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Cerebrovascular Events in Systemic Lupus Erythematosus: Results From an International Inception Cohort Study
Objective To determine the frequency, characteristics, and outcomes of cerebrovascular events (CerVEs), as well as clinical and autoantibody associations in a multiethnic/racial inception cohort of patients with systemic lupus erythematosus (SLE). Methods A total of 1,826 patients were assessed annu...
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Published in: | Arthritis care & research (2010) 2018-10, Vol.70 (10), p.1478-1487 |
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creator | Hanly, John G. Li, Qiuju Su, Li Urowitz, Murray B. Gordon, Caroline Bae, Sang‐Cheol Romero‐Diaz, Juanita Sanchez‐Guerrero, Jorge Bernatsky, Sasha Clarke, Ann E. Wallace, Daniel J. Isenberg, David A. Rahman, Anisur Merrill, Joan T. Fortin, Paul Gladman, Dafna D. Bruce, Ian N. Petri, Michelle Ginzler, Ellen M. Dooley, M. A. Steinsson, Kristjan Ramsey‐Goldman, Rosalind Zoma, Asad A. Manzi, Susan Nived, Ola Jonsen, Andreas Khamashta, Munther A. Alarcón, Graciela S. Chatham, Winn Vollenhoven, Ronald F. Aranow, Cynthia Mackay, Meggan Ruiz‐Irastorza, Guillermo Ramos‐Casals, Manuel Lim, S. Sam Inanc, Murat Kalunian, Kenneth C. Jacobsen, Soren Peschken, Christine A. Kamen, Diane L. Askanase, Anca Theriault, Chris Farewell, Vernon |
description | Objective
To determine the frequency, characteristics, and outcomes of cerebrovascular events (CerVEs), as well as clinical and autoantibody associations in a multiethnic/racial inception cohort of patients with systemic lupus erythematosus (SLE).
Methods
A total of 1,826 patients were assessed annually for 19 neuropsychiatric (NP) events, including 5 types of CerVEs: 1) stroke, 2) transient ischemia, 3) chronic multifocal ischemia, 4) subarachnoid/intracranial hemorrhage, and 5) sinus thrombosis. Global disease activity (Systemic Lupus Erythematosus Disease [SLE] Activity Index 2000), damage scores (SLE International Collaborating Clinics/American College of Rheumatology Damage Index), and Short Form 36 (SF‐36) scores were collected. Time to event, linear and logistic regressions, and multistate models were used as appropriate.
Results
CerVEs were the fourth most frequent NP event: 82 of 1,826 patients had 109 events; of these events, 103 were attributed to SLE, and 44 were identified at the time of enrollment. The predominant events were stroke (60 of 109 patients) and transient ischemia (28 of 109 patients). CerVEs were associated with other NP events attributed to SLE, non–SLE‐attributed NP events, African ancestry (at US SLICC sites), and increased organ damage scores. Lupus anticoagulant increased the risk of first stroke and sinus thrombosis and transient ischemic attack. Physician assessment indicated resolution or improvement in the majority of patients, but patients reported sustained reduction in SF‐36 summary and subscale scores following a CerVE.
Conclusion
CerVEs, the fourth most frequent NP event in SLE, are usually attributable to lupus. In contrast to good physician‐reported outcomes, patients reported a sustained reduction in health‐related quality of life following a CerVE. |
doi_str_mv | 10.1002/acr.23509 |
format | article |
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To determine the frequency, characteristics, and outcomes of cerebrovascular events (CerVEs), as well as clinical and autoantibody associations in a multiethnic/racial inception cohort of patients with systemic lupus erythematosus (SLE).
Methods
A total of 1,826 patients were assessed annually for 19 neuropsychiatric (NP) events, including 5 types of CerVEs: 1) stroke, 2) transient ischemia, 3) chronic multifocal ischemia, 4) subarachnoid/intracranial hemorrhage, and 5) sinus thrombosis. Global disease activity (Systemic Lupus Erythematosus Disease [SLE] Activity Index 2000), damage scores (SLE International Collaborating Clinics/American College of Rheumatology Damage Index), and Short Form 36 (SF‐36) scores were collected. Time to event, linear and logistic regressions, and multistate models were used as appropriate.
