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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 |
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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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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 < 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 >$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 & 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 (>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 < 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 >$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><subject>Central nervous system</subject><subject>Cognition</subject><subject>Cognitive ability</subject><subject>Ethnicity</subject><subject>Lupus</subject><subject>Minority & ethnic groups</subject><subject>Systemic lupus erythematosus</subject><issn>0961-2033</issn><issn>1477-0962</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp1kM1LAzEQxYMotlbvnmTBi5fVJJtNNsdSahUKHqrgbckmszVlP2qyK_rfm6VVoeBpYN7vvRkeQpcE3xIixB2WnFCcJCQTqWRUHqExYULEYU-P0XiQ40EfoTPvNxjjhEh-ikZUMs4lScbodaUdQGObdVS2LtLturGd_YDI1ltlXQ1NF9kmWi3nUe8HqnuDaAVVGU9NbRvrO3BgogW49s87_1T1OTopVeXhYj8n6OV-_jx7iJdPi8fZdBnrhKddXBghTWaoMoymJJOG8cRoxbQsiAZOCk0Jl2mGOSUZ4WBSKnVRpJSKolBlmUzQzS5369r3HnyX19ZrqCrVQNv7nGIsWOiAsoBeH6CbtndN-C5QLMso40wGCu8o7VrvHZT51tlaua-c4HxoPT9sPViu9sF9UYP5NfzUHIB4B3i1hr-r_wZ-A6bGiNk</recordid><startdate>201807</startdate><enddate>201807</enddate><creator>Meara, A</creator><creator>Davidson, N</creator><creator>Steigelman, H</creator><creator>Zhao, S</creator><creator>Brock, G</creator><creator>Jarjour, W N</creator><creator>Rovin, B H</creator><creator>Madhoun, H</creator><creator>Parikh, S</creator><creator>Hebert, L</creator><creator>Ayoub, I</creator><creator>Ardoin, S P</creator><general>SAGE Publications</general><general>Sage Publications Ltd</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>H94</scope><scope>K9.</scope><scope>7X8</scope></search><sort><creationdate>201807</creationdate><title>Screening for cognitive impairment in SLE using the Self-Administered Gerocognitive Exam</title><author>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</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c365t-bd79d8d2ad425189d463dca4c9b1ce61bc2169580621816ed529cbb5227bbaff3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Central nervous system</topic><topic>Cognition</topic><topic>Cognitive ability</topic><topic>Ethnicity</topic><topic>Lupus</topic><topic>Minority & ethnic groups</topic><topic>Systemic lupus erythematosus</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><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><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Lupus</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Meara, A</au><au>Davidson, N</au><au>Steigelman, H</au><au>Zhao, S</au><au>Brock, G</au><au>Jarjour, W N</au><au>Rovin, B H</au><au>Madhoun, H</au><au>Parikh, S</au><au>Hebert, L</au><au>Ayoub, I</au><au>Ardoin, S P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Screening for cognitive impairment in SLE using the Self-Administered Gerocognitive Exam</atitle><jtitle>Lupus</jtitle><addtitle>Lupus</addtitle><date>2018-07</date><risdate>2018</risdate><volume>27</volume><issue>8</issue><spage>1363</spage><epage>1367</epage><pages>1363-1367</pages><issn>0961-2033</issn><eissn>1477-0962</eissn><abstract>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 < 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 >$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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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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