Medizinische Universität Graz Austria/Österreich - Forschungsportal - Medical University of Graz
Gewählte Publikation:
SHR Neuro Krebs Kardio Lipid Stoffw Microb
Trummer, O; Schwetz, V; Walter-Finell, D; Lerchbaum, E; Renner, W; Gugatschka, M; Dobnig, H; Pieber, TR; Obermayer-Pietsch, B.
Allelic Determinants of Vitamin D Insufficiency, Bone Mineral Density, and Bone Fractures.
J Clin Endocrinol Metab. 2012; 97(7): E1234-E1240.
Doi: 10.1210/jc.2011-3088
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- Führende Autor*innen der Med Uni Graz
- Obermayer-Pietsch Barbara
- Trummer Olivia
- Co-Autor*innen der Med Uni Graz
- Dobnig Harald
- Gugatschka Markus
- Lerchbaum Elisabeth
- Pieber Thomas
- Renner Wilfried
- Theiler-Schwetz Verena
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- Abstract:
- Context: Low 25-hydroxycholecalciferol [25(OH) vitamin D] status is known to play an important role in many diseases with focus on bone health. Objective: Based on recently reported genetic determinants of vitamin D insufficiency, we aimed to analyze genetic variants of group-specific component (GC), 7-dehydrocholesterol reductase (DHCR7), and cytochrome P450IIR-1 (CYP2R1) for association with vitamin D levels, bone mineral density (BMD), and bone fractures. Design: We conducted a cross-sectional BMD and fracture study and a prospective cohort study. Setting: The cross-sectional study comprised participants of a BMD screening study, and the prospective cohort study comprised nursing home subjects. Patients: The cross-sectional study included 342 subjects (mean age, 55.3 +/- 12.0 yr), and the prospective study included 1093 subjects (mean age, 84.0 +/- 6.0 yr). Interventions: Patients were stratified by GC, DHCR7, and CYP2R1 genotypes. For each gene, the allele associated with lower 25(OH) vitamin D levels was designated as "risk allele." The potential role of these risk alleles in fracture risk was analyzed by logistic regression analysis including age and sex as confounders. Main Outcome Measures: We measured BMD and fractures. Results: GC genotypes were significantly associated with lower mean 25(OH) vitamin D levels in both cohorts (P = 0.001 and P = 0.048, respectively). There was no significant association of BMD with any of the genotypes. None of the alleles was associated with past fractures, whereas the DHCR7 G-allele was significantly associated with prospective fractures (odds ratio, 0.68; 95% confidence interval, 0.51-0.92; P = 0.011). Conclusions: The DHCR7 gene polymorphism may be a predictor for fracture risk. (J Clin Endocrinol Metab 97: E1234-E1240, 2012)
- Find related publications in this database (using NLM MeSH Indexing)
- Adolescent -
- Adult -
- Aged -
- Aged, 80 and over -
- Algorithms -
- Alleles -
- Alleles - epidemiology
- Bone Density - genetics Bone Density - physiology
- Cohort Studies -
- Cross-Sectional Studies -
- Female -
- Fractures, Bone - blood Fractures, Bone - epidemiology Fractures, Bone - etiology Fractures, Bone - genetics
- Genetic Association Studies -
- Genetic Predisposition to Disease -
- Humans -
- Male -
- Middle Aged -
- Vitamin D Deficiency - blood Vitamin D Deficiency - complications Vitamin D Deficiency - epidemiology Vitamin D Deficiency - genetics
- Young Adult -