Literature DB >> 876911

Paget's disease of bone--a clinical and genetic study.

H J Galbraith, E C Evans, J Lacey.   

Abstract

An unselected series of 285 patients with Paget's disease of bone has been studied, of whom 54% were male and 46% female. The youngest was aged 25 years at diagnosis and the oldest 95. Of the patients 109 (38-2%) had never suffered serious symptoms. These diagnosed cases certainly represent only a small proportion, perhaps 10-15%, of all those with Paget's disease in the community from which they came. Few of the undiagnosed cases are likely to be suffering from serious symptoms or complications so it is apparent that the majority (probably over 80 or 90%) of those with the pathological state are relatively untroubled by their disease. The most common complication (8-8%) was pathological fracture. The fracture involved the shaft of the femur in 62% occurring in this section of the bone almost seven times more frequently in the patients with Paget's disease than in the general population. Because of the large number of undiagnosed cases in the community, the true incidence of pathological fracture and of sarcoma of bone in all patients with Paget's disease is probably only 1% and 0-1% respectively. Simultaneous estimates of the serum alkaline phosphatase and ESR were made in 128 of the patients. It was shown that the ESR is valueless as a measure of activity or extent of the disease. In many patients the level of the serum alkaline phosphatase changed very little over periods of several years. A history of the disease in one or more close relatives was found in three families, a lower incidence than was expected from previously recorded studies. The ABO blood groups were determined in 215 of the patients; 50% were of group A compared with 46% in a control group. The difference in distribution of blood groups in the two series of subjects is small and well within chance limits. The secretor status of 138 patients was investigated; 77% were secretors. This is similar to the proportion in control series. There is evidence to suggest that the degree of severity of Paget's disease does not vary, once it has developed in any particular individual, and that the more severe and extensive forms may have a stronger genetic basis.

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Year:  1977        PMID: 876911      PMCID: PMC2496530          DOI: 10.1136/pgmj.53.615.33

Source DB:  PubMed          Journal:  Postgrad Med J        ISSN: 0032-5473            Impact factor:   2.401


  19 in total

1.  INCIDENCE OF FRACTURES IN PERSONS OVER 35 YEARS OF AGE. A REPORT TO THE M.R.C. WORKING PARTY ON FRACTURES IN THE ELDERLY.

Authors:  J KNOWELDEN; A J BUHR; O DUNBAR
Journal:  Br J Prev Soc Med       Date:  1964-07

Review 2.  PAGET'S DISEASE OF BONE: CLINICAL AND METABOLIC OBSERVATIONS.

Authors:  C N DE DEUXCHAISNES; S M KRANE
Journal:  Medicine (Baltimore)       Date:  1964-05       Impact factor: 1.889

3.  Secretor status in carcinoma of the breast.

Authors:  C G BREMNER
Journal:  Lancet       Date:  1961-12-16       Impact factor: 79.321

4.  Secretion of blood-group substances in rheumatic fever. A genetic requirement for susceptibility?

Authors:  A A GLYNN; L E GLYNN; E J HOLBOROW
Journal:  Br Med J       Date:  1959-08-29

5.  Paget's disease; active or quiescent?

Authors:  R G GRAINGER; J W LAWS
Journal:  Br J Radiol       Date:  1957-03       Impact factor: 3.039

6.  Paget's disease of bone associated with Hashimoto's struma lymphomatosa; a clue to the pathogenesis of Paget's disease?

Authors:  R W LUXTON
Journal:  Lancet       Date:  1957-03-02       Impact factor: 79.321

7.  ANGIOID STREAKS, AND THEIR RELATION TO A FORM OF CENTRAL CHOROIDAL DISEASE.

Authors:  R D Batten
Journal:  Br J Ophthalmol       Date:  1931-05       Impact factor: 4.638

8.  ABO groups and Rh genotypes in the elderly.

Authors:  S MURRAY
Journal:  Br Med J       Date:  1961-12-02

9.  Increase in the incidence of non-secretors of ABH blood group substances among alcoholic patients.

Authors:  F E Camps; B E Dodd
Journal:  Br Med J       Date:  1967-01-07

10.  Secretion of blood group substances in duodenal, gastric and stomal ulcer, gastric carcinoma, and diabetes mellitus.

Authors:  R DOLL; H DRANE; A C NEWELL
Journal:  Gut       Date:  1961-12       Impact factor: 23.059

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  5 in total

1.  Guidelines for diagnosis and management of Paget's disease of bone in Japan.

Authors:  Shinjiro Takata; Jun Hashimoto; Kiyoshi Nakatsuka; Noriko Yoshimura; Kousei Yoh; Ikko Ohno; Hiroo Yabe; Satoshi Abe; Masao Fukunaga; Masaki Terada; Masaaki Zamma; Stuart H Ralston; Hirotoshi Morii; Hideki Yoshikawa
Journal:  J Bone Miner Metab       Date:  2006       Impact factor: 2.626

2.  [Osteitis deformans (Paget)--or a tarda-type of a hereditary hyperphosphatasia (author's transl)].

Authors:  A Enderle; S von Gumppenberg
Journal:  Arch Orthop Trauma Surg       Date:  1979-07-31

3.  A family study of Paget's disease of bone.

Authors:  J A Sofaer; S M Holloway; A E Emery
Journal:  J Epidemiol Community Health       Date:  1983-09       Impact factor: 3.710

4.  Osteosarcoma complicating familial Paget's disease.

Authors:  D P Brenton; D A Isenberg; J Bertram
Journal:  Postgrad Med J       Date:  1980-04       Impact factor: 2.401

5.  A statistical study of sarcoma complicating Paget's disease of bone in three countries.

Authors:  C J Brackenridge
Journal:  Br J Cancer       Date:  1979-08       Impact factor: 7.640

  5 in total

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