(Circulation. 2000;102:1470.)
© 2000 American Heart Association, Inc.
Brief Rapid Communication |
From the Departments of Rheumatology (K.R., A.R.E., C.H., A.F., D.M.C., P.A.B.) and Cardiology (J.T., J.N.T.), University of Birmingham, Birmingham, UK.
Correspondence to Dr K. Raza, Department of Rheumatology, University of Birmingham, Birmingham B15 2TT, UK. E-mail K.Raza{at}bham.ac.uk
BackgroundChronic inflammatory rheumatic disorders are associated with excess cardiovascular mortality. This may result from arteriosclerosis following inflammatory damage to the vessel wall by vasculitis. Our hypothesis that vasculitis results in arteriosclerosis by causing vascular endothelial dysfunction was tested in patients with primary systemic necrotizing vasculitis (SNV).
Methods and ResultsEndothelial function was assessed in cross-sectional and longitudinal studies of patients with primary SNV by measuring flow-mediated, endothelium-dependent brachial artery vasodilatation. These patients exhibited marked endothelial dysfunction compared with controls. Remission induction in patients with active primary SNV restored endothelial function.
ConclusionsEndothelial function is significantly impaired in adults with primary SNV, supporting the hypothesis that premature arteriosclerosis in chronic inflammatory rheumatic disorders results from endothelial dysfunction secondary to vasculitis. Normalization of endothelial function after the treatment of primary SNV suggests that early suppression of disease activity in chronic inflammatory rheumatic disorders may reduce long-term vascular damage. The role of inflammation in atheroma formation is increasingly appreciated; this work raises questions regarding the potential for anti-inflammatory therapy in atherosclerosis itself.
Key Words: inflammation endothelium atherosclerosis
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