Evidence map›Paper›PMID 28516329›Full record

ArticleJournal of neurology2017

Screening for lipoprotein receptor-related protein 4-, agrin-, and titin-antibodies and exploring the autoimmune spectrum in myasthenia gravis.

Isabell Cordts, Nicolas Bodart, Kathi Hartmann, Katerina Karagiorgou, John S Tzartos, Lin Mei, Jens Reimann, Philip Van Damme, Michael H Rivner, Alain Vigneron and 4 more

Abstract read
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In one paragraph

Article in Journal of neurology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
5.1field-weighted citation impact, top 4% 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

22 citing papers in PubMed, 57 citations in OpenAlex.

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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

14 authors at 8 institutions in 4 countries.

Isabell CordtsDepartment of Neurology, RWTH Aachen University, Aachen, Germany.
Nicolas BodartD-Tek, Mons, Belgium.
Kathi HartmannDepartment of Ophthalmology, RWTH Aachen University, Aachen, Germany.
Katerina KaragiorgouHellenic Pasteur Institute, Athens, Greece.
John S TzartosHellenic Pasteur Institute, Athens, Greece.
Lin MeiDepartment of Neuroscience and Regenerative Medicine, Medical College of Georgia, Augusta University, Augusta, GA, USA.
Jens ReimannDepartment of Neurology, University Hospital Bonn, Bonn, Germany.
Philip Van DammeDepartment of Neurology, University Hospitals Leuven, Leuven, Belgium.
Michael H RivnerDepartment of Neurology, Medical College of Georgia, Augusta University, Augusta, GA, USA.
Alain VigneronD-Tek, Mons, Belgium.
Joachim WeisInstitute of Neuropathology, RWTH Aachen University, Aachen, Germany.
Jörg B SchulzDepartment of Neurology, RWTH Aachen University, Aachen, Germany.
Socrates J TzartosHellenic Pasteur Institute, Athens, Greece.
Kristl G ClaeysDepartment of Neurology, RWTH Aachen University, Aachen, Germany. Kristl.Claeys@uzleuven.be.
Pasteur Hellenic Institute · GRRWTH Aachen University · DEKU Leuven · BEUniversity of Mons · BEAugusta University · USCharlie Norwood VA Medical Center · USJülich Aachen Research Alliance · DEUniversity Hospital Bonn · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In autoimmune myasthenia gravis (MG), the identification of antibodies and characterization of serological subgroups is of great importance for diagnosis and management of the disease. Our aims were to study the frequency of antibodies against lipoprotein-related protein 4 (LRP4), agrin, and titin using the most recent techniques, and to characterize corresponding clinical features and autoimmune diseases (AID) in 100 MG-patients. The antibody frequencies in the 55 AChR-antibody positive patients were 7% LRP4, 5% agrin, 53% titin, and in the 45 AChR-antibody negative patients 2% MuSK, 2% LRP4, 2% agrin, and 27% titin. LRP4-MG presented late-onset age, mild symptoms, good therapeutic response, and no thymic changes. Agrin-MG showed early onset age, mild-to-severe symptoms, and moderate treatment response. The phenotype of titin-MG depended on AChR-antibodies: AChR-antibody negative patients presented with mostly mild limb muscle weakness, whereas AChR-antibody positive patients showed more frequently severe symptoms, including myasthenic crisis, bulbar predominance, and thymoma. Additional AID were detected in 32% of MG-patients, most frequently Hashimoto's thyroiditis (21%). Based on our data, we recommend the detection of LRP4-antibodies for at least AChR-antibody negative MG-patients and titin-antibodies for all MG-patients. We propose taking an accurate medical history for typical symptoms of Hashimoto's thyroiditis in MG-patients.

Indexed as

AdolescentAdultAgedAgrinAutoantibodiesChildConnectinFemaleHumansLDL-Receptor Related ProteinsMaleMiddle AgedMyasthenia GravisRadioimmunoassayReceptor Protein-Tyrosine KinasesReceptors, CholinergicAgrinAutoantibodiesConnectinLDL-Receptor Related ProteinsLRP4 protein, humanMUSK protein, humanReceptor Protein-Tyrosine KinasesReceptors, CholinergicAntibodiesAutoimmune diseasesLRP4SeronegativeThyroidTitin RIPA

Identifiers

PMID28516329
OpenAlexW2615980857

What OpenQuestion holds

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Read underepoch 390

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.