Literature DB >> 6750206

Effect of alternate-day prednisone on plasma lipids in renal transplant recipients.

J J Curtis, J H Galla, S Y Woodford, B A Lucas, R G Luke.   

Abstract

While numerous groups have reported high prevalences of plasma lipid abnormalities in their renal transplant recipients, we have been unable to confirm this finding. We have suggested that the routine use of alternate-day steroids (ADS) in our patients may be responsible. To test that hypothesis, a prospective controlled trial of equal total dose ADS versus daily steroids (DS) was conducted. Four months after transplant and before entering the trial, transplant study patients had significantly higher serum cholesterol (243 +/- 9 mg/dl) than either normal controls (cholesterol 200 +/- 7 mg/dl, alpha = 0.01) or hemodialysis patients (cholesterol 211 +/- 9 mg/dl, alpha = 0.01). They also had higher serum triglyceride than controls (129 +/- 7 mg/dl vs. 98 +/- 8 mg/dl, alpha = 0.01). After randomization to DS or ADS and 1 year of further followup study, the ADS group had a significant decrease in both serum triglyceride (139 +/- 9 to 100 +/- 7 mg/dl, P less than 0.01) and cholesterol (251 +/- 16 to 220 +/- 9 mg/dl, P less than 0.05) while the DS group's serum triglyceride and cholesterol values remained unchanged. Serum triglyceride and cholesterol in the ADS group had decreased to values that were not significantly different from 41 normal healthy controls. Dose spacing per se, and not the use of a lower total dose of prednisone, appears to result in a lower prevalence of abnormal plasma lipids after successful renal transplantation.

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Year:  1982        PMID: 6750206     DOI: 10.1038/ki.1982.130

Source DB:  PubMed          Journal:  Kidney Int        ISSN: 0085-2538            Impact factor:   10.612


  8 in total

Review 1.  Post-transplant hyperlipidaemia.

Authors:  R M Jindal
Journal:  Postgrad Med J       Date:  1997-12       Impact factor: 2.401

Review 2.  Safety of low dose glucocorticoid treatment in rheumatoid arthritis: published evidence and prospective trial data.

Authors:  J A P Da Silva; J W G Jacobs; J R Kirwan; M Boers; K G Saag; L B S Inês; E J P de Koning; F Buttgereit; M Cutolo; H Capell; R Rau; J W J Bijlsma
Journal:  Ann Rheum Dis       Date:  2005-08-17       Impact factor: 19.103

Review 3.  [Pathophysiology and therapy of lipid metabolism disorders in kidney diseases].

Authors:  C J Olbricht
Journal:  Klin Wochenschr       Date:  1991-08-01

4.  Cardiovascular pathology in renal transplant recipients.

Authors:  E B Frye; N D Vaziri; D C Martin; S Farooqui
Journal:  J Natl Med Assoc       Date:  1986-12       Impact factor: 1.798

5.  Dyslipidemia can be controlled in diabetic as well as nondiabetic recipients after kidney transplant.

Authors:  Vijay Shivaswamy; R Brian Stevens; Ramona Zephier; Myhra Zephier; Junfeng Sun; Gerald Groggel; Judi Erickson; Jennifer Larsen
Journal:  Transplantation       Date:  2008-05-15       Impact factor: 4.939

Review 6.  The influence of long-term morbidity on health status and rehabilitation following paediatric organ transplantation.

Authors:  P A Keown; C R Shackleton; B M Ferguson
Journal:  Eur J Pediatr       Date:  1992       Impact factor: 3.183

Review 7.  Endocrine and metabolic abnormalities following kidney transplantation.

Authors:  W H Hörl; W Riegel; C Wanner; M Haag-Weber; P Schollmeyer; H Wieland; H Wilms
Journal:  Klin Wochenschr       Date:  1989-09-01

Review 8.  HMG CoA reductase inhibitors (statins) for kidney transplant recipients.

Authors:  Suetonia C Palmer; Sankar D Navaneethan; Jonathan C Craig; Vlado Perkovic; David W Johnson; Sagar U Nigwekar; Jorgen Hegbrant; Giovanni Fm Strippoli
Journal:  Cochrane Database Syst Rev       Date:  2014-01-28
  8 in total

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