Lupus low disease activity state within 12 months is associated with favourable outcomes in severely active systemic lupus erythematosus.

low disease activity lupus low disease activity state outcome measure remission induction therapy systemic lupus erythematosus treatment target

Journal

Rheumatology (Oxford, England)
ISSN: 1462-0332
Titre abrégé: Rheumatology (Oxford)
Pays: England
ID NLM: 100883501

Informations de publication

Date de publication:
30 08 2022
Historique:
received: 09 09 2021
revised: 31 12 2021
pubmed: 12 1 2022
medline: 9 9 2022
entrez: 11 1 2022
Statut: ppublish

Résumé

To demonstrate the significance of the time to attain lupus low disease activity state (LLDAS) after remission induction therapy in patients with severely active SLE. We enrolled 79 patients starting prednisolone ≥0.4 mg/kg/day for active lupus with a BILAG 2004 index of A ≥ 1 or B ≥ 2, or for severe flare based on the Safety of Estrogens in Lupus Erythematosus National Assessment-SLE Disease Activity Index (SELENA-SLEDAI). The time to LLDAS attainment was divided into ≤6, 6-12 and >12 months and non-LLDAS; associations between the timing of LLDAS and flares, damage accrual and ≥50% LLDAS attainment were examined. The mean SLEDAI was 17; median starting dose of prednisolone, 0.95 mg/kg/day; and mean observational period, 39.7 months. Six (7.6%) and 41 (51.9%) patients achieved LLDAS within 6 and 12 months. Patients with a shorter time to LLDAS achievement were more likely to spend ≥50% of the time in LLDAS and had a lower cumulative prednisolone dose; no differences were observed in damage accrual. Patients requiring longer than 12 months to achieve LLDAS had a higher prevalence of thrombocytopenia and those with non-LLDAS had lower renal function and a higher starting dose of prednisolone and steroid pulse therapy than those who achieved LLDAS within 12 months. Achieving LLDAS within 12 months of induction therapy may be favourable in patients with severely active SLE. The low frequency of LLDAS attainment in high-risk populations highlights the need for a new strategy for SLE treatment.

Identifiants

pubmed: 35015824
pii: 6500278
doi: 10.1093/rheumatology/keac002
doi:

Substances chimiques

Prednisolone 9PHQ9Y1OLM

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

3777-3791

Informations de copyright

© The Author(s) 2022. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Auteurs

Jun Kikuchi (J)

Division of Rheumatology, Department of Internal Medicine, School of Medicine, Keio University, Tokyo, Japan.

Hironari Hanaoka (H)

Division of Rheumatology, Department of Internal Medicine, School of Medicine, Keio University, Tokyo, Japan.

Shuntaro Saito (S)

Division of Rheumatology, Department of Internal Medicine, School of Medicine, Keio University, Tokyo, Japan.

Tatsuhiro Oshige (T)

Division of Rheumatology, Department of Internal Medicine, School of Medicine, Keio University, Tokyo, Japan.

Kazuoto Hiramoto (K)

Division of Rheumatology, Department of Internal Medicine, School of Medicine, Keio University, Tokyo, Japan.

Yuko Kaneko (Y)

Division of Rheumatology, Department of Internal Medicine, School of Medicine, Keio University, Tokyo, Japan.

Tsutomu Takeuchi (T)

Division of Rheumatology, Department of Internal Medicine, School of Medicine, Keio University, Tokyo, Japan.

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Classifications MeSH