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线粒体疾病的生物标志物。

Biomarkers of mitochondrial disorders.

机构信息

Division of Medical Genetics, Department of Pediatrics, University of Utah, Salt Lake City, UT, USA.

出版信息

Neurotherapeutics. 2024 Jan;21(1):e00325. doi: 10.1016/j.neurot.2024.e00325. Epub 2024 Jan 30.

Abstract

Mitochondrial diseases encompass a heterogeneous group of disorders with a wide range of clinical manifestations, most classically resulting in neurological, muscular, and metabolic abnormalities, but having the potential to affect any organ system. Over the years, substantial progress has been made in identifying and characterizing various biomarkers associated with mitochondrial diseases. This review summarizes the current knowledge of mitochondrial biomarkers based on a literature review and discusses the evidence behind their use in clinical practice. A total of 13 biomarkers were thoroughly reviewed including lactate, pyruvate, lactate:pyruvate ratio, creatine kinase, creatine, amino acid profiles, glutathione, malondialdehyde, GDF-15, FGF-21, gelsolin, neurofilament light-chain, and circulating cell-free mtDNA. Most biomarkers had mixed findings depending on the study, especially when considering their utility for specific mitochondrial diseases versus mitochondrial conditions in general. However, in large biomarker comparison studies, GDF-15 followed by FGF-21, seem to have the greatest value though they are still not perfect. As such, additional studies are needed, especially in light of newer biomarkers that have not yet been thoroughly investigated. Understanding the landscape of biomarkers in mitochondrial diseases is crucial for advancing early detection, improving patient management, and developing targeted therapies.

摘要

线粒体疾病包括一组具有广泛临床表现的异质性疾病,最典型的表现为神经、肌肉和代谢异常,但也有可能影响任何器官系统。多年来,在识别和描述与线粒体疾病相关的各种生物标志物方面取得了重大进展。本综述通过文献回顾总结了目前基于线粒体生物标志物的知识,并讨论了其在临床实践中应用的证据。总共彻底审查了 13 种生物标志物,包括乳酸、丙酮酸、乳酸:丙酮酸比值、肌酸激酶、肌酸、氨基酸谱、谷胱甘肽、丙二醛、GDF-15、FGF-21、凝胶蛋白、神经丝轻链和循环细胞游离 mtDNA。大多数生物标志物的研究结果不一致,特别是在考虑它们对特定线粒体疾病与一般线粒体疾病的应用时。然而,在大型生物标志物比较研究中,GDF-15 之后是 FGF-21,似乎具有最大的价值,尽管它们并不完美。因此,需要开展更多的研究,特别是针对尚未得到充分研究的新型生物标志物。了解线粒体疾病中的生物标志物全景对于早期检测、改善患者管理和开发靶向治疗至关重要。

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