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Neuropsychological Impairment in Systemic Lupus Erythematosus: A Comparison with Multiple Sclerosis

机译:系统性红斑狼疮的神经心理障碍:与多发性硬化症的比较。

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摘要

In this manuscript, we review literature describing the neuropsychological and brain imaging characteristics of systemic lupus erythematosus (SLE) patients. The findings are compared and contrasted with multiple sclerosis (MS) studies, revealing similarities and differences of interest to clinicians and researchers. While cognitive impairment is somewhat less common in SLE than MS, the diseases share a similar cognitive profile with deficits most prominent on tests emphasizing the speed of information processing, working memory, and visual/spatial learning, and memory. In early or more mildly affected patients, diffuse white matter damage, which may not be apparent on conventional brain imaging, plays a major role in clinical presentation and cognitive testing. The causes of white matter damage are very different, however, and in later stages of the disease MS and SLE appear to give rise to different forms of cerebral pathology. MS may be characterized by increasing brain atrophy affecting especially the cortical and deep gray matter, at least after conversion to secondary progressive course. There is less evidence for neurodegenerative changes in SLE, but patients are increasingly at risk for cerebrovascular disease. We conclude by offering some suggestions for future clinical and imaging research.
机译:在本手稿中,我们回顾了描述系统性红斑狼疮(SLE)患者的神经心理学和脑成像特征的文献。将这些发现与多发性硬化症(MS)研究进行比较和对比,揭示临床医生和研究人员感兴趣的异同。尽管在SLE中认知障碍在某种程度上不如在MS中常见,但这些疾病具有相似的认知特征,其缺陷在强调信息处理,工作记忆以及视觉/空间学习和记忆速度的测试中最为突出。在早期或更轻​​度受影响的患者中,弥散性白质损伤(在常规脑成像中可能不明显)在临床表现和认知测试中起主要作用。然而,白质损害的原因非常不同,在疾病的晚期,MS和SLE似乎引起了不同形式的脑病理。 MS的特征可能是至少在转换为继发性进行性病程后,脑萎缩增加,尤其是影响皮质和深灰质。 SLE发生神经退行性改变的证据较少,但患者患脑血管疾病的风险越来越高。最后,我们为将来的临床和影像学研究提供了一些建议。

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