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A Mechanistic, Stochastic Model Helps Understand Multiple Sclerosis Course and Pathogenesis
Heritable and nonheritable factors play a role in multiple sclerosis, but their effect size appears too small, explaining relatively little about disease etiology. Assuming that the factors that trigger the onset of the disease are, to some extent, also those that generate its remissions and relapse...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3647536/ https://www.ncbi.nlm.nih.gov/pubmed/23671846 http://dx.doi.org/10.1155/2013/910321 |
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author | Bordi, Isabella Umeton, Renato Ricigliano, Vito A. G. Annibali, Viviana Mechelli, Rosella Ristori, Giovanni Grassi, Francesca Salvetti, Marco Sutera, Alfonso |
author_facet | Bordi, Isabella Umeton, Renato Ricigliano, Vito A. G. Annibali, Viviana Mechelli, Rosella Ristori, Giovanni Grassi, Francesca Salvetti, Marco Sutera, Alfonso |
author_sort | Bordi, Isabella |
collection | PubMed |
description | Heritable and nonheritable factors play a role in multiple sclerosis, but their effect size appears too small, explaining relatively little about disease etiology. Assuming that the factors that trigger the onset of the disease are, to some extent, also those that generate its remissions and relapses, we attempted to model the erratic behaviour of the disease course as observed on a dataset containing the time series of relapses and remissions of 70 patients free of disease-modifying therapies. We show that relapses and remissions follow exponential decaying distributions, excluding periodic recurrences and confirming that relapses manifest randomly in time. It is found that a mechanistic model with a random forcing describes in a satisfactory manner the occurrence of relapses and remissions, and the differences in the length of time spent in each one of the two states. This model may describe how interactions between “soft” etiologic factors occasionally reach the disease threshold thanks to comparably small external random perturbations. The model offers a new context to rethink key problems such as “missing heritability” and “hidden environmental structure” in the etiology of complex traits. |
format | Online Article Text |
id | pubmed-3647536 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-36475362013-05-13 A Mechanistic, Stochastic Model Helps Understand Multiple Sclerosis Course and Pathogenesis Bordi, Isabella Umeton, Renato Ricigliano, Vito A. G. Annibali, Viviana Mechelli, Rosella Ristori, Giovanni Grassi, Francesca Salvetti, Marco Sutera, Alfonso Int J Genomics Research Article Heritable and nonheritable factors play a role in multiple sclerosis, but their effect size appears too small, explaining relatively little about disease etiology. Assuming that the factors that trigger the onset of the disease are, to some extent, also those that generate its remissions and relapses, we attempted to model the erratic behaviour of the disease course as observed on a dataset containing the time series of relapses and remissions of 70 patients free of disease-modifying therapies. We show that relapses and remissions follow exponential decaying distributions, excluding periodic recurrences and confirming that relapses manifest randomly in time. It is found that a mechanistic model with a random forcing describes in a satisfactory manner the occurrence of relapses and remissions, and the differences in the length of time spent in each one of the two states. This model may describe how interactions between “soft” etiologic factors occasionally reach the disease threshold thanks to comparably small external random perturbations. The model offers a new context to rethink key problems such as “missing heritability” and “hidden environmental structure” in the etiology of complex traits. Hindawi Publishing Corporation 2013 2013-03-12 /pmc/articles/PMC3647536/ /pubmed/23671846 http://dx.doi.org/10.1155/2013/910321 Text en Copyright © 2013 Isabella Bordi et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Bordi, Isabella Umeton, Renato Ricigliano, Vito A. G. Annibali, Viviana Mechelli, Rosella Ristori, Giovanni Grassi, Francesca Salvetti, Marco Sutera, Alfonso A Mechanistic, Stochastic Model Helps Understand Multiple Sclerosis Course and Pathogenesis |
title | A Mechanistic, Stochastic Model Helps Understand Multiple Sclerosis Course and Pathogenesis |
title_full | A Mechanistic, Stochastic Model Helps Understand Multiple Sclerosis Course and Pathogenesis |
title_fullStr | A Mechanistic, Stochastic Model Helps Understand Multiple Sclerosis Course and Pathogenesis |
title_full_unstemmed | A Mechanistic, Stochastic Model Helps Understand Multiple Sclerosis Course and Pathogenesis |
title_short | A Mechanistic, Stochastic Model Helps Understand Multiple Sclerosis Course and Pathogenesis |
title_sort | mechanistic, stochastic model helps understand multiple sclerosis course and pathogenesis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3647536/ https://www.ncbi.nlm.nih.gov/pubmed/23671846 http://dx.doi.org/10.1155/2013/910321 |
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