TY - JOUR
T1 - Genome-wide association identifies three new susceptibility loci for Paget's disease of bone
AU - Albagha, Omar M.E.
AU - Wani, Sachin E.
AU - Visconti, Micaela R.
AU - Alonso, Nerea
AU - Goodman, Kirsteen
AU - Brandi, Maria Luisa
AU - Cundy, Tim
AU - Chung, Pui Yan Jenny
AU - Dargie, Rosemary
AU - Devogelaer, Jean Pierre
AU - Falchetti, Alberto
AU - Fraser, William D.
AU - Gennari, Luigi
AU - Gianfrancesco, Fernando
AU - Hooper, Michael J.
AU - Van Hul, Wim
AU - Isaia, Gianluca
AU - Nicholson, Geoff C.
AU - Nuti, Ranuccio
AU - Papapoulos, Socrates
AU - Montes, Javier Del Pino
AU - Ratajczak, Thomas
AU - Rea, Sarah L.
AU - Rendina, Domenico
AU - Gonzalez-Sarmiento, Rogelio
AU - Di Stefano, Marco
AU - Ward, Lynley C.
AU - Walsh, John P.
AU - Ralston, Stuart H.
PY - 2011/7
Y1 - 2011/7
N2 - Paget's disease of bone (PDB) is a common disorder characterized by focal abnormalities of bone remodeling. We previously identified variants at the CSF1, OPTN and TNFRSF11A loci as risk factors for PDB by genome-wide association study. Here we extended this study, identified three new loci and confirmed their association with PDB in 2,215 affected individuals (cases) and 4,370 controls from seven independent populations. The new associations were with rs5742915 within PML on 15q24 (odds ratio (OR) = 1.34, P = 1.6 × 10 -14), rs10498635 within RIN3 on 14q32 (OR = 1.44, P = 2.55 × 10-11) and rs4294134 within NUP205 on 7q33 (OR = 1.45, P = 8.45 × 10-10). Our data also confirmed the association of TM7SF4 (rs2458413, OR = 1.40, P = 7.38 × 10-17) with PDB. These seven loci explained μ13% of the familial risk of PDB. These studies provide new insights into the genetic architecture and pathophysiology of PDB.
AB - Paget's disease of bone (PDB) is a common disorder characterized by focal abnormalities of bone remodeling. We previously identified variants at the CSF1, OPTN and TNFRSF11A loci as risk factors for PDB by genome-wide association study. Here we extended this study, identified three new loci and confirmed their association with PDB in 2,215 affected individuals (cases) and 4,370 controls from seven independent populations. The new associations were with rs5742915 within PML on 15q24 (odds ratio (OR) = 1.34, P = 1.6 × 10 -14), rs10498635 within RIN3 on 14q32 (OR = 1.44, P = 2.55 × 10-11) and rs4294134 within NUP205 on 7q33 (OR = 1.45, P = 8.45 × 10-10). Our data also confirmed the association of TM7SF4 (rs2458413, OR = 1.40, P = 7.38 × 10-17) with PDB. These seven loci explained μ13% of the familial risk of PDB. These studies provide new insights into the genetic architecture and pathophysiology of PDB.
UR - http://www.scopus.com/inward/record.url?scp=79959745220&partnerID=8YFLogxK
U2 - 10.1038/ng.845
DO - 10.1038/ng.845
M3 - Article
C2 - 21623375
AN - SCOPUS:79959745220
SN - 1061-4036
VL - 43
SP - 685
EP - 689
JO - Nature Genetics
JF - Nature Genetics
IS - 7
ER -