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Inflammatory Pathogenesis of Coronary Atherosclerosis in HIV

Primary Purpose

Coronary Artery Disease, Human Immunodeficiency Virus

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Colchicine
Placebo
Sponsored by
Johns Hopkins University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Coronary Artery Disease

Eligibility Criteria

21 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients of either gender who are 21 years of age (no upper age limit), HIV positive and taking stable ART (no change in ART regimen in last 3 months),
  • HIV viral load <100 copies/mL (plasma HIV RNA concentration),
  • Abnormal CEF at baseline (<7ml/min change in CBF during IHE as compared to resting value).

Exclusion Criteria:

  • Patients unable to understand the risks, benefits, and alternatives of participation and give meaningful consent,
  • Patients with contraindications to MRI such as implanted metallic objects (pre-existing cardiac pacemakers, cerebral clips) or indwelling metallic projectiles,
  • History of clinical CAD, including acute coronary syndrome, myocardial infarction or revascularization,
  • Resting ECG with evidence of Q wave myocardial infarction,
  • Pregnant women,
  • Recent history, within the past 3 months, of cocaine or heroin use,
  • Moderate or greater renal impairment (estimated glomerular filtration rate <45ml/min),
  • Moderate-severe hepatic disease (elevation in hepatic transaminases >3x upper limit of normal),
  • Leukopenia (<3000/mm3) or thrombocytopenia (<100,000/mm3),
  • CD4<200 cell/mm3,
  • Chronic inflammatory condition such as lupus or rheumatoid arthritis, ulcerative colitis or Crohn's disease,
  • Requirement for, or intolerance to, colchicine,
  • Women of childbearing potential (even if using oral contraceptive agents) or intention to breastfeed,
  • Chronic, continuous use of oral or IV steroid therapy or other immunosuppressive or biologic response modifiers or anti-inflammatory agents (chronic NSAIDs or acetylsalicylic acid (ASA) >81mg daily),
  • History of chronic pericardial effusion, pleural effusion, ascites or peripheral neuropathy manifested by both signs and symptoms,
  • Taking protease inhibitors (PI), cobicistat, or CYP3A4 inhibitors.

Sites / Locations

  • Johns Hopkins Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Colchicine

Placebo

Arm Description

Colchicine 0.6 mg daily by mouth

Placebo for colchicine 1 tablet by mouth daily

Outcomes

Primary Outcome Measures

Coronary Endothelial Function Measured by Percent Change in Coronary Blood Flow With Exercise (%) at 8 Weeks
Percent change in coronary blood flow (CBF) from rest to that during isometric handgrip exercise (IHE) stress at 8 weeks.

Secondary Outcome Measures

Coronary Endothelial Function at 24 Weeks;
Change in coronary blood flow (CBF) from rest to that during isometric handgrip exercise (IHE) stress at 24 weeks.
Change in Coronary Artery Cross-sectional Area (CSA) at 8 Weeks
Change in CSA as measured by the difference between CSA at rest and under IHE stress at 8 weeks
Change in Coronary Artery Cross-sectional Area (CSA) at 24 Weeks
Change in CSA as measured by the difference between CSA at rest and under IHE stress at 24 weeks
High-sensitivity C-reactive Protein (hsCRP) at 8 Weeks.
High-sensitivity C-reactive protein (hsCRP) at 8 weeks
Brachial Flow Mediated Dilatation (FMD) at 8 Weeks.
Brachial flow mediated dilatation (FMD) at 8 weeks.
Interleukin-6 (IL-6) at 8 Weeks
Interleukin-6 (IL-6) at 8 weeks
High-sensitivity C-reactive Protein (hsCRP) at 24 Weeks
High-sensitivity C-reactive Protein (hsCRP) at 24 weeks
Brachial Flow Mediated Dilatation (FMD) at 24 Weeks.
Brachial Flow Mediated Dilatation (FMD) at 24 Weeks.

Full Information

First Posted
November 11, 2015
Last Updated
September 20, 2021
Sponsor
Johns Hopkins University
Collaborators
National Heart, Lung, and Blood Institute (NHLBI)
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1. Study Identification

Unique Protocol Identification Number
NCT02624180
Brief Title
Inflammatory Pathogenesis of Coronary Atherosclerosis in HIV
Official Title
Inflammatory Pathogenesis of Coronary Atherosclerosis in HIV
Study Type
Interventional

