Evidence map›Paper›PMID 31368393›Full record

ArticleMultiple sclerosis (Houndmills, Basingstoke, England)2020

The genetic diversity of multiple sclerosis risk among Hispanic and African American populations living in the United States.

A H Beecham, L Amezcua, A Chinea, C P Manrique, C Rubi, N Isobe, B T Lund, A Santaniello, G W Beecham, E G Burchard and 9 more

Abstract read
In one paragraph

Article in Multiple sclerosis (Houndmills, Basingstoke, England), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
–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

25 citing papers in PubMed.

  1. Trial
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  7. Frontiers in pharmacology · 2025
    Review
  8. GWAS highlights the neuronal contribution to multiple sclerosis susceptibility.medRxiv : the preprint server for health sciences · 2024
    Article
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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

19 authors.

A H BeechamJohn P. Hussman Institute for Human Genomics, Miller School of Medicine, University of Miami, Miami, FL, USA/The Dr. John T. Macdonald Foundation Department of Human Genetics, Miller School of Medicine, University of Miami, Miami, FL, USA.
L AmezcuaDepartment of Neurology, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.ORCID 0000-0003-1542-7819
A ChineaSan Juan MS Center, Guaynabo, Puerto Rico, USA; Universidad Central del Caribe, Bayamon, Puerto Rico, USA.
C P ManriqueJohn P. Hussman Institute for Human Genomics, Miller School of Medicine, University of Miami, Miami, FL, USA.
C RubiSan Juan MS Center, Guaynabo, Puerto Rico, USA; Universidad Central del Caribe, Bayamon, Puerto Rico, USA.
N IsobeDepartment of Neurological Therapeutics, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
B T LundDepartment of Neurology, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.
A SantanielloDepartment of Neurology, University of California at San Francisco, San Francisco, CA, USA.
G W BeechamJohn P. Hussman Institute for Human Genomics, Miller School of Medicine, University of Miami, Miami, FL, USA/The Dr. John T. Macdonald Foundation Department of Human Genetics, Miller School of Medicine, University of Miami, Miami, FL, USA.
E G BurchardDepartments of Medicine and Bioengineering and Therapeutic Sciences, University of California at San Francisco, San Francisco, CA, USA.
M ComabellaServei de Neurologia-Neuroimmunologia, Centre d'Esclerosi Múltiple de Catalunya (Cemcat), Institut de Recerca Vall d'Hebron (VHIR), Hospital Universitari Vall d'Hebron, Universitat Autònoma de Barcelona, Barcelona, Spain.
N PatsopoulosDepartment of Neurology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
K FitzgeraldDepartment of Neurology and The Solomon H. Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
P A CalabresiDepartment of Neurology and The Solomon H. Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
P De JagerCenter for Translational and Computational Neuroimmunology, Department of Neurology, Columbia University Medical Center, New York, NY, USA.
D V ContiDepartment of Preventive Medicine, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.
S R DelgadoMultiple Sclerosis Division, Department of Neurology, Miller School of Medicine, University of Miami, Miami, FL, USA.
J R OksenbergDepartment of Neurology, University of California at San Francisco, San Francisco, CA, USA.
J L McCauleyJohn P. Hussman Institute for Human Genomics, Miller School of Medicine, University of Miami, Miami, FL, USA/The Dr. John T. Macdonald Foundation Department of Human Genetics, Miller School of Medicine, University of Miami, Miami, FL, USA.

Funding

Southern California Clinical and Translational Science InstituteUL1TR001855 · NCATS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI Thomas A Buchanan, Michele D. Kipke · 2016 to 2026
$81.3M
Imaging Neurodegeneration in Multiple SclerosisR01NS082347 · NINDS · JOHNS HOPKINS UNIVERSITY · PI PETER A CALABRESI, Shiv Saidha · 2013 to 2026
$7.0M
GENE LINKAGE STUDY OF MULTIPLE SCLEROSIS SIBLING PAIRSR01NS026799 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI HAUSER, STEPHEN L, OKSENBERG, JORGE R. · 1989 to 2018
$6.8M
Individualized Risk Stratification Using the Genomic ContributionR01HL102487 · NHLBI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI BEECHAM, GARY WAYNE, SEO, DAVID M · 2010 to 2014
$3.7M
Genetic and Phenotypic Analysis of Multiple Sclerosis in HispanicsR01NS096212 · NINDS · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI MCCAULEY, JACOB L · 2016 to 2021
$3.1M
Southern California Clinical and Translational Science InstituteKL2TR000131 · NCATS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI BUCHANAN, THOMAS A · 2012 to 2015
$2.1M
NCATS NIH HHS KL2 TR000131NCATS NIH HHS UL1 TR001855NHLBI NIH HHS R01 HL102487NINDS NIH HHS R01 NS026799NINDS NIH HHS R01 NS082347NINDS NIH HHS R01 NS096212
6 · The paper itself

Abstract

backgroundSubstantial progress has been made toward unraveling the genetic architecture of multiple sclerosis (MS) within populations of European ancestry, but few genetic studies have focused on Hispanic and African American populations within the United States.

objectiveWe sought to test the relevance of common European MS risk variants outside of the major histocompatibility complex (

methodsGenotype data were available on 2652 Hispanics (1298 with MS, 1354 controls) and 2435 African Americans (1298 with MS, 1137 controls). We conducted single variant, pathway, and cumulative genetic risk score analyses.

resultsWe found less replication than statistical power suggested, particularly among African Americans. This could be due to limited correlation between the tested and causal variants within the sample or alternatively could indicate allelic and locus heterogeneity. Differences were observed between pathways enriched among the replicating versus all 200 variants. Although these differences should be examined in larger samples, a potential role exists for gene-environment or gene-gene interactions which alter phenotype differentially across racial and ethnic groups. Cumulative genetic risk scores were associated with MS within each study sample but showed limited diagnostic capability.

conclusionThese findings provide a framework for fine-mapping efforts in multi-ethnic populations of MS.

Indexed as

Black or African AmericanMultiple SclerosisAllelesGenetic VariationHispanic or LatinoHumansPolymorphism, Single NucleotideUnited Statesadmixtureallelic heterogeneitygeneticslocus heterogeneitymulti-ethnicMultiple sclerosispathway analysisrisk score

Identifiers

PMID31368393
PMCPMC6994382

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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.