4.7 Article

Metabolomic identification of α-ketoglutaric acid elevation in pediatric chronic graft-versus-host disease

期刊

BLOOD
卷 139, 期 2, 页码 287-299

出版社

AMER SOC HEMATOLOGY
DOI: 10.1182/blood.2021013244

关键词

-

资金

  1. Canadian Institutes of Health Research (CIHR) Team grant
  2. CIHR Foundation grant
  3. Leukemia Lymphoma Canada

向作者/读者索取更多资源

This study longitudinally evaluated the metabolomic patterns of chronic graft-versus-host disease (cGVHD) and late acute graft-versus-host disease (aGVHD) in pediatric hematopoietic stem cell transplant recipients. The results showed that plasma alpha-ketoglutaric acid levels were consistently elevated before and at the onset of cGVHD, and late aGVHD had a unique metabolomic pattern at an early stage compared to cGVHD.
Chronic graft-versus-host disease (cGVHD) is the most common cause for non-relapse mortality postallogeneic hematopoietic stem cell transplant (HSCT). However, there are no well-defined biomarkers for cGVHD or late acute GVHD (aGVHD). This study is a longitudinal evaluation of metabolomic patterns of cGVHD and late aGVHD in pediatric HSCT recipients. A quantitative analysis of plasma metabolites was performed on 222 evaluable pediatric subjects from the ABLE/PBMTC1202 study. We performed a risk-assignment analysis at day 1 100 (D100) on subjects who later developed either cGVHD or late aGVHD after day 114 to non-cGVHD controls. A second analysis at diagnosis used fixed and mixed multiple regression to compare cGVHD at onset to time-matched non-cGVHD controls. A metabolomic biomarker was considered biologically relevant only if it met all 3 selection criteria: (1) P <= .05; (2) effect ratio of >= 1.3 or <= 0.75; and (3) receiver operator characteristic AUC >= 0.60. We found a consistent elevation in plasma alpha-ketoglutaric acid before (D100) and at the onset of cGVHD, not impacted by cGVHD severity, pubertal status, or previous aGVHD. In addition, late aGVHD had a unique metabolomic pattern at D100 compared with cGVHD. Additional metabolomic correlation patterns were seen with the clinical presentation of pulmonary, de novo, and progressive cGVHD. alpha-ketoglutaric acid emerged as the single most significant metabolite associated with cGVHD, both in the D100 risk-assignment and later diagnostic onset analysis. These distinctive metabolic patterns may lead to improved subclassification of cGVHD. Future validation of these exploratory results is needed.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据