Congenital abnormalities and multiple sclerosis

Background: There is a strong maternal parent-of-origin effect in determining susceptibility to multiple sclerosis (MS). One hypothesis is that an abnormal intrauterine milieu leading to impaired fetal development could plausibly also result in increased susceptibility to MS. A possible marker for t...

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主要な著者: Ramagopalan, S, Guimond, C, Criscuoli, M, Dyment, D, Orton, S, Irene M. Yee, Ebers, G, Sadovnick, D
フォーマット: Journal article
言語:English
出版事項: BioMed Central 2010
主題:
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author Ramagopalan, S
Guimond, C
Criscuoli, M
Dyment, D
Orton, S
Irene M. Yee
Ebers, G
Sadovnick, D
author_facet Ramagopalan, S
Guimond, C
Criscuoli, M
Dyment, D
Orton, S
Irene M. Yee
Ebers, G
Sadovnick, D
author_sort Ramagopalan, S
collection OXFORD
description Background: There is a strong maternal parent-of-origin effect in determining susceptibility to multiple sclerosis (MS). One hypothesis is that an abnormal intrauterine milieu leading to impaired fetal development could plausibly also result in increased susceptibility to MS. A possible marker for this intrauterine insult is the presence of a non-fatal congenital anomaly. Methods: We investigated whether or not congenital anomalies are associated with MS in a population-based cohort. We identified 7063 MS index cases and 2655 spousal controls with congenital anomaly information from the Canadian Collaborative Project on Genetic Susceptibility to MS (CCPGSMS). Results: The frequency of congenital anomalies were compared between index cases and controls. No significant differences were found. Conclusions: Congenital anomalies thus do not appear to be associated with MS. However, we did not have complete data on types and severity of congenital anomalies or on maternal birth history and thus this study should be regarded as preliminary.
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spelling oxford-uuid:3d0b7d2f-3a95-489e-9787-71de3319bd072022-03-26T14:17:18ZCongenital abnormalities and multiple sclerosisJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:3d0b7d2f-3a95-489e-9787-71de3319bd07Genetics (medical sciences)Multiple SclerosisEnglishOxford University Research Archive - ValetBioMed Central2010Ramagopalan, SGuimond, CCriscuoli, MDyment, DOrton, SIrene M. YeeEbers, GSadovnick, DBackground: There is a strong maternal parent-of-origin effect in determining susceptibility to multiple sclerosis (MS). One hypothesis is that an abnormal intrauterine milieu leading to impaired fetal development could plausibly also result in increased susceptibility to MS. A possible marker for this intrauterine insult is the presence of a non-fatal congenital anomaly. Methods: We investigated whether or not congenital anomalies are associated with MS in a population-based cohort. We identified 7063 MS index cases and 2655 spousal controls with congenital anomaly information from the Canadian Collaborative Project on Genetic Susceptibility to MS (CCPGSMS). Results: The frequency of congenital anomalies were compared between index cases and controls. No significant differences were found. Conclusions: Congenital anomalies thus do not appear to be associated with MS. However, we did not have complete data on types and severity of congenital anomalies or on maternal birth history and thus this study should be regarded as preliminary.
spellingShingle Genetics (medical sciences)
Multiple Sclerosis
Ramagopalan, S
Guimond, C
Criscuoli, M
Dyment, D
Orton, S
Irene M. Yee
Ebers, G
Sadovnick, D
Congenital abnormalities and multiple sclerosis
title Congenital abnormalities and multiple sclerosis
title_full Congenital abnormalities and multiple sclerosis
title_fullStr Congenital abnormalities and multiple sclerosis
title_full_unstemmed Congenital abnormalities and multiple sclerosis
title_short Congenital abnormalities and multiple sclerosis
title_sort congenital abnormalities and multiple sclerosis
topic Genetics (medical sciences)
Multiple Sclerosis
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AT criscuolim congenitalabnormalitiesandmultiplesclerosis
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AT ortons congenitalabnormalitiesandmultiplesclerosis
AT irenemyee congenitalabnormalitiesandmultiplesclerosis
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