The Department of Clinical Laboratory, Zhejiang Hospital, Hangzhou, P. R. China.
The Department of Geriatrics, Zhejiang Hospital, Hangzhou, P. R. China.
Proteomics Clin Appl. 2024 May;18(3):e2300035. doi: 10.1002/prca.202300035. Epub 2024 Jan 9.
This study was aimed to analyze serum amino acid metabolite profiles in frailty patients, gain a better understanding of the metabolic mechanisms in frailty, and assess the diagnostic value of metabolomics-based biomarkers of frailty.
This study utilized the ultra-performance liquid chromatography tandem mass spectrometry to examine amino acids associated with frailty. Additionally, we employed multivariate statistical methods, metabolomic data analysis, receiver operating characteristic (ROC) curve analysis, and pathway enrichment analysis.
Among the assayed amino acid metabolites, we identified biomarkers for frailty. ROC curve analysis for frailty diagnosis based on the modified Fried's frailty index showed that the areas under ROC curve of tryptophan, phenylalanine, aspartic acid, and combination were 0.775, 0.679, 0.667, and 0.807, respectively. ROC curve analysis for frailty diagnosis based on Frail Scale showed that the areas under ROC curve of cystine, phenylalanine, and combination of amino acids (cystine, L-Glutamine, citrulline, tyrosine, kynurenine, phenylalanine, glutamin acid) were 0.834, 0.708, and 0.854 respectively.
In this study, we explored the serum amino acid metabolite profiles in frailty patients. These present metabolic analyses may provide valuable information on the potential biomarkers and the possible pathogenic mechanisms of frailty.
Frailty is a clinical syndrome, as a consequence it is challenging to identify at early course of the disease, even based on the existing frailty scales. Early diagnosis and appropriate patient management are the key to improve the survival and limit disabilities in frailty patients. Proven by the extensive laboratory and clinical studies on frailty, comprehensive analysis of metabolic levels in frail patients, identification of biomarkers and study of pathogenic pathways of metabolites contribute to the prediction and early diagnosis of frailty. In this study, we explored the serum amino acid metabolite profiles in frailty patients. These present metabolic analyses may provide valuable information on the potential biomarkers and the possible pathogenic mechanisms of frailty.
本研究旨在分析衰弱患者的血清氨基酸代谢物谱,深入了解衰弱的代谢机制,并评估基于代谢组学的衰弱生物标志物的诊断价值。
本研究采用超高效液相色谱串联质谱法检测与衰弱相关的氨基酸。此外,我们还采用了多变量统计方法、代谢组学数据分析、接受者操作特征(ROC)曲线分析和途径富集分析。
在测定的氨基酸代谢物中,我们确定了与衰弱相关的生物标志物。基于改良的 Fried 衰弱指数进行衰弱诊断的 ROC 曲线分析显示,色氨酸、苯丙氨酸、天冬氨酸和组合的 ROC 曲线下面积分别为 0.775、0.679、0.667 和 0.807。基于 Frail Scale 进行衰弱诊断的 ROC 曲线分析显示,胱氨酸、苯丙氨酸和氨基酸组合(胱氨酸、L-谷氨酰胺、瓜氨酸、酪氨酸、犬尿氨酸、苯丙氨酸、谷氨酸)的 ROC 曲线下面积分别为 0.834、0.708 和 0.854。
本研究探讨了衰弱患者的血清氨基酸代谢物谱。这些代谢分析可能为衰弱的潜在生物标志物和可能的发病机制提供有价值的信息。
衰弱是一种临床综合征,因此即使基于现有的衰弱量表,在疾病早期也难以识别。早期诊断和适当的患者管理是改善衰弱患者生存和限制残疾的关键。大量的实验室和临床研究证明,全面分析衰弱患者的代谢水平,确定生物标志物,研究代谢物的致病途径,有助于预测和早期诊断衰弱。在本研究中,我们探讨了衰弱患者的血清氨基酸代谢物谱。这些代谢分析可能为衰弱的潜在生物标志物和可能的发病机制提供有价值的信息。