Horn Mitchell J, Gokcal Elif, Becker Alex J, Das Alvin S, Warren Andrew D, Schwab Kristin, Goldstein Joshua N, Biffi Alessandro, Rosand Jonathan, Polimeni Jonathan R, Viswanathan Anand, Greenberg Steven M, Gurol M Edip
J Philip Kistler Stroke Research Center, Department of Neurology, Massachusetts General Hospital, Boston, MA, USA.
Radiology, Massachusetts General Hospital, Boston, Massachusetts, USA.
J Neurol Neurosurg Psychiatry. 2022 May 9. doi: 10.1136/jnnp-2021-328553.
Recent data suggest that cerebral amyloid angiopathy (CAA) causes haemorrhagic lesions in cerebellar cortex as well as subcortical cerebral atrophy. However, the potential effect of CAA on cerebellar tissue loss and its clinical implications have not been investigated.
Our study included 70 non-demented patients with probable CAA, 70 age-matched healthy controls (HCs) and 70 age-matched patients with Alzheimer's disease (AD). The cerebellum was segmented into percent of cerebellar subcortical volume (pCbll-ScV) and percent of cerebellar cortical volume (pCbll-CV) represented as percent (p) of estimated total intracranial volume. We compared pCbll-ScV and pCbll-CV between patients with CAA, HCs and those with AD. Gait velocity (metres/second) was used to investigate gait function in patients with CAA.
Patients with CAA had significantly lower pCbll-ScV compared with both HC (1.49±0.1 vs 1.73±0.2, p<0.001) and AD (1.49±0.1 vs 1.66±0.24, p<0.001) and lower pCbll-CV compared with HCs (6.03±0.5 vs 6.23±0.6, p=0.028). Diagnosis of CAA was independently associated with lower pCbll-ScV compared with HCs (p<0.001) and patients with AD (p<0.001) in separate linear regression models adjusted for age, sex and presence of hypertension. Lower pCbll-ScV was independently associated with worse gait velocity (β=0.736, 95% CI 0.28 to 1.19, p=0.002) in a stepwise linear regression analysis including pCbll-CV along with other relevant variables.
Patients with CAA show more subcortical cerebellar atrophy than HC or patients with AD and more cortical cerebellar atrophy than HCs. Reduced pCbll-ScV correlated with lower gait velocity in regression models including other relevant variables. Overall, this study suggests that CAA causes cerebellar injury, which might contribute to gait disturbance.
近期数据表明,脑淀粉样血管病(CAA)可导致小脑皮质出血性病变以及皮质下脑萎缩。然而,CAA对小脑组织丢失的潜在影响及其临床意义尚未得到研究。
我们的研究纳入了70例可能患有CAA的非痴呆患者、70例年龄匹配的健康对照者(HCs)以及70例年龄匹配的阿尔茨海默病(AD)患者。将小脑分割为小脑皮质下体积百分比(pCbll-ScV)和小脑皮质体积百分比(pCbll-CV),以估计的总颅内体积的百分比(p)表示。我们比较了CAA患者、HCs和AD患者之间的pCbll-ScV和pCbll-CV。使用步态速度(米/秒)来研究CAA患者的步态功能。
与HCs(1.49±0.1对1.73±0.2,p<0.001)和AD患者(1.49±0.1对1.66±0.24,p<0.001)相比,CAA患者的pCbll-ScV显著更低;与HCs相比,CAA患者的pCbll-CV更低(6.03±0.5对6.23±0.6,p=0.028)。在针对年龄、性别和高血压存在情况进行调整的单独线性回归模型中,与HCs(p<0.001)和AD患者(p<0.001)相比,CAA诊断与更低的pCbll-ScV独立相关。在包括pCbll-CV以及其他相关变量的逐步线性回归分析中,更低的pCbll-ScV与更差的步态速度独立相关(β=0.736,95%置信区间0.28至1.19,p=0.002)。
CAA患者的皮质下小脑萎缩比HCs或AD患者更严重,皮质小脑萎缩比HCs更严重。在包括其他相关变量的回归模型中,pCbll-ScV降低与更低的步态速度相关。总体而言,本研究表明CAA会导致小脑损伤,这可能导致步态障碍。