Genetic Contribution of Femoral Neck Bone Geometry to the Risk of Developing Osteoporosis: A Family-Based Study

被引:4
作者
Hernandez-de Sosa, Nerea [1 ]
Athanasiadis, Georgios [2 ,3 ]
Malouf, Jorge [1 ]
Laiz, Ana [1 ]
Marin, Ana [1 ]
Herrera, Silvia [1 ]
Farrerons, Jordi [1 ]
Soria, Jose Manuel [2 ]
Casademont, Jordi [1 ]
机构
[1] Univ Autonoma Barcelona, Hosp Santa Creu & St Pau, Dept Internal Med, E-08193 Barcelona, Spain
[2] Hosp Santa Creu & Sant Pau, Res Inst, Dept Genom Complex Dis, Barcelona, Spain
[3] Aarhus Univ, Bioinformat Res Ctr, Aarhus, Denmark
关键词
GENOME-WIDE ASSOCIATION; MINERAL DENSITY; HIP FRACTURE; LINKAGE ANALYSIS; PHOTON-ABSORPTIOMETRY; POSTMENOPAUSAL WOMEN; GENDER-DIFFERENCES; NUCLEAR FAMILIES; STRENGTH; MEN;
D O I
10.1371/journal.pone.0154833
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Femoral neck geometry parameters are believed to be as good as bone mineral density as independent factors in predicting hip fracture risk. This study was conducted to analyze the roles of genetic and environmental factors in femoral properties measured in a sample of Spanish families with osteoporotic fractures and extended genealogy. The "Genetic Analysis of Osteoporosis (GAO) Project" involved 11 extended families with a total number of 376 individuals. We studied three categorical phenotypes of particular clinical interest and we used a Hip structural analysis based on DXA to analyze 17 strength and geometrical phenotypes of the hip. All the femoral properties had highly significant heritability, ranging from 0.252 to 0.586. The most significant correlations were observed at the genetic level (rho(G)). Osteoporotic fracture status (Affected 2) and, particularly, low bone mass and osteoporotic condition (Affected 3) had the highest number of significant genetic correlations with diverse femoral properties. In conclusion, our findings suggest that a relatively simple and easy to use method based on DXA studies can provide useful data on properties of the Hip in clinical practice. Furthermore, our results provide a strong motivation for further studies in order to improve the understanding of the pathophysiological mechanism underlying bone architecture and the genetics of osteoporosis.
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页数:13
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