An interventional study of extended release niacin in HIV Infections, Dyslipidemia and Endothelial Dysfunction, sponsored by University of Hawaii. Completed at 1 site in United States. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2012-12-18.
Sponsored by University of Hawaii · Not applicable, Interventional, and Treatment
This study is a pilot study examining the effect of extended-release niacin (Niaspan ®) on flow-mediated vasodilation (FMD) of the brachial artery, among human immunodeficiency virus (HIV)-1 infected individuals with low high density lipoprotein (HDL). Brachial artery diameter will be measured by high-resolution ultrasound at entry and week 12 of study. The primary comparisons will be change in FMD from baseline to 12 weeks within each of the two arms. The second specific aim will be to investigate the proportion of the effect of extended-release niacin on other known cardiovascular markers.
Low high density lipoprotein (HDL) and a lipid pattern consistent with atherogenic dyslipidemia are also common in the human immunodeficiency virus (HIV)infected population and is likely due, in large part, to the chronic inflammatory effect of HIV infection per se. While highly active antiretroviral therapy (HAART) and the resultant reconstitution of the immune system might be expected to lead to improvement in this lipid profile, studies from our own research as well as others clearly demonstrate that such therapy fails to fully correct the low HDL pattern. This coronary artery disease (CAD) risk in the HIV population is then further compounded by the dyslipidemic effects of various protease inhibitors and other antiretroviral medications used to treat HIV.
Endothelial dysfunction is an early marker of atherosclerosis that can be determined non-invasively utilizing assessment of flow-mediated vasodilation (FMD) of the brachial artery, which may be analogous to blood flow through coronary arteries. Using this novel technology and HIV as a model of a chronic inflammatory state, we propose to determine if increasing HDL in subjects with low HDL but no LDL elevation may have potential beneficial effects. Our overall hypothesis for this pilot project is that increasing HDL levels in HIV-infected subjects with low HDL by the use of extended-release niacin over a 12 week period will lead to an identifiable improvement in endothelial function.
Specific Aim 1. To compare endothelial function, measured by flow-mediated vasodilation (FMD) of the brachial artery, among HIV-1 infected individuals with low high density lipoprotein (HDL) before and after treatment with extended-release niacin (Niaspan ®)
Hypothesis to be tested:
Use of extended-release niacin will improve FMD among HIV-1 infected individuals with low HDL
Specific Aim 2. To evaluate changes in lipid parameters, insulin sensitivity and cardiovascular risk markers with changes in FMD among the treatment and control arms
Hypothesis to be tested:
There will be a correlation between improvements in lipid, insulin sensitivity and cardiovascular risk markers and FMD in the extended niacin treatment arm
SIGNIFICANCE and RATIONALE: Low HDL cholesterol levels elevate CAD risk independent of low density lipoprotein (LDL) cholesterol levels. In association with high triglyceride levels and with small LDL particle size, low HDL is part of the syndrome of atherogenic dyslipidemia. This form of dyslipidemia is characteristic of the underlying dyslipidemia found in HIV-infected subjects, likely represents the consequences of chronic inflammatory changes due to HIV, and contributes substantively to the CAD risk in this population even without the added risk from dyslipidemic antiretroviral medications. Primary CAD preventive modalities may be warranted for patients in the HIV population as well as in the general population who manifest this type of dyslipidemia. Niacin is currently the best medication available to elevate HDL cholesterol levels. Thus, using the novel technique of assessing flow-mediated dilatation of the brachial artery, a pilot project is proposed to assess whether the use of extended release niacin will lead to short term improvement in endothelial function. If successful, this study may lay the foundation for further studies into the potential use of niacin for prevention of CAD in patients who are particularly at risk for CAD due to low HDL cholesterol levels.
1,073 studies on the registry are indexed under Dyslipidemias; 158 are open to participants now.
This study's enrollment of 20 is below the median of 99 across 842 interventional studies indexed under Dyslipidemias.
Browse Dyslipidemias studies →University of Hawaii is the lead sponsor of 95 studies on the registry; 20 are open to participants now.
Of its 7 completed or terminated interventional studies of FDA-regulated products, 3 (43%) have results posted.
