The clinically quiescent phase in early-diagnosed SLE patients: Inception cohort study

© The Author 2014. Objectives: The aims of this study were to evaluate the incidence of clinical quiescence in early-diagnosed SLE patients and to determine factors associated with a prolonged clinically quiescent phase. Methods: We used an inception cohort of SLE patients seen between May 2007 and...

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Main Authors: Kasitanon N., Intaniwet T., Wangkaew S., Pantana S., Sukitawut W., Louthrenoo W.
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Published: Oxford University Press 2015
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http://cmuir.cmu.ac.th/handle/6653943832/38500
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spelling th-cmuir.6653943832-385002015-06-16T07:47:21Z The clinically quiescent phase in early-diagnosed SLE patients: Inception cohort study Kasitanon N. Intaniwet T. Wangkaew S. Pantana S. Sukitawut W. Louthrenoo W. Medicine (all) Pharmacology (medical) Medicine (all) Pharmacology (medical) Rheumatology © The Author 2014. Objectives: The aims of this study were to evaluate the incidence of clinical quiescence in early-diagnosed SLE patients and to determine factors associated with a prolonged clinically quiescent phase. Methods: We used an inception cohort of SLE patients seen between May 2007 and June 2012. All patients were assessed for clinical quiescence [modified SLEDAI 2000 (mSLEDAI-2K) score = 0, no new features of lupus activity o increase in treatment] then evaluated for the occurrence of flare (mSLEDAI-2K increase ≥4 and increased disease activity in one or more organ systems or an increase in treatment). Results: Ninety-five patients (88 females) with a mean age of 33.22 years (S.D. 13.24) and mean disease duration 2.79 months (S.D. 3.19) at cohort entry were enrolled during a mean observation period of 3.04 years (S.D. 1.38). Sixty-six patients (69.5%) reached clinical quiescence within 11.31 months (S.D. 1.10) of enrolment. Thirty-six patients (54.5%) had a disease flare during the observation period. The clinically quiescent phase was 28.2 months (S.D. 3.4). Cox regression analysis revealed that age ≥25 years at diagnosis [hazard ratio (HR) 2.57 (95% CI 1.23, 5.40)] and continued antimalarial drug treatment [HR 2.80 (95% CI 1.40, 5.58)] were associated with a longer clinically quiescent phase. Conclusion: Most early-diagnosed SLE patients could have a good prognosis. Age at diagnosis ≥25 years or continued treatment with antimalarial drugs after reaching clinical quiescence may result in a longer clinically quiescent phase. More studies are needed to elucidate the mechanism of action for these protective effects. 2015-06-16T07:47:21Z 2015-06-16T07:47:21Z 2014-01-01 Article 14620324 2-s2.0-84929664049 10.1093/rheumatology/keu406 http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84929664049&origin=inward http://cmuir.cmu.ac.th/handle/6653943832/38500 Oxford University Press
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
topic Medicine (all)
Pharmacology (medical)
Medicine (all)
Pharmacology (medical)
Rheumatology
spellingShingle Medicine (all)
Pharmacology (medical)
Medicine (all)
Pharmacology (medical)
Rheumatology
Kasitanon N.
Intaniwet T.
Wangkaew S.
Pantana S.
Sukitawut W.
Louthrenoo W.
The clinically quiescent phase in early-diagnosed SLE patients: Inception cohort study
description © The Author 2014. Objectives: The aims of this study were to evaluate the incidence of clinical quiescence in early-diagnosed SLE patients and to determine factors associated with a prolonged clinically quiescent phase. Methods: We used an inception cohort of SLE patients seen between May 2007 and June 2012. All patients were assessed for clinical quiescence [modified SLEDAI 2000 (mSLEDAI-2K) score = 0, no new features of lupus activity o increase in treatment] then evaluated for the occurrence of flare (mSLEDAI-2K increase ≥4 and increased disease activity in one or more organ systems or an increase in treatment). Results: Ninety-five patients (88 females) with a mean age of 33.22 years (S.D. 13.24) and mean disease duration 2.79 months (S.D. 3.19) at cohort entry were enrolled during a mean observation period of 3.04 years (S.D. 1.38). Sixty-six patients (69.5%) reached clinical quiescence within 11.31 months (S.D. 1.10) of enrolment. Thirty-six patients (54.5%) had a disease flare during the observation period. The clinically quiescent phase was 28.2 months (S.D. 3.4). Cox regression analysis revealed that age ≥25 years at diagnosis [hazard ratio (HR) 2.57 (95% CI 1.23, 5.40)] and continued antimalarial drug treatment [HR 2.80 (95% CI 1.40, 5.58)] were associated with a longer clinically quiescent phase. Conclusion: Most early-diagnosed SLE patients could have a good prognosis. Age at diagnosis ≥25 years or continued treatment with antimalarial drugs after reaching clinical quiescence may result in a longer clinically quiescent phase. More studies are needed to elucidate the mechanism of action for these protective effects.
format Article
author Kasitanon N.
Intaniwet T.
Wangkaew S.
Pantana S.
Sukitawut W.
Louthrenoo W.
author_facet Kasitanon N.
Intaniwet T.
Wangkaew S.
Pantana S.
Sukitawut W.
Louthrenoo W.
author_sort Kasitanon N.
title The clinically quiescent phase in early-diagnosed SLE patients: Inception cohort study
title_short The clinically quiescent phase in early-diagnosed SLE patients: Inception cohort study
title_full The clinically quiescent phase in early-diagnosed SLE patients: Inception cohort study
title_fullStr The clinically quiescent phase in early-diagnosed SLE patients: Inception cohort study
title_full_unstemmed The clinically quiescent phase in early-diagnosed SLE patients: Inception cohort study
title_sort clinically quiescent phase in early-diagnosed sle patients: inception cohort study
publisher Oxford University Press
publishDate 2015
url http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84929664049&origin=inward
http://cmuir.cmu.ac.th/handle/6653943832/38500
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