预测进展性多发性硬化症残疾恶化的血液生物标志物:一个跨国,个体参与者级别分析
Ahmed Abdelhak1, Franziska Bachhuber2, Kiarra Ning3
1Department of Neurology, University of California San Francisco (UCSF), San Francisco, California, USA Ahmed.Abdelhak@ucsf.edu.
Journal of neurology, neurosurgery, and psychiatry
|June 12, 2025
概括
状纤维酸蛋白 (GFAP) 预测在渐进的多发性硬化症 (MS) 中残疾恶化,特别是在次级渐进的MS (SPMS) 中. 神经纤维光链 (NfL) 预测只有在初级渐进性MS (PPMS) 中恶化.
科学领域:
- 神经科学是一个神经科学.
- 生物标志物 生物标志物
- 神经学 神经学
背景情况:
- 像状纤维酸蛋白 (GFAP) 和神经纤维光链 (NfL) 这样的生物信息标志物对于预测多发性硬化症 (MS) 确定的残疾恶化 (CDW) 至关重要.
- 有限的数据和差异存在于血清GFAP和NfL在渐进性MS (PMS) 的预后值.
- 这项研究利用国际个人参与者数据来澄清PMS患者血清GFAP和NfL的预后价值.
研究的目的:
- 确定血清GFAP和NfL的预后值,用于预测进展性多发性硬化症 (pwPMS) 患者的确诊残疾恶化 (CDW).
- 调查GFAP和NfL在初级渐进性MS (PPMS) 与次级渐进性MS (SPMS) 中的不同预测能力.
主要方法:
- 分析了来自国际BioMS-eu网络中心和合作队伍的个人参与者数据.
- 包括pwPMS与PPMS或SPMS,至少有一个GFAP值和三个后续EDSS分数.
- 考克斯回归模型评估了CDW年龄和性别调整的GFAP和NfL Z-score的预后值,控制共变量.
主要成果:
- 纳入了1058名参与者 (平均年龄为53岁,57%为女性),有7530次接触,平均随访时间为4.6年.
- 增加的GFAP Z-分数与~10%的CDW风险增加有关 (aHR 1.107,p=0.049),主要是由SPMS参与者驱动的 (aHR 1.242,p=0.004).
- 在PPMS参与者中,较高的NfL Z-score仅在PPMS参与者中预测了CDW (aHR为1.236,p=0.001).
结论:
- 血清GFAP是pwPMS中未来CDW的显著预后指标,在pwSPMS中观察到更强效应.
- 血清NfL仅在pwPPMS中证明了CDW的预测价值.
- 这些发现凸显了GFAP和NfL在不同的渐进性MS亚型中作为生物标志物的差异效用.
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