Your browser doesn't support javascript.
loading
Strong Genetic Effects on Bone Mineral Density in Multiple Locations with Two Different Techniques: Results from a Cross-Sectional Twin Study.
Piroska, Marton; Tarnoki, David Laszlo; Szabo, Helga; Jokkel, Zsofia; Meszaros, Szilvia; Horvath, Csaba; Tarnoki, Adam Domonkos.
Afiliação
  • Piroska M; Medical Imaging Centre, Faculty of Medicine, Semmelweis University, 1082 Budapest, Hungary.
  • Tarnoki DL; Medical Imaging Centre, Faculty of Medicine, Semmelweis University, 1082 Budapest, Hungary.
  • Szabo H; Hungarian Twin Registry, 1082 Budapest, Hungary.
  • Jokkel Z; Medical Imaging Centre, Faculty of Medicine, Semmelweis University, 1082 Budapest, Hungary.
  • Meszaros S; Central Radiological Diagnostic Department, Medical Centre Hungarian Defence Forces, 1134 Budapest, Hungary.
  • Horvath C; Medical Imaging Centre, Faculty of Medicine, Semmelweis University, 1082 Budapest, Hungary.
  • Tarnoki AD; Department of Internal Medicine and Oncology, Faculty of Medicine, Semmelweis University, 1085 Budapest, Hungary.
Medicina (Kaunas) ; 57(3)2021 Mar 08.
Article em En | MEDLINE | ID: mdl-33800136
ABSTRACT
Background and

Objectives:

Previous studies have demonstrated that risk of hip fracture is at least partly heritable. The aim of this study was to determine the magnitude of the genetic component of bone mineral density (BMD), using both X-ray and ultrasound assessment at multiple sites. Materials and

Methods:

216 adult, healthy Hungarian twins (124 monozygotic, MZ, 92 dizygotic, DZ; mean age 54.2 ± 14.3 years), recruited from the Hungarian Twin Registry with no history of oncologic disease underwent cross-sectional BMD studies. We measured BMD, T- and Z-scores with dual energy X-ray absorptiometry (DEXA) at multiple sites (lumbar spine, femoral neck, total hip and radius). Quantitative bone ultrasound (QUS) was also performed, resulting in a calculated value of estimated bone mineral density (eBMD) in the heel bone. Heritability was calculated using the univariate ACE model.

Results:

Bone density had a strong genetic component at all sites with estimates of heritability ranging from 0.613 to 0.838 in the total sample. Lumbar BMD and calcaneus eBMD had major genetic components with estimates of 0.828 and 0.838 respectively, and least heritable (0.653) at the total hip. BMD of the radius had also a strong genetic component with an estimate of 0.806. No common environmental effect was found. The remaining variance was influenced by unique environment (0.162 to 0.387). In females only, slightly higher additive genetic estimates were found, especially in the case of the femoral neck and total hip.

Conclusion:

Bone mineral density is strongly heritable, especially in females at all locations using both DEXA and QUS, which may explain the importance of family history as a risk factor for bone fractures. Unshared environmental effects account for the rest of the variance with slight differences in magnitude across various bone regions, supporting the role of lifestyle in preventing osteoporotic fractures with various efficacy in different bone regions.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Calcâneo / Densidade Óssea Tipo de estudo: Diagnostic_studies / Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Middle aged Idioma: En Revista: Medicina (Kaunas) Assunto da revista: MEDICINA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Hungria

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Calcâneo / Densidade Óssea Tipo de estudo: Diagnostic_studies / Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Middle aged Idioma: En Revista: Medicina (Kaunas) Assunto da revista: MEDICINA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Hungria