Literature DB >> 15455187

Paget's disease of bone in New Zealand: continued decline in disease severity.

H R Cundy1, G Gamble, D Wattie, M Rutland, T Cundy.   

Abstract

We have reported previously that severe Paget's disease of bone had become less common at our center between 1973 and 1993. Data from several countries support the view that there are important secular trends in the prevalence and severity of Paget's disease. In this paper we describe recent trends in the demography of newly referred patients with Paget's disease to determine if the secular trend toward milder disease has continued. A database of all newly referred patients (n = 1487) with Paget's disease (1973 to 2002 inclusive, 30 years) was examined. Of these, 832 subjects (56%) had scintiscans. Plasma total alkaline phosphatase (total ALP) activity, disease extent on scintiscan, and a derived index of average ALP activity of pagetic bone were used as indices of severity. The number of new referrals with Paget's disease declined sharply from 1994 onward and is currently at half the rate seen 20 years earlier, while the mean age at presentation has progressively increased by 4 years per decade (P < 0.0001). Total ALP at diagnosis, disease extent on scintiscan, and the number of bones involved were all negatively correlated with both date of birth (P < 0.0001) and year of presentation (P < 0.0001), indicating that more recently born and presenting subjects had substantially less severe bone disease. The average activity of pagetic bone was only weakly correlated with year of presentation, but not with year of birth or age at presentation. Although there are a number of potential biases, these data are consistent with a continued secular trend to presentation in older subjects with less extensive skeletal involvement, and a declining prevalence of Paget's disease.

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Year:  2004        PMID: 15455187     DOI: 10.1007/s00223-004-0281-z

Source DB:  PubMed          Journal:  Calcif Tissue Int        ISSN: 0171-967X            Impact factor:   4.333


  19 in total

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Journal:  Hum Genet       Date:  2010-09-14       Impact factor: 4.132

2.  The Implications of the Sequestosome 1 Mutation P392L in Patients with Paget's Disease in a United States Cohort.

Authors:  Margaret Seton; Marc Hansen; Daniel H Solomon
Journal:  Calcif Tissue Int       Date:  2015-12-28       Impact factor: 4.333

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Journal:  Curr Osteoporos Rep       Date:  2008-12       Impact factor: 5.096

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Review 5.  Paget's Disease of Bone among Various Ethnic Groups.

Authors:  Mira Merashli; Ali Jawad
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6.  Paget's Disease of Bone: A Review of Epidemiology, Pathophysiology and Management.

Authors:  Joseph L Shaker
Journal:  Ther Adv Musculoskelet Dis       Date:  2009-04       Impact factor: 5.346

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Authors:  Pietro Ruggieri; Teresa Calabrò; Maurizio Montalti; Mario Mercuri
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8.  Management of patients with Paget's disease: a consensus document of the Belgian Bone Club.

Authors:  J-P Devogelaer; P Bergmann; J-J Body; Y Boutsen; S Goemaere; J-M Kaufman; J-Y Reginster; S Rozenberg; S Boonen
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Review 9.  Dental Manifestations of Pediatric Bone Disorders.

Authors:  Juan F Yepes
Journal:  Curr Osteoporos Rep       Date:  2017-12       Impact factor: 5.096

10.  Morbidity and mortality associated with Paget's disease of bone: a population-based study.

Authors:  Robert A Wermers; Robert D Tiegs; Elizabeth J Atkinson; Sara J Achenbach; L Joseph Melton
Journal:  J Bone Miner Res       Date:  2008-06       Impact factor: 6.741

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