Evidence map›Paper›PMID 42811191›Full record

ArticleRheumatology (Oxford, England)2026

Ability of SLE-DAS and SLEDAI-2K to predict damage accrual in SLE: a real-world 7-year cohort study from Sweden.

Rama Andraos, Alexander Tsoi, Alf Kastbom, Martina Frodlund, Diogo Jesus, Luís Sousa Inês, Ioannis Parodis, Christopher Sjöwall

Abstract read
In one paragraph

Article in Rheumatology (Oxford, England), 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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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Rama AndraosDivision of Inflammation and Infection/Rheumatology, Department of Biomedical and Clinical Sciences, Linköping University, Linköping, Sweden.ORCID 0000-0002-5433-3885
Alexander TsoiDivision of Rheumatology, Department of Medicine Solna, Karolinska Institutet, Karolinska University Hospital, and Center for Molecular Medicine (CMM), Stockholm, Sweden.
Alf KastbomDivision of Inflammation and Infection/Rheumatology, Department of Biomedical and Clinical Sciences, Linköping University, Linköping, Sweden.ORCID 0000-0001-7187-1477
Martina FrodlundDivision of Inflammation and Infection/Rheumatology, Department of Biomedical and Clinical Sciences, Linköping University, Linköping, Sweden.ORCID 0000-0001-7522-5069
Diogo JesusRheumatology Department, ULS Região de Leiria, Leiria, Portugal.ORCID 0000-0003-3136-0722
Luís Sousa InêsFaculty of Health Sciences, University of Beira Interior, Covilhã, Portugal.ORCID 0000-0003-3172-3570
Ioannis ParodisDivision of Rheumatology, Department of Medicine Solna, Karolinska Institutet, Karolinska University Hospital, and Center for Molecular Medicine (CMM), Stockholm, Sweden.ORCID 0000-0002-4875-5395
Christopher SjöwallDivision of Inflammation and Infection/Rheumatology, Department of Biomedical and Clinical Sciences, Linköping University, Linköping, Sweden.ORCID 0000-0003-0900-2048

Funding

Karolinska InstitutetRegion Stockholm FoUI-977096
6 · The paper itself

Abstract

objectivesSLE remains a heterogeneous autoimmune disease that can lead to irreversible organ damage. SLE Disease Activity Score (SLE-DAS) is a recently developed tool with higher sensitivity to change than SLE Disease Activity Index-2000 (SLEDAI-2K). We compared SLE-DAS with other activity measures in terms of ability to predict organ damage.

methodsPatients from Linköping University Hospital with ≥2 visits between 2008 and 2025 were included. SLEDAI-2K and Physician's Global Assessment (PhGA) were assessed prospectively, and SLE-DAS retrospectively. Organ damage was estimated annually using the SLICC/ACR Damage Index (SDI). Adjusted mean scores of SLEDAI-2K (amSLEDAI-2K), PhGA (amPhGA) and SLE-DAS (amSLE-DAS) were determined for each time interval between consecutive visits, and their ability to predict damage accrual was evaluated using time-dependent multivariable Cox regression models. Predictive ability was compared across measures using Akaike Information Criterion (AIC) and Bayesian Information Criterion (BIC).

resultsIn total, 335 patients with 3582 outpatient visits contributed data. amSLE-DAS was an independent predictor of SDI increase at the 3- (HR; 95% CI: 1.04; 1.00-1.08), 5- (1.05; 1.01-1.09) and 7-year follow-up (1.04; 1.00-1.08). amSLEDAI-2K was predictive at the 5-year follow-up only (1.12; 1.02-1.22), and amPhGA at 5 (1.99; 1.19-3.36) and 7 (1.84; 1.02-3.30) years. amSLE-DAS showed a higher predictive ability for damage accrual than amSLEDAI-2K at the 3-, 5- and 7-year follow-up, as indicated by lower AIC and BIC.

conclusionIn this real-world Swedish setting, we demonstrate that SLE-DAS outperforms SLEDAI-2K in predicting organ damage accrual in SLE, substantiating its clinical relevance.

Indexed as

Lupus Erythematosus, SystemicSeverity of Illness IndexAdultCohort StudiesDisease ProgressionFemaleHumansMaleMiddle AgedPredictive Value of TestsRetrospective StudiesSwedendisease activityorgan damageSLEDAI-2KSLE-DASsystemic lupus erythematosus

Identifiers

PMID42811191
PMCPMC13661249

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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.