The antinuclear antibody assay: developing criteria for reflexive anti-dsDNA antibody testing in a laboratory setting
Background: We examined the relationship between antinuclear antibody (ANA) data and the presence of anti-double stranded DNA antibodies (anti-dsDNA). Methods: De-identified demographic, ANA and anti-dsDNA data were available for 30,196 individuals aged ≥20 years, whose sera were submitted sequentia...
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Veröffentlicht in: | Clinical chemistry and laboratory medicine 2011-07, Vol.49 (7), p.1205-1211 |
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description | Background: We examined the relationship between antinuclear antibody (ANA) data and the presence of anti-double stranded DNA antibodies (anti-dsDNA). Methods: De-identified demographic, ANA and anti-dsDNA data were available for 30,196 individuals aged ≥20 years, whose sera were submitted sequentially to our laboratory. When multiple sera were received for the same subject, data from the earliest sample were used. Anti-dsDNA frequency was stratified by ANA titer and pattern, sample referral source, and by the patient's age, gender, and diagnosis. Results: For sera with ANA titer ≥256 and an accompanying diagnosis of systemic lupus erythematosus, anti-dsDNA frequency was 53.7%, 35.3%, and 37.5% for homogeneous, speckled, or multiple ANA patterns, respectively. Among remaining sera with ANA titer ≥256, anti-dsDNA frequency was highest for the homogeneous pattern (15.9%). Anti-dsDNA frequency was three-fold higher among sera submitted by rheumatologists compared with other providers. However, its relative distribution by ANA pattern and titer was similar between these groups. Patient age and gender had no significant effect on anti-dsDNA frequency after ANA data were taken into account. Conclusions: ANA pattern and titer, together with the diagnosis submitted with the serum sample, can be used to guide decisions for reflexive anti-dsDNA testing in a clinical laboratory setting. |
doi_str_mv | 10.1515/CCLM.2011.613 |
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Methods: De-identified demographic, ANA and anti-dsDNA data were available for 30,196 individuals aged ≥20 years, whose sera were submitted sequentially to our laboratory. When multiple sera were received for the same subject, data from the earliest sample were used. Anti-dsDNA frequency was stratified by ANA titer and pattern, sample referral source, and by the patient's age, gender, and diagnosis. Results: For sera with ANA titer ≥256 and an accompanying diagnosis of systemic lupus erythematosus, anti-dsDNA frequency was 53.7%, 35.3%, and 37.5% for homogeneous, speckled, or multiple ANA patterns, respectively. Among remaining sera with ANA titer ≥256, anti-dsDNA frequency was highest for the homogeneous pattern (15.9%). Anti-dsDNA frequency was three-fold higher among sera submitted by rheumatologists compared with other providers. However, its relative distribution by ANA pattern and titer was similar between these groups. Patient age and gender had no significant effect on anti-dsDNA frequency after ANA data were taken into account. Conclusions: ANA pattern and titer, together with the diagnosis submitted with the serum sample, can be used to guide decisions for reflexive anti-dsDNA testing in a clinical laboratory setting.</description><identifier>ISSN: 1434-6621</identifier><identifier>EISSN: 1437-4331</identifier><identifier>DOI: 10.1515/CCLM.2011.613</identifier><identifier>PMID: 21612543</identifier><language>eng</language><publisher>Berlin: Walter de Gruyter</publisher><subject>Adult ; Age Factors ; Aged ; Aged, 80 and over ; anti-dsDNA antibody ; Antibodies, Antinuclear - blood ; Antibodies, Antinuclear - immunology ; antinuclear antibody ; Biological and medical sciences ; DNA - immunology ; Female ; General aspects ; Humans ; indirect immunofluorescence assay ; Investigative techniques, diagnostic techniques (general aspects) ; Male ; Medical sciences ; Middle Aged ; Rheumatic Diseases - blood ; Rheumatic Diseases - diagnosis ; Serologic Tests - methods ; Sex Factors ; Young Adult</subject><ispartof>Clinical chemistry and laboratory medicine, 2011-07, Vol.49 (7), p.1205-1211</ispartof><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c445t-4ea815a249182a3c4c8d77dbf49c41c1bf276bb4ee3786885a246dade82f246b3</citedby><cites>FETCH-LOGICAL-c445t-4ea815a249182a3c4c8d77dbf49c41c1bf276bb4ee3786885a246dade82f246b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.degruyter.com/document/doi/10.1515/CCLM.2011.613/pdf$$EPDF$$P50$$Gwalterdegruyter$$H</linktopdf><linktohtml>$$Uhttps://www.degruyter.com/document/doi/10.1515/CCLM.2011.613/html$$EHTML$$P50$$Gwalterdegruyter$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,66754,68538</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=24358114$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21612543$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Craig, Wendy Y.</creatorcontrib><creatorcontrib>Ledue, Thomas B.</creatorcontrib><title>The antinuclear antibody assay: developing criteria for reflexive anti-dsDNA antibody testing in a laboratory setting</title><title>Clinical chemistry and laboratory medicine</title><addtitle>Clin Chem Lab Med</addtitle><description>Background: We examined the relationship between antinuclear antibody (ANA) data and the presence of anti-double stranded DNA antibodies (anti-dsDNA). Methods: De-identified demographic, ANA and anti-dsDNA data were available for 30,196 individuals aged ≥20 years, whose sera were submitted sequentially to our laboratory. When multiple sera were received for the same subject, data from the earliest sample were used. Anti-dsDNA frequency was stratified by ANA titer and pattern, sample referral source, and by the patient's age, gender, and diagnosis. Results: For sera with ANA titer ≥256 and an accompanying diagnosis of systemic lupus erythematosus, anti-dsDNA frequency was 53.7%, 35.3%, and 37.5% for homogeneous, speckled, or multiple ANA patterns, respectively. Among remaining sera with ANA titer ≥256, anti-dsDNA frequency was highest for the homogeneous pattern (15.9%). Anti-dsDNA frequency was three-fold higher among sera submitted by rheumatologists compared with other providers. However, its relative distribution by ANA pattern and titer was similar between these groups. Patient age and gender had no significant effect on anti-dsDNA frequency after ANA data were taken into account. Conclusions: ANA pattern and titer, together with the diagnosis submitted with the serum sample, can be used to guide decisions for reflexive anti-dsDNA testing in a clinical laboratory setting.</description><subject>Adult</subject><subject>Age Factors</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>anti-dsDNA antibody</subject><subject>Antibodies, Antinuclear - blood</subject><subject>Antibodies, Antinuclear - immunology</subject><subject>antinuclear antibody</subject><subject>Biological and medical sciences</subject><subject>DNA - immunology</subject><subject>Female</subject><subject>General aspects</subject><subject>Humans</subject><subject>indirect immunofluorescence assay</subject><subject>Investigative techniques, diagnostic techniques (general aspects)</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Rheumatic Diseases - blood</subject><subject>Rheumatic Diseases - diagnosis</subject><subject>Serologic Tests - methods</subject><subject>Sex Factors</subject><subject>Young Adult</subject><issn>1434-6621</issn><issn>1437-4331</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1v1DAQhi0EomXhyBXlgjhl8cc4dhCXavkoaAEhLRy4WBPHKS7ZZGsnpfn3ON2le0Hi5FfW845G8xDylNElk0y-XK3Wn5acMrYsmLhHThkIlYMQ7P5thrwoODshj2K8pJRJCeohOeGsYFyCOCXj5qfLsBt8N9rWYbjNVV9PGcaI06usdteu7Xe-u8hs8IMLHrOmD1lwTetu_PW-ndfxzeezY3lwcZgrvsswa7HqAw59mLLohvn_MXnQYBvdk8O7IN_evd2szvP1l_cfVmfr3ALIIQeHmknkUDLNUViwulaqrhooLTDLqoaroqrAOaF0ofWMFjXWTvMmpUosyIv93F3or8a0k9n6aF3bYuf6MZqSAijNhfgvqRXoUnM6k_metKGPMZ3B7ILfYpgMo2ZWYmYlZlZikpLEPztMHqutq-_ovw4S8PwAYLTYNgE76-ORAyE1SyoX5PWe-41t8lC7izBOKZjLfgxdOuO_F4BSMU7lcW8fB3dzNx7DL1MooaT5ugFDf1B9Xn7_aED8AR1atv0</recordid><startdate>20110701</startdate><enddate>20110701</enddate><creator>Craig, Wendy Y.</creator><creator>Ledue, Thomas B.