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A population-based study of multiple sclerosis in twins.
Ebers GC,
Bulman DE,
Sadovnick AD,
Paty DW,
Warren S,
Hader W,
Murray TJ,
Seland TP,
Duquette P,
Grey T, et al.
Results from studies of twin concordance in multiple sclerosis have not conclusively differentiated between environmental and genetic factors that determine susceptibility to the disease. Published studies that have been based on case finding by public appeal have been characterized by difficulties in ascertainment. The data reported here are from a large population-based study of multiple sclerosis in twins, in which ascertainment has been relatively unbiased and the cooperation of patients nearly complete. A total of 5463 patients attending 10 multiple sclerosis clinics across Canada were surveyed. Twenty-seven monozygotic and 43 dizygotic twin pairs were identified, and the diagnosis of multiple sclerosis was verified by examination and laboratory investigation. Seven of 27 monozygotic pairs (25.9 percent) and 1 of 43 dizygotic pairs (2.3 percent) were concordant for multiple sclerosis. The concordance rate for 4582 nontwin siblings of patients at two multiple sclerosis clinics was 1.9 percent, closely paralleling the concordance rate in dizygotic twins. To the extent that the difference in concordance rates between monozygotic and dizygotic twins indicates genetic susceptibility, the results of this study show a major genetic component in susceptibility to multiple sclerosis.
PMID: 3785335 [PubMed - indexed for MEDLINE]
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Cited by 44 PubMed Central articles
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Variants of ST8SIA1 are associated with risk of developing multiple sclerosis.
Husain S, Yildirim-Toruner C, Rubio JP, Field J, Southern MS Genetics Consortium, Schwalb M, Cook S, Devoto M, Vitale E.
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[PLoS One. 2008]
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Avasarala JR, Chittur SV, George AD, Tine JA.
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[BMC Med Genomics. 2008]
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Walsh KB, Lodoen MB, Edwards RA, Lanier LL, Lane TE.
J Virol. 2008 Mar; 82(6):3021-30. Epub 2007 Dec 19.
[J Virol. 2008]
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