Evidence map›Paper›PMID 26769066›Full record

ArticleMultiple sclerosis (Houndmills, Basingstoke, England)2016

Genetic predictors of relapse rate in pediatric MS.

Jennifer S Graves, Lisa F Barcellos, Xiaorong Shao, Janelle Noble, Ellen M Mowry, Hong Quach, Anita Belman, T Charles Casper, Lauren B Krupp, Emmanuelle Waubant and 1 more

Open access · greenAbstract read
In one paragraph

Article in Multiple sclerosis (Houndmills, Basingstoke, England), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
4.2field-weighted citation impact, top 6% 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

13 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
  2. Review
  3. Epigenetic age and telomere length correlations in pediatric-onset multiple sclerosis.Multiple sclerosis (Houndmills, Basingstoke, England) · 2025
    Article
  4. Article
  5. Review
  6. Vitamin D genes influence MS relapses in children.Multiple sclerosis (Houndmills, Basingstoke, England) · 2020
    Article
  7. Article
  8. Article
  9. Review
  10. Pediatric multiple sclerosis: current perspectives on health behaviors.Pediatric health, medicine and therapeutics · 2018
    Review
  11. Article
  12. Observational
  13. Multiple sclerosis journal - experimental, translational and clinical
    Article
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 at 5 institutions in 1 country.

Jennifer S GravesUCSF Pediatric Multiple Sclerosis Center, San Francisco, CA, USA Jennifer.Graves@ucsf.edu.
Lisa F BarcellosGenetic Epidemiology and Genomics Lab, School of Public Health, and California Institute for Quantitative Biosciences, University of California-Berkeley, Berkeley, CA, USA.
Xiaorong ShaoGenetic Epidemiology and Genomics Lab, School of Public Health, and California Institute for Quantitative Biosciences, University of California-Berkeley, Berkeley, CA, USA.
Janelle NobleChildren's Hospital Oakland Research Institute, Oakland, CA, USA.
Ellen M MowryThe Multiple Sclerosis Center, Johns Hopkins University, Baltimore, MD, USA.
Hong QuachGenetic Epidemiology and Genomics Lab, School of Public Health, and California Institute for Quantitative Biosciences, University of California-Berkeley, Berkeley, CA, USA.
Anita BelmanNational Pediatric Multiple Sclerosis Center, Stony Brook, NY, USA.
T Charles CasperData Coordinating and Analysis Center, University of Utah, Salt Lake City, UT, USA.
Lauren B KruppNational Pediatric Multiple Sclerosis Center, Stony Brook, NY, USA.
Emmanuelle WaubantUCSF Pediatric Multiple Sclerosis Center, San Francisco, CA, USA.
U.S. Network of Pediatric MS Centers
National Multiple Sclerosis Society · USUniversity of California, Berkeley · USJohns Hopkins University · USQB3 · USUniversity of Utah · US

Funding

UCSF/Kaiser-DOR Program for Developing Independent Women's Health ResearchersK12HD052163 · NICHD · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ADLER, NANCY E, BRINDIS, CLAIRE D. · 2005 to 2023
$9.3M
The Identification of Risk Factors for the Complex MS PhenotypeR01AI076544 · NIAID · UNIVERSITY OF CALIFORNIA BERKELEY · PI BARCELLOS, LISA F · 2008 to 2012
$3.6M
Novel Strategies to Identify GxE Contributions to MS PathogenesisR01ES017080 · NIEHS · UNIVERSITY OF CALIFORNIA BERKELEY · PI BARCELLOS, LISA F · 2011 to 2015
$3.0M
Environmental and genetic risk factors for pediatric MSR01NS071463 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI WAUBANT, EMMANUELLE LAURENCE · 2010 to 2015
$2.8M
Genetic and non-genetic risk factors in MSR01NS049510 · NINDS · UNIVERSITY OF CALIFORNIA BERKELEY · PI BARCELLOS, LISA F · 2005 to 2009
$2.7M
NIAID NIH HHS R01 AI076544NICHD NIH HHS K12 HD052163NIEHS NIH HHS R01 ES017080NINDS NIH HHS R01 NS049510NINDS NIH HHS R01 NS071463
6 · The paper itself

Abstract

backgroundGenetic ancestry, sex, and individual alleles have been associated with multiple sclerosis (MS) susceptibility.

objectiveTo determine whether established risk factors for disease onset are associated with relapse rate in pediatric MS.

methodsWhole-genome genotyping was performed for 181 MS or high-risk clinically isolated syndrome patients from two pediatric MS centers. Relapses and disease-modifying therapies were recorded as part of continued follow-up. Participants were characterized for 25-hydroxyvitamin D serum status. Ancestral estimates (STRUCTURE v2.3.1), human leukocyte antigen (HLA)-DRB1*15 carrier status (direct sequencing), sex, and a genetic risk score (GRS) of 110 non-HLA susceptibility single-nucleotide polymorphisms (SNPs) were evaluated for association with relapse rate with Cox and negative binomial regression models.

resultsOver 622 patient-years, 408 relapses were captured. Girls had greater relapse rate than boys (incident rate ratio (IRR) = 1.40, 95% confidence interval (CI) = 1.04-1.87, p = 0.026). Participants were genetically diverse; ~40% (N = 75) had <50% European ancestry. HLA-DRB1*15 status modified the association of vitamin D status (p

conclusionWe demonstrate that HLA-DRB1*15 modifies the association of vitamin D status with relapse rate. Our findings emphasize the need to pursue disease-modifying effects of MS genes in the context of environmental factors.

Indexed as

AdolescentAge of OnsetCalcitriolChildFemaleFollow-Up StudiesGenotyping TechniquesHLA-DRB1 ChainsHumansMaleMultiple SclerosisRecurrenceSex FactorsCalcitriolHLA-DRB1*15 antigenHLA-DRB1 ChainsGeneticsmultiple sclerosisoutcome measurementrelapsing/remittingvitamin D

Identifiers

PMID26769066
PMCPMC4945462
OpenAlexW2408123531

What OpenQuestion holds

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LicenceTDM
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.