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Exclusion Criteria:
Subjects in this arm will be given 12 weeks of extended release niacin. Intervention: extended release niacin (Niaspan) starting at 500 mg by mouth daily and titrated to a maximum dose of 1500 mg by mouth daily. Titration will depend on patient tolerability.
Drug: extended release niacin
Subjects in this arm will be monitored for 12 weeks and will not receive extended release niacin
Active arm subjects will start extended release niacin (Niaspan) at 500 mg per night (by mouth once a daily) and titrate to a maximum tolerated dose (not exceeding 1500 mg per night (by mouth once a day) for 12 weeks. Titration will depend on patient tolerability of Niaspan.
Also known as: Niaspan
Change in Flow-mediated Vasodilation (FMD) From Baseline to Study Week 12
Brachial arterial flow-mediated dilation (FMD), assessed by high-resolution ultrasonography, reflects endothelium-dependent vasodilator function. The primary outcome is the change in FMD from baseline to study week 12.
Time frame: Two time points (baseline and study week 12)
Flow Mediated Vasodilation
Flow mediated vasodilation is a marker of endothelial function
Time frame: 12 weeks
High-density Lipoprotein Cholesterol (HDL) Change From Baseline to Study Week 12
HDL, often referred to "Good cholesterol levels", will be obtained in both arms. HDL is a marker of coronary heart disease.
Time frame: Two time points (baseline and study week 12)
HDL
Time frame: 12 weeks
Recruitment was through the University of Hawaii, Hawaii Center for AIDS
| Milestone | Active Drug (Extended Release Niacin) | Observation |
|---|---|---|
| Started | 10 | 10 |
| Completed | 10 | 9 |
| Not completed | 0 | 1 |
| Withdrew: Lost to follow-up | 0 | 1 |
Brachial arterial flow-mediated dilation (FMD), assessed by high-resolution ultrasonography, reflects endothelium-dependent vasodilator function. The primary outcome is the change in FMD from baseline to study week 12.
| percentage change in FMD | Extended Release Niacin | Observation |
|---|---|---|
| Change in Flow-mediated Vasodilation (FMD) From Baseline to Study Week 12 | 6.36 (4.85 to 7.87) | 2.73 (0.95 to 4.51) |
HDL, often referred to "Good cholesterol levels", will be obtained in both arms. HDL is a marker of coronary heart disease.
| mg/dl | Active Drug (Extended Release Niacin) | Observation |
|---|---|---|
| High-density Lipoprotein Cholesterol (HDL) Change From Baseline to Study Week 12 | 42.0 (39.3 to 43.5) | 27.0 (24.0 to 39.0) |
Flow mediated vasodilation is a marker of endothelial function
| percentage change in FMD | Active Drug (Extended Release Niacin) | Observation |
|---|---|---|
| Flow Mediated Vasodilation | 4.51 (4.46 to 8.32) | 3.25 (1.95 to 4.85) |
Results for this outcome have not been posted.
Collected over 2 years. Non-serious events are listed at a 5% frequency threshold.
| Group | Deaths | Serious | Other |
|---|---|---|---|
| Active Drug (Extended Release Niacin) | — | 0/10 (0%) | 0/10 (0%) |
| Observation | — | 0/10 (0%) | 0/10 (0%) |
| Age, Categorical(Participants) | Active Drug (Extended Release Niacin) | Observation | Total |
|---|---|---|---|
| <=18 years | 0 | 0 | 0 |
| Between 18 and 65 years | 10 | 10 | 20 |
| >=65 years | 0 | 0 | 0 |
| Age Continuous(years) | Active Drug (Extended Release Niacin) | Observation | Total |
|---|---|---|---|
| Mean | 49.96 ± 11.60 | 47.72 ± 10.81 | 48.84 ± 10.94 |
| Sex: Female, Male(Participants) | Active Drug (Extended Release Niacin) | Observation | Total |
|---|---|---|---|
| Female | 0 | 2 | 2 |
| Male | 10 | 8 | 18 |
| Region of Enrollment(participants) | Active Drug (Extended Release Niacin) | Observation | Total |
|---|---|---|---|
| United States | 10 | 10 | 20 |
This study is completed, as verified in Jul 2012. You cannot join it, but the record below documents what was studied.
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University of Hawaii