Please use this identifier to cite or link to this item: http://cuir.car.chula.ac.th/handle/123456789/61831
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dc.contributor.authorMananya Techapatiphandee-
dc.contributor.authorNattapol Tammachote-
dc.contributor.authorRachaneekorn Tammachote-
dc.contributor.authorAnna Wongkularb-
dc.contributor.authorPattamawadee Yanatatsaneejit-
dc.contributor.otherChulalongkorn University. Faculty of Science-
dc.date.accessioned2019-05-15T10:52:59Z-
dc.date.available2019-05-15T10:52:59Z-
dc.date.issued2018-08-01-
dc.identifier.citationBiomedical Reports. Vol.9, Issue 4 (Oct, 2018), p.350-356en_US
dc.identifier.issn2049-9434 (Print)-
dc.identifier.issn2049-9442 (Online)-
dc.identifier.urihttp://cuir.car.chula.ac.th/handle/123456789/61831-
dc.description.abstractDetermining molecular markers for osteoporosis may be valuable for improving the quality of life of affected elderly patients by aiding in early detection and disease management. In the present study, the association between single nucleotide polymorphisms (SNPs) of the vitamin D receptor (VDR) and tumour necrosis factor superfamily number 11 (TNFSF11) genes and the susceptibility of developing osteoporosis was investigated in a Thai female cohort. The study group consisted of 105 Thai postmenopausal patients diagnosed with osteoporosis and 132 healthy Thai postmenopausal female volunteers. DNA extracted from blood samples was used to genotype the VDR and TNFSF11 genes using polymerase chain reaction‑restriction fragment length polymorphism and sequencing analysis. For VDR, the frequencies of the genotypes TT, CT and CC for the TaqI SNP (rs731236) were 87.88, 11.36 and 0.76%, respectively, in the control group, while in the osteoporosis cohort were 92.38, 5.71 and 1.91%, respectively. For the FokI SNP (rs2228570), the frequencies of the genotypes CC, CT and TT were 31.06, 55.30 and 13.64%, respectively, in the control group, and in the osteoporosis group were 29.52, 43.81 and 26.67%, respectively. For BsmI SNP (rs1544410), the frequencies of the genotypes GG, GA and AA were 78.03, 18.94 and 3.03%, respectively, in control group, and in the osteoporosis group were 80.95, 18.10 and 0.95%, respectively. The significant risk of osteoporosis associated with the FokI SNP was determined. The odds ratio (95% confidence interval) was 2.30 (1.14‑4.69; P=0.01) among patients with osteoporosis with TT as the susceptibility genotype. For TNFSF11, the frequencies of the genotypes TT, CT and CC for the ‑290C>T SNP (rs9525641) in the control group were 36.36, 50.76 and 12.88%, respectively, while in the osteoporosis group were 31.43, 56.19 and 12.38%, respectively. For the ‑643C>T SNP (rs9533156), the frequencies of the genotypes TT, CT and CC in the control group were 35.61, 48.48 and 15.91%, respectively, while in the osteoporosis group were 32.38, 55.24 and 12.38%, respectively. For the ‑693G>C SNP (rs9533155), the frequencies of the genotypes CC, CG, and GG in the control group were 39.39, 46.97 and 13.64%, respectively, and in the osteoporosis group were 36.19, 53.33 and 10.48%, respectively. No significant associations of the TNFSF11 SNPs with osteoporosis were determined; however, it was notable that the GCT haplotype of TNFSF11 may be a protective haplotype for osteoporosis. Therefore, it was concluded that the SNP FokI of VDR may be a potential molecular biomarker for the development of osteoporosis in Thai females.en_US
dc.language.isoenen_US
dc.publisherSpandidos Publicationsen_US
dc.relation.urihttps://doi.org/10.3892/br.2018.1137-
dc.relation.urihttps://www.spandidos-publications.com/10.3892/br.2018.1137-
dc.rights© Spandidos Publications UK Ltden_US
dc.titleVDR and TNFSF11 polymorphisms are associated with osteoporosis in Thai patientsen_US
dc.typeArticleen_US
dc.email.authorNo information provided-
dc.email.authorNo information provided-
dc.email.authorRatchaneekorn.T@Chula.ac.th-
dc.email.authorNo information provided-
dc.email.authorPattamawadee.Y@Chula.ac.th-
dc.subject.keywordosteoporosisen_US
dc.subject.keywordpostmenopauseen_US
dc.subject.keywordvitamin D receptoren_US
dc.subject.keywordtumour necrosis factor superfamily member 11en_US
dc.subject.keywordgenotypingen_US
dc.identifier.DOI10.3892/br.2018.1137-
Appears in Collections:Chula Scholars - 2018

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