Data for: Proteomics reveal biomarkers for diagnosis, disease activity and long-term disability outcomes in multiple sclerosis

SND-ID: 2024-400. Version: 1. DOI: https://doi.org/10.48360/jcps-gw67

Associated documentation

Citation

Creator/Principal investigator(s)

Mika Gustafsson - Linköping University

Jan Ernerudh - Linköping University orcid

Tomas Olsson - Karoinska Institute orcid

Research principal

Linköping University rorId

Description

Protein levels were measured in cerebrospinal fluid samples (CSF; n = 186) and plasma samples (n = 165) from persons with multiple sclerosis and healthy controls. CSF samples and plasma samples were taken from 92 persons with CIS or RRMS at Linköping University Hospital, Sweden and 51 persons with CIS or RRMS at the Karolinska University Hospital, Sweden. Everyone fulfilled the revised McDonald criteria from 2010 and 2017 for CIS or Multiple sclerosis (MS). Age-matched healthy controls (HC) were recruited from healthy blood donors (23 at the Linköping University hospital and 20 at the Karolinska University Hospital). The concentration of 1463 proteins were measured using the Olink Explore platform which uses Proximity Extension Assay (PEA) technology. The proteins were preselected from four Olink panels: Explore 384 Cardiometabolic, Explore 384 Inflammation, Explore 384 Neurology, and Explore 384 Oncology. The protein concentrations are given as Olink’s relative protein quantification unit on log2 scale: Normalized Protein Expression (NPX). The NPX values were intensity normalized by Olink.

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Protein levels were measured in cerebrospinal fluid samples (CSF; n = 186) and plasma samples (n = 165) from persons with multiple sclerosis and healthy controls. CSF samples and plasma samples were taken from 92 persons with CIS or RRMS at Linköping University Hospital, Sweden and 51 persons with CIS or RRMS at the Karolinska University Hospital, Sweden. Everyone fulfilled the revised McDonald criteria from 2010 and 2017 for CIS or Multiple sclerosis (MS). Age-matched healthy controls (HC) were recruited from healthy blood donors (23 at the Linköping University hospital and 20 at the Karolinska University Hospital). The concentration of 1463 proteins were measured using the Olink Explore platform which uses Proximity Extension Assay (PEA) technology. The proteins were preselected from four Olink panels: Explore 384 Cardiometabolic, Explore 384 Inflammation, Explore 384 Neurology, and Explore 384 Oncology. The protein concentrations are given as Olink’s relative protein quantification unit on log2 scale: Normalized Protein Expression (NPX). The NPX values were intensity normalized by Olink.

Raw data: supplementary information to publication

For access to dataset, please contact mika.gustafsson@liu.se for further information.

Research funders:
Swedish Foundation for Strategic Research (SB16-0011)
Swedish Brain Foundation
Knut and Alice Wallenberg Foundation
Margareth AF Ugglas Foundation
Swedish Research Council (2019-04193, 2018-02776, 2020-02700, 2021-03092)
Swedish Knowledge Foundation (2020-0014)
Medical Research Council of Southeast Sweden (FORSS-315121)
NEURO Sweden (F2018-0052)
ALF grants
Region Östergötland
Swedish Foundation for MS Research
European Union's Marie Sklodowska-Curie (813863)

The dataset was originally published in DiVA and moved to SND in 2024. Show less..

Data contains personal data

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Language

Method and outcome

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Data collection
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Topic and keywords

Research area

Bioinformatics (computational biology) (Standard för svensk indelning av forskningsämnen 2011)

Bioinformatics and systems biology (Standard för svensk indelning av forskningsämnen 2011)

Neurology (Standard för svensk indelning av forskningsämnen 2011)

Rheumatology and autoimmunity (Standard för svensk indelning av forskningsämnen 2011)

Publications

Åkesson, J., Hojjati, S., Hellberg, S., Raffetseder, J., Khademi, M., Rynkowski, R., … Gustafsson, M. (2023). Proteomics reveal biomarkers for diagnosis, disease activity and long-term disability outcomes in multiple sclerosis. Nature Communications, 14(1). https://doi.org/10.1038/s41467-023-42682-9

If you have published anything based on these data, please notify us with a reference to your publication(s). If you are responsible for the catalogue entry, you can update the metadata/data description in DORIS.

Versions

Version 1. 2024-08-29

Version 1: 2024-08-29

DOI: https://doi.org/10.48360/jcps-gw67

Contact for questions about the data

Mika Gustafsson

mika.gustafsson@liu.se

This resource has the following relations

Published: 2024-08-29