Viswanathan A, Gschwendtner A, Guichard J-P, Buffon F, Cumurciuc R, O'Sullivan M, Holtmannspötter M, Pachai C, Bousser M-G, Dichgans M, Chabriat H
Departments of Neurology, Centre Hospitalier Universitaire Lariboisière, Assistance Publique des Hôpitaux de Paris, France.
Neurology. 2007 Jul 10;69(2):172-9. doi: 10.1212/01.wnl.0000265221.05610.70.
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a hereditary arteriopathy caused by mutations of the Notch3 gene. The disease is characterized by T2-hyperintense lesions (subcortical white matter lesions), T1-hypointense lesions (lacunar lesions), and T2*-weighted gradient-echo (GE) lesions (cerebral microhemorrhages [CMs]) visualized on clinical MRI sequences and is considered as a model of "pure" subcortical ischemic vascular dementia. Although numerous studies have investigated the impact of white matter lesions in patients with CADASIL, the clinical importance of lacunar lesions remains unknown. Our purpose was to examine the influence of the visible MRI markers in the disease, including the load of lacunar lesions on cognitive impairment and disability in CADASIL.
We collected clinical data from 147 consecutive patients enrolled in an ongoing two-center prospective cohort study. Degree of disability was assessed by modified Rankin scale and Barthel index. Degree of cognitive impairment was assessed by Mattis Dementia Rating Scale and Mini-Mental Status Examination. T1-weighted, fluid-attenuated inversion recovery, and GE images were obtained on a 1.5-T MRI. Volume and location of lacunar lesions, white matter hyperintensities (WMHs), and CMs were assessed.
There was a significant independent association between age, volume of lacunar lesions, and global cognitive function scales when analyzed in a multivariable model. In contrast, WMHs and CMs had no independent influence on cognitive function. Disability in this cohort was associated with volume of lacunar lesions, CMs, systolic blood pressure, and age but not with WMHs.
Among the lesions observed on conventional MRI in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), the overall lacunar lesion burden seems to have the most important impact on cognitive function and disability. These findings suggest that preventive strategies to decrease the risk of lacunar lesions as observed on MRI may reduce disease-related impairment in CADASIL. These results suggest that lacunar lesions may also play a key role in disability and cognitive impairment in more common forms of small-vessel disease.
大脑常染色体显性遗传性动脉病伴皮质下梗死和白质脑病(CADASIL)是一种由Notch3基因突变引起的遗传性动脉病。该疾病的特征是在临床MRI序列上可见T2高信号病变(皮质下白质病变)、T1低信号病变(腔隙性病变)和T2*加权梯度回波(GE)病变(脑微出血[CMs]),被认为是“纯”皮质下缺血性血管性痴呆的模型。尽管众多研究调查了CADASIL患者白质病变的影响,但腔隙性病变的临床重要性仍不明确。我们的目的是研究该疾病中可见的MRI标志物的影响,包括腔隙性病变负荷对CADASIL患者认知障碍和残疾的影响。
我们收集了正在进行的一项两中心前瞻性队列研究中连续纳入的147例患者的临床数据。残疾程度通过改良Rankin量表和Barthel指数进行评估。认知障碍程度通过Mattis痴呆评定量表和简易精神状态检查进行评估。在1.5-T MRI上获取T1加权、液体衰减反转恢复和GE图像。评估腔隙性病变、白质高信号(WMHs)和CMs的体积及位置。
在多变量模型分析中,年龄、腔隙性病变体积与整体认知功能量表之间存在显著的独立关联。相比之下,WMHs和CMs对认知功能没有独立影响。该队列中的残疾与腔隙性病变体积、CMs、收缩压和年龄相关,但与WMHs无关。
在大脑常染色体显性遗传性动脉病伴皮质下梗死和白质脑病(CADASIL)患者常规MRI上观察到的病变中,总的腔隙性病变负荷似乎对认知功能和残疾影响最大。这些发现表明,降低MRI上观察到的腔隙性病变风险的预防策略可能会减少CADASIL患者与疾病相关的损害。这些结果表明,腔隙性病变在更常见的小血管疾病形式的残疾和认知障碍中也可能起关键作用。