Evidence map›Paper›PMID 24955287›Full record

ArticleJournal of clinical & cellular immunology2014

Autoantibodies against C1q as a Diagnostic Measure of Lupus Nephritis: Systematic Review and Meta-analysis.

Paul Eggleton, Obioha C Ukoumunne, Isabel Cottrell, Asma Khan, Sidra Maqsood, Jemma Thornes, Elizabeth Perry, David Isenberg

Open access · greenAbstract read
In one paragraph

Article in Journal of clinical & cellular immunology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.1field-weighted citation impact, top 9% of its field
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

15 citing papers in PubMed, 27 citations in OpenAlex.

  1. Review
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  7. Anti-Idiotype scFv Localizes an Autoepitope in the Globular Domain of C1q.International journal of molecular sciences · 2021
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  15. Pediatric lupus nephritis.Jornal brasileiro de nefrologia
    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

8 authors at 1 institution in 1 country.

Paul EggletonInstitute of Biomedical and Clinical Sciences, University of Exeter Medical School, University of Exeter, Exeter, UK.
Obioha C UkoumunneNIHR CLAHRC South West Peninsula (PenCLAHRC),University of Exeter Medical School, University of Exeter, Exeter, UK.
Isabel CottrellInstitute of Biomedical and Clinical Sciences, University of Exeter Medical School, University of Exeter, Exeter, UK.
Asma KhanInstitute of Biomedical and Clinical Sciences, University of Exeter Medical School, University of Exeter, Exeter, UK.
Sidra MaqsoodInstitute of Biomedical and Clinical Sciences, University of Exeter Medical School, University of Exeter, Exeter, UK.
Jemma ThornesInstitute of Biomedical and Clinical Sciences, University of Exeter Medical School, University of Exeter, Exeter, UK.
Elizabeth PerryInstitute of Biomedical and Clinical Sciences, University of Exeter Medical School, University of Exeter, Exeter, UK.
David IsenbergCentre for Rheumatology, Department of Medicine University College London, UK.
University College London · GB

Funding

Arthritis Research UK 19894
6 · The paper itself

Abstract

objectivesTo evaluate the diagnostic accuracy of C1q autoantibodies in identifying lupus nephritis (LN) in patients with systemic lupus erythematosus (SLE). DATA SOURCES AND

methodsCitation indexes were searched and 370 articles published from 1977 to 2013 were evaluated. The 31 selected studies included in the meta-analysis were cross-sectional in design. Among the 31 studies, 28 compared anti-C1q antibodies in 2769 SLE patients with (n=1442) and without a history of LN (n=1327). Nine studies examined anti-C1q in 517 SLE patients with active (n=249) and inactive LN (n=268). Hierarchical summary receiver operating characteristic (HSROC) random effects models were fitted to pool estimates of accuracy across the studies.

resultsAnti-C1q antibodies discriminated between patients with and without a history of LN, with a median specificity of 73.5%. The HSROC model estimated the corresponding sensitivity to be 70.4%. A hypothetical patient with a 55% prior probability of having a history of LN as opposed to no history (the median prevalence across 28 eligible studies) would have a post-test probability of 76.4% following a positive test result (positive predictive value) or 33.0% following a negative test result (negative predictive value). For discriminating active from inactive LN the median specificity of anti-C1q antibodies was 80%, with a corresponding estimated sensitivity value 75.7% based on the HSROC model. A hypothetical patient with a 56% prior probability of active as opposed to inactive LN (the median prevalence across the 9 eligible studies) would have a post-test probability of 82.8% following a positive test result or 27.9% following a negative test result.

conclusionsAlthough C1q antibodies are associated with lupus nephritis the post-test probabilities are not sufficiently convincing to provide reasonable certainty of the presence or absence of history of disease/active disease.

Indexed as

AutoantibodyBiopsyDiagnosisEnzyme-linked immunosorbent assay (ELISA)First component of complement (C1q)Hierarchical summary receiver operating characteristic (HSROC)Systemic lupus erythematosus (SLE)

Identifiers

PMID24955287
PMCPMC4062947
OpenAlexW2152804742

What OpenQuestion holds

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LicenceCC BY
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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.