From the Department of Anatomy & Neurosciences, Amsterdam Neuroscience, MS Center Amsterdam, VU University Medical Center, PO Box 7057, 1007 MB, Amsterdam, the Netherlands.
Radiology. 2018 Aug;288(2):544-551. doi: 10.1148/radiol.2018172808. Epub 2018 May 22.
Purpose To investigate the discrepancy between patients with multiple sclerosis (MS) without atrophy who have already developed cognitive impairment and patients with MS with atrophy who have preserved cognitive function. Materials and Methods This retrospective imaging study, with imaging acquired between 2008 and 2012, included 332 patients with MS (106 men and 226 women; mean age, 48.1 years; range, 23.0-72.5 years) and 96 healthy control participants. Cognitive impairment was defined as cognitive performance of z less than -1.5 compared with that in control participants in greater than or equal to two cognitive domains. Atrophy was defined as cortical and deep gray matter volumes of z less than -1.5 compared with that in control participants. White matter lesions were assessed with T2-imaging, tract fractional anisotropy (ie, integrity) with diffusion MRI, and regional centrality (ie, importance within network) with functional MRI. Within each atrophy group, patients with cognitive impairment and preserved cognitive function were compared and regression analyses were performed to predict cognitive impairment. Results A total of 132 of 328 patients with MS had no atrophy; of these, 42 of 132 (32%) had cognitive impairment. Cognitive impairment in patients without atrophy was predicted by level of education (Wald test, 11.63; P < .01) and posterior cingulate centrality (Wald test, 6.82; P < .01). A total of 65 of 328 patients with MS had atrophy; of these, 49 of 65 (75%) had cognitive impairment. Cognitive impairment in patients with atrophy was predicted by white matter tract fractional anisotropy (Wald test, 4.89; P = .03) and posterior cingulate centrality (Wald test, 7.19; P < .01). Conclusion Cognitive impairment was related to white matter damage, but only in patients with MS with atrophy. In patients without atrophy, a lower level of education was most important for cognitive impairment. Posterior cingulate cortex showed functional abnormalities in all MS groups with cognitive impairment, regardless of atrophy.
研究已经出现认知障碍的无萎缩多发性硬化症(MS)患者与认知功能正常的伴萎缩 MS 患者之间的差异。
本回顾性影像学研究纳入了 332 例 MS 患者(106 名男性,226 名女性;平均年龄 48.1 岁;范围:23.0-72.5 岁)和 96 名健康对照参与者,这些参与者的影像资料采集于 2008 年至 2012 年之间。认知障碍定义为认知表现 z 评分低于对照参与者的-1.5,且至少在两个认知领域中出现这种情况。萎缩定义为皮质和深部灰质体积 z 评分低于对照参与者的-1.5。采用 T2 成像评估白质病变,采用弥散 MRI 评估束状分数各向异性(即完整性),采用功能 MRI 评估区域中心性(即网络内的重要性)。在每个萎缩组内,比较有认知障碍和认知功能正常的患者,并进行回归分析以预测认知障碍。
328 例 MS 患者中共有 132 例无萎缩,其中 42 例(32%)有认知障碍。无萎缩患者的认知障碍由受教育程度(Wald 检验,11.63;P <.01)和后扣带回中心性(Wald 检验,6.82;P <.01)预测。328 例 MS 患者中共有 65 例有萎缩,其中 49 例(75%)有认知障碍。萎缩患者的认知障碍由白质束状分数各向异性(Wald 检验,4.89;P =.03)和后扣带回中心性(Wald 检验,7.19;P <.01)预测。
认知障碍与白质损伤有关,但仅存在于伴萎缩的 MS 患者中。在无萎缩的患者中,较低的受教育程度对认知障碍最重要。后扣带回皮质在所有伴有认知障碍的 MS 患者组中均显示出功能异常,无论是否有萎缩。