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Atherosclerosis and Lipoproteins |
From The University of Washington, Departments of Epidemiology (C.L.C.), Biostatistics (P.H.), and Medicine (Division of Medical Genetics) (K.N., E.C.M., J.L., D.L., E.B., B.R.S., J.R., T.B., C.F., G.P.J.), Seattle, Wash; Puget Sound Veterans Affairs Health Care System (C.M.-G.), Seattle, Wash.
Correspondence to Gail P. Jarvik, MD, PhD, University of Washington Medical Center, Division of Medical Genetics, Box 357720, Seattle, WA 98195-7720. E-mail pair{at}u.washington.edu
Objective Inflammatory markers are associated with vascular disease; however, variation in the acute phase response (APR) has not been evaluated. We evaluated whether the APR magnitude in men with severe carotid artery disease (CAAD) (>80% stenosis) differed from that of men without stenosis (<15% stenosis).
Methods and Results White males with (n=43) and without (n=61) severe CAAD receiving clinical influenza vaccinations were recruited. Their baseline and 24-hour after -vaccination blood samples were assayed for C-reactive protein (CRP), IL-6, and serum amyloid-a (SAA). In vivo APR to vaccination was measurable and varied among subjects. Adjusted for age, smoking, oral hypoglycemics, aspirin, and stain use, the relative 24-hour changes in levels of ln(CRP), ln(IL-6), and ln(SAA) were higher in men with CAAD than in men without, but only the SAA response was significant (P=0.02); the relative SAA response was 1.6 (95% confidence interval, 1.1 to 2.5) times higher in men with than without CAAD. The APR for all markers appeared to be independent of baseline levels.
Conclusions Influenza vaccination results in a mild, but measurable, APR in men with and without CAAD. SAA APR variability may be a predictor of severe vascular disease that is independent of basal SAA level.
Influenza vaccination results in acute phase response (APR) in men with and without severe carotid artery disease. Increased serum amyloid A (SAA) APR predicted severe vascular disease. APR magnitude may be a marker of CAAD.
Key Words: acute phase response inflammation carotid artery disease
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