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Association of VDBP rs4701 Variant, but not VDR/RXR-α Over-Expression with Bone Mineral Density in Pediatric Well-Chelated ß-Thalassemia Patients.
Sahmoud, Shaimaa; Ibrahim, Mostafa S; Toraih, Eman A; Kamel, Noha; Fawzy, Manal S; Elfiky, Samar.
Afiliação
  • Sahmoud S; Pediatric Department, Faculty of Medicine, Suez Canal University, Ismailia, Egypt.
  • Ibrahim MS; Diagnostic Radiology Department, Faculty of Medicine, Suez Canal University, Ismailia, Egypt.
  • Toraih EA; Genetics Unit, Histology and Cell Biology Department, Faculty of Medicine, Suez Canal University, Ismailia, Egypt.
  • Kamel N; Department of Surgery, Tulane University, School of Medicine, New Orleans, Louisiana, USA.
  • Fawzy MS; Clinical Pathology Department, Faculty of Medicine, Suez Canal University, Ismailia, Egypt.
  • Elfiky S; Medical Biochemistry and Molecular Biology Department, Faculty of Medicine, Suez Canal University, Ismailia, Egypt.
Mediterr J Hematol Infect Dis ; 12(1): e2020037, 2020.
Article em En | MEDLINE | ID: mdl-32670515
BACKGROUND: The reduced rate of bone formation despite the availability of vitamin D has been reported in ß-thalassemia. Genetic factors, together with environmental ones, could be implicated in this condition. Since vitamin D binding protein (VDBP) maintains bioavailability of vitamin D which binds to vitamin D receptor (VDR)-retinoid X receptor alpha (RXRA) heterodimer to exert its molecular actions, we speculated that vitamin D metabolic-axis expression signature and variants could be potential molecular candidates for bone turnover/disease in thalassemia. To this end, this study aims to analyze VDR/RXRA expression signature, and two VDBP variants in a pilot sample of Egyptian ß-thalassemia children in correlation with bone mineral density (BMD). PATIENTS AND METHODS: Forty-four well-chelated ß-thalassemia children and 40 unrelated controls were enrolled. The serum bone chemistry profile was measured. Peripheral blood mononuclear cells (PBMN) VDR/RXRA expression levels were quantified by Real-Time quantitative reverse transcription-polymerase chain reaction (qRT-PCR). VDBP rs7041 and rs4588 variants were identified by Real-Time allelic discrimination assay. All patients were subjected to lumbar-spine Dual-energy X-ray absorptiometry (DEXA). RESULTS: VDR/RXRA expressions were significantly higher in ß-thalassemia children compared to controls (P = 0.001 and <0.001, respectively) and showed higher values in ß-thalassemia major relative to ß-thalassemia intermedia. Expression levels of both genes were not associated with sex or BMD. However, VDBP rs4701 genotyping revealed lower BMD-L4 and a higher frequency of osteoporosis. CONCLUSIONS: ß-Thalassemia children had higher expression levels of PBMN VDR/RXRA. VDBP rs4701 variant was associated with osteoporosis in our ß-thalassemia patients on vitamin D supplementation. Further large-scale studies in other ethnic populations are warranted.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Mediterr J Hematol Infect Dis Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Mediterr J Hematol Infect Dis Ano de publicação: 2020 Tipo de documento: Article