Indart Sandrine, Hugon Jacques, Guillausseau Pierre Jean, Gilbert Alice, Dumurgier Julien, Paquet Claire, Sène Damien
aCognitive Neurology Center AP-HP, Hôpital Lariboisière bINSERM, U942 cUniversity of Paris Diderot, Sorbonne Paris Cité dDepartment of Internal Medicine, AP-HP, Hôpital Lariboisière, INSERM eDepartment of Biochemistry and Molecular Biology, AP-HP, Hôpital Lariboisière, Paris, France.
Medicine (Baltimore). 2017 Apr;96(16):e6384. doi: 10.1097/MD.0000000000006384.
Primary Sjögren syndrome (pSS) is a chronic systemic autoimmune disease characterized by xerophthalmia, xerostomia, and potential peripheral or central neurological involvement. In pSS, the prevalence of cognitive disorders is generally sparse across literature and the impact of pain on cognitive profile is unclear. The aim of this study was to determine the relation between pain, cognitive complaint, and impairment in a very homogenous population of 10 pSS patients with painful small fiber neuropathy (PSFN) and spontaneous cognitive complaint. Neurological exam, neuropsychological assessment, clinical evaluation measuring pain level, fatigue, anxiety, depression, and cognitive complaint were performed. Our results showed that 100% of patients had cognitive dysfunction especially in executive domain (80%). The most sensitive test was the Wisconsin Card Sorting Test (WCST), abnormal in 70% of our population. Moreover, we found clear cut significant correlations between pain levels and 3 measures of WCST: the number of errors (R = -0.768, P = .0062), perseverations (R = 0.831, P = .0042), and categories (R = 0.705, P = .02). In the literature review, the impact of pain is underexplored and results could be discordant. In a homogeneous cohort of pSS patients with PSFN, a cognitive complaint seems to be a valid reflection of cognitive dysfunction marked by a specific executive profile found with the WCST. In this preliminary study, this profile is linked to the level of pain and highlights that an appropriate management of pain control and a cognitive readaptation in patients could improve the quality of life.
原发性干燥综合征(pSS)是一种慢性全身性自身免疫性疾病,其特征为干眼症、口干症以及可能出现的外周或中枢神经系统受累。在原发性干燥综合征中,认知障碍的患病率在文献中普遍较少提及,且疼痛对认知状况的影响尚不清楚。本研究的目的是确定10例患有疼痛性小纤维神经病变(PSFN)且有自发认知主诉的原发性干燥综合征患者这一非常同质的群体中,疼痛、认知主诉与功能损害之间的关系。进行了神经学检查、神经心理学评估、测量疼痛程度、疲劳、焦虑、抑郁和认知主诉的临床评估。我们的结果显示,100%的患者存在认知功能障碍,尤其是在执行领域(80%)。最敏感的测试是威斯康星卡片分类测验(WCST),我们群体中有70%的结果异常。此外,我们发现疼痛程度与WCST的3项指标之间存在明显的显著相关性:错误数量(R = -0.768,P = 0.0062)、持续性错误(R = 0.831,P = 0.0042)和分类(R = 0.705,P = 0.02)。在文献综述中,疼痛的影响研究不足且结果可能不一致。在一组患有PSFN的原发性干燥综合征患者的同质队列中,认知主诉似乎是认知功能障碍的有效反映,这种障碍以WCST发现的特定执行特征为标志。在这项初步研究中,这种特征与疼痛程度相关,并突出表明对患者进行适当的疼痛控制管理和认知再适应可以提高生活质量。