Evidence map›Paper›PMID 37628757›Full record

ArticleInternational journal of molecular sciences2023

DNA Methylation Signatures of Multiple Sclerosis Occur Independently of Known Genetic Risk and Are Primarily Attributed to B Cells and Monocytes.

Alexandre Xavier, Vicki E Maltby, Ewoud Ewing, Maria Pia Campagna, Sean M Burnard, Jesper N Tegner, Mark Slee, Helmut Butzkueven, Ingrid Kockum, Lara Kular and 10 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

14 citing papers in PubMed, 12 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

20 authors at 9 institutions in 3 countries.

Alexandre XavierSchool of Biomedical Sciences and Pharmacy, Hunter Medical Research Institute, University of Newcastle, New Lambton Heights, NSW 2305, Australia.ORCID 0000-0002-6397-051X
Vicki E MaltbySchool of Medicine and Public Health, Hunter Medical Research Institute, University of Newcastle, New Lambton Heights, NSW 2305, Australia.
Ewoud EwingDepartment of Clinical Neuroscience, Karolinska Institutet, Center for Molecular Medicine, Karolinska University Hospital, 17176 Stockholm, Sweden.ORCID 0000-0001-8644-366X
Maria Pia CampagnaDepartment of Neuroscience, Central Clinical School, Monash University, Melbourne, VIC 3004, Australia.ORCID 0000-0001-8148-8228
Sean M BurnardSchool of Biomedical Sciences and Pharmacy, Hunter Medical Research Institute, University of Newcastle, New Lambton Heights, NSW 2305, Australia.ORCID 0000-0003-2149-3556
Jesper N TegnerBiological and Environmental Science and Engineering Division, King Abdullah University of Science and Technology (KAUST), Thuwal 23955-6900, Saudi Arabia.
Mark SleeCollege of Medicine and Public Health, Flinders University, Bedford Park, SA 5042, Australia.ORCID 0000-0003-4323-2453
Helmut ButzkuevenDepartment of Neuroscience, Central Clinical School, Monash University, Melbourne, VIC 3004, Australia.ORCID 0000-0003-3940-8727
Ingrid KockumDepartment of Clinical Neuroscience, Karolinska Institutet, Center for Molecular Medicine, Karolinska University Hospital, 17176 Stockholm, Sweden.
Lara KularDepartment of Clinical Neuroscience, Karolinska Institutet, Center for Molecular Medicine, Karolinska University Hospital, 17176 Stockholm, Sweden.ORCID 0000-0002-2907-6071
Ausimmune/AusLong Investigators Group
Vilija G JokubaitisDepartment of Neuroscience, Central Clinical School, Monash University, Melbourne, VIC 3004, Australia.ORCID 0000-0002-3942-4340
Trevor KilpatrickFlorey Institute of Neuroscience and Mental Health, The University of Melbourne, Melbourne, VIC 3052, Australia.
Lars AlfredssonDepartment of Clinical Neuroscience, Karolinska Institutet, Center for Molecular Medicine, Karolinska University Hospital, 17176 Stockholm, Sweden.ORCID 0000-0003-1688-6697
Maja JagodicDepartment of Clinical Neuroscience, Karolinska Institutet, Center for Molecular Medicine, Karolinska University Hospital, 17176 Stockholm, Sweden.
Anne-Louise PonsonbyFlorey Institute of Neuroscience and Mental Health, The University of Melbourne, Melbourne, VIC 3052, Australia.ORCID 0000-0002-6581-3657
Bruce V TaylorMenzies Institute for Medical Research, University of Tasmania, Hobart, TAS 7000, Australia.ORCID 0000-0003-2807-0070
Rodney J ScottSchool of Biomedical Sciences and Pharmacy, Hunter Medical Research Institute, University of Newcastle, New Lambton Heights, NSW 2305, Australia.ORCID 0000-0001-7724-3404
Rodney A LeaSchool of Medicine and Public Health, Hunter Medical Research Institute, University of Newcastle, New Lambton Heights, NSW 2305, Australia.
Jeannette Lechner-ScottSchool of Medicine and Public Health, Hunter Medical Research Institute, University of Newcastle, New Lambton Heights, NSW 2305, Australia.
Karolinska University Hospital · SEMonash University · AUAustralian National University · AUHunter Medical Research Institute · AUJohn Hunter Hospital · AUQueensland University of Technology · AUFlinders University · AUThe University of Melbourne · AUUniversity of Tasmania · AU

Funding

MS Australia 18-0424National Health and Medical Research Council APP1127819National Multiple Sclerosis Society RG-1803-30499
6 · The paper itself

Abstract

Epigenetic mechanisms can regulate how DNA is expressed independently of sequence and are known to be associated with various diseases. Among those epigenetic mechanisms, DNA methylation (DNAm) is influenced by genotype and the environment, making it an important molecular interface for studying disease etiology and progression. In this study, we examined the whole blood DNA methylation profiles of a large group of people with (pw) multiple sclerosis (MS) compared to those of controls. We reveal that methylation differences in pwMS occur independently of known genetic risk loci and show that they more strongly differentiate disease (AUC = 0.85, 95% CI 0.82-0.89,

Indexed as

MonocytesMultiple SclerosisB-LymphocytesDNA MethylationEpigenesis, GeneticHumanscell deconvolutionepigeneticsepigenome-wide association studiesgenetic riskmethylationmultiple sclerosis

Identifiers

PMID37628757
PMCPMC10454485
OpenAlexW4385665872

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.