Relationship of antihypertensive treatment to plasma markers of vascular inflammation and remodeling in the Comparison of Amlodipine versus Enalapril to Limit Occurrences of Thrombosis study.
Abstract
BACKGROUND
Antihypertensive agents lower the risk of cardiovascular events, but whether they affect pathways important in inflammation
and plaque remodeling in atherosclerosis is uncertain. We assessed whether 2 commonly used antihypertensive agents affected
plasma biomarkers reflecting specific inflammatory and remodeling processes over 2 years in the Comparison of Amlodipine versus
Enalapril to Limit Occurrences of Thrombosis (CAMELOT) study.
METHODS
The study was a randomized controlled trial of 2 antihypertensives (amlodipine and enalapril) compared with placebo in patients
with coronary artery disease and diastolic blood pressure less than 100 mm Hg. In 196 subjects who had baseline and 2-year
intravascular coronary ultrasound examinations, we measured plasma interleukin 18, interleukin 1 receptor antagonist, matrix
metalloproteinase 9, neopterin, and C-reactive protein. Results for both treatment groups were pooled and compared with placebo.
RESULTS
Antihypertensive treatment with either agent significantly lowered diastolic blood pressure (-4.7 vs placebo 1.3 mm Hg, P
= .002) and progression of coronary atheroma (Δ percent atheroma volume 0.6 vs placebo 2.1, P = .031). Antihypertensive therapy
did not affect plasma biomarkers of inflammation or plaque remodeling in the 135 subjects with baseline and 2-year biomarker
samples. Progression in percent atheroma volume was significantly less in subjects taking statins at baseline (-2.5%, P =
.0008).
CONCLUSIONS
In patients with coronary artery disease and well-controlled risk factors, antihypertensive therapy lowered blood pressure
and progression of coronary atherosclerosis but did not affect plasma biomarkers of inflammation and remodeling. Antihypertensives
may decrease atheroma progression by mechanisms other than those reflected by these plasma biomarkers.
Links
Authors
Zamani P, Ganz P, Libby P, Sutradhar SC, Rifai N, Nicholls SJ, Nissen SE, Kinlay S
Institution
Cardiovascular Division, University of California, San Diego, CA, USA.
Source
American heart journal 163:4 2012 Apr pg 735-40MeSH
AmlodipineAntihypertensive Agents
Biological Markers
C-Reactive Protein
Coronary Artery Disease
Coronary Thrombosis
Disease Progression
Enalapril
Humans
Interleukin-18
Matrix Metalloproteinase 9
Neopterin
Receptors, Interleukin-1
Recurrence
Ultrasonography, Interventional
Pub Type(s)
Journal ArticleRandomized Controlled Trial
Language
eng
PubMed ID
22520542
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