Evidence map›Paper›PMID 38978729›Full record

ArticleBrain communications2024

Potential biomarkers for multiple sclerosis stage from targeted proteomics and microRNA sequencing.

Ineke L Tan, Rutger Modderman, Anna Stachurska, Rodrigo Almeida, Riemer de Vries, Dorothea J Heersema, Ranko Gacesa, Cisca Wijmenga, Iris H Jonkers, Jan F Meilof and 1 more

Abstract read
In one paragraph

Article in Brain communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

8 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. 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

11 authors.

Ineke L TanDepartment of Genetics, University of Groningen, University Medical Center Groningen, 9713 GZ Groningen, The Netherlands.ORCID https://orcid.org/0000-0001-8159-2367
Rutger ModdermanDepartment of Genetics, University of Groningen, University Medical Center Groningen, 9713 GZ Groningen, The Netherlands.
Anna StachurskaDepartment of Genetics, University of Groningen, University Medical Center Groningen, 9713 GZ Groningen, The Netherlands.
Rodrigo AlmeidaTelespazio Belgium S.R.L. for the European Space Agency (ESA), 2200AG Noordwijk, The Netherlands.
Riemer de VriesDepartment of Neurology, University of Groningen, University Medical Center Groningen, 9713 GZ Groningen, The Netherlands.
Dorothea J HeersemaDepartment of Neurology, University of Groningen, University Medical Center Groningen, 9713 GZ Groningen, The Netherlands.
Ranko GacesaDepartment of Genetics, University of Groningen, University Medical Center Groningen, 9713 GZ Groningen, The Netherlands.ORCID https://orcid.org/0000-0003-2119-0539
Cisca WijmengaDepartment of Genetics, University of Groningen, University Medical Center Groningen, 9713 GZ Groningen, The Netherlands.
Iris H JonkersDepartment of Genetics, University of Groningen, University Medical Center Groningen, 9713 GZ Groningen, The Netherlands.
Jan F MeilofMS Center Noord Nederland, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
Sebo WithoffDepartment of Genetics, University of Groningen, University Medical Center Groningen, 9713 GZ Groningen, The Netherlands.ORCID https://orcid.org/0000-0001-7704-3437

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple sclerosis is a chronic demyelinating disease of the central nervous system. There is a need for new circulating biomarkers for multiple sclerosis, in particular, markers that differentiate multiple sclerosis subtypes (relapsing-remitting, secondary progressive and primary progressive multiple sclerosis), as this can help in making treatment decisions. In this study, we explore two classes of potential multiple sclerosis biomarkers-proteins and microRNAs-circulating in the cerebrospinal fluid and serum. Targeted medium-throughput proteomics (92 proteins) and microRNA sequencing were performed on serum samples collected in a cross-sectional case-control cohort (cohort I, controls

Indexed as

biomarkerdisease stagemicroRNA sequencingmultiple sclerosisproteomics

Identifiers

PMID38978729
PMCPMC11229703

What OpenQuestion holds

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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.