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Attainment of low disease activity and remission targets reduces the risk of severe flare and new damage in childhood lupus.
Smith, Eve M D; Tharmaratnam, Kukatharmini; Al-Abadi, Eslam; Armon, Kate; Bailey, Kathryn; Brennan, Mary; Ciurtin, Coziana; Gardner-Medwin, Janet; Haslam, Kirsty E; Hawley, Daniel; Leahy, Alice; Leone, Valentina; Malik, Gulshan; McLaren, Zoe; Pilkington, Clarissa; Ramanan, Athimalaipet V; Rangaraj, Satyapal; Ratcliffe, Annie; Riley, Philip; Sen, Ethan; Sridhar, Arani; Wilkinson, Nick; Hedrich, Christian M; Jorgensen, Andrea; Beresford, Michael W.
Afiliación
  • Smith EMD; Department of Women's & Children's Health, Institute of Life Course and Medical Sciences, University of Liverpool.
  • Tharmaratnam K; Department of Paediatric Rheumatology, Alder Hey Children's NHS Foundation Trust Hospital.
  • Al-Abadi E; Department of Health Data Science, Institute of Population Health, University of Liverpool, Liverpool.
  • Armon K; Department of Rheumatology, Birmingham Children's Hospital, Birmingham.
  • Bailey K; Department of Paediatric Rheumatology, Cambridge University Hospitals, Cambridge.
  • Brennan M; Department of Paediatric Rheumatology, Oxford University Hospitals NHS Foundation Trust, Oxford.
  • Ciurtin C; Department of Paediatric Rheumatology, Royal Hospital for Sick Children, Edinburgh.
  • Gardner-Medwin J; Department of Rheumatology, Centre for Adolescent Rheumatology, University College London, London.
  • Haslam KE; Department of Child Health, University of Glasgow, Glasgow.
  • Hawley D; Department of Paediatrics, Bradford Royal Infirmary, Bradford.
  • Leahy A; Department of Paediatric Rheumatology, Sheffield Children's Hospital, Sheffield.
  • Leone V; Department of Paediatric Rheumatology, Southampton General Hospital, Southampton.
  • Malik G; Department of Paediatric Rheumatology, Leeds Children Hospital, Leeds.
  • McLaren Z; Department of Paediatrics, Royal Aberdeen Children's Hospital, Aberdeen.
  • Pilkington C; Rheumatology Department, Aintree University Hospital, Liverpool.
  • Ramanan AV; Department of Paediatric Rheumatology, Great Ormond Street Hospital, London.
  • Rangaraj S; Department of Paediatric Rheumatology, University Hospitals Bristol NHS Foundation Trust & Bristol Medical School, University of Bristol, Bristol.
  • Ratcliffe A; Department of Paediatric Rheumatology, Nottingham University Hospitals, Nottingham.
  • Riley P; Department of Paediatrics, Musgrove Park Hospital, Taunton.
  • Sen E; Department of Paediatric Rheumatology, Royal Manchester Children's Hospital, Manchester.
  • Sridhar A; Department of Paediatric Rheumatology, Great North Children's Hospital & Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne.
  • Wilkinson N; Department of Paediatrics, Leicester Children's Hospital, University Hospitals of Leicester NHS trust, Leicester.
  • Hedrich CM; Department of Paediatric Rheumatology, Guy's & St Thomas's NHS Foundation Trust, Evelina Children's Hospital, London, UK.
  • Jorgensen A; Department of Women's & Children's Health, Institute of Life Course and Medical Sciences, University of Liverpool.
  • Beresford MW; Department of Paediatric Rheumatology, Alder Hey Children's NHS Foundation Trust Hospital.
Rheumatology (Oxford) ; 61(8): 3378-3389, 2022 08 03.
Article en En | MEDLINE | ID: mdl-34894234
ABSTRACT

OBJECTIVES:

To assess the achievability and effect of attaining low disease activity (LDA) or remission in childhood-onset SLE (cSLE).

METHODS:

Attainment of three adult-SLE derived definitions of LDA (LLDAS, LA, Toronto-LDA), and four definitions of remission (clinical-SLEDAI-defined remission on/off treatment, pBILAG-defined remission on/off treatment) was assessed in UK JSLE Cohort Study patients longitudinally. Prentice-Williams-Petersen gap recurrent event models assessed the impact of LDA/remission attainment on severe flare/new damage.

RESULTS:

LLDAS, LA and Toronto-LDA targets were reached in 67%, 73% and 32% of patients, after a median of 18, 15 or 17 months, respectively. Cumulatively, LLDAS, LA and Toronto-LDA was attained for a median of 23%, 31% and 19% of total follow-up-time, respectively. Remission on-treatment was more common (61% cSLEDAI-defined, 42% pBILAG-defined) than remission off-treatment (31% cSLEDAI-defined, 21% pBILAG-defined). Attainment of all target states, and disease duration (>1 year), significantly reduced the hazard of severe flare (P < 0.001). As cumulative time in each target increased, hazard of severe flare progressively reduced. LLDAS attainment reduced the hazard of severe flare more than LA or Toronto-LDA (P < 0.001). Attainment of LLDAS and all remission definitions led to a statistically comparable reduction in the hazards of severe flare (P > 0.05). Attainment of all targets reduced the hazards of new damage (P < 0.05).

CONCLUSIONS:

This is the first study demonstrating that adult-SLE-derived definitions of LDA/remission are achievable in cSLE, significantly reducing risk of severe flare/new damage. Of the LDA definitions, LLDAS performed best, leading to a statistically comparable reduction in the hazards of severe flare to attainment of clinical remission.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Lupus Eritematoso Sistémico Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Humans Idioma: En Revista: Rheumatology (Oxford) Asunto de la revista: REUMATOLOGIA Año: 2022 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Lupus Eritematoso Sistémico Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Humans Idioma: En Revista: Rheumatology (Oxford) Asunto de la revista: REUMATOLOGIA Año: 2022 Tipo del documento: Article
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