Literature DB >> 24334171

Linkage and association analyses using families identified a locus affecting an osteoporosis-related trait.

Georgios Athanasiadis1, Jorge Malouf2, Nerea Hernandez-Sosa2, Laura Martin-Fernandez1, Marta Catalan1, Jordi Casademont2, Jose Manuel Soria3.   

Abstract

Osteoporosis is a common disorder characterized by low bone mass and microarchitectural deterioration of bone tissue, resulting in an increase in bone fragility and in susceptibility to fractures. The genetic basis of osteoporosis is complex and involves multiple genes and environmental factors. Here we introduce a family-based study of the genetics of osteoporosis - the Genetic Analysis of Osteoporosis (GAO) Project - to discover genetic variants affecting osteoporosis-related phenotypes. The GAO Project involved 11 extended families from Barcelona, Spain selected through a proband with osteoporosis (N=367). We performed spine, femur and whole body densitometry for all participants and also analyzed strength and geometrical properties of the hip. Our study focused on 23 densitometric phenotypes that we considered of high clinical relevance and four definitions of low bone mass and fracture status. Pedigree validation was carried out through microsatellite genotyping. The same microsatellites were used to interrogate our data (i) for the replication of previous linkage signals and (ii) for the potential discovery of new linkage signals. The linkage analysis identified one region marked by microsatellite D17S787 showing a strong and significant signal of linkage with femoral shaft cross-sectional moment of inertia (CSMI; LOD=3.18; p=6.5×10(-5)). The chromosomal location marked by microsatellite D17S787 includes several genes, among which two are of particular interest: COL1A1 and SOST, coding for collagen alpha-1 (I) chain and sclerostin, respectively. Follow-up association analysis resulted in only one significant result for rs4792909 from the SOST genomic region (p=0.00248). As a result, we provide strong and significant evidence from both linkage and association analyses that the SOST gene may affect the strength of the femoral shaft. Future investigations should study the relationship between bone mass formation and strength properties of the bones.
Copyright © 2013 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Association; Bone mineral density; Dual energy X-ray absorptiometry; Linkage; Osteoporosis

Mesh:

Year:  2013        PMID: 24334171     DOI: 10.1016/j.bone.2013.12.010

Source DB:  PubMed          Journal:  Bone        ISSN: 1873-2763            Impact factor:   4.398


  3 in total

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

Authors:  Nerea Hernandez-de Sosa; Georgios Athanasiadis; Jorge Malouf; Ana Laiz; Ana Marin; Silvia Herrera; Jordi Farrerons; Jose Manuel Soria; Jordi Casademont
Journal:  PLoS One       Date:  2016-05-10       Impact factor: 3.240

2.  Identification of candidate genes in osteoporosis by integrated microarray analysis.

Authors:  J J Li; B Q Wang; Q Fei; Y Yang; D Li
Journal:  Bone Joint Res       Date:  2016-12       Impact factor: 5.853

3.  Spitting for Science: Danish High School Students Commit to a Large-Scale Self-Reported Genetic Study.

Authors:  Georgios Athanasiadis; Frank G Jørgensen; Jade Y Cheng; Peter C Kjærgaard; Mikkel H Schierup; Thomas Mailund
Journal:  PLoS One       Date:  2016-08-29       Impact factor: 3.240

  3 in total

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