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Effects of Niacin on Good Cholesterol in People With Peripheral Arterial Disease

The Effects of Chronic High-density Lipoprotein (HDL) Elevation With Extended Release Niacin on Peripheral Arterial Disease

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01391377
Enrollment
7
Registered
2011-07-12
Start date
2011-07-31
Completion date
2014-12-31
Last updated
2013-02-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Peripheral Arterial Disease

Keywords

HDL, High density Lipoprotein, Peripheral arterial disease, Tredaptive, Niacin, Laropiprant, Plaque, Atherosclerosis, Lipid content

Brief summary

Atherosclerosis is a disorder in the body that is characterized by cholesterol plaque formation in various arteries, causing narrowing of the artery and a limitation in blood flow. Depending on which artery the plaque is in, different clinical conditions occur. In adults common areas include in the heart arteries, in the neck arteries and in the aorta and lower leg arteries. When it affects the lower limbs it is known as peripheral arterial disease - PAD. The main symptom of PAD is called claudication and is described as pain or discomfort in the legs when walking. The aim of PAD treatment is to improve walking distance and quality of life in those with intermittent claudication, and to decrease long term complications including illness and death. An important controlling factor of these cholesterol plaques is a type of cholesterol called HDL (High density lipoprotein). This study aims to look at the effect that raising HDL for a prolonged period has on blood markers of inflammation and on the cholesterol plaque composition in patients with PAD. This investigation will also have relevance to the effects of HDL elevation on plaque composition and inflammation in other areas of the body including the heart, neck and brain arteries. Twenty (20) PAD patients with will be recruited into the study. The investigators anticipate recruitment of all 20 patients within 12 months. The 20 PAD patients all must have significant leg pains when walking, and after review by a doctor, be determined to have narrowings in the leg artery that they will plan to operate on. Patients will be randomized to either niacin (Tredaptive, 1g/day) or matching placebo for 8 weeks (prior to operation) After the 8 week period they will then go on to receive the normal interventional treatment as planned. Blood samples will be taken at enrollment and at the 8 week mark prior to surgery. The plaque that is removed at the time of operation will also be sent to the lab for analysis. The investigators hope to show with this study that by raising the levels of HDL with extended release niacin, there are positive effects on the amount of cholesterol in the plaque, and on the markers in the blood of inflammation and thrombosis. The hypothesis is that elevation of HDL with Niacin will have anti-atherosclerotic actions including: Lower plaque lipid content, Reduced plaque macrophage infiltration, Reduced monocyte activation, Reduced neutrophil adhesion, Inhibition of inflammation and Inhibition of thrombotic markers.

Interventions

DRUGNiacin/Laropiprant combination

Niacin 1g / Laropiprant 20mg for 4 weeks followed by Niacin 2g / Laropiprant 20mg for 4 weeks

DRUGSugar pill

Placebo

Sponsors

National Health and Medical Research Council, Australia
CollaboratorOTHER
Bayside Health
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
40 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* age \>40 years * ankle-brachial index (ABI) of \<0.9 at rest in at least one leg, * symptom limiting intermittent claudication (unilateral or bilateral) and stable for the previous 6 months, * superficial femoral artery disease amenable to percutaneous revascularisation, * serum HDL \<1.0 mmol/l * a stable medication regime for at least 6 months

Exclusion criteria

* acute myocardial infarction or presentation with angina within 1 month of enrolment, * serum creatinine \>0.2mmol/l, * significant co-morbidity with expected survival \<6 months, * current niacin or fibrate therapy * unable to give informed consent

Design outcomes

Primary

MeasureTime frameDescription
Plaque composition8 weeks after recruitment.After femoral arthrectomy the excised plaque will analysed for histological studies, for lipid content, immunohistochemistry, macrophage content and size and VCAM-1 staining.

Secondary

MeasureTime frameDescription
Platelet Aggregation Assays8 weeks after recruitment
Plasma Thrombotic Markers8 weeks after recruitment
Size distribution and composition of HDL8 weeks after recruitment
Plasma Neutrophil Adhesion to Immobilized Fibrinogen8 weeks after recruitment
Plasma Monocyte Activation8 weeks after recruitmentCd11b expression on peripheral blood monocytes will be measured as a marker of monocyte activation.
Plasma lipid parameters and inflammatory markers8 weeks after recruitmentLipid levels including total cholesterol, HDL, LDL and TGs, will be measured as well as ApoA1 protien and Plasma soluble ICAM-1 and soluble VCAM-1. TNF-A levels will also be measured and CRP.
Ex vivo cholesterol efflux8 weeks after recruitment

Countries

Australia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026