Statins and the Urinary Proteome

NCT ID: NCT00464503

Last Updated: 2008-04-08

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 7 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2007-09-30
• Study Completion Date: 2007-10-31

Brief Summary

This study aims to investigate whether statines (rosuva- and pravastatin) induce tubular proteinuria.

Detailed Description

The proximal tubular cells of the kidney are responsible for reabsorption of proteins from the tubular lumen. In a study using Opossum kidney (OK) cells, receptor-mediated protein endocytosis was reduced by statins, inhibitors of 3-hydroxy-3-methylglutaryl CoA (HMG-CoA) reductase, which are widely used for therapeutic reduction of plasma cholesterol levels (1). In a subsequent in vitro study protein endocytosis in human mixed proximal/distal kidney tubular cells was investigated in the presence and absence of statins to explore the possible clinical relevance of the observations in OK cells (2). The uptake of FITC-labeled albumin in these cultures occurred selectively into proximal tubular cells while it was absent in distal tubular/collecting duct cells. Three statins (simvastatin, pravastatin, and rosuvastatin) significantly inhibited the uptake of protein in a concentration-dependent way. This inhibitory effect of statins could be prevented by the co-addition of mevalonate, the product of HMG-CoA reductase. This effect was not the result of a statin-induced cytotoxicity since cell-viability was unaffected.

These data suggest that statins have the potential to inhibit albumin uptake by the human proximal nephron as a result of inhibition of HMG-CoA reductase in the proximal tubule cells. A reduced prenylation of some proteins critically involved in endocytosis has been put forward as the underlying mechanism.

Knowing these data it has been suggested that the occurrence of proteinuria in some patients treated with high statin doses is the result of a reduced tubular reabsorption/endocytosis of normally filtered proteins. To further explore the clinical relevance of such a mechanism, the composition of the urinary proteome under statin treatment will be investigated in normal healthy volunteers by two-dimensional gel electrophoresis based proteomics analysis.

Conditions

Statin Induced Proteinuria

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: DIAGNOSTIC
• Blinding Strategy: DOUBLE

Interventions

Rosuvastatin-Crestor

Intervention Type: DRUG

Pravastatin-Pravasine

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Male, age range: 25 - 65 years
• Non-smoker
• Proteinuria: < 60 mg/24 hours
• Dipstick negative hematuria
• Bloodpressure: < 135 mm systolic, < 85 mm dyastolic
• Waist circumference: < 94 cm

Exclusion Criteria

• Treatment with lipid-lowering drugs <1 year prior to the study
• Known history of diabetes or fasting glucose level: < 110 mg/dl
• Anti-hypertensive medication
• Life-expectancy < 1 year
• Pharmacological treatment with inotropes
• Acute or chronic inflammatory process, use if anti-inflammatory drugs or immunosuppression
• Clinically active malignant disease
• Administration of any investigational drug within 30 days preceding study start and during the study
• Known intolerance to rosuvastatin or other statins
• Acute or chronic liver disease or ALAT>2.0 x upper limit of normal (ULN) at enrolment visit.
• Chronic muscle disease such as dermatomyositis or polymyositis or unexplained creatinine kinase (CK) above 3 x ULN at enrolment.
• Uncontrolled hypothyroidism as indicated by a thyroid stimulating hormone (TSH) > 2 x ULN at enrolment.
• Renal insufficiency: creatinine > 2.0mg/dl
• Known or suspect alcohol or drug abuse.

• Minimum Eligible Age: 25 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: MALE
• Accepts Healthy Volunteers: Yes

Sponsors

Universiteit Antwerpen

OTHER

Sponsor Role: lead

Principal Investigators

Patrick C D'Haese, Prof

Role: STUDY_DIRECTOR

Universiteit Antwerpen

Locations

University of Antwerp

Antwerp, Antwerp, Belgium

Countries

Belgium

Other Identifiers

STAT-AZ-01

Identifier Type: -

Identifier Source: org_study_id