2. Study Status

Record Verification Date
September 2021
Overall Recruitment Status
Completed
Study Start Date
November 2015 (undefined)
Primary Completion Date
August 1, 2020 (Actual)
Study Completion Date
September 1, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Johns Hopkins University
Collaborators
National Heart, Lung, and Blood Institute (NHLBI)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The investigators are studying whether an anti-inflammatory intervention improves impaired coronary endothelial function (CEF) in HIV+ people with no clinical coronary artery disease (CAD).
Detailed Description
Survival in people with HIV has significantly improved with the use of antiretroviral therapy (ART) but HIV+ people now experience an increasing burden of chronic diseases, including coronary atherosclerosis and coronary artery disease (CAD). HIV patients manifest an increased risk of CAD and its consequences possibly due to interplay of inflammation with traditional risk factors (smoking, high cholesterol, and poor diet), some of the latter accentuated by ART. What the investigators are studying in this program is the function of the coronary arteries and in particular the inner lining of the arteries called the endothelium in patients with HIV. The endothelium has several important functions; one of them is that under conditions of stress it releases a substance called nitric oxide which increases the size of the artery and increases blood flow. When it is not functioning normally the artery does not increase as much and blood flow does not increase during stress. The investigators study coronary artery function with magnetic resonance imaging, or MRI. MRI is a method of obtaining images of what is happening inside the body. MRI does not involve radiation, x-ray, or injection of contrast. The investigators can measure flow in the artery and the dimension of the artery at rest and with a handgrip stress and learn the extent to which the artery dilates and flow increases with the stress. The investigators believe that inflammation can interfere with normal function and that by decreasing inflammation abnormal endothelial function may be improved. Colchicine is an anti-inflammatory agent approved by the Food and Drug Administration (FDA) to treat arthritis and some other conditions. This drug is not approved for use to suppress inflammation in patients with coronary artery disease and improve coronary artery endothelial function. The FDA is allowing the use of colchicine or a placebo in this research study. This study will involve 24 weeks of colchicine or placebo and 3 Magnetic Resonance Imaging (MRI) scans of the heart and other study procedures.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Coronary Artery Disease, Human Immunodeficiency Virus

