Pan Jie J, Lee Michelle, Honig Lawrence S, Vonsattel Jean-Paul G, Faust Phyllis L, Louis Elan D
Department of Epidemiology, Mailman School of Public Health, Columbia University, New York, NY, USA.
G.H. Sergievsky Center, College of Physicians and Surgeons, Columbia University, New York, NY, USA.
Parkinsonism Relat Disord. 2014 Jun;20(6):655-8. doi: 10.1016/j.parkreldis.2014.03.003. Epub 2014 Mar 12.
In addition to tremor, patients with essential tremor (ET) may exhibit non-motor features, including a range of cognitive deficits. Several prospective, population-based epidemiological studies have reported an association between ET and incident dementia, especially Alzheimer's disease (AD). Moreover, in a brain repository-based study, a larger than expected proportion of ET patients also developed pathological changes characteristic of progressive supranuclear palsy, further suggesting a link between ET and tau pathology.
We selected a group of ET patients that were free of dementia clinically and without AD on postmortem examination. Our hypothesis was that neuronal tauopathic burden would be higher in the brains of these ET patients compared to controls. We compared Braak stage for neuronal tangles and Consortium to Establish a Registry for Alzheimer's Disease (CERAD) scores for neuritic plaques in the two groups.
The two groups were similar in age (82.6 ± 6.0 vs. 80.4 ± 8.1, p = 0.22). The 40 ET patients had a higher Braak neurofibrillary stage than 32 controls (means: 2.2 ± 1.2 vs. 1.2 ± 1.1; medians: 2.0 vs. 1.0, p < 0.001). Meanwhile, CERAD scores for neuritic plaques were similar in patients and controls (means: 0.6 ± 0.9 vs. 0.5 ± 0.6; medians: 0.0 vs. 0.0, p = 0.83).
While ET itself is not a tauopathy (i.e., a neurodegenerative disorder among whose main features are accumulation of hyperphosphorylated tau protein), ET may predispose individuals to accumulate more widespread cellular tau aggregates, and thus tau could play a central role in the cognitive impairment that can accompany ET.
除震颤外,特发性震颤(ET)患者可能表现出非运动特征,包括一系列认知缺陷。几项基于人群的前瞻性流行病学研究报告了ET与新发痴呆,尤其是阿尔茨海默病(AD)之间的关联。此外,在一项基于脑库的研究中,ET患者中出现进行性核上性麻痹特征性病理改变的比例高于预期,这进一步表明ET与tau病理之间存在联系。
我们选择了一组临床上无痴呆且死后检查无AD的ET患者。我们的假设是,与对照组相比,这些ET患者大脑中的神经元tau病变负担会更高。我们比较了两组中神经元缠结的Braak分期和阿尔茨海默病注册协会(CERAD)神经炎性斑块评分。
两组年龄相似(82.6±6.0岁对80.4±8.1岁,p = 0.22)。40例ET患者的Braak神经原纤维分期高于32例对照组(均值:2.2±1.2对1.2±1.1;中位数:2.0对1.0,p < 0.001)。同时,患者和对照组的神经炎性斑块CERAD评分相似(均值:0.6±0.9对0.5±0.6;中位数:0.0对0.0,p = 0.83)。
虽然ET本身不是tau病(即一种主要特征为过度磷酸化tau蛋白积累的神经退行性疾病),但ET可能使个体更容易积累更广泛的细胞tau聚集体,因此tau可能在ET伴发的认知障碍中起核心作用。