Hebei Medical University-National University of Ireland Galway Stem Cell Research Center, Hebei Medical University, Shijiazhuang, 050017, Hebei Province, China.
Hebei Research Center for Stem Cell Medical Translational Engineering, Hebei Medical University, Shijiazhuang, 050017, Hebei Province, China.
Stem Cell Res Ther. 2023 Jan 5;14(1):3. doi: 10.1186/s13287-022-03231-1.
Alzheimer's disease (AD) is a common progressive neurodegenerative disease characterized by memory impairments, and there is no effective therapy. Neural stem/progenitor cell (NSPC) has emerged as potential novel therapy for AD, and we aim to explore whether neural stem/progenitor cell therapy was effective for rodent models of AD.
We searched PubMed, Embase, Cochrane Library and Web of Science up to December 6, 2022. The outcomes included cognitive function, pathological features and BDNF. The GetData Graph Digitizer software (version 2.26) was applied to extract numerical values, and RevMan 5.3 and Stata 16 were used to analyze data. The SYRCLE risk of bias tool was used to assess study quality.
We evaluated 22 mice studies and 8 rat studies. Compared to control groups, cognitive function of NSPC groups of both mice studies (SMD = - 1.96, 95% CI - 2.47 to - 1.45, I = 75%, P < 0.00001) and rat studies (SMD = - 1.35, 95% CI - 2.11 to - 0.59, I = 77%, P = 0.0005) was apparently improved. In mice studies, NSPC group has lower Aβ deposition (SMD = - 0.96, 95% CI - 1.40 to - 0.52, P < 0.0001) and p-tau level (SMD = - 4.94, 95% CI - 7.29 to - 2.95, P < 0.0001), higher synaptic density (SMD = 2.02, 95% CI 0.50-3.55, P = 0.009) and BDNF (SMD = 1.69, 95% CI 0.61-2.77, P = 0.002). Combined with nanoformulation (SMD = - 1.29, 95% CI - 2.26 to - 0.32, I = 65%, P = 0.009) and genetically modified (SMD = - 1.29, 95% CI - 1.92 to - 0.66, I = 60%, P < 0.0001) could improve the effect of NSPC. In addition, both xenogeneic and allogeneic transplant of NSPC could reverse the cognitive impairment of AD animal models.
Our results suggested that NSPC therapy could improve the cognitive function and slow down the progression of AD. Due to the limitations of models, more animal trials and clinical trials are needed.
阿尔茨海默病(AD)是一种常见的进行性神经退行性疾病,其特征是记忆障碍,目前尚无有效的治疗方法。神经干细胞/祖细胞(NSPC)已成为 AD 的潜在新型治疗方法,我们旨在探讨 NSPC 治疗是否对 AD 啮齿动物模型有效。
我们检索了 PubMed、Embase、Cochrane 图书馆和 Web of Science 截至 2022 年 12 月 6 日的文献。结局指标包括认知功能、病理特征和 BDNF。使用 GetData Graph Digitizer 软件(版本 2.26)提取数值,采用 RevMan 5.3 和 Stata 16 进行数据分析。使用 SYRCLE 偏倚风险工具评估研究质量。
我们评估了 22 项小鼠研究和 8 项大鼠研究。与对照组相比,NSPC 组的认知功能在两项小鼠研究(SMD = -1.96,95%CI -2.47 至 -1.45,I = 75%,P < 0.00001)和两项大鼠研究(SMD = -1.35,95%CI -2.11 至 -0.59,I = 77%,P = 0.0005)中均明显改善。在小鼠研究中,NSPC 组的 Aβ 沉积(SMD = -0.96,95%CI -1.40 至 -0.52,P < 0.0001)和 p-tau 水平(SMD = -4.94,95%CI -7.29 至 -2.95,P < 0.0001)更低,突触密度(SMD = 2.02,95%CI 0.50-3.55,P = 0.009)和 BDNF(SMD = 1.69,95%CI 0.61-2.77,P = 0.002)更高。与纳米制剂(SMD = -1.29,95%CI -2.26 至 -0.32,I = 65%,P = 0.009)和基因修饰(SMD = -1.29,95%CI -1.92 至 -0.66,I = 60%,P < 0.0001)联合使用可提高 NSPC 的效果。此外,NSPC 的异种和同种移植均可逆转 AD 动物模型的认知障碍。
我们的结果表明,NSPC 治疗可改善 AD 患者的认知功能并减缓疾病进展。由于模型的局限性,还需要更多的动物试验和临床试验。