Human Atherosclerotic Plaque Inflammation Imaged Using PDG-PET/CT

NCT ID: NCT00958815

Last Updated: 2012-06-26

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

14 participants

Study Classification

OBSERVATIONAL

Study Start Date

2009-03-31

Study Completion Date

2010-03-31

Brief Summary

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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.

Detailed Description

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Conditions

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Insulin Resistance Atherosclerosis Cardiovascular Disease HIV/AIDS HIV Infections

Study Design

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Observational Model Type

COHORT

Study Time Perspective

CROSS_SECTIONAL

Study Groups

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HIV-seronegative with no CVD risk factors

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).

No interventions assigned to this group

HIV+ with CVD risk factors

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

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* 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

* 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
Minimum Eligible Age

35 Years

Maximum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

NIH

Sponsor Role lead

Responsible Party

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Kevin Yarasheski

Professor of Medicine, Cell Biology & Physiology, Physical Therapy

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Kevin E Yarasheski, PhD

Role: PRINCIPAL_INVESTIGATOR

Washington University School of Medicine

Locations

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Washington University School of Medicine

St Louis, Missouri, United States

Site Status

Countries

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United States

References

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Yarasheski KE, Laciny E, Overton ET, Reeds DN, Harrod M, Baldwin S, Davila-Roman VG. 18FDG PET-CT imaging detects arterial inflammation and early atherosclerosis in HIV-infected adults with cardiovascular disease risk factors. J Inflamm (Lond). 2012 Jun 22;9(1):26. doi: 10.1186/1476-9255-9-26.

Reference Type RESULT
PMID: 22726233 (View on PubMed)

Related Links

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Other Identifiers

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DK-020579

Identifier Type: -

Identifier Source: secondary_id

18FDG (completed)

Identifier Type: -

Identifier Source: org_study_id

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