Use of exogenous estrogens in systemic lupus erythematosus
Objective: To review the current literature on the safety of using exogenous estrogens in patients with systemic lupus erythematosus (SLE). Method: A MEDLINE search for articles published between 1970 and 2000 regarding the relationship between estrogens and SLE was performed. Emphasis was put on hu...
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description | Objective: To review the current literature on the safety of using exogenous estrogens in patients with systemic lupus erythematosus (SLE). Method: A MEDLINE search for articles published between 1970 and 2000 regarding the relationship between estrogens and SLE was performed. Emphasis was put on human studies, treatment trials, and epidemiologic surveys. Results: The use of exogenous estrogens in healthy women increases the risk of SLE development. For patients with established SLE, a hypoestrogenemic state appears to be protective against severe flares, whereas exogenous estrogen administration or hyperestrogenemia induced by hormonal manipulation may exacerbate the disease in certain individuals. Both the use of oral contraceptives and the use of hormonal replacement therapy (HRT) increase the chance of venous thromboembolism. The presence of antiphospholipid antibodies may aggravate the risk of thrombosis in SLE. In retrospective studies, HRT appears to be well tolerated in postmenopausal SLE patients. Conclusions: There are no prospective data that show a deleterious effect of exogenous estrogens on disease activity in human SLE. Oral contraceptives may be considered for patients with SLE in the absence of active nephritis or antiphospholipid antibodies. The slight increase in venous thromboembolic risk should not be the chief deterrent to the use of HRT in postmenopausal SLE patients, considering its various health benefits. Semin Arthritis Rheum 30:426-435. Copyright © 2001 by W.B. Saunders Company |
doi_str_mv | 10.1053/sarh.2001.22498 |
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Method: A MEDLINE search for articles published between 1970 and 2000 regarding the relationship between estrogens and SLE was performed. Emphasis was put on human studies, treatment trials, and epidemiologic surveys. Results: The use of exogenous estrogens in healthy women increases the risk of SLE development. For patients with established SLE, a hypoestrogenemic state appears to be protective against severe flares, whereas exogenous estrogen administration or hyperestrogenemia induced by hormonal manipulation may exacerbate the disease in certain individuals. Both the use of oral contraceptives and the use of hormonal replacement therapy (HRT) increase the chance of venous thromboembolism. The presence of antiphospholipid antibodies may aggravate the risk of thrombosis in SLE. In retrospective studies, HRT appears to be well tolerated in postmenopausal SLE patients. Conclusions: There are no prospective data that show a deleterious effect of exogenous estrogens on disease activity in human SLE. Oral contraceptives may be considered for patients with SLE in the absence of active nephritis or antiphospholipid antibodies. The slight increase in venous thromboembolic risk should not be the chief deterrent to the use of HRT in postmenopausal SLE patients, considering its various health benefits. Semin Arthritis Rheum 30:426-435. Copyright © 2001 by W.B. Saunders Company</description><identifier>ISSN: 0049-0172</identifier><identifier>EISSN: 1532-866X</identifier><identifier>DOI: 10.1053/sarh.2001.22498</identifier><identifier>PMID: 11404826</identifier><identifier>CODEN: SAHRBF</identifier><language>eng</language><publisher>Philadelphia, PA: Elsevier Inc</publisher><subject>Biological and medical sciences ; contraception ; Estrogens - adverse effects ; Estrogens - therapeutic use ; Female ; flare ; hormone ; Hormones. Endocrine system ; Humans ; Immune System - drug effects ; Lupus Erythematosus, Systemic - chemically induced ; Lupus Erythematosus, Systemic - physiopathology ; Medical sciences ; Menopause ; Pharmacology. Drug treatments ; Prognosis ; Risk Factors ; Safety ; Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis ; SLE ; Thrombosis - chemically induced</subject><ispartof>Seminars in arthritis and rheumatism, 2001-06, Vol.30 (6), p.426-435</ispartof><rights>2001 W.B. Saunders Company</rights><rights>2001 INIST-CNRS</rights><rights>Copyright 2001 by W.B. Saunders Company</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c316t-a4c88d8e51de363c8219d44a9b9268abff00145cc234231dd6084c4a5ead7513</citedby><cites>FETCH-LOGICAL-c316t-a4c88d8e51de363c8219d44a9b9268abff00145cc234231dd6084c4a5ead7513</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1053/sarh.2001.22498$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,777,781,3537,27905,27906,45976</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1059952$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11404826$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mok, Chi Chiu</creatorcontrib><creatorcontrib>Lau, Chak Sing</creatorcontrib><creatorcontrib>Wong, Raymond Woon Sing</creatorcontrib><title>Use of exogenous estrogens in systemic lupus erythematosus</title><title>Seminars in arthritis and rheumatism</title><addtitle>Semin Arthritis Rheum</addtitle><description>Objective: To review the current literature on the safety of using exogenous estrogens in patients with systemic lupus erythematosus (SLE). Method: A MEDLINE search for articles published between 1970 and 2000 regarding the relationship between estrogens and SLE was performed. Emphasis was put on human studies, treatment trials, and epidemiologic surveys. Results: The use of exogenous estrogens in healthy women increases the risk of SLE development. For patients with established SLE, a hypoestrogenemic state appears to be protective against severe flares, whereas exogenous estrogen administration or hyperestrogenemia induced by hormonal manipulation may exacerbate the disease in certain individuals. Both the use of oral contraceptives and the use of hormonal replacement therapy (HRT) increase the chance of venous thromboembolism. The presence of antiphospholipid antibodies may aggravate the risk of thrombosis in SLE. In retrospective studies, HRT appears to be well tolerated in postmenopausal SLE patients. Conclusions: There are no prospective data that show a deleterious effect of exogenous estrogens on disease activity in human SLE. Oral contraceptives may be considered for patients with SLE in the absence of active nephritis or antiphospholipid antibodies. The slight increase in venous thromboembolic risk should not be the chief deterrent to the use of HRT in postmenopausal SLE patients, considering its various health benefits. Semin Arthritis Rheum 30:426-435. Copyright © 2001 by W.B. Saunders Company</description><subject>Biological and medical sciences</subject><subject>contraception</subject><subject>Estrogens - adverse effects</subject><subject>Estrogens - therapeutic use</subject><subject>Female</subject><subject>flare</subject><subject>hormone</subject><subject>Hormones. Endocrine system</subject><subject>Humans</subject><subject>Immune System - drug effects</subject><subject>Lupus Erythematosus, Systemic - chemically induced</subject><subject>Lupus Erythematosus, Systemic - physiopathology</subject><subject>Medical sciences</subject><subject>Menopause</subject><subject>Pharmacology. Drug treatments</subject><subject>Prognosis</subject><subject>Risk Factors</subject><subject>Safety</subject><subject>Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis</subject><subject>SLE</subject><subject>Thrombosis - chemically induced</subject><issn>0049-0172</issn><issn>1532-866X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kM1LAzEQxYMotlbP3mQPXrdNskmaeBPxCwpeKngLaTJrI93dktkV-9-7awt68TQD83uPeY-QS0anjMpihi6tp5xSNuVcGH1ExkwWPNdKvR2TMaXC5JTN-YicIX70GFN0fkpGjAkqNFdjcvOKkDVlBl_NO9RNhxlgm4Yds1hnuMMWquizTbcdbmnXrqFybYMdnpOT0m0QLg5zQpYP98u7p3zx8vh8d7vIfcFUmzvhtQ4aJAtQqMJrzkwQwpmV4Uq7VVn2fwnpPS8EL1gIimrhhZPgwlyyYkJme1ufGsQEpd2mWLm0s4zaoQQ7lGCHEuxPCb3iaq_YdqsKwi9_SN0D1wfAoXebMrnaR_zjK42RvMfMHoM-3WeEZNFHqD2EmMC3NjTx3x--AbSPeME</recordid><startdate>200106</startdate><enddate>200106</enddate><creator>Mok, Chi Chiu</creator><creator>Lau, Chak Sing</creator><creator>Wong, Raymond Woon Sing</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>200106</creationdate><title>Use