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Multiple sclerosis genomic map implicates peripheral immune cells and microglia in susceptibility
- Source :
- Science, 365(6460):eaav7188, 1417-+. American Association for the Advancement of Science, Science
- Publication Year :
- 2019
-
Abstract
- Genetic roots of multiple sclerosis The genetics underlying who develops multiple sclerosis (MS) have been difficult to work out. Examining more than 47,000 cases and 68,000 controls with multiple genome-wide association studies, the International Multiple Sclerosis Genetics Consortium identified more than 200 risk loci in MS (see the Perspective by Briggs). Focusing on the best candidate genes, including a model of the major histocompatibility complex region, the authors identified statistically independent effects at the genome level. Gene expression studies detected that every major immune cell type is enriched for MS susceptibility genes and that MS risk variants are enriched in brain-resident immune cells, especially microglia. Up to 48% of the genetic contribution of MS can be explained through this analysis. Science , this issue p. eaav7188 ; see also p. 1383
- Subjects :
- 0301 basic medicine
Multiple Sclerosis
Quantitative Trait Loci
Inheritance Patterns
Cell Cycle Proteins
Genome-wide association study
Biology
Major histocompatibility complex
Polymorphism, Single Nucleotide
Major Histocompatibility Complex
Transcriptome
03 medical and health sciences
0302 clinical medicine
Immune system
Gene Frequency
Autoimmune Process
medicine
Humans
RNA-Seq
X chromosome
Genetics
Chromosomes, Human, X
Multidisciplinary
Microglia
Multiple sclerosis
GTPase-Activating Proteins
Chromosome Mapping
Genomics
medicine.disease
3. Good health
030104 developmental biology
medicine.anatomical_structure
Genetic Loci
Case-Control Studies
biology.protein
Genome-Wide Association Study
030217 neurology & neurosurgery
Subjects
Details
- Language :
- English
- ISSN :
- 10959203 and 00368075
- Volume :
- 365
- Issue :
- 6460
- Database :
- OpenAIRE
- Journal :
- Science
- Accession number :
- edsair.doi.dedup.....94bb28899c26c0aa3a4abb4b13a1087c