Evidence map›Paper›PMID 42203250›Full record

ArticleLupus science & medicine2026

Beyond renal response: sustained systemic disease control protects against adverse long-term outcomes in lupus nephritis.

Konstantinos Drougkas, Spyridon Katechis, Myrto Kostopoulou, Christina Tsalapaki, Sofia Flouda, Maria Pappa, Marija Bakula, Ivan Padjen, Myrto Nikoloudaki, Pinelopi Konstantopoulou and 6 more

Abstract readMulticenter Study
In one paragraph

Article in Lupus science & medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

16 authors.

Konstantinos DrougkasRheumatology and Clinical Immunology Unit, Attikon University Hospital, National and Kapodistrian University of Athens, School of Medicine, Athens, Greece.ORCID 0009-0003-0143-6404
Spyridon KatechisRheumatology and Clinical Immunology Unit, Attikon University Hospital, National and Kapodistrian University of Athens, School of Medicine, Athens, Greece.
Myrto KostopoulouDepartment of Nephrology, "G. Gennimatas" General Hospital, Athens, Greece.
Christina TsalapakiClinical Immunology- Rheumatology Unit, 2nd Department of Medicine and Laboratory, General Hospital of Athens Hippokration, National and Kapodistrian University of Athens, School of Medicine, Athens, Greece.
Sofia FloudaRheumatology and Clinical Immunology Unit, Attikon University Hospital, National and Kapodistrian University of Athens, School of Medicine, Athens, Greece.ORCID 0000-0002-5423-5847
Maria PappaRheumatology and Clinical Immunology Unit, Attikon University Hospital, National and Kapodistrian University of Athens, School of Medicine, Athens, Greece.ORCID 0000-0003-1296-0693
Marija BakulaDivision of Clinical Immunology and Rheumatology, Croatian Referral Centre for SLE and Related Diseases, Department of Internal Medicine, University Hospital Centre Zagreb, University of Zagreb, School of Medicine, Zagreb, Croatia.
Ivan PadjenDivision of Clinical Immunology and Rheumatology, Croatian Referral Centre for SLE and Related Diseases, Department of Internal Medicine, University Hospital Centre Zagreb, University of Zagreb, School of Medicine, Zagreb, Croatia.
Myrto NikoloudakiRheumatology, Clinical Immunology and Allergy Department, University Hospital of Heraklion, University of Crete, School of Medicine, Heraklion, Greece.
Pinelopi KonstantopoulouDepartment of Rheumatology, "G. Gennimatas" General Hospital, Athens, Greece.
George MoustakasDepartment of Nephrology, "G. Gennimatas" General Hospital, Athens, Greece.
Dimitrios VassilopoulosClinical Immunology- Rheumatology Unit, 2nd Department of Medicine and Laboratory, General Hospital of Athens Hippokration, National and Kapodistrian University of Athens, School of Medicine, Athens, Greece.
George BertsiasRheumatology, Clinical Immunology and Allergy Department, University Hospital of Heraklion, University of Crete, School of Medicine, Heraklion, Greece.ORCID 0000-0001-5299-1406
Paraskevi V VoulgariDepartment of Rheumatology, University of Ioannina, Faculty of Medicine, Ioannina, Greece.
Dimitrios T BoumpasRheumatology and Clinical Immunology Unit, Attikon University Hospital, National and Kapodistrian University of Athens, School of Medicine, Athens, Greece.ORCID 0000-0002-9812-4671
Antonis FanouriakisRheumatology and Clinical Immunology Unit, Attikon University Hospital, National and Kapodistrian University of Athens, School of Medicine, Athens, Greece afanour@med.uoa.gr.ORCID 0000-0003-2696-031X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesLupus Low Disease Activity State (LLDAS) and Definition of Remission in SLE (DORIS) are associated with improved outcomes in SLE; however, their value in lupus nephritis (LN) remains unexplored. We sought to evaluate their prognostic value on organ damage accrual, renal flares and chronic kidney disease in patients with LN.

methodsMulticentre retrospective cohort study of patients with biopsy-proven LN who achieved renal response. Enrolment date was the time of first renal response. Longitudinal data were analysed using Cox proportional hazards models. Modified LLDAS (mLLDAS) and DORIS (mDORIS) attainment and sustained durations were evaluated.

results155 patients with 1703 visits were included. During a median follow-up of 3.5 years (IQR 4.5), 127 patients (81.9%) achieved mLLDAS and 92 (59.4%) achieved mDORIS. Both states demonstrated robust protective effects across all outcomes. For organ damage, mLLDAS attainment was associated with 85% risk reduction (adjusted HR (aHR 0.15, 95% CI 0.07 to 0.32), while mDORIS conferred a 79% reduction (aHR 0.21, 95% CI 0.08 to 0.55). Periods under mLLDAS were also associated with a 73% reduction in renal flare risk (aHR 0.27, 95% CI 0.14 to 0.51), with similar effects for mDORIS. Sustained achievement resulted in progressively greater protection, with the strongest effects seen for ≥24 consecutive months. Early attainment protected against damage accrual (aHR 0.31, 95% CI 0.16 to 0.61) and renal flares (aHR 0.51, 95% CI 0.29 to 1.00).

conclusionsFollowing renal response, achievement of mLLDAS and mDORIS is strongly associated with improved outcomes in LN patients. Earlier attainment and longer duration in these states confer progressively greater protection.

Indexed as

Lupus NephritisAdultDisease ProgressionFemaleHumansKidneyMaleMiddle AgedPrognosisProportional Hazards ModelsRemission InductionRenal Insufficiency, ChronicRetrospective StudiesSeverity of Illness IndexLupus Erythematosus, SystemicLupus NephritisOutcome Assessment, Health Care

Identifiers

PMID42203250
PMCPMC13218096

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