Evidence map›Paper›PMID 26402865›Full record

ArticlePloS one2015

Elevated Concentrations of Serum Immunoglobulin Free Light Chains in Systemic Lupus Erythematosus Patients in Relation to Disease Activity, Inflammatory Status, B Cell Activity and Epstein-Barr Virus Antibodies.

Anette H Draborg, Magnus C Lydolph, Marie Westergaard, Severin Olesen Larsen, Christoffer T Nielsen, Karen Duus, Søren Jacobsen, Gunnar Houen

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
3.8field-weighted citation impact, top 7% 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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 39 citations in OpenAlex.

  1. Pooled it
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  4. Free Light ChainsInternational journal of molecular sciences · 2023
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

Anette H DraborgDepartment of Autoimmunology and Biomarkers, Statens Serum Institut, Copenhagen, Denmark.
Magnus C LydolphDepartment of Autoimmunology and Biomarkers, Statens Serum Institut, Copenhagen, Denmark.
Marie WestergaardDepartment of Autoimmunology and Biomarkers, Statens Serum Institut, Copenhagen, Denmark.
Severin Olesen LarsenDepartment of Autoimmunology and Biomarkers, Statens Serum Institut, Copenhagen, Denmark.
Christoffer T NielsenDepartment of Autoimmunology and Biomarkers, Statens Serum Institut, Copenhagen, Denmark; Department of Infectious Diseases and Rheumatology, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.
Karen DuusDepartment of Autoimmunology and Biomarkers, Statens Serum Institut, Copenhagen, Denmark.
Søren JacobsenDepartment of Infectious Diseases and Rheumatology, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.
Gunnar HouenDepartment of Autoimmunology and Biomarkers, Statens Serum Institut, Copenhagen, Denmark.
Statens Serum Institut · DKRigshospitalet · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveIn this study, we examined the concentration of serum immunoglobulin free light chains (FLCs) in systemic lupus erythematosus (SLE) patients and investigated its association with various disease parameters in order to evaluate the role of FLCs as a potential biomarker in SLE. Furthermore, FLCs' association with Epstein-Barr virus (EBV) antibodies was examined.

methodsUsing a nephelometric assay, κFLC and λFLC concentrations were quantified in sera from 45 SLE patients and 40 healthy controls. SLE patients with renal insufficiency were excluded in order to preclude high concentrations of serum FLCs due to decreased clearance.

resultsSerum FLC concentrations were significantly elevated in SLE patients compared to healthy controls (p<0.0001) also after adjusting for Ig levels (p<0.0001). The concentration of serum FLCs correlated with a global disease activity (SLE disease activity index (SLEDAI)) score of the SLE patients (r = 0.399, p = 0.007). Furthermore, concentrations of FLCs correlated with titers of dsDNA antibodies (r = 0.383, p = 0.009), and FLC levels and SLEDAI scores correlated in the anti-dsDNA-positive SLE patients, but not in anti-dsDNA-negative SLE patients. Total immunoglobulin (IgG and IgA) concentrations correlated with FLC concentrations and elevated FLC levels were additionally shown to associate with the inflammatory marker C-reactive protein and also with complement consumption determined by low C4 in SLE patients. Collectively, results indicated that elevated serum FLCs reflects increased B cell activity in relation to inflammation. SLE patients had an increased seropositivity of EBV-directed antibodies that did not associate with elevated FLC concentrations. An explanation for this could be that serum FLC concentrations reflect the current EBV activity (reactivation) whereas EBV-directed antibodies reflect the extent of previous infection/reactivations.

conclusionSLE patients have elevated concentrations of serum FLCs that correlate with global disease activity scores and especially serologic markers for active disease. These findings are suggestive of circulating FLCs having potential as a new supplementary serologic biomarker in SLE.

Indexed as

AdultAgedAntibodies, AntinuclearAntibodies, ViralAutoantibodiesBiomarkersB-LymphocytesCase-Control StudiesComplement System ProteinsC-Reactive ProteinFemaleHerpesvirus 4, HumanHumansImmunoglobulin Light ChainsInflammationLupus Erythematosus, SystemicAntibodies, AntinuclearAntibodies, ViralAutoantibodiesBiomarkersComplement System ProteinsC-Reactive ProteinImmunoglobulin Light Chains

Identifiers

PMID26402865
PMCPMC4581754
OpenAlexW2181155886

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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.