Effect of Rosuvastatin on Left Ventricular Remodeling

University of Oslo (UIO)

Status and phase

Completed

Phase 3

Conditions

Dilated Cardiomyopathy

Treatments

Drug: placebo

Drug: Rosuvastatin

Study type

Interventional

Funder types

Other

Identifiers

NCT00505154

LG012007

Details and patient eligibility

About

The purpose of this study is to examine the the effect of the HMG-CoA reductase inhibitor Rosuvastatin on left ventricular remodeling in patients with dilated cardiomyopathy.

Full description

Chronic heart failure (HF) is one of the most important public health problems in cardiovascular medicine.
Idioatic dilated cardiomyopathy (CMP) represents the final common expression of primary myocardial damage produced by a variety of as yet undefined myocardial insults, producing areas of interstitial and perivascular fibrosis, particularly of the left ventricle. Chronic HF, including CMP, is a progressive disease with high morbidity and mortality, suggesting that important pathogenic mechanisms remain active and unmodified by the present treatment modalities. The presence of chronic inflammation in patients with chronic heart failure has been widely recognized and coupled with persistent immune activation may represent such unmodified mechanisms.

The effect of statin therapy on lipids are well known, but recent studies suggest that the beneficial effects of statins also may be related to their anti-inflammatory properties.

To further elucidate this issue we want to study the potent new statin Rosuvastatin on myocardial function and remodeling and their relation to inflammatory markers in patients with IDCM. As hyperlipidemia is not involved in the pathogenesis of IDCM, as opposed to HF secondary to CAD, such studies will also be an interesting approach in separating the lipid lowering from other effects of these medications in HF.

Enrollment

75 patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Age of 18-80 years
Have clinical or symptomatic evidence of HF, in NYHA class II-IV, for at least 3 months
Have LVEF <40%
On optimal medical treatment and considered unsuitable for surgical intervention.
Have given written informed consent
No planned heart transplantation
Female of potential childbearing age must have a negative serum pregnancy test within 7 days prior to enrollment. Effective contraception must be used during the trial and for 6 weeks following discontinuation of the study medication, even where there has been a history of infertility.

Exclusion criteria

Evidence of unstable disease
Evidence of ischemic etiology on the basis of history (diagnosed myocardial infarction), echocardiography or angiography)
Evidence of clinical significant valvular disease based on echocardiography
Significant concomitant diseases such as infections, pulmonary disease or connective tissue disease.
Contraindication against statin therapy
- Hypersensitivity against statins
- Liver disease with SGOT and SGPT > 2 timer upper normal limit
- Baseline elevations of CK 3 times upper normal values at any time during the course of the study
- Serum creatinine above 2.0 mg/dL (177 umol/L) at any time during the course of the study
- Pregnancy or breast feeding