Genetics of multiple sclerosis [published erratum appears in Hum Mol Genet 1997 Nov;6(12):2189]
Abstract
Multiple Sclerosis (MS) is a common chronic central nervous system disease in young adults. Relative familial risk appears to be determined largely by genes while population risk is strongly influenced by environmental factors. This is supported by genetic epidemiological studies which also suggest an oligogenic inheritance of susceptibility. The HLA DRB1*1501, DQA1*0102, DQB1 0602 haplotype is associated with the disease but HLA contributes only modestly to overall susceptibility. The results of three genomic searches are concordant with the genetic epidemiology and imply a number of genes with interacting effects will be found. Importantly, no single region has been identified with a major influence on familial risk.
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Candidate gene studies in multiple sclerosis produced inconsistent findings.
“Candidate gene studies in cohorts of tens or hundreds of individuals at the loci encoding T‐cell receptor alpha12, 13 and beta14, 15 loci, the immunoglobulin heavy‐chain genes16, 17 and the gene for myelin basic protein,18, 19 among others, produced inconsistent findings.20, 21”
From Genome‐wide association studies of multiple sclerosis (2018) · cites this paper as [21]
Cites
Axonal transection in the lesions of multiple sclerosis
Trapp, B. D., Peterson, J., Ransohoff, R. M., Rudick, R., Mörk, S., & Bö, L. (1998) · New England Journal of Medicine · doi:10.1056/nejm199801293380502 · Cited by 4,029 · see citing works
Epidemiologic evidence for multiple sclerosis as an infection
Kurtzke, J. F. (1993) · Clinical Microbiology Reviews · doi:10.1128/cmr.6.4.382 · Cited by 472 · see citing works
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The burden of complex genetics in brain disorders
Uhl, G. R., & Grow, R. W. (2004) · Archives of General Psychiatry · doi:10.1001/archpsyc.61.3.223 · Cited by 176 · see citing works
Genome‐wide association studies of multiple sclerosis
Cotsapas, C., & Mitrovic, M. (2018) · Clinical & Translational Immunology · doi:10.1002/cti2.1018 · Cited by 89 · see citing works
- Authors
- Dyment, D.
- Affiliations
- Western University (CA)
- Corresponding author
- Dyment, D.
- Venue
- Human Molecular Genetics
- Publisher
- Oxford University Press (OUP)
- Published
- 1997-09-01
- Volume
- 6
- Issue
- 10
- Pages
- 1693-1698
- ISSN
- 0964-6906 (ISSN-L)
- 1460-2083
- OpenAlex
- W2116104996
- Cited by
- 152
- References
- 2
- Citations by year
- 2024: 1 · 2023: 4 · 2022: 4 · 2021: 1 · 2020: 5 · 2019: 3 · 2018: 6 · 2017: 5 · 2016: 2 · 2015: 3 · 2014: 4 · 2013: 7 · 2012: 2
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Human Molecular Genetics (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Pathology and Forensic Medicine › 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, genetic susceptibility, HLA-DRB1*1501, HLA-DQA1*0102, HLA-DQB1*0602, HLA haplotypes, oligogenic inheritance, familial risk, environmental risk factors, genetic epidemiology, genome-wide search
- MeSH terms
- Adult, Chromosome Mapping, Chromosomes, Human, Disease Susceptibility, Diseases in Twins, Environment, Family, Genetic Markers, HLA-D Antigens, HLA-DQ Antigens, HLA-DR Antigens, Humans, Multiple Sclerosis, Risk Factors, HLA-DRB1 Chains, HLA-DQ alpha-Chains, HLA-DQ beta-Chains
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