Duke University School of Medicine, Duke University, DUMC 3710, Durham, NC 27710, United States; Duke Molecular Physiology Institute, Duke University, 300 N. Duke St, Durham, NC 27701, United States.
Duke Molecular Physiology Institute, Duke University, 300 N. Duke St, Durham, NC 27701, United States.
J Neuroimmunol. 2021 May 15;354:577541. doi: 10.1016/j.jneuroim.2021.577541. Epub 2021 Mar 5.
This study examined the utility of serum neurofilament light chain (sNfL) and glial fibrillary acidic protein (sGFAP) as biomarkers in primary progressive multiple sclerosis in context with clinical severity, progression, and treatment. Using a single-molecule array (Quanterix), serum protein concentrations were measured from twenty-five participants semiannually for five years. There was no association between levels of either biomarker and disease severity, disease duration, or treatment group. Enrollment sNfL level was not associated with future clinical worsening. Precedent clinical worsening was not associated with last sGFAP measurement. These results suggest a limited role for these biomarkers in primary progressive disease management.
本研究考察了血清神经丝轻链(sNfL)和神经胶质纤维酸性蛋白(sGFAP)作为原发性进展性多发性硬化症的生物标志物在临床严重程度、进展和治疗方面的效用。使用单分子阵列(Quanterix),对 25 名参与者的血清蛋白浓度进行了五年半的半年一次的测量。这两种生物标志物的水平与疾病严重程度、疾病持续时间或治疗组之间均无关联。入组时的 sNfL 水平与未来的临床恶化无关。既往临床恶化与最后一次 sGFAP 测量无关。这些结果表明这些生物标志物在原发性进行性疾病管理中的作用有限。