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Published on: November 10, 2017
Niacin improves lipid profile but not endothelial function in patients with coronary artery disease on high dose
Andrew C Philpott1, Jaroslav Hubacek, Yichun C Sun
1Department of Cardiology, Lyell McEwin Hospital, Elizabeth Vale, Adelaide, South Australia 5000, Australia. aphilp02@gmail.com
Insights
Extended-release niacin improved lipid profiles in coronary artery disease patients on statins but did not enhance endothelial or microvascular function. This study evaluated niacin
Area of Science:
- Cardiovascular Medicine
- Pharmacology
- Vascular Biology
Background:
- Endothelial dysfunction is prevalent in coronary artery disease (CAD) and impacts prognosis.
- Niacin demonstrates clinical benefits in CAD patients, but its added value alongside statin therapy requires investigation.
- The effect of niacin on endothelial function with optimal LDL cholesterol levels remains unclear.
Purpose of the Study:
- To assess the impact of extended-release (ER) niacin on endothelial and vascular function in CAD patients receiving high-dose statins.
- To evaluate changes in brachial flow-mediated dilatation (FMD), peak hyperemic velocity (VTiRH), and pulse arterial tonometry (PAT).
Main Methods:
- A randomized crossover study involving 66 CAD patients treated with atorvastatin 80 mg daily.
- Patients received ER niacin (1500 mg/day) or placebo for 3 months each.
- Endothelial and vascular function were measured using FMD, VTiRH, and PAT at baseline and after each treatment period.
Main Results:
- Niacin significantly improved lipid profiles, lowering LDL and raising HDL cholesterol compared to placebo.
- No significant improvements were observed in FMD, VTiRH, or PAT measurements with niacin treatment.
- Lipid profile improvements did not correlate with enhanced endothelial or microvascular function.
Conclusions:
- ER niacin as an adjunct to high-dose statins in CAD patients effectively improves lipid profiles.
- Despite lipid improvements, niacin did not enhance endothelial or microvascular function in this patient cohort.
- Further research is needed to understand niacin's role in vascular health for CAD patients on statins.
Aims:
To determine the effect of extended release (ER) niacin on endothelial and vascular function assessed by brachial flow-mediated dilatation (FMD), peak hyperemic velocity (VTiRH) and pulse arterial tonometry (PAT) in patients with established coronary artery disease (CAD), already treated with high dose statins. Endothelial dysfunction is common in patients with established coronary artery disease (CAD) and has prognostic implications. Niacin has proven clinical benefit in patients with CAD, but its additive effect in patients on statin therapy is being evaluated. The effect of niacin on endothelial function, in the presence of optimal LDL cholesterol is unclear.
Methods And Results:
Sixty-six patients with CAD (mean age 57.9 ± 8.5 yrs) received ER niacin (1500 mg per day) and placebo in a randomized crossover fashion for 3 months of each therapy. All patients received atorvastatin 80 mg per day. FMD, VTiRH and PAT measurements were performed at baseline and after each treatment period. Treatment with niacin improved dyslipidemia parameters (LDL placebo 1.52 ± 0.51 vs. niacin 1.30 ± 0.43; p = 0.004; HDL placebo 0.95 ± 0.16 vs. niacin 1.11 ± 0.22; p < 0.001). However, there was no observed improvement in endothelial function as assessed by FMD (placebo 6.1 ± 4.9 vs. niacin 6.6 ± 4.8%; p = 0.48), VTiRH (placebo 75 ± 28 vs. niacin 78 ± 26 cm; p = 0.23) or PAT (placebo 1.8 ± 0.42 vs. niacin 1.79 ± 0.5; p = 0.43).
Conclusion:
Niacin as add-on treatment to high dose statins in patients with established CAD significantly improves lipid profile. However, these changes were not associated with improved endothelial or microvascular function. Registered clinical trial with clinicaltrials.gov: NCT00150722.
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