Clinical criteria for systemic lupus erythematosus precede diagnosis, and associated autoantibodies are present before clinical symptoms
Objective Specific events that occur during the development of systemic lupus erythematosus (SLE) can be quite variable among individual patients. The aim of this study was to identify patterns that distinguish early clinical events in SLE and to assess whether the presence of associated autoantibod...
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Veröffentlicht in: | Arthritis and rheumatism 2007-07, Vol.56 (7), p.2344-2351 |
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creator | Heinlen, Latisha D. McClain, Micah T. Merrill, Joan Akbarali, Yasmin W. Edgerton, Colin C. Harley, John B. James, Judith A. |
description | Objective
Specific events that occur during the development of systemic lupus erythematosus (SLE) can be quite variable among individual patients. The aim of this study was to identify patterns that distinguish early clinical events in SLE and to assess whether the presence of associated autoantibodies precedes the fulfillment of clinical criteria.
Methods
Through a retrospective chart review of military medical records, 130 patients who met the American College of Rheumatology (ACR) criteria for the classification of SLE were identified. The initial time at which each criterion was fulfilled was recorded. Autoantibody analysis was performed on serum samples, using enzyme‐linked immunosorbent assays or immunofluorescence.
Results
The clinical features that were observed earliest were discoid rash and seizures, which developed a mean 1.74 and 1.70 years, respectively, before the diagnosis of SLE; however, arthritis was the criterion that was most commonly observed before diagnosis. The presence of IgG rheumatoid factor (IgG‐RF) preceded the development of arthritis in 15 (94%) of the 16 patients who were positive for IgG‐RF and in whom arthritis developed (Z = 10.2, P < 0.0001). Analogously, IgM‐RF appeared before the development of arthritis in 13 (76%) of 17 patients. Anti–double‐stranded DNA antibodies were associated with renal disease and appeared before evidence of nephritis in most patients (92%) (Z = 13.3, P < 0.0001). An analysis of the appearance of autoantibodies compared with the appearance of clinical criteria not associated with them revealed no significant temporal relationship.
Conclusion
Symptoms associated with the ACR criteria for classification of SLE are commonly present before the diagnosis of SLE, and development of organ‐associated autoantibodies generally precedes the appearance of their associated clinical features. |
doi_str_mv | 10.1002/art.22665 |
format | Article |
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Specific events that occur during the development of systemic lupus erythematosus (SLE) can be quite variable among individual patients. The aim of this study was to identify patterns that distinguish early clinical events in SLE and to assess whether the presence of associated autoantibodies precedes the fulfillment of clinical criteria.
Methods
Through a retrospective chart review of military medical records, 130 patients who met the American College of Rheumatology (ACR) criteria for the classification of SLE were identified. The initial time at which each criterion was fulfilled was recorded. Autoantibody analysis was performed on serum samples, using enzyme‐linked immunosorbent assays or immunofluorescence.
Results
The clinical features that were observed earliest were discoid rash and seizures, which developed a mean 1.74 and 1.70 years, respectively, before the diagnosis of SLE; however, arthritis was the criterion that was most commonly observed before diagnosis. The presence of IgG rheumatoid factor (IgG‐RF) preceded the development of arthritis in 15 (94%) of the 16 patients who were positive for IgG‐RF and in whom arthritis developed (Z = 10.2, P < 0.0001). Analogously, IgM‐RF appeared before the development of arthritis in 13 (76%) of 17 patients. Anti–double‐stranded DNA antibodies were associated with renal disease and appeared before evidence of nephritis in most patients (92%) (Z = 13.3, P < 0.0001). An analysis of the appearance of autoantibodies compared with the appearance of clinical criteria not associated with them revealed no significant temporal relationship.
Conclusion
Symptoms associated with the ACR criteria for classification of SLE are commonly present before the diagnosis of SLE, and development of organ‐associated autoantibodies generally precedes the appearance of their associated clinical features.</description><identifier>ISSN: 0004-3591</identifier><identifier>EISSN: 1529-0131</identifier><identifier>DOI: 10.1002/art.22665</identifier><identifier>PMID: 17599763</identifier><identifier>CODEN: ARHEAW</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Autoantibodies - blood ; Biological and medical sciences ; Biomarkers - blood ; Complement C1q - immunology ; Diagnosis, Differential ; Diseases of the osteoarticular system ; Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy ; Humans ; Immunoglobulin G - blood ; Lupus Erythematosus, Systemic - diagnosis ; Lupus Erythematosus, Systemic - immunology ; Medical sciences ; Military Personnel ; Miscellaneous. Osteoarticular involvement in other diseases ; Nervous system (semeiology, syndromes) ; Neurology ; Reproducibility of Results ; Retrospective Studies ; Rheumatoid Factor - blood ; Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis ; United States</subject><ispartof>Arthritis and rheumatism, 2007-07, Vol.56 (7), p.2344-2351</ispartof><rights>Copyright © 2007 by the American College of Rheumatology</rights><rights>2007 INIST-CNRS</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3845-fab42d8a5d790d21e30d86725995f93927603695d2a29229d9774ea5c37b4ac13</citedby><cites>FETCH-LOGICAL-c3845-fab42d8a5d790d21e30d86725995f93927603695d2a29229d9774ea5c37b4ac13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fart.22665$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fart.22665$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=18913203$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17599763$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Heinlen, Latisha D.</creatorcontrib><creatorcontrib>McClain, Micah T.</creatorcontrib><creatorcontrib>Merrill, Joan</creatorcontrib><creatorcontrib>Akbarali, Yasmin W.</creatorcontrib><creatorcontrib>Edgerton, Colin C.</creatorcontrib><creatorcontrib>Harley, John B.</creatorcontrib><creatorcontrib>James, Judith A.</creatorcontrib><title>Clinical criteria for systemic lupus erythematosus precede diagnosis, and associated autoantibodies are present before clinical symptoms</title><title>Arthritis and rheumatism</title><addtitle>Arthritis Rheum</addtitle><description>Objective
Specific events that occur during the development of systemic lupus erythematosus (SLE) can be quite variable among individual patients. The aim of this study was to identify patterns that distinguish early clinical events in SLE and to assess whether the presence of associated autoantibodies precedes the fulfillment of clinical criteria.
