Jonas Children's Vision Care and Bernard & Shirlee Brown Glaucoma Laboratory, Department of Ophthalmology, Columbia University, New York, NY, USA.
Edward S. Harkness Eye Institute, New York-Presbyterian Hospital, New York, NY, USA.
Cell Mol Life Sci. 2018 May;75(9):1559-1566. doi: 10.1007/s00018-018-2744-9. Epub 2018 Jan 13.
Metabolomics studies in the context of ophthalmology have largely focused on identifying metabolite concentrations that characterize specific retinal diseases. Studies involving mass spectrometry (MS) and nuclear magnetic resonance (NMR) spectroscopy have shown that individuals suffering from retinal diseases exhibit metabolic profiles that markedly differ from those of control individuals, supporting the notion that metabolites may serve as easily identifiable biomarkers for specific conditions. An emerging branch of metabolomics resulting from biomarker studies, however, involves the study of retinal metabolic dysfunction as causes of degeneration. Recent publications have identified a number of metabolic processes-including but not limited to glucose and oxygen metabolism-that, when perturbed, play a role in the degeneration of photoreceptor cells. As a result, such studies have led to further research elucidating methods for prolonging photoreceptor survival in an effort to halt degeneration in its early stages. This review will explore the ways in which metabolomics has deepened our understanding of the causes of retinal degeneration and discuss how metabolomics can be used to prevent retinal degeneration from progressing to its later disease stages.
代谢组学研究在眼科学领域主要集中在鉴定能够表征特定视网膜疾病的代谢物浓度上。涉及质谱(MS)和核磁共振(NMR)光谱的研究表明,患有视网膜疾病的个体表现出的代谢特征与对照组个体明显不同,这支持了代谢物可以作为特定疾病的易于识别的生物标志物的观点。然而,代谢组学作为生物标志物研究的一个新兴分支,涉及到视网膜代谢功能障碍作为退行性变的原因的研究。最近的出版物已经确定了许多代谢过程——包括但不限于葡萄糖和氧气代谢——当受到干扰时,在感光细胞的退行性变中发挥作用。因此,这些研究导致了进一步的研究,阐明了延长感光细胞存活的方法,以努力在退行性变的早期阶段阻止其进展。这篇综述将探讨代谢组学如何加深我们对视网膜退行性变原因的理解,并讨论如何利用代谢组学来防止视网膜退行性变进展到后期疾病阶段。