Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
Texas Children's Hospital, Houston, TX, USA.
Genet Med. 2019 Sep;21(9):1977-1986. doi: 10.1038/s41436-019-0442-0. Epub 2019 Jan 23.
Untargeted metabolomic analysis is increasingly being used in the screening and management of individuals with inborn errors of metabolism (IEM). We aimed to test whether untargeted metabolomic analysis in plasma might be useful for monitoring the disease course and management of urea cycle disorders (UCDs).
Untargeted mass spectrometry-based metabolomic analysis was used to generate z-scores for more than 900 metabolites in plasma from 48 individuals with various UCDs. Pathway analysis was used to identify common pathways that were perturbed in each UCD.
Our metabolomic analysis in plasma identified multiple potentially neurotoxic metabolites of arginine in arginase deficiency and, thus, may have utility in monitoring the efficacy of treatment in arginase deficiency. In addition, we were also able to detect multiple biochemical perturbations in all UCDs that likely reflect clinical management, including metabolite alterations secondary to dietary and medication management.
In addition to utility in screening for IEM, our results suggest that untargeted metabolomic analysis in plasma may be beneficial for monitoring efficacy of clinical management and off-target effects of medications in UCDs and potentially other IEM.
非靶向代谢组学分析越来越多地用于代谢性疾病(IEM)患者的筛查和管理。我们旨在测试血浆中的非靶向代谢组学分析是否可用于监测尿素循环障碍(UCD)的疾病进程和管理。
使用基于质谱的非靶向代谢组学分析,对 48 名患有各种 UCD 的个体的血浆中超过 900 种代谢物生成 z 值。通过途径分析确定在每种 UCD 中受到干扰的常见途径。
我们对血浆的代谢组学分析鉴定出精氨酸酶缺乏症中精氨酸的多种潜在神经毒性代谢物,因此可能对监测精氨酸酶缺乏症的治疗效果有用。此外,我们还能够检测到所有 UCD 中的多种生化干扰,这可能反映了临床管理,包括饮食和药物管理引起的代谢物改变。
除了在 IEM 的筛查中有应用价值外,我们的结果表明,血浆中的非靶向代谢组学分析可能有助于监测 UCD 及其他潜在 IEM 中临床管理的疗效和药物的脱靶效应。