Results
CerVEs were the fourth most frequent NP event: 82 of 1,826 patients had 109 events; of these events, 103 were attributed to SLE, and 44 were identified at the time of enrollment. The predominant events were stroke (60 of 109 patients) and transient ischemia (28 of 109 patients). CerVEs were associated with other NP events attributed to SLE, non–SLE‐attributed NP events, African ancestry (at US SLICC sites), and increased organ damage scores. Lupus anticoagulant increased the risk of first stroke and sinus thrombosis and transient ischemic attack. Physician assessment indicated resolution or improvement in the majority of patients, but patients reported sustained reduction in SF‐36 summary and subscale scores following a CerVE.
Conclusion
CerVEs, the fourth most frequent NP event in SLE, are usually attributable to lupus. In contrast to good physician‐reported outcomes, patients reported a sustained reduction in health‐related quality of life following a CerVE.</description><identifier>ISSN: 2151-464X</identifier><identifier>EISSN: 2151-4658</identifier><identifier>DOI: 10.1002/acr.23509</identifier><identifier>PMID: 29316357</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>Adult ; Autoantibodies ; Cerebrovascular Disorders - epidemiology ; Cerebrovascular Disorders - immunology ; Clinical Medicine ; Cohort analysis ; Female ; Hemorrhage ; Humans ; Ischemia ; Klinisk medicin ; Lupus ; Lupus Erythematosus, Systemic - complications ; Male ; Medical and Health Sciences ; Medicin och hälsovetenskap ; Middle Aged ; Prospective Studies ; Quality of Life ; Reumatologi och inflammation ; Rheumatology and Autoimmunity ; Stroke ; Systemic lupus erythematosus ; Thrombosis ; Transient ischemic attack ; Young Adult</subject><ispartof>Arthritis care & research (2010), 2018-10, Vol.70 (10), p.1478-1487</ispartof><rights>2018, American College of Rheumatology</rights><rights>2018, American College of Rheumatology.</rights><rights>2018 American College of Rheumatology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c6169-6d09ece22c031c6661f779abe5cc25847bad265c9156cbfd4e3ead94a613bfef3</citedby><cites>FETCH-LOGICAL-c6169-6d09ece22c031c6661f779abe5cc25847bad265c9156cbfd4e3ead94a613bfef3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29316357$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://lup.lub.lu.se/record/227e0c06-4693-44cb-8e97-809669d8f8b6$$DView record from Swedish Publication Index$$Hfree_for_read</backlink><backlink>$$Uhttp://kipublications.ki.se/Default.aspx?queryparsed=id:139259444$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Hanly, John G.</creatorcontrib><creatorcontrib>Li, Qiuju</creatorcontrib><creatorcontrib>Su, Li</creatorcontrib><creatorcontrib>Urowitz, Murray B.</creatorcontrib><creatorcontrib>Gordon, Caroline</creatorcontrib><creatorcontrib>Bae, Sang‐Cheol</creatorcontrib><creatorcontrib>Romero‐Diaz, Juanita</creatorcontrib><creatorcontrib>Sanchez‐Guerrero, Jorge</creatorcontrib><creatorcontrib>Bernatsky, Sasha</creatorcontrib><creatorcontrib>Clarke, Ann E.</creatorcontrib><creatorcontrib>Wallace, Daniel J.</creatorcontrib><creatorcontrib>Isenberg, David A.</creatorcontrib><creatorcontrib>Rahman, Anisur</creatorcontrib><creatorcontrib>Merrill, Joan T.</creatorcontrib><creatorcontrib>Fortin, Paul</creatorcontrib><creatorcontrib>Gladman, Dafna D.</creatorcontrib><creatorcontrib>Bruce, Ian N.</creatorcontrib><creatorcontrib>Petri, Michelle</creatorcontrib><creatorcontrib>Ginzler, Ellen M.</creatorcontrib><creatorcontrib>Dooley, M. A.</creatorcontrib><creatorcontrib>Steinsson, Kristjan</creatorcontrib><creatorcontrib>Ramsey‐Goldman, Rosalind</creatorcontrib><creatorcontrib>Zoma, Asad A.