线粒体DNA中m.3243A >g变异患者的认知障碍概况

IF 2.2 3区 医学 Q3 CLINICAL NEUROLOGY
Satu Winqvist, Mikko Kärppä, Jukka S Moilanen, Kari Majamaa
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引用次数: 0

摘要

背景:线粒体DNA中的m.3243A >g变异与广泛的临床特征相关,从无症状的受试者到有严重症状的患者。认知受累是临床特征之一,但其严重程度和频率尚不清楚。在这里,我们描述与m.3243相关的神经心理学特征a b> g。方法:对45例成年m.3243患者进行研究一个b> G和45个健康受试者。采用综合神经心理测试组。如果与匹配的对照组相比,七个认知领域中至少有五个受损,则定义为认知障碍。如果认知障碍在各个领域普遍存在,则诊断为严重认知障碍。结果:m.3243患者16例(36%)其中有1名儿童被诊断为认知障碍,其中6名(13%)有严重认知障碍。诊断为认知障碍的中位年龄为53岁(范围25-64岁)。包括抽象推理障碍、记忆问题、运动功能缺陷和执行问题。执行功能受影响最大,言语记忆受影响最小。较高的变异异质性和更严重的整体表型与认知障碍相关,而年龄和性别无关。结论:m.3243患者认知功能障碍发生率高但严重的认知障碍并不常见。这种损伤影响所有的神经心理学领域,没有特定的特征可以确定。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Cognitive impairment profile in patients with the m.3243A> G variant in mitochondrial DNA.

Cognitive impairment profile in patients with the m.3243A> G variant in mitochondrial DNA.

Cognitive impairment profile in patients with the m.3243A> G variant in mitochondrial DNA.

Background: The m.3243A>G variant in mitochondrial DNA is associated with a wide spectrum of clinical features ranging from asymptomatic subjects to severely symptomatic patients. Cognitive involvement is one of the clinical features, but its severity and frequency are not properly known. Here we describe neuropsychological features associated with m.3243 A > G.

Methods: We studied 45 adult patients with m.3243 A > G and 45 healthy subjects. Comprehensive neuropsychological test battery was applied. Cognitive impairment was defined, if at least five out of seven cognitive domains were impaired compared to matched controls. Major cognitive impairment was diagnosed, if the impairment was general across the domains.

Results: Sixteen patients (36%) with m.3243 A > G were diagnosed with cognitive impairment, and six of them (13%) had a major cognitive impairment. The median age at diagnosis of cognitive impairment was 53 years (range, 25-64). The profile consisted of impaired abstract reasoning, memory problems, motor function defects and executive problems. Executive functions were affected most, and verbal memory was affected the least. Higher variant heteroplasmy and more severe global phenotype were associated with cognitive impairment, whereas age and sex were not.

Conclusion: Cognitive impairment is found frequently in patients with m.3243 A > G, but major cognitive impairment is not common. The impairment affects all neuropsychological domains and no specific profile could be identified.

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来源期刊
BMC Neurology
BMC Neurology 医学-临床神经学
CiteScore
4.20
自引率
0.00%
发文量
428
审稿时长
3-8 weeks
期刊介绍: BMC Neurology is an open access, peer-reviewed journal that considers articles on all aspects of the prevention, diagnosis and management of neurological disorders, as well as related molecular genetics, pathophysiology, and epidemiology.
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