of exogenous estrogens in systemic lupus erythematosus</title><author>Mok, Chi Chiu ; Lau, Chak Sing ; Wong, Raymond Woon Sing</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c316t-a4c88d8e51de363c8219d44a9b9268abff00145cc234231dd6084c4a5ead7513</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Biological and medical sciences</topic><topic>contraception</topic><topic>Estrogens - adverse effects</topic><topic>Estrogens - therapeutic use</topic><topic>Female</topic><topic>flare</topic><topic>hormone</topic><topic>Hormones. Endocrine system</topic><topic>Humans</topic><topic>Immune System - drug effects</topic><topic>Lupus Erythematosus, Systemic - chemically induced</topic><topic>Lupus Erythematosus, Systemic - physiopathology</topic><topic>Medical sciences</topic><topic>Menopause</topic><topic>Pharmacology. Drug treatments</topic><topic>Prognosis</topic><topic>Risk Factors</topic><topic>Safety</topic><topic>Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis</topic><topic>SLE</topic><topic>Thrombosis - chemically induced</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mok, Chi Chiu</creatorcontrib><creatorcontrib>Lau, Chak Sing</creatorcontrib><creatorcontrib>Wong, Raymond Woon Sing</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Seminars in arthritis and rheumatism</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mok, Chi Chiu</au><au>Lau, Chak Sing</au><au>Wong, Raymond Woon Sing</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Use of exogenous estrogens in systemic lupus erythematosus</atitle><jtitle>Seminars in arthritis and rheumatism</jtitle><addtitle>Semin Arthritis Rheum</addtitle><date>2001-06</date><risdate>2001</risdate><volume>30</volume><issue>6</issue><spage>426</spage><epage>435</epage><pages>426-435</pages><issn>0049-0172</issn><eissn>1532-866X</eissn><coden>SAHRBF</coden><abstract>Objective: To review the current literature on the safety of using exogenous estrogens in patients with systemic lupus erythematosus (SLE). Method: A MEDLINE search for articles published between 1970 and 2000 regarding the relationship between estrogens and SLE was performed. Emphasis was put on human studies, treatment trials, and epidemiologic surveys. Results: The use of exogenous estrogens in healthy women increases the risk of SLE development. For patients with established SLE, a hypoestrogenemic state appears to be protective against severe flares, whereas exogenous estrogen administration or hyperestrogenemia induced by hormonal manipulation may exacerbate the disease in certain individuals. Both the use of oral contraceptives and the use of hormonal replacement therapy (HRT) increase the chance of venous thromboembolism. The presence of antiphospholipid antibodies may aggravate the risk of thrombosis in SLE. In retrospective studies, HRT appears to be well tolerated in postmenopausal SLE patients. Conclusions: There are no prospective data that show a deleterious effect of exogenous estrogens on disease activity in human SLE. Oral contraceptives may be considered for patients with SLE in the absence of active nephritis or antiphospholipid antibodies. The slight increase in venous thromboembolic risk should not be the chief deterrent to the use of HRT in postmenopausal SLE patients, considering its various health benefits. Semin Arthritis Rheum 30:426-435. Copyright © 2001 by W.B. Saunders Company</abstract><cop>Philadelphia, PA</cop><pub>Elsevier Inc</pub><pmid>11404826</pmid><doi>10.1053/sarh.2001.22498</doi><tpages>10</tpages></addata></record> |
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subjects | Biological and medical sciences contraception Estrogens - adverse effects Estrogens - therapeutic use Female flare hormone Hormones. Endocrine system Humans Immune System - drug effects Lupus Erythematosus, Systemic - chemically induced Lupus Erythematosus, Systemic - physiopathology Medical sciences Menopause Pharmacology. Drug treatments Prognosis Risk Factors Safety Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis SLE Thrombosis - chemically induced |
title | Use of exogenous estrogens in systemic lupus erythematosus |
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