Ferumoxytol-enhanced Imaging and Mapping in neuroAIDS



Status:Completed
Conditions:Neurology
Therapuetic Areas:Neurology
Healthy:No
Age Range:40 - 65
Updated:10/29/2017
Start Date:February 2015
End Date:September 2017

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Ferumoxytol-enhanced Imaging and Quantitative Susceptibility Mapping in neuroAIDS

This project will investigate the ability of a novel MRI contrast agent to identify and
quantitate ongoing monocyte/macrophage (M/MΦ)-mediated inflammation in the brains of
HIV-infected individuals.

HIV-associated neurocognitive disorders (HAND) continue to be prevalent despite effective
combination antiretroviral therapy (cART) and have a significant impact on morbidity and
quality of life. Monocytes/macrophages (M/MΦ) are believed to play a critical role in the
pathogenesis of HAND. Neuroimaging HIV research has not focused on assessing M/MΦ-mediated
inflammation in the brain. Currently, no neuroimaging modality exists that can define the
extent of active inflammation due to M/MΦ in HAND either as a clinical diagnostic tool or to
assist in defining objective improvement in clinical trials addressing HAND. Ferumoxytol is
an ultra-small iron oxide MRI contrast agent avidly taken up by circulating M/MΦ. The
investigators hypothesize that ferumoxytol-based imaging can identify ongoing inflammation
due to perivascular M/MΦ which is believed to represent a key pathologic correlate of HAND.

Inclusion Criteria:

- Age 40-65 years

- Plasma HIV RNA < 48 copies/ml (HIV+ subjects only)

- On stable cART >= 1 year (HIV+ subjects only)

- Global neuropsychological (NP) score <-0.5 in at least one cognitive domain known to
be affected by HIV (neurocognitively impaired subjects only)

- Documentation of negative HIV infection by an FDA approved test (HIV- subjects only)

Exclusion Criteria:

- Active substance use

- History of myocardial infarct or stroke

- Diabetes

- Chronic hepatitis C virus (HCV) infection

- Uncontrolled major affective disorder, active psychosis, central nervous system
disease that affects the brain structure, or other uncontrolled chronic medical
condition that in the opinion of the investigator may impact NP testing or the study
outcome

- Psychoactive or other medications which may impact NP testing

- Factors that preclude MRI

- Known hypersensitivity to ferumoxytol

- History of laboratory measurements consistent with an iron overload syndrome

- Medical conditions that require frequent blood transfusions

- Taking oral iron supplements

- Elevated iron levels

- Any condition, which in the opinion of the investigator, would compromise the
subject's ability to participate

- Multiple drug allergies that may pose a greater risk of anaphylaxis associated with
ferumoxytol

- Pregnant, unwillingness to practice birth control, or breastfeeding

- Unable to give informed consent
We found this trial at
1
site
Honolulu, Hawaii 96816
Phone: 808-692-1335
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Honolulu, HI
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