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
. 2007;10(2):181-7.
doi: 10.1007/s11102-007-0025-y.

Utility of free IGF-I measurements

Affiliations
Review

Utility of free IGF-I measurements

Jan Frystyk. Pituitary. 2007.

Abstract

For nearly 30 years, the endogenous bioactivity of insulin-like growth factor I (IGF-I) has been estimated by its circulating concentrations of immunoreactive IGF-I, obtained after either removal or inactivation of the IGF-binding proteins (IGFBPs), and today serum/plasma total IGF-I serves as a useful parameter in the diagnosis and clinical control of growth hormone (GH) disorders. Different assays for the measurement of free, unbound IGF-I were introduced more than a decade ago. Nevertheless, this measurement remains controversial, and in daily clinical practice serum total IGF-I has retained its position as the most widely used IGF-related measurement in GH disorders. This review will provide a survey of data on free versus total IGF-I, with particular reference to GH disorders. As it will be clear, there is reasonable clinical evidence to conclude that both in the diagnosis of as well as during treatment of patients with GH disorders, serum/plasma total IGF-I should remain the primary IGF-related measurement. However, in certain patients the inclusion of free IGF-I may be useful and therefore, some guidelines for the inclusion of free IGF-I measurements will be given.

PubMed Disclaimer

Similar articles

Cited by

References

    1. J Clin Endocrinol Metab. 2005 Oct;90(10):5627-31 - PubMed
    1. N Engl J Med. 2000 Apr 20;342(16):1171-7 - PubMed
    1. Metabolism. 1995 Oct;44(10 Suppl 4):37-44 - PubMed
    1. Lancet. 1994 Apr 30;343(8905):1064-8 - PubMed
    1. Growth Horm IGF Res. 2001 Apr;11(2):117-27 - PubMed

Publication types

MeSH terms

Substances

LinkOut - more resources