The DOI matches its Crossref record; 41 of the 41 references it cites were found in a registry or an index.
Multiple sclerosis risk loci and disease severity in 7,125 individuals from 10 studies
Open accessAbstract
OBJECTIVE: We investigated the association between 52 risk variants identified through genome-wide association studies and disease severity in multiple sclerosis (MS). METHODS: Ten unique MS case data sets were analyzed. The Multiple Sclerosis Severity Score (MSSS) was calculated using the Expanded Disability Status Scale at study entry and disease duration. MSSS was considered as a continuous variable and as 2 dichotomous variables (median and extreme ends; MSSS of ≤5 vs >5 and MSSS of <2.5 vs ≥7.5, respectively). Single nucleotide polymorphisms (SNPs) were examined individually and as both combined weighted genetic risk score (wGRS) and unweighted genetic risk score (GRS) for association with disease severity. Random-effects meta-analyses were conducted and adjusted for cohort, sex, age at onset, and HLA-DRB1*15:01. RESULTS: A total of 7,125 MS cases were analyzed. The wGRS and GRS were not strongly associated with disease severity after accounting for cohort, sex, age at onset, and HLA-DRB1*15:01. After restricting analyses to cases with disease duration ≥10 years, associations were null (p value ≥0.05). No SNP was associated with disease severity after adjusting for multiple testing. CONCLUSIONS: The largest meta-analysis of established MS genetic risk variants and disease severity, to date, was performed. Results suggest that the investigated MS genetic risk variants are not associated with MSSS, even after controlling for potential confounders. Further research in large cohorts is needed to identify genetic determinants of disease severity using sensitive clinical and MRI measures, which are critical to understanding disease mechanisms and guiding development of effective treatments.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Although these risk variants have been found to reduce the age at onset5, it is notable that they do not appear to have any impact on disease severity6.”
From Locus for severity implicates CNS resilience in progression of multiple sclerosis (2023) · cites this paper as [6]
Experimental — accuracy not yet measured
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
McDonald, W. I., Compston, A., Edan, G., Goodkin, D., Hartung, H., Lublin, F. D., McFarland, H. F., Paty, D. W., Polman, C. H., Reingold, S. C., et al. (2001) · Annals of Neurology · doi:10.1002/ana.1032 · Cited by 6,969
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis
The International Multiple Sclerosis Genetics Consortium & The Wellcome Trust Case Control Consortium 2 (2011) · Nature · doi:10.1038/nature10251 · Cited by 2,697
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis
International Multiple Sclerosis Genetics Consortium (IMSGC) (2013) · Nature Genetics · doi:10.1038/ng.2770 · Cited by 1,386
Self-citationMultiple Sclerosis Severity Score: Using disability and disease duration to rate disease severity
Roxburgh, R. H. S. R., Seaman, S. R., Masterman, T., Hensiek, A. E., Sawcer, S. J., Vukusic, S., Achiti, I., Confavreux, C., Coustans, M., le Page, E., et al. (2005) · Neurology · doi:10.1212/01.wnl.0000156155.19270.f8 · Cited by 963
Self-citationVitamin D and multiple sclerosis
Ascherio, A., Munger, K. L., & Simon, K. C. (2010) · The Lancet Neurology · doi:10.1016/s1474-4422(10)70086-7 · Cited by 614
Body size and risk of MS in two cohorts of US women
Munger, K. L., Chitnis, T., & Ascherio, A. (2009) · Neurology · doi:10.1212/wnl.0b013e3181c0d6e0 · Cited by 441
