Serological evolution in women with positive antiphospholipid antibodies
Abstract Objectives To explore the clinical and serological course of fertile women with positive aPL, and the factors and therapeutic implications associated with aPL negativization. Methods Retrospective study including 105 women with a positive aPL serology between 1995 and 2013 attending the obs...
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Veröffentlicht in: | Seminars in arthritis and rheumatism 2017-12, Vol.47 (3), p.397-402 |
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creator | Riancho-Zarrabeitia, Leyre, MD, PhD Daroca, Germán, MD Muñoz, Pedro, MD, PhD López-Hoyos, Marcos, MD, PhD Haya, Ana, MD Martínez-Taboada, Víctor M., MD, PhD |
description | Abstract Objectives To explore the clinical and serological course of fertile women with positive aPL, and the factors and therapeutic implications associated with aPL negativization. Methods Retrospective study including 105 women with a positive aPL serology between 1995 and 2013 attending the obstetric autoimmune pathology clinic of a tertiary-facility. Patients were classified into 3 groups: patients with primary antiphospholipid syndrome (pAPS, 49), patients with a positive serology for aPL, not meeting clinical criteria (42) and patients with systemic lupus erythematosus and a positive aPL serology (14). They were also classified, according to the serological aPL evolution: persistently negative aPL, transiently positive serology and persistently positive serology according to established criteria. Results After a mean follow-up of 114.4 ± 37.2 months, 59% patients had persistently negative antibodies, while 25.7% patients presented persistently positive aPL serology. Multivariate analysis confirmed that smoking (OR 4, 95%CI 1.45–11.08, p=0.008) was an independent risk factor for positive persistence. Persistent positivity, as well as a higher antibody load was associated with higher risk for further pregnancy morbidity. In 29 patients, with persistently negative serology who were asymptomatic, treatment with low-dose aspirin was discontinued. No clinical events related to APS were reported after treatment withdrawal, during the 40.95 months of follow-up. Conclusions A significant proportion of fertile women with aPL antibodies became negative during follow-up. Tobacco use and the number of positive antibodies are associated with persistently positive serology. Patients with persistently positive aPL serology suffer more obstetric complications. Treatment withdrawal might be safe in selected patients. |
doi_str_mv | 10.1016/j.semarthrit.2017.05.001 |
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Methods Retrospective study including 105 women with a positive aPL serology between 1995 and 2013 attending the obstetric autoimmune pathology clinic of a tertiary-facility. Patients were classified into 3 groups: patients with primary antiphospholipid syndrome (pAPS, 49), patients with a positive serology for aPL, not meeting clinical criteria (42) and patients with systemic lupus erythematosus and a positive aPL serology (14). They were also classified, according to the serological aPL evolution: persistently negative aPL, transiently positive serology and persistently positive serology according to established criteria. Results After a mean follow-up of 114.4 ± 37.2 months, 59% patients had persistently negative antibodies, while 25.7% patients presented persistently positive aPL serology. Multivariate analysis confirmed that smoking (OR 4, 95%CI 1.45–11.08, p=0.008) was an independent risk factor for positive persistence. Persistent positivity, as well as a higher antibody load was associated with higher risk for further pregnancy morbidity. In 29 patients, with persistently negative serology who were asymptomatic, treatment with low-dose aspirin was discontinued. No clinical events related to APS were reported after treatment withdrawal, during the 40.95 months of follow-up. Conclusions A significant proportion of fertile women with aPL antibodies became negative during follow-up. Tobacco use and the number of positive antibodies are associated with persistently positive serology. Patients with persistently positive aPL serology suffer more obstetric complications. Treatment withdrawal might be safe in selected patients.