Subacute cutaneous lupus erythematosus and its association with drugs: a population-based matched case-control study of 234 patients in Sweden

Summary Background  Numerous case reports about drug‐induced (DI) subacute cutaneous lupus erythematosus (SCLE) have been published. Various drug types with different latencies has been proposed as triggers for this autoimmune skin disease. Objectives  To evaluate the association between exposure to...

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Veröffentlicht in:British journal of dermatology (1951) 2012-08, Vol.167 (2), p.296-305
Hauptverfasser: Grönhagen, C.M., Fored, C.M., Linder, M., Granath, F., Nyberg, F.
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container_issue 2
container_start_page 296
container_title British journal of dermatology (1951)
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creator Grönhagen, C.M.
Fored, C.M.
Linder, M.
Granath, F.
Nyberg, F.
description Summary Background  Numerous case reports about drug‐induced (DI) subacute cutaneous lupus erythematosus (SCLE) have been published. Various drug types with different latencies has been proposed as triggers for this autoimmune skin disease. Objectives  To evaluate the association between exposure to certain suspected drugs (previously implicated to induce SCLE) and a subsequent diagnosis of SCLE. Methods  We performed a population‐based matched case–control study in which all incident cases of SCLE (n = 234) from 2006 to 2009 were derived from the National Patient Register. The control group was selected from the general population, matched (1 : 10) for gender, age and county of residence. The data were linked to the Prescribed Drug Register. Odds ratios (ORs) and 95% confidence intervals (CIs) were calculated for the association between exposures to certain suspected drugs and the development of SCLE. Results  During the 6 months preceding SCLE diagnosis, 166 (71%) of the patients with SCLE had at least one filled prescription of the suspected drugs. The most increased ORs were found for terbinafine (OR 52·9, 95% CI 6·6–∞), tumour necrosis factor‐α inhibitors (OR 8·0, 95% CI 1·6–37·2), antiepileptics (OR 3·4, 95% CI 1·9–5·8) and proton pump inhibitors (OR 2·9, 95% CI 2·0–4·0). Conclusions  We found an association between drug exposure and SCLE. More than one third of the SCLE cases could be attributed to drug exposure. No significant OR was found for thiazides, which might be due to longer latency and therefore missed with this study design. DI‐SCLE is reversible once the drug is discontinued, indicating the importance of screening patients with SCLE for potentially triggering drugs. A causal relationship cannot be established from this study and the underlying pathogenesis remains unclear.
doi_str_mv 10.1111/j.1365-2133.2012.10969.x
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Various drug types with different latencies has been proposed as triggers for this autoimmune skin disease. Objectives  To evaluate the association between exposure to certain suspected drugs (previously implicated to induce SCLE) and a subsequent diagnosis of SCLE. Methods  We performed a population‐based matched case–control study in which all incident cases of SCLE (n = 234) from 2006 to 2009 were derived from the National Patient Register. The control group was selected from the general population, matched (1 : 10) for gender, age and county of residence. The data were linked to the Prescribed Drug Register. Odds ratios (ORs) and 95% confidence intervals (CIs) were calculated for the association between exposures to certain suspected drugs and the development of SCLE. Results  During the 6 months preceding SCLE diagnosis, 166 (71%) of the patients with SCLE had at least one filled prescription of the suspected drugs. The most increased ORs were found for terbinafine (OR 52·9, 95% CI 6·6–∞), tumour necrosis factor‐α inhibitors (OR 8·0, 95% CI 1·6–37·2), antiepileptics (OR 3·4, 95% CI 1·9–5·8) and proton pump inhibitors (OR 2·9, 95% CI 2·0–4·0). Conclusions  We found an association between drug exposure and SCLE. More than one third of the SCLE cases could be attributed to drug exposure. No significant OR was found for thiazides, which might be due to longer latency and therefore missed with this study design. DI‐SCLE is reversible once the drug is discontinued, indicating the importance of screening patients with SCLE for potentially triggering drugs. A causal relationship cannot be established from this study and the underlying pathogenesis remains unclear.