Clinical Hospital Centre Split, 21000 Split, Croatia.
Clinical Hospital Centre Sisters of Mercy, 10000 Zagreb, Croatia.
Molecules. 2022 Mar 8;27(6):1774. doi: 10.3390/molecules27061774.
The pathogenesis of age-related macular degeneration (AMD) remains elusive, despite numerous research studies. Therefore, we aimed to investigate the changes of plasma and IgG-specific -glycosylation across the disease severity spectrum. We examined 2835 subjects from the 10.001 Dalmatians project, originating from the isolated Croatian islands of Vis and Korčula. All subjects were classified into four groups, namely (i) bilateral AMD, (ii) unilateral AMD, (iii) early-onset drusen, and (iv) controls. We analysed plasma and IgG -glycans measured by HPLC and their association with retinal fundus photographs. There were 106 (3.7%) detected cases of AMD; 66 of them were bilateral. In addition, 45 (0.9%) subjects were recorded as having early-onset retinal drusen. We detected several interesting differences across the analysed groups, suggesting that -glycans can be used as a biomarker for AMD. Multivariate analysis suggested a significant decrease in the immunomodulatory bi-antennary glycan structures in unilateral AMD (adjusted odds ratio 0.43 (95% confidence interval 0.22-0.79)). We also detected a substantial increase in the pro-inflammatory tetra-antennary plasma glycans in bilateral AMD (7.90 (2.94-20.95)). Notably, some of these associations were not identified in the aggregated analysis, where all three disease stages were collapsed into a single category, suggesting the need for better-refined phenotypes and the use of disease severity stages in the analysis of more complex diseases. Age-related macular degeneration progression is characterised by the complex interplay of various mechanisms, some of which can be detected by measuring plasma and IgG -glycans. As opposed to a simple case-control study, more advanced and refined study designs are needed to understand the pathogenesis of complex diseases.
年龄相关性黄斑变性(AMD)的发病机制仍然难以捉摸,尽管有许多研究。因此,我们旨在研究疾病严重程度谱中血浆和 IgG 特异性 -糖基化的变化。我们检查了来自孤立的克罗地亚维斯岛和科尔丘拉岛的 10.001 达尔马提亚犬项目的 2835 名受试者。所有受试者分为四组,即(i)双侧 AMD,(ii)单侧 AMD,(iii)早发性玻璃膜疣和(iv)对照组。我们分析了通过 HPLC 测量的血浆和 IgG -聚糖及其与视网膜眼底照片的关联。有 106 例(3.7%)被诊断为 AMD;其中 66 例为双侧。此外,有 45 例(0.9%)被记录为有早发性视网膜玻璃膜疣。我们在分析的组中发现了一些有趣的差异,表明 -聚糖可以作为 AMD 的生物标志物。多变量分析表明,单侧 AMD 中免疫调节双天线聚糖结构显著减少(调整后的优势比 0.43(95%置信区间 0.22-0.79))。我们还发现双侧 AMD 中促炎四天线血浆聚糖显著增加(7.90(2.94-20.95))。值得注意的是,在聚合分析中没有发现其中一些关联,在聚合分析中,将所有三个疾病阶段合并为一个类别,这表明需要更好地细化表型,并在分析更复杂的疾病时使用疾病严重程度阶段。年龄相关性黄斑变性的进展是由各种机制的复杂相互作用所决定的,其中一些可以通过测量血浆和 IgG -聚糖来检测。与简单的病例对照研究相比,需要更先进和精细的研究设计来了解复杂疾病的发病机制。