Insulin-like growth factor-I in growth and metabolism

Research output: Contribution to journalJournal articleResearch

Standard

Insulin-like growth factor-I in growth and metabolism. / Backeljauw, P; Bang, P; Dunger, D B; Juul, A; Le Bouc, Y; Rosenfeld, R.

In: Journal of Pediatric Endocrinology and Metabolism, Vol. 23, No. 1-2, 2010, p. 3-16.

Research output: Contribution to journalJournal articleResearch

Harvard

Backeljauw, P, Bang, P, Dunger, DB, Juul, A, Le Bouc, Y & Rosenfeld, R 2010, 'Insulin-like growth factor-I in growth and metabolism', Journal of Pediatric Endocrinology and Metabolism, vol. 23, no. 1-2, pp. 3-16. https://doi.org/10.1515/JPEM.2010.23.1-2.3

APA

Backeljauw, P., Bang, P., Dunger, D. B., Juul, A., Le Bouc, Y., & Rosenfeld, R. (2010). Insulin-like growth factor-I in growth and metabolism. Journal of Pediatric Endocrinology and Metabolism, 23(1-2), 3-16. https://doi.org/10.1515/JPEM.2010.23.1-2.3

Vancouver

Backeljauw P, Bang P, Dunger DB, Juul A, Le Bouc Y, Rosenfeld R. Insulin-like growth factor-I in growth and metabolism. Journal of Pediatric Endocrinology and Metabolism. 2010;23(1-2):3-16. https://doi.org/10.1515/JPEM.2010.23.1-2.3

Author

Backeljauw, P ; Bang, P ; Dunger, D B ; Juul, A ; Le Bouc, Y ; Rosenfeld, R. / Insulin-like growth factor-I in growth and metabolism. In: Journal of Pediatric Endocrinology and Metabolism. 2010 ; Vol. 23, No. 1-2. pp. 3-16.

Bibtex

@article{5311d8301c9e456aab2add3d9a2372bb,
title = "Insulin-like growth factor-I in growth and metabolism",
abstract = "Deficiency of insulin-like growth factor-I (IGF-I) results in growth failure. A variety of molecular defects have been found to underlie severe primary IGF-I deficiency (IGFD), in which serum IGF-I concentrations are substantially decreased and fail to respond to GH therapy. Identification of more patients with primary or secondary IGFD is likely with investigative and diagnostic progress, particularly in the assessment of children with idiopathic short stature. Diagnosis of IGFD requires accurate and reliable IGF-I assays, adequate normative data for reference, and knowledge of IGF-I physiology for proper interpretation of data. Recombinant human IGF-I (rhIGF-I) treatment improves stature in patients with severe primary IGFD, and has also been shown to improve glycaemic control and insulin sensitivity in patients with severe insulin resistance. Ongoing studies of patients receiving rhIGF-I will allow further evaluation of the clinical utility of this treatment, with concurrent increase in our understanding of IGF-I and conditions of IGFD.",
author = "P Backeljauw and P Bang and Dunger, {D B} and A Juul and {Le Bouc}, Y and R Rosenfeld",
year = "2010",
doi = "10.1515/JPEM.2010.23.1-2.3",
language = "English",
volume = "23",
pages = "3--16",
journal = "Journal of Pediatric Endocrinology and Metabolism",
issn = "0334-018X",
publisher = "Walterde Gruyter GmbH",
number = "1-2",

}

RIS

TY - JOUR

T1 - Insulin-like growth factor-I in growth and metabolism

AU - Backeljauw, P

AU - Bang, P

AU - Dunger, D B

AU - Juul, A

AU - Le Bouc, Y

AU - Rosenfeld, R

PY - 2010

Y1 - 2010

N2 - Deficiency of insulin-like growth factor-I (IGF-I) results in growth failure. A variety of molecular defects have been found to underlie severe primary IGF-I deficiency (IGFD), in which serum IGF-I concentrations are substantially decreased and fail to respond to GH therapy. Identification of more patients with primary or secondary IGFD is likely with investigative and diagnostic progress, particularly in the assessment of children with idiopathic short stature. Diagnosis of IGFD requires accurate and reliable IGF-I assays, adequate normative data for reference, and knowledge of IGF-I physiology for proper interpretation of data. Recombinant human IGF-I (rhIGF-I) treatment improves stature in patients with severe primary IGFD, and has also been shown to improve glycaemic control and insulin sensitivity in patients with severe insulin resistance. Ongoing studies of patients receiving rhIGF-I will allow further evaluation of the clinical utility of this treatment, with concurrent increase in our understanding of IGF-I and conditions of IGFD.

AB - Deficiency of insulin-like growth factor-I (IGF-I) results in growth failure. A variety of molecular defects have been found to underlie severe primary IGF-I deficiency (IGFD), in which serum IGF-I concentrations are substantially decreased and fail to respond to GH therapy. Identification of more patients with primary or secondary IGFD is likely with investigative and diagnostic progress, particularly in the assessment of children with idiopathic short stature. Diagnosis of IGFD requires accurate and reliable IGF-I assays, adequate normative data for reference, and knowledge of IGF-I physiology for proper interpretation of data. Recombinant human IGF-I (rhIGF-I) treatment improves stature in patients with severe primary IGFD, and has also been shown to improve glycaemic control and insulin sensitivity in patients with severe insulin resistance. Ongoing studies of patients receiving rhIGF-I will allow further evaluation of the clinical utility of this treatment, with concurrent increase in our understanding of IGF-I and conditions of IGFD.

U2 - 10.1515/JPEM.2010.23.1-2.3

DO - 10.1515/JPEM.2010.23.1-2.3

M3 - Journal article

VL - 23

SP - 3

EP - 16

JO - Journal of Pediatric Endocrinology and Metabolism

JF - Journal of Pediatric Endocrinology and Metabolism

SN - 0334-018X

IS - 1-2

ER -

ID: 34047679