Atherosclerotic Cardiovascular Disease Clinical Trial
Official title:
Cardiovascular Inflammation Reduction Trial (CIRT) - Inflammation Imaging Study
Vascular inflammation, a central feature of atherosclerosis, participates in the initiation,
perpetuation and instability of plaques. Multiple clinical trials of cholesterol lowering
therapy with statins have demonstrated that reductions in atherosclerotic cardiovascular
disease (CVD) events are associated with reductions in both LDL cholesterol (LDL-C) and the
systemic inflammatory mediator C-reactive protein (CRP). The Cardiovascular Inflammation
Reduction Trial (CIRT) investigates if an anti-inflammatory agent commonly used in rheumatoid
arthritis (low dose methotrexate (LDM)) can reduce CV morbidity and mortality among patients
with a prior myocardial infarction or angiographically demonstrated multivessel coronary
artery disease (GCO#13-1467).
In this ancillary CIRT imaging study, the investigators propose to use this well validated
approach by non-invasive serial FDG-PET/CT imaging in a subset of patients enrolled in the
main CIRT trial to directly visualize vascular inflammation. Once the subjects are enrolled
in the main CIRT trial, baseline imaging will be done and follow up imaging will be done
approximately 8 months after the baseline imaging.
18FDG-PET imaging data will be acquired, analyzed centrally and results incorporated into the
main CIRT database. The investigators hypothesize that LDM treatment will result in a
significant decrease in plaque inflammation as measured by 18-FDG-PET/CT after 8 months as
compared to placebo.
The NHLBI funded (Ridker 5U01HL101422) Cardiovascular Inflammation Reduction Trial (CIRT)
provides a unique opportunity to investigate whether a commonly used anti-inflammatory agent
used in rheumatoid arthritis (low dose methotrexate (LDM)) can reduce CVD morbidity and
mortality among patients with stable coronary artery disease. CIRT, is a randomized,
double-blind, placebo-controlled, multi-center trial among 7,000 men and women with prior
myocardial infarction or angiographically demonstrated multivessel coronary artery disease.
Eligible participants will be randomly allocated over a three to four year period to usual
care plus placebo or usual care plus LDM (average dose of 15-20 mg po/weekly. CIRT proposes
that the reduction in CVD events with methotrexate derives from its effect on vascular
inflammation, thus it is crucial to incorporate a measure of vascular inflammation imaging
for confirmation of the primary mechanism of action underlying CIRT. As such, the direct
evaluation of arterial inflammation would enhance the scientific value of the CIRT trial.
The inclusion of the proposed vascular inflammation imaging substudy has widespread
implications that will allow this imaging modality to serve as a surrogate measure of
disease, and thereby provide an opportunity for stratification in individuals at risk for CVD
and evaluation of other interventions with presumed anti-inflammatory effects.
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