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Clinical Trials/NCT02874703
NCT02874703
Completed
Not Applicable

Mechanisms of Diastolic Dysfunction Among Persons With HIV Compared With Non-HIV Control Subjects

Massachusetts General Hospital1 site in 1 country48 target enrollmentAugust 2016

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
HIV
Sponsor
Massachusetts General Hospital
Enrollment
48
Locations
1
Primary Endpoint
Extracellular Volume (ECV), a measure of myocardial fibrosis on Cardiac MRI
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

In this study, investigators plan to test two potential mechanisms contributing to diastolic dysfunction among asymptomatic persons with HIV who are on cART. The first proposed mechanism is that heightened systemic immune activation/inflammation in HIV contributes to myocardial inflammation, which in turn promotes myocardial fibrosis. The second mechanism is that ectopic fat deposition (increased visceral adiposity) in HIV relates to increased intramyocardial lipid content, which in turn contributes to diastolic dysfunction. Both HIV positive and HIV-negative participants will undergo cardiac MRI/ MRS imaging studies for evaluation of myocardial fibrosis, myocardial inflammation, and intramyocardial lipid content. Traditional markers of CVD risk, inflammatory markers/immune, hormonal markers, and markers of myocardial stretch/injury will be assessed in relation to cardiac MRI/MRS outcomes. Additionally, a small subset of participants with HIV will undergo longitudinal evaluations to assess effects of a clinically prescribed hormonal therapy on myocardial structure and function.

Registry
clinicaltrials.gov
Start Date
August 2016
End Date
August 2019
Last Updated
6 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Tomas Neilan, MD

MD

Massachusetts General Hospital

Eligibility Criteria

Inclusion Criteria

  • age ≥40 and ≤75 years
  • documented HIV infection
  • participant report that combination antiretroviral therapy (cART) (any regimen) has been taken stably without \> 4 week interruption for at least 180 days prior to study entry (report of switching regimens in that time frame is permissible)

Exclusion Criteria

  • CD4 \< 100 cell/mm3
  • current active AIDS-defining illness
  • current active or recent (not fully resolved within 30 days prior to study entry) systemic bacterial, fungal, parasitic, or viral infections (except HIV, HBV, human papillomavirus \[HPV\], or HCV)
  • current active cancer
  • clinical ASCVD, as defined by 2013 ACC/AHA guidelines (including previous diagnosis of AMI, ACS, stable or unstable angina, coronary or other arterial revascularization, stroke, TIA, PAD), by subject report
  • clinical diagnosis of HFpEF or HFrEF, by subject report
  • diagnosed DM on antihyperglycemic medication
  • current, active use of immune suppressant medication including oral or intravenous corticosteroid or injectable biologic (oral ASA or NSAID use permitted)
  • eGFR \<45 ml/min/1.73 m2 calculated by CDK-EPI
  • standard contraindications to MRI procedure based on MGH MRI Patient Procedure Screening Form - including history of severe allergy to gadolinium

Outcomes

Primary Outcomes

Extracellular Volume (ECV), a measure of myocardial fibrosis on Cardiac MRI

Time Frame: 3 weeks

Secondary Outcomes

  • Markers of myocardial stretch(3 weeks)
  • Inflammation/ immune markers(3 weeks)
  • Diastolic function on Cardiac MRI(3 weeks)
  • Myocardial Inflammation on Cardiac MRI(3 weeks)
  • Hormonal markers(3 weeks)
  • Intramyocardial fat on Cardiac MRI/MRS(3 weeks)
  • Visceral Adiposity on MRI(3 weeks)

Study Sites (1)

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