Analysis of Inducible Nitric Oxide Synthase Gene Polymorphisms in Vitiligo in Han Chinese People 英文参考文献.docVIP
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Analysis of Inducible Nitric Oxide Synthase Gene Polymorphisms in Vitiligo in Han Chinese People 英文参考文献
AnalysisofInducibleNitricOxideSynthaseGene
PolymorphismsinVitiligoinHanChinesePeople
YingZhang,ChunyingLi*,KaiLi,LingLiu,ZheJian,TianwenGao*
DepartmentofDermatology,XijingHospital,TheFourthMilitaryMedicalUniversity,Xi’an,China
Abstract
Background:Vitiligoisachronicdepigmentedskindisorderwithregionalmelanocytesdepletion.Thepathogenesiswas
notcompletelyclarified.Recently,moreandmoreevidencesuggestedthatpolymorphismsofsomegenesareassociated
with vitiligo risk. Here, we want to examine the association between the inducible nitric oxide synthase (iNOS) gene
polymorphismsandtheriskofvitiligoinChinesepopulations.
MethodsandPrincipalFindings:Inahospital-basedcase-controlstudyof749patientswithvitiligoand763age-andsex-
matchedhealthycontrols,threepolymorphismsofiNOSgeneweregenotypedbyusingthePCR-restrictionfragmentlength
polymorphism (PCR-RFLP) and mutagenically separated PCR (MS-PCR) methods, respectively. We found the iNOS-954
polymorphism was associated with a significantly higher risk of vitiligo (adjusted OR=1.36, 95% CI=1.02–1.81).
Furthermore,thisassociationismorepronouncedinvulgarisvitiligo,activevitiligoandvitiligowithoutotherautoimmune
diseasesinthestratificationstudy.AnalysisofhaplotypesshowedincreasedriskfortheC
C
C
(OR=1.44,95%
-1173
-954
Ex16+14
CI=1.01–1.74).Inaddition,theserumiNOSactivityissignificantlyassociatedwithiNOS-954combinedgenotype(GC+CC)
andismuchhigherinvitiligopatientsthaninthecontrols(P,0.01).LogisticregressionanalysisofiNOSactivityshowed
increasedriskbetweenhigheractivityandiNOS-954GRCvariantgenotypecarriers(Ptrend,0.001).
ConclusionsandSignificance:INOSgenepolymorphismsmayplayanimportantroleinthegeneticsusceptibilitytothe
developmentofvitiligo.
Citation:ZhangY,LiC,LiK,LiuL,JianZ,etal.(2011)AnalysisofInducibleNitricOxideSynthaseGenePolymorphismsinVitiligoinHanChinesePeople.PLoS
ONE6(12):e27077.doi:10.1371/journal.pone.0027077
Editor:PaulWrede,Charite′-Universita¨tsmedizin Berlin,Germany
ReceivedApril14,2011;AcceptedOctober10,2011;PublishedDe
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