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(Circulation. 2003;108:678.)
© 2003 American Heart Association, Inc.
Clinical Investigation and Reports |
From the Department of Epidemiology and Public Health, University College London, London, UK (N.N.C., H.M.C.); the Department of Virology, Royal Free and University College School of Medicine, Royal Free Campus, London, UK (D.A., V.E.); the Department of Medicine, Royal Free and University College Medical School, London, UK (C.G.-C., D.J.B., P.V.); and the Department of Clinical Microbiology, University College London Hospitals, London, UK (G.L.R.).
Correspondence to Dr Patrick Vallance, Centre for Clinical Pharmacology, Department of Medicine, BHF Laboratories, University College London, 5 University St, London, WC1E 6JJ, UK. E-mail Patrick.Vallance{at}ucl.ac.uk
Received September 17, 2002; de novo received March 11, 2003; revision received May 13, 2003; accepted May 14, 2003.
Background Herpesvirus infection is a possible risk factor for atherogenesis, and diabetics may be at particular risk. Endothelial dysfunction is an early marker for atherosclerosis, and the present study tests the hypotheses that (1) prior infection with cytomegalovirus (CMV) and herpes simplex virus (HSV) is associated with endothelial dysfunction and (2) this may be more marked in diabetics.
Methods and Results Serum samples were tested for anti-IgG antibodies to CMV and HSV from 400 subjects (mean age for diabetics and nondiabetics, 37.8±4.3 and 37.9±3.7 [SD]). We also assessed Helicobacter pylori and Chlamydia pneumoniae serology. Coronary atheroma was quantified by means of electron beam computed tomography. Subjects (n=157) underwent venous occlusion plethysmography with acetylcholine, bradykinin, glyceryl trinitrate, norepinephrine, and L-NG-monomethyl-L-arginine. Individuals who were seropositive for CMV had reduced responses to bradykinin (P=0.005) and glyceryl trinitrate (P=0.006). The reduced response to bradykinin remained significant (P=0.045) after adjusting for the response to glyceryl trinitrate and was independent of conventional risk factors. Positive serology for the other organisms did not have an independent effect on reactivity. There was a weaker association between CMV and coronary artery calcification (P=0.09). Positive serology for each of the other pathogens did not affect reactivity, but there was a relation between total pathogen burden and impaired vascular reactivity. No significant differences were found between diabetics and nondiabetics.
Conclusions This study shows that CMV-seropositive individuals have endothelial dysfunction and impaired responses to NO. This association was independent of conventional risk factors and may be associated with increased atherosclerosis burden.
Key Words: atherosclerosis risk factors viruses endothelium
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