Human Atherosclerotic Plaque Inflammation Imaged Using PDG-PET/CT

National Institutes of Health (NIH)

Status: Completed

Conditions: Insulin Resistance; HIV Infections; Atherosclerosis; HIV/AIDS; Cardiovascular Disease

Study type: Observational

Funder types: NIH

Identifiers

NCT00958815

DK-020579

18FDG (completed)

Details and patient eligibility

About

People with diabetes are at increased risk for atherosclerosis and have high CVD morbidity and mortality rates. Tools for detecting and quantifying atherosclerotic pro/regression in people with diabetes and other CVD risk factors lack sensitivity and specificity for molecular level events that occur during the early stages of atherogenesis. Inflammatory macrophage infiltration in the vessel endothelium is an early, molecular level proatherogenic event. Activated macrophages consume glucose at a high rate. Novel in vivo radiotracer PET/CT techniques have been developed to detect, image and quantify molecular level events like macrophage inflammation and glucose utilization (18FDG) in human vessels. We propose to develop and test this novel technique in the Center for Clinical Imaging Research (CCIR) at WUMS. We propose that HIV-infected people with significant CVD risk profiles are a suitable, unique human model for testing these novel imaging techniques. HIV-infected people taking anti-HIV medications develop insulin resistance, T2DM, dyslipidemia, central adiposity, and hypertension. HIV replicates in macrophages and represents a chronic proinflammatory condition. Recent data indicate that HIV+ CVD risk have greater risk for atherosclerosis and MI than HIV-negative people. To test feasibility, we hypothesize that: a.18FDG-PET/CT imaging will detect more macrophage glucose uptake and inflammation in the carotid and aorta arteries of HIV-infected people with CVD risk than in HIV-negative controls; b. radiotracer PET/CT measures of proatherogenic processes will correlate with carotid intima media thickness; a standard measure of carotid atherosclerotic burden. We propose to obtain pilot data that shows feasibility for a novel analytical approach that will expand capabilities for researchers interested in studying the links between diabetes, inflammation, and CVD in humans.

Enrollment: 14 patients

Sex: All

Ages: 35 to 60 years old

Volunteers: Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria for HIV+ group:

• confirmed HIV+ status
• 35-60 years old
• stable ART for at least the past 4 mos
• CD4 count >200 cells/µL
• HIV RNA <40copies/mL
• fasting glucose=100-126 mg/dL
• 2hr-oGTT glucose=140-200mg/dL
• fasting triglycerides >150mg/dL
• HDL-cholesterol <40mg/dL (men), <50mg/dL (women)
• resting blood pressure>130/85mmHg
• waist circumference >102cm(men), >88cm(women)
• BMI 25-35 kg/m2

For HIV-negative control group:

• Confirmed HIV negative status
• 35-60 years old
• fasting glucose<100mg/dL,
• 2hr-oGTT glucose<140mg/dL
• fasting triglycerides<150mg/dL
• HDL-cholesterol >40mg/dL (men), >50mg/dL(women)
• normal BP (<130/85mmHg)
• no central adiposity (waist circ.<102cm(men), <88cm(women)
• BMI (25-35 kg/m2)

Exclusion Criteria for both groups:

• history of heart disease, MI, stroke, transient ischemic attack, kidney or liver disease (active hepatitis B or C), dementia
• statins, fibrates, TZDs, antihypertensives, low dose aspirin, or other prescribed/over-the-counter agents with anti-inflammatory properties
• cocaine and methamphetamine users
• serum creatinine >1.5 mg/dL
• pregnant women
• cognitive impairment that limits ability to provide voluntary informed consent

Trial design

14 participants in 2 patient groups

HIV-seronegative with no CVD risk factors

Description:

Healthy, 35-60 yr old HIV-seronegative men and women with no CVD risk factors (normal fasting glucose tolerance, normal fasting lipid/lipoprotein levels, normotensive, waist circumference \<102cm (men) and \<88cm (women).

HIV+ with CVD risk factors

Description:

35-60 yr old HIV-infected men and women with insulin resistance, dyslipidemia, hypertension, and central adiposity.