Pellicano Clelia, Kane Robert L, Gallo Antonio, Xiaobai Li, Stern Susan K, Ikonomidou Vasiliki N, Evangelou Iordanis E, Ohayon Joan M, Ehrmantraut Mary, Cantor Fredric K, Bagnato Francesca
Neuroimmunology Branch (NIB), National Institute of Neurological Disorders and Stroke (NINDS), NIH, Bethesda, MD, USA.
J Neuroimaging. 2013 Jul;23(3):445-52. doi: 10.1111/j.1552-6569.2011.00687.x. Epub 2012 Dec 10.
Cognitive impairment (CI) is an important component of multiple sclerosis (MS) disability. A complex biological interplay between white matter (WM) and gray matter (GM) disease likely sustains CI. This study aims to address this issue by exploring the association between the extent of normal WM and GM disease and CI.
Cognitive function of 24 MS patients and 24 healthy volunteers (HVs) was studied using the Automated Neuropsychological Assessment Metrics (ANAM) battery. WM focal lesions and normal appearing WM (NAWM) volume in patients, cortical thickness (CTh) and deep GM structure volumes in both patients and HVs were measured by high field strength (3.0-Tesla; 3T) imaging.
An analysis of covariance showed that patients performed worse than HVs on Code Substitution Delayed Memory (P = .04) and Procedural Reaction Time (P = .05) indicative of reduced performance in memory, cognitive flexibility, and processing speed. A summary score (Index of Cognitive Efficiency) indicating global test battery performance was also lower for the patient group (P = .04). Significant associations, as determined by the Spearman rank correlation tests, were noted between each of these 3 cognitive scores and measures of NAWM volume [CDD-TP1(r = .609; P = .0035), PRO-TP1 (r = .456; P = .029) and ICE (r = .489; P = .0129)], CTh (r = .5; P ≤ .05) and volume of subcortical normal appearing GM (NAGM) structures (r = .4; P≤ .04), but not WM lesions.
Both NAWM and NAGM volumes are related to CI in MS. The results highlight once again the urgent need to develop pharmacological strategies protecting patients from widespread neurodegeneration as possible preventive strategies of CI development.
认知障碍(CI)是多发性硬化症(MS)致残的重要组成部分。白质(WM)和灰质(GM)疾病之间复杂的生物学相互作用可能导致CI持续存在。本研究旨在通过探讨正常WM和GM疾病的程度与CI之间的关联来解决这一问题。
使用自动神经心理评估指标(ANAM)电池对24例MS患者和24名健康志愿者(HV)的认知功能进行研究。通过高场强(3.0特斯拉;3T)成像测量患者的WM局灶性病变和正常外观WM(NAWM)体积、患者和HV的皮质厚度(CTh)以及深部GM结构体积。
协方差分析显示,患者在代码替换延迟记忆(P = 0.04)和程序反应时间(P = 0.05)方面的表现比HV差,表明在记忆、认知灵活性和处理速度方面表现降低。患者组的一个表明整体测试电池性能的综合评分(认知效率指数)也较低(P = 0.04)。通过Spearman等级相关检验确定,这3个认知评分中的每一个与NAWM体积测量值[CDD - TP1(r = 0.609;P = 0.0035)、PRO - TP1(r = 0.456;P = 0.029)和ICE(r = 0.489;P = 0.0129)]、CTh(r = 0.5;P≤0.05)以及皮质下正常外观GM(NAGM)结构体积(r = 0.4;P≤0.04)之间均存在显著相关性,但与WM病变无关。
NAWM和NAGM体积均与MS中的CI相关。结果再次强调迫切需要制定药物策略,保护患者免受广泛的神经退行性变,作为CI发展的可能预防策略。