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Early bilirubinemia after allogeneic stem cell transplantation-an endothelial complication

机译:同种异体干细胞移植后早期胆红素血症 - 内皮复杂性

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摘要

Hyperbilirubinemia occurs frequently after allogeneic stem cell transplantation. Causes include primary liver damage and endothelial complications as major contributors. Here, we have investigated the impact of early bilirubinemia (EB) on posttransplant outcomes. Maximum total bilirubin levels (days 0-28) were categorized using maximally selected log rank statistics to identify a cut off for the endpoint non-relapse mortality (NRM) in a training cohort of 873 patients. EB above this cut off was correlated with NRM and overall survival (OS) and with pre- and posttransplant Angiopoietin-2, interleukin (IL)18, CXCL8 and suppressor of tumorigenicity-2 (ST2) serum levels, and the endothelial activation and stress index (EASIX). Clinical correlations were validated in a sample of 388 patients transplanted in an independent institution. The EB cut off was determined at 3.6 mg/dL (61.6 mu M). EB predicted OS (HR 1.60, 95% CI 1.21-2.12, p < 0.001), and NRM (CSHR 2.14; 1.28-3.56, p = 0.004), also independent of typical endothelial complications such as veno-occlusive disease, refractory acute graft-versus-host disease, or transplant-associated microangiopathy. However, EB correlated with high Angiopoietin-2, EASIX-pre and EASIX-day 0, as well as increased levels of posttransplant CXCL8, IL18, and ST2. In summary, EB indicates a poor prognosis. The association of EB with endothelial biomarkers suggests an endothelial pathomechanism also for this posttransplant complication.
机译:同种异体干细胞移植后经常发生高胆管血症。原因包括原发性肝损伤和内皮并发症作为主要贡献者。在这里,我们研究了早期胆红素血症(EB)对后翻境结果的影响。使用最大选择的日志等级统计分类为最大总胆红素水平(天0-28),以识别873名患者培训队列的端点非复发死亡率(NRM)的切断。在该切断上方的EB与NRM和整体存活(OS)相关,并且具有前后血管生成素-2,白细胞介素(IL)18,CXCL8和肿瘤血清-2(ST2)血清水平的抑制剂,以及内皮活化和应力索引(Easix)。在一个独立机构移植的388名患者的样本中验证了临床相关性。在3.6mg / dl(61.6μm)下测定EB切断。 EB预测OS(HR 1.60,95%CI 1.21-2.12,P <0.001)和NRM(CSHR 2.14; 1.28-3.56,P = 0.004),也与典型的内皮并发症如静脉闭塞性疾病,难治性急性移植物无关 - 宿主病,或移植相关的微疗病。然而,EB与高血管发射素-2,Easix-pre和Easix-Day 0相关,以及后翻版物CXCL8,IL18和ST2的水平增加。总之,EB表明预后差。 EB与内皮生物标志物的关联表明,内皮病理学机制也适用于这种后翻转并发症。

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  • 来源
    《Bone marrow transplantation》 |2021年第7期|共11页
  • 作者单位

    German Canc Res Ctr Epidemiol Heidelberg Germany;

    Charite Univ Med Berlin Hematol Oncol &

    Tumor Immunol Berlin Germany;

    Univ Hosp Heidelberg Dept Med Hematol Oncol &

    Rheumatol 5 Heidelberg Germany;

    Univ Hosp Heidelberg Dept Med Hematol Oncol &

    Rheumatol 5 Heidelberg Germany;

    Univ Hosp Heidelberg Dept Med Hematol Oncol &

    Rheumatol 5 Heidelberg Germany;

    Charite Univ Med Berlin Hematol Oncol &

    Tumor Immunol Berlin Germany;

    Charite Univ Med Berlin Hematol Oncol &

    Tumor Immunol Berlin Germany;

    Charite Univ Med Berlin Hematol Oncol &

    Tumor Immunol Berlin Germany;

    Univ Hosp Heidelberg Dept Med Hematol Oncol &

    Rheumatol 5 Heidelberg Germany;

    Univ Hosp Heidelberg Dept Med Hematol Oncol &

    Rheumatol 5 Heidelberg Germany;

    Univ Hosp Heidelberg Dept Med Hematol Oncol &

    Rheumatol 5 Heidelberg Germany;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 治疗学;
  • 关键词

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