@article{ChupeerachHarnroongrojPhonratetal.2011,
  author    = {Chupeerach, Chaowanee and Harnroongroj, Talabporn and Phonrat, Benjaluck and Tungtrongchitr, Anchalee and Schweigert, Florian J. and Tungtrongchitr, Rungsunn and Preutthipan, Sangchai},
  title     = {Decreased retinol transport proteins in thai post-menopausal women with Osteporosis},
  series = {The Southeast Asian journal of tropical medicine and public health : official publication of the SEAMEO Regional Tropical Medicine and Public Health Project (TROPMED)},
  volume    = {42},
  journal   = {The Southeast Asian journal of tropical medicine and public health : official publication of the SEAMEO Regional Tropical Medicine and Public Health Project (TROPMED)},
  number    = {6},
  publisher = {SEAMEO},
  address   = {Bangkok},
  issn      = {0125-1562},
  pages     = {1515 -- 1520},
  year      = {2011},
  abstract  = {High vitamin A ingestion or high serum retinol have been postulated to increase the risk of fractures and osteoporosis by reduced bone mineral density (BMD). Retinol is carried and transported to the tissues bound to retinol binding protein 4 (RBP4) and transthyretin (TTR). The relationships between retinol, retinol transport protein, retinol binding protein 4 (RBP4) and transthyretin (TTR) and BMD and osteoporosis are unclear. To examine the association between retinol and RBP4 and TTR and osteoporosis, 73 osteoporotic and 71 normal Thai postmenopausal women were studied. RBP4 and retinol levels did not differ between the groups. Serum TTR was significantly higher in control than osteoporotic subjects (89.47 and 144.53 mu g/ml, respectively, p=0.003, Mann-Whitney U test). TTR was positively correlated with BMD at several sites, such as the total radius bone (r=0.172, p=0.008, Spearman rank test). Osteoporosis risk was analyzed with binary logistic regression. Lean elderly Thais with lower TTR levels had a higher risk of osteoporosis. RBP4 and retinol levels had no relationship with disease status among Thai post-menopausal women. These results suggest calcium, minerals, vitamins and the retinol transport protein, transthyretin may be involved in the pathogenesis of osteoporosis.},
  language  = {en}
}
@article{ChupeerachTungtrongchitrPhonratetal.2012,
  author    = {Chupeerach, Chaowanee and Tungtrongchitr, Anchalee and Phonrat, Benjaluck and Schweigert, Florian J. and Tungtrongchitr, Rungsunn and Preutthipan, Sangchai},
  title     = {Association of Thr420Lys polymorphism in DBP gene with fat-soluble vitamins and low radial bone mineral density in postmenopausal Thai women},
  series = {Biomarkers in medicine},
  volume    = {6},
  journal   = {Biomarkers in medicine},
  number    = {1},
  publisher = {Future Medicine},
  address   = {London},
  issn      = {1752-0363},
  doi       = {10.2217/BMM.11.88},
  pages     = {103 -- 108},
  year      = {2012},
  abstract  = {Aims: 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 alpha-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 alpha-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.},
  language  = {en}
}