Literature DB >> 656293

Prednisone or prednisolone for the treatment of chronic active hepatitis? A comparison of plasma availability.

M Davis, R Williams, J Chakraborty, J English, V Marks, G Ideo, S Tempini.   

Abstract

1 The plasma availability of prednisolone after oral doses of prednisolone and its precursor, prednisone, were compared in ten normal controls and twenty-five patients with chronic active hepatitis by estimation of the area under the plasma concentration--time curve for the drug (AUC). 2 In controls, values for AUC were significantly more variable after prednisone than prednisolone, and two subjects showed markedly inefficient conversion of prednisone to prednisolone. In patients, variability was similarly wide after both preparations, but overall bioavailability after both prednisone and prednisolone was similar to that found in controls, although three patients showed subnormal values after both preparations, possibly as a result of impaired intestinal absorption. 3 Patients with biochemical and histological evidence of active hepatocellular necrosis showed evidence of impaired activation of prednisone, but this was compensated for by a decreased rate of elimination of prednisolone from the plasma. 4 It is concluded that plasma prednisolone levels will be more predictable after prednisolone than after prednisone in subjects without hepatic dysfunction. In the presence of liver disease, because of the marked variability in plasma prednisolone levels after either drug, estimation of these could be of value in those patients whose disease cannot be controlled by normal maintenance doses.

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Year:  1978        PMID: 656293      PMCID: PMC1429358          DOI: 10.1111/j.1365-2125.1978.tb01664.x

Source DB:  PubMed          Journal:  Br J Clin Pharmacol        ISSN: 0306-5251            Impact factor:   4.335


  8 in total

1.  Bioavailability and pharmacokinetics of prednisone in humans.

Authors:  A R Disanto; K A Desante
Journal:  J Pharm Sci       Date:  1975-01       Impact factor: 3.534

Review 2.  Treatment of chronic hepatitis.

Authors:  S P Mistilis; K C Lam
Journal:  Prog Liver Dis       Date:  1972

Review 3.  Polygenic factors controlling drug response.

Authors:  E S Vesell
Journal:  Med Clin North Am       Date:  1974-09       Impact factor: 5.456

4.  A classification of chronic hepatitis.

Authors:  J De Groote; V J Desmet; P Gedigk; G Korb; H Popper; H Poulsen; P J Scheuer; M Schmid; H Thaler; E Uehlinger
Journal:  Lancet       Date:  1968-09-14       Impact factor: 79.321

5.  Phenylbutazone and isoniazid metabolism in patients with liver disease in relation to previous drug therapy.

Authors:  A J Levi; S Sherlock; D Walker
Journal:  Lancet       Date:  1968-06-15       Impact factor: 79.321

6.  Increased hepatic microsomal activity induced by spironolactone and other steroids.

Authors:  B Solymoss; H G Classen; S Varga
Journal:  Proc Soc Exp Biol Med       Date:  1969-12

7.  Conversion of cortisone to cortisol and prednisone to prednisolone.

Authors:  J S Jenkins; P A Sampson
Journal:  Br Med J       Date:  1967-04-22

8.  Corticosteroids in liver disease: studies on the biological conversion of prednisone to prednisolone and plasma protein binding.

Authors:  L W Powell; E Axelsen
Journal:  Gut       Date:  1972-09       Impact factor: 23.059

  8 in total
  23 in total

1.  Acute gout: oral steroids work as well as NSAIDs.

Authors:  Shailendra Prasad; Bernard Ewigman
Journal:  J Fam Pract       Date:  2008-10       Impact factor: 0.493

Review 2.  Review article: The pharmacokinetics and pharmacodynamics of drugs used in inflammatory bowel disease treatment.

Authors:  E G Quetglas; A Armuzzi; S Wigge; G Fiorino; L Barnscheid; M Froelich; Silvio Danese
Journal:  Eur J Clin Pharmacol       Date:  2015-05-27       Impact factor: 2.953

Review 3.  Clinical pharmacokinetics of prednisone and prednisolone.

Authors:  B M Frey; F J Frey
Journal:  Clin Pharmacokinet       Date:  1990-08       Impact factor: 6.447

4.  Alterations of glucocorticoid actions by other drugs and disease states.

Authors:  W Jubiz; A W Meikle
Journal:  Drugs       Date:  1979-08       Impact factor: 9.546

5.  Prednisone compared to methylprednisolone in the polymyalgia rheumatica treatment.

Authors:  Ombretta Viapiana; Davide Gatti; Sonila Troplini; Silvano Adami; Elena Fracassi; Luca Idolazzi; Maurizio Rossini
Journal:  Rheumatol Int       Date:  2014-08-23       Impact factor: 2.631

Review 6.  Corticosteroids in liver disease: possible mechanisms of action, pharmacology, and rational use.

Authors:  A R Tanner; L W Powell
Journal:  Gut       Date:  1979-12       Impact factor: 23.059

Review 7.  Clinical Pharmacokinetic and Pharmacodynamic Considerations in the Treatment of Inflammatory Bowel Disease.

Authors:  Luc J J Derijks; Dennis R Wong; Daniel W Hommes; Adriaan A van Bodegraven
Journal:  Clin Pharmacokinet       Date:  2018-09       Impact factor: 6.447

8.  Prednisolone absorption in coeliac disease.

Authors:  M E Pickup; F Farah; J R Lowe; J S Dixon; C O Record
Journal:  Eur J Drug Metab Pharmacokinet       Date:  1979       Impact factor: 2.441

9.  Intra-individual consistency of prednisolone kinetics during long-term prednisone treatment.

Authors:  E Langhoff; H Flachs; J Ladefoged; E F Hvidberg
Journal:  Eur J Clin Pharmacol       Date:  1984       Impact factor: 2.953

10.  Methylprednisolone versus prednisolone pharmacokinetics in relation to dose in adults.

Authors:  S J Szefler; W F Ebling; J W Georgitis; W J Jusko
Journal:  Eur J Clin Pharmacol       Date:  1986       Impact factor: 2.953

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