Methods
Through a retrospective chart review of military medical records, 130 patients who met the American College of Rheumatology (ACR) criteria for the classification of SLE were identified. The initial time at which each criterion was fulfilled was recorded. Autoantibody analysis was performed on serum samples, using enzyme‐linked immunosorbent assays or immunofluorescence.
Results
The clinical features that were observed earliest were discoid rash and seizures, which developed a mean 1.74 and 1.70 years, respectively, before the diagnosis of SLE; however, arthritis was the criterion that was most commonly observed before diagnosis. The presence of IgG rheumatoid factor (IgG‐RF) preceded the development of arthritis in 15 (94%) of the 16 patients who were positive for IgG‐RF and in whom arthritis developed (Z = 10.2, P < 0.0001). Analogously, IgM‐RF appeared before the development of arthritis in 13 (76%) of 17 patients. Anti–double‐stranded DNA antibodies were associated with renal disease and appeared before evidence of nephritis in most patients (92%) (Z = 13.3, P < 0.0001). An analysis of the appearance of autoantibodies compared with the appearance of clinical criteria not associated with them revealed no significant temporal relationship.
Conclusion
Symptoms associated with the ACR criteria for classification of SLE are commonly present before the diagnosis of SLE, and development of organ‐associated autoantibodies generally precedes the appearance of their associated clinical features.</description><subject>Autoantibodies - blood</subject><subject>Biological and medical sciences</subject><subject>Biomarkers - blood</subject><subject>Complement C1q - immunology</subject><subject>Diagnosis, Differential</subject><subject>Diseases of the osteoarticular system</subject><subject>Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy</subject><subject>Humans</subject><subject>Immunoglobulin G - blood</subject><subject>Lupus Erythematosus, Systemic - diagnosis</subject><subject>Lupus Erythematosus, Systemic - immunology</subject><subject>Medical sciences</subject><subject>Military Personnel</subject><subject>Miscellaneous. Osteoarticular involvement in other diseases</subject><subject>Nervous system (semeiology, syndromes)</subject><subject>Neurology</subject><subject>Reproducibility of Results</subject><subject>Retrospective Studies</subject><subject>Rheumatoid Factor - blood</subject><subject>Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis</subject><subject>United States</subject><issn>0004-3591</issn><issn>1529-0131</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0d2K1TAQB_AgintcvfAFJDcKgmc3H03bXC4Hv2BBkPW6TJOpRtqmZlKkb-Bjm-M5slfiVTLwywyTP2PPpbiSQqhrSPlKqbo2D9hOGmX3Qmr5kO2EENVeGysv2BOi76VU2ujH7EI2xtqm1jv26zCGOTgYuUshYwrAh5g4bZRxCo6P67ISx7TlbzhBjlSqJaFDj9wH-DpHCvSGw-w5EEUXIGO5rjnCnEMffUDikPD4iHDOvMfSH7n7O5a2aclxoqfs0QAj4bPzecm-vHt7d_iwv_30_uPh5nbvdFuZ_QB9pXwLxjdWeCVRC9_WjSr7mMFqq5pa6Noar0BZpay3TVMhGKebvgIn9SV7deq7pPhjRcrdFMjhOMKMcaWubqUwjVL_hUpUbZG2wNcn6FIkSjh0SwoTpK2Tojvm05V8uj_5FPvi3HTtJ_T38hxIAS_PAKh8z5BgdoHuXWulVuLork_uZxhx-_fE7ubz3Wn0bwtvqU8</recordid><startdate>200707</startdate><enddate>200707</enddate><creator>Heinlen, Latisha D.</creator><creator>McClain, Micah T.</creator><creator>Merrill, Joan</creator><creator>Akbarali, Yasmin W.</creator><creator>Edgerton, Colin C.</creator><creator>Harley, John B.</creator><creator>James, Judith A.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley</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><scope>7T5</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>200707</creationdate><title>Clinical criteria for systemic lupus erythematosus precede diagnosis, and associated autoantibodies are present before clinical symptoms</title><author>Heinlen, Latisha D. ; McClain, Micah T. ; Merrill, Joan ; Akbarali, Yasmin W. ; Edgerton, Colin C. ; Harley, John B. ; James, Judith A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3845-fab42d8a5d790d21e30d86725995f93927603695d2a29229d9774ea5c37b4ac13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Autoantibodies - blood</topic><topic>Biological and medical sciences</topic><topic>Biomarkers - blood</topic><topic>Complement C1q - immunology</topic><topic>Diagnosis, Differential</topic><topic>Diseases of the osteoarticular system</topic><topic>Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy</topic><topic>Humans</topic><topic>Immunoglobulin G - blood</topic><topic>Lupus Erythematosus, Systemic - diagnosis</topic><topic>Lupus Erythematosus, Systemic - immunology</topic><topic>Medical sciences</topic><topic>Military Personnel</topic><topic>Miscellaneous. Osteoarticular involvement in other diseases</topic><topic>Nervous system (semeiology, syndromes)</topic><topic>Neurology</topic><topic>Reproducibility of Results</topic><topic>Retrospective Studies</topic><topic>Rheumatoid Factor - blood</topic><topic>Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis</topic><topic>United States</topic><toplevel>online_resources</toplevel><creatorcontrib>Heinlen, Latisha D.