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Screening for cognitive impairment in SLE using the Self-Administered Gerocognitive Exam

Objective Systemic lupus erythematosus (SLE) is a multisystem autoimmune disease that can affect the central nervous system in multiple ways, including causing cognitive dysfunction. Cognitive dysfunction is a common complaint of SLE patients yet diagnosis is challenging, time consuming, and costly....

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Published in:Lupus 2018-07, Vol.27 (8), p.1363-1367
Main Authors: Meara, A, Davidson, N, Steigelman, H, Zhao, S, Brock, G, Jarjour, W N, Rovin, B H, Madhoun, H, Parikh, S, Hebert, L, Ayoub, I, Ardoin, S P
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cited_by cdi_FETCH-LOGICAL-c365t-bd79d8d2ad425189d463dca4c9b1ce61bc2169580621816ed529cbb5227bbaff3
cites cdi_FETCH-LOGICAL-c365t-bd79d8d2ad425189d463dca4c9b1ce61bc2169580621816ed529cbb5227bbaff3
container_end_page 1367
container_issue 8
container_start_page 1363
container_title Lupus
container_volume 27
creator Meara, A
Davidson, N
Steigelman, H
Zhao, S
Brock, G
Jarjour, W N
Rovin, B H
Madhoun, H
Parikh, S
Hebert, L
Ayoub, I
Ardoin, S P
description Objective Systemic lupus erythematosus (SLE) is a multisystem autoimmune disease that can affect the central nervous system in multiple ways, including causing cognitive dysfunction. Cognitive dysfunction is a common complaint of SLE patients yet diagnosis is challenging, time consuming, and costly. This study evaluated the Self-Administered Gerocognitive Exam (SAGE) as a screening test for cognitive impairment in a cohort of SLE patients. Methods A total of 118 SLE patients completed the SAGE. Providers completed the Systemic Lupus Erythematosus Disease Activity Index (SLEDAI) and the Systemic Lupus International Collaborative Clinics Damage Index (SLICC-DI). SAGE scores were grouped into normal (>16) and abnormal (≤16) categories. Univariate and multivariate analyses were performed. Results Of the 118 participants, 21(18%) scored ≤16 on the SAGE instrument. In univariate analysis, race, ethnicity, household income, and SLICC-DI scores were associated with the SAGE (p $50,000, 95% CI 2.45–57, p = 0.002). Conclusions In SLE patients, this study demonstrates an independent relationship between neurocognitive impairment (as measured by the SAGE) and higher lupus-related damage, as measured by the SLICC-DI, and lower household income. Abnormal SAGE scores were also associated with Hispanic ethnicity. A language barrier could explain this because the SAGE instrument was conducted in English only. The SAGE was feasible to measure in the clinic setting.
doi_str_mv 10.1177/0961203318759429
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Cognitive dysfunction is a common complaint of SLE patients yet diagnosis is challenging, time consuming, and costly. This study evaluated the Self-Administered Gerocognitive Exam (SAGE) as a screening test for cognitive impairment in a cohort of SLE patients. Methods A total of 118 SLE patients completed the SAGE. Providers completed the Systemic Lupus Erythematosus Disease Activity Index (SLEDAI) and the Systemic Lupus International Collaborative Clinics Damage Index (SLICC-DI). SAGE scores were grouped into normal (&gt;16) and abnormal (≤16) categories. Univariate and multivariate analyses were performed. Results Of the 118 participants, 21(18%) scored ≤16 on the SAGE instrument. In univariate analysis, race, ethnicity, household income, and SLICC-DI scores were associated with the SAGE (p &lt; 0.05). In multivariable analysis, abnormal SAGE score was independently associated with higher SLICC-DI score (odds ratio (OR) = 1.44, 95% confidence intervals 1.04–1.99, p = 0.03)), Hispanic ethnicity (OR = 43.4, 95% CI 3.1–601, p = 0.005), and lower household income (OR = 11.9 for ≤$15,000 vs &gt;$50,000, 95% CI 2.45–57, p = 0.002). Conclusions In SLE patients, this study demonstrates an independent relationship between neurocognitive impairment (as measured by the SAGE) and higher lupus-related damage, as measured by the SLICC-DI, and lower household income. Abnormal SAGE scores were also associated with Hispanic ethnicity. A language barrier could explain this because the SAGE instrument was conducted in English only. The SAGE was feasible to measure in the clinic setting.