风湿性多肌痛
代谢组
巨细胞动脉炎
血沉
医学
代谢组学
内科学
生物标志物
肌酐
炎症
疾病
免疫学
内分泌学
代谢物
生物
生物信息学
血管炎
生物化学
作者
Aikaterini Iliou,Ourania D Argyropoulou,Dimitris Anastasios Palamidas,Marianna Karagiannakou,Dimitra Benaki,Konstantina Ismini Tsezou,Panayiotis G. Vlachoyiannopoulos,Emmanuel Mikros,Athanasios G. Tzioufas
出处
期刊:Rheumatology
[Oxford University Press]
日期:2023-11-03
被引量:1
标识
DOI:10.1093/rheumatology/kead590
摘要
Giant Cell Arteritis-(GCA) is an inflammatory disease following a chronic, relapsing course. The metabolic alterations related to the intense inflammatory process during the active phase and to the rapid impact of steroid treatment, remain unknown. The study aims to investigate the serum metabolome in active and inactive disease state.110 serum samples from 50 patients [33-GCA and 17-Polymyalgia rheumatica-(PMR)] at 3 time points, 0-(V1: active disease), 1 and 6 months-(V2 and V3: remission) of treatment with glucocorticosteroids (GCs), were subjected to Nuclear Magnetic Resonance (NMR)-based metabolomic analysis. Multi- and univariate statistical analyses were utilized to unveil metabolome alterations following treatment.Distinct metabolic profiles were identified between activity and remission, independently to disease type. N-acetylglycoproteins and cholines of bound phospholipids, emerged as predictive markers of disease activity. Altered levels of 4 out of the 21 small molecules were also observed, including increased levels of phenylalanine, and decreased of glutamine, alanine, and creatinine in active disease. Metabolic fingerprinting discriminated GCA from PMR in remission. GCA and PMR patients exhibited characteristic lipid alterations as a response and/or adverse effect of GCs treatment. Correlation analysis showed that several identified biomarkers were further associated with acute phase reactants, C-Reactive Protein and Erythrocyte Sedimentation Rate.The NMR profile of serum metabolome could identify and propose sensitive biomarkers of inflammation. Metabolome alterations, following GCs treatment, could provide predictors for future steroid-induced side effects.
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