Efficacy, safety, and tolerability of once-daily niacin for the treatment of dyslipidemia associated with type 2 diabetes - Results of the assessment of diabetes control and evaluation of the efficacy of niaspan trial

被引:373
作者
Grundy, SM
Vega, GL
McGovern, ME
Tulloch, BR
Kendall, DM
Fitz-Patrick, D
Ganda, OP
Rosenson, RS
Buse, JB
Robertson, DD
Sheehan, JP
机构
[1] Univ Texas, SW Med Ctr, Ctr Human Nutr, Dallas, TX USA
[2] Kos Pharmaceut, Miami, FL USA
[3] Diagnost Clin Houston, Houston, TX USA
[4] Int Diabet Ctr, St Louis Pk, MN USA
[5] EW Med Res Inst, Honolulu, HI USA
[6] Harvard Univ, Sch Med, Dept Med, Joslin Diabet Ctr, Boston, MA 02115 USA
[7] Northwestern Univ, Sch Med, Prevent Cardiol Clin, Chicago, IL 60614 USA
[8] Univ N Carolina, Sch Med, Diabet Care Ctr, Chapel Hill, NC 27599 USA
[9] Atlanta Diabet Assoc, Atlanta, GA USA
[10] N Coast Inst Diabet & Endocrinol, Westlake, OH USA
关键词
D O I
10.1001/archinte.162.14.1568
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Diabetic dyslipidemia is characterized by high triglyceride levels; low high-density lipoprotein cholesterol levels; small, dense low-density lipoprotein particles; and high free fatty acid levels. Niacin reduces concentrations of triglyceride-rich and small low-density lipoprotein particles while increasing high-density lipoprotein cholesterol levels. It also lowers levels of free fatty acids and lipoprotein(a). However, the use of niacin in patients with diabetes has been discouraged because high doses can worsen glycemic control. We evaluated the efficacy and safety of once-daily extended-release (ER) niacin in patients with diabetic dyslipidemia. Methods: During a 16-week, double-blind, placebo-controlled trial, 148 patients were randomized to placebo (n=49) or 1000 (n=45) or 1500 mg/d (n=52) of ER niacin. Sixty-nine patients (47%) were also receiving concomitant therapy with statins. Results: Dose-dependent increases in high-density lipoprotein cholesterol levels (+19% to +24% [P<.05] vs placebo for both niacin dosages) and reductions in triglyceride levels (-13% to -28% [P<.05] vs placebo for the 1500-mg ER niacin) were observed. Baseline and week 16 values for glycosylated hemoglobin levels were 7.13% and 7.11%, respectively, in the placebo group; 7.28% and 7.35%, respectively, in the 1000-mg ER niacin group (P=.16 vs placebo); and 7.2% and 7.5%, respectively, in the 1500-mg ER niacin group (P=.048 vs placebo). Four patients discontinued participation because of inadequate glucose control. Rates of adverse event rates other than flushing were similar for the niacin and placebo groups. Four patients discontinued participation owing to flushing (including 1 receiving placebo). No hepatotoxic effects or myopathy were observed. Conclusion: Low doses of ER niacin (1000 or 1500 mg/d) are a treatment option for dyslipidemia in patients with type 2 diabetes.
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页码:1568 / 1576
页数:9
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