Details

Autor(en) / Beteiligte

• ALBAGHA, Omar M. E
• WANI, Sachin E
• FALCHETTI, Alberto
• FRASER, William D
• GENNARI, Luigi
• GIANFRANCESCO, Fernando
• HOOPER, Michael J
• VAN HUL, Wim
• ISAIA, Gianluca
• NICHOLSON, Geoff C
• NUTI, Ranuccio
• PAPAPOULOS, Socrates
• VISCONTI, Micaela R
• DEL PINO MONTES, Javier
• RATAJCZAK, Thomas
• REA, Sarah L
• RENDINA, Domenico
• GONZALEZ-SARMIENTO, Rogelio
• DI STEFANO, Marco
• WARD, Lynley C
• WALSH, John P
• RALSTON, Stuart H
• ALONSO, Nerea
• GOODMAN, Kirsteen
• BRANDI, Maria Luisa
• CUNDY, Tim
• CHUNG, Pui Yan Jenny
• DARGIE, Rosemary
• DEVOGELAER, Jean-Pierre

Titel

Genome-wide association identifies three new susceptibility loci for Paget's disease of bone

Ist Teil von

• Nature genetics, 2011-07, Vol.43 (7), p.685-689

Ort / Verlag

New York: Nature Publishing Group US

Erscheinungsjahr

2011

Quelle

MEDLINE

Beschreibungen/Notizen

• 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 ∼13% of the familial risk of PDB. These studies provide new insights into the genetic architecture and pathophysiology of PDB.