Suppr超能文献

用于局灶节段性肾小球硬化的其他免疫抑制剂。

Other immunosuppressive agents for focal segmental glomerulosclerosis.

作者信息

Ponticelli Claudio, Passerini Patrizia

机构信息

Division of Nephrology, IRCCS, Ospedale Maggiore, Milano, Italy.

出版信息

Semin Nephrol. 2003 Mar;23(2):242-8. doi: 10.1053/snep.2003.50023.

Abstract

A prolonged course with corticosteroids represents the first therapeutic approach for nephrotic patients with focal segmental glomerulosclerosis (FSGS). In patients with contraindications to steroids or in those who do not respond to steroids or cyclosporine, cytotoxic agents, mycophenolate mofetil (MMF), plasmapheresis, and low-density lipoprotein (LDL) apheresis have been tried as alternative treatments. A short-term treatment with cytotoxic agents often is ineffective in steroid-resistant patients However, an aggressive and prolonged treatment with cytotoxic agents combined with corticosteroids proved to be effective in more than half of steroid-resistant children. In adults, the response to cytotoxic agents was good in steroid-responsive patients, but was poor in steroid-resistant patients. Better results were observed when cytotoxic therapy was prolonged for several months. The problem with these drugs is that long-term immunosuppression may be complicated by severe side effects including a major risk for cancer. Uncontrolled studies reported that MMF can induce some reduction of proteinuria, but complete remission of proteinuria was rare and no data on long-term follow-up evaluation with this drug are available. Good results have been reported with plasmapheresis, immunoadsorption, and lipopheresis. However, all the reports were uncontrolled, small sized, and with short-term follow-up evaluation. In conclusion, there are several therapeutic options for patients who respond to steroids and have further relapses of nephrotic syndrome, but how to treat steroid-resistant patients is still a matter of debate. Nevertheless, a 6-month trial with cytotoxic agents or MMF can be offered to steroid-resistant patients to identify the few patients who respond to these agents. The preliminary results with plasmapheresis or lipopheresis are promising but further studies are needed to assess the role of these treatments.

摘要

长期使用皮质类固醇是局灶节段性肾小球硬化(FSGS)肾病患者的首要治疗方法。对于有类固醇禁忌证的患者,或对类固醇或环孢素无反应的患者,已尝试使用细胞毒性药物、霉酚酸酯(MMF)、血浆置换和低密度脂蛋白(LDL)去除术作为替代治疗。细胞毒性药物的短期治疗在类固醇抵抗患者中往往无效。然而,对细胞毒性药物联合皮质类固醇进行积极且长期的治疗在超过一半的类固醇抵抗儿童中被证明是有效的。在成人中,细胞毒性药物对类固醇反应性患者效果良好,但对类固醇抵抗患者效果不佳。当细胞毒性治疗延长数月时,观察到了更好的结果。这些药物的问题在于长期免疫抑制可能会因严重副作用而变得复杂,包括患癌症的重大风险。非对照研究报告称,MMF可使蛋白尿有所减少,但蛋白尿完全缓解的情况很少见,且尚无关于该药物长期随访评估的数据。血浆置换、免疫吸附和脂质分离术已报告有良好效果。然而,所有报告均为非对照、小样本且短期随访评估。总之,对于对类固醇有反应但肾病综合征进一步复发的患者有多种治疗选择,但如何治疗类固醇抵抗患者仍是一个有争议的问题。尽管如此,可对类固醇抵抗患者进行为期6个月的细胞毒性药物或MMF试验,以确定少数对这些药物有反应的患者。血浆置换或脂质分离术的初步结果很有前景,但需要进一步研究来评估这些治疗方法的作用。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验