Evidence map›Paper›PMID 18050213›Full record

ArticleArthritis and rheumatism2007

British Isles Lupus Assessment Group 2004 index is valid for assessment of disease activity in systemic lupus erythematosus.

Chee-Seng Yee, Vernon Farewell, David A Isenberg, Anisur Rahman, Lee-Suan Teh, Bridget Griffiths, Ian N Bruce, Yasmeen Ahmad, Athiveeraramapandian Prabu, Mohammed Akil and 5 more

Abstract readMulticenter StudyValidation Study
In one paragraph

Article in Arthritis and rheumatism, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed, 1 pooled it
–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.

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

43 citing papers in PubMed, 1 synthesis or guideline pooled it.

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  6. [What is proven in the treatment of systemic lupus erythematosus?]Innere Medizin (Heidelberg, Germany) · 2023
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  7. Lupus clinical trials and the promise of future therapies.Rheumatology and immunology research · 2023
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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

15 authors.

Chee-Seng YeeDepartment of Rheumatology, Division of Infection and Immunity, Medical School, University of Birmingham, Birmingham, UK. csyee@blueyonder.co.uk
Vernon Farewell
David A Isenberg
Anisur Rahman
Lee-Suan Teh
Bridget Griffiths
Ian N Bruce
Yasmeen Ahmad
Athiveeraramapandian Prabu
Mohammed Akil
Neil McHugh
David D'Cruz
Munther A Khamashta
Peter Maddison
Caroline Gordon

Funding

Medical Research Council MC_U105261167Wellcome Trust
6 · The paper itself

Abstract

objectiveTo determine the construct and criterion validity of the British Isles Lupus Assessment Group 2004 (BILAG-2004) index for assessing disease activity in systemic lupus erythematosus (SLE).

methodsPatients with SLE were recruited into a multicenter cross-sectional study. Data on SLE disease activity (scores on the BILAG-2004 index, Classic BILAG index, and Systemic Lupus Erythematosus Disease Activity Index 2000 [SLEDAI-2K]), investigations, and therapy were collected. Overall BILAG-2004 and overall Classic BILAG scores were determined by the highest score achieved in any of the individual systems in the respective index. Erythrocyte sedimentation rates (ESRs), C3 levels, C4 levels, anti-double-stranded DNA (anti-dsDNA) levels, and SLEDAI-2K scores were used in the analysis of construct validity, and increase in therapy was used as the criterion for active disease in the analysis of criterion validity. Statistical analyses were performed using ordinal logistic regression for construct validity and logistic regression for criterion validity. Sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) were calculated.

resultsOf the 369 patients with SLE, 92.7% were women, 59.9% were white, 18.4% were Afro-Caribbean and 18.4% were South Asian. Their mean +/- SD age was 41.6 +/- 13.2 years and mean disease duration was 8.8 +/- 7.7 years. More than 1 assessment was obtained on 88.6% of the patients, and a total of 1,510 assessments were obtained. Increasing overall scores on the BILAG-2004 index were associated with increasing ESRs, decreasing C3 levels, decreasing C4 levels, elevated anti-dsDNA levels, and increasing SLEDAI-2K scores (all P < 0.01). Increase in therapy was observed more frequently in patients with overall BILAG-2004 scores reflecting higher disease activity. Scores indicating active disease (overall BILAG-2004 scores of A and B) were significantly associated with increase in therapy (odds ratio [OR] 19.3, P < 0.01). The BILAG-2004 and Classic BILAG indices had comparable sensitivity, specificity, PPV, and NPV.

conclusionThese findings show that the BILAG-2004 index has construct and criterion validity.

Indexed as

Disability EvaluationSeverity of Illness IndexAdultBlood SedimentationComplement C3Complement C4Cross-Sectional StudiesFemaleHumansLogistic ModelsLupus Erythematosus, SystemicMaleMiddle AgedPredictive Value of TestsSensitivity and SpecificityUnited KingdomComplement C3Complement C4

Identifiers

PMID18050213
PMCPMC2659367

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Registered trials

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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.