Literature DB >> 10848878

The use of insulin-like growth factor 1 reference values for the diagnosis of growth hormone deficiency in prepubertal children.

L Bussières1, J C Souberbielle, G Pinto, L Adan, M Noel, R Brauner.   

Abstract

OBJECTIVE: This study was done to determine whether the use of reference values obtained in children with idiopathic short stature (ISS) improved the clinical value of serum insulin-like growth factor I (IGF-1) as a tool for diagnosing GH deficiency (GHD) in prepubertal children. PATIENTS AND METHODS: Serum IGF-1 was measured with a new IRMA kit (IGFI-RIA CT, Cis Bio, Gif sur Yvette, France) in 168 prepubertal normal children and in prepubertal children with ISS (n = 68), organic GHD due to a craniopharyngioma (oGHD, n = 15) and permanent idiopathic GHD (iGHD, n = 28).
RESULTS: IGF-1 was lower (P < 0.001) in iGHD than in either ISS or oGHD and was below the fifth percentile of the normal range in 29/68 ISS (43%), 8/15 oGHD (53%) and 28/28 (100%) iGHD patients. Three oGHD (20%) and two iGHD (7%) patients had a serum IGF-1 below the fifth percentile of the normal group but above the fifth percentile of the ISS group. Thus, a serum IGF-1 below the fifth percentile of the normal group distinguished between normal children and iGHD with 100% sensitivity, between normal and oGHD with 53% sensitivity and between normal and all GHD (idiopathic + organic) with 84% sensitivity; the overall specificity was only 57%. Conversely, a serum IGF-1 below the fifth percentile of the ISS population distinguished between ISS and iGHD with 93% sensitivity, between ISS and oGHD with 33% sensitivity and between ISS and all GHD with 72% sensitivity; the overall specificity was then 95%.
CONCLUSIONS: A serum IGF-1 within the normal range virtually excludes idiopathic GHD but does not rule out organic GHD, whereas an IGF-1 below the ISS range is strongly in favour of GHD, after exclusion of poor nutritional status and/or liver disease. An IGF-1 below the normal range but in the idiopathic short stature range gives no definitive conclusion even when it is associated with a low GH peak. Thus, whereas reference values obtained in normal children must be used to interpret serum IGF-1 in short prepubertal children, reference data obtained in idiopathic short stature children should also be taken into account.

Entities:  

Mesh:

Substances:

Year:  2000        PMID: 10848878     DOI: 10.1046/j.1365-2265.2000.00999.x

Source DB:  PubMed          Journal:  Clin Endocrinol (Oxf)        ISSN: 0300-0664            Impact factor:   3.478


  10 in total

Review 1.  Assessment of serum IGF-I concentrations in the diagnosis of isolated childhood-onset GH deficiency: a proposal of the Italian Society for Pediatric Endocrinology and Diabetes (SIEDP/ISPED).

Authors:  G Federico; M E Street; M Maghnie; M Caruso-Nicoletti; S Loche; S Bertelloni; S Cianfarani
Journal:  J Endocrinol Invest       Date:  2006-09       Impact factor: 4.256

2.  Insulin-like growth factor I correlates with lean body mass in cystic fibrosis patients.

Authors:  I Sermet-Gaudelus; J C Souberbielle; I Azhar; J C Ruiz; P Magnine; V Colomb; C Le Bihan; D Folio; G Lenoir
Journal:  Arch Dis Child       Date:  2003-11       Impact factor: 3.791

3.  Insulin-Like Growth Factor Dysregulation Both Preceding and Following Type 1 Diabetes Diagnosis.

Authors:  Melanie R Shapiro; Clive H Wasserfall; Sean M McGrail; Amanda L Posgai; Rhonda Bacher; Andrew Muir; Michael J Haller; Desmond A Schatz; Johnna D Wesley; Matthias von Herrath; William A Hagopian; Cate Speake; Mark A Atkinson; Todd M Brusko
Journal:  Diabetes       Date:  2019-12-11       Impact factor: 9.461

4.  Metabolomics in plasma of Malawian children 7 years after surviving severe acute malnutrition: "ChroSAM" a cohort study.

Authors:  Celine Bourdon; Natasha Lelijveld; Debbie Thompson; Prasad S Dalvi; Gerard Bryan Gonzales; Dominic Wang; Misagh Alipour; Eytan Wine; Emmanuel Chimwezi; Jonathan C Wells; Marko Kerac; Robert Bandsma; Moffat J Nyirenda
Journal:  EBioMedicine       Date:  2019-06-27       Impact factor: 11.205

Review 5.  Diagnosis of GH Deficiency Without GH Stimulation Tests.

Authors:  Anastasia Ibba; Sandro Loche
Journal:  Front Endocrinol (Lausanne)       Date:  2022-02-18       Impact factor: 5.555

6.  Childhood craniopharyngioma: greater hypothalamic involvement before surgery is associated with higher homeostasis model insulin resistance index.

Authors:  Christine Trivin; Kanetee Busiah; Nizar Mahlaoui; Christophe Recasens; Jean-Claude Souberbielle; Michel Zerah; Christian Sainte-Rose; Raja Brauner
Journal:  BMC Pediatr       Date:  2009-04-02       Impact factor: 2.125

7.  Diagnosis of growth hormone (GH) deficiency: comparison of pituitary stalk interruption syndrome and transient GH deficiency.

Authors:  Murielle Louvel; Mariana Marcu; Christine Trivin; Jean-Claude Souberbielle; Raja Brauner
Journal:  BMC Pediatr       Date:  2009-05-06       Impact factor: 2.125

8.  Selecting short-statured children needing growth hormone testing: derivation and validation of a clinical decision rule.

Authors:  Laëtitia Duché; Christine Trivin; Wassim Chemaitilly; Jean Claude Souberbielle; Gérard Bréart; Raja Brauner; Martin Chalumeau
Journal:  BMC Pediatr       Date:  2008-07-16       Impact factor: 2.125

9.  Factors influencing the growth hormone peak and plasma insulin-like growth factor I in young adults with pituitary stalk interruption syndrome.

Authors:  Mariana Marcu; Christine Trivin; Jean-Claude Souberbielle; Raja Brauner
Journal:  BMC Endocr Disord       Date:  2008-07-11       Impact factor: 2.763

10.  IGF1 for the diagnosis of growth hormone deficiency in children and adolescents: a reappraisal.

Authors:  Anastasia Ibba; Francesca Corrias; Chiara Guzzetti; Letizia Casula; Mariacarolina Salerno; Natascia di Iorgi; Gianluca Tornese; Giuseppa Patti; Giorgio Radetti; Mohamad Maghnie; Marco Cappa; Sandro Loche
Journal:  Endocr Connect       Date:  2020-11       Impact factor: 3.335

  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.