Mosora Oana, Maier Smaranda, Manu Doina, Bărcuțean Laura, Roman Medeea, Dumitreasă Mihai, Bălașa Rodica
Doctoral School, "George Emil Palade" University of Medicine, Pharmacy, Science, and Technology of Targu Mures, 540142 Targu Mures, Romania.
Ist Neurology Clinical, Emergency Clinical County Hospital Targu Mures, 540136 Targu Mures, Romania.
Int J Mol Sci. 2025 Apr 20;26(8):3889. doi: 10.3390/ijms26083889.
Multiple sclerosis (MS) is a chronic, immune-mediated disease that affects young adults, leading to neurological disability. Regardless of the studies and the research involved in developing an efficient disease-modifying therapy (DMT), relapsing-remitting multiple sclerosis (RRMS) will transition to a progressive multiple sclerosis phenotype. The moment of transition from RRMS to secondary progressive multiple sclerosis (SPMS) is difficult to predict, and the diagnosis is based on the accumulation of disabilities in the evolution of the disease. Research on microRNAs' (miRNAs) role in MS began in the early 2000s, with miR-155 frequently cited for its link to blood-brain barrier dysfunction and neurodegeneration, making it an early transition biomarker from RRMS to SPMS. The purpose of this review is to reveal the importance of finding a biomarker from the molecular field that will be able to identify the transition phase so patients can receive high-efficacy treatments and to cease the clinical progression.
多发性硬化症(MS)是一种影响年轻人的慢性免疫介导疾病,会导致神经功能残疾。尽管在开发有效的疾病修正疗法(DMT)方面进行了诸多研究,但复发缓解型多发性硬化症(RRMS)仍会转变为进展型多发性硬化症表型。从RRMS转变为继发进展型多发性硬化症(SPMS)的时间难以预测,诊断基于疾病发展过程中残疾的累积情况。关于微小RNA(miRNA)在MS中作用的研究始于21世纪初,miR-155因其与血脑屏障功能障碍和神经退行性变的关联而经常被提及,使其成为从RRMS到SPMS的早期转变生物标志物。本综述的目的是揭示从分子领域寻找一种能够识别转变阶段的生物标志物的重要性,以便患者能够接受高效治疗并停止临床进展。