Chaowanee ChupeerachAnchalee TungtrongchitrBenjaluck PhonratFlorian J. SchweigertRungsunn TungtrongchitrSangchai PreutthipanMahidol UniversityUniversitat Potsdam2018-06-112018-06-112012-02-01Biomarkers in Medicine. Vol.6, No.1 (2012), 103-10817520371175203632-s2.0-84856609038https://repository.li.mahidol.ac.th/handle/123456789/13813Aims: To investigate the genetic markers for osteoporosis bone mineral density by the genotyping of rs7041, rs4588 and rs1352845 in the DBP gene with either bone mineral density or serum 25-hydroxycholecalciferol, retinol and α-tocopherol, among 365 postmenopausal Thai women. Materials & methods: The DBP genotypes were analyzed by a PCR restriction fragment-length polymorphism method. Serum 25-hydroxycholecalciferol was assessed using a commercial chemiluminescent immunoassay. Serum retinol and α-tocopherol were measured by reverse-phase high-performance liquid chromatography. Results: After adjustment for age > 50 years, elder Thai subjects with low BMI (≤25 kg/m 2 ) and carrying the rs4588 CC genotype had a higher risk of radial bone mineral density osteoporosis (odds ratio: 6.29; p = 0.048). The rs1352845 genotype also had a statistical association with total hip bone mineral density; however, it disappeared after adjustment for age and BMI. No association was found in fat-soluble vitamins with bone mineral density. Conclusion: DBP genotypes may influence the osteoporosis bone mineral density in postmenopausal Thai women. © 2012 Future Medicine Ltd.Mahidol UniversityBiochemistry, Genetics and Molecular BiologyMedicinePharmacology, Toxicology and PharmaceuticsAssociation of Thr420Lys polymorphism in DBP gene with fat-soluble vitamins and low radial bone mineral density in postmenopausal Thai womenArticleSCOPUS10.2217/bmm.11.88