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The genetic basis of multiple sclerosis: a model for MS susceptibility

ABSTACT: BACKGROUND: MS-pathogenesis is known to involve both multiple environmental events, and several independent genetic risk-factors. METHODS: A model of susceptibility is developed and a mathematical analysis undertaken to elucidate the nature of genetic susceptibility to MS and to understand...

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Autor principal: Goodin, Douglas S
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2994805/
https://www.ncbi.nlm.nih.gov/pubmed/21029420
http://dx.doi.org/10.1186/1471-2377-10-101
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author Goodin, Douglas S
author_facet Goodin, Douglas S
author_sort Goodin, Douglas S
collection PubMed
description ABSTACT: BACKGROUND: MS-pathogenesis is known to involve both multiple environmental events, and several independent genetic risk-factors. METHODS: A model of susceptibility is developed and a mathematical analysis undertaken to elucidate the nature of genetic susceptibility to MS and to understand the constraints that are placed on the genetic basis of MS, both by the known epidemiological facts of this disease and by the known frequency of the HLA DRB1*1501 allele in the general populations of northern Europe and North America. RESULTS: For the large majority of cases (possibly all), MS develops, in part, because an individual is genetically susceptible. Nevertheless, 2.2% or less of the general population is genetically susceptible. Moreover, from the model, the number of susceptibility-loci that need to be in a "susceptible allelic state" to produce MS-susceptibility is small (11-18), whereas the total number of such susceptibility-loci is large (50-200), and their "frequency of susceptibility" is low (i.e., ≤ 0.12). The optimal solution to the model equations (which occurs when 80% of the loci are recessive) predicts the epidemiological data quite closely. CONCLUSIONS: The model suggests that combinations of only a small number of genetic loci in a "susceptible allelic state" produce MS-susceptibility. Nevertheless, genome-wide associations studies with hundreds of thousands of SNPs, are plagued by both false-positive and false-negative identifications and, consequently, emphasis has been rightly placed on the replicability of findings. Nevertheless, because genome-wide screens don't distinguish between true susceptibility-loci and disease-modifying-loci, and because only true susceptibility-loci are constrained by the model, unraveling the two will not be possible using this approach. The model also suggests that HLA DRB1 may not be as uniquely important for MS-susceptibility as currently believed. Thus, this allele is only one among a hundred or more loci involved in MS susceptibility. Even though the "frequency of susceptibility" at the HLA DRB1 locus is four-fold that of other loci, the penetrance of those susceptible genotypes that include this allele is no different from those that don't. Also, almost 50% of genetically-susceptible individuals, lack this allele. Moreover, of those who have it, only a small fraction (≤ 5.2%) are even susceptible to getting MS.
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spelling pubmed-29948052011-01-05 The genetic basis of multiple sclerosis: a model for MS susceptibility Goodin, Douglas S BMC Neurol Research Article ABSTACT: BACKGROUND: MS-pathogenesis is known to involve both multiple environmental events, and several independent genetic risk-factors. METHODS: A model of susceptibility is developed and a mathematical analysis undertaken to elucidate the nature of genetic susceptibility to MS and to understand the constraints that are placed on the genetic basis of MS, both by the known epidemiological facts of this disease and by the known frequency of the HLA DRB1*1501 allele in the general populations of northern Europe and North America. RESULTS: For the large majority of cases (possibly all), MS develops, in part, because an individual is genetically susceptible. Nevertheless, 2.2% or less of the general population is genetically susceptible. Moreover, from the model, the number of susceptibility-loci that need to be in a "susceptible allelic state" to produce MS-susceptibility is small (11-18), whereas the total number of such susceptibility-loci is large (50-200), and their "frequency of susceptibility" is low (i.e., ≤ 0.12). The optimal solution to the model equations (which occurs when 80% of the loci are recessive) predicts the epidemiological data quite closely. CONCLUSIONS: The model suggests that combinations of only a small number of genetic loci in a "susceptible allelic state" produce MS-susceptibility. Nevertheless, genome-wide associations studies with hundreds of thousands of SNPs, are plagued by both false-positive and false-negative identifications and, consequently, emphasis has been rightly placed on the replicability of findings. Nevertheless, because genome-wide screens don't distinguish between true susceptibility-loci and disease-modifying-loci, and because only true susceptibility-loci are constrained by the model, unraveling the two will not be possible using this approach. The model also suggests that HLA DRB1 may not be as uniquely important for MS-susceptibility as currently believed. Thus, this allele is only one among a hundred or more loci involved in MS susceptibility. Even though the "frequency of susceptibility" at the HLA DRB1 locus is four-fold that of other loci, the penetrance of those susceptible genotypes that include this allele is no different from those that don't. Also, almost 50% of genetically-susceptible individuals, lack this allele. Moreover, of those who have it, only a small fraction (≤ 5.2%) are even susceptible to getting MS. BioMed Central 2010-10-28 /pmc/articles/PMC2994805/ /pubmed/21029420 http://dx.doi.org/10.1186/1471-2377-10-101 Text en Copyright ©2010 Goodin; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Goodin, Douglas S
The genetic basis of multiple sclerosis: a model for MS susceptibility
title The genetic basis of multiple sclerosis: a model for MS susceptibility
title_full The genetic basis of multiple sclerosis: a model for MS susceptibility
title_fullStr The genetic basis of multiple sclerosis: a model for MS susceptibility
title_full_unstemmed The genetic basis of multiple sclerosis: a model for MS susceptibility
title_short The genetic basis of multiple sclerosis: a model for MS susceptibility
title_sort genetic basis of multiple sclerosis: a model for ms susceptibility
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2994805/
https://www.ncbi.nlm.nih.gov/pubmed/21029420
http://dx.doi.org/10.1186/1471-2377-10-101
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