Li Zhi-Hui, Xia Tuan-Hong, Duan Cui-Rong, Wu Tian-Hui, Xun Mai, Yin Yan, Ding Yun-Feng, Zhang Yi, Zhang Liang
Department of Nephrology, Hunan Children's Hospital, Changsha 410007, China.
Zhongguo Dang Dai Er Ke Za Zhi. 2015 Mar;17(3):222-6.
To study the significance of trace immunoglobulin M (IgM) deposits in glomerular mesangium in children with minimal change primary nephrotic syndrome (PNS).
One hundred and six children who were clinically diagnosed with PNS and pathologically diagnosed with minimal change disease (MCD) and trace deposition of IgM in renal tissues were enrolled as subjects. Eighty-one PNS children with MCD but no deposition of immune complexes were used as the control group. The clinical characteristics and efficacies of glucocorticoids and immunosuppressants were retrospectively analyzed in the two groups. All patients were given full-dose prednisone by oral administration, and patients with glucocorticoid resistance or frequent relapses were additionally given immunosuppressants.
The incidence of glucocorticoid resistance in the IgM deposit group was significantly higher than that in the control group (27.2% vs 12.3%; P<0.05). The incidence of frequent relapses in the IgM deposit group was also significantly higher than that in the control group (48.1% vs 10.4%; P<0.05). The complete remission rate for glucocorticoid-resistant patients treated with prednisone combined with mycophenolate mofetil (MMF) was 68% and 62% respectively in the IgM deposit and control groups (P>0.05). The relapse frequency in patients with frequent relapses was significantly reduced in both groups after treatment with prednisone and MMF in combination (P<0.05).
Trace deposition of IgM in renal tissues may be an important factor for glucocorticoid resistance and frequent relapses in PNS children with MCD. Prednisone combined with MMF may be a better choice in the treatment of patients with glucocorticoid resistance or frequent relapses.
探讨原发性微小病变型肾病综合征(PNS)患儿肾小球系膜区微量免疫球蛋白M(IgM)沉积的意义。
选取106例临床诊断为PNS且病理诊断为微小病变病(MCD)、肾组织有微量IgM沉积的患儿作为研究对象。选取81例MCD且无免疫复合物沉积的PNS患儿作为对照组。回顾性分析两组患儿的临床特征以及糖皮质激素和免疫抑制剂的疗效。所有患儿均口服足量泼尼松,对糖皮质激素抵抗或频繁复发的患儿加用免疫抑制剂。
IgM沉积组糖皮质激素抵抗发生率显著高于对照组(27.2% 对12.3%;P<0.05)。IgM沉积组频繁复发发生率也显著高于对照组(48.1% 对10.4%;P<0.05)。IgM沉积组和对照组中泼尼松联合霉酚酸酯(MMF)治疗糖皮质激素抵抗患儿的完全缓解率分别为68%和62%(P>0.05)。两组频繁复发患儿经泼尼松和MMF联合治疗后复发频率均显著降低(P<0.05)。
肾组织微量IgM沉积可能是MCD型PNS患儿糖皮质激素抵抗和频繁复发的重要因素。泼尼松联合MMF可能是治疗糖皮质激素抵抗或频繁复发患儿的较好选择。