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原发性干燥综合征中的认知功能障碍与痴呆

Cognitive Dysfunction and Dementia in Primary Sjögren's Syndrome.

作者信息

Blanc Frederic, Longato Nadine, Jung Barbara, Kleitz Catherine, Di Bitonto Laure, Cretin Benjamin, Collongues Nicolas, Sordet Christelle, Fleury Marie, Poindron Vincent, Gottenberg Jacques-Eric, Anne Olivier, Lipsker Dan, Martin Thierry, Sibilia Jean, de Seze Jérôme

机构信息

Neuropsychology Unit, Service of Neurology, University Hospital of Strasbourg, 1 avenue Molière, 67000 Strasbourg, France ; ICube Laboratory and Strasbourg Federation of Translational Medicine (FMTS), University of Strasbourg and CNRS, Strasbourg, France ; Memory Resource and Research Centre (CMRR) from Alsace, University Hospital of Strasbourg, 1 avenue Molière, 67000 Strasbourg, France.

出版信息

ISRN Neurol. 2013 Sep 19;2013:501327. doi: 10.1155/2013/501327. eCollection 2013.

Abstract

Background. Primary Sjögren's syndrome (PSS) is a frequent systemic autoimmune disease. In this study, we aimed to explore the cognitive impairment and the correlations with brain MRI. Methods. Twenty-five patients (mean age 55 ± 11.8 years, 21 females) with PSS were prospectively selected and tested with a French translation of the Brief Repeatable Battery for Neuropsychological Examination. The results were compared with the scores for 25 matched patients with multiple sclerosis (MS) and 25 controls. Brain lesions were assessed by brain MRI using the Wahlund classification. Results. Fifteen of the 25 PSS patients (60%) presented with cognitive disorders versus 19/25 MS patients (76%). Five patients had dementia in the PSS group. Speed of information processing, attention, immediate and long-term memory, and executive functions were frequently impaired. The mean duration of cognitive complaints was 5.6 ± 6.1 years, and the mean duration of PSS was 15.8 ± 14.0 years. A trend towards a correlation was found between the severity of cognitive impairment and the degree of white matter lesions (WML) (P = 0.03, rho = 0.43). Conclusion. Cognitive impairment-mild or dementia-exists in patients with PSS. Further MRI studies are needed to better understand the precise neural basis of cognitive impairment in PSS patients.

摘要

背景。原发性干燥综合征(PSS)是一种常见的全身性自身免疫性疾病。在本研究中,我们旨在探讨认知障碍及其与脑部磁共振成像(MRI)的相关性。方法。前瞻性选取25例PSS患者(平均年龄55±11.8岁,21例女性),使用神经心理学检查简式可重复成套测验的法语翻译版本进行测试。将结果与25例匹配的多发性硬化症(MS)患者及25例对照者的得分进行比较。采用瓦伦德分类法通过脑部MRI评估脑损伤情况。结果。25例PSS患者中有15例(60%)存在认知障碍,而25例MS患者中有19例(76%)存在认知障碍。PSS组中有5例患者患有痴呆。信息处理速度、注意力、即刻和长期记忆以及执行功能经常受损。认知主诉的平均持续时间为5.6±6.1年,PSS的平均病程为15.8±14.0年。发现认知障碍的严重程度与白质病变(WML)程度之间存在相关性趋势(P = 0.03,rho = 0.43)。结论。PSS患者存在认知障碍——轻度或痴呆。需要进一步的MRI研究以更好地理解PSS患者认知障碍的确切神经基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe5d/3793286/c86b12f750d6/ISRN.NEUROLOGY2013-501327.001.jpg

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