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Alcohol-related cerebellar degeneration: not all down to toxicity?

机译:酒精相关性小脑变性:不是全部归结为毒性吗?

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BackgroundAlcohol-related cerebellar degeneration is one of the commonest acquired forms of cerebellar ataxia. The exact pathogenic mechanisms by which alcohol leads to cerebellar damage remain unknown. Possible autoreactive immune mediated mechanisms have not been explored previously. In this study, we aim to investigate the potential role of alcohol-induced immune mediated cerebellar degeneration. MethodsPatients with ataxia and a history of alcohol misuse were recruited from the Ataxia and Hepatology tertiary clinics at Sheffield Teaching Hospitals NHS Trust. We determined the pattern of cerebellar involvement both on clinical (SARA score) and imaging (MRI volumetry and MR spectroscopy) parameters. In addition, HLA genotyping, serological markers for gluten-related disorders and serological reactivity on rat cerebellar tissue using indirect immunohistochemistry were assessed. ResultsThirty-eight patients were included in the study all of whom had ataxia. The gait (97?%), stance (89?%) and heel-shin slide (89?%) were the predominant SARA elements affected. MRI volumetric and spectroscopy techniques demonstrated significant structural, volumetric and functional deficits of the cerebellum with particular involvement of the cerebellar vermis. Circulating anti-gliadin antibodies were detected in 34?% patients vs. 12?% in healthy controls. Antibodies to transglutaminase 6 (TG6) were detected in 39?% of patients and 4?% of healthy control subjects. Using immunohistochemistry, Purkinje cell and/or granular layer reactivity was demonstrated in 71?% of patient sera. ConclusionsAlcohol induced tissue injury to the CNS leading to cerebellar degeneration may also involve immune mediated mechanisms, including sensitisation to gluten.
机译:背景与酒精有关的小脑变性是小脑共济失调最常见的获得形式之一。酒精导致小脑损伤的确切致病机制尚不清楚。先前尚未探讨可能的自身反应性免疫介导的机制。在这项研究中,我们旨在调查酒精诱导的免疫介导的小脑变性的潜在作用。方法从谢菲尔德教学医院NHS Trust的共济失调和肝病三级诊所招募有共济失调和酗酒史的患者。我们确定了小脑受累的临床(SARA评分)和影像学(MRI容量法和MR光谱)参数的模式。此外,使用间接免疫组织化学方法评估了HLA基因分型,面筋相关疾病的血清学标志物以及大鼠小脑组织的血清反应性。结果共纳入38例共济失调患者。步态(97%),姿势(89%)和后跟跟滑(89 %%)是受影响的主要SARA元素。 MRI体积和光谱技术显示出小脑的明显结构,体积和功能缺陷,特别是小脑ver骨受累。在34%的患者中检测到循环中的抗麦醇溶蛋白抗体,而在健康对照组中则为12%。在39%的患者和4%的健康对照组中检出了转谷氨酰胺酶6(TG6)抗体。使用免疫组织化学,在71%的患者血清中证实了浦肯野细胞和/或颗粒层反应性。结论酒精引起的中枢神经系统组织损伤导致小脑变性可能还涉及免疫介导的机制,包括对面筋的致敏作用。

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