Effects of mesenchymal stem cells in renovascular disease of preclinical and clinical studies: a systematic review and meta-analysis.

Effects of mesenchymal stem cells in renovascular disease of preclinical and clinical studies: a systematic review and meta-analysis.
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间充质干细胞在肾血管疾病中的作用的临床前和临床研究:系统评价和荟萃分析

DOI:
10.1038/s41598-022-23059-2
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发表时间:
2022-10-27
期刊:
影响因子:
4.6
通讯作者:
--
中科院分区:
综合性期刊3区
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--
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肾动脉狭窄(RAS)会导致严重的肾血管性高血压、肾功能恶化和心血管并发症的增加。根据最近的研究,间充质干细胞(MSCs)移植是改善RAS预后的一种有前途的治疗方法。Meta分析旨在评价MSC治疗RAS的疗效。我们检索了MEDLINE、Web of Science、Embase和Cochrane图书馆,检索时间为2022年10月5日。我们在这项荟萃分析中纳入了16项临床前研究和3项临床研究。在临床前研究中,综合结果表明,接受骨髓间充质干细胞处理的动物的收缩压(Smd = − 1.019,95%CI− 1.434至− 0.604,I2 = 37.2%,P = 0.000)、血清肌酐(Smd = − 1.112,95%CI− 1.932至− 0.293,I2 = 72.0%,P = 0.008)水平较低,血浆肾素活性( = − )为0.477,95%CI− 为0.913~0.042,I2 = 为43.4%,P = 为0.032。狭窄组肾血流量增加( = 0.774,95%CI− 0.351~1.197,I2 = 0%,P = 0.000),肾小球滤过率增加( = 1.825,95%CI 0.963~2.688,I2 = 72.6%,P = 0.000)。在临床研究中,MSC治疗可以减轻对侧肾(CLK)的皮质灌注和部分缺氧。综上所述,这项荟萃分析显示,骨髓间充质干细胞疗法可能是治疗RAS的一种有前途的疗法。然而,由于临床前研究和早期临床试验结果之间的差异,目前还不能推荐使用MSC治疗,需要更多高质量的随机对照临床试验来验证我们的结论并规范MSCs方案。
Renal artery stenosis (RAS) causes severe renovascular hypertension, worsening kidney function, and increased cardiovascular morbidity. According to recent studies, mesenchymal stem cells (MSCs) administration is a promising therapy for the improvement of RAS outcomes. The meta-analysis aims to evaluate the therapeutic effects of MSC therapy on RAS. We performed a search in MEDLINE, Web of Science, Embase, and Cochrane Library from inception to 5, October 2022. We included 16 preclinical and 3 clinical studies in this meta-analysis. In preclinical studies, the pooled results indicated that animals treated with MSCs had lower levels of systolic blood pressure (SBP) (SMD = − 1.019, 95% CI − 1.434 to − 0.604, I2 = 37.2%, P = 0.000), serum creatinine (Scr) (SMD = − 1.112, 95% CI − 1.932 to − 0.293, I2 = 72.0%, P = 0.008), and plasma renin activity (PRA) (SMD = − 0.477, 95% CI − 0.913 to 0.042, I2 = 43.4%, P = 0.032). The studies also revealed increased levels of renal blood flow (RBF) in stenotic kidney (STK) (SMD = 0.774, 95% CI − 0.351 to 1.197, I2 = 0%, P = 0.000) and the glomerular filtration rate (GFR) of STK (SMD = 1.825, 95% CI 0.963 to 2.688, I2 = 72.6%, P = 0.000). In clinical studies, the cortical perfusion and fractional hypoxia of the contralateral kidney (CLK) were alleviated by MSC therapy. Taken together, this meta-analysis revealed that MSCs therapy might be a promising treatment for RAS. However, due to the discrepancy between preclinical studies and early clinical trials outcomes, MSC therapy couldn’t be recommended in clinical care for the moment, more high-quality randomized controlled clinical trials are needed to validate our conclusions and standardize MSCs protocols.
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