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Identification of New Biomarkers of Low-Dose GH Replacement Therapy in GH-Deficient Patients
Author(s) -
Diana CruzTopete,
Jens Otto Lunde Jørgensen,
Britt Christensen,
Lucila SackmannSala,
Thomas Krusenstjerna-Hafstrøm,
Adam Jara,
Shigeru Okada,
John J. Kopchick
Publication year - 2011
Publication title -
the journal of clinical endocrinology and metabolism
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.206
H-Index - 353
eISSN - 1945-7197
pISSN - 0021-972X
DOI - 10.1210/jc.2011-0197
Subject(s) - medicine , haptoglobin , endocrinology , apolipoprotein b , gene isoform , biology , biochemistry , cholesterol , gene
GH secretion peaks at puberty and continues to be secreted in adulthood, albeit at a declining rate. Profound GH deficiency (GHD) in adults with pituitary disease is associated with symptoms that improve with GH substitution, but it is important to tailor the GH dose to avoid overtreatment. Measurement of serum IGF-I levels is an important clinical tool in this regard, but it is well recognized that some patients receiving GH treatment do not show an increase in IGF-I.

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