Literature DB >> 21619381

Niacin extended-release therapy in phase III clinical trials is associated with relatively low rates of drug discontinuation due to flushing and treatment-related adverse events: a pooled analysis.

Eliot A Brinton1, Moti L Kashyap, Anthony N Vo, Roopal B Thakkar, Ping Jiang, Robert J Padley.   

Abstract

BACKGROUND AND
OBJECTIVE: Niacin is a highly effective agent for increasing low high-density lipoprotein cholesterol (HDL-C) levels. It also has beneficial effects on key pro-atherogenic lipoprotein parameters. However, the side effect of flushing can challenge patient adherence to treatment. In this study, we pooled safety data from available trials of at least 16 weeks' duration to evaluate the impact of flushing on patient adherence to niacin extended-release (NER) therapy.
METHODS: Data were pooled from eight NER studies (administered as NER with a maximum dosage of 1000, 1500, and 2000 mg/day, either as monotherapy or in combination with simvastatin 20 or 40 mg/day [NER/S], or lovastatin 20 or 40 mg/day [NER/L]) to evaluate rates of study discontinuation due to flushing or any treatment-related adverse events.
RESULTS: While 66.6% of patients experienced flushing, only 5.2% of patients discontinued treatment due to flushing. Of the total number of patients treated with NER (n = 307), NER/S (n = 912), or NER/L (n = 928), 34 (11%), 105 (11%), and 127 (14%) patients discontinued due to any treatment-related adverse event, respectively, while 14 (5%), 43 (5%), and 55 (6%) discontinued due to flushing. Discontinuation for flushing did not differ with regard to maximum dose, or to the presence or type of statin combined with NER.
CONCLUSION: Although flushing was common with NER treatment, discontinuation due to flushing occurred in only 5-6% of patients in this pooled analysis. This could be due to several factors, including the fact that all patients in the NER trials were educated about flushing and its management. Translation of methodology employed in these trials into clinical practice may improve long-term adherence to NER therapy, which would enhance the therapeutic benefit of NER for reducing cardiovascular risk.

Entities:  

Mesh:

Substances:

Year:  2011        PMID: 21619381     DOI: 10.2165/11592560-000000000-00000

Source DB:  PubMed          Journal:  Am J Cardiovasc Drugs        ISSN: 1175-3277            Impact factor:   3.571


  5 in total

Review 1.  Niacin in cardiovascular disease: recent preclinical and clinical developments.

Authors:  Janet E Digby; Neil Ruparelia; Robin P Choudhury
Journal:  Arterioscler Thromb Vasc Biol       Date:  2011-12-29       Impact factor: 8.311

Review 2.  Niacin: the evidence, clinical use, and future directions.

Authors:  Todd C Villines; Andrew S Kim; Rosco S Gore; Allen J Taylor
Journal:  Curr Atheroscler Rep       Date:  2012-02       Impact factor: 5.113

Review 3.  Pharmacotherapies for lipid modification: beyond the statins.

Authors:  Antonio M Gotto; Jennifer E Moon
Journal:  Nat Rev Cardiol       Date:  2013-08-20       Impact factor: 32.419

4.  Effect of oral niacin on central retinal vein occlusion.

Authors:  Michael W Gaynon; Yannis M Paulus; Ehsan Rahimy; Janet L Alexander; Sam E Mansour
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2017-02-04       Impact factor: 3.117

5.  Laropiprant attenuates EP3 and TP prostanoid receptor-mediated thrombus formation.

Authors:  Sonia Philipose; Viktoria Konya; Mirjana Lazarevic; Lisa M Pasterk; Gunther Marsche; Sasa Frank; Bernhard A Peskar; Akos Heinemann; Rufina Schuligoi
Journal:  PLoS One       Date:  2012-08-01       Impact factor: 3.240

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.