Suppr超能文献

自体骨髓单个核细胞移植治疗失代偿期酒精性肝病患者的随机对照研究。

Autologous bone marrow mononuclear cell transplantation in patients with decompensated alcoholic liver disease: a randomized controlled trial.

机构信息

Division of Gastroenterology and Hepatology, University Hospitals and Faculty of Medicine, Geneva, Switzerland.

出版信息

PLoS One. 2013;8(1):e53719. doi: 10.1371/journal.pone.0053719. Epub 2013 Jan 14.

Abstract

OBJECTIVE

Impaired liver regeneration is associated with a poor outcome in patients with decompensated alcoholic liver disease (ALD). We assessed whether autologous bone marrow mononuclear cell transplantation (BMMCT) improved liver function in decompensated ALD.

DESIGN

58 patients (mean age 54 yrs; mean MELD score 19, all with cirrhosis, 81% with alcoholic steatohepatitis at baseline liver biopsy) were randomized early after hospital admission to standard medical therapy (SMT) alone (n = 30), including steroids in patients with a Maddrey's score ≥32, or combined with G-CSF injections and autologous BMMCT into the hepatic artery (n = 28). Bone marrow cells were harvested, isolated and reinfused the same day. The primary endpoint was a ≥3 points decrease in the MELD score at 3 months, corresponding to a clinically relevant improvement in liver function. Liver biopsy was repeated at week 4 to assess changes in Ki67+/CK7+ hepatic progenitor cells (HPC) compartment.

RESULTS

Both study groups were comparable at baseline. After 3 months, 2 and 4 patients died in the BMMCT and SMT groups, respectively. Adverse events were equally distributed between groups. Moderate alcohol relapse occurred in 31% of patients. The MELD score improved in parallel in both groups during follow-up with 18 patients (64%) from the BMMCT group and 18 patients (53%) from the SMT group reaching the primary endpoint (p = 0.43 (OR 1.6, CI 0.49-5.4) in an intention to treat analysis. Comparing liver biopsy at 4 weeks to baseline, steatosis improved (p<0.001), and proliferating HPC tended to decrease in both groups (-35 and -33%, respectively).

CONCLUSION

Autologous BMMCT, compared to SMT is a safe procedure but did not result in an expanded HPC compartment or improved liver function. These data suggest either insufficient regenerative stimulation after BMMCT or resistance to liver regenerative drive in patients with decompensated alcoholic cirrhosis.

TRIAL REGISTRATION

Controlled-Trials.com ISRCTN83972743.

摘要

目的

肝再生受损与失代偿性酒精性肝病(ALD)患者的预后不良相关。我们评估了自体骨髓单个核细胞移植(BMMCT)是否改善失代偿性 ALD 的肝功能。

设计

58 名患者(平均年龄 54 岁;平均 MELD 评分 19,所有患者均为肝硬化,基线肝活检 81%为酒精性脂肪性肝炎)在入院后早期被随机分为单纯标准医学治疗(SMT)组(n=30),包括 Maddrey 评分≥32 的患者使用类固醇,或联合 G-CSF 注射和自体 BMMCT 肝动脉内给药(n=28)。骨髓细胞采集、分离并当天回输。主要终点是 3 个月时 MELD 评分下降≥3 分,对应于肝功能的临床相关改善。第 4 周重复肝活检以评估 Ki67+/CK7+肝祖细胞(HPC)区的变化。

结果

两组在基线时具有可比性。3 个月后,BMMCT 组和 SMT 组各有 2 例和 4 例患者死亡。不良事件在两组之间分布均匀。31%的患者出现中度酒精复发。两组在随访过程中 MELD 评分均同步改善,BMMCT 组 18 例(64%)和 SMT 组 18 例(53%)患者达到主要终点(意向治疗分析中 p=0.43(OR 1.6,CI 0.49-5.4)。与基线相比,4 周时肝活检显示脂肪变性改善(p<0.001),两组的增殖 HPC 均有下降趋势(分别减少-35%和-33%)。

结论

与 SMT 相比,自体 BMMCT 是一种安全的方法,但并未导致 HPC 区扩大或改善肝功能。这些数据表明,BMMCT 后再生刺激不足,或失代偿性酒精性肝硬化患者对肝再生驱动的抵抗。

试验注册

controlled-trials.com ISRCTN83972743。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6a3/3544843/e230eacaa3fd/pone.0053719.g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验