Blood and digital biomarkers in MG.

International review of neurobiology Pub Date : 2025-01-01 Epub Date: 2025-05-09 DOI:10.1016/bs.irn.2025.04.030
Amol K Bhandage, Jiaxin Chen, Henry J Kaminski, Anna Rostedt Punga
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Abstract

Biomarkers are measurable indicators to assess physiological processes, disease states, or therapy responses. In myasthenia gravis (MG), biomarkers are critical for diagnosis, monitoring, and treatment optimization. Despite advances in MG diagnostics and therapies, predictive biomarkers to personalize treatment remain underdeveloped. Key diagnostic blood biomarkers include antibodies against acetylcholine receptors (AChR) or muscle-specific tyrosine kinase (MuSK), confirming MG diagnosis and guiding treatment decisions. Prognostic markers, such as microRNAs (e.g., miR-150-5p and miR-30e-5p), show promise in predicting disease progression. Pharmacodynamic biomarkers enhance treatment precision, including CD20+ B cell counts for Rituximab and the CYP3A5 gene for Tacrolimus. Emerging research on metabolites, T and B-cell markers, complement factors, and proteomics may help distinguish MG's autoimmune profile. Digital biomarkers, using wearables and sensors, offer innovative patient monitoring. Future efforts integrating multi-omics and big data could revolutionize biomarker discovery, advancing personalized care and improving outcomes for MG patients.

MG血液及数字生物标志物。
生物标志物是评估生理过程、疾病状态或治疗反应的可测量指标。在重症肌无力(MG)中,生物标志物对诊断、监测和治疗优化至关重要。尽管在MG诊断和治疗方面取得了进展,但用于个性化治疗的预测性生物标志物仍然不发达。关键的诊断血液生物标志物包括针对乙酰胆碱受体(AChR)或肌肉特异性酪氨酸激酶(MuSK)的抗体,可确认MG的诊断并指导治疗决策。预后标志物,如microrna(如miR-150-5p和miR-30e-5p),在预测疾病进展方面显示出希望。药效学生物标志物提高了治疗精度,包括利妥昔单抗的CD20+ B细胞计数和他克莫司的CYP3A5基因。代谢物、T细胞和b细胞标记物、补体因子和蛋白质组学的新兴研究可能有助于区分MG的自身免疫特征。使用可穿戴设备和传感器的数字生物标志物提供了创新的患者监测。未来整合多组学和大数据的努力可能会彻底改变生物标志物的发现,推进个性化护理,改善MG患者的预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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