Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2001 Jan;2(1):117-27.
doi: 10.1023/a:1010067326811.

Animal models for osteoporosis

Collaborators, Affiliations
Review

Animal models for osteoporosis

R T Turner et al. Rev Endocr Metab Disord. 2001 Jan.

Abstract

Animal models will continue to be important tools in the quest to understand the contribution of specific genes to establishment of peak bone mass and optimal bone architecture, as well as the genetic basis for a predisposition toward accelerated bone loss in the presence of co-morbidity factors such as estrogen deficiency. Existing animal models will continue to be useful for modeling changes in bone metabolism and architecture induced by well-defined local and systemic factors. However, there is a critical unfulfilled need to develop and validate better animal models to allow fruitful investigation of the interaction of the multitude of factors which precipitate senile osteoporosis. Well characterized and validated animal models that can be recommended for investigation of the etiology, prevention and treatment of several forms of osteoporosis have been listed in Table 1. Also listed are models which are provisionally recommended. These latter models have potential but are inadequately characterized, deviate significantly from the human response, require careful choice of strain or age, or are not practical for most investigators to adopt. It cannot be stressed strongly enough that the enormous potential of laboratory animals as models for osteoporosis can only be realized if great care is taken in the choice of an appropriate species, age, experimental design, and measurements. Poor choices will results in misinterpretation of results which ultimately can bring harm to patients who suffer from osteoporosis by delaying advancement of knowledge.

PubMed Disclaimer

References

    1. J Bone Miner Res. 1999 Nov;14 (11):1952-62 - PubMed
    1. J Endocrinol. 1989 May;121(2):293-8 - PubMed
    1. Breast Cancer Res Treat. 1987 Oct;10(1):31-5 - PubMed
    1. J Bone Miner Res. 1999 Nov;14(11):1934-42 - PubMed
    1. Calcif Tissue Int. 1985 May;37(3):324-8 - PubMed

Publication types

LinkOut - more resources