</description><identifier>ISSN: 0049-0172</identifier><identifier>EISSN: 1532-866X</identifier><identifier>DOI: 10.1016/j.semarthrit.2017.05.001</identifier><identifier>PMID: 28576307</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adult ; Antibodies, Antiphospholipid - blood ; Antibodies, Antiphospholipid - immunology ; Anticoagulants - therapeutic use ; Antiphospholipid antibodies ; Antiphospholipid syndrome ; Antiphospholipid Syndrome - blood ; Antiphospholipid Syndrome - drug therapy ; Antiphospholipid Syndrome - immunology ; Aspirin - therapeutic use ; Biomarkers - blood ; Female ; Follow-Up Studies ; Heparin - therapeutic use ; Humans ; Lupus Erythematosus, Systemic - blood ; Lupus Erythematosus, Systemic - drug therapy ; Middle Aged ; Multivariate Analysis ; Platelet Aggregation Inhibitors - therapeutic use ; Pregnancy ; Pregnancy Complications - blood ; Pregnancy Complications - immunology ; Retrospective Studies ; Rheumatology ; Risk Factors ; Seroepidemiologic Studies ; Serological evolution ; Smoking - adverse effects ; Thrombosis - drug therapy ; Thrombosis - immunology ; Thrombosis - prevention & control</subject><ispartof>Seminars in arthritis and rheumatism, 2017-12, Vol.47 (3), p.397-402</ispartof><rights>2017 Elsevier Inc.</rights><rights>Copyright © 2017 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c479t-718bca9380b92037921d809ff56a2b30d037f06c924898be9c65d1714dcf5c223</citedby><cites>FETCH-LOGICAL-c479t-718bca9380b92037921d809ff56a2b30d037f06c924898be9c65d1714dcf5c223</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.semarthrit.2017.05.001$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,781,785,3551,27929,27930,46000</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28576307$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Riancho-Zarrabeitia, Leyre, MD, PhD</creatorcontrib><creatorcontrib>Daroca, Germán, MD</creatorcontrib><creatorcontrib>Muñoz, Pedro, MD, PhD</creatorcontrib><creatorcontrib>López-Hoyos, Marcos, MD, PhD</creatorcontrib><creatorcontrib>Haya, Ana, MD</creatorcontrib><creatorcontrib>Martínez-Taboada, Víctor M., MD, PhD</creatorcontrib><title>Serological evolution in women with positive antiphospholipid antibodies</title><title>Seminars in arthritis and rheumatism</title><addtitle>Semin Arthritis Rheum</addtitle><description>Abstract Objectives To explore the clinical and serological course of fertile women with positive aPL, and the factors and therapeutic implications associated with aPL negativization. Methods Retrospective study including 105 women with a positive aPL serology between 1995 and 2013 attending the obstetric autoimmune pathology clinic of a tertiary-facility. Patients were classified into 3 groups: patients with primary antiphospholipid syndrome (pAPS, 49), patients with a positive serology for aPL, not meeting clinical criteria (42) and patients with systemic lupus erythematosus and a positive aPL serology (14). They were also classified, according to the serological aPL evolution: persistently negative aPL, transiently positive serology and persistently positive serology according to established criteria. Results After a mean follow-up of 114.4 ± 37.2 months, 59% patients had persistently negative antibodies, while 25.7% patients presented persistently positive aPL serology. Multivariate analysis confirmed that smoking (OR 4, 95%CI 1.45–11.08, p=0.008) was an independent risk factor for positive persistence. Persistent positivity, as well as a higher antibody load was associated with higher risk for further pregnancy morbidity. In 29 patients, with persistently negative serology who were asymptomatic, treatment with low-dose aspirin was discontinued. No clinical events related to APS were reported after treatment withdrawal, during the 40.95 months of follow-up. Conclusions A significant proportion of fertile women with aPL antibodies became negative during follow-up. Tobacco use and the number of positive antibodies are associated with persistently positive serology. Patients with persistently positive aPL serology suffer more obstetric complications. Treatment withdrawal might be safe in selected patients.