Neuropathological correlates of memory dysfunction in the Wernicke-Korsakoff syndrome.

G Halliday, K Cullen, A Harding
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Abstract

The Wernicke-Korsakoff syndrome is a neuropathological term which encompasses two clinical syndromes in thiamine-deficient alcoholics, Wernicke's encephalopathy and Korsakoff's psychosis. Wernicke's encephalopathy is characterised by eye and gait disorders and mental confusion, and can lead to the profound and permanent amnesia known as Korsakoff's psychosis. Despite this specific difference, both conditions appear to have identical neuropathology with haemorrhages and other lesions around the ventricular system. The memory deficit has been attributed to a number of brain lesions, including a recent suggestion that brain pathways utilising particular neurotransmitters are specifically damaged. To examine this, the number of chemically identified neurons in particular brain regions was quantified in patients with Wernicke's encephalopathy alone or in combination with Korsakoff's psychosis and compared with age- and sex-matched controls. Noradrenaline, a neurotransmitter thought to be involved in the process of selective attention, is localised in pathways projecting to the cortex. Our patients with either Wernicke's encephalopathy or additional Korsakoff's psychosis do not differ from controls in the distribution and number of these cells. Serotonin is another neurotransmitter that has been linked with alcohol dependency. Both patient groups have a profound loss of serotonin-containing neurons compared with controls. The loss of forebrain neurons containing acetylcholine in patients with Alzheimer's disease has implicated this neurotransmitter in the maintenance of memory functions. There was a large variation in the number of these forebrain neurons in thiamine-deficient alcoholics compared with controls. Cholinergic cell loss reflected the severity of cognitive dysfunction, but was not exclusive to patients with amnesia. Two thalamic nuclei are involved in relaying memories for storage and retrieval, the anterior and mediodorsal thalamic nuclei. While patients with Wernicke's encephalopathy often had neuronal loss in the mediodorsal nucleus, only patients with Korsakoff's psychosis had cell loss in both medial thalamic nuclei. The results suggest that cumulative lesions contribute to the amnesia seen in thiamine-deficient alcoholics, including deficits in serotonergic, cholinergic and medial thalamic pathways.

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Wernicke-Korsakoff综合征中记忆功能障碍的神经病理学相关性。
Wernicke-Korsakoff综合征是一个神经病理学术语,包括两种硫胺素缺乏症的临床综合征,即Wernicke脑病和Korsakoff精神病。韦尼克脑病的特点是眼睛和步态紊乱以及精神错乱,并可能导致被称为科萨科夫精神病的严重和永久性健忘症。尽管有这种特殊的差异,但两种情况似乎都有相同的神经病理,出血和心室系统周围的其他病变。记忆缺陷被认为是由一些大脑损伤引起的,包括最近的一项研究表明,利用特定神经递质的大脑通路受到了特别的损害。为了检验这一点,在单独患有韦尼克脑病或合并Korsakoff精神病的患者中,对特定大脑区域化学鉴定的神经元数量进行了量化,并与年龄和性别匹配的对照组进行了比较。去甲肾上腺素,一种被认为与选择性注意过程有关的神经递质,被定位于投射到大脑皮层的通路中。我们的患者无论是韦尼克脑病还是附加的Korsakoff精神病,在这些细胞的分布和数量上与对照组没有区别。血清素是另一种与酒精依赖有关的神经递质。与对照组相比,两组患者都有含血清素神经元的严重缺失。阿尔茨海默病患者含有乙酰胆碱的前脑神经元的丧失暗示了这种神经递质在维持记忆功能中的作用。与对照组相比,缺乏硫胺素的酗酒者的前脑神经元数量有很大变化。胆碱能细胞丧失反映了认知功能障碍的严重程度,但并非健忘症患者所独有。两个丘脑核参与传递记忆的存储和检索,即丘脑前核和丘脑中背核。Wernicke脑病患者通常在中背侧核有神经元丢失,而只有Korsakoff精神病患者在丘脑内侧核有细胞丢失。结果表明,累积性损伤导致了硫胺素缺乏症酗酒者的健忘症,包括血清素能、胆碱能和内侧丘脑通路的缺陷。
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