An atlas of genetic determinants of forearm fracture

Author:

Nethander MariaORCID,Movérare-Skrtic SofiaORCID,Kämpe AndersORCID,Coward Eivind,Reimann EneORCID,Grahnemo LouiseORCID,Borbély Éva,Helyes Zsuzsanna,Funck-Brentano Thomas,Cohen-Solal MartineORCID,Tuukkanen JuhaORCID,Koskela Antti,Wu Jianyao,Li Lei,Lu TianyuanORCID,Gabrielsen Maiken E.,Mägi ReedikORCID,Hoff Mari,Lerner Ulf H.,Henning Petra,Ullum Henrik,Erikstrup ChristianORCID,Brunak SørenORCID,Langhammer ArnulfORCID,Tuomi TiinamaijaORCID,Oddsson AsmundurORCID,Stefansson Kari,Pettersson-Kymmer Ulrika,Ostrowski Sisse RyeORCID,Pedersen Ole Birger VesteragerORCID,Styrkarsdottir Unnur,Mäkitie OutiORCID,Hveem Kristian,Richards J. BrentORCID,Ohlsson ClaesORCID, ,

Abstract

AbstractOsteoporotic fracture is among the most common and costly of diseases. While reasonably heritable, its genetic determinants have remained elusive. Forearm fractures are the most common clinically recognized osteoporotic fractures with a relatively high heritability. To establish an atlas of the genetic determinants of forearm fractures, we performed genome-wide association analyses including 100,026 forearm fracture cases. We identified 43 loci, including 26 new fracture loci. Although most fracture loci associated with bone mineral density, we also identified loci that primarily regulate bone quality parameters. Functional studies of one such locus, at TAC4, revealed that Tac4/ mice have reduced mechanical bone strength. The strongest forearm fracture signal, at WNT16, displayed remarkable bone-site-specificity with no association with hip fractures. Tall stature and low body mass index were identified as new causal risk factors for fractures. The insights from this atlas may improve fracture prediction and enable therapeutic development to prevent fractures.

Publisher

Springer Science and Business Media LLC

Subject

Genetics

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