University of Montpellier, INM, INSERM, MS referral center & reference center for adult-onset leukodystrophies, CHU Montpellier, Montpellier, France.
Clinical Research and Epidemiology Unit, CHU Montpellier, Univ Montpellier, Montpellier, France.
Mult Scler Relat Disord. 2024 Sep;89:105747. doi: 10.1016/j.msard.2024.105747. Epub 2024 Jun 24.
Serum neurofilament light chain (sNfL) and glial fibrillary acidic protein (sGFAP) are promising biomarkers that might be associated with clinical and radiological markers of multiple sclerosis (MS) severity. However, it is not known whether they can accurately identify patients at risk of disability progression in the medium and long term.
We wanted to determine the association between sNfL and sGFAP, Expanded Disability Status Scale score changes, and conversion to secondary progressive MS (SPMS) in a cohort of 133 patients with relapsing remitting MS.
Blood samples were collected at inclusion to measure SNfL and sGFAP by single molecule array and their prognostic value was assessed using a linear mixed model.
In this cohort, 37 patients (27.8 % of 133) experienced disability progression and 12 patients (9.0 %) converted to SPMS during the follow-up (mean follow-up duration: 6.4 years). Only sNfL (p = 0.03) was associated with conversion to SPMS, and neither SNfL nor sGFAP was associated with disability progression.
Serum NfL and GFAP do not seem to accurately predict MS outcome in the long term. More studies are needed to determine how serum biomarkers, associated with other clinical and MRI biomarkers, might be used to improve MS prognostication.
血清神经丝轻链(sNfL)和胶质纤维酸性蛋白(sGFAP)是很有前途的生物标志物,可能与多发性硬化症(MS)严重程度的临床和影像学标志物相关。然而,目前尚不清楚它们是否能准确识别出有残疾进展风险的患者。
我们旨在确定血清神经丝轻链(sNfL)和 sGFAP 与扩展残疾状况量表评分变化之间的关系,并在 133 例复发缓解型多发性硬化症(RRMS)患者队列中评估其与向继发性进展型多发性硬化症(SPMS)转化的关系。
在纳入时采集血样以通过单分子阵列测量 sNfL 和 sGFAP,并使用线性混合模型评估其预后价值。
在该队列中,37 例患者(133 例的 27.8%)经历了残疾进展,12 例患者(9.0%)在随访期间转化为 SPMS(平均随访时间:6.4 年)。只有 sNfL(p=0.03)与向 SPMS 转化相关,而 sNfL 和 sGFAP 均与残疾进展无关。
血清 NfL 和 GFAP 似乎不能准确预测 MS 的长期预后。需要更多的研究来确定与其他临床和 MRI 生物标志物相关的血清生物标志物如何用于改善 MS 的预后判断。