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New classification criteria for systemic lupus erythematosus correlate with disease activity

AIM: To determine the prevalence of American College of Rheumatology (ACR) and Systemic Lupus International Collaborating Clinics (SLICC) classification criteria among systemic lupus erythematosus (SLE) patients; to determine disease activity and severity; and to investigate the correlation of class...

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Autores principales: Anić, Felina, Žuvić-Butorac, Marta, Štimac, Davor, Novak, Srđan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Croatian Medical Schools 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4228292/
https://www.ncbi.nlm.nih.gov/pubmed/25358884
http://dx.doi.org/10.3325/cmj.2014.55.514
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author Anić, Felina
Žuvić-Butorac, Marta
Štimac, Davor
Novak, Srđan
author_facet Anić, Felina
Žuvić-Butorac, Marta
Štimac, Davor
Novak, Srđan
author_sort Anić, Felina
collection PubMed
description AIM: To determine the prevalence of American College of Rheumatology (ACR) and Systemic Lupus International Collaborating Clinics (SLICC) classification criteria among systemic lupus erythematosus (SLE) patients; to determine disease activity and severity; and to investigate the correlation of classification criteria with disease activity, and of disease activity and damage index with disease duration. METHODS: We performed a cross-sectional study on 110 SLE patients from the Division of Rheumatology and Clinical Immunology, University Hospital Centre Rijeka, Croatia in the period from September to December 2013 and determined disease duration and the total number of ACR and SLICC classification criteria. Disease activity was assessed by Systemic Lupus Erythematosus Disease Activity Index (SLEDAI) index and organ damage by Systemic Lupus International Collaborating Clinics/American College of Rheumatology (SLICC/ACR) damage index. RESULTS: The number of SLICC classification criteria met per patient was significantly higher than the number of ACR criteria (7 [IQR 6-8] vs 5 [IQR 4-6], P < 0.001). Moderate correlations were detected between the number of SLICC classification criteria and disease activity index, both in case of active (r = 0.48, P = 0.003) and inactive disease (r = 0.43, P < 0.001). We neither found a correlation between the number of ACR criteria and disease activity nor between disease activity and disease duration. However, there was a good correlation between SLICC/ACR damage index and disease duration (r = 0.63, P < 0.001). CONCLUSION: New SLICC classification criteria correlate with disease activity because they capture more manifestations also included in the SLEDAI index. Patients with longer disease duration had a larger damage index score.
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spelling pubmed-42282922014-11-17 New classification criteria for systemic lupus erythematosus correlate with disease activity Anić, Felina Žuvić-Butorac, Marta Štimac, Davor Novak, Srđan Croat Med J Clinical Science AIM: To determine the prevalence of American College of Rheumatology (ACR) and Systemic Lupus International Collaborating Clinics (SLICC) classification criteria among systemic lupus erythematosus (SLE) patients; to determine disease activity and severity; and to investigate the correlation of classification criteria with disease activity, and of disease activity and damage index with disease duration. METHODS: We performed a cross-sectional study on 110 SLE patients from the Division of Rheumatology and Clinical Immunology, University Hospital Centre Rijeka, Croatia in the period from September to December 2013 and determined disease duration and the total number of ACR and SLICC classification criteria. Disease activity was assessed by Systemic Lupus Erythematosus Disease Activity Index (SLEDAI) index and organ damage by Systemic Lupus International Collaborating Clinics/American College of Rheumatology (SLICC/ACR) damage index. RESULTS: The number of SLICC classification criteria met per patient was significantly higher than the number of ACR criteria (7 [IQR 6-8] vs 5 [IQR 4-6], P < 0.001). Moderate correlations were detected between the number of SLICC classification criteria and disease activity index, both in case of active (r = 0.48, P = 0.003) and inactive disease (r = 0.43, P < 0.001). We neither found a correlation between the number of ACR criteria and disease activity nor between disease activity and disease duration. However, there was a good correlation between SLICC/ACR damage index and disease duration (r = 0.63, P < 0.001). CONCLUSION: New SLICC classification criteria correlate with disease activity because they capture more manifestations also included in the SLEDAI index. Patients with longer disease duration had a larger damage index score. Croatian Medical Schools 2014-10 /pmc/articles/PMC4228292/ /pubmed/25358884 http://dx.doi.org/10.3325/cmj.2014.55.514 Text en Copyright © 2014 by the Croatian Medical Journal. All rights reserved. http://creativecommons.org/licenses/by/2.5/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Science
Anić, Felina
Žuvić-Butorac, Marta
Štimac, Davor
Novak, Srđan
New classification criteria for systemic lupus erythematosus correlate with disease activity
title New classification criteria for systemic lupus erythematosus correlate with disease activity
title_full New classification criteria for systemic lupus erythematosus correlate with disease activity
title_fullStr New classification criteria for systemic lupus erythematosus correlate with disease activity
title_full_unstemmed New classification criteria for systemic lupus erythematosus correlate with disease activity
title_short New classification criteria for systemic lupus erythematosus correlate with disease activity
title_sort new classification criteria for systemic lupus erythematosus correlate with disease activity
topic Clinical Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4228292/
https://www.ncbi.nlm.nih.gov/pubmed/25358884
http://dx.doi.org/10.3325/cmj.2014.55.514
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