Bone Marrow-Derived Stem Cells for Patients with Liver Cirrhosis: A Systematic Review and Meta-analysis

Bone Marrow-Derived Stem Cells for Patients with Liver Cirrhosis: A Systematic Review and Meta-analysis
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骨髓干细胞治疗肝硬化患者:系统评价和荟萃分析

DOI:
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发表时间:
2021
期刊:
Turk J Gastroenterol
影响因子:
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通讯作者:
Li Ban
Li Ban
中科院分区:
其他
文献类型:
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作者:
Shi Ouyang;Lei Ouyang;Yuanqi Li;Yaling Ye;Li Ban

文献摘要

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背景资料:迄今为止,研究显示骨髓源性干细胞(BMDSC)治疗肝硬化患者的结果不一致。本研究旨在比较BMDSC与标准疗法治疗肝硬化的有效性和安全性。方法:从PubMed、Embase和科克伦图书馆检索自成立至2018年4月的文献。指标包括终末期肝病模型(MELD)、丙氨酸转氨酶(ALT)、白蛋白、总胆红素(TBIL)、凝血酶原时间(PT)、Child-Pugh评分和全因死亡率。结果:共纳入9篇研究,共424例肝硬化患者。BMDSC治疗与3个月内较低的MELD相关(P = .010),而6个月后对MELD无显著影响(P = .074)。BMDSC和标准治疗在3个月内(P = 0.336)和6个月后(P = 0.379)对ALT的影响were.no差异。BMDSC在3个月内(P = 0.196)和6个月后(P = 0.840)不影响白蛋白水平。BMDSC在3个月内降低了TBIL水平(P = .037),6个月后与TBIL水平无关(P = .914)。BMDSC和标准治疗之间没有差异。PT在3个月内(P = 0.167)和6个月后(P = 0.484)。3个月内(P = .342)和6个月后的Child-Pugh评分。(P = .133)与肝硬化患者的BMDSC治疗无关。最后,与标准治疗相比,BMDSC与全因死亡风险无关(P = 0.622)。结论:与标准治疗相比,BMDSC治疗肝硬化患者可改善短期MELD和TBIL,但不能降低死亡风险。
Background: To date, studies have shown inconsistent results of treatment with bone marrow-derived stem cells (BMDSC) for patients.with liver cirrhosis. This study aims to compare the efficacy and safety of BMDSC and standard therapy for liver cirrhosis..Methods: Articles from PubMed, Embase, and the Cochrane library were searched from inception to April 2018. The index included Model.for End-stage Liver Disease (MELD), alanine aminotransferase (ALT), albumin, total bilirubin (TBIL), prothrombin time (PT), Child–Pugh.score, and all-cause mortality..Results: A total of 9 studies with a total of 424 patients with liver cirrhosis were included in final meta-analysis. BMDSC therapy was.associated with lower MELD within 3 months (P = .010), while it had no significant impact on MELD after 6 months (P = .074). There were.no differences between BMDSC and standard therapy for ALT within 3 months (P = .336) and after 6 months (P = .379). BMDSC did not.affect albumin level within 3 months (P = .196) and after 6 months (P = .840). BMDSC reduced the TBIL level within 3 months (P = .037).and was not associated with the TBIL level after 6 months (P = .914). There were no differences between BMDSC and standard therapy.for PT within 3 months (P = .167) and after 6 months (P = .484). The Child–Pugh scores within 3 months (P = .342) and after 6 months.(P = .133) were not associated with BMDSC treatment for liver cirrhosis patients. Finally, the BMDSC was not associated with the risk of.all-cause mortality, as compared with standard therapy (P = .622)..Conclusions: BMDSC treatment for patients with liver cirrhosis could improve short-term MELD and TBIL, but not the risk of mortality,.as compared with standard therapy.