Concise reports
Effects of moderate renal insufficiency on pharmacokinetics of
methotrexate in rheumatoid arthritis patients
a Laboratoire de Pharmacocinétique, Faculté de
Pharmacie, Montpellier, and Laboratoire de Pharmacocinétique, CHU
Carémeau, Nîmes, France, b Fédération de Rhumatologie, CHU Lapeyronie, Montpellier,
France
Correspondence to: Professor B Combe, Fédération de Rhumatologie, CHU Lapeyronie, 34295 Montpellier Cedex 5, France.
Accepted for publication 6
January 1998
OBJECTIVES
To determine the effects of impaired
renal function on the pharmacokinetics of methotrexate (MTX) in
rheumatoid arthritis (RA) patients.
METHODS
77 RA patients were included in this
study. MTX was administered intramuscularly (7.5 to 15 mg). Subjects
were divided into four groups, according to their creatinine clearance
(CLCR); group 1: CLCR lower than 45 ml/min;
group 2: CLCR between 45 and 60 ml/min, group 3:
CLCR between 61 and 80 ml/min and group 4: CLCR higher than 80 ml/min. Blood samples were collected from each subject
before drug administration and at two and eight hours after
administration. Individual pharmacokinetic parameters were estimated
using a Bayesian approach.
RESULTS
MTX concentrations (total and free) were
1.3 to 1.6-times higher in group 1 than in groups 2, 3, and 4. For
total and free MTX, t1/2 eliminations were 22.7 hours in
group 1, 13.5 hours in group 2, 12 hours in group 3, and 11 hours in
group 4. Clearance of total MTX was 64, 92, 96, 115 ml/min in groups 1 to 4, respectively, it was 118, 163, 171, 206 ml/min in groups 1 to 4 for the free MTX, respectively. Volume of distribution averaged 2.16 l/kg in group 1, 1.92 l/kg in group 2, 1.61 l/kg in group 3, and 1.56 l/kg in group 4. Elimination half life was significantly increased and
total clearance was significantly reduced with the degree of renal
impairment. Linear regression revealed good correlations between
clearance values of MTX and creatinine clearance.
CONCLUSION
Individual testing is required rather
than a general decrease of the MTX dose based only on
CLCR.
© 1998 by Annals of the Rheumatic Diseases
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