Azzimonti Matteo, Preziosa Paolo, Pagani Elisabetta, Meani Alessandro, Margoni Monica, Rubin Martina, Gueye Mor, Esposito Federica, Filippi Massimo, Rocca Maria A
Neuroimaging Research Unit, Division of Neuroscience, IRCCS San Raffaele Scientific Institute, Via Olgettina, 60, 20132, Milan, Italy.
Neurology Unit, IRCCS San Raffaele Scientific Institute, Milan, Italy.
J Neurol. 2025 Feb 25;272(3):228. doi: 10.1007/s00415-025-12979-4.
Cervical spinal cord (cSC) gray matter (GM) damage is associated with current disability in multiple sclerosis (MS), but its prognostic value remains unexplored. We aimed to investigate whether cSC GM damage may predict disability worsening in MS.
Seventy-nine MS patients and 49 healthy controls (HC) underwent 3 T brain and cSC MRI at baseline and two neurological evaluations after median follow-up of 1.3 years. Total and GM cSC lesions were identified on axial T2-weighted sequences, whereas global and GM cSC cross-sectional areas (CSAs) at C3-C4 level were quantified on phase-sensitive inversion recovery sequences. Brain lesional and volumetric measures were also assessed. At follow-up, disability worsening was defined as deterioration on ≥ 1/3 components of the Expanded Disability Status Scale (EDSS)-plus score (EDSS worsening or ≥ 20% change in timed 25-foot walk [T25FWT] or 9-hole peg test [9-HPT]).
At follow-up, 40/79 (50.6%) patients showed EDSS-plus worsening, with 13/79 (16.4%) worsening at EDSS score, 13/79 (16.4%) at 9-HPT, and 29/79 (36.7%) at T25FWT. Progressive phenotype (odds ratio [OR] = 8.65) predicted EDSS worsening (p = 0.001, C-index = 0.79). Progressive phenotype (OR = 5.56), lower cortical volume (OR = 0.41), and higher cSC GM T2-hyperintense lesion volume (OR = 2.28) (p ≤ 0.035, C-index = 0.88) predicted 9-HPT worsening. Longer disease duration (OR = 1.64), progressive phenotype (OR = 4.74), and lower cSC GM CSA (OR = 0.51) predicted T25FWT worsening (p ≤ 0.050, C-index = 0.77). Male sex (OR = 6.12), older age (OR = 1.71), progressive phenotype (OR = 7.40), and lower cSC GM CSA (OR = 0.47) predicted EDSS-plus worsening (p ≤ 0.055, C-index = 0.83).
cSC GM damage emerged as a relevant MRI predictor of disability worsening in MS, highlighting its prognostic relevance.
颈脊髓(cSC)灰质(GM)损伤与多发性硬化症(MS)当前的残疾状况相关,但其预后价值仍未得到探索。我们旨在研究cSC GM损伤是否可预测MS患者残疾状况的恶化。
79例MS患者和49名健康对照者(HC)在基线时接受了3T脑部和cSC MRI检查,并在中位随访1.3年后进行了两次神经学评估。在轴向T2加权序列上识别cSC的总病变和GM病变,而在相位敏感反转恢复序列上对C3 - C4水平的cSC整体和GM横截面积(CSA)进行量化。还评估了脑部病变和体积测量指标。在随访时,残疾状况恶化定义为扩展残疾状态量表(EDSS)加分评分中≥1/3项指标恶化(EDSS恶化或定时25英尺步行试验[T25FWT]或9孔插钉试验[9 - HPT]变化≥20%)。
随访时,40/79(50.6%)例患者出现EDSS加分评分恶化,其中13/79(16.4%)例EDSS评分恶化,13/79(16.4%)例9 - HPT恶化,29/79(36.7%)例T25FWT恶化。进展型表型(优势比[OR]=8.65)可预测EDSS恶化(p = 0.001,C指数=0.79)。进展型表型(OR = 5.56)、较低的皮质体积(OR = 0.41)和较高的cSC GM T2高信号病变体积(OR = 2.28)可预测9 - HPT恶化(p≤0.035,C指数=0.88)。病程较长(OR = 1.64)、进展型表型(OR = 4.74)和较低的cSC GM CSA(OR = 0.51)可预测T25FWT恶化(p≤0.050,C指数=0.77)。男性(OR = 6.12)、年龄较大(OR = 1.71)、进展型表型(OR = 7.40)和较低的cSC GM CSA(OR = 0.47)可预测EDSS加分评分恶化(p≤0.055,C指数=0.83)。
cSC GM损伤是MS患者残疾状况恶化的一个重要MRI预测指标,凸显了其预后相关性。