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Evaluation of Hydroxychloroquine Blood Concentrations and Effects in Childhood-Onset Systemic Lupus Erythematosus.
Zahr, Noël; Urien, Saik; Funck-Brentano, Christian; Vantomme, Hélène; Garcelon, Nicolas; Melki, Isabelle; Boistault, Margaux; Boyer, Olivia; Bader-Meunier, Brigitte.
Affiliation
  • Zahr N; Clinical Investigation Center, Department of Pharmacology, INSERM, CIC-1901, UMR ICAN 1166, Pitié-Salpêtrière Hospital, Sorbonne Université, AP-HP, F-75013 Paris, France.
  • Urien S; Department of Pediatric and Perinatal Pharmacology, Necker Hospital, Université de Paris, AP-HP, F-75015 Paris, France.
  • Funck-Brentano C; Clinical Investigation Center, Department of Pharmacology, INSERM, CIC-1901, UMR ICAN 1166, Pitié-Salpêtrière Hospital, Sorbonne Université, AP-HP, F-75013 Paris, France.
  • Vantomme H; Clinical Investigation Center, Department of Pharmacology, INSERM, CIC-1901, UMR ICAN 1166, Pitié-Salpêtrière Hospital, Sorbonne Université, AP-HP, F-75013 Paris, France.
  • Garcelon N; Data Science Platform, INSERM UMR 1163, Imagine Institute, Université de Paris, AP-HP, F-75015 Paris, France.
  • Melki I; Infectious Disease and Internal Medicine Reference Center for Rheumatic, AutoImmune and Systemic Diseases in Children (RAISE), Department of General Pediatrics, Robert Debré Hospital, Nord-Université de Paris, AP-HP, F-75019 Paris, France.
  • Boistault M; Reference Center MARHEA, Department of Pediatric Nephrology, Imagine Institute, INSERM U1163, Necker Hospital, Université de Paris, AP-HP, F-75015 Paris, France.
  • Boyer O; Reference Center MARHEA, Department of Pediatric Nephrology, Imagine Institute, INSERM U1163, Necker Hospital, Université de Paris, AP-HP, F-75015 Paris, France.
  • Bader-Meunier B; Department of Pediatric Immunology, Hematology and Rheumatology, INSERM U1163, Imagine Institute, Necker Hospital, Université de Paris, AP-HP, F-75015 Paris, France.
Pharmaceuticals (Basel) ; 14(3)2021 Mar 17.
Article in En | MEDLINE | ID: mdl-33802811
ABSTRACT

BACKGROUND:

Hydroxychloroquine (HCQ) is an antimalarial agent given to patients with systemic lupus erythematosus (SLE) as first-line therapy. It alleviates childhood-onset systemic lupus erythematosus cSLE skin and musculoskeletal disease, decreasing disease activity and flares. HCQ concentration-effect relationships in children remains unknown. This study aimed to investigate the pharmacokinetics of HCQ and possible concentration-effect relationships.

METHODS:

HCQ blood concentrations and effects were obtained during clinical follow-up on different occasions. cSLE flares were defined using the SLE Disease Activity Index (SLEDAI); flare was denoted by a SLEDAI score > 6. Blood concentration was measured using high-performance liquid chromatography with fluorometric detection. Statistical analysis was performed using a nonlinear mixed-effect approach with the Monolix software.

RESULTS:

A total of 168 blood samples were obtained from 55 pediatric patients. HCQ apparent blood clearance (CL/F) was dependent on patients' bodyweight and platelet count. Patients with active cSLE had a lower mean blood HCQ concentration compared with inactive cSLE patients (536 ± 294 vs. 758 ± 490 ng/mL, p = 5 × 10-6). Among patients with HCQ blood concentration ≥750 ng/mL, 87.6% had inactive cSLE. Moreover, HCQ blood concentration was a significant predictor of disease status.

CONCLUSION:

We developed the first HCQ blood concentration-effect relationship for cSLE associated with active or non-active disease status. A prospective randomized study is necessary to confirm these results.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Clinical_trials / Prognostic_studies Language: En Journal: Pharmaceuticals (Basel) Year: 2021 Document type: Article Affiliation country: France

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Clinical_trials / Prognostic_studies Language: En Journal: Pharmaceuticals (Basel) Year: 2021 Document type: Article Affiliation country: France