Volume 5, Issue 1 pp. 30-34

Microalbuminuria in cerebrovascular disease: a modifiable risk factor?

A. Rocco

Corresponding Author

A. Rocco

Department of Neurology, Ruprecht-Karls-University Heidelberg, Heidelberg, Germany

A. Rocco*, Department of Neurology, Ruprecht-Karls University Heidelberg, Im Neuenheimer Feld 400, D69120 Heidelberg, Germany. E-mail: [email protected]Search for more papers by this author
K. Heerlein

K. Heerlein

Department of Neurology, Ruprecht-Karls-University Heidelberg, Heidelberg, Germany

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J. Diedler

J. Diedler

Department of Neurology, Ruprecht-Karls-University Heidelberg, Heidelberg, Germany

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M. Sykora

M. Sykora

Department of Neurology, Ruprecht-Karls-University Heidelberg, Heidelberg, Germany

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R. Barrows

R. Barrows

Department of Neurology, Ruprecht-Karls-University Heidelberg, Heidelberg, Germany

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W. Hacke

W. Hacke

Department of Neurology, Ruprecht-Karls-University Heidelberg, Heidelberg, Germany

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Th. Steiner

Th. Steiner

Department of Neurology, Ruprecht-Karls-University Heidelberg, Heidelberg, Germany

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First published: 07 January 2010
Citations: 1

Conflicts of interest: None.

Abstract

Stroke is potentially preventable through risk factor modification. Over the past decade, there has been considerable interest on microalbuminuria as a risk factor for chronic diseases. The concept of microalbuminuria was originally introduced, about 25 years ago, to clinical practice as a useful marker of nephropathy. Since then various studies reported an association of microalbuminuria with the increased risk of cardiovascular events and all cause of mortality in subjects with or without diabetes. The presence of microalbuminuria was related to left ventricular dysfunction, stroke, and myocardial infarction. Microalbuminuria may be a predictor of stroke but further studies are required. However data on prognostic significance and therapeutic consequence, particularly in haemorrhagic stroke are lacking. This review focuses on the importance of microalbuminuria for cerebrovascular disease, stressing the clinical and therapeutic implications using antihypertensive therapy to control the urinary albumin excretion.

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