Evidence map›Paper›PMID 40256631›Full record

ArticleRheumatology advances in practice2025

Predicting EQ-5D full health state in systemic lupus erythematosus using machine learning algorithms.

João Botto, Nursen Cetrez, Dionysis Nikolopoulos, Malin Regardt, Emelie Heintz, Julius Lindblom, Ioannis Parodis

2 registry-linked trialsAbstract read
In one paragraph

Article in Rheumatology advances in practice, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are 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.

NCT00410384 phase3completednot on this map

A Phase 3, Multi-Center, Randomized, Double-Blind, Placebo-Controlled, 76-Week Study to Evaluate the Efficacy and Safety of Belimumab (HGS1006, LymphoStat-B™), a Fully Human Monoclonal Anti-BLyS Antibody, in Subjects With Systemic Lupus Erythematosus (SLE)

TypeinterventionalSponsorHuman Genome Sciences Inc.Ran2006 to 2010Enrolled819ConditionsSystemic Lupus ErythematosusArmsPlacebo, Belimumab 1 mg/kg, Belimumab 10 mg/kg
NCT00424476 phase3completednot on this map

A Phase 3, Multi-Center, Randomized, Double-Blind, Placebo-Controlled, 52-Wk Study to Evaluate the Efficacy and Safety of Belimumab (HGS1006, LymphoStat-B™), a Fully Human Monoclonal Anti-BLyS Antibody, in Subjects With Systemic Lupus Erythematosus (SLE)

TypeinterventionalSponsorHuman Genome Sciences Inc.Ran2007 to 2010Enrolled865ConditionsSystemic Lupus ErythematosusArmsPlacebo, Belimumab 1 mg/kg, Belimumab 10 mg/kg
3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Lessons Learnt from the Belimumab Trials in Systemic Lupus Erythematosus.International journal of molecular sciences · 2025
    Review
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

7 authors.

João BottoDivision of Rheumatology, Department of Medicine Solna, Karolinska Institutet, Stockholm, Sweden.
Nursen CetrezDivision of Rheumatology, Department of Medicine Solna, Karolinska Institutet, Stockholm, Sweden.
Dionysis NikolopoulosDivision of Rheumatology, Department of Medicine Solna, Karolinska Institutet, Stockholm, Sweden.
Malin RegardtDepartment of Neurobiology, Care Sciences and Society, Division of Occupational Therapy, Karolinska Institutet, Stockholm, Sweden.
Emelie HeintzDepartment of Learning, Informatics, Management and Ethics (LIME), Karolinska Institutet, Stockholm, Sweden.
Julius LindblomDivision of Rheumatology, Department of Medicine Solna, Karolinska Institutet, Stockholm, Sweden.ORCID https://orcid.org/0000-0003-1582-9471
Ioannis ParodisDivision of Rheumatology, Department of Medicine Solna, Karolinska Institutet, Stockholm, Sweden.ORCID https://orcid.org/0000-0002-4875-5395

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: To determine factors associated with reports of EuroQol 5-Dimensions (EQ-5D) full health state (FHS) before and after a trial intervention in patients with SLE, resorting to machine learning algorithms. Methods: We conducted a post hoc analysis of two phase 3 clinical trials of belimumab (BLISS-52, BLISS-76). Demographic, laboratory and clinical features were retrieved and the Monte Carlo Feature Selection algorithm was employed, then further refined upon consideration of collinearity and clinical relevance. We used support vector machine with radial basis function kernel (SVMRadial), least absolute shrinkage and selection operator (LASSO), neural network (NNet) and logistic regression (LR) to capture both linear and non-linear relationships while ensuring interpretability and robustness. Results: Among 1642 SLE patients, 12.9% reported FHS at baseline and 23.1% at week 52. Selected features were age, sex, Asian ancestry, baseline cSLEDAI-2K, SELENA-SLEDAI PGA, and urine protein:creatinine ratio (UPCR) and baseline EQ-5D 3-Levels (EQ-5D-3L) index score (week 52 models only). The models predicting FHS demonstrated comparable performance at baseline and week 52. A maximum area under the curve of 0.73 was seen for the baseline LASSO and LR models and a maximum of 0.77 for the week 52 LASSO and NNet models. Negative predictive values were high for all models (0.88-0.94). Calibration showed marginal improvement in week 52 models. Conclusion: Machine learning identified older age, female sex, non-Asian ancestry, high disease activity and low UPCR to be associated with a lack of FHS experience in SLE patients at baseline and week 52. High baseline EQ-5D-3L index scores constituted the strongest predictor of FHS at week 52. Trial registration: The BLISS-52 and BLISS-76 trials are registered at www.clinicaltrials.gov (NCT00424476 and NCT00410384, respectively).

Indexed as

EQ-5Dmachine learningpatient-reported outcomesquality of lifesystemic lupus erythematosus

Identifiers

PMID40256631
PMCPMC12007597

What OpenQuestion holds

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LicenceCC BY
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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.