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Growth hormone variants : a potential avenue for a better diagnostic characterization of growth hormone deficiency in children

Articolo
Data di Pubblicazione:
2012
Abstract:
Human GH (hGH) is a heterogeneous protein hormone consisting of several isoforms. This heterogeneity is the consequence of multiple hGH genes, mRNA splicing, post-translational modifications, and peripheral metabolism, and it represents one important reason for the disparity among GH assay results from different laboratories. However, other factors are involved: a) interference from endogenous GH binding proteins; b) different specificities of anti- GH (monoclonal and polyclonal) antibodies; c) different matrix effects among the calibrators; d) the use of different calibrators. The measurement of GH levels in response to provocative testing is an essential part of the diagnosis of GH deficiency. For this purpose, an accurate, reproducible and universally valid GH measurement would be highly desirable, but, despite a huge number of efforts in clinical biochemistry, this goal remains elusive.
Tipologia CRIS:
1.1 Articolo in rivista
Keywords:
Human Growth Hormone; Multigene Family; Humans; Growth Disorders; Biological Assay; Protein Isoforms; analytical methods; biochemical diagnosis; GH deficiency; OH isoforms
Elenco autori:
A. E., Rigamonti; M., Bozzola; Banfi, Giuseppe; C., Meazza; E. E., Müller; S. G., Cella
Autori di Ateneo:
BANFI GIUSEPPE
Link alla scheda completa:
https://iris.unisr.it/handle/20.500.11768/13425
Pubblicato in:
JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
Journal
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