</description><subject>Adult</subject><subject>Antibodies, Antiphospholipid - blood</subject><subject>Antibodies, Antiphospholipid - immunology</subject><subject>Anticoagulants - therapeutic use</subject><subject>Antiphospholipid antibodies</subject><subject>Antiphospholipid syndrome</subject><subject>Antiphospholipid Syndrome - blood</subject><subject>Antiphospholipid Syndrome - drug therapy</subject><subject>Antiphospholipid Syndrome - immunology</subject><subject>Aspirin - therapeutic use</subject><subject>Biomarkers - blood</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Heparin - therapeutic use</subject><subject>Humans</subject><subject>Lupus Erythematosus, Systemic - blood</subject><subject>Lupus Erythematosus, Systemic - drug therapy</subject><subject>Middle Aged</subject><subject>Multivariate Analysis</subject><subject>Platelet Aggregation Inhibitors - therapeutic use</subject><subject>Pregnancy</subject><subject>Pregnancy Complications - blood</subject><subject>Pregnancy Complications - immunology</subject><subject>Retrospective Studies</subject><subject>Rheumatology</subject><subject>Risk Factors</subject><subject>Seroepidemiologic Studies</subject><subject>Serological evolution</subject><subject>Smoking - adverse effects</subject><subject>Thrombosis - drug therapy</subject><subject>Thrombosis - immunology</subject><subject>Thrombosis - prevention & control</subject><issn>0049-0172</issn><issn>1532-866X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkcFu1DAQhi0EotuFV0A5ckkY2-vYviBBBbRSJQ4FiZuV2BPWSzYOtrOob4_DFpA4cZgZafzPjPz9hFQUGgq0fXVoEh67mPfR54YBlQ2IBoA-IhsqOKtV2355TDYAO12XV3ZBLlM6FAFtQT4lF0wJ2XKQG3J9hzGM4au33VjhKYxL9mGq_FT9CEcs2ed9NYfksz9h1U3Zz_uQSox-9u5Xow_OY3pGngzdmPD5Q92Sz-_ffbq6rm8_fri5enNb253UuZZU9bbTXEGvGXCpGXUK9DCItmM9B1d6A7RWs53SqkdtW-GopDtnB2EZ41vy8rx3juH7gimbo08Wx7GbMCzJUA1CcqVL2hJ1ltoYUoo4mDn6gu3eUDArR3MwfzmalaMBYQqmMvri4crSH9H9GfwNrgjengVY_nryGE2yHieLzke02bjg_-fK63-W2NFPqxXf8B7TISxxKiwNNYkZMHern6udVHKgQgj-EyYVnuo</recordid><startdate>20171201</startdate><enddate>20171201</enddate><creator>Riancho-Zarrabeitia, Leyre, MD, PhD</creator><creator>Daroca, Germán, MD</creator><creator>Muñoz, Pedro, MD, PhD</creator><creator>López-Hoyos, Marcos, MD, PhD</creator><creator>Haya, Ana, MD</creator><creator>Martínez-Taboada, Víctor M., MD, PhD</creator><general>Elsevier 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>7X8</scope></search><sort><creationdate>20171201</creationdate><title>Serological evolution in women with positive antiphospholipid antibodies</title><author>Riancho-Zarrabeitia, Leyre, MD, PhD ; Daroca, Germán, MD ; Muñoz, Pedro, MD, PhD ; López-Hoyos, Marcos, MD, PhD ; Haya, Ana, MD ; Martínez-Taboada, Víctor M., MD, PhD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c479t-718bca9380b92037921d809ff56a2b30d037f06c924898be9c65d1714dcf5c223</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Adult</topic><topic>Antibodies, Antiphospholipid - blood</topic><topic>Antibodies, Antiphospholipid - immunology</topic><topic>Anticoagulants - therapeutic use</topic><topic>Antiphospholipid antibodies</topic><topic>Antiphospholipid syndrome</topic><topic>Antiphospholipid Syndrome - blood</topic><topic>Antiphospholipid Syndrome - drug therapy</topic><topic>Antiphospholipid Syndrome - immunology</topic><topic>Aspirin - therapeutic use</topic><topic>Biomarkers - blood</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Heparin - therapeutic use</topic><topic>Humans</topic><topic>Lupus Erythematosus, Systemic - blood</topic><topic>Lupus Erythematosus, Systemic - drug therapy</topic><topic>Middle Aged</topic><topic>Multivariate Analysis</topic><topic>Platelet Aggregation Inhibitors - therapeutic use</topic><topic>Pregnancy</topic><topic>Pregnancy Complications - blood</topic><topic>Pregnancy Complications - immunology</topic><topic>Retrospective Studies</topic><topic>Rheumatology</topic><topic>Risk Factors</topic><topic>Seroepidemiologic Studies</topic><topic>Serological evolution</topic><topic>Smoking - adverse effects</topic><topic>Thrombosis - drug