Macrostructural Brain Abnormalities in Spinal Muscular Atrophy

被引:0
|
作者
Groulx-Boivin, Emilie [1 ,2 ]
Oliveira-Carneiro, Andrea [3 ]
Carlson, Helen [4 ,5 ]
Floer, Amalia [4 ,5 ]
Kirton, Adam [4 ,5 ]
Mah, Jean [4 ,5 ]
Saint-Martin, Christine [6 ]
La Piana, Roberta [7 ,8 ]
Oskoui, Maryam [1 ,2 ,3 ]
机构
[1] McGill Univ, Montreal Childrens Hosp, Dept Pediat, Montreal, PQ, Canada
[2] McGill Univ, Montreal Childrens Hosp, Dept Neurol & Neurosurg, Montreal, PQ, Canada
[3] McGill Univ, Res Inst, Hlth Ctr, Montreal, PQ, Canada
[4] Alberta Childrens Hosp Res Inst, Calgary, AB, Canada
[5] Univ Calgary, Cumming Sch Med, Dept Pediat, Calgary, AB, Canada
[6] Montreal Childrens Hosp, Dept Radiol, Div Pediat Med Imaging, Montreal, PQ, Canada
[7] Montreal Neurol Inst, Dept Neurol & Neurosurg, Montreal, PQ, Canada
[8] McGill Univ, Dept Diagnost Radiol, Montreal, PQ, Canada
关键词
EXPRESSION; GENE; MRI;
D O I
10.1212/NXG.0000000000200193
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Background and ObjectivesMost individuals with spinal muscular atrophy (SMA) on disease-modifying therapies continue to have chronic motor impairment. Insights into brain involvement in SMA may open new pathways for adjunctive therapies to optimize outcomes. We aimed to characterize macrostructural brain abnormalities detected by MRI in individuals with SMA compared with peer controls.MethodsWe conducted a cross-sectional case-control study of children and adults with a confirmed genetic diagnosis of 5q SMA, and peer controls matched by age and sex. Brain MRIs acquired on a 3T MRI scanner through a standardized research protocol were reviewed to qualitatively assess the presence of macrostructural changes. The primary outcome was the presence of any structural brain anomaly on MRI. In addition, the total volume of each participant's lateral ventricles was quantified by volumetry using MRIcron. Genetic and clinical variables, including SMN2 copy number and motor function (Hammersmith Functional Motor Scale Expanded and Revised Upper Limb Module scores), were then correlated with neuroimaging findings.ResultsA total of 42 participants completed the study (mean age 17.4, range 7-40; 67% male). Of the 21 individuals with 5q SMA, 9 (43%) had macrostructural brain abnormalities identified on MRI compared with 2 of 21 (10%) peer controls (odds ratio 7.1, 95% confidence interval 1.4-34.0). In patients with SMA, the most common structural changes were widening of the arachnoid spaces (n = 4) and ventriculomegaly (n = 4). Individuals with SMA had larger median lateral ventricular volume than their normally developing peers (9.3 mL, interquartile range [IQR] 5.5-13.1 vs 5.3 mL, IQR 3.8-9.8; p = 0.034). Structural brain abnormalities were more frequent in those with 2 SMN2 copies (3/5, 60%) compared with 3 or 4 SMN2 copies (4/10, 40% and 2/6, 33% respectively), not reaching significance. We found no association between structural changes and motor function scores.DiscussionIndividuals with SMA have higher rates of macrostructural brain abnormalities than their neurotypical peers, suggesting CNS involvement in SMA. Understanding changes in the brain architecture of the SMA population can inform the development of adjunct therapies targeting the CNS and potentially guide rehabilitation strategies.
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页数:9
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