</description><identifier>ISSN: 0007-0963</identifier><identifier>ISSN: 1365-2133</identifier><identifier>EISSN: 1365-2133</identifier><identifier>DOI: 10.1111/j.1365-2133.2012.10969.x</identifier><identifier>PMID: 22458771</identifier><identifier>CODEN: BJDEAZ</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Aged ; Biological and medical sciences ; Case-Control Studies ; Dermatology ; Female ; Humans ; Lupus Erythematosus, Cutaneous - chemically induced ; Lupus Erythematosus, Cutaneous - epidemiology ; Male ; Medical sciences ; Medicin och hälsovetenskap ; Middle Aged ; Odds Ratio ; Prescription Drugs - adverse effects ; Registries ; Sweden - epidemiology</subject><ispartof>British journal of dermatology (1951), 2012-08, Vol.167 (2), p.296-305</ispartof><rights>2012 The Authors. BJD © 2012 British Association of Dermatologists</rights><rights>2015 INIST-CNRS</rights><rights>2012 The Authors. BJD © 2012 British Association of Dermatologists.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5149-cb4f4555e7b58fb653fdd3bcb71e3dbc480c2dfbc65628fbda80cfce203f09fa3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1365-2133.2012.10969.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1365-2133.2012.10969.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,314,780,784,885,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=26225095$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22458771$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-180276$$DView record from Swedish Publication Index$$Hfree_for_read</backlink><backlink>$$Uhttp://kipublications.ki.se/Default.aspx?queryparsed=id:125000640$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Grönhagen, C.M.</creatorcontrib><creatorcontrib>Fored, C.M.</creatorcontrib><creatorcontrib>Linder, M.</creatorcontrib><creatorcontrib>Granath, F.</creatorcontrib><creatorcontrib>Nyberg, F.</creatorcontrib><title>Subacute cutaneous lupus erythematosus and its association with drugs: a population-based matched case-control study of 234 patients in Sweden</title><title>British journal of dermatology (1951)</title><addtitle>Br J Dermatol</addtitle><description>Summary Background  Numerous case reports about drug‐induced (DI) subacute cutaneous lupus erythematosus (SCLE) have been published. Various drug types with different latencies has been proposed as triggers for this autoimmune skin disease. Objectives  To evaluate the association between exposure to certain suspected drugs (previously implicated to induce SCLE) and a subsequent diagnosis of SCLE. Methods  We performed a population‐based matched case–control study in which all incident cases of SCLE (n = 234) from 2006 to 2009 were derived from the National Patient Register. The control group was selected from the general population, matched (1 : 10) for gender, age and county of residence. The data were linked to the Prescribed Drug Register. Odds ratios (ORs) and 95% confidence intervals (CIs) were calculated for the association between exposures to certain suspected drugs and the development of SCLE. Results  During the 6 months preceding SCLE diagnosis, 166 (71%) of the patients with SCLE had at least one filled prescription of the suspected drugs. The most increased ORs were found for terbinafine (OR 52·9, 95% CI 6·6–∞), tumour necrosis factor‐α inhibitors (OR 8·0, 95% CI 1·6–37·2), antiepileptics (OR 3·4, 95% CI 1·9–5·8) and proton pump inhibitors (OR 2·9, 95% CI 2·0–4·0). Conclusions  We found an association between drug exposure and SCLE. More than one third of the SCLE cases could be attributed to drug exposure. No significant OR was found for thiazides, which might be due to longer latency and therefore missed with this study design. DI‐SCLE is reversible once the drug is discontinued, indicating the importance of screening patients with SCLE for potentially triggering drugs. A causal relationship cannot be established from this study and the underlying pathogenesis remains unclear.</description><subject>Aged</subject><subject>Biological and medical sciences</subject><subject>Case-Control Studies</subject><subject>Dermatology</subject><subject>Female</subject><subject>Humans</subject><subject>Lupus Erythematosus, Cutaneous - chemically induced</subject><subject>Lupus Erythematosus, Cutaneous - epidemiology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Medicin och hälsovetenskap</subject><subject>Middle Aged</subject><subject>Odds Ratio</subject><subject>Prescription Drugs - adverse effects</subject><subject>Registries</subject><subject>Sweden - epidemiology</subject><issn>0007-0963</issn><issn>1365-2133</issn><issn>1365-2133</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kttu1DAQhiMEokvhFZBvkLggwYc4By6QyhZaUAVSC4U7y6d0vc3GIY61uy_BMzN76O5VfeEZe77_lzWeJEEEZwTW-3lGWMFTShjLKCY0I7gu6mz1JJkcCk-TCca4TKHCTpIXIcwxJgxz_Dw5oTTnVVmSSfLvJiqp42gRbLKzPgbUxh52O6zHmV3I0Qc4yc4gN0IMwWsnR-c7tHTjDJkh3oUPSKLe97HdFlIlgzUIpHoGUcMp1b4bB9-iMEazRr5BlOWoB9x24Oo6dLO0xnYvk2eNbIN9tY-nya8vn39OL9OrHxdfp2dXqeYkr1Ot8ibnnNtS8apRBWeNMUxpVRLLjNJ5hTU1jdIFLygARsJFoy3FrMF1I9lpku58w9L2UYl-cAs5rIWXTuyv7iGzgrMK1xXw9aN8P3hzFD0ICeXQ_iLHoH33qPbc3Z4JP9yJGAWpMC0LwN_ucPD9G20YxcIFbdt29zuCYIZxhQuyedXrPRrVwpqD88P3AvBmD8igZdsMstMuHLmCwitrDtzHHbd0rV0f6gSLzbiJudhMldhMldiMm9iOm1iJT9_Ot-mxny6MdnUwkMO9KEpWcvH7-4X4M60vb6_pNTT1P_qT3Gk</recordid><startdate>201208</startdate><enddate>201208</enddate><creator>Grönhagen, C.M.</creator><creator>Fored, C.M.</creator><creator>Linder, M.</creator><creator>Granath, F.