Abstract
Several studies have reported a defective Fas function in patients with multiple sclerosis (MS). We were interested whether this could result from a genetically altered Fas regulation. We examined the FAS-670 polymorphism in 382 patients with MS and 206 controls, and found that the carriership of allele FAS-670*G was significantly less frequent in patients than in controls. We found no association between the carriership of FAS-670*G and clinical features. For a subgroup of patients, longitudinal MRI data were available. We observed similar brain and lesion volumes in carriers and noncarriers of FAS-670*G. These data suggest that FAS-670*G decreases the risk of developing MS, but does not affect the course of disease.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Adult
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Age of Onset
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Brain / immunology
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Brain / pathology
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Brain / physiopathology
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DNA Mutational Analysis
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Fas Ligand Protein
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Female
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Gene Frequency
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Genetic Predisposition to Disease / genetics*
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Genetic Testing
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Humans
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Interferon-beta / therapeutic use
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Magnetic Resonance Imaging
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Male
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Membrane Glycoproteins / genetics*
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Membrane Glycoproteins / immunology
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Middle Aged
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Multiple Sclerosis / genetics*
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Multiple Sclerosis / immunology
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Multiple Sclerosis / physiopathology
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Polymorphism, Genetic / genetics*
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Polymorphism, Genetic / immunology
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Sex Factors
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fas Receptor / genetics*
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fas Receptor / immunology
Substances
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FASLG protein, human
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Fas Ligand Protein
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Membrane Glycoproteins
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fas Receptor
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Interferon-beta