Kersten Eveline, Paun Constantin C, Schellevis Rosa L, Hoyng Carel B, Delcourt Cécile, Lengyel Imre, Peto Tunde, Ueffing Marius, Klaver Caroline C W, Dammeier Sascha, den Hollander Anneke I, de Jong Eiko K
Department of Ophthalmology, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, the Netherlands.
Université de Bordeaux, ISPED, Bordeaux, France; INSERM, U1219-Bordeaux Population Health Research Center, Bordeaux, France.
Surv Ophthalmol. 2018 Jan-Feb;63(1):9-39. doi: 10.1016/j.survophthal.2017.05.003. Epub 2017 May 15.
Biomarkers can help unravel mechanisms of disease and identify new targets for therapy. They can also be useful in clinical practice for monitoring disease progression, evaluation of treatment efficacy, and risk assessment in multifactorial diseases, such as age-related macular degeneration (AMD). AMD is a highly prevalent progressive retinal disorder for which multiple genetic and environmental risk factors have been described, but the exact etiology is not yet fully understood. Many compounds have been evaluated for their association with AMD. We performed an extensive literature review of all compounds measured in serum, plasma, vitreous, aqueous humor, and urine of AMD patients. Over 3600 articles were screened, resulting in more than 100 different compounds analyzed in AMD studies, involved in neovascularization, immunity, lipid metabolism, extracellular matrix, oxidative stress, diet, hormones, and comorbidities (such as kidney disease). For each compound, we provide a short description of its function and discuss the results of the studies in relation to its usefulness as AMD biomarker. In addition, biomarkers identified by hypothesis-free techniques, including metabolomics, proteomics, and epigenomics, are covered. In summary, compounds belonging to the oxidative stress pathway, the complement system, and lipid metabolism are the most promising biomarker candidates for AMD. We hope that this comprehensive survey of the literature on systemic and ocular fluid compounds as potential biomarkers in AMD will provide a stepping stone for future research and possible implementation in clinical practice.
生物标志物有助于揭示疾病机制并确定新的治疗靶点。它们在临床实践中也可用于监测疾病进展、评估治疗效果以及对多因素疾病(如年龄相关性黄斑变性,AMD)进行风险评估。AMD是一种高度常见的进行性视网膜疾病,已描述了多种遗传和环境风险因素,但其确切病因尚未完全明确。许多化合物已被评估与AMD的关联。我们对在AMD患者血清、血浆、玻璃体、房水和尿液中检测的所有化合物进行了广泛的文献综述。筛选了超过3600篇文章,在AMD研究中分析了100多种不同的化合物,这些化合物涉及血管生成、免疫、脂质代谢、细胞外基质、氧化应激、饮食、激素和合并症(如肾脏疾病)。对于每种化合物,我们提供其功能的简短描述,并讨论与其作为AMD生物标志物的有用性相关的研究结果。此外,还涵盖了通过无假设技术(包括代谢组学、蛋白质组学和表观基因组学)鉴定的生物标志物。总之,属于氧化应激途径、补体系统和脂质代谢的化合物是AMD最有前景的生物标志物候选物。我们希望,对作为AMD潜在生物标志物的全身和眼液化合物的文献进行的全面调查将为未来研究以及可能在临床实践中的应用提供一个跳板。