Mercadillo Roberto E, Galvez Víctor, Díaz Rosalinda, Hernández-Castillo Carlos Roberto, Campos-Romo Aurelio, Boll Marie-Catherine, Pasaye Erick H, Fernandez-Ruiz Juan
Laboratorio de Neuropsicología, Departamento de Fisiología, Facultad de Medicina, Universidad Nacional Autónoma de México, Mexico.
Instituto de Neuroetología, Universidad Veracruzana, Mexico.
J Neurol Sci. 2014 Dec 15;347(1-2):50-8. doi: 10.1016/j.jns.2014.09.018. Epub 2014 Sep 19.
Spinocerebellar Ataxia Type 2 (SCA2) is a genetic disorder causing cerebellar degeneration that result in motor and cognitive alterations. Voxel-based morphometry (VBM) analyses have found neurodegenerative patterns associated to SCA2, but they show some discrepancies. Moreover, behavioral deficits related to non-cerebellar functions are scarcely discussed in those reports. In this work we use behavioral and cognitive tests and VBM to identify and confirm cognitive and gray matter alterations in SCA2 patients compared with control subjects. Also, we discuss the cerebellar and non-cerebellar functions affected by this disease. Our results confirmed gray matter reduction in the cerebellar vermis, pons, and insular, frontal, parietal and temporal cortices. However, our analysis also found unreported loss of gray matter in the parahippocampal gyrus bilaterally. Motor performance test ratings correlated with total gray and white matter reductions, but executive performance and clinical features such as CAG repetitions and disease progression did not show any correlation. This pattern of cerebellar and non-cerebellar morphological alterations associated with SCA2 has to be considered to fully understand the motor and non-motor deficits that include language production and comprehension and some social skill changes that occur in these patients.
2型脊髓小脑共济失调(SCA2)是一种导致小脑变性的遗传性疾病,会引起运动和认知改变。基于体素的形态测量(VBM)分析发现了与SCA2相关的神经退行性模式,但这些模式存在一些差异。此外,这些报告很少讨论与非小脑功能相关的行为缺陷。在这项研究中,我们使用行为和认知测试以及VBM来识别和确认SCA2患者与对照受试者相比的认知和灰质改变。此外,我们还讨论了受该疾病影响的小脑和非小脑功能。我们的结果证实了小脑蚓部、脑桥以及岛叶、额叶、顶叶和颞叶皮质的灰质减少。然而,我们的分析还发现双侧海马旁回存在未报告的灰质丢失。运动性能测试评分与总灰质和白质减少相关,但执行性能以及诸如CAG重复和疾病进展等临床特征未显示出任何相关性。必须考虑这种与SCA2相关的小脑和非小脑形态学改变模式,以便全面理解这些患者出现的运动和非运动缺陷,包括语言产生和理解以及一些社交技能变化。