Li Hanluo, Chen Cheng, Wang Yuansheng, Yi Wei, Guo Peipei, Yao Chenguang, Liu Jinbiao, Wei Yanhong, Hu Kanghong, Shang Xiaoke, Kang Sini
National "111" Center for Cellular Regulation and Molecular Pharmaceutics, Cooperative Innovation Center of Industrial Fermentation (Ministry of Education & Hubei Province), Hubei University of Technology, Wuhan, 430068, China.
Wuhan Vickor Medical Technology Co. Ltd., Building 3-3, 3-4, and 3-5, Zhaoshang·High-Tech Network Valley, No. 16, Luzling Third Road, East Lake High-Tech Development Zone, Wuhan (Wuhan Area of the Pilot Free Trade Zone), Wuhan, 430015, China.
Stem Cell Res Ther. 2025 May 19;16(1):249. doi: 10.1186/s13287-025-04377-4.
Diabetes mellitus (DM) is a grave autoimmune disorder because of no insulin self-generation. Currently, mainly clinical methods exist, serious adverse effects leading to stem cell therapy are considered. The mesenchymal stem cells (MSCs), require high differentiation capacity and are judged as crucial in DM treatment. The meta-analysis aimed to systemically analyze the particular types of MSCs which play a more important role in DM and which DM is treated more effectively.
A systematic review was conducted on the published literature, clinical trials and observational studies, utilizing databases such as PubMed, Embase, Cochrane and clinicaltrial.gov. RevMan software was adopted to draw Forest Plot and Funnel Plot, and subgroup analysis were employed to evaluate heterogeneity between different groups.
We identified the meta-analyses of 34 unique random controlled trials and divided our own systematic reviews into 8 groups. The MSCs were associated with placebo (OR = 2.79, 95% CI [1.63, 4.75]), Standard Clinical Treatment (SCT) (OR = 4.12, 95% CI [2.76, 6.14]), and monocyte (OR = 6.52, 95% CI [3.56, 9.48]). The comparison between Autologous MSCs and Allogenic MSCs (OR = 4.64, 95% CI [3.42, 6.31]), Autologous BMMSCs and other MSCs (OR = 5.28, 95% CI [3.64, 7.66]), Allogenic ASCs and UCMSCs (OR = 3.54, 95% CI [1.83, 6.86]), Type I DM and Type II DM (OR = 3.10, 95% CI [1.79, 5.38]), intravenous injection and other injections (OR = 4.81, 95% CI [3.34, 6.94]), diabetic foot ulcers and diabetic neurological disease (OR = 3.88,,95% CI [2.53,5.95]).
Current evidence suggests that MSCs hold significant potential for treating DM, demonstrating considerably high safety and efficacy. MSCs exhibit higher therapeutic benefits compared to monocytes, with autologous MSCs offering better clinical outcomes than allogenic sources. MSCs (BMMSCs) proved more effective than other types of MSCs. However, no significant differences were observed between adipose-derived MSCs (ASCs) and umbilical cord-derived MSCs (UCMSCs) in the allogeneic setting. Moreover, MSCs show more pronounced therapeutic effects in Type II DM, and the difference among the injection methods is minimally observed. In conclusion, the research scope on DM is relatively limited in this study and further research is necessary to improve the reliability of the estimates.
糖尿病(DM)是一种严重的自身免疫性疾病,因为无法自身产生胰岛素。目前,主要存在临床治疗方法,但会产生严重不良反应,因此干细胞疗法受到关注。间充质干细胞(MSCs)具有高分化能力,被认为在糖尿病治疗中至关重要。本荟萃分析旨在系统分析在糖尿病治疗中发挥更重要作用且能更有效治疗糖尿病的特定类型的间充质干细胞。
对已发表的文献、临床试验和观察性研究进行系统评价,利用PubMed、Embase、Cochrane和clinicaltrial.gov等数据库。采用RevMan软件绘制森林图和漏斗图,并进行亚组分析以评估不同组之间的异质性。
我们纳入了34项独特随机对照试验的荟萃分析,并将我们自己的系统评价分为8组。间充质干细胞与安慰剂(OR = 2.79,95% CI [1.63, 4.75])、标准临床治疗(SCT)(OR = 4.12,95% CI [2.76, 6.14])和单核细胞(OR = 6.52,95% CI [3.56, 9.48])相关。自体间充质干细胞与异体间充质干细胞的比较(OR = 4.64,95% CI [3.42, 6.31])、自体骨髓间充质干细胞与其他间充质干细胞(OR = 5.28,95% CI [3.64, 7.66])、异体脂肪干细胞与脐带间充质干细胞(OR = 3.54,95% CI [1.83, 6.86])、1型糖尿病与2型糖尿病(OR = 3.10,95% CI [1.79, 5.38])、静脉注射与其他注射方式(OR = 4.81,95% CI [3.34, 6.94])、糖尿病足溃疡与糖尿病神经病变(OR = 3.88,95% CI [2.53, 5.95])。
目前的证据表明,间充质干细胞在治疗糖尿病方面具有显著潜力,显示出相当高的安全性和有效性。与单核细胞相比,间充质干细胞具有更高的治疗效果,自体间充质干细胞比异体来源的临床效果更好。间充质干细胞(BMMSCs)被证明比其他类型的间充质干细胞更有效。然而,在异体情况下,脂肪来源的间充质干细胞(ASCs)和脐带来源的间充质干细胞(UCMSCs)之间未观察到显著差异。此外,间充质干细胞在2型糖尿病中显示出更明显的治疗效果,且注射方式之间的差异最小。总之,本研究中关于糖尿病的研究范围相对有限,需要进一步研究以提高估计的可靠性。