Evidence map›Paper›PMID 41219118›Full record

Observational studyLupus science & medicine2025

Impact of glucocorticoid dose threshold in definition of lupus low disease activity state: a multinational observational cohort study.

Rangi Kandane-Rathnayake, Alberta Hoi, Worawit Louthrenoo, Vera Golder, Yi-Hsing Chen, Jiacai Cho, Aisha Lateef, Laniyati Hamijoyo, Shue-Fen Luo, Yeong-Jian Jan Wu and 30 more

Registry-linked trialAbstract readObservational StudyMulticenter Study
In one paragraph

Observational study in Lupus science & medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03138941 (Validation of the Lupus Low Disease Activity State), which is not on this map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT03138941 recruitingnot on this map

Validation of the Lupus Low Disease Activity State (LLDAS) in the Asia Pacific Region

Typeobservational_patient_registrySponsorMonash UniversityRan2013 to 2032Enrolled5,000ConditionsSystemic Lupus Erythematosus
3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

40 authors.

Rangi Kandane-RathnayakeCentre for Inflammatory Diseases, Monash University, Clayton, Victoria, Australia rangi.kandane-rathnayake@monash.edu.ORCID 0000-0001-5397-1482
Alberta HoiCentre for Inflammatory Diseases, Monash University, Clayton, Victoria, Australia.ORCID 0000-0002-9416-7383
Worawit LouthrenooDivision of Rheumatology, Department of Internal Medicine, Chiang Mai University, Chiang Mai, Thailand.ORCID 0000-0003-3105-6122
Vera GolderCentre for Inflammatory Diseases, Monash University, Clayton, Victoria, Australia.
Yi-Hsing ChenDivision of Allergy, Immunology and Rheumatology, Taichung Veterans General Hospital, Taichung, Taichung City, Taiwan.
Jiacai ChoRheumatology Division, Department of Medicine, National University Hospital, Singapore.ORCID 0000-0002-4477-3430
Aisha LateefDepartment of Medicine, Woodlands Health, Singapore.ORCID 0000-0002-0838-7495
Laniyati HamijoyoDepartment of Internal Medicine, Faculty of Medicine, Padjadjaran University, Bandung, Indonesia.ORCID 0000-0002-1310-674X
Shue-Fen LuoDepartment of Rheumatology, Allergy and Immunology, Chang Gung Memorial Hospital, Taipei, Taiwan.
Yeong-Jian Jan WuDepartment of Rheumatology, Allergy and Immunology, Chang Gung Memorial Hospital, Keelung, Taiwan.
Sandra NavarraSection of Rheumatology, University of Santo Tomas Hospital, Manila, Philippines.ORCID 0000-0003-0094-8654
Leonid ZamoraSection of Rheumatology, University of Santo Tomas Hospital, Manila, Philippines.
Zhanguo LiDepartment of Rheumatology and Immunology, Peking University People's Hospital, Beijing, China.
Haihong YaoDepartment of Rheumatology and Immunology, Peking University People's Hospital, Beijing, China.
Sargunan SockalingamDepartment of Medicine, Universiti Malaya Medical Centre, Kuala Lumpur, Malaysia.
Yasuhiro KatsumataDepartment of Rheumatology, Tokyo Women's Medical University, Tokyo, Japan.ORCID 0000-0003-1654-0119
Yanjie HaoDepartment of Rheumatology and Clinical Immunology, Peking University First Hospital, Beijing, China.
Zhuoli ZhangDepartment of Rheumatology and Clinical Immunology, Peking University First Hospital, Beijing, China.ORCID 0000-0001-7219-9141
B M D B BasnayakeDepartment of Nephrology, Teaching Hospital Kandy, Kandy, Sri Lanka.
Madelynn ChanDepartment of Rheumatology, Allergy & Immunology, Tan Tock Seng Hospital, Singapore.
Jun KikuchiDepartment of Internal Medicine, Keio University, Tokyo, Japan.ORCID 0000-0003-3231-8841
Yuko KanekoDepartment of Internal Medicine, Keio University, Tokyo, Japan.ORCID 0000-0003-2646-5765
Tsutomu TakeuchiDepartment of Internal Medicine, Keio University, Tokyo, Japan.
Shereen OonDepartment of Rheumatology, St Vincent's Hospital Melbourne, Fitzroy, Victoria, Australia.
Sang-Cheol BaeRheumatology, Hanyang University Hospital for Rheumatic Diseases, Seongdong-gu, Seoul, Republic of Korea.ORCID 0000-0003-4658-1093
Sean O'NeillRheumatology Department, Liverpool Hospital, Liverpool, New South Wales, Australia.
Geraldine HassettRheumatology Department, Liverpool Hospital, Liverpool, New South Wales, Australia.
Fiona GoldblattDepartment of Rheumatology, Flinders Medical Centre, Bedford Park, South Australia, Australia.
Kristine Pek Ling NgNorth Shore Hospital, Te Whatu Ora Health New Zealand Waitemata, Auckland, New Zealand.ORCID 0009-0006-6225-2715
Yih Jia PohDepartment of Rheumatology and Immunology, Singapore General Hospital, Singapore.ORCID 0000-0002-0003-8338
Nicola TugnetGreenlane Clinical Centre, Te Whatu Ora Health New Zealand Te Toka Tumai Auckland, Auckland, New Zealand.
Mark SapsfordMiddlemore Hospital, Te Whatu Ora Health New Zealand Counties Manukau, Auckland, New Zealand.
Shirley ChanDepartment of Medicine, The University of Hong Kong, Pok fu lam, Hong Kong.ORCID 0000-0002-0640-0676
Cherica TeeDepartment of Pediatrics, College of Medicine, University of the Philippines, Manila, Philippines.
Michael Lucas TeeDepartment of Internal Medicine, Rheumatology, University of the Philippines, Manila, Philippines.
Naoaki OhkuboThe First Department of Internal Medicine, University of Occupational and Environmental Health Japan, Kitakyushu, Japan.
Yoshiya TanakaThe First Department of Internal Medicine, University of Occupational and Environmental Health Japan, Kitakyushu, Japan.ORCID 0000-0002-0807-7139
Chak Sing LauDepartment of Medicine, The University of Hong Kong, Pok fu lam, Hong Kong.ORCID 0000-0001-6698-8355
Mandana NikpourDepartment of Rheumatology, St Vincent's Hospital Melbourne, Fitzroy, Victoria, Australia.
Eric MorandCentre for Inflammatory Diseases, Monash University, Clayton, Victoria, Australia.ORCID 0000-0002-9507-3338

