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Combination of niacin extended-release and simvastatin results in a less atherogenic lipid profile than atorvastatin monotherapy.
Insull, William; Toth, Peter P; Superko, H Robert; Thakkar, Roopal B; Krause, Scott; Jiang, Ping; Parreno, Rhea A; Padley, Robert J.
Afiliação
  • Insull W; Baylor College of Medicine and Methodist Hospital, Houston, Texas, USA.
Vasc Health Risk Manag ; 6: 1065-75, 2010 Nov 24.
Article em En | MEDLINE | ID: mdl-21191426
ABSTRACT

OBJECTIVE:

To compare the effects of combination niacin extended-release + simvastatin (NER/S) versus atorvastatin alone on apolipoproteins and lipid fractions in a post hoc analysis from SUPREME, a study which compared the lipid effects of niacin extended-release + simvastatin and atorvastatin in patients with hyperlipidemia or mixed dyslipidemia. PATIENTS AND

METHODS:

Patients (n = 137) with dyslipidemia (not previously receiving statin therapy or having discontinued any lipid-altering treatment 4-5 weeks prior to the study) received NER/S (1000/40 mg/day for four weeks, then 2000/40 mg/day for eight weeks) or atorvastatin 40 mg/day for 12 weeks. Median percent changes in apolipoprotein (apo) A-1, apo B, and the apo BA-I ratio, and nuclear magnetic resonance lipoprotein subclasses from baseline to week 12 were compared using the Wilcoxon rank-sum test and Fisher's exact test.

RESULTS:

NER/S treatment produced significantly greater percent changes in apo A-I and apo BA-I, and, at the final visit, apo B < 80 mg/dL was attained by 59% versus 33% of patients, compared with atorvastatin treatment (P = 0.003). NER/S treatment resulted in greater percent reductions in calculated particle numbers for low-density lipoprotein (LDL, 52% versus 43%; P = 0.022), small LDL (55% versus 45%; P = 0.011), very low-density lipoprotein (VLDL) and total chylomicrons (63% versus 39%; P < 0.001), and greater increases in particle size for LDL (2.7% versus 1.0%; P = 0.007) and VLDL (9.3% versus 0.1%; P < 0.001), compared with atorvastatin.

CONCLUSION:

NER/S treatment significantly improved apo A-I levels and the apo BA-I ratio, significantly lowered the number of atherogenic LDL particles and VLDL and chylomicron particles, and increased the mean size of LDL and VLDL particles, compared with atorvastatin.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Pirróis / Sinvastatina / Aterosclerose / Dislipidemias / Ácidos Heptanoicos / Hipolipemiantes / Niacina Idioma: En Ano de publicação: 2010 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Pirróis / Sinvastatina / Aterosclerose / Dislipidemias / Ácidos Heptanoicos / Hipolipemiantes / Niacina Idioma: En Ano de publicação: 2010 Tipo de documento: Article