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Risk factors for reaching renal endpoints in the Assessment of Lescol in Renal Transplantation (ALERT) trial

Fellström, Bengt, 1942- (author)
Uppsala universitet,Institutionen för medicinska vetenskaper,The Assessment of LEscol in Renal Transplantation (ALERT) Study Investigators,Fellström, B., University Hospital, Uppsala, Sweden, Department of Medical Science, Renal Unit, University Hospital, Uppsala, Sweden
Holdaas, H. (author)
Rikshospitalet, Oslo, Norway,the Assessment of LEscol in Renal Transplantation (ALERT) Study Investigators,Univ. Klin. Charité, Berlin, Germany
Jardine, A.G. (author)
University of Glasgow, Glasgow, United Kingdom,the Assessment of LEscol in Renal Transplantation (ALERT) Study Investigators
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Nyberg, G. (author)
Sahlgrenska University Hospital, Göteborg, Sweden,the Assessment of LEscol in Renal Transplantation (ALERT) Study Investigators
Gronhagen-Riska, C. (author)
Grönhagen-Riska, C., University Hospital, Helsinki, Finland
Madsen, S. (author)
Skejby Hospital, Aarhus, Denmark
Neumayer, H.-H. (author)
Univ. Klin. Charité, Berlin, Germany
Cole, E. (author)
Toronto General Hospital, Toronto, Ont., Canada
Maes, B. (author)
University Hospital, Leuven, Belgium
Ambuhl, P. (author)
Ambühl, P., University Hospital, Zürich, Switzerland
Olsson, Anders (author)
Östergötlands Läns Landsting,Linköpings universitet,Hälsouniversitetet,Internmedicin,Endokrin- och magtarmmedicinska kliniken US
Staffler, B. (author)
Novartis, Basel, Switzerland
Pedersen, T.R. (author)
Preventive Medicine Clinic, Ullevaal University Hospital, Oslo, Norway
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 (creator_code:org_t)
2005
2005
English.
In: Transplantation. - 0041-1337 .- 1534-6080. ; 79:2, s. 205-212
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Background. The aim of the study was to identity risk factors for long-term renal transplant function and development of chronic allograft nephropathy (CAN) in renal transplant recipients included in the Assessment of Lescol in Renal Transplantation (ALERT) trial. Methods. The ALERT trial was a randomized, double-blind, placebo-controlled study of the effect of fluvastatin, 40 and 80 mg/day, in renal transplant recipients who were randomized to receive fluvastatin (Lescol) (n=1,050) or placebo (n=1,052) over 5 to 6 years of follow-up. Renal endpoints including graft loss or doubling of serum creatinine or death were analyzed by univariate and multivariate regression analysis in the placebo group. Results. There were 137 graft losses (13.5%) in the placebo group, mainly caused by CAN (82%). Univariate risk factors for graft loss or doubling of serum creatinine were as follows: serum creatinine, proteinuria, hypertension, pulse pressure, time since transplantation, donor age, human leukocyte antigen-DR mismatches, treatment for rejection, low high-density lipoprotein cholesterol, and smoking. Multivariate analysis revealed independent risk factors for graft loss as follows: serum creatinine (relative risk [RR], 3.12 per 100-µM increase), proteinuria (RR, 1.64 per 1-g/24 hr increase), and pulse pressure (RR, 1.12 per 10 mm Hg), whereas age was a protective factor. With patient death in the composite endpoint, diabetes mellitus, smoking, age, and number of transplantations were also risk factors. Conclusions. Independent risk factors for graft loss or doubling of serum creatinine or patient death are mainly related to renal transplant function, proteinuria, and blood pressure, which emphasizes the importance of renoprotective treatment regimens in this population.

Subject headings

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

Keyword

Chronic rejection
Graft loss
Renal transplantation
Risk factors
MEDICINE
MEDICIN
Kidney diseases
Medicin

Publication and Content Type

ref (subject category)
art (subject category)

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