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CompletedNCT00986986Updated Dec 18, 2012Results posted

Study of Niacin on Endothelial Function in HIV-infected Subjects With Low High Density Lipoprotein Cholesterol Levels

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

Phase
Not applicable
Study type
Interventional
Enrollment
20
Allocation
Randomized
Ages
18 Years and older
Sex
All
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Study summary

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.

Read the detailed description

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 ®)

  • Conduct a prospective randomized 12-week clinical trial on HIV-1 infected individuals with low HDL and normal low density lipoprotein levels who plan to continue their current anti-retroviral regimens
  • Subjects will be randomized to either a treatment or control arm
  • Subjects randomized to the treatment arm will receive extended-release niacin (Niaspan ®) starting at 500 mg per night and titrated to a maximum tolerated dose (not exceeding 1500 mg per night)
  • Assess changes in FMD of the brachial artery using high-resolution ultrasound from baseline to week 12 (Total of 2 FMD assessments)
  • Correlate changes in HDL with changes in FMD

Hypothesis to be tested:

Use of extended-release niacin will improve FMD among HIV-1 infected individuals with low HDL

  • Following 12 weeks of therapy, subjects treated with extended-release niacin will show a 8% improvement in FMD compared to controls
  • There will be a positive correlation between changes in HDL with changes in FMD

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

  • Assess and compare changes in non-HDL lipid and lipoprotein parameters with changes in FMD among the two arms
  • Assess and compare changes in insulin sensitivity by homeostasis model assessment (HOMA) with changes in FMD among the two arms
  • Assess and compare changes in cardiovascular risk markers such as adhesion molecules and C-reactive protein with changes in FMD among the two 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.

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Conditions studied

  • HIV Infections
  • Dyslipidemia
  • Endothelial Dysfunction

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Keywords

  • Human immunodeficiency virus
  • Low high density lipoprotein
  • Endothelial function
  • Flow-mediated vasodilation
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In context

Dyslipidemias

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 →

Lead sponsor

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.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Age ≥18 years
  • Documented HIV infection
  • Subjects must have taken HAART 6 months prior to study entry and must be on stable HAART (no dose change to antiretroviral medications) for at least 30 days immediately prior to study entry
  • HDL \< 40 mg/dL • LDL \< 130 mg/dL
  • All subjects with reproductive potential should utilize adequate contraception for the duration of this study and for at least 12 weeks following permanent discontinuation of study treatment. Acceptable methods include male condom, female condom, diaphragm, or intra-uterine device (IUD)

Exclusion criteria

Exclusion Criteria:

  • Known cardiac disease
  • Arrhythmia
  • History of angina
  • Uncontrolled hypertension
  • Pregnancy
  • Breast-feeding
  • Medication known to influence vasodilatation such as nitrates, metformin, pioglitazone, and rosiglitazone
  • Heavy use of vitamin supplements
  • Diagnosis of diabetes mellitus
  • Treatment with lipid-lowering drugs within 6 weeks prior to study
  • Hemoglobin \<9.0 mg/dL
  • Absolute neutrophil count \<750 cells/mm3
  • Platelet count \<75,000 platelets/ mm3
  • Alanine aminotransferase (ALT or SGOT)/ aspartate aminotransferase (AST or SGPT) / alkaline phosphatase > 2.5 x upper limit of normal (ULN)
  • Creatinine >1.5 x ULN
  • Individuals with an infection or other medical illness requiring hospitalization within 14 days prior to study entry
  • Individuals who have active alcohol or drug abuse which, in the investigator's opinion, is sufficient to prevent adequate compliance with study therapy and evaluations
  • Prior history of hypersensitivity reaction to niacin or any other component of the study drug
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Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
20 participants (actual)

Study arms

  • Experimental
    Active Drug (extended release niacin)

    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

  • No intervention
    Observation

    Subjects in this arm will be monitored for 12 weeks and will not receive extended release niacin

Interventions

  • Drugextended 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

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What researchers measure

Primary outcomes

  1. 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)

