GLUCOCORTICOID THERAPY SUPPRESSES ABNORMAL SECRETION OF BIG IGF-II BYNON-ISLET CELL TUMORS INDUCING HYPOGLYCEMIA (NICTH)

Authors
Citation
Jd. Teale et V. Marks, GLUCOCORTICOID THERAPY SUPPRESSES ABNORMAL SECRETION OF BIG IGF-II BYNON-ISLET CELL TUMORS INDUCING HYPOGLYCEMIA (NICTH), Clinical endocrinology, 49(4), 1998, pp. 491-498
Citations number
19
Categorie Soggetti
Endocrynology & Metabolism
Journal title
ISSN journal
03000664
Volume
49
Issue
4
Year of publication
1998
Pages
491 - 498
Database
ISI
SICI code
0300-0664(1998)49:4<491:GTSASO>2.0.ZU;2-J
Abstract
OBJECTIVE To assess the relative efficacy of hGH and glucocorticoids i n the treatment of non-islet cell tumour hypoglycaemia (NICTH) by exam ination of their influence on the composition of the various molecular species involving tumour and mature forms of IGF-II in association wi th IGFBP-3. DESIGN Two groups each of 4 patients, all diagnosed as cas es of NICTH, were treated with either hGH or glucocorticoids. Through the use of acidic size exclusion chromatography serum levels of tumour (big) and mature IGF-II were evaluated. Neutral size exclusion chroma tography was used in the separation of molecular species before assay for immunoreactive IGF-II and IGFBP-3 content. RESULTS High-dose hGH t reatment produced increases in serum levels of big and mature IGF-II a nd IGFBP-3 but without generation of high molecular weight complexes, Glucocorticoid treatment suppressed big IGF-II permitting re-establish ment of normal IGF/IGFBP association patterns. CONCLUSION Glucocortico id therapy has been demonstrated to consistently reverse the biochemic al abnormalities caused by tumour-derived big IGF-II compared with the potentially adverse stimulatory effects of hGH treatment in causing i ncreases in serum levels of big IGF-II.