</creatorcontrib><creatorcontrib>Manzi, Susan</creatorcontrib><creatorcontrib>Nived, Ola</creatorcontrib><creatorcontrib>Jonsen, Andreas</creatorcontrib><creatorcontrib>Khamashta, Munther A.</creatorcontrib><creatorcontrib>Alarcón, Graciela S.</creatorcontrib><creatorcontrib>Chatham, Winn</creatorcontrib><creatorcontrib>Vollenhoven, Ronald F.</creatorcontrib><creatorcontrib>Aranow, Cynthia</creatorcontrib><creatorcontrib>Mackay, Meggan</creatorcontrib><creatorcontrib>Ruiz‐Irastorza, Guillermo</creatorcontrib><creatorcontrib>Ramos‐Casals, Manuel</creatorcontrib><creatorcontrib>Lim, S. Sam</creatorcontrib><creatorcontrib>Inanc, Murat</creatorcontrib><creatorcontrib>Kalunian, Kenneth C.</creatorcontrib><creatorcontrib>Jacobsen, Soren</creatorcontrib><creatorcontrib>Peschken, Christine A.</creatorcontrib><creatorcontrib>Kamen, Diane L.</creatorcontrib><creatorcontrib>Askanase, Anca</creatorcontrib><creatorcontrib>Theriault, Chris</creatorcontrib><creatorcontrib>Farewell, Vernon</creatorcontrib><title>Cerebrovascular Events in Systemic Lupus Erythematosus: Results From an International Inception Cohort Study</title><title>Arthritis care & research (2010)</title><addtitle>Arthritis Care Res (Hoboken)</addtitle><description>Objective
To determine the frequency, characteristics, and outcomes of cerebrovascular events (CerVEs), as well as clinical and autoantibody associations in a multiethnic/racial inception cohort of patients with systemic lupus erythematosus (SLE).
Methods
A total of 1,826 patients were assessed annually for 19 neuropsychiatric (NP) events, including 5 types of CerVEs: 1) stroke, 2) transient ischemia, 3) chronic multifocal ischemia, 4) subarachnoid/intracranial hemorrhage, and 5) sinus thrombosis. Global disease activity (Systemic Lupus Erythematosus Disease [SLE] Activity Index 2000), damage scores (SLE International Collaborating Clinics/American College of Rheumatology Damage Index), and Short Form 36 (SF‐36) scores were collected. Time to event, linear and logistic regressions, and multistate models were used as appropriate.
Results
CerVEs were the fourth most frequent NP event: 82 of 1,826 patients had 109 events; of these events, 103 were attributed to SLE, and 44 were identified at the time of enrollment. The predominant events were stroke (60 of 109 patients) and transient ischemia (28 of 109 patients). CerVEs were associated with other NP events attributed to SLE, non–SLE‐attributed NP events, African ancestry (at US SLICC sites), and increased organ damage scores. Lupus anticoagulant increased the risk of first stroke and sinus thrombosis and transient ischemic attack. Physician assessment indicated resolution or improvement in the majority of patients, but patients reported sustained reduction in SF‐36 summary and subscale scores following a CerVE.
Conclusion
CerVEs, the fourth most frequent NP event in SLE, are usually attributable to lupus. In contrast to good physician‐reported outcomes, patients reported a sustained reduction in health‐related quality of life following a CerVE.</description><subject>Adult</subject><subject>Autoantibodies</subject><subject>Cerebrovascular Disorders - epidemiology</subject><subject>Cerebrovascular Disorders - immunology</subject><subject>Clinical Medicine</subject><subject>Cohort analysis</subject><subject>Female</subject><subject>Hemorrhage</subject><subject>Humans</subject><subject>Ischemia</subject><subject>Klinisk medicin</subject><subject>Lupus</subject><subject>Lupus Erythematosus, Systemic - complications</subject><subject>Male</subject><subject>Medical and Health Sciences</subject><subject>Medicin och hälsovetenskap</subject><subject>Middle Aged</subject><subject>Prospective