The purpose of this study is to determine individual susceptibility factors (drug interactions, genetic factors such as enzyme polymorphism…) to explain wide interindividual variability towards corticosteroids (prednisone, prednisolone, methylprednisolone, hydrocortisone) in children, which could establish a base for therapeutic monitoring.
Corticosteroids are widely used in children. A large interindividual variability exists concerning both efficacity and tolerance. Pharmacokinetic is poorly known. A knowledge of individual susceptibility factors would allow to better adapt therapy in each case. Drugs evaluated here are used in routine care in children and will be prescribed according to department practices concerning treated disease. Medical checks will be done during usual follow-up. Several features will be collected: reason of treatment, drug chosen and prescription modalities, observance, concomitant treatments, side effects, clinical examination, photography, score… Blood samples will be performed at different interval during usual biological follow-up. Three samples per patient will be required for pharmacokinetic and pharmacogenetic. 170 children under prednisone/prednisolone,130 under methylprednisolone, and 100 children under hydrocortisone will be recruited in four pediatric medical departments: immuno-hematology, nephrology,dermatology, and pediatric neurology.
Study Type
OBSERVATIONAL
Enrollment
146
Blood sample of 2 ml at enrolment and then at following visits. Buccal cell collection swab
AP-HP Necker
Paris, France
Composite of Pharmacokinetic parameter for Prednisone, Prednisolone, Methylprednisolone, hydrocortisone
Assessed by: * Volume of distribution of creatinine * Creatinine clearance
Time frame: 24 months
Side effects
Ferryman and Gallwey score
Time frame: 24 months
Side effects
Dermaphot® score
Time frame: 24 months
Analysis of genetic polymorphism of proteins taking part in glucocorticoids metabolism
Time frame: 24 months
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