Cardiovascular Inflammation Reduction Trial - Inflammation Imaging Study

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.

Inclusion criteria

• Age > 18 years at screening
• Documented MI in the past or past evidence of multivessel coronary artery disease by angiography must have completed any planned coronary revascularization procedures associated with the qualifying event, and must be clinically stable for at least 60 d before screening; the qualifying prior MI must be documented either by hospital records or by evidence on current electrocardiogram of Q waves in 2 contiguous leads and/or an imaging test demonstrating wall motion abnormality or scar; the qualifying documentation of multivessel coronary disease must include angiographic evidence of atherosclerosis in at least 2 major epicardial vessels defined either as the presence of a stent, a coronary bypass graft, or an angiographic lesion of 60% or greater. Left main coronary artery disease that has been revascularized with a stent or bypass graft will qualify as multivessel disease, as will the presence of a 50% or greater isolated left main stenosis.
• History of type 2 diabetes or metabolic syndrome at the time of study enrollment
• Willing to participate as evidence by signing the study informed consent

Exclusion criteria

• Prior history of chronic infectious disease, including tuberculosis, severe fungal disease, or known HIV positive
• Chronic hepatitis B or C infection
• Interstitial pneumonitis, bronchiectasis, or pulmonary fibrosis. Chest x-ray evidence in the past 12 months of interstitial pneumonitis, bronchiectasis, or pulmonary fibrosis.
• Prior history of non basal cell malignancy or myeloproliferative or lymphoproliferative disease within the past 5 years
• White blood cell count <3,500/mm3, hematocrit <32%, or platelet count <75000/mm3
• Liver transaminase levels (AST/ALT) greater than the upper limit of normal or albumin less than the lower limit of normal
• Creatinine clearance (CrCl) <40 mL/min as estimated by the Cockcroft-Gault equation
• History of alcohol abuse or unwillingness to limit alcohol consumption to <4 drinks per week
• Women of child bearing potential, even if currently using contraception, and women intending to breastfeed
• Men who plan to father children during the study period or who are unwilling to use contraception
• Requirement for use of drugs that alter folate metabolism (trimethoprim/sulfamethoxazoyl) or reduce tubular excretion (probenecid) or known allergies to antibiotics making avoidance of trimethoprim impossible
• Current indication for methotrexate therapy
• Chronic use of oral steroid therapy or other immunosuppressive or biologic response modifiers
• Known chronic pericardial effusion, pleural effusion, or ascites
• New York Heart Association class IV congestive heart failure
• Life expectancy of <3 years

The study population for the ancillary study will be the same as the main trial with the following additional exclusion criteria

• Subjects with a history of multiple imaging studies associated with radiation exposure
• Insulin-dependent diabetics
• If subject is Type 2 diabetic, hemoglobin A1c greater than 8% as determined by patient medical record review in the one year prior to the date of consent to this study.
• BMI greater than 37 kg/m2 or weight greater than 350 pounds