Environmental factors in multiple sclerosis
Ascherio, A. (2013) · Expert Review of Neurotherapeutics · doi:10.1586/14737175.2013.865866 · Cited by 331
Tobacco smoking, but not Swedish snuff use, increases the risk of multiple sclerosis
Hedström, A. K., Bäärnhielm, M., Olsson, T. P., & Alfredsson, L. S. (2009) · Neurology · doi:10.1212/wnl.0b013e3181b59c40 · Cited by 323
Self-citationPatsopoulos, N. A., Barcellos, L. F., Hintzen, R. Q., Schaefer, C., van Duijn, C. M., Noble, J. A., Raj, T., IMSGC, ANZgene, Gourraud, P.-A., et al. (2013) · PLoS Genetics · doi:10.1371/journal.pgen.1003926 · Cited by 312
Self-citationHeterogeneity at the HLA-DRB1 locus and risk for multiple sclerosis
Barcellos, L. F., Sawcer, S. J., Ramsay, P. P., Baranzini, S. E., Thomson, G. J., Briggs, F. B. S., Cree, B., Begovich, A. B., Villoslada, P., Montalbán, X., et al. (2006) · Human Molecular Genetics · doi:10.1093/hmg/ddl223 · Cited by 312
Self-citation
Flagged first, then by citations
Cited by
Sorted by citations
Multiple sclerosis genomic map implicates peripheral immune cells and microglia in susceptibility
International Multiple Sclerosis Genetics Consortium, Patsopoulos, N. A., Baranzini, S. E., Santaniello, A., Shoostari, P., Cotsapas, C., Wong, G., Beecham, A. H., James, T., Replogle, J., et al. (2019) · Science · doi:10.1126/science.aav7188 · Cited by 1,471
“Further investigationmay lead to the identification of variants that have an effect on the neurodegenerative component of MS, which is largely genetically distinct from MS susceptibility (41).”
BackgroundSelf-citationEnvironmental and genetic risk factors for MS: an integrated review
Waubant, E. L., Lucas, R. M., Mowry, E. M., Graves, J., Olsson, T. P., Alfredsson, L. S., & Langer-Gould, A. M. (2019) · Annals of Clinical and Translational Neurology · doi:10.1002/acn3.50862 · Cited by 368
Self-citationLocus for severity implicates CNS resilience in progression of multiple sclerosis
International Multiple Sclerosis Genetics Consortium, Harroud, A., Stridh, P., McCauley, J. L., Saarela, J., van den Bosch, A. M. R., Engelenburg, H. J., Beecham, A. H., Alfredsson, L., Alikhani, K., et al. (2023) · Nature · doi:10.1038/s41586-023-06250-x · Cited by 243
Self-citationGenetics of Multiple Sclerosis: An Overview and New DirectionsPreprint
Patsopoulos, N. A. (2018) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a028951 · Cited by 188
Self-citationGenetics of multiple sclerosis: lessons from polygenicity
Goris, A., Vandebergh, M., McCauley, J. L., Saarela, J., & Cotsapas, C. J. (2022) · The Lancet Neurology · doi:10.1016/s1474-4422(22)00255-1 · Cited by 116
Metadata
- Authors
- George, M. F., Briggs, F. B. S., Shao, X., Gianfrancesco, M. A., Kockum, I., Harbo, H. F., Celius, E. G., Bos, S. D., Hedström, A., Shen, L., Bernstein, A., Alfredsson, L., Hillert, J., Olsson, T., Patsopoulos, N. A., De Jager, P. L., Oturai, A. B., Søndergaard, H. B., Sellebjerg, F., Sorensen, P. S., Gomez, R., Caillier, S. J., Cree, B. A. C., Oksenberg, J. R., Hauser, S. L., D'Alfonso, S., Leone, M. A., Boneschi, F. M., Sorosina, M., van der Mei, I., Taylor, B. V., Zhou, Y., Schaefer, C., & Barcellos, L. F.
- Affiliations
- Author affiliations are listed at the end of the article.
- Corresponding author
- Barcellos, Lisa F.
- ORCID
- George, Michaela F.
- Briggs, Farren B.S.
- Gianfrancesco, Milena A.
- Kockum, Ingrid
- Harbo, Hanne F.
- Celius, Elisabeth G.
- Bos, Steffan D.
- Hedström, Anna
- Bernstein, Allan
- Alfredsson, Lars
- Hillert, Jan
- Olsson, Tomas
- Patsopoulos, Nikolaos A.
- Søndergaard, Helle B.
