<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Dobrowolski C</submitter><funding>Arthritis Society, Young Investigator Award</funding><funding>Province of Ontario Early Research Award</funding><funding>NCATS NIH HHS</funding><funding>Canadian Rheumatology Association–Arthritis Society Clinician Investigator Award</funding><funding>Department of Medicine, University of Toronto</funding><funding>National Center for Advancing Translational Science</funding><funding>Lupus Research Alliance</funding><funding>National Institutes of Health</funding><funding>Lupus Ontario and Schroeder Arthritis Institute</funding><funding>Arthritis Society of Canada, Canadian Institutes of Health Research, Physician’s Services Incorporated</funding><pagination>1860-1869</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10152298</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>62(5)</volume><pubmed_abstract>&lt;h4>Objectives&lt;/h4>Cognitive dysfunction (CD) is a common manifestation of SLE that can have detrimental consequences for those affected. To date, no treatments have been approved for SLE-CD. This study aims to assess the association of azathioprine (AZA) and mycophenolate (MMF) use with SLE-CD, given that these medications have demonstrated neuroprotective qualities in prior studies.&lt;h4>Methods&lt;/h4>Consecutive adult SLE patients presenting to a single healthcare center were considered for participation. The ACR neuropsychological battery for SLE was administered to consenting patients at 0, 6 and 12 months. Scores were compared with age- and sex-matched controls. Primary outcome was CD, defined as a z-score ≤-1.5 in two or more cognitive domains. Mixed-effects logistic regression models w</pubmed_abstract><journal>Rheumatology (Oxford, England)</journal><pubmed_title>Association of mycophenolate and azathioprine use with cognitive function in systemic lupus.</pubmed_title><pmcid>PMC10152298</pmcid><funding_grant_id>UL1TR002556</funding_grant_id><funding_grant_id>UL1 TR002556</funding_grant_id><pubmed_authors>Diaz Martinez JP</pubmed_authors><pubmed_authors>Wither JE</pubmed_authors><pubmed_authors>Katz P</pubmed_authors><pubmed_authors>Dobrowolski C</pubmed_authors><pubmed_authors>Ruttan L</pubmed_authors><pubmed_authors>Choi MY</pubmed_authors><pubmed_authors>Su J</pubmed_authors><pubmed_authors>Kakvan M</pubmed_authors><pubmed_authors>Bingham KS</pubmed_authors><pubmed_authors>Touma Z</pubmed_authors><pubmed_authors>McGinley J</pubmed_authors><pubmed_authors>Beaton DE</pubmed_authors><pubmed_authors>Green R</pubmed_authors><pubmed_authors>Anderson N</pubmed_authors><pubmed_authors>Putterman C</pubmed_authors><pubmed_authors>Fazzari M</pubmed_authors><pubmed_authors>Bonilla D</pubmed_authors><pubmed_authors>Fritzler MJ</pubmed_authors><pubmed_authors>Tartaglia MC</pubmed_authors></additional><is_claimable>false</is_claimable><name>Association of mycophenolate and azathioprine use with cognitive function in systemic lupus.</name><description>&lt;h4>Objectives&lt;/h4>Cognitive dysfunction (CD) is a common manifestation of SLE that can have detrimental consequences for those affected. To date, no treatments have been approved for SLE-CD. This study aims to assess the association of azathioprine (AZA) and mycophenolate (MMF) use with SLE-CD, given that these medications have demonstrated neuroprotective qualities in prior studies.&lt;h4>Methods&lt;/h4>Consecutive adult SLE patients presenting to a single healthcare center were considered for participation. The ACR neuropsychological battery for SLE was administered to consenting patients at 0, 6 and 12 months. Scores were compared with age- and sex-matched controls. Primary outcome was CD, defined as a z-score ≤-1.5 in two or more cognitive domains. Mixed-effects logistic regression models w</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 May</publication><modification>2026-07-14T23:02:14.588Z</modification><creation>2025-04-06T00:47:21.925Z</creation></dates><accession>S-EPMC10152298</accession><cross_references><pubmed>36135792</pubmed><doi>10.1093/rheumatology/keac540</doi></cross_references></HashMap>