PAGETS-DISEASE OF BONE - INDICATIONS FOR TREATMENT AND GOALS OF THERAPY

Authors
Citation
Rd. Tiegs, PAGETS-DISEASE OF BONE - INDICATIONS FOR TREATMENT AND GOALS OF THERAPY, Clinical therapeutics, 19(6), 1997, pp. 1309-1329
Citations number
111
Categorie Soggetti
Pharmacology & Pharmacy
Journal title
ISSN journal
01492918
Volume
19
Issue
6
Year of publication
1997
Pages
1309 - 1329
Database
ISI
SICI code
0149-2918(1997)19:6<1309:POB-IF>2.0.ZU;2-8
Abstract
Paget's disease of bone is a common disorder of unknown etiology chara cterized by increased bone remodeling and abnormal bone architecture. The pathologic process is initiated by an increase in osteoclast-media ted bone resorption, accompanied by a compensatory increase in bone fo rmation. The increased bone remodeling results in a disorganized mosai c of woven and lamellar bone. This bone is highly vascular and gradual ly becomes enlarged and structurally weakened. Paget's disease is gene rally diagnosed in patients older than 40 years of age, usually as an incidental finding. The disease may be monostotic or polyostotic. The pelvis, femur, spine, tibia, skull, and humerus are most commonly invo lved. Most patients with Paget's disease are asymptomatic. Pain is the most common presenting symptom. Complications of the disease include bowing deformity of the long bones, fracture, and a variety of nerve c ompression syndromes. Malignant degeneration of Paget's disease is a r are complication. As safer, more effective therapies have become avail able, the indications for treatment and goals of therapy have changed. The difficult issue that clinicians are currently facing is whether t o treat patients with asymptomatic disease. The progressive nature of the disease, the severity of its complications, its potential negative impact on quality of life, and the availability of therapy capable of controlling its activity have led many experts in the field to recomm end treatment of asymptomatic patients who have active disease at site s where complications are likely to develop. There are, however, no da ta to prove that complications can be prevented by decreasing the rate of bone remodeling in Pager's disease, nor any data to define who is at risk for complications. Until more information is available, the ma nagement of patients with Paget's disease will continue to be based on clinical observation and theoretical considerations. This review exam ines the present understanding of Paget's disease, the rationale for t he proposed indications for treatment, and the goals of therapy.