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Impact of Rosuvastatin on Endothelial Function and Inflammation in Patients With Chronic Heart Failure

U

University of Leipzig

Status and phase

Completed
Phase 2

Conditions

Heart Failure

Treatments

Drug: rosuvastatin

Study type

Interventional

Funder types

Other
Industry

Identifiers

NCT00176332
121/2003

Details and patient eligibility

About

Statin therapy has been shown to efficiently reduce mortality in patients with coronary artery disease and myocardial infarction, partially as a result of the lipid-lowering properties of statins. However, especially the pleiotropic effects of statins, e.g. their anti-inflammatory and anti-oxidative properties, might be of interest in the treatment of patients with chronic heart failure that are limited in their exercise capacity due to alterations of the skeletal muscle and peripheral endothelial dysfunction.

Aim of this trial is therefore to assess the effects of three months of rosuvastatin treatment on markers of inflammation and oxidative stress in the skeletal muscle and the blood, on postnatal vasculogenesis, and endothelial function of the radial artery in patients with severe chronic heart failure.

Full description

A total of 40 patients with severe chronic heart failure are prospectively randomized to either 3 months of rosuvastatin or placebo treatment.

Before and after the intervention period maximal exercise capacity is measured by ergospirometry and endothelial function is determined by high-resolution A-mode ultrasound. Skeletal muscle biopsies are obtained at begin and after 3 months and are analyzed for inflammatory markers, measures of oxidative stress and vasculogenesis. Blood samples are assessed with regard to markers of inflammation and oxidative stress as well.

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • chronic heart failure (NYHA class III or IV)
  • peak oxygen uptake <20 mL/min/kg body weight
  • left ventricular ejection fraction <30 %
  • left ventricular end-diastolic diameter >55 mm
  • stable medication within the last 4 weeks

Exclusion criteria

  • elevated GOT and GPT levels as a sign of hepatic dysfunction
  • elevated creatinine levels as a sign of renal dysfunction
  • insulin-dependent diabetes mellitus
  • arterial hypertension
  • muscle disease or elevated CK levels
  • treatment with fibrates
  • co-treatment with drugs that are metabolized by Cyp3A4
  • diseases that disallow a participation in the study

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Single Group Assignment

Masking

Double Blind

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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