</description><identifier>ISSN: 0961-2033</identifier><identifier>EISSN: 1477-0962</identifier><identifier>DOI: 10.1177/0961203318759429</identifier><identifier>PMID: 29466913</identifier><language>eng</language><publisher>London, England: SAGE Publications</publisher><subject>Central nervous system ; Cognition ; Cognitive ability ; Ethnicity ; Lupus ; Minority &amp; ethnic groups ; Systemic lupus erythematosus</subject><ispartof>Lupus, 2018-07, Vol.27 (8), p.1363-1367</ispartof><rights>The Author(s) 2018</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c365t-bd79d8d2ad425189d463dca4c9b1ce61bc2169580621816ed529cbb5227bbaff3</citedby><cites>FETCH-LOGICAL-c365t-bd79d8d2ad425189d463dca4c9b1ce61bc2169580621816ed529cbb5227bbaff3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925,79364</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29466913$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Meara, A</creatorcontrib><creatorcontrib>Davidson, N</creatorcontrib><creatorcontrib>Steigelman, H</creatorcontrib><creatorcontrib>Zhao, S</creatorcontrib><creatorcontrib>Brock, G</creatorcontrib><creatorcontrib>Jarjour, W N</creatorcontrib><creatorcontrib>Rovin, B H</creatorcontrib><creatorcontrib>Madhoun, H</creatorcontrib><creatorcontrib>Parikh, S</creatorcontrib><creatorcontrib>Hebert, L</creatorcontrib><creatorcontrib>Ayoub, I</creatorcontrib><creatorcontrib>Ardoin, S P</creatorcontrib><title>Screening for cognitive impairment in SLE using the Self-Administered Gerocognitive Exam</title><title>Lupus</title><addtitle>Lupus</addtitle><description>Objective Systemic lupus erythematosus (SLE) is a multisystem autoimmune disease that can affect the central nervous system in multiple ways, including causing cognitive dysfunction. Cognitive dysfunction is a common complaint of SLE patients yet diagnosis is challenging, time consuming, and costly. This study evaluated the Self-Administered Gerocognitive Exam (SAGE) as a screening test for cognitive impairment in a cohort of SLE patients. Methods A total of 118 SLE patients completed the SAGE. Providers completed the Systemic Lupus Erythematosus Disease Activity Index (SLEDAI) and the Systemic Lupus International Collaborative Clinics Damage Index (SLICC-DI). SAGE scores were grouped into normal (&gt;16) and abnormal (≤16) categories. Univariate and multivariate analyses were performed. Results Of the 118 participants, 21(18%) scored ≤16 on the SAGE instrument. In univariate analysis, race, ethnicity, household income, and SLICC-DI scores were associated with the SAGE (p &lt; 0.05). In multivariable analysis, abnormal SAGE score was independently associated with higher SLICC-DI score (odds ratio (OR) = 1.44, 95% confidence intervals 1.04–1.99, p = 0.03)), Hispanic ethnicity (OR = 43.4, 95% CI 3.1–601, p = 0.005), and lower household income (OR = 11.9 for ≤$15,000 vs &gt;$50,000, 95% CI 2.45–57, p = 0.002). Conclusions In SLE patients, this study demonstrates an independent relationship between neurocognitive impairment (as measured by the SAGE) and higher lupus-related damage, as measured by the SLICC-DI, and lower household income. Abnormal SAGE scores were also associated with Hispanic ethnicity. A language barrier could explain this because the SAGE instrument was conducted in English only. 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Cognitive dysfunction is a common complaint of SLE patients yet diagnosis is challenging, time consuming, and costly. This study evaluated the Self-Administered Gerocognitive Exam (SAGE) as a screening test for cognitive impairment in a cohort of SLE patients. Methods A total of 118 SLE patients completed the SAGE. Providers completed the Systemic Lupus Erythematosus Disease Activity Index (SLEDAI) and the Systemic Lupus International Collaborative Clinics Damage Index (SLICC-DI). SAGE scores were grouped into normal (&gt;16) and abnormal (≤16) categories. Univariate and multivariate analyses were performed. Results Of the 118 participants, 21(18%) scored ≤16 on the SAGE instrument. In univariate analysis, race, ethnicity, household income, and SLICC-DI scores were associated with the SAGE (p &lt; 0.05). In multivariable analysis, abnormal SAGE score was independently associated with higher SLICC-DI score (odds ratio (OR) = 1.44, 95% confidence intervals 1.04–1.99, p = 0.03)), Hispanic ethnicity (OR = 43.4, 95% CI 3.1–601, p = 0.005), and lower household income (OR = 11.9 for ≤$15,000 vs &gt;$50,000, 95% CI 2.45–57, p = 0.002). Conclusions In SLE patients, this study demonstrates an independent relationship between neurocognitive impairment (as measured by the SAGE) and higher lupus-related damage, as measured by the SLICC-DI, and lower household income. Abnormal SAGE scores were also associated with Hispanic ethnicity. A language barrier could explain this because the SAGE instrument was conducted in English only. The SAGE was feasible to measure in the clinic setting.</abstract><cop>London, England</cop><pub>SAGE Publications</pub><pmid>29466913</pmid><doi>10.1177/0961203318759429</doi><tpages>5</tpages></addata></record>
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source Sage Journals Online
subjects Central nervous system
Cognition
Cognitive ability
Ethnicity
Lupus
Minority & ethnic groups
Systemic lupus erythematosus
title Screening for cognitive impairment in SLE using the Self-Administered Gerocognitive Exam
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