Canosa Antonio, Manera Umberto, Vasta Rosario, Zocco Grazia, Di Pede Francesca, Cabras Sara, De Mattei Filippo, Palumbo Francesca, Iazzolino Barbara, Minerva Emilio, Sbaiz Luca, Brunetti Maura, Gallone Salvatore, Grassano Maurizio, Matteoni Enrico, Polverari Giulia, Fuda Giuseppe, Casale Federico, Salamone Paolina, De Marco Giovanni, Marchese Giulia, Moglia Cristina, Calvo Andrea, Pagani Marco, Chiò Adriano
ALS Center, 'Rita Levi Montalcini' Department of Neuroscience, University of Turin, Turin, Italy.
Azienda Ospedaliero-Universitaria Città della Salute e della Scienza di Torino, Neurology Unit 1U, Turin, Italy.
Ann Neurol. 2025 Jun;97(6):1134-1143. doi: 10.1002/ana.27201. Epub 2025 Feb 20.
We aimed at evaluating the brain metabolic features of fused in sarcoma amyotrophic lateral sclerosis (FUS-ALS) compared with sporadic ALS (sALS), using 2-[fluorine-18] fluoro-2-deoxy-D-glucose positron emission tomography (2-[F]FDG-PET).
We employed the 2-sample t-test model of SPM12, implemented in MATLAB, to compare 12 FUS-ALS cases with 40 healthy controls (HC) and 48 sALS, randomly collected from the series of patients who underwent brain 2-[F]FDG-PET at the ALS Center of Turin (Italy) at diagnosis from 2009 to 2019. In the comparisons between cases and HC, we included age at PET and sex as covariates. Because FUS-ALS usually shows early onset in spinal regions, in the comparison between FUS-ALS and sALS, we included singularly the following covariates in a second step, to evaluate the determinants of eventual metabolic differences: age at PET, sex, and onset (spinal/bulbar).
sALS patients showed significant relative hypometabolism in bilateral fronto-temporo-occipital cortex and right insula as compared with FUS-ALS. After adjusting for age, the relative hypometabolism remained in the bilateral precentral gyrus and in the right middle and inferior temporal gyrus. As compared with HC, FUS patients displayed a significant relative hypermetabolism in the pontobulbar region and right cerebellar tonsil, dentate nucleus, and uvula, while sALS showed relative hypometabolism in bilateral frontal and occipital cortices and in left temporal and parietal regions.
Patients with FUS-ALS show relative preservation of motor cortex metabolism compared with those with sALS, possibly reflecting the prevalence of lower motor neuron impairment in their phenotype. Prospective studies are necessary to investigate the possible role of 2-[F]FDG-PET as a biomarker to track disease spreading in clinical trials. ANN NEUROL 2025;97:1134-1143.
我们旨在通过使用2-[氟-18]氟-2-脱氧-D-葡萄糖正电子发射断层扫描(2-[F]FDG-PET),评估与散发性肌萎缩侧索硬化症(sALS)相比,融合性肉瘤肌萎缩侧索硬化症(FUS-ALS)的脑代谢特征。
我们采用在MATLAB中实现的SPM12的双样本t检验模型,将12例FUS-ALS患者与40名健康对照(HC)以及48例sALS患者进行比较,这些病例是从2009年至2019年在意大利都灵ALS中心接受脑部2-[F]FDG-PET检查的患者系列中随机收集的。在病例与HC的比较中,我们将PET时的年龄和性别作为协变量纳入。由于FUS-ALS通常在脊髓区域表现为早发,在FUS-ALS与sALS的比较中,我们在第二步单独纳入以下协变量,以评估最终代谢差异的决定因素:PET时的年龄、性别和发病部位(脊髓/延髓)。
与FUS-ALS相比,sALS患者在双侧额颞枕叶皮质和右侧岛叶显示出明显的相对代谢减低。在调整年龄后,相对代谢减低仍存在于双侧中央前回以及右侧颞中回和颞下回。与HC相比,FUS患者在脑桥延髓区域以及右侧小脑扁桃体、齿状核和小舌显示出明显的相对代谢增高,而sALS在双侧额叶和枕叶皮质以及左侧颞叶和顶叶区域显示出相对代谢减低。
与sALS患者相比,FUS-ALS患者的运动皮质代谢相对保留,这可能反映了其表型中下运动神经元损伤的普遍性。有必要进行前瞻性研究,以调查2-[F]FDG-PET作为生物标志物在临床试验中追踪疾病传播的可能作用。《神经病学年鉴》2025年;97:1134 - 1143。