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系统评价:免疫球蛋白 G-聚糖作为常见慢性疾病的下一代诊断生物标志物。

Systematic Review: Immunoglobulin G -Glycans as Next-Generation Diagnostic Biomarkers for Common Chronic Diseases.

机构信息

Beijing Key Laboratory of Clinical Epidemiology, School of Public Health, Capital Medical University, Beijing, China.

School of Medical and Health Sciences, Edith Cowan University, Perth, Australia.

出版信息

OMICS. 2019 Dec;23(12):607-614. doi: 10.1089/omi.2019.0032. Epub 2019 Aug 16.

Abstract

Glycomics is a new subspecialty in omics systems sciences that offers significant promise for next-generation biomarkers on disease susceptibility, drug target discovery, and precision medicine. In this context, alternative immunoglobulin G (IgG) -glycosylation has been reportedly implicated in several common chronic diseases, although systematic assessment is currently lacking in the literature. We conducted a systematic review of observational studies on IgG -glycan variability and susceptibility to common chronic diseases. Observational studies reporting an association between diseases (such as colorectal cancer, dyslipidemia, ischemic stroke, rheumatoid arthritis, and systemic lupus erythematosus) and IgG -glycans quantified by ultraperformance liquid chromatography were included. The glycans were categorized into 24 initial IgG glycan peaks (GPs). Notably, aging positively correlated with GP1, GP2, GP4-7, GP10, GP11, GP19, and GP24, while negatively correlated with GP8, GP12-15, GP17, GP18, GP20, GP21, and GP23 ( < 0.05). The absolute value of significant correlation coefficients of age and IgG glycans ranged from 0.043 to 0.645. We found that the high levels of GP1-4, GP6, GP7, and GP24 and low levels of GP9, GP13-15, GP18, and GP23 could potentially increase the risk of disease. In conclusion, the present systematic review suggests that the field of glycomics, and GP1-4, GP6, GP7, GP9, GP13-15, GP18, GP23, and GP24 in particular, holds promise for further candidate biomarker research on susceptibility to common chronic diseases.

摘要

糖组学是组学系统科学的一个新分支,它为疾病易感性、药物靶点发现和精准医学的下一代生物标志物提供了巨大的潜力。在这种情况下,替代免疫球蛋白 G(IgG)-糖基化据称与几种常见的慢性疾病有关,尽管目前文献中缺乏系统评估。我们对 IgG-聚糖变异性与常见慢性疾病易感性的观察性研究进行了系统评价。纳入了报告疾病(如结直肠癌、血脂异常、缺血性中风、类风湿关节炎和系统性红斑狼疮)与通过超高效液相色谱法定量的 IgG-聚糖之间存在关联的观察性研究。将聚糖分为 24 个初始 IgG 聚糖峰(GP)。值得注意的是,随着年龄的增长,GP1、GP2、GP4-7、GP10、GP11、GP19 和 GP24 呈正相关,而 GP8、GP12-15、GP17、GP18、GP20、GP21 和 GP23 则呈负相关(<0.05)。年龄与 IgG 聚糖的显著相关系数的绝对值范围为 0.043 至 0.645。我们发现,GP1-4、GP6、GP7 和 GP24 水平较高,而 GP9、GP13-15、GP18 和 GP23 水平较低,可能会增加患病风险。总之,本系统评价表明,糖组学领域,特别是 GP1-4、GP6、GP7、GP9、GP13-15、GP18、GP23 和 GP24,有望进一步开展常见慢性疾病易感性候选生物标志物研究。

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