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Subventricular Zone Microstructure in Pediatric-Onset Multiple Sclerosis
被引:0
|作者:
Margoni, Monica
[1
,2
,3
]
Storelli, Loredana
[1
]
Pagani, Elisabetta
[1
]
Preziosa, Paolo
[1
,2
,4
]
Mistri, Damiano
[1
]
Gueye, Mor
[1
,2
,4
]
Rubin, Martina
[1
,2
,4
]
Moiola, Lucia
[2
]
Filippi, Massimo
[1
,2
,3
,4
,5
]
Rocca, Maria Assunta
[1
,2
,4
]
机构:
[1] IRCCS San Raffaele Sci Inst, Div Neurosci, Neuroimaging Res Unit, Milan, Italy
[2] IRCCS San Raffaele Sci Inst, Neurol Unit, Milan, Italy
[3] IRCCS San Raffaele Sci Inst, Neurorehabil Unit, Milan, Italy
[4] Univ Vita Salute San Raffaele, Milan, Italy
[5] IRCCS San Raffaele Sci Inst, Neurophysiol Serv, Milan, Italy
来源:
关键词:
NEURAL STEM-CELLS;
HUMAN BRAIN;
COGNITIVE IMPAIRMENT;
CHILDHOOD;
NEURONS;
PROLIFERATION;
REMYELINATION;
NEUROGENESIS;
INFLAMMATION;
PROGENITORS;
D O I:
10.1002/ana.27180
中图分类号:
R74 [神经病学与精神病学];
学科分类号:
摘要:
Objective: The aim of this study was to explore the microstructural dynamics of the subventricular zone (SVZ) with aging and their associations with clinical disability and brain structural damage in pediatric-onset multiple sclerosis (MS) patients. Methods: One-hundred and forty-one pediatric-onset MS patients (67 pediatric and 74 adults with pediatric-onset) and 233 healthy controls (HC) underwent neurological and 3.0 T MRI assessment. Fractional anisotropy (FA) and mean diffusivity (MD) were extracted from the SVZ and the thalamus (as control region). Results: In HC, SVZ FA was higher until age 40 then declined, whereas MD was lower until age 35 before rising (false discovery rate p value [pFDR] <= 0.008). Thalamic FA was higher until age 30 and then declined, whereas MD was higher until age 50 (pFDR <= 0.007). Pediatric MS patients showed significantly higher SVZ FA than pediatric HC (pFDR < 0.001), while adult patients showed no differences compared to adult HC (pFDR <= 0.724). Adult patients had lower thalamic FA and higher MD (pFDR < 0.001). Adults had lower SVZ FA and MD, but higher thalamic MD compared to pediatric patients (pFDR < 0.001). In pediatric MS, higher SVZ FA and MD were associated with higher white matter (WM) lesion volume (LV) and choroid plexus volume and lower brain and thalamic volumes (pFDR <= 0.047). In adult patients, higher SVZ MD associated with higher WM LV, lower brain volumes, and lower z-SDMT (pFDR <= 0.019). Thalamic microstructural abnormalities were associated with more severe disability and brain damage in both groups (pFDR <= 0.018). Interpretation: Our findings suggest that microstructural changes in the SVZ occur early in pediatric MS and are associated with brain structural damage but not with clinical impairment. ANN NEUROL 2025
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