therapy</topic><topic>Thrombosis - immunology</topic><topic>Thrombosis - prevention & control</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Riancho-Zarrabeitia, Leyre, MD, PhD</creatorcontrib><creatorcontrib>Daroca, Germán, MD</creatorcontrib><creatorcontrib>Muñoz, Pedro, MD, PhD</creatorcontrib><creatorcontrib>López-Hoyos, Marcos, MD, PhD</creatorcontrib><creatorcontrib>Haya, Ana, MD</creatorcontrib><creatorcontrib>Martínez-Taboada, Víctor M., MD, PhD</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Seminars in arthritis and rheumatism</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Riancho-Zarrabeitia, Leyre, MD, PhD</au><au>Daroca, Germán, MD</au><au>Muñoz, Pedro, MD, PhD</au><au>López-Hoyos, Marcos, MD, PhD</au><au>Haya, Ana, MD</au><au>Martínez-Taboada, Víctor M., MD, PhD</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Serological evolution in women with positive antiphospholipid antibodies</atitle><jtitle>Seminars in arthritis and rheumatism</jtitle><addtitle>Semin Arthritis Rheum</addtitle><date>2017-12-01</date><risdate>2017</risdate><volume>47</volume><issue>3</issue><spage>397</spage><epage>402</epage><pages>397-402</pages><issn>0049-0172</issn><eissn>1532-866X</eissn><abstract>Abstract Objectives To explore the clinical and serological course of fertile women with positive aPL, and the factors and therapeutic implications associated with aPL negativization. Methods Retrospective study including 105 women with a positive aPL serology between 1995 and 2013 attending the obstetric autoimmune pathology clinic of a tertiary-facility. Patients were classified into 3 groups: patients with primary antiphospholipid syndrome (pAPS, 49), patients with a positive serology for aPL, not meeting clinical criteria (42) and patients with systemic lupus erythematosus and a positive aPL serology (14). They were also classified, according to the serological aPL evolution: persistently negative aPL, transiently positive serology and persistently positive serology according to established criteria. Results After a mean follow-up of 114.4 ± 37.2 months, 59% patients had persistently negative antibodies, while 25.7% patients presented persistently positive aPL serology. Multivariate analysis confirmed that smoking (OR 4, 95%CI 1.45–11.08, p=0.008) was an independent risk factor for positive persistence. Persistent positivity, as well as a higher antibody load was associated with higher risk for further pregnancy morbidity. In 29 patients, with persistently negative serology who were asymptomatic, treatment with low-dose aspirin was discontinued. No clinical events related to APS were reported after treatment withdrawal, during the 40.95 months of follow-up. Conclusions A significant proportion of fertile women with aPL antibodies became negative during follow-up. Tobacco use and the number of positive antibodies are associated with persistently positive serology. Patients with persistently positive aPL serology suffer more obstetric complications. Treatment withdrawal might be safe in selected patients.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>28576307</pmid><doi>10.1016/j.semarthrit.2017.05.001</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Antibodies, Antiphospholipid - blood Antibodies, Antiphospholipid - immunology Anticoagulants - therapeutic use Antiphospholipid antibodies Antiphospholipid syndrome Antiphospholipid Syndrome - blood Antiphospholipid Syndrome - drug therapy Antiphospholipid Syndrome - immunology Aspirin - therapeutic use Biomarkers - blood Female Follow-Up Studies Heparin - therapeutic use Humans Lupus Erythematosus, Systemic - blood Lupus Erythematosus, Systemic - drug therapy Middle Aged Multivariate Analysis Platelet Aggregation Inhibitors - therapeutic use Pregnancy Pregnancy Complications - blood Pregnancy Complications - immunology Retrospective Studies Rheumatology Risk Factors Seroepidemiologic Studies Serological evolution Smoking - adverse effects Thrombosis - drug therapy Thrombosis - immunology Thrombosis - prevention & control |
title | Serological evolution in women with positive antiphospholipid antibodies |
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