Chronic Renal Failure, Hyperlipidemia, Hypertension
Conditions
Brief summary
This study was done to determine whether Simvastatin (a medication commonly used to treat patients with high cholesterol levels in the blood increases blood flow to the kidneys and improves renal function in normal volunteers and patients with impaired renal function secondary to polycystic kidney diseases.
Interventions
DRUGSimvastatin
Sponsors
Mayo Clinic
Study design
Primary purpose
TREATMENT
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes
Inclusion criteria
Patients with chronic renal failure: 1. Age 18 or older 2. Chronic renal failure secondary to Autosomal Dominant Polycystic Kidney Disease 3. Serum creatinine ≥ 1.4 but ≤ 2.0 mg/dl 4. Creatinine or iothalamate clearance between 35-70 ml/min per 1.73m2 5. Stable renal function for the three preceding months 6. Blood pressure needs to be adequately controlled (\< 140/90 mm Hg), with or without the use of antihypertensive agents. However, ACE inhibitors or AT1 receptor blockers must not be initiated, or have their dose increased during the study period. Patients with normal renal function: 1. Age 18 or older 2. Normal renal function and diagnosed with Autosomal Dominant Polycystic Kidney Disease 3. Serum creatinine ≤ 1.4 4. Creatinine or iothalamate clearance ≥70 ml/min per 1.73m2 5. Renal function has to be stable for the three preceding months 6. Blood pressure needs to be adequately controlled (\< 140/90 mm Hg), with or without the use of antihypertensive agents. However, ACE inhibitors or AT1 receptor blockers must not be initiated, or have their dose increased during the study period.
Exclusion criteria
include: 1. Patients using corticosteroids, cytotoxic drugs (alkylating agents, chlorambucil, cyclophosphamide), CellCept, or cyclosporin A therapy 2. Positive hepatitis B surface antigen (HBsAg) or hepatitis C antibody (HCV-Ab) 3. Serum transaminase levels (AST, ALT) 2 times the upper limit of normal 4. Clinically significant medical conditions 5. Pregnant patients, patients who are breast-feeding, or women intending to conceive during the course of the study 6. Presence or suspicion of active infection, recent serious infection or chronic/recurrent viral or bacterial infection 7. Presence of concomitant renal artery stenosis.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Effect of short term HMG-CoA reductase treatment | 4 weeks | Differences between mean values for RPF, GFR and FF at baseline versus mean values obtained for these same parameters after 4 weeks of treatment will be analyzed using two-tailed Student's paired t-test. A similar analysis will be performed regarding patient's profiles for creatinine clearance, serum creatinine, urinary protein excretion and serum lipids. All results will be expressed as mean ± standard deviations. Differences will be considered significant at P \<0.05. |
Outcome results
None listed