Evidence map›Paper›PMID 31839982›Full record

ArticleMultiple sclerosis journal - experimental, translational and clinical

Is multiple sclerosis progression associated with the HLA-DR15 haplotype?

Klarissa Hanja Stürner, Inessa Siembab, Gerhard Schön, Jan-Patrick Stellmann, Nika Heidari, Boris Fehse, Christoph Heesen, Thomas H Eiermann, Roland Martin, Thomas Mc Binder

Open access · goldAbstract read
In one paragraph

Article in Multiple sclerosis journal - experimental, translational and clinical. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

11 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
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  9. A review of possible therapies for multiple sclerosis.Molecular and cellular biochemistry · 2021
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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

10 authors at 1 institution in 2 countries.

Klarissa Hanja StürnerInstitute for Neuroimmunology and Clinical MS Research, University Medical Center Hamburg-Eppendorf, Germany.ORCID https://orcid.org/0000-0003-2199-3315
Inessa SiembabInstitute for Neuroimmunology and Clinical MS Research, University Medical Center Hamburg-Eppendorf, Germany.
Gerhard SchönDepartment of Medical Biometry and Epidemiology, University Medical Center Hamburg-Eppendorf, Germany.
Jan-Patrick StellmannInstitute for Neuroimmunology and Clinical MS Research, University Medical Center Hamburg-Eppendorf, Germany.
Nika HeidariInstitute for Neuroimmunology and Clinical MS Research, University Medical Center Hamburg-Eppendorf, Germany.
Boris FehseResearch Department Cell and Gene Therapy, University Medical Center Hamburg-Eppendorf, Germany.
Christoph HeesenInstitute for Neuroimmunology and Clinical MS Research, University Medical Center Hamburg-Eppendorf, Germany.ORCID https://orcid.org/0000-0001-8131-9467
Thomas H EiermannHLA Laboratory, University Medical Center Hamburg-Eppendorf, Germany.ORCID https://orcid.org/0000-0002-5193-0297
Roland MartinInstitute for Neuroimmunology and Clinical MS Research, University Medical Center Hamburg-Eppendorf, Germany.
Thomas Mc BinderHLA Laboratory, University Medical Center Hamburg-Eppendorf, Germany.
Universität Hamburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe prevalence of multiple sclerosis is associated with the major histocompatibility complex class II DR15 haplotype HLA-DRB1*15:01∼HLA-DRB5*01:01.

objectiveTo assess whether multiple sclerosis progression is associated with the main susceptibility haplotype HLA-DRB1*15:01∼HLA-DRB5*01:01.

methodsPatients (

resultsAfter follow-up of the consecutive cohort 349 patients were classified as having clinical isolated syndrome and 881 patients as having multiple sclerosis. The susceptibility allele HLA-DRB1*15:01 was more frequent in clinical isolated syndrome (odds ratio 1.56) and multiple sclerosis (odds ratio 3.17) compared to controls. HLA- DRB1*15:01 was the only enriched HLA-DRB1 allele in multiple sclerosis patients. Comparison of clinical characteristics between HLA-DRB1*15:01∼HLA-DRB5*01:01 negative and positive patients with multiple sclerosis showed that baseline EDSS score, disease duration and frequency of the category secondary progressive multiple sclerosis with relapse were increased in the HLA-DRB1*15:01∼HLA-DRB5*01:01 positive group.

conclusionThe study confirmed HLA-DRB1*15:01 and HLA-DRB5*01:01 as the main susceptibility alleles and showed weak indirect evidence for a role in progression of the disease.

Indexed as

EDSSHLA-DRB1*15:01HLA-DRB5*01:01Multiple sclerosisprogression

Identifiers

PMID31839982
PMCPMC6902395
OpenAlexW2994012519

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.