Hossen Md Munnaf, Fleiss Bobbi, Zakaria Rosita
School of Health and Biomedical Sciences, RMIT University, Bundoora, Victoria, Australia.
Inserm, NeuroDiderot, Université Paris-Cité, Paris, France.
Crit Rev Clin Lab Sci. 2025 Apr 29:1-17. doi: 10.1080/10408363.2025.2495160.
Kynurenine pathway (KP) metabolites are implicated in various disorders, including Alzheimer's disease, schizophrenia, and adverse pregnancy outcomes. Simultaneous measurement of multiple KP metabolites offers valuable insight into the pathway's role in health and disease, would improve this relatively undeveloped field. This systematic review aim was to summarize the state of the art for measuring the eight key KP metabolites, using liquid chromatography-mass spectrometry (LC-MS), explicitly focusing on whether methods were validated using established guidelines with superior sensitivity and selectivity. We undertook a comprehensive review of the literature using the PRISMA guidelines. Our search uncovered 66 publications, and 39 qualified the defined key criteria. We summarized each publication's method development parameters, analytical design, and method performance specifications. We found notable variability in sample preparation techniques and analytical design across biological matrices, underscoring a lack of universally established and validated methods for KP metabolite quantification. We also identified significant gaps in the basic method evaluation. Our findings highlight that no single method has been evaluated for quantifying the eight key KP metabolites across three or more biological sample types, revealing a critical gap in the field. Our review emphasizes the need for robust analytical methods to quantify KP metabolites across multiple biological matrices, facilitating a better understanding of their roles in health and disease. Given the diversity of disorders involving the KP in the clinical testing lab, developing such methods will reduce diagnostic errors and advance KP metabolite research, supporting more precise, and personalized medical care.
犬尿氨酸途径(KP)代谢产物与多种疾病有关,包括阿尔茨海默病、精神分裂症和不良妊娠结局。同时测量多种KP代谢产物有助于深入了解该途径在健康和疾病中的作用,将改善这个相对未充分发展的领域。本系统综述旨在总结使用液相色谱 - 质谱联用(LC - MS)测量八种关键KP代谢产物的最新技术水平,特别关注方法是否按照既定指南进行验证,具有卓越的灵敏度和选择性。我们使用PRISMA指南对文献进行了全面综述。我们的检索发现了66篇出版物,其中39篇符合定义的关键标准。我们总结了每篇出版物的方法开发参数、分析设计和方法性能规格。我们发现不同生物基质的样品制备技术和分析设计存在显著差异,这突出表明缺乏普遍确立和验证的KP代谢产物定量方法。我们还发现基本方法评估存在重大差距。我们的研究结果表明,尚未对单一方法进行评估以跨三种或更多种生物样品类型定量八种关键KP代谢产物,这揭示了该领域的一个关键差距。我们的综述强调需要强大的分析方法来跨多种生物基质定量KP代谢产物,以便更好地理解它们在健康和疾病中的作用。鉴于临床检测实验室中涉及KP的疾病多样性,开发此类方法将减少诊断错误并推进KP代谢产物研究,支持更精确和个性化的医疗护理。