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Can simvastatin reduce COPD exacerbations? A randomised double-blind controlled study.
Schenk, Peter; Spiel, Alexander O; Hüttinger, Felix; Gmeiner, Micheline; Fugger, Josefine; Pichler, Martina; Pichler, Gernot; Schmeikal, Susanne; Janistyn, Wolfgang; Schügerl, Stefan; Sajdik, Constantin; Herkner, Harald.
Afiliação
  • Schenk P; Landesklinikum Hochegg, Pulmologische Abteilung, Grimmenstein, Austria peter.schenk@hochegg.lknoe.at.
  • Spiel AO; Medical University Vienna, Dept of Emergency Medicine, Vienna, Austria.
  • Hüttinger F; Central Emergency Dept, Ottakring Clinic, Vienna, Austria.
  • Gmeiner M; Landesklinikum Hochegg, Pulmologische Abteilung, Grimmenstein, Austria.
  • Fugger J; Landesklinikum Hochegg, Pulmologische Abteilung, Grimmenstein, Austria.
  • Pichler M; Landesklinikum Mödling, Pharmacy, Mödling, Austria.
  • Pichler G; Landesklinikum Hochegg, Pulmologische Abteilung, Grimmenstein, Austria.
  • Schmeikal S; Landesklinikum Hochegg, Pulmologische Abteilung, Grimmenstein, Austria.
  • Janistyn W; Baden, Austria.
  • Schügerl S; Wr. Neustadt, Austria.
  • Sajdik C; Neunkirchen, Austria.
  • Herkner H; Landesklinikum Hochegg, Pulmologische Abteilung, Grimmenstein, Austria.
Eur Respir J ; 58(1)2021 07.
Article em En | MEDLINE | ID: mdl-33574076
ABSTRACT

BACKGROUND:

Several studies have shown that statins have beneficial effects in COPD regarding lung function decline, rates and severity of exacerbation, hospitalisation and need for mechanical ventilation.

METHODS:

We performed a randomised double-blind placebo-controlled single-centre trial of simvastatin at a daily dose of 40 mg versus placebo in patients with Global Initiative for Chronic Obstructive Lung Disease criteria grades 2-4 at a tertiary care pulmonology department in Austria. Scheduled treatment duration was 12 months and the main outcome parameter was time to first exacerbation.

RESULTS:

Overall, 209 patients were enrolled. In the 105 patients taking simvastatin, time to first exacerbation was significantly longer compared to the 104 patients taking placebo median 341 versus 140 days (log-rank test p<0.001). Hazard ratio for risk of first exacerbation for the simvastatin group was 0.51 (95% CI 0.34-0.75; p=0.001). Rate of exacerbations was significantly lower with simvastatin 103 (41%) versus 147 (59%) (p=0.003). The annualised exacerbation rate was 1.45 events per patient-year in the simvastatin group and 1.9 events per patient-year in the placebo group (incidence rate ratio 0.77, 95% CI 0.60-0.99). We found no effect on quality of life, lung function, 6-min walk test and high-sensitivity C-reactive protein. More patients dropped out in the simvastatin group compared to the placebo group (39 versus 29).

CONCLUSION:

In our single-centre RCT, simvastatin at a dose of 40 mg daily significantly prolonged time to first COPD exacerbation and reduced exacerbation rate.
Assuntos

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Inibidores de Hidroximetilglutaril-CoA Redutases / Doença Pulmonar Obstrutiva Crônica Tipo de estudo: Clinical_trials Limite: Humans Idioma: En Revista: Eur Respir J Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Áustria

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Inibidores de Hidroximetilglutaril-CoA Redutases / Doença Pulmonar Obstrutiva Crônica Tipo de estudo: Clinical_trials Limite: Humans Idioma: En Revista: Eur Respir J Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Áustria