Fang Xiao-Jing, Yu Meng, Wu Yuan, Zhang Zi-Hao, Wang Wei-Wei, Wang Zhao-Xia, Yuan Yun
Department of Neurology, Peking University First Hospital, Beijing 100034, China.
Department of Ophthalmology, Peking University First Hospital, Beijing 100034, China.
Chin Med J (Engl). 2017 May 5;130(9):1042-1048. doi: 10.4103/0366-6999.204935.
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a hereditary small artery disease caused by NOTCH3 gene mutation. We performed enhanced depth imaging optical coherence tomography (EDI-OCT) to evaluate the retinal vessel changes in CADASIL patients and assessed their consonance with brain magnetic resonance imaging (MRI) findings.
Of 27 genetically confirmed patients and an equal number of controls were recruited at the Peking University First Hospital from January 2015 to August 2016. All patients underwent 7T-MRI of the brain. Fazekas score, number of small infarcts and microbleeds were evaluated. All patients and controls underwent EDI-OCT to measure subfoveal choroidal thickness (SFCT), inner and outer diameters as well as arterial and venous wall thickness, and arterial venous ratio of the inner (AVRin) and outer diameters (AVRout). The relation between retinal vessel changes and Fazekas scores, numbers of small infarcts, or microbleeds was analyzed. Paired t-test was used to compare the SFCT and retinal vessel measurement data between patients and controls. Spearman's correlation was used to investigate the correlation between retinal vessel changes and MRI lesions.
In CADASIL patients, mean SFCT (268.37 ± 46.50 μm) and mean arterial inner diameter (93.46 ± 9.70 μm) were significantly lower than that in controls (P < 0.001,P = 0.048, respectively). Mean arterial outer diameter (131.74 ± 10.87 μm), venous inner (128.99 ± 13.62 μm) and outer diameter (164.82 ± 14.77 μm), and mean arterial (19.13 ± 1.85 μm) and venous (17.91 ± 2.76 μm) wall thickness were significantly higher than that in controls (P = 0.023,P = 0.004,P < 0.001,P < 0.001, respectively). Arterial inner diameter (rs= -0.39, P= 0.044), AVRin (rs= -0.65,P < 0.001), and AVRout (rs= -0.56, P= 0.002) showed a negative correlation with the number of small infarcts. Venous inner diameter (rs = 0.46, P= 0.016) showed a positive correlation with the number of small infarcts. Venous inner diameter (rs = 0.59, P= 0.002), outer diameter (rs = 0.47, P= 0.017), showed a positive correlation with the number of cerebral microbleeds (CMBs). AVRin (rs= -0.52, P= 0.007) and AVRout (rs= -0.40, P= 0.048) showed a negative correlation with the number of CMBs.
Measurement of retinal vessels using EDI-OCT correlates moderately well with MRI parameters. EDI-OCT might be a useful evaluation tool for CADASIL patients.
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小动脉疾病。我们进行了增强深度成像光学相干断层扫描(EDI-OCT)以评估CADASIL患者的视网膜血管变化,并评估其与脑磁共振成像(MRI)结果的一致性。
2015年1月至2016年8月,北京大学第一医院招募了27例基因确诊患者及同等数量的对照。所有患者均接受脑部7T-MRI检查。评估Fazekas评分、小梗死灶数量和微出血情况。所有患者及对照均接受EDI-OCT检查,以测量黄斑中心凹下脉络膜厚度(SFCT)、内径和外径以及动静脉壁厚度,以及内径(AVRin)和外径(AVRout)的动静脉比。分析视网膜血管变化与Fazekas评分、小梗死灶数量或微出血情况之间的关系。采用配对t检验比较患者与对照之间的SFCT和视网膜血管测量数据。采用Spearman相关性分析研究视网膜血管变化与MRI病变之间的相关性。
CADASIL患者的平均SFCT(268.37±46.50μm)和平均动脉内径(93.46±9.70μm)显著低于对照(分别为P<0.001,P=0.048)。平均动脉外径(131.74±10.87μm)、静脉内径(128.99±13.62μm)和外径(164.82±14.77μm),以及平均动脉壁厚度(19.13±1.85μm)和静脉壁厚度(17.91±2.76μm)显著高于对照(分别为P=0.023,P=0.004,P<0.001,P<0.001)。动脉内径(rs=-0.39,P=0.044)、AVRin(rs=-0.65,P<0.001)和AVRout(rs=-0.56,P=0.002)与小梗死灶数量呈负相关。静脉内径(rs=0.46,P=0.016)与小梗死灶数量呈正相关。静脉内径(rs=0.59,P=0.002)、外径(rs=0.47,P=0.017)与脑微出血(CMB)数量呈正相关。AVRin(rs=-0.52,P=0.007)和AVRout(rs=-0.40,P=0.048)与CMB数量呈负相关。
使用EDI-OCT测量视网膜血管与MRI参数具有较好的相关性。EDI-OCT可能是CADASIL患者的一种有用的评估工具。