SQSTM1 gene analysis and gene-environment interaction in Paget's disease of bone

Luigi Gennari, Fernando Gianfrancesco, Marco Di Stefano, Domenico Rendina, Daniela Merlotti, Teresa Esposito, Salvatore Gallone, Pina Fusco, Innocenzo Rainero, Pierpaola Fenoglio, Maria Mancini, Giuseppe Martini, Simona Bergui, Gianpaolo De Filippo, Giancarlo Isaia, Pasquale Strazzullo, Ranuccio Nuti, Giuseppe Mossetti

Research output: Contribution to journalArticle

Abstract

Even though SQSTM1 gene mutations have been identified in a consistent number of patients, the etiology of Paget's disease of bone (PDB) remains in part unknown. In this study we analyzed SQSTM1 mutations in 533 of 608 consecutive PDB patients from several regions, including the high-prevalence area of Campania (also characterized by increased severity of PDB, higher number of familial cases, and peculiar phenotypic characteristics as giant cell tumor). Eleven different mutations (Y383X, P387L, P392L, E396X, M401V, M404V, G411S, D423X, G425E, G425R, and A427D) were observed in 34 of 92 (37%) and 43 of 441 (10%) of familial and sporadic PDB patients, respectively. All five patients with giant cell tumor complicating familial PDB were negative for SQSTM1 mutations. An increased heterogeneity and a different distribution of mutations were observed in southern Italy (showing 9 of the 11 mutations) than in central and northern Italy. Genotype-phenotype analysis showed only a modest reduction in age at diagnosis in patients with truncating versus missense mutations, whereas the number of affected skeletal sites did not differ significantly. Patients from Campania had the highest prevalence of animal contacts (i.e., working or living on a farm or pet ownership) without any difference between patients with or without mutation. However, when familial cases from Campania were considered, animal contacts were observed in 90% of families without mutations. Interestingly, a progressive age-related decrease in the prevalence of animal contacts, as well as a parallel increase in the prevalence of SQSTM1 mutations, was observed in most regions except in the subgroup of patients from Campania. Moreover, patients reporting animal contacts showed an increased number of affected sites (2.54±2.0 versus 2.19±1.9, p

Original languageEnglish
Pages (from-to)1375-1384
Number of pages10
JournalJournal of Bone and Mineral Research
Volume25
Issue number6
DOIs
Publication statusPublished - Jun 2010

Keywords

  • Environment
  • Genetics
  • Giant cell tumor
  • Paget's disease of bone
  • SQSTM1

ASJC Scopus subject areas

  • Orthopedics and Sports Medicine
  • Endocrinology, Diabetes and Metabolism

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  • Cite this

    Gennari, L., Gianfrancesco, F., Di Stefano, M., Rendina, D., Merlotti, D., Esposito, T., Gallone, S., Fusco, P., Rainero, I., Fenoglio, P., Mancini, M., Martini, G., Bergui, S., De Filippo, G., Isaia, G., Strazzullo, P., Nuti, R., & Mossetti, G. (2010). SQSTM1 gene analysis and gene-environment interaction in Paget's disease of bone. Journal of Bone and Mineral Research, 25(6), 1375-1384. https://doi.org/10.1002/jbmr.31