Literature DB >> 1423044

The increased susceptibility of women to multiple sclerosis.

P Duquette1, J Pleines, M Girard, L Charest, M Senecal-Quevillon, C Masse.   

Abstract

Many diseases with an auto-immune etiology have a skewed sex distribution. In the majority of instances, women are affected more frequently than men. A review of population studies demonstrates that the preponderance of women in multiple sclerosis (MS) is almost constant. We show that this preponderance is further increased in early as well as in late-onset cases, in familial cases as well as in MS twin pairs and that the HLA-DR2 allele, which has been associated with MS in Caucasian populations, is significantly more frequent in women than in men with MS. "Rules" have been established for multifactorial diseases; MS contravenes most of those rules. The skewed sex distribution in MS could be attributed to the known hormonal and gender influences on the immune response, as well as to genetic influences.

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Year:  1992        PMID: 1423044

Source DB:  PubMed          Journal:  Can J Neurol Sci        ISSN: 0317-1671            Impact factor:   2.104


  30 in total

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3.  Gene expression analyses reveal molecular relationships among 20 regions of the human CNS.

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4.  Enhancing the ability of experimental autoimmune encephalomyelitis to serve as a more rigorous model of multiple sclerosis through refinement of the experimental design.

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Journal:  Comp Med       Date:  2009-04       Impact factor: 0.982

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Review 6.  Estrogen and testosterone therapies in multiple sclerosis.

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Review 7.  Spatiotemporal changes in the human lens proteome: Critical insights into long-lived proteins.

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8.  Gender-specific expression of beta1 integrin of VLA-4 in myelin basic protein-primed T cells: implications for gender bias in multiple sclerosis.

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Journal:  J Immunol       Date:  2010-05-05       Impact factor: 5.422

9.  Breakdown of multiple sclerosis genetics to identify an integrated disease network and potential variant mechanisms.

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10.  Optic neuritis in different strains of mice by a recombinant HSV-1 expressing murine interleukin-2.

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