Studies</subject><subject>Quality of Life</subject><subject>Reumatologi och inflammation</subject><subject>Rheumatology and Autoimmunity</subject><subject>Stroke</subject><subject>Systemic lupus erythematosus</subject><subject>Thrombosis</subject><subject>Transient ischemic attack</subject><subject>Young Adult</subject><issn>2151-464X</issn><issn>2151-4658</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp1kt9r1TAUgIsobsw9-A9IwRd96JZfTRofhFHudHBB2BR8C2l66u1Mm2vS3NH_3lx7vThhgUNOki9fQnKy7DVGFxghcqmNvyC0RPJZdkpwiQvGy-r5MWffT7LzEO5RapRUFZUvsxMiKea0FKeZrcFD491OBxOt9vlqB-MU8n7M7-YwwdCbfB23MeQrP08bGPTkQgwf8lsI0Sbw2rsh12N-M07gRz31btQ2jQxs93leu43zU343xXZ-lb3otA1wfujPsm_Xq6_152L95dNNfbUuDMdcFrxFEgwQYhDFhnOOOyGkbqA0hpQVE41uCS-NxCU3TdcyoKBbyTTHtOmgo2dZsXjDA2xjo7a-H7SfldO9Okz9TBkoJjHlNPHrJ3kbtymaFPsNhAhABnHFuKSKMdOoCqRQFZKcy7bqqoYn3cdFl1wDtCY9qNf2kfXxythv1A-3UxxRmrxJ8O4g8O5XhDCpoQ8GrNUjuBgUlpUsuajE_qy3_6H3LqZ_sEERjInATBCWqPcLZbwLwUN3vAxGal9FKlWR-lNFiX3z7-2P5N-aScDlAjz0FuanTeqqvl2UvwE689OT</recordid><startdate>201810</startdate><enddate>201810</enddate><creator>Hanly, John G.</creator><creator>Li, Qiuju</creator><creator>Su, Li</creator><creator>Urowitz, Murray B.</creator><creator>Gordon, Caroline</creator><creator>Bae, Sang‐Cheol</creator><creator>Romero‐Diaz, Juanita</creator><creator>Sanchez‐Guerrero, Jorge</creator><creator>Bernatsky, Sasha</creator><creator>Clarke, Ann E.</creator><creator>Wallace, Daniel J.</creator><creator>Isenberg, David A.</creator><creator>Rahman, Anisur</creator><creator>Merrill, Joan T.</creator><creator>Fortin, Paul</creator><creator>Gladman, Dafna D.</creator><creator>Bruce, Ian N.</creator><creator>Petri, Michelle</creator><creator>Ginzler, Ellen M.</creator><creator>Dooley, M. A.</creator><creator>Steinsson, Kristjan</creator><creator>Ramsey‐Goldman, Rosalind</creator><creator>Zoma, Asad A.</creator><creator>Manzi, Susan</creator><creator>Nived, Ola</creator><creator>Jonsen, Andreas</creator><creator>Khamashta, Munther A.</creator><creator>Alarcón, Graciela S.</creator><creator>Chatham, Winn</creator><creator>Vollenhoven, Ronald F.</creator><creator>Aranow, Cynthia</creator><creator>Mackay, Meggan</creator><creator>Ruiz‐Irastorza, Guillermo</creator><creator>Ramos‐Casals, Manuel</creator><creator>Lim, S. Sam</creator><creator>Inanc, Murat</creator><creator>Kalunian, Kenneth C.</creator><creator>Jacobsen, Soren</creator><creator>Peschken, Christine A.</creator><creator>Kamen, Diane L.</creator><creator>Askanase, Anca</creator><creator>Theriault, Chris</creator><creator>Farewell, Vernon</creator><general>Wiley Subscription Services, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>NAPCQ</scope><scope>7X8</scope><scope>5PM</scope><scope>ADTPV</scope><scope>AOWAS</scope><scope>D95</scope><scope>D8T</scope><scope>ZZAVC</scope></search><sort><creationdate>201810</creationdate><title>Cerebrovascular Events in Systemic Lupus Erythematosus: Results From an International Inception Cohort Study</title><author>Hanly, John G. ; Li, Qiuju ; Su, Li ; Urowitz, Murray B. ; Gordon, Caroline ; Bae, Sang‐Cheol ; Romero‐Diaz, Juanita ; Sanchez‐Guerrero, Jorge ; Bernatsky, Sasha ; Clarke, Ann E. ; Wallace, Daniel J. ; Isenberg, David A. ; Rahman, Anisur ; Merrill, Joan T. ; Fortin, Paul ; Gladman, Dafna D. ; Bruce, Ian N. ; Petri, Michelle ; Ginzler, Ellen M. ; Dooley, M. A. ; Steinsson, Kristjan ; Ramsey‐Goldman, Rosalind ; Zoma, Asad A. ; Manzi, Susan ; Nived, Ola ; Jonsen, Andreas ; Khamashta, Munther A. ; Alarcón, Graciela S. ; Chatham, Winn ; Vollenhoven, Ronald F. ; Aranow, Cynthia ; Mackay, Meggan ; Ruiz‐Irastorza, Guillermo ; Ramos‐Casals, Manuel ; Lim, S. Sam ; Inanc, Murat ; Kalunian, Kenneth C. ; Jacobsen, Soren ; Peschken, Christine A. ; Kamen, Diane L. ; Askanase, Anca ; Theriault, Chris ; Farewell, Vernon</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c6169-6d09ece22c031c6661f779abe5cc25847bad265c9156cbfd4e3ead94a613bfef3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Adult</topic><topic>Autoantibodies</topic><topic>Cerebrovascular Disorders - epidemiology</topic><topic>Cerebrovascular Disorders - immunology</topic><topic>Clinical Medicine</topic><topic>Cohort analysis</topic><topic>Female</topic><topic>Hemorrhage</topic><topic>Humans</topic><topic>Ischemia</topic><topic>Klinisk medicin</topic><topic>Lupus</topic><topic>Lupus Erythematosus, Systemic - complications</topic><topic>Male</topic><topic>Medical and Health Sciences</topic><topic>Medicin och hälsovetenskap</topic><topic>Middle Aged</topic><topic>Prospective Studies</topic><topic>Quality of Life</topic><topic>Reumatologi och inflammation</topic><topic>Rheumatology and Autoimmunity</topic><topic>Stroke</topic><topic>Systemic lupus erythematosus</topic><topic>Thrombosis</topic><topic>Transient ischemic attack</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hanly, John G.</creatorcontrib><creatorcontrib>Li, Qiuju</creatorcontrib><creatorcontrib>Su, Li</creatorcontrib><creatorcontrib>Urowitz, Murray B.</creatorcontrib><creatorcontrib>Gordon, Caroline</creatorcontrib><creatorcontrib>Bae, Sang‐Cheol</creatorcontrib><creatorcontrib>Romero‐Diaz, Juanita</creatorcontrib><creatorcontrib>Sanchez‐Guerrero, Jorge</creatorcontrib><creatorcontrib>Bernatsky, Sasha</creatorcontrib><creatorcontrib>Clarke, Ann E.</creatorcontrib><creatorcontrib>Wallace, Daniel J.</creatorcontrib><creatorcontrib>Isenberg, David A.</creatorcontrib><creatorcontrib>Rahman, Anisur</creatorcontrib><creatorcontrib>Merrill, Joan T.</creatorcontrib><creatorcontrib>Fortin, Paul</creatorcontrib><creatorcontrib>Gladman, Dafna D.</creatorcontrib><creatorcontrib>Bruce, Ian N.</creatorcontrib><creatorcontrib>Petri, Michelle</creatorcontrib><creatorcontrib>Ginzler, Ellen M.</creatorcontrib><creatorcontrib>Dooley, M. 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Sam</creatorcontrib><creatorcontrib>Inanc, Murat</creatorcontrib><creatorcontrib>Kalunian, Kenneth C.</creatorcontrib><creatorcontrib>Jacobsen, Soren</creatorcontrib><creatorcontrib>Peschken, Christine A.</creatorcontrib><creatorcontrib>Kamen, Diane L.</creatorcontrib><creatorcontrib>Askanase, Anca</creatorcontrib><creatorcontrib>Theriault, Chris</creatorcontrib><creatorcontrib>Farewell, Vernon</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Nursing & Allied Health Premium</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>SwePub</collection><collection>SwePub Articles</collection><collection>SWEPUB Lunds universitet</collection><collection>SWEPUB Freely available online</collection><collection>SwePub Articles full text</collection><jtitle>Arthritis care & research (2010)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hanly, John G.</au><au>Li, Qiuju</au><au>Su, Li</au><au>Urowitz, Murray B.</au><au>Gordon, Caroline</au><au>Bae, Sang‐Cheol</au><au>Romero‐Diaz, Juanita</au><au>Sanchez‐Guerrero, Jorge</au><au>Bernatsky, Sasha</au><au>Clarke, Ann E.</au><au>Wallace, Daniel J.</au><au>Isenberg, David A.</au><au>Rahman, Anisur</au><au>Merrill, Joan T.</au><au>Fortin, Paul</au><au>Gladman, Dafna D.</au><au>Bruce, Ian N.</au><au>Petri, Michelle</au><au>Ginzler, Ellen M.</au><au>Dooley, M. A.</au><au>Steinsson, Kristjan</au><au>Ramsey‐Goldman, Rosalind</au><au>Zoma, Asad A.</au><au>Manzi, Susan</au><au>Nived, Ola</au><au>Jonsen, Andreas</au><au>Khamashta, Munther A.</au><au>Alarcón, Graciela S.</au><au>Chatham, Winn</au><au>Vollenhoven, Ronald F.