</creator><general>Walter de Gruyter</general><general>De Gruyter</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>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7TM</scope></search><sort><creationdate>20110701</creationdate><title>The antinuclear antibody assay: developing criteria for reflexive anti-dsDNA antibody testing in a laboratory setting</title><author>Craig, Wendy Y. ; Ledue, Thomas B.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c445t-4ea815a249182a3c4c8d77dbf49c41c1bf276bb4ee3786885a246dade82f246b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Adult</topic><topic>Age Factors</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>anti-dsDNA antibody</topic><topic>Antibodies, Antinuclear - blood</topic><topic>Antibodies, Antinuclear - immunology</topic><topic>antinuclear antibody</topic><topic>Biological and medical sciences</topic><topic>DNA - immunology</topic><topic>Female</topic><topic>General aspects</topic><topic>Humans</topic><topic>indirect immunofluorescence assay</topic><topic>Investigative techniques, diagnostic techniques (general aspects)</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Rheumatic Diseases - blood</topic><topic>Rheumatic Diseases - diagnosis</topic><topic>Serologic Tests - methods</topic><topic>Sex Factors</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Craig, Wendy Y.</creatorcontrib><creatorcontrib>Ledue, Thomas B.</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>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Nucleic Acids Abstracts</collection><jtitle>Clinical chemistry and laboratory medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Craig, Wendy Y.</au><au>Ledue, Thomas B.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The antinuclear antibody assay: developing criteria for reflexive anti-dsDNA antibody testing in a laboratory setting</atitle><jtitle>Clinical chemistry and laboratory medicine</jtitle><addtitle>Clin Chem Lab Med</addtitle><date>2011-07-01</date><risdate>2011</risdate><volume>49</volume><issue>7</issue><spage>1205</spage><epage>1211</epage><pages>1205-1211</pages><issn>1434-6621</issn><eissn>1437-4331</eissn><abstract>Background: We examined the relationship between antinuclear antibody (ANA) data and the presence of anti-double stranded DNA antibodies (anti-dsDNA). Methods: De-identified demographic, ANA and anti-dsDNA data were available for 30,196 individuals aged ≥20 years, whose sera were submitted sequentially to our laboratory. When multiple sera were received for the same subject, data from the earliest sample were used. Anti-dsDNA frequency was stratified by ANA titer and pattern, sample referral source, and by the patient's age, gender, and diagnosis. Results: For sera with ANA titer ≥256 and an accompanying diagnosis of systemic lupus erythematosus, anti-dsDNA frequency was 53.7%, 35.3%, and 37.5% for homogeneous, speckled, or multiple ANA patterns, respectively. Among remaining sera with ANA titer ≥256, anti-dsDNA frequency was highest for the homogeneous pattern (15.9%). Anti-dsDNA frequency was three-fold higher among sera submitted by rheumatologists compared with other providers. However, its relative distribution by ANA pattern and titer was similar between these groups. Patient age and gender had no significant effect on anti-dsDNA frequency after ANA data were taken into account. Conclusions: ANA pattern and titer, together with the diagnosis submitted with the serum sample, can be used to guide decisions for reflexive anti-dsDNA testing in a clinical laboratory setting.</abstract><cop>Berlin</cop><pub>Walter de Gruyter</pub><pmid>21612543</pmid><doi>10.1515/CCLM.2011.613</doi><tpages>7</tpages></addata></record> |
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subjects | Adult Age Factors Aged Aged, 80 and over anti-dsDNA antibody Antibodies, Antinuclear - blood Antibodies, Antinuclear - immunology antinuclear antibody Biological and medical sciences DNA - immunology Female General aspects Humans indirect immunofluorescence assay Investigative techniques, diagnostic techniques (general aspects) Male Medical sciences Middle Aged Rheumatic Diseases - blood Rheumatic Diseases - diagnosis Serologic Tests - methods Sex Factors Young Adult |
title | The antinuclear antibody assay: developing criteria for reflexive anti-dsDNA antibody testing in a laboratory setting |
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