Clinical Efficacy of Induction Therapy Using Mycophenolate Mofetil for Diffuse Proliferative Lupus Nephritis
Wei Xin
Abstract:Objective To evaluate clinical efficacy and safety of treating diffuse proliferative lupus nephritis (LN)with mycophenolate mofetil(MMF). Methods 74 patients diagnosed as LN by renal biopsy were selected,clini-cal types of whom were type Ⅳ with formation of crescents(≥15% ). They were randomly assigned to control group and treatment group with 37 cases in each group. Intermittent intravenous cyclophosphamide(Ⅳ - CTX)and MMF in-duction therapy were used in two groups respectively. Remission rate differences were compared 6 months after induc-tion therapy. Serum immune indicators were measured and safety of medication was evaluated. Results Total remis-sion rate was higher in treatment group than that in control group after 6 months induction in 60 patients with crescents< 50%(P < 0. 05). There was no significant difference in total remission rate between treatment group and control group in 14 patients with crescents≥50%(P > 0. 05). C3 recovery rate was significantly better in treatment group than that in control group 6 months after induction(P < 0. 05). There was no significant difference in ds - DNA nega-tive conversion rate and complement C4 recovery rate between the two groups(P > 0. 05). There were no serious com-plications in the two groups during treatment. There were less patients with white blood cells reduction in treatment group than that in control group(P < 0. 05). Conclusion MMF induction treatment can promote remission rate and has less adverse reactions for patients with type Ⅳ LN with formation of crescents.
Keywords:Diffuse proliferative lupus nephritisMycophenolate mofetilCyclophosphamide
Publication Date:2016-01-01
Online Publishing Date:2025-08-15(First online date of this platform, not the publication date of the document)
Pages:3( 116-118 )
