Wu Qian, Zheng Shuai, Qin Yao, Zheng Xuqin, Chen Heng, Yang Tao, Zhang Mei
Department of Endocrinology, The First Affiliated Hospital with Nanjing Medical University, Nanjing Medical University, Nanjing, 210029, China.
Department of Endocrinology, Taikang Xianlin Drum Tower Hospital, Nanjing University School of Medicine, Nanjing, 210046, China.
Endocr J. 2020 Aug 28;67(8):827-840. doi: 10.1507/endocrj.EJ20-0050. Epub 2020 May 23.
Stem cells (SCs) therapy is a new promising therapeutic modality for type 1 diabetes (T1DM). We performed a systematic review and meta-analysis to evaluate the efficacy and safety of stem cells transplantation (SCT) in patients with T1DM. We searched five literature databases (MEDLINE, EMBASE, Web of Science, WanFang and CENTRAL) up to 31 October 2019. 29 studies (487 patients with T1DM) were included in our meta-analysis. There was no substantial publication bias. Meta-analysis showed the SCT had significant effect to decrease HbA1c (SMD, 1.40; 95% CI, 0.93 to 1.86; p < 0.00001; I = 89%) and to improve C-peptide levels (SMD, -0.62; 95% CI, -1.22 to -0.02; p = 0.04; I = 92%) at 1 year follow-up. Subgroup analyses showed the heterogeneity level of the results was high. Significant improvement of metabolic outcomes was observed in the subgroups of mesenchymal stem cells (MSCs) combined with hematopoietic stem cells (HSCs) and HSCs. The older age showed significant association with the efficacy in HSCs subgroup. The higher GADA positive rate before treatment also significantly associated with the decrease of daily insulin requirement. The transient insulin independence rate at last follow-up was 9.6 per 100 person-years (95% CI: 5.8-13.5%). The mean length of insulin independence was 15.6 months (95% CI: 12.3-18.9). The mortality of SCT was 3.4% (95% CI: 2.1-5.5%). Therefore, SCT is an efficacious and safe method for treating patients with T1DM especially in the subgroups of MSCs + HSCs and HSCs. Well designed, double blind and randomized controlled trails with large sample size and long-term follow-up are needed for further evaluation.
干细胞(SCs)疗法是1型糖尿病(T1DM)一种新的、有前景的治疗方式。我们进行了一项系统评价和荟萃分析,以评估干细胞移植(SCT)治疗T1DM患者的疗效和安全性。我们检索了截至2019年10月31日的五个文献数据库(MEDLINE、EMBASE、Web of Science、万方和CENTRAL)。我们的荟萃分析纳入了29项研究(487例T1DM患者)。不存在实质性的发表偏倚。荟萃分析显示,在1年随访时,SCT对降低糖化血红蛋白(HbA1c)有显著效果(标准化均数差[SMD],1.40;95%可信区间[CI],0.93至1.86;p<0.00001;I² = 89%),并能改善C肽水平(SMD,-0.62;95% CI,-1.22至-0.02;p = 0.04;I² = 92%)。亚组分析显示结果的异质性水平较高。在间充质干细胞(MSCs)联合造血干细胞(HSCs)和HSCs亚组中观察到代谢结果有显著改善。年龄较大在HSCs亚组中与疗效显著相关。治疗前较高的谷氨酸脱羧酶自身抗体(GADA)阳性率也与每日胰岛素需求量的降低显著相关。最后随访时的短暂胰岛素停用率为每100人年9.6%(95% CI:5.8 - 13.5%)。胰岛素停用的平均时长为15.6个月(95% CI:12.3 - 18.9)。SCT死亡率为3.4%(95% CI: