinical atherosclerosis in those with hypertension (OR 1.58 [95% CI 1.08, 2.30]) or diabetes (OR 2.51 [95% CI 1.27, 4.94]). Conclusion: In the absence of hypertension or diabetes, MA was associated with clinical CVD but not with subclinical atherosclerosis. Thus, a hypothesis may be made that the mechanism of association of MA with clinical vascular disease involves destabilization of the vasculature, leading to clinical disease. (c) 2005 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:372 / 377
页数:6
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