Eduarda Scoto Dias , José Henrique Tercziany Vanzin , Eduardo Augusto Borba , Mahara Freitas dos Santos , Thiago Alberto F.G. dos Santos , Thelma Skare , Renato Nisihara
{"title":"Cognitive dysfunction in systemic lupus erythematosus: Insights from a two-year longitudinal study in a Brazilian cohort","authors":"Eduarda Scoto Dias , José Henrique Tercziany Vanzin , Eduardo Augusto Borba , Mahara Freitas dos Santos , Thiago Alberto F.G. dos Santos , Thelma Skare , Renato Nisihara","doi":"10.1016/j.reuma.2025.501941","DOIUrl":null,"url":null,"abstract":"<div><h3>Objectives</h3><div>The objective of this study was to examine cognitive dysfunction in a Brazilian sample of SLE patients for two years.</div></div><div><h3>Methods</h3><div>A sample of 50 individuals with SLE was assessed at baseline for epidemiological and treatment data, disease activity by SLEDAI 2K (SLE disease activity 2000), cumulative damage by SLICC/ACR DI (Systemic Lupus International Collaborating Clinics/American College of Rheumatology Damage Index), depression by CES-D (Center for Epidemiological Studies-Depression) and cognitive function through MoCA (Montreal Cognitive Assessment). The same assessment was repeated after two years.</div></div><div><h3>Results</h3><div>The prevalence of cognitive impairment at baseline was 68%. The baseline cognitive assessment showed impairment in visuospatial/executive function (<em>p</em> <!-->=<!--> <!-->0.002), naming (<em>p</em> <!-->=<!--> <!-->0.04), attention (<em>p</em> <!--><<!--> <!-->0.0001) and delayed recall (<em>p</em> <!--><<!--> <!-->0.0001). The median MoCA results did not change in two years (<em>p</em> <!-->=<!--> <!-->0.45), but 6 individuals (12%) that had normal cognitive function at baseline developed mild cognitive impairment and two (4%) that had mild cognitive impairment, improved. When considering the MoCA domains the only significant difference was improvement in abstraction (<em>p</em> <!-->=<!--> <!-->0.001). No correlations between MoCA delta (difference between second and first value) and delta SLEDAI, delta SLICC and delta CES-D were found (all with <em>p</em> <!-->><!--> <!-->0.05). Also, no associations were found with used treatment or autoantibodies profile.</div></div><div><h3>Conclusions</h3><div>Cognitive dysfunction in SLE is dynamic and may require periodic re-assessments. Changes in cognition were not associated with disease activity, depression or cumulative damage in this sample.</div></div>","PeriodicalId":47115,"journal":{"name":"Reumatologia Clinica","volume":"21 7","pages":"Article 501941"},"PeriodicalIF":1.3000,"publicationDate":"2025-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Reumatologia Clinica","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1699258X25001354","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"RHEUMATOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Objectives
The objective of this study was to examine cognitive dysfunction in a Brazilian sample of SLE patients for two years.
Methods
A sample of 50 individuals with SLE was assessed at baseline for epidemiological and treatment data, disease activity by SLEDAI 2K (SLE disease activity 2000), cumulative damage by SLICC/ACR DI (Systemic Lupus International Collaborating Clinics/American College of Rheumatology Damage Index), depression by CES-D (Center for Epidemiological Studies-Depression) and cognitive function through MoCA (Montreal Cognitive Assessment). The same assessment was repeated after two years.
Results
The prevalence of cognitive impairment at baseline was 68%. The baseline cognitive assessment showed impairment in visuospatial/executive function (p = 0.002), naming (p = 0.04), attention (p < 0.0001) and delayed recall (p < 0.0001). The median MoCA results did not change in two years (p = 0.45), but 6 individuals (12%) that had normal cognitive function at baseline developed mild cognitive impairment and two (4%) that had mild cognitive impairment, improved. When considering the MoCA domains the only significant difference was improvement in abstraction (p = 0.001). No correlations between MoCA delta (difference between second and first value) and delta SLEDAI, delta SLICC and delta CES-D were found (all with p > 0.05). Also, no associations were found with used treatment or autoantibodies profile.
Conclusions
Cognitive dysfunction in SLE is dynamic and may require periodic re-assessments. Changes in cognition were not associated with disease activity, depression or cumulative damage in this sample.
期刊介绍:
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