Efficacy of Umbilical Cord-Derived Mesenchymal Stem Cells in the Treatment of Type 2 Diabetes Assessed by Retrospective Continuous Glucose Monitoring.

IF 5.4 2区 医学 Q1 CELL & TISSUE ENGINEERING Stem Cells Translational Medicine Pub Date : 2023-12-18 DOI:10.1093/stcltm/szad060
Li Zang, Yijun Li, Haojie Hao, Jiejie Liu, Qian Zhang, Fei Gao, Haibin Wang, Yulong Chen, Weijun Gu, Jin Du, Junhua Meng, Saichun Zhang, Zhaohui Lyu, Jingtao Dou, Yiming Mu
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Abstract

Umbilical cord-derived mesenchymal stem cells (UC-MSCs) have been proved a promising clinical strategy for the treatment of diabetes, and time in range (TIR) has been demonstrated a new metric of glycemic control links to diabetes complications. To further assess the therapeutic effect of UC-MSCs on TIR, a phase II study investigating the efficacy of UC-MSCs in Chinese adults with type 2 diabetes (T2D) assessed by retrospective continuous glucose monitoring (CGM) was conducted. In this randomized and placebo-controlled trial, a total of 73 patients were randomly assigned to receive intravenous infusion of UC-MSCs (n = 37) or placebo (n = 36) 3 times at 4-week intervals and followed up for 48 weeks. The primary endpoint was the changes in TIR and glycosylated hemoglobin (HbA1c). TIR and HbA1c were both significantly improved in UC-MSCs and placebo groups after 48 weeks of therapy compared with baseline. Compared with placebo group, UC-MSCs group exhibited more pronounced changes at 9 and 48 weeks from baseline in TIR (26.54 vs. 15.84 and 21.36 vs. 6.32) and HbA1c (-1.79 vs. -0.96 and -1.36 vs. -0.51). More patients in UC-MSCs group achieved the glycemic control target of TIR ≥ 70% and HbA1c < 7% at 9 and 48 weeks than in placebo group (59.5% vs. 27.8% and 43.2% vs. 11.1%). The C-peptide area under the curve (AUCC-pep) was an independent risk factor associated with efficacy in T2D undergoing UC-MSCs intervention. These results illustrate that UC-MSCs administration via intravenous infusion is an effective approach for ameliorating TIR.

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通过回顾性连续血糖监测评估脐带间充质干细胞治疗2型糖尿病的疗效。
脐带来源的间充质干细胞(UC-MSCs)已被证明是治疗糖尿病的一种很有前途的临床策略,时间范围(TIR)已被证实是血糖控制与糖尿病并发症联系的一种新指标。为了进一步评估UC间充质干细胞对TIR的治疗效果,进行了一项II期研究,通过回顾性连续血糖监测(CGM)评估UC间质干细胞在中国成人2型糖尿病(T2D)患者中的疗效。在这项随机和安慰剂对照试验中,共有73名患者被随机分配接受静脉输注UC MSCs(n = 37)或安慰剂(n = 36)间隔4周3次,随访48周。主要终点是TIR和糖化血红蛋白(HbA1c)的变化。与基线相比,治疗48周后,UC MSC和安慰剂组的TIR和HbA1c均显著改善。与安慰剂组相比,UC MSCs组在第9周和第48周的TIR(26.54 vs.15.84和21.36 vs.6.32)和HbA1c(-1.79 vs.-0.96和-1.36 vs.-0.51)发生了更明显的变化 ≥ 70%和HbA1c
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来源期刊
Stem Cells Translational Medicine
Stem Cells Translational Medicine CELL & TISSUE ENGINEERING-
CiteScore
12.90
自引率
3.30%
发文量
140
审稿时长
6-12 weeks
期刊介绍: STEM CELLS Translational Medicine is a monthly, peer-reviewed, largely online, open access journal. STEM CELLS Translational Medicine works to advance the utilization of cells for clinical therapy. By bridging stem cell molecular and biological research and helping speed translations of emerging lab discoveries into clinical trials, STEM CELLS Translational Medicine will help move applications of these critical investigations closer to accepted best patient practices and ultimately improve outcomes. The journal encourages original research articles and concise reviews describing laboratory investigations of stem cells, including their characterization and manipulation, and the translation of their clinical aspects of from the bench to patient care. STEM CELLS Translational Medicine covers all aspects of translational cell studies, including bench research, first-in-human case studies, and relevant clinical trials.
期刊最新文献
Endostatin-expressing endometrial mesenchymal stem cells inhibit angiogenesis in endometriosis through the miRNA-21-5p/TIMP3/PI3K/Akt/mTOR pathway. Tailoring cell therapies for diabetic metabolic phenotypes: a comparative study on the efficacy of various umbilical cord-derived cell regimens. Human umbilical cord mesenchymal stem cells small extracellular vesicles-derived miR-370-3p inhibits cervical precancerous lesions by targeting DHCR24. Exploring mesenchymal stem cells homing mechanisms and improvement strategies. Progranulin enhances the engraftment of transplanted human iPS cell-derived cerebral neurons.
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