pubmed-article:9930632 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:9930632 | lifeskim:mentions | umls-concept:C0030705 | lld:lifeskim |
pubmed-article:9930632 | lifeskim:mentions | umls-concept:C0001675 | lld:lifeskim |
pubmed-article:9930632 | lifeskim:mentions | umls-concept:C0020517 | lld:lifeskim |
pubmed-article:9930632 | lifeskim:mentions | umls-concept:C1522496 | lld:lifeskim |
pubmed-article:9930632 | lifeskim:mentions | umls-concept:C0037663 | lld:lifeskim |
pubmed-article:9930632 | lifeskim:mentions | umls-concept:C0037668 | lld:lifeskim |
pubmed-article:9930632 | lifeskim:mentions | umls-concept:C0018270 | lld:lifeskim |
pubmed-article:9930632 | lifeskim:mentions | umls-concept:C1258192 | lld:lifeskim |
pubmed-article:9930632 | lifeskim:mentions | umls-concept:C0205099 | lld:lifeskim |
pubmed-article:9930632 | lifeskim:mentions | umls-concept:C0332120 | lld:lifeskim |
pubmed-article:9930632 | pubmed:issue | 12 | lld:pubmed |
pubmed-article:9930632 | pubmed:dateCreated | 1999-4-1 | lld:pubmed |
pubmed-article:9930632 | pubmed:abstractText | The aim of this study was to assess the GH-IGFI axis, GH receptor availability, as reflected by the levels of GH-BP, and the amount of GH-dependent IGFBP-3 in adult IDDM patients with different degrees of metabolic control. Thus, 10 adult well-controlled IDDMs (HbA1 7.8 +/- 0.4%), 10 adult non-ketotic poorly controlled IDDMs (HbA1 13.3 +/- 7%) and 14 sex- and age-matched healthy controls were subjected to two intravenous GH-RH stimulation tests with 0.1 and 1.0 microg/kg body weight respectively, and a plasma IGF-1 generation test induced by the administration of hGH. Poorly controlled IDDM patients exhibited an exaggerated GH response to 1.0 microg/kg of GH-RH when compared to healthy control subjects. Low fasting plasma IGF-1 levels and a blunted IGF-1 response to exogenously administered hGH were also found in poorly controlled IDDMs when compared to the healthy control group. GH-BP levels were significantly lower in IDDMs than in normal controls, and correlated positively with the IGF-1 generation capacity after hGH. Serum IGFBP-3 levels measured by RIA were similar in IDDM and control groups. Good glycemic control for 5.7 +/- 0.9 months did not correct the above mentioned abnormalities of the GH-IGF-1 axis. Our findings suggest that IDDM is associated with a diminished availability of GH receptors and synthesis of IGF-1. GH might then increase as a compensatory mechanism, further down-regulating liver GH receptors, and thus perpetuating the initial abnormality. | lld:pubmed |
pubmed-article:9930632 | pubmed:language | eng | lld:pubmed |
pubmed-article:9930632 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:9930632 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:9930632 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:9930632 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:9930632 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:9930632 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:9930632 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:9930632 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:9930632 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:9930632 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:9930632 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:9930632 | pubmed:month | Dec | lld:pubmed |
pubmed-article:9930632 | pubmed:issn | 0018-5043 | lld:pubmed |
pubmed-article:9930632 | pubmed:author | pubmed-author:GutmanR ARA | lld:pubmed |
pubmed-article:9930632 | pubmed:author | pubmed-author:FabioG PGP | lld:pubmed |
pubmed-article:9930632 | pubmed:author | pubmed-author:Fainstein... | lld:pubmed |
pubmed-article:9930632 | pubmed:author | pubmed-author:LitwakL ELE | lld:pubmed |
pubmed-article:9930632 | pubmed:author | pubmed-author:VaglioR MRM | lld:pubmed |
pubmed-article:9930632 | pubmed:author | pubmed-author:PicassoM FMF | lld:pubmed |
pubmed-article:9930632 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:9930632 | pubmed:volume | 30 | lld:pubmed |
pubmed-article:9930632 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:9930632 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:9930632 | pubmed:pagination | 737-42 | lld:pubmed |
pubmed-article:9930632 | pubmed:dateRevised | 2009-2-19 | lld:pubmed |
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pubmed-article:9930632 | pubmed:year | 1998 | lld:pubmed |
pubmed-article:9930632 | pubmed:articleTitle | Growth hormone-insulin-like growth factor-I axis in adult insulin-dependent diabetic patients: evidence for central hypersensitivity to growth hormone-releasing hormone and peripheral resistance to growth hormone. | lld:pubmed |
pubmed-article:9930632 | pubmed:affiliation | Division of Endocrinology and Nuclear Medicine, Hospital Italiano de Buenos Aires, Argentina. pfainstein@intramed.net.ar | lld:pubmed |
pubmed-article:9930632 | pubmed:publicationType | Journal Article | lld:pubmed |