Bonacchi Raffaello, Meani Alessandro, Pagani Elisabetta, Marchesi Olga, Falini Andrea, Filippi Massimo, Rocca Maria A
From the Neuroimaging Research Unit, Division of Neuroscience (R.B., A.M., E.P., O.M., M.F., M.A.R.), Neurology Unit (R.B., M.F., M.A.R.), Neuroradiology Unit (A.F.), Neurorehabilitation Unit (M.F.), and Neurophysiology Service (M.F.), IRCCS San Raffaele Scientific Institute; and Vita-Salute San Raffaele University (A.F., M.F., M.A.R.), Milan, Italy.
Neurology. 2021 Nov 16;97(20):e2007-e2019. doi: 10.1212/WNL.0000000000012869. Epub 2021 Oct 4.
To investigate whether age at onset influences brain gray matter volume (GMV) and white matter (WM) microstructural abnormalities in adult patients with multiple sclerosis (MS), given its influence on clinical phenotype and disease course.
In this hypothesis-driven cross-sectional study, we enrolled 67 patients with pediatric-onset MS (POMS) and 143 sex- and disease duration (DD)-matched randomly selected patients with adult-onset MS (AOMS), together with 208 healthy controls. All participants underwent neurologic evaluation and 3T MRI acquisition. MRI variables were standardized based on healthy controls, to remove effects of age and sex. Associations with DD in patients with POMS and patients with AOMS were studied with linear models. Time to reach clinical and MRI milestones was assessed with product-limit approach.
At DD 1 year, GMV and WM fractional anisotropy (FA) were abnormal in AOMS but not in POMS. Significant interaction of age at onset (POMS vs AOMS) into the association with DD was found for GMV and WM FA. The crossing point of regression lines in POMS and AOMS was at 20 years of DD for GMV and 14 for WM FA. For POMS and AOMS, median DD was 29 and 19 years to reach Expanded Disability Status Scale score 3 ( < 0.001), 31 and 26 years to reach abnormal Paced Auditory Serial Addition Task, 3-second version ( = 0.01), 24 and 18 years to reach abnormal GMV ( = 0.04), and 19 and 17 years to reach abnormal WM FA ( = 0.36).
Younger patients are initially resilient to MS-related damage. Then, compensatory mechanisms start failing with loss of WM integrity, followed by GM atrophy and finally disability.
鉴于发病年龄对成年多发性硬化症(MS)患者临床表型和病程的影响,研究发病年龄是否会影响其脑灰质体积(GMV)和白质(WM)微观结构异常。
在这项基于假设的横断面研究中,我们纳入了67例儿童期发病的MS(POMS)患者和143例按性别和病程(DD)匹配的随机选取的成年期发病的MS(AOMS)患者,以及208名健康对照者。所有参与者均接受了神经学评估和3T磁共振成像(MRI)检查。MRI变量根据健康对照者进行标准化,以消除年龄和性别的影响。采用线性模型研究POMS患者和AOMS患者中DD与各指标的关联。采用乘积限法评估达到临床和MRI里程碑的时间。
在病程1年时,AOMS患者的GMV和WM分数各向异性(FA)异常,而POMS患者无异常。发现发病年龄(POMS与AOMS)与DD的关联中,GMV和WM FA存在显著交互作用。POMS和AOMS回归线的交叉点在病程20年时为GMV,病程14年时为WM FA。对于POMS和AOMS患者,达到扩展残疾状态量表评分3的中位病程分别为29年和19年(<0.001),达到异常的3秒版听觉序列加法任务的中位病程分别为31年和26年(=0.01),达到异常GMV的中位病程分别为24年和18年(=0.04),达到异常WM FA的中位病程分别为19年和17年(=0.36)。
年轻患者最初对MS相关损伤具有抵抗力。然后,随着WM完整性丧失,代偿机制开始失效,随后出现GM萎缩,最终导致残疾。