- Sellebjerg, Finn
- Gomez, Refujia
- Caillier, Stacy J.
- Cree, Bruce A.C.
- Oksenberg, Jorge R.
- Hauser, Stephen L.
- Leone, Maurizio A.
- Boneschi, Filippo Martinelli
- Sorosina, Melissa
- van der Mei, Ingrid
- Taylor, Bruce V.
- Zhou, Yuan
- Schaefer, Catherine
- Barcellos, Lisa F.
- Venue
- Neurology Genetics
- Published
- 2016-08
- Volume
- 2
- Issue
- 4
- Pages
- e87-e87
- ISSN
- 2376-7839 (ISSN-L)
- PMC
- PMC4974846
- OpenAlex
- W2476223773
- Cited by
- 86
- References
- 41
- Citations by year
- 2026: 5 · 2025: 5 · 2024: 6 · 2023: 3 · 2022: 14 · 2021: 8 · 2020: 12 · 2019: 10 · 2018: 12 · 2017: 8 · 2016: 2
- FWCI
- 9.70
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- cc-by-nc-nd
- Locations
- Neurology Genetics (publishedVersion, cc-by-nc-nd)
- Europe PMC (PubMed Central) (publishedVersion, cc-by-nc-nd)
- PubMed Central (publishedVersion, cc-by-nc-nd)
- PubMed (publishedVersion)
- Research at the University of Copenhagen (University of Copenhagen) (publishedVersion, cc-by-nc-nd)
- eCite Digital Repository (University of Tasmania) (submittedVersion, cc-by-nc-nd)
- Dominican Scholar (Dominican University of California) (submittedVersion, cc-by-nc-nd)
- Archivio Istituzionale della Ricerca (Universita Degli Studi Di Milano) (submittedVersion, other-oa)
- eScholarship (California Digital Library) (submittedVersion)
- eScholarship (California Digital Library) (submittedVersion, cc-by-nc-nd)
- Figshare (submittedVersion, cc-by-nc-nd)
- Funders
- U.S. Environmental Protection Agency
- National Multiple Sclerosis Society
- Harvard NeuroDiscovery Center
- Intel Corporation
- Eli Lilly and Company
- Pfizer
- AstraZeneca
- GlaxoSmithKline
- Sanofi
- Biogen
- Teva Pharmaceutical Industries
- Strategiske Forskningsråd
- Scleroseforeningen
- Sundhed og Sygdom, Det Frie Forskningsråd
- Association of Fraternity/Sorority Advisors Foundation
- Acorda Therapeutics
- Multiple Sclerosis Society
- European Commission
- Multiple Sclerosis Australia
- AFA Försäkring
- Fondazione Cariplo (2010-0728)
- Ministero della Salute
- Ministero dell’Istruzione, dell’Università e della Ricerca
- Karolinska Institutet
- Novo Nordisk
- Vetenskapsrådet
- Universitetet i Oslo
- Norges Forskningsråd
- A.P. Møller og Hustru Chastine Mc-Kinney Møllers Fond til almene Formaal
- H. Lundbeck A/S
- National Institutes of Health
- Genentech
- EMD Serono
- University of California, San Francisco
- Medical Research Council
- Australian Research Council
- National Health and Medical Research Council
- Strategic Research Council
- National Institute of Mental Health
- National Cancer Institute
- National Institute of Allergy and Infectious Diseases (R01AI076544)
- National Institute of Neurological Disorders and Stroke (R01NS026799, R01NS049510, R01NS049477)
- National Institute of Environmental Health Sciences (R01ES017080)
- Topics
- Health Sciences › Medicine › Clinical Neurology › Multiple Sclerosis Research Studies
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Associations and Epidemiology
- Life Sciences › Immunology and Microbiology › Immunology › Psoriasis: Treatment and Pathogenesis
- Keywords
- multiple sclerosis, disease severity, genetic risk variants, Multiple Sclerosis Severity Score, Expanded Disability Status Scale, polygenic risk score, single nucleotide polymorphisms, HLA-DRB1*1501, disease duration
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review