Attainment of low disease activity and remission targets reduces the risk of severe flare and new damage in childhood lupus

Author:

Smith Eve M D12ORCID,Tharmaratnam Kukatharmini3,Al-Abadi Eslam4ORCID,Armon Kate5,Bailey Kathryn6,Brennan Mary7,Ciurtin Coziana8ORCID,Gardner-Medwin Janet9,Haslam Kirsty E10,Hawley Daniel11,Leahy Alice12,Leone Valentina13,Malik Gulshan14,McLaren Zoe15,Pilkington Clarissa16,Ramanan Athimalaipet V17,Rangaraj Satyapal18,Ratcliffe Annie19,Riley Philip20,Sen Ethan21,Sridhar Arani22,Wilkinson Nick23,Hedrich Christian M12,Jorgensen Andrea3,Beresford Michael W12ORCID

Affiliation:

1. Department of Women's & Children's Health, Institute of Life Course and Medical Sciences, University of Liverpool

2. Department of Paediatric Rheumatology, Alder Hey Children's NHS Foundation Trust Hospital

3. Department of Health Data Science, Institute of Population Health, University of Liverpool, Liverpool

4. Department of Rheumatology, Birmingham Children’s Hospital, Birmingham

5. Department of Paediatric Rheumatology, Cambridge University Hospitals, Cambridge

6. Department of Paediatric Rheumatology, Oxford University Hospitals NHS Foundation Trust, Oxford

7. Department of Paediatric Rheumatology, Royal Hospital for Sick Children, Edinburgh

8. Department of Rheumatology, Centre for Adolescent Rheumatology, University College London, London

9. Department of Child Health, University of Glasgow, Glasgow

10. Department of Paediatrics, Bradford Royal Infirmary, Bradford

11. Department of Paediatric Rheumatology, Sheffield Children’s Hospital, Sheffield

12. Department of Paediatric Rheumatology, Southampton General Hospital, Southampton

13. Department of Paediatric Rheumatology, Leeds Children Hospital, Leeds

14. Department of Paediatrics, Royal Aberdeen Children’s Hospital, Aberdeen

15. Rheumatology Department, Aintree University Hospital, Liverpool

16. Department of Paediatric Rheumatology, Great Ormond Street Hospital, London

17. Department of Paediatric Rheumatology, University Hospitals Bristol NHS Foundation Trust & Bristol Medical School, University of Bristol, Bristol

18. Department of Paediatric Rheumatology, Nottingham University Hospitals, Nottingham

19. Department of Paediatrics, Musgrove Park Hospital, Taunton

20. Department of Paediatric Rheumatology, Royal Manchester Children’s Hospital, Manchester

21. Department of Paediatric Rheumatology, Great North Children’s Hospital & Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne

22. Department of Paediatrics, Leicester Children’s Hospital, University Hospitals of Leicester NHS trust, Leicester

23. Department of Paediatric Rheumatology, Guy's & St Thomas's NHS Foundation Trust, Evelina Children's Hospital, London, UK

Abstract

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.

Funder

Wellcome Trust Institutional Strategic Support Fund

Faculty of Health and Life Sciences, University of Liverpool’

UK JSLE Cohort Study

Versus Arthritis

University of Liverpool, Alder Hey Children’s NHS Foundation Trust and the Alder Hey Charity

University of Liverpool and Alder Hey Children’s NHS Foundation Trust

Publisher

Oxford University Press (OUP)

Subject

Pharmacology (medical),Rheumatology

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