» Articles » PMID: 3156705

Paget's Disease of Bone: Clinical Features and Treatment

Overview
Specialty Rheumatology
Date 1985 Jan 1
PMID 3156705
Citations 7
Authors
Affiliations
Soon will be listed here.
Abstract

Paget's disease of bone is often discovered incidentally, but can have extensive metabolic and local mechanical complications. Treatment is not required for all patients and should only be undertaken for certain indications, and with a clear understanding of the three types of drugs available. Bone pain unmanageable with analgesics and pathologic fractures are the most common indications, while neurologic symptoms, hypercalcemia and congestive heart failure are less frequent ones. Calcitonin or mithramycin is used for the more urgent indications, and calcitonin or the diphosphonate, etidronate sodium (EHDP), for the more chronic ones. The drugs are generally efficacious and well tolerated.

Citing Articles

Sphingolipid-Induced Bone Regulation and Its Emerging Role in Dysfunction Due to Disease and Infection.

Seal A, Hughes M, Wei F, Pugazhendhi A, Ngo C, Ruiz J Int J Mol Sci. 2024; 25(5).

PMID: 38474268 PMC: 10932382. DOI: 10.3390/ijms25053024.


Increased S1P expression in osteoclasts enhances bone formation in an animal model of Paget's disease.

Nagata Y, Miyagawa K, Ohata Y, Petrusca D, Pagnotti G, Mohammad K J Cell Biochem. 2020; 122(3-4):335-348.

PMID: 33107091 PMC: 7887003. DOI: 10.1002/jcb.29861.


Osteoclast-derived IGF1 is required for pagetic lesion formation in vivo.

Miyagawa K, Ohata Y, Delgado-Calle J, Teramachi J, Zhou H, Dempster D JCI Insight. 2020; 5(6).

PMID: 32078587 PMC: 7213785. DOI: 10.1172/jci.insight.133113.


Measles virus nucleocapsid protein increases osteoblast differentiation in Paget's disease.

Teramachi J, Nagata Y, Mohammad K, Inagaki Y, Ohata Y, Guise T J Clin Invest. 2016; 126(3):1012-22.

PMID: 26878170 PMC: 4767344. DOI: 10.1172/JCI82012.


CHMP5 controls bone turnover rates by dampening NF-κB activity in osteoclasts.

Greenblatt M, Park K, Oh H, Kim J, Shin D, Lee J J Exp Med. 2015; 212(8):1283-301.

PMID: 26195726 PMC: 4516796. DOI: 10.1084/jem.20150407.