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesThis study examined if lowering the glucocorticoid (GC) ceiling in the definition of lupus low disease activity state (LLDAS) from 7.5 mg/day to 5 mg/day (LLDAS-5) was associated with better outcomes in patients with systemic lupus erythematosus (SLE).

methodsData from a 13-country longitudinal SLE cohort (American College of Rheumatology/Systemic Lupus International Collaborating Clinics criteria), collected prospectively between 2013 and 2020, were analysed. Survival analyses were used to examine the longitudinal associations of LLDAS definitions with flare, organ damage accrual (frailty models) and mortality (Cox regression models).

results3801 patients with ≥2 visits were studied, with a median of 2.8 years (IQR: 1.0-5.4) of follow-up data (total visits: 40 949). 2141 (56.3%) patients experienced mild-moderate/severe flares; 717 (20.8%) accrued organ damage, and 80 (2.1%) died. 3072 (80%) patients attained LLDAS in 19 293 (47%) visits, while 2858 (75%) patients attained LLDAS-5 in 17 403 (42%) visits. Most patients in LLDAS were also in LLDAS-5; 214 patients (5.6%) attained LLDAS on at least one occasion, but never attained LLDAS-5. The magnitude of protection provided by LLDAS attainment against flare, irreversible organ damage accrual and mortality was similar with both GC thresholds. HRs (95% CIs) of damage accrual subsequent to spending 12 months in sustained LLDAS and LLDAS-5 were 0.42 (0.33 to 0.54, p<0.0001) and 0.43 (0.34 to 0.55, p<0.001), respectively. Likewise, HRs of flare and mortality corresponding to 12 months in LLDAS and LLDAS-5 were similar.

conclusionsNo evidence was found to support revising the GC dose threshold of the LLDAS definition. Regardless, minimising GC exposure remains a key goal of SLE management. TRIAL REGISTRATION NUMBER: NCT03138941.

Indexed as

GlucocorticoidsLupus Erythematosus, SystemicAdultDose-Response Relationship, DrugFemaleHumansLongitudinal StudiesMaleMiddle AgedProspective StudiesSeverity of Illness IndexSymptom Flare UpGlucocorticoidsGlucocorticoidsLupus Erythematosus, SystemicMortalityOutcome Assessment, Health Care

Identifiers

PMID41219118
PMCPMC12606472

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.