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Clinical Efficacy of Mycophenolic Acid in the Treatment of Lupus Nephritis

黴菌酚酸(mycophenolic acid)治療狼瘡性腎炎的臨床經驗

摘要


目的:近期的研究已證實在狼瘡性腎炎急性誘導期使用口服黴菌酚酸(MMF或MPA),其效果和環磷醯胺(CYC)脈衝療法類似或更好但副作用顯著減少。在台灣,探討狼瘡性腎炎病患的療效及安全治療劑量之相關研究很少。方法:收集門診37位狼瘡腎炎患者,依據其服用黴菌酚酸劑量分成兩組並收集實驗室檢查報告,包括全血細胞計數、血清肌酸酐、白蛋白、補體、抗雙鏈去氧核糖核酸抗體,及二十四小時尿蛋白。回溯性分析這二組病患使用MMF/MPA類藥物後之治療反應及副作用。結果:每日口服MMF 1克或MPA 720毫克這一組有26人,另一組每日口服MMF 2 克或MPA 1440 毫克有11人。在這兩組中,第12和24週各有1人達到完全緩解(CR)。第一組在第12週達到部分緩解(PR)有33%,第24週有43%。第二組在第12週達到部分緩解(PR)有67%,第24週有75%。這兩組的血清肌酸酐下降百分比在第12週為5%和20% (p=0.02),第24週為0%和26% (p=0.007)。除了血清肌酸酐下降百分比之外,這兩組數據在二十四小時尿蛋白、血清白蛋白、補體、和抗雙鏈去氧核糖核酸抗體都未達到統計學上的意義,但卻有明顯改善的趨勢,而且都沒有嚴重的副作用。結論:我們的研究發現使用MMF 2g/day或MPA 1440mg/day治療的這一組病人,有較好的療效。

並列摘要


Objective: To demonstrate the efficacy and safety of mycophenolic acid (MPA) as an induction therapy for lupus nephritis (LN) due to the availability of limited data in Taiwan. Materials and Methods: This retrospective study included subjects who were treated with MPA for LN at the rheumatology outpatient clinic in Chang Gung Memorial Hospital-Kaohsiung and Linkou Medical Centers between January 2005 and July 2007. Subjects were categorized into 2 groups according to the dose of MPA. We measured complete blood count (CBC), levels of serum creatinine (Scr), albumin, complement (C3 and C4), anti-double-stranded DNA (anti-dsDNA) antibody titer, and daily urinary protein at the baseline, 12 weeks, and 24 weeks after MPA therapy, and therapeutic response and adverse effects were analyzed. Results: A total of 37 subjects were enrolled: 26 in group Ⅰ (Gr Ⅰ) and Ⅱ in group Ⅱ (Gr Ⅱ). At both 12 and 24 weeks, 1 subject from each group achieved a complete response (CR). One-third of the subjects in Gr Ⅰ achieved partial response (PR) at 12 weeks and 43% achieved it at 24 weeks, while 67% and 75% of subjects in Gr Ⅱ achieved CR at 12 and 24 weeks, respectively. Except for a significant improvement in percent changes in the Scr levels in Gr Ⅱ, the changes in the daily urinary protein, serum albumin, complement, and anti-dsDNA levels of both the groups were not statistically significant but showed a similar trend of improvement. Only one serious adverse event occurred in each group. Conclusions: Compared to treatment with mycophenolate mofetil (MMF) at 1 g/day or MPA at 720 mg/day, treatment with either MMF at 2 g/day or MPA at 1440 mg/day had a better therapeutic effect on LN. In general, the regimen followed in our investigation was safe.

並列關鍵字

Mycophenolic acid lupus nephritis

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