Genetic Association of Multiple Sclerosis with the Marker rs391745 near the Endogenous Retroviral Locus HERV-Fc1 Analysis of Disease Subtypes 英文参考文献.docVIP
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Genetic Association of Multiple Sclerosis with the Marker rs391745 near the Endogenous Retroviral Locus HERV-Fc1 Analysis of Disease Subtypes 英文参考文献
GeneticAssociationofMultipleSclerosiswiththeMarker
rs391745neartheEndogenousRetroviralLocusHERV-
Fc1:AnalysisofDiseaseSubtypes
BettinaHansen1,AnnetteB.Oturai2,HanneF.Harbo3,4,ElisabethG.Celius3,KariK.Nissen1,
MagdalenaJ.Laska1,HelleB.S?ndergaard2,ThorPetersen5,Bj?rnA.Nex?1*
1Department of Biomedicine, Aarhus University, Aarhus C, Denmark, 2Danish Multiple Sclerosis Center, Department of Neurology, Copenhagen University Hospital
Rigshospitalet, Copenhagen, Denmark, 3Department of Neurology, Oslo University Hospital, Oslo, Norway, 4Institute of Clinical Medicine, University of Oslo, Oslo,
Norway,5Neurology,AarhusUniversityHospital,AarhusC,Denmark
Abstract
We have previously described the occurrence of multiple sclerosis (MS) to be associated with human endogenous
retroviruses,specificallytheX-linkedvirallocusHERV-Fc1.Theaimofthisstudywastoinvestigateapossibleassociationof
theHERV-Fc1locuswithsubtypesofMS.MSpatientsaregenerallysubdividedintothreecategories:Remitting/Relapsing
andSecondaryProgressive,whichtogetherconstituteBoutOnsetMS,andPrimaryProgressive.Inthisstudyof1181MS
patientsand1886controlswefoundthatBoutOnsetMSwasassociatedwiththeC-alleleofthemarkerrs391745nearthe
HERV-Fc1 locus (p=0.003), while primary progressive disease was not. The ability to see genetic differences between
subtypesofMSnearthisgenespeaksfortheinvolvementofthevirusHERV-Fc1locusinmodifyingthediseasecourseof
MS.
Citation: Hansen B, Oturai AB, Harbo HF, Celius EG, Nissen KK, et al. (2011) Genetic Association of Multiple Sclerosis with the Marker rs391745 near the
EndogenousRetroviralLocusHERV-Fc1:AnalysisofDiseaseSubtypes.PLoSONE6(10):e26438.doi:10.1371/journal.pone.0026438
Editor:WelkinE.Johnson,HarvardMedicalSchool,UnitedStatesofAmerica
ReceivedJuly25,2011;AcceptedSeptember27,2011;PublishedOctober25,2011
Copyright: ? 2011 Hansen et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits
unrestricteduse,distribution,andreprod
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