</creator><creator>Nyberg, F.</creator><general>Blackwell Publishing Ltd</general><general>Wiley-Blackwell</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope><scope>ADTPV</scope><scope>AOWAS</scope><scope>DF2</scope></search><sort><creationdate>201208</creationdate><title>Subacute cutaneous lupus erythematosus and its association with drugs: a population-based matched case-control study of 234 patients in Sweden</title><author>Grönhagen, C.M. ; Fored, C.M. ; Linder, M. ; Granath, F. ; Nyberg, F.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5149-cb4f4555e7b58fb653fdd3bcb71e3dbc480c2dfbc65628fbda80cfce203f09fa3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Aged</topic><topic>Biological and medical sciences</topic><topic>Case-Control Studies</topic><topic>Dermatology</topic><topic>Female</topic><topic>Humans</topic><topic>Lupus Erythematosus, Cutaneous - chemically induced</topic><topic>Lupus Erythematosus, Cutaneous - epidemiology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Medicin och hälsovetenskap</topic><topic>Middle Aged</topic><topic>Odds Ratio</topic><topic>Prescription Drugs - adverse effects</topic><topic>Registries</topic><topic>Sweden - epidemiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Grönhagen, C.M.</creatorcontrib><creatorcontrib>Fored, C.M.</creatorcontrib><creatorcontrib>Linder, M.</creatorcontrib><creatorcontrib>Granath, F.</creatorcontrib><creatorcontrib>Nyberg, F.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><collection>SwePub</collection><collection>SwePub Articles</collection><collection>SWEPUB Uppsala universitet</collection><jtitle>British journal of dermatology (1951)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Grönhagen, C.M.</au><au>Fored, C.M.</au><au>Linder, M.</au><au>Granath, F.</au><au>Nyberg, F.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Subacute cutaneous lupus erythematosus and its association with drugs: a population-based matched case-control study of 234 patients in Sweden</atitle><jtitle>British journal of dermatology (1951)</jtitle><addtitle>Br J Dermatol</addtitle><date>2012-08</date><risdate>2012</risdate><volume>167</volume><issue>2</issue><spage>296</spage><epage>305</epage><pages>296-305</pages><issn>0007-0963</issn><issn>1365-2133</issn><eissn>1365-2133</eissn><coden>BJDEAZ</coden><abstract>Summary Background  Numerous case reports about drug‐induced (DI) subacute cutaneous lupus erythematosus (SCLE) have been published. Various drug types with different latencies has been proposed as triggers for this autoimmune skin disease. Objectives  To evaluate the association between exposure to certain suspected drugs (previously implicated to induce SCLE) and a subsequent diagnosis of SCLE. Methods  We performed a population‐based matched case–control study in which all incident cases of SCLE (n = 234) from 2006 to 2009 were derived from the National Patient Register. The control group was selected from the general population, matched (1 : 10) for gender, age and county of residence. The data were linked to the Prescribed Drug Register. Odds ratios (ORs) and 95% confidence intervals (CIs) were calculated for the association between exposures to certain suspected drugs and the development of SCLE. Results  During the 6 months preceding SCLE diagnosis, 166 (71%) of the patients with SCLE had at least one filled prescription of the suspected drugs. The most increased ORs were found for terbinafine (OR 52·9, 95% CI 6·6–∞), tumour necrosis factor‐α inhibitors (OR 8·0, 95% CI 1·6–37·2), antiepileptics (OR 3·4, 95% CI 1·9–5·8) and proton pump inhibitors (OR 2·9, 95% CI 2·0–4·0). Conclusions  We found an association between drug exposure and SCLE. More than one third of the SCLE cases could be attributed to drug exposure. No significant OR was found for thiazides, which might be due to longer latency and therefore missed with this study design. DI‐SCLE is reversible once the drug is discontinued, indicating the importance of screening patients with SCLE for potentially triggering drugs. A causal relationship cannot be established from this study and the underlying pathogenesis remains unclear.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>22458771</pmid><doi>10.1111/j.1365-2133.2012.10969.x</doi><tpages>10</tpages></addata></record>
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source MEDLINE; Access via Wiley Online Library; Oxford University Press Journals All Titles (1996-Current)
subjects Aged
Biological and medical sciences
Case-Control Studies
Dermatology
Female
Humans
Lupus Erythematosus, Cutaneous - chemically induced
Lupus Erythematosus, Cutaneous - epidemiology
Male
Medical sciences
Medicin och hälsovetenskap
Middle Aged
Odds Ratio
Prescription Drugs - adverse effects
Registries
Sweden - epidemiology
title Subacute cutaneous lupus erythematosus and its association with drugs: a population-based matched case-control study of 234 patients in Sweden
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