scholarly journals Genetic Determinants of Paget’s Disease of Bone

Author(s):  
Navnit S. Makaram ◽  
Stuart H. Ralston

Abstract Purpose of Review To provide an overview of the role of genes and loci that predispose to Paget’s disease of bone and related disorders. Recent Findings Studies over the past ten years have seen major advances in knowledge on the role of genetic factors in Paget’s disease of bone (PDB). Genome wide association studies have identified six loci that predispose to the disease whereas family based studies have identified a further eight genes that cause PDB. This brings the total number of genes and loci implicated in PDB to fourteen. Emerging evidence has shown that a number of these genes also predispose to multisystem proteinopathy syndromes where PDB is accompanied by neurodegeneration and myopathy due to the accumulation of abnormal protein aggregates, emphasising the importance of defects in autophagy in the pathogenesis of PDB. Summary Genetic factors play a key role in the pathogenesis of PDB and the studies in this area have identified several genes previously not suspected to play a role in bone metabolism. Genetic testing coupled to targeted therapeutic intervention is being explored as a way of halting disease progression and improving outcome before irreversible skeletal damage has occurred.

IBMS BoneKEy ◽  
2010 ◽  
Vol 7 (3) ◽  
pp. 124-133
Author(s):  
Pui Yan Jenny Chung ◽  
Wim Van Hul

Bone ◽  
2010 ◽  
Vol 47 ◽  
pp. S229 ◽  
Author(s):  
L.J. Hocking ◽  
F.P. Coxon ◽  
E. Azzam ◽  
D.S. Miranda de Stegmann ◽  
J.G. Greenhorn ◽  
...  

2021 ◽  
Vol 14 (6) ◽  
pp. 516
Author(s):  
Félix Javier Jiménez-Jiménez ◽  
Hortensia Alonso-Navarro ◽  
Elena García-Martín ◽  
Ignacio Álvarez ◽  
Pau Pastor ◽  
...  

There are many reports suggesting an important role of genetic factors in the etiopathogenesis of essential tremor (ET), encouraging continuing the research for possible genetic markers. Linkage studies in families with ET have identified 4 genes/loci for familial ET, although the responsible gene(s) have not been identified. Genome-wide association studies (GWAS) described several variants in LINGO1, SLC1A2, STK32B, PPARGC1A, and CTNNA3, related with ET, but none of them have been confirmed in replication studies. In addition, the case-control association studies performed for candidate variants have not convincingly linked any gene with the risk for ET. Exome studies described the association of several genes with familial ET (FUS, HTRA2, TENM4, SORT1, SCN11A, NOTCH2NLC, NOS3, KCNS2, HAPLN4, USP46, CACNA1G, SLIT3, CCDC183, MMP10, and GPR151), but they were found only in singular families and, again, not found in other families or other populations, suggesting that some can be private polymorphisms. The search for responsible genes for ET is still ongoing.


Bone ◽  
2001 ◽  
Vol 28 (1) ◽  
pp. 104-107 ◽  
Author(s):  
W Wuyts ◽  
L Van Wesenbeeck ◽  
A Morales-Piga ◽  
S Ralston ◽  
L Hocking ◽  
...  

Bone ◽  
2009 ◽  
Vol 44 ◽  
pp. S224-S225 ◽  
Author(s):  
O.M.E. Albagha ◽  
M.R. Visconti ◽  
N. Alonso ◽  
P.L. Riches ◽  
A.L. Langston ◽  
...  

2013 ◽  
Vol 34 (4) ◽  
pp. 501-524 ◽  
Author(s):  
Sarah L. Rea ◽  
John P. Walsh ◽  
Robert Layfield ◽  
Thomas Ratajczak ◽  
Jiake Xu

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