7. Study Design

Primary Purpose
Other
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
81 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Colchicine
Arm Type
Experimental
Arm Description
Colchicine 0.6 mg daily by mouth
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo for colchicine 1 tablet by mouth daily
Intervention Type
Drug
Intervention Name(s)
Colchicine
Other Intervention Name(s)
Colcrys
Intervention Description
Administered to determine the effect of anti-inflammatory agents on coronary and systemic endothelial function in patients with coronary artery disease.
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
A substance containing no medication
Primary Outcome Measure Information:
Title
Coronary Endothelial Function Measured by Percent Change in Coronary Blood Flow With Exercise (%) at 8 Weeks
Description
Percent change in coronary blood flow (CBF) from rest to that during isometric handgrip exercise (IHE) stress at 8 weeks.
Time Frame
Difference between measurements at baseline compared to measurement at 8 weeks
Secondary Outcome Measure Information:
Title
Coronary Endothelial Function at 24 Weeks;
Description
Change in coronary blood flow (CBF) from rest to that during isometric handgrip exercise (IHE) stress at 24 weeks.
Time Frame
At 24 weeks.
Title
Change in Coronary Artery Cross-sectional Area (CSA) at 8 Weeks
Description
Change in CSA as measured by the difference between CSA at rest and under IHE stress at 8 weeks
Time Frame
Difference between measurements at baseline compared to measurement at 8 weeks
Title
Change in Coronary Artery Cross-sectional Area (CSA) at 24 Weeks
Description
Change in CSA as measured by the difference between CSA at rest and under IHE stress at 24 weeks
Time Frame
At 24 weeks
Title
High-sensitivity C-reactive Protein (hsCRP) at 8 Weeks.
Description
High-sensitivity C-reactive protein (hsCRP) at 8 weeks
Time Frame
At 8 weeks.
Title
Brachial Flow Mediated Dilatation (FMD) at 8 Weeks.
Description
Brachial flow mediated dilatation (FMD) at 8 weeks.
Time Frame
At 8 weeks
Title
Interleukin-6 (IL-6) at 8 Weeks
Description
Interleukin-6 (IL-6) at 8 weeks
Time Frame
At 8 weeks
Title
High-sensitivity C-reactive Protein (hsCRP) at 24 Weeks
Description
High-sensitivity C-reactive Protein (hsCRP) at 24 weeks
Time Frame
At 24 weeks
Title
Brachial Flow Mediated Dilatation (FMD) at 24 Weeks.
Description
Brachial Flow Mediated Dilatation (FMD) at 24 Weeks.
Time Frame
At 24 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients of either gender who are 21 years of age (no upper age limit), HIV positive and taking stable ART (no change in ART regimen in last 3 months), HIV viral load <100 copies/mL (plasma HIV RNA concentration), Abnormal CEF at baseline (<7ml/min change in CBF during IHE as compared to resting value). Exclusion Criteria: Patients unable to understand the risks, benefits, and alternatives of participation and give meaningful consent, Patients with contraindications to MRI such as implanted metallic objects (pre-existing cardiac pacemakers, cerebral clips) or indwelling metallic projectiles, History of clinical CAD, including acute coronary syndrome, myocardial infarction or revascularization, Resting ECG with evidence of Q wave myocardial infarction, Pregnant women, Recent history, within the past 3 months, of cocaine or heroin use, Moderate or greater renal impairment (estimated glomerular filtration rate <45ml/min), Moderate-severe hepatic disease (elevation in hepatic transaminases >3x upper limit of normal), Leukopenia (<3000/mm3) or thrombocytopenia (<100,000/mm3), CD4<200 cell/mm3, Chronic inflammatory condition such as lupus or rheumatoid arthritis, ulcerative colitis or Crohn's disease, Requirement for, or intolerance to, colchicine, Women of childbearing potential (even if using oral contraceptive agents) or intention to breastfeed, Chronic, continuous use of oral or IV steroid therapy or other immunosuppressive or biologic response modifiers or anti-inflammatory agents (chronic NSAIDs or acetylsalicylic acid (ASA) >81mg daily), History of chronic pericardial effusion, pleural effusion, ascites or peripheral neuropathy manifested by both signs and symptoms, Taking protease inhibitors (PI), cobicistat, or CYP3A4 inhibitors.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Robert G Weiss, MD
Organizational Affiliation
Johns Hopkins University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Johns Hopkins Hospital
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21287
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
17353456
Citation
Deanfield JE, Halcox JP, Rabelink TJ. Endothelial function and dysfunction: testing and clinical relevance. Circulation. 2007 Mar 13;115(10):1285-95. doi: 10.1161/CIRCULATIONAHA.106.652859. No abstract available.
Results Reference
background
PubMed Identifier
14522472
Citation
Widlansky ME, Gokce N, Keaney JF Jr, Vita JA. The clinical implications of endothelial dysfunction. J Am Coll Cardiol. 2003 Oct 1;42(7):1149-60. doi: 10.1016/s0735-1097(03)00994-x.
Results Reference
background
PubMed Identifier
21050976
Citation
Hays AG, Hirsch GA, Kelle S, Gerstenblith G, Weiss RG, Stuber M. Noninvasive visualization of coronary artery endothelial function in healthy subjects and in patients with coronary artery disease. J Am Coll Cardiol. 2010 Nov 9;56(20):1657-65. doi: 10.1016/j.jacc.2010.06.036.
Results Reference
background
PubMed Identifier
23536782
Citation
Hays AG, Stuber M, Hirsch GA, Yu J, Schar M, Weiss RG, Gerstenblith G, Kelle S. Non-invasive detection of coronary endothelial response to sequential handgrip exercise in coronary artery disease patients and healthy adults. PLoS One. 2013;8(3):e58047. doi: 10.1371/journal.pone.0058047. Epub 2013 Mar 11.
Results Reference
background
PubMed Identifier
22492483
Citation
Hays AG, Kelle S, Hirsch GA, Soleimanifard S, Yu J, Agarwal HK, Gerstenblith G, Schar M, Stuber M, Weiss RG. Regional coronary endothelial function is closely related to local early coronary atherosclerosis in patients with mild coronary artery disease: pilot study. Circ Cardiovasc Imaging. 2012 May 1;5(3):341-8. doi: 10.1161/CIRCIMAGING.111.969691. Epub 2012 Apr 5.
Results Reference
background
PubMed Identifier
23265346
Citation
Nidorf SM, Eikelboom JW, Budgeon CA, Thompson PL. Low-dose colchicine for secondary prevention of cardiovascular disease. J Am Coll Cardiol. 2013 Jan 29;61(4):404-410. doi: 10.1016/j.jacc.2012.10.027. Epub 2012 Dec 19.
Results Reference
background
PubMed Identifier
6426817
Citation
Brown BG, Lee AB, Bolson EL, Dodge HT. Reflex constriction of significant coronary stenosis as a mechanism contributing to ischemic left ventricular dysfunction during isometric exercise. Circulation. 1984 Jul;70(1):18-24. doi: 10.1161/01.cir.70.1.18.
Results Reference
background
PubMed Identifier
33587443
Citation
Hays AG, Schar M, Barditch-Crovo P, Bagchi S, Bonanno G, Meyer J, Afework Y, Streeb V, Stradley S, Kelly S, Anders NM, Margolick JB, Lai S, Gerstenblith G, Weiss RG. A randomized, placebo-controlled, double-blinded clinical trial of colchicine to improve vascular health in people living with HIV. AIDS. 2021 Jun 1;35(7):1041-1050. doi: 10.1097/QAD.0000000000002845.
Results Reference
derived

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Inflammatory Pathogenesis of Coronary Atherosclerosis in HIV

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