Department of Neurology, University of Washington School of Medicine, 1959 NE Pacific St., Seattle, WA, 98195, USA.
Department of Neurology, Veterans Affairs Boston Healthcare System, Jamaica Plain Campus, 150 S. Huntington Ave., Boston, MA, USA.
Cerebellum. 2018 Apr;17(2):143-151. doi: 10.1007/s12311-017-0882-5.
Spinocerebellar ataxias are a genetically heterogeneous group of degenerative diseases typically characterized by progressive ataxia and to various degrees, neuropathy, amyotrophy, and ocular abnormalities. There is increasing evidence for non-motor manifestations associated with cerebellar syndromes including cognitive and psychiatric features. We studied a retrospective clinical case series of eight subjects with spinocerebellar ataxias (SCAs) 2, 3, 7, and 17, all displaying features of psychosis, and also measured tyrosine hydroxylase (TH) staining of the substantia nigra (SN) at autopsy, among four of the subjects. We hypothesized that increased dopamine production in the SN may underlie the pathophysiology of psychosis in SCAs, given evidence of increased dopamine production in the SN in schizophrenia, as measured by TH staining. We analyzed differences in TH staining between the SCA psychosis cohort (n = 4), a heterogeneous ataxic cohort without psychosis (n = 22), and non-diseased age- and sex-matched control group (n = 12). SCA subjects with psychosis did not differ significantly in TH staining versus ataxic cases without psychosis. There was, however, increased TH staining in the ataxic cohort with and without psychosis (n = 26), compared to non-diseased controls (n = 12). Psychotic features were similar across subjects, with the presence of delusions, paranoia, and auditory hallucinations. Our findings are preliminary because of small numbers of subjects and variable neuropathology; however, they suggest that psychosis is a clinical feature of SCAs and may be under-recognized. While the underlying pathophysiology remains to be fully established, it may be related to extra-cerebellar pathology, including a possible propensity for increased dopamine activity in the SN.
脊髓小脑共济失调是一组遗传异质性退行性疾病,通常表现为进行性共济失调,并伴有不同程度的神经病、肌萎缩和眼部异常。越来越多的证据表明,与小脑综合征相关的非运动表现包括认知和精神特征。我们研究了 8 例脊髓小脑共济失调(SCA)2、3、7 和 17 患者的回顾性临床病例系列,所有患者均表现出精神病特征,并且还在其中 4 名患者死后测量了黑质(SN)中的酪氨酸羟化酶(TH)染色。我们假设,鉴于精神分裂症中 SN 中多巴胺生成增加的证据,SN 中多巴胺生成增加可能是 SCA 中精神病的病理生理学基础,TH 染色测量。我们分析了 SCA 精神病队列(n=4)、无精神病共济失调队列(n=22)和非疾病年龄和性别匹配对照组(n=12)之间 TH 染色的差异。与无精神病的共济失调病例相比,精神病 SCA 患者的 TH 染色无显著差异。然而,有和没有精神病的共济失调队列(n=26)中的 TH 染色均增加,与非疾病对照组(n=12)相比。精神症状在各个患者之间相似,存在妄想、偏执和幻听。由于患者数量少和神经病理学变化多样,我们的发现是初步的;然而,它们表明精神病是 SCA 的一种临床特征,可能被低估了。虽然潜在的病理生理学仍有待充分确定,但它可能与小脑外病理学有关,包括 SN 中多巴胺活性增加的可能性。