Evidence map›Paper›PMID 27102765›Full record

ArticleClinical immunology (Orlando, Fla.)2016

IgM antibodies against malondialdehyde and phosphorylcholine are together strong protection markers for atherosclerosis in systemic lupus erythematosus: Regulation and underlying mechanisms.

Mizanur Rahman, Sudhir Sing, Zahra Golabkesh, Roland Fiskesund, Thomas Gustafsson, Tomas Jogestrand, Anna G Frostegård, Ingiäld Hafström, Anquan Liu, Johan Frostegård

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Article in Clinical immunology (Orlando, Fla.), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
4.2field-weighted citation impact, top 6% 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

43 citing papers in PubMed, 74 citations in OpenAlex.

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  18. Cardiovascular disease in systemic lupus erythematosus.Rheumatology and immunology research · 2021
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 1 country.

Mizanur RahmanIMM, Unit of Immunology and Chronic Disease, Karolinska Institutet, 171 65 Stockholm, Sweden.
Sudhir SingIMM, Unit of Immunology and Chronic Disease, Karolinska Institutet, 171 65 Stockholm, Sweden.
Zahra GolabkeshIMM, Unit of Immunology and Chronic Disease, Karolinska Institutet, 171 65 Stockholm, Sweden.
Roland FiskesundIMM, Unit of Immunology and Chronic Disease, Karolinska Institutet, 171 65 Stockholm, Sweden.
Thomas GustafssonDepartment of Laboratory Medicine, Division of Clinical Physiology, Karolinska Institutet at Karolinska University Hospital, Huddinge, 141 86 Stockholm, Sweden.
Tomas JogestrandDepartment of Laboratory Medicine, Division of Clinical Physiology, Karolinska Institutet at Karolinska University Hospital, Huddinge, 141 86 Stockholm, Sweden.
Anna G FrostegårdIMM, Unit of Immunology and Chronic Disease, Karolinska Institutet, 171 65 Stockholm, Sweden.
Ingiäld HafströmDepartment of Rheumatology, Karolinska Institutet at Karolinska University Hospital, Huddinge, 141 86 Stockholm, Sweden.
Anquan LiuIMM, Unit of Immunology and Chronic Disease, Karolinska Institutet, 171 65 Stockholm, Sweden.
Johan FrostegårdIMM, Unit of Immunology and Chronic Disease, Karolinska Institutet, 171 65 Stockholm, Sweden. Electronic address: johan.frostegard@ki.se.
Karolinska Institutet · SEKarolinska University Hospital · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesPhosphorylcholine (PC) and malondialdehyde (MDA) are generated during lipid peroxidation and form adducts with proteins as albumin as studied herein. Atherosclerosis and cardiovascular disease (CVD) are increased in systemic lupus erythematosus (SLE). We here investigate the role and regulation of IgM antibodies against PC (anti-PC) and MDA (anti-MDA).

methodsIgM anti-PC and anti-MDA in SLE patients (n=114) were compared with age- and sex-matched population-based controls (n=108). Common carotid intima-media thickness (IMT) and plaque occurrence were determined by B-mode ultrasound. Plaques were graded according to echogenicity (potentially vulnerability). Production of IgM anti-PC and anti-MDA by B cells was determined by ELISA and ELISPOT. The effect of anti-PC and anti-MDA on macrophage uptake of apoptotic cells and oxidative stress was studied by flow cytometry.

resultsAbove 66rd percentile together, IgM anti-PC and anti-MDA were striking protection markers for plaque prevalence and echolucency in SLE (OR: 0.08, CI: 0.01-0.46 and OR: 0.10, CI: 0.01-0.82), respectively, and risk markers for plaque prevalence when below 33rd percentile: OR: 3.79, CI: (1.10-13.00). In vitro, IgM anti-PC and anti-MDA were much higher when B cells were co-cultured with CD3 T cells. Anti-HLA-, anti-CD40 antibody or CD40 silencing abolished these effects. Uptake of apoptotic cells was increased by IgM anti-PC and anti-MDA. MDA induced increased oxidative stress, which was inhibited by IgM anti-MDA.

conclusionsUnexpectedly, both IgM anti-MDA and IgM anti-PC are T-cell dependent and especially together, are strong protection markers for atherosclerosis in SLE. Underlying mechanisms include increased phagocytosis of apoptotic cells and decrease of oxidative stress.

Indexed as

AdultApoptosisAtherosclerosisBiomarkersB-LymphocytesCarotid Intima-Media ThicknessCD3 ComplexCells, CulturedCoculture TechniquesEnzyme-Linked Immunosorbent AssayEnzyme-Linked Immunospot AssayFemaleHumansImmunoglobulin MJurkat CellsLupus Erythematosus, SystemicBiomarkersCD3 ComplexImmunoglobulin MMalondialdehydePhosphorylcholineAntibodiesAtherosclerosisMalondialdehydePhosphorylcholineSystemic lupus erythematosusT-cellsVulnerable plaque

Identifiers

PMID27102765
OpenAlexW2340112205

What OpenQuestion holds

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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.