Evaluation of the role of Valosin-containing protein in the pathogenesis of familial and sporadic Paget's disease of bone

Lucas, Gavin J A, Mehta, Sarju G, Hocking, Lynne J, Stewart, Tracy L, Cundy, Tim, Nicholson, Geoff C, Walsh, John P, Fraser, William D, Watts, Giles D J, Ralston, Stuart H and Kimonis, Virginia E (2006) Evaluation of the role of Valosin-containing protein in the pathogenesis of familial and sporadic Paget's disease of bone. Bone, 38 (2). pp. 280-285. ISSN 1873-2763

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Paget's disease of bone (PDB) is a common metabolic bone disease of late onset with a strong genetic component. Rarely, PDB can occur as part of a syndrome in which the disease is accompanied by inclusion body myopathy and frontotemporal dementia (inclusion body myopathy, Paget's disease and frontotemporal dementia, IBMPFD). Recently, IBMPFD has been shown to be caused by mutations in Valosin-containing Protein (VCP), which is required for the proteasomal degradation of phosphorylated I?B-a, a necessary step in the activation of the transcription factor NF-?B. Here, we evaluated the role of VCP in the pathogenesis of typical PDB. We conducted mutation screening of VCP in 44 kindreds with familial Paget's disease recruited mainly through clinic referrals in the UK, Australia and New Zealand. We also performed an association study of VCP haplotypes in patients with PDB who did not have a family history of the disease (sporadic PDB). No mutations were found in VCP in three PDB families where there was evidence of allele sharing between affected subjects in the VCP critical region on chromosome 9p13. We failed to detect disease-associated mutations in any of the three exons previously reported to contain IBMPFD mutations in a further 41 PDB families. We found no evidence of allelic association between common VCP haplotypes in a case-control study of 179 sporadic PDB patients and 172 age- and sex-matched controls. Genetic variation in VCP does not appear to be a common cause of familial or sporadic PDB in the absence of myopathy and dementia.

Item Type: Article
Uncontrolled Keywords: adenosine triphosphatases,alleles,case-control studies,cell cycle proteins,dna mutational analysis,databases, nucleic acid,female,gene frequency,genetic predisposition to disease,genetic testing,haplotypes,humans,male,mutation,osteitis deformans,pedigree,polymorphism, single nucleotide
Faculty \ School: Faculty of Medicine and Health Sciences > Norwich Medical School
UEA Research Groups: Faculty of Medicine and Health Sciences > Research Groups > Musculoskeletal Medicine
Faculty of Medicine and Health Sciences > Research Centres > Metabolic Health
Depositing User: Rhiannon Harvey
Date Deposited: 08 Jun 2011 12:59
Last Modified: 19 Oct 2023 00:50
URI: https://ueaeprints.uea.ac.uk/id/eprint/32060
DOI: 10.1016/j.bone.2005.07.014

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