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Time correlation between mononucleosis and initial symptoms of MS
OBJECTIVE: To determine the average age of MS onset vs the age at which Epstein-Barr infection has previously occurred and stratify this analysis by sex and the blood level of Epstein-Barr nuclear antigen 1 (EBNA1) antibody. METHODS: Using infectious mononucleosis (IM) as a temporal marker in data f...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Lippincott Williams & Wilkins
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5330199/ https://www.ncbi.nlm.nih.gov/pubmed/28271078 http://dx.doi.org/10.1212/NXI.0000000000000308 |
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author | Endriz, John Ho, Peggy P. Steinman, Lawrence |
author_facet | Endriz, John Ho, Peggy P. Steinman, Lawrence |
author_sort | Endriz, John |
collection | PubMed |
description | OBJECTIVE: To determine the average age of MS onset vs the age at which Epstein-Barr infection has previously occurred and stratify this analysis by sex and the blood level of Epstein-Barr nuclear antigen 1 (EBNA1) antibody. METHODS: Using infectious mononucleosis (IM) as a temporal marker in data from the Swedish epidemiologic investigation of MS, 259 adult IM/MS cases were identified and then augmented to account for “missing” childhood data so that the average age of MS onset could be determined for cases binned by age of IM (as stratified by sex and EBNA1 titer level). RESULTS: Mean age of IM vs mean age of MS reveals a positive time correlation for all IM ages (from ∼5 to ∼30 years), with IM-to-MS delay decreasing with increased age. When bifurcated by sex or EBNA1 blood titer levels, males and high-titer subpopulations show even stronger positive time correlation, while females and low-titer populations show negative time correlation in early childhood (long IM/MS delay). The correlation becomes positive in females beyond puberty. CONCLUSIONS: IM/MS time correlation implies causality if IM is time random. Alternative confounding models seem implausible, in light of constraints imposed by time-invariant delay observed here. Childhood infection with Epstein-Barr virus (EBV) in females and/or those genetically prone to low EBNA1 blood titers will develop MS slowly. Males and/or high EBNA1-prone develop MS more rapidly following IM infection at all ages. For all, postpubescent EBV infection is critical for the initiation and rapid development of MS. |
format | Online Article Text |
id | pubmed-5330199 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-53301992017-03-07 Time correlation between mononucleosis and initial symptoms of MS Endriz, John Ho, Peggy P. Steinman, Lawrence Neurol Neuroimmunol Neuroinflamm Article OBJECTIVE: To determine the average age of MS onset vs the age at which Epstein-Barr infection has previously occurred and stratify this analysis by sex and the blood level of Epstein-Barr nuclear antigen 1 (EBNA1) antibody. METHODS: Using infectious mononucleosis (IM) as a temporal marker in data from the Swedish epidemiologic investigation of MS, 259 adult IM/MS cases were identified and then augmented to account for “missing” childhood data so that the average age of MS onset could be determined for cases binned by age of IM (as stratified by sex and EBNA1 titer level). RESULTS: Mean age of IM vs mean age of MS reveals a positive time correlation for all IM ages (from ∼5 to ∼30 years), with IM-to-MS delay decreasing with increased age. When bifurcated by sex or EBNA1 blood titer levels, males and high-titer subpopulations show even stronger positive time correlation, while females and low-titer populations show negative time correlation in early childhood (long IM/MS delay). The correlation becomes positive in females beyond puberty. CONCLUSIONS: IM/MS time correlation implies causality if IM is time random. Alternative confounding models seem implausible, in light of constraints imposed by time-invariant delay observed here. Childhood infection with Epstein-Barr virus (EBV) in females and/or those genetically prone to low EBNA1 blood titers will develop MS slowly. Males and/or high EBNA1-prone develop MS more rapidly following IM infection at all ages. For all, postpubescent EBV infection is critical for the initiation and rapid development of MS. Lippincott Williams & Wilkins 2017-02-27 /pmc/articles/PMC5330199/ /pubmed/28271078 http://dx.doi.org/10.1212/NXI.0000000000000308 Text en Copyright © 2017 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits downloading and sharing the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. |
spellingShingle | Article Endriz, John Ho, Peggy P. Steinman, Lawrence Time correlation between mononucleosis and initial symptoms of MS |
title | Time correlation between mononucleosis and initial symptoms of MS |
title_full | Time correlation between mononucleosis and initial symptoms of MS |
title_fullStr | Time correlation between mononucleosis and initial symptoms of MS |
title_full_unstemmed | Time correlation between mononucleosis and initial symptoms of MS |
title_short | Time correlation between mononucleosis and initial symptoms of MS |
title_sort | time correlation between mononucleosis and initial symptoms of ms |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5330199/ https://www.ncbi.nlm.nih.gov/pubmed/28271078 http://dx.doi.org/10.1212/NXI.0000000000000308 |
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