Article
Effects of niacin on glucose control in patients with dyslipidemia.
Lipid Disorders Clinic, Division of Endocrinology, Diabetes, and Metabolism, University of Miami Leonard M. Miller School of Medicine, 1450 NW 10th Ave, Miami, FL 33136, USA.
Mayo Clinic Proceedings (impact factor:
5.7).
05/2008;
83(4):470-8.
DOI:10.4065/83.4.470
pp.470-8
Source: PubMed
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Citations (0)
- Cited In (2)
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Article: Lipid management in the geriatric patient.
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ABSTRACT: Elderly individuals are at higher risk for cardiovascular events, and thus this population stands to gain a greater reduction in events from lipid therapy than younger individuals. Multiple primary and secondary prevention trials have demonstrated that the benefits of statins in geriatric patients are equivalent to, or greater than, those seen in younger patients. Combination therapy with non-statin agents should be considered in patients who do not meet cholesterol goals or who have concomitant hypertriglyceridemia or low levels of high-density lipoprotein cholesterol. Although increased side effects may occur with high-dose statin therapy, careful vigilance of drug interactions and limiting polypharmacy can reduce these effects.Endocrinology and metabolism clinics of North America 04/2009; 38(1):185-206. · 3.56 Impact Factor -
Article: Effect of niacin ER/lovastatin on claudication symptoms in patients with peripheral artery disease.
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ABSTRACT: In patients with peripheral artery disease (PAD), statins may improve the symptoms of claudication. The Intermittent Claudication Proof of Principle (ICPOP) study tested the hypothesis that the combination of extended release niacin plus lovastatin would improve exercise performance in patients with PAD and claudication compared with a diet intervention. A phase 3 double-blind, parallel-group, multi-center, 28-week multi-national study evaluated subjects with a history of claudication who had an ankle-brachial index (ABI) < or = 0.90, a reproducible peak treadmill walking time (PWT) of 1-20 minutes, and a low-density lipoprotein (LDL)-cholesterol level < 160 mg/dl (< 4.1 mmol/l). Subjects were randomly assigned to low-dose niacin 1000 mg plus lovastatin 40 mg (low niacin-statin), high-dose niacin 2000 mg plus lovastatin 40 mg (high niacin-statin), or diet intervention (diet). The co-primary efficacy endpoint of percent change in PWT and claudication onset time (COT) at 28 weeks was assessed using a graded treadmill protocol. At completion, 385 subjects were analyzed for safety and 370 subjects were analyzed for efficacy. The primary efficacy analysis showed no statistical significance for overall treatment effect at week 28 for the co-primary endpoint of PWT and COT. The PWT component of the primary endpoint increased 26.5% on diet, 37.8% on high niacin-statin (p = 0.137) and 38.6% on low niacin-statin (p = 0.096). Flushing as the most common event leading to discontinuation and treatment was associated with increases in liver enzymes, fasting blood glucose concentration and a decrease in platelet count.Vascular Medicine 03/2010; 15(3):171-9. · 1.46 Impact Factor
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Keywords
clinical benefits
discontinuing niacin
dyslipidemic patients
effective available pharmacotherapy
fasting glucose
glucose control
incident diabetes
key words
long-term niacin
mild effects
monitoring glycemic control
new insulin prescriptions
niacin-statin regimens
observational studies
open-label studies
oral hypoglycemic regimens
residual cardiovascular risk
search terms
significant reductions
title words niacin