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Low-dose atorvastatin in severe chronic kidney disease patients : a randomized, controlled endpoint study

Stegmayr, Bernd (author)
Umeå universitet,Medicin
Brännström, M (author)
Bucht, S (author)
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Crougneau, V (author)
Umeå universitet,Medicin
Dimeny, Emöke (author)
Umeå universitet,Medicin
Ekspong, A (author)
Eriksson, Marie (author)
Umeå universitet,Medicin
Granroth, B (author)
Gröntoft, KC (author)
Hadimeri, H (author)
Holmberg, Benny (author)
Umeå universitet,Medicin
Ingman, B (author)
Isaksson, B (author)
Johansson, G (author)
Lindberger, K (author)
Lundberg, Lennart (author)
Umeå universitet,Medicin
Mikaelsson, L (author)
Olausson, E (author)
Persson, B (author)
Stenlund, Hans (author)
Umeå universitet,Epidemiologi och global hälsa
Wikdahl, A-M (author)
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 (creator_code:org_t)
2005
2005
English.
In: Scandinavian Journal of Urology and Nephrology. - 0036-5599 .- 1651-2065. ; 39:6, s. 489-497
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Objective. There have been no endpoint studies with statins for patients with severe renal failure. The purpose of this prospective, open, randomized, controlled study was to investigate whether atorvastatin (10 mg/day) would alter cardiovascular endpoints and the overall mortality rate of patients with chronic kidney disease stage 4 or 5 (creatinine clearance < 30 ml/min).Material and methods. The study subjects comprised 143 patients who were randomized either to placebo (controls; n=73; mean age 69.5 years) or to treatment with atorvastatin (n=70; mean age 67.9 years). The patients included were either non-dialysis (n=33), haemodialysis (n=97) or peritoneal dialysis (n=13) patients. Analysis focused on the primary endpoints of all-cause mortality, non-lethal acute myocardial infarction, coronary artery bypass graft surgery and percutaneous transluminal coronary angioplasty. Statistical analysis for endpoint data was mainly by intention-to-treat.Results. Primary endpoints occurred in 74% of the subjects. There was no difference in outcome between the control and atorvastatin groups. The 5-year endpoint-free survival rate from study entry was 20%. Atorvastatin was withdrawn in 20% of patients due to unacceptable side-effects. In the atorvastatin group, low-density lipoprotein (LDL) cholesterol was reduced by 35% at 1 month and then sustained. The controls showed a progressive reduction in LDL cholesterol until 36 months.Conclusions. Although atorvastatin reduced total and LDL cholesterol effectively it was not beneficial regarding the long-term outcomes of cardiovascular endpoints or survival. In contrast to other patient groups, patients with severe chronic kidney disease, especially those on dialysis, seem to derive limited benefit from this lower dose of atorvastatin.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Urologi och njurmedicin (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Urology and Nephrology (hsv//eng)

Keyword

Atorvastatin; cholesterol; chronic kidney disease; hemodialysis; high-density lipoprotein cholesterol; lipids; low-density lipoprotein cholesterol; peritoneal dialysis; risk factors; statins; triglyceride
Kidney diseases
Njursjukdomar

Publication and Content Type

ref (subject category)
art (subject category)

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