ORIGINAL ARTICLE
Prospective study of low-dose cyclosporine A in patients with refractory lupus nephritis
Authors
Hiroe Ogawa1, Hideto Kameda1, Hayato Nagasawa1, Naoya Sekiguchi1, Hirofumi Takei1, Kensei Tsuzaka1, Koichi Amano1 and Tsutomu Takeuchi1
- Department of Internal Medicine, Division of Rheumatology and Clinical Immunology, Saitama Medical Center, Saitama Medical University, 1981 Kamoda, Tsujido-machi, Kawagoe 350-8550, Japan
Received:
29 May 2006
Accepted:
10 November 2006
Full Text
Download (PDF)
Abstract
We evaluated the efficacy and safety of low-dose cyclosporine A (CsA) in patients with refractory lupus nephritis. Nine patients with systemic lupus erythematosus who had lupus nephritis resistant to previous treatment with glucocorticoids and immunosuppressants other than CsA were enrolled in a prospective, open-label study. All patients initially received 2.5mg/kg per day of CsA; the dosage was adjusted to reach a blood trough level of 80-150ng/ml. The urinary protein concentration decreased significantly 2 weeks after the initiation of treatment. After 30 weeks of CsA treatment, the mean urinary protein concentration was more than 50% lower than the baseline value, and urinary casts had decreased significantly. There were no significant changes in the levels of serum creatinine, serum anti-double-stranded DNA antibodies, or CH50 during any part of the study. The dose of glucocorticoids was significantly tapered by approximately 50%, without any disease flare. Hypertension developed in one patient, but was controlled with antihypertensive agents. Our results suggest that low-dose CsA therapy is an effective and less toxic alternative to conventional cyclophosphamide therapy for the management of refractory lupus nephritis.
Key words
Cyclosporine A - Immunosuppressive drugs - Lupus nephritis - Systemic lupus erythematosus