</au><au>Aranow, Cynthia</au><au>Mackay, Meggan</au><au>Ruiz‐Irastorza, Guillermo</au><au>Ramos‐Casals, Manuel</au><au>Lim, S. Sam</au><au>Inanc, Murat</au><au>Kalunian, Kenneth C.</au><au>Jacobsen, Soren</au><au>Peschken, Christine A.</au><au>Kamen, Diane L.</au><au>Askanase, Anca</au><au>Theriault, Chris</au><au>Farewell, Vernon</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cerebrovascular Events in Systemic Lupus Erythematosus: Results From an International Inception Cohort Study</atitle><jtitle>Arthritis care & research (2010)</jtitle><addtitle>Arthritis Care Res (Hoboken)</addtitle><date>2018-10</date><risdate>2018</risdate><volume>70</volume><issue>10</issue><spage>1478</spage><epage>1487</epage><pages>1478-1487</pages><issn>2151-464X</issn><eissn>2151-4658</eissn><abstract>Objective
To determine the frequency, characteristics, and outcomes of cerebrovascular events (CerVEs), as well as clinical and autoantibody associations in a multiethnic/racial inception cohort of patients with systemic lupus erythematosus (SLE).
Methods
A total of 1,826 patients were assessed annually for 19 neuropsychiatric (NP) events, including 5 types of CerVEs: 1) stroke, 2) transient ischemia, 3) chronic multifocal ischemia, 4) subarachnoid/intracranial hemorrhage, and 5) sinus thrombosis. Global disease activity (Systemic Lupus Erythematosus Disease [SLE] Activity Index 2000), damage scores (SLE International Collaborating Clinics/American College of Rheumatology Damage Index), and Short Form 36 (SF‐36) scores were collected. Time to event, linear and logistic regressions, and multistate models were used as appropriate.
Results
CerVEs were the fourth most frequent NP event: 82 of 1,826 patients had 109 events; of these events, 103 were attributed to SLE, and 44 were identified at the time of enrollment. The predominant events were stroke (60 of 109 patients) and transient ischemia (28 of 109 patients). CerVEs were associated with other NP events attributed to SLE, non–SLE‐attributed NP events, African ancestry (at US SLICC sites), and increased organ damage scores. Lupus anticoagulant increased the risk of first stroke and sinus thrombosis and transient ischemic attack. Physician assessment indicated resolution or improvement in the majority of patients, but patients reported sustained reduction in SF‐36 summary and subscale scores following a CerVE.
Conclusion
CerVEs, the fourth most frequent NP event in SLE, are usually attributable to lupus. In contrast to good physician‐reported outcomes, patients reported a sustained reduction in health‐related quality of life following a CerVE.</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>29316357</pmid><doi>10.1002/acr.23509</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2151-464X |
ispartof | Arthritis care & research (2010), 2018-10, Vol.70 (10), p.1478-1487 |
issn | 2151-464X 2151-4658 |
language | eng |
recordid | cdi_swepub_primary_oai_swepub_ki_se_491363 |
source | Wiley-Blackwell Read & Publish Collection |
subjects | Adult Autoantibodies Cerebrovascular Disorders - epidemiology Cerebrovascular Disorders - immunology Clinical Medicine Cohort analysis Female Hemorrhage Humans Ischemia Klinisk medicin Lupus Lupus Erythematosus, Systemic - complications Male Medical and Health Sciences Medicin och hälsovetenskap Middle Aged Prospective Studies Quality of Life Reumatologi och inflammation Rheumatology and Autoimmunity Stroke Systemic lupus erythematosus Thrombosis Transient ischemic attack Young Adult |
title | Cerebrovascular Events in Systemic Lupus Erythematosus: Results From an International Inception Cohort Study |
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