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Rate of T alleles and TT genotype at MTHFR 677C->T locus or C alleles and CC genotype at MTHFR 1298A->C locus among healthy subjects in Turkey: Impact on homocysteine and folic acid status and reference intervals

dc.contributor.authorSucu, Derya Kaynak
dc.contributor.authorAslan, Diler
dc.contributor.buuauthorİlçöl, Yeşim Özarda
dc.contributor.buuauthorHızlı, Banu Zafer
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentBiyokimya Ana Bilim Dalı
dc.contributor.researcheridAAL-8873-2021
dc.contributor.scopusid35741320500
dc.contributor.scopusid14019332100
dc.date.accessioned2021-12-07T06:01:50Z
dc.date.available2021-12-07T06:01:50Z
dc.date.issued2009-12
dc.description.abstractMethylenetetrahydrofolate reductase (MTHFR) is important for folate and homocysteine (Hcy) metabolism. MTHFR 677C->T and 1298A->C MTHFR are two most common mutations which can affect. folate and total homocysteine (tHcy) status This study was designed to determine the rate of,MTHFR 677C->T and 1298A->C mutations. and their Influence Oil serum folate, Hcy and vitamin B12 Status and the reference intervals in 402 healthy Turkish adults. The rate of MTHFR 677C->T or 1298A->C mutations was 50 7% or 54 7%. respectively. The MTHFR 677C->T mutation-specific reference intervals for serum folate and tHcy were characterized by marked shifts in their upper limits In homozygote subjects for MTHFR 677C->T serum folate concentration was lower and serum tHcy concentration was higher than those in the wild genotype. all subjects had lower serum folate and 54% of the subjects had higher tHcy concentration,; than the cutoff Values of <= 10 nmol/L and >= 12 mu mol/L, respectively. Serum vitamin 1312 status was similar in all genotypes Serum tHcy concentrations were inversely correlated with serum folate and vitamin B12 concentrations in all genotypes These data show that the rate of MTHFR 677C->T and 1298A->C mutations is very high in Turks and serum folate and tHcy status are impaired by these mutations.
dc.identifier.citationİlçöl, Y. Ö. vd. (2009). "Rate of T alleles and TT genotype at MTHFR 677C->T locus or C alleles and CC genotype at MTHFR 1298A->C locus among healthy subjects in Turkey: Impact on homocysteine and folic acid status and reference intervals". Cell Biochemistry and Function, 27(8), 568-577.
dc.identifier.doi10.1002/cbf.1610
dc.identifier.endpage577
dc.identifier.issn0263-6484
dc.identifier.issue8
dc.identifier.pubmed19764044
dc.identifier.scopus2-s2.0-71949087027
dc.identifier.startpage568
dc.identifier.urihttps://doi.org/10.1002/cbf.1610
dc.identifier.urihttps://onlinelibrary.wiley.com/doi/10.1002/cbf.1610
dc.identifier.urihttp://hdl.handle.net/11452/23020
dc.identifier.volume27
dc.identifier.wos000272576800010
dc.indexed.wosSCIE
dc.language.isoen
dc.publisherWiley
dc.relation.bap2002/34
dc.relation.collaborationYurt içi
dc.relation.journalCell Biochemistry and Function
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectFolate
dc.subjectHomocysteine
dc.subjectMTHFR
dc.subjectMutations
dc.subjectReference intervals
dc.subjectTurkey
dc.subjectVitamin B12
dc.subjectMethylenetetrahydrofolate reductase gene
dc.subjectApproved recommendation 1987
dc.subjectCollected reference values
dc.subjectCoronary-artery-disease
dc.subject3rd national-health
dc.subjectPlasma homocysteine
dc.subjectCardiovascular-disease
dc.subjectCommon mutation
dc.subjectRisk-factor
dc.subjectStatistical treatment
dc.subjectBiochemistry & molecular biology
dc.subjectCell biology
dc.subject.emtree5,10 methylenetetrahydrofolate reductase (FADH2)
dc.subject.emtreeAlanine
dc.subject.emtreeCyanocobalamin
dc.subject.emtreeCysteine
dc.subject.emtreeFolic acid
dc.subject.emtreeHomocysteine
dc.subject.emtreeMethionine
dc.subject.emtreeThreonine
dc.subject.emtreeAdult
dc.subject.emtreeAllele
dc.subject.emtreeAmino acid blood level
dc.subject.emtreeArticle
dc.subject.emtreeControlled study
dc.subject.emtreeFemale
dc.subject.emtreeFolic acid blood level
dc.subject.emtreeGene locus
dc.subject.emtreeGene mutation
dc.subject.emtreeGenetic polymorphism
dc.subject.emtreeGenotype
dc.subject.emtreeHomozygote
dc.subject.emtreeHuman
dc.subject.emtreeHuman experiment
dc.subject.emtreeMale
dc.subject.emtreeMethylation
dc.subject.emtreeMutation rate
dc.subject.emtreeNormal human
dc.subject.emtreePriority journal
dc.subject.emtreeReference value
dc.subject.emtreeTurkey (republic)
dc.subject.emtreeVitamin blood level
dc.subject.emtreeVitamin metabolism
dc.subject.meshAdolescent
dc.subject.meshAdult
dc.subject.meshAlleles
dc.subject.meshFemale
dc.subject.meshFolic acid
dc.subject.meshGenotype
dc.subject.meshHealth status
dc.subject.meshHomocysteine
dc.subject.meshHumans
dc.subject.meshMale
dc.subject.meshMethylenetetrahydrofolate reductase (NADPH2)
dc.subject.meshMiddle aged
dc.subject.meshPoint mutation
dc.subject.meshTurkey
dc.subject.meshVitamin B 12
dc.subject.meshYoung adult
dc.subject.scopusClinical Chemistry; Thyrotropin; Nonparametric Methods
dc.subject.wosBiochemistry & molecular biology
dc.subject.wosCell biology
dc.titleRate of T alleles and TT genotype at MTHFR 677C->T locus or C alleles and CC genotype at MTHFR 1298A->C locus among healthy subjects in Turkey: Impact on homocysteine and folic acid status and reference intervals
dc.typeArticle
dc.wos.quartileQ4
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/Biyokimya Ana Bilim Dalı
local.indexed.atScopus
local.indexed.atWOS

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