Assessment of growth hormone status in acromegaly: what biochemical markers to measure and how?

Citation
C. Camacho-hubner, Assessment of growth hormone status in acromegaly: what biochemical markers to measure and how?, GROWTH H I, 10, 2000, pp. 125-129
Citations number
37
Categorie Soggetti
Endocrinology, Nutrition & Metabolism
Journal title
GROWTH HORMONE & IGF RESEARCH
ISSN journal
10966374 → ACNP
Volume
10
Year of publication
2000
Supplement
B
Pages
125 - 129
Database
ISI
SICI code
1096-6374(200004)10:<125:AOGHSI>2.0.ZU;2-0
Abstract
Various studies have evaluated the usefulness of measuring insulin-like gro wth factor I (IGF-I) and IGF-binding proteins, compared with growth hormone (GH), in the diagnosis and follow-up of patients with acromegaly. The clin ical use of recently developed, highly sensitive GH assays has improved our understanding of the secretion of GH at very low concentrations. Studies e xamining the GH nadir after oral glucose administration in healthy adults s uggest that GH values should be suppressed to no more than 0.14 mu g/l afte r oral glucose administration. The highly sensitive GH assays are now being used in the diagnosis of patients with acromegaly and in post-treatment fo llow-up. In addition, the use of IGF-I immunoassays has confirmed that seru m IGF-I level is a reliable and useful biochemical marker for determining G H excess. The widespread use of highly sensitive, carefully validated assay s offers accurate and reproducible biochemical information that will help i n the overall clinical management of patients with acromegaly, including th e monitoring of disease remission, disease cure and treatment titration reg imen, as well as the early recognition of patients with residual disease. ( C) 2000 Harcourt Publishers Ltd.