Clinical Medicine III. Posters
Dr. Piroska, Márton
Semmelweis University, Medical Imaging Centre
+36205491303
piroskamarton94@gmail.com
Cross Sectional Twin Study Shows Significant Heritability in the Background of Bone Mineral Density
Marton Piroska1, Zsofia Jokkel1, Helga Szabo1, Szilvia Meszaros3, Csaba Horvath3, David Laszlo Tarnoki1,2, Adam Domonkos Tarnoki1,2
1 Medical Imaging Centre, Semmelweis University, Budapest, Hungary
2 Hungarian Twin Registry, Budapest, Hungary
3 1st Department of Internal Medicine, Semmelweis University, Budapest, Hungary
Clinical Medicine III. Posters
English
Clinical Medicine
Theoretical and Translational Medicine
Purpose: Previous studies have demonstrated that risk of hip fracture is heritable. The aim of this study was to determine the genetic component of bone mineral density (BMD), using both X-ray and ultrasound assessment at multiple sites.
Methods and Materials: 160 adult, healthy Hungarian twins (97 monozygotic, MZ, 62 dizygotic, DZ; mean age 50.6±14.7 years), recruited from the Hungarian Twin Registry with no history of oncologic disease underwent cross sectional BMD studies in 2019. We measured X-ray BMD at multiple sites (lumbar spine, femur, hip and radius), whileas broadband ultrasound attenuation of the calcaneus was also determined. Heritability was calculated using univariate ACE model.
Results: Bone density had a strong genetic component at all sites with estimates of heritability ranging from 0.619 to 0.829. Lumbar and calcaneus BMD had major genetic components with estimates of 0.828 and 0.829 respectively, and least heritable (0.619) at femur. Broadband ultrasound attenuation at calcaneus had also a strong genetic component with an estimate of 0.816. No common environmental effect was found. The remaining variance was influenced by unique environment (0.171 to 0.381).
Conclusion: Bone mineral density is strongly heritable at all sights which may explain the importance of family history as a risk factor for bone fractures. Our results might stimulate further studies in family risk based osteoporosis screening.
Semmelweis University STIA fund was received for this work.
The local ethical committee approved the study (approval number: 189-4/2014). All participants gave informed consent.
Supervisor: Dr Tárnoki Ádám
E-mail address: tarnoki2@gmail.com
Szóbeli
Szabad
elfogadva
poszter
nem rendelkezett róla
4777
12:43
12:46
Marton Piroska1, Zsofia Jokkel1, Helga Szabo1, Szilvia Meszaros3, Csaba Horvath3, David Laszlo Tarnoki1,2, Adam Domonkos Tarnoki1,2
1 Medical Imaging Centre, Semmelweis University, Budapest, Hungary
2 Hungarian Twin Registry, Budapest, Hungary
3 1st Department of Internal Medicine, Semmelweis University, Budapest, Hungary