Xu Lin, Liu Zhong-Cheng, Guan Guang-Ju, Lv Xue-Ai, Luo Qing
Department of Nephrology, The Second Hospital of Shandong University, Shandong University, Jinan, China; Department of Nephrology, Taian Central Hospital, Taian, China.
Department of Neurosurgery, The First People's Hospital of Taian, Taian, China.
Kaohsiung J Med Sci. 2014 Aug;30(8):390-5. doi: 10.1016/j.kjms.2014.04.002. Epub 2014 May 27.
The aim of the present study was to evaluate the efficacy of cyclosporine A (CsA) combined with medium/low dose prednisone in the treatment of progressive immunoglobulin A nephropathy (IgAN). Ninety-six patients who satisfied the inclusion criteria were enrolled in a prospective controlled clinical study. They were assigned into two groups and initially given either 0.6-0.8 mg/kg/day prednisone (maximum 40 mg/day) plus 3 mg/kg/day CsA (CsA group), or 1 mg/kg/day prednisone (maximum 60 mg/day) alone (steroid group). During therapy, the dose of prednisone was reduced in both groups and the dose of CsA was gradually tailed off over the first 3 months and maintained at 2 mg/kg/day in the CsA group. Urinary protein excretion, serum biochemical indexes, clinical efficacy and side effects of CsA were assayed. A significant decline in mean 24-hour urinary protein excretion (p < 0.05) was observed 1 month after treatment in patients in the CsA group, which was observed 2 months after treatment in the steroid group. The decline in mean 24-hour urinary protein excretion in the CsA group was more significant than in the steroid group. Serum albumin level increased significantly in the CsA group 2 months after therapy (p < 0.05). Moreover, at the end of the course, a higher remission rate was observed in patients with Lee's Grade III IgAN after combined treatment with prednisone and CsA (p < 0.05). No significant difference in clinical efficacy was observed in patients with Lee's Grade IV and Grade V IgAN between the two groups (p > 0.05). CsA at a dose of 2-3 mg/kg/day in combination with medium/low dose prednisone was effective in inducing remission of IgAN, especially for patients with Lee's Grade III IgAN, and is a safe and effective choice for short-term treatment of patients with progressive IgAN.
本研究旨在评估环孢素A(CsA)联合中/低剂量泼尼松治疗进行性免疫球蛋白A肾病(IgAN)的疗效。96例符合纳入标准的患者被纳入一项前瞻性对照临床研究。他们被分为两组,初始分别给予0.6 - 0.8 mg/kg/天泼尼松(最大剂量40 mg/天)加3 mg/kg/天CsA(CsA组),或仅给予1 mg/kg/天泼尼松(最大剂量60 mg/天)(激素组)。治疗期间,两组泼尼松剂量均减少,CsA组在前3个月逐渐减量并维持在2 mg/kg/天。检测尿蛋白排泄、血清生化指标、CsA的临床疗效及副作用。CsA组患者治疗1个月后平均24小时尿蛋白排泄显著下降(p < 0.05),激素组在治疗2个月后出现该情况。CsA组平均24小时尿蛋白排泄的下降幅度比激素组更显著。治疗2个月后CsA组血清白蛋白水平显著升高(p < 0.05)。此外,疗程结束时,泼尼松和CsA联合治疗后Lee氏III级IgAN患者的缓解率更高(p < 0.05)。两组Lee氏IV级和V级IgAN患者的临床疗效无显著差异(p > 0.05)。2 - 3 mg/kg/天的CsA联合中/低剂量泼尼松能有效诱导IgAN缓解,尤其对于Lee氏III级IgAN患者,是进行性IgAN患者短期治疗的安全有效选择。