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
Hauptverfasser: Heinlen, Latisha D., McClain, Micah T., Merrill, Joan, Akbarali, Yasmin W., Edgerton, Colin C., Harley, John B., James, Judith A.
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container_end_page 2351
container_issue 7
container_start_page 2344
container_title Arthritis and rheumatism
container_volume 56
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
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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 &lt; 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 &lt; 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. 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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 &lt; 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 &lt; 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. 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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. 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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 &lt; 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 &lt; 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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source MEDLINE; Wiley Journals
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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