Drs. Zahr and Arnaud contributed equally to this work.
Systemic Lupus Erythematosus
Mycophenolic acid area under the curve correlates with disease activity in lupus patients treated with mycophenolate mofetil
Article first published online: 6 APR 2010
Copyright © 2010 by the American College of Rheumatology
Arthritis & Rheumatism
Volume 62, Issue 7, pages 2047–2054, July 2010
How to Cite
Zahr, N., Arnaud, L., Marquet, P., Haroche, J., Costedoat-Chalumeau, N., Hulot, J.-S., Funck-Brentano, C., Piette, J.-C. and Amoura, Z. (2010), Mycophenolic acid area under the curve correlates with disease activity in lupus patients treated with mycophenolate mofetil. Arthritis & Rheumatism, 62: 2047–2054. doi: 10.1002/art.27495
- Issue published online: 29 JUN 2010
- Article first published online: 6 APR 2010
- Manuscript Accepted: 30 MAR 2010
- Manuscript Received: 23 DEC 2009
Mycophenolic acid (MPA) is the active metabolite of mycophenolate mofetil (MMF), which is widely used to treat systemic lupus erythematosus (SLE). In transplantation, MPA area under the plasma concentration–time curve from 0 to 12 hours (MPA AUC0–12) is correlated with clinical outcome. We undertook the present study to assess possible relationships between SLE activity and MPA AUC0–12.
Using a Bayesian estimator, MPA AUC0–12 was determined in 71 consecutive SLE patients (61 women and 10 men; mean ± SD age 34 ± 10 years) receiving a stable MMF dose. On the same day, SLE activity was assessed using the SLE Disease Activity Index (SLEDAI; active disease defined as a SLEDAI score ≥6) and the British Isles Lupus Assessment Group (BILAG) index (active disease defined as BILAG A or B).
Two groups were studied: patients with active SLE (mean ± SD SLEDAI score 11.6 ± 4.4; n = 26) and patients with inactive SLE (mean ± SD SLEDAI score 1.9 ± 1.6; n = 45). MPA AUC0–12 correlated weakly with the dose of MMF (r = 0.33, P = 0.005). Mean ± SD MPA AUC0–12 in the group with active SLE was significantly lower than that in the group with inactive SLE (26.8 ± 13.6 μg.hour/ml versus 46.5 ± 16.3 μg.hour/ml; P < 0.0001). MPA AUC0–12 was negatively correlated with the SLEDAI (r = –0.64, P < 0.0001). In multivariate analysis, MPA AUC0–12 was the sole parameter associated with SLE activity (odds ratio 0.89 [95% confidence interval 0.83–0.96], P = 0.002). The MPA AUC0–12 threshold value of 35 μg.hour/ml was associated with the lowest risk of active SLE.
Our data show that SLE activity is strongly correlated with MPA AUC0–12. An individualized dosing regimen of MMF, with a target AUC0–12 of 35 μg.hour/ml, should be considered for SLE patients.