Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/124630
Title: Genetic analysis of high bone mass cases from the BARCOS cohort of spanish postmenopausal women
Author: Sarrión Pérez-Caballero, Patricia
Mellivobsky, Leonardo
Urreizti Frexedas, Roser
Civit Vives, Sergi
Cols Coll, Neus
Garcia Giralt, Natàlia
Yoskovitz, Guy
Aranguren, Alvaro
Malouf, Jorge
Di Gregorio, Silvana
Río y Lara, Luis del
Güerri, Roberto
Nogués Solán, Xavier
Diez Pérez, Adolfo
Grinberg Vaisman, Daniel Raúl
Balcells Comas, Susana
Keywords: Ossos
Genètica molecular
Mutació (Biologia)
Bones
Molecular genetics
Mutation (Biology)
Issue Date: 15-Apr-2014
Publisher: Public Library of Science (PLoS)
Abstract: The aims of the study were to establish the prevalence of high bone mass (HBM) in a cohort of Spanish postmenopausal women (BARCOS) and to assess the contribution of LRP5 and DKK1 mutations and of common bone mineral density (BMD) variants to a HBM phenotype. Furthermore, we describe the expression of several osteoblast-specific and Wnt-pathway genes in primary osteoblasts from two HBM cases. A 0.6% of individuals (10/1600) displayed Z-scores in the HBM range (sum Z-score >4). While no mutation in the relevant exons of LRP5 was detected, a rare missense change in DKK1 was found (p.Y74F), which cosegregated with the phenotype in a small pedigree. Fifty-five BMD SNPs from Estrada et al. [NatGenet 44:491-501,2012] were genotyped in the HBM cases to obtain risk scores for each individual. In this small group of samples, Z-scores were found inversely related to risk scores, suggestive of a polygenic etiology. There was a single exception, which may be explained by a rare penetrant genetic variant, counterbalancing the additive effect of the risk alleles. The expression analysis in primary osteoblasts from two HBM cases and five controls suggested that IL6R, DLX3, TWIST1 and PPARG are negatively related to Z-score. One HBM case presented with high levels of RUNX2, while the other displayed very low SOX6. In conclusion, we provide evidence of lack of LRP5 mutations and of a putative HBM-causing mutation in DKK1. Additionally, we present SNP genotyping and expression results that suggest additive effects of several genes for HBM.
Note: Reproducció del document publicat a: https://doi.org/10.1371/journal.pone.0094607
It is part of: PLoS One, 2014, vol. 9, num. 4, p. 1-9
URI: http://hdl.handle.net/2445/124630
Related resource: https://doi.org/10.1371/journal.pone.0094607
ISSN: 1932-6203
Appears in Collections:Articles publicats en revistes (Genètica, Microbiologia i Estadística)

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