</creatorcontrib><creatorcontrib>McClain, Micah T.</creatorcontrib><creatorcontrib>Merrill, Joan</creatorcontrib><creatorcontrib>Akbarali, Yasmin W.</creatorcontrib><creatorcontrib>Edgerton, Colin C.</creatorcontrib><creatorcontrib>Harley, John B.</creatorcontrib><creatorcontrib>James, Judith A.</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><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Arthritis and rheumatism</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Heinlen, Latisha D.</au><au>McClain, Micah T.</au><au>Merrill, Joan</au><au>Akbarali, Yasmin W.</au><au>Edgerton, Colin C.</au><au>Harley, John B.</au><au>James, Judith A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Clinical criteria for systemic lupus erythematosus precede diagnosis, and associated autoantibodies are present before clinical symptoms</atitle><jtitle>Arthritis and rheumatism</jtitle><addtitle>Arthritis Rheum</addtitle><date>2007-07</date><risdate>2007</risdate><volume>56</volume><issue>7</issue><spage>2344</spage><epage>2351</epage><pages>2344-2351</pages><issn>0004-3591</issn><eissn>1529-0131</eissn><coden>ARHEAW</coden><abstract>Objective
Specific events that occur during the development of systemic lupus erythematosus (SLE) can be quite variable among individual patients. The aim of this study was to identify patterns that distinguish early clinical events in SLE and to assess whether the presence of associated autoantibodies precedes the fulfillment of clinical criteria.
Methods
Through a retrospective chart review of military medical records, 130 patients who met the American College of Rheumatology (ACR) criteria for the classification of SLE were identified. The initial time at which each criterion was fulfilled was recorded. Autoantibody analysis was performed on serum samples, using enzyme‐linked immunosorbent assays or immunofluorescence.
Results
The clinical features that were observed earliest were discoid rash and seizures, which developed a mean 1.74 and 1.70 years, respectively, before the diagnosis of SLE; however, arthritis was the criterion that was most commonly observed before diagnosis. The presence of IgG rheumatoid factor (IgG‐RF) preceded the development of arthritis in 15 (94%) of the 16 patients who were positive for IgG‐RF and in whom arthritis developed (Z = 10.2, P < 0.0001). Analogously, IgM‐RF appeared before the development of arthritis in 13 (76%) of 17 patients. Anti–double‐stranded DNA antibodies were associated with renal disease and appeared before evidence of nephritis in most patients (92%) (Z = 13.3, P < 0.0001). An analysis of the appearance of autoantibodies compared with the appearance of clinical criteria not associated with them revealed no significant temporal relationship.
Conclusion
Symptoms associated with the ACR criteria for classification of SLE are commonly present before the diagnosis of SLE, and development of organ‐associated autoantibodies generally precedes the appearance of their associated clinical features.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>17599763</pmid><doi>10.1002/art.22665</doi><tpages>8</tpages></addata></record> |
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subjects | Autoantibodies - blood Biological and medical sciences Biomarkers - blood Complement C1q - immunology Diagnosis, Differential Diseases of the osteoarticular system Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy Humans Immunoglobulin G - blood Lupus Erythematosus, Systemic - diagnosis Lupus Erythematosus, Systemic - immunology Medical sciences Military Personnel Miscellaneous. Osteoarticular involvement in other diseases Nervous system (semeiology, syndromes) Neurology Reproducibility of Results Retrospective Studies Rheumatoid Factor - blood Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis United States |
title | Clinical criteria for systemic lupus erythematosus precede diagnosis, and associated autoantibodies are present before clinical symptoms |
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