  2. Flow Mediated Vasodilation

    Flow mediated vasodilation is a marker of endothelial function

    Time frame: 12 weeks

Secondary outcomes

  1. 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)

  2. HDL

    Time frame: 12 weeks

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Results

Posted Dec 18, 2012
Limitations and caveats
* Small sample size * Un-blinded pilot study * Increase in HDL was less than predicted in a non-HIV infected population

Participant flow

Recruitment was through the University of Hawaii, Hawaii Center for AIDS

Participant flow — Overall Study
MilestoneActive Drug (Extended Release Niacin)Observation
Started1010
Completed109
Not completed01
Withdrew: Lost to follow-up01

Outcome measures

PrimaryChange 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)
Reported as:
Median · percentage change in FMD
Change in Flow-mediated Vasodilation (FMD) From Baseline to Study Week 12
percentage change in FMDExtended Release NiacinObservation
Change in Flow-mediated Vasodilation (FMD) From Baseline to Study Week 126.36 (4.85 to 7.87)2.73 (0.95 to 4.51)
SecondaryHigh-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)
Reported as:
Median · mg/dl
High-density Lipoprotein Cholesterol (HDL) Change From Baseline to Study Week 12
mg/dlActive Drug (Extended Release Niacin)Observation
High-density Lipoprotein Cholesterol (HDL) Change From Baseline to Study Week 1242.0 (39.3 to 43.5)27.0 (24.0 to 39.0)
PrimaryFlow Mediated Vasodilation

Flow mediated vasodilation is a marker of endothelial function

Time frame:
12 weeks
Reported as:
Median · percentage change in FMD
Flow Mediated Vasodilation
percentage change in FMDActive Drug (Extended Release Niacin)Observation
Flow Mediated Vasodilation4.51 (4.46 to 8.32)3.25 (1.95 to 4.85)
SecondaryHDL
Time frame:
12 weeks

Results for this outcome have not been posted.

Adverse events

Collected over 2 years. Non-serious events are listed at a 5% frequency threshold.

Adverse event summary by group
GroupDeathsSeriousOther
Active Drug (Extended Release Niacin)—0/10 (0%)0/10 (0%)
Observation—0/10 (0%)0/10 (0%)

Baseline characteristics

Age, Categorical
Age, Categorical(Participants)Active Drug (Extended Release Niacin)ObservationTotal
<=18 years000
Between 18 and 65 years101020
>=65 years000
Age Continuous
Age Continuous(years)Active Drug (Extended Release Niacin)ObservationTotal
Mean49.96 ± 11.6047.72 ± 10.8148.84 ± 10.94
Sex: Female, Male
Sex: Female, Male(Participants)Active Drug (Extended Release Niacin)ObservationTotal
Female022
Male10818
Region of Enrollment
Region of Enrollment(participants)Active Drug (Extended Release Niacin)ObservationTotal
United States101020
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Study locations

1 site
  • University of Hawaii - Hawaii Center for AIDS
    Honolulu, Hawaii 96816, United States
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References and documents

Publications

  • Chow DC, Stein JH, Seto TB, Mitchell C, Sriratanaviriyakul N, Grandinetti A, Gerschenson M, Shiramizu B, Souza S, Shikuma C. Short-term effects of extended-release niacin on endothelial function in HIV-infected patients on stable antiretroviral therapy. AIDS. 2010 Apr 24;24(7):1019-23. doi: 10.1097/QAD.0b013e3283383016. PubMed 20216298 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 18, 2012, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT00986986
Lead sponsor
University of Hawaii
Collaborators
United States Department of Defense
Responsible party
Dominic Chow (Associate Professor of Medicine and Pediatrics, University of Hawaii) — Principal investigator
First posted
Sep 30, 2009
Start date
Nov 2007
Primary completion
Apr 2010
Completion
Apr 2010
Results posted
Dec 18, 2012
Last update
Dec 18, 2012

Study contacts

Dominic C Chow, MD
principal investigator · University of Hawaii - Hawaii Center for AIDS

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

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