IGF-I and IGF-binding protein-3 measurements on filter paper blood spots in children and adolescents on GH treatment: use in monitoring and as markers of growth performance
- PMID: 12943519
- DOI: 10.1530/eje.0.1490179
IGF-I and IGF-binding protein-3 measurements on filter paper blood spots in children and adolescents on GH treatment: use in monitoring and as markers of growth performance
Abstract
Background/aim: In childhood an appropriate response to GH treatment is achieved by titration of growth response against dose administered, with careful observation for side-effects. In order to evaluate the potential use of IGF monitoring in children treated with GH, a cross-sectional study has been carried in 215 children and adolescents (134 with GH deficiency (GHD), 54 with Turner syndrome (TS) and 27 with non-GHD growth disorders) treated with GH for 0.2-13.7 years.
Methods: IGF-I and IGF-binding protein-3 (IGFBP-3) were measured in ELISAs, using dried capillary blood collected onto filter papers. Results were expressed as the mean S.D. range (SDS). Values of either analyte < -2 or > +2 SDS were considered abnormal.
Results: IGF-I and IGFBP-3 SDS were higher in the TS and non-GHD groups (mean +0.01 and +0.1 respectively) than in those with GHD (mean value -0.6). Nineteen per cent of the IGF-I values (13% low, 6% high) and 12% of IGFBP-3 values were abnormal (10% low, 2% high). Abnormalities, either low or high, were most common in the GHD group. There was a weak but significant relationship between change in height SDS over the Year up to the time of sampling in the whole group and IGF-I SDS. Satisfactory growth performance (+0.5>change in height SDS> -0.5) was found in those with high (7.2%), normal (60%) and low (9.3%) IGF-I levels. Overall, it was estimated that 26% of the tests would indicate that an adjustment to GH dose (up in 18% and down in 8%) could be considered.
Conclusions: From this cross-sectional study of IGF monitoring across a broad range of diagnoses and ages, it can be concluded that the majority of children on GH have normal levels of IGF-I and IGFBP-3, but 26% of tests could suggest that a change of GH dose should be considered. Regular monitoring of IGF-I and IGFBP-3 should be considered in any child on GH treatment.
Similar articles
-
Monitoring serum insulin-like growth factor-I (IGF-I), IGF binding protein-3 (IGFBP-3), IGF-I/IGFBP-3 molar ratio and leptin during growth hormone treatment for disordered growth.Clin Endocrinol (Oxf). 2000 Sep;53(3):329-36. doi: 10.1046/j.1365-2265.2000.01105.x. Clin Endocrinol (Oxf). 2000. PMID: 10971450
-
Elevated insulin-like growth factor-I values in children with Prader-Willi syndrome compared with growth hormone (GH) deficiency children over two years of GH treatment.J Clin Endocrinol Metab. 2010 Oct;95(10):4600-8. doi: 10.1210/jc.2009-1831. J Clin Endocrinol Metab. 2010. PMID: 20926543
-
Circulating IGF-I, IGFBP-3 and the IGF-I/IGFBP-3 Molar Ratio Concentration and Height Outcome in Prepubertal Short Children on rhGH Treatment over Two Years of Therapy.Horm Res Paediatr. 2017;88(5):354-363. doi: 10.1159/000479691. Epub 2017 Sep 19. Horm Res Paediatr. 2017. PMID: 28926833
-
IGF-I and IGFBP-3 assessment in the management of childhood onset growth hormone deficiency.Endocr Dev. 2005;9:66-75. doi: 10.1159/000085757. Endocr Dev. 2005. PMID: 15879689 Review.
-
Clinical information on serum IGFBP-3 levels and IGFBP-3 proteolytic activity in childhood.Prog Growth Factor Res. 1995;6(2-4):457-63. doi: 10.1016/0955-2235(96)00005-1. Prog Growth Factor Res. 1995. PMID: 8817690 Review.
Cited by
-
IGF-I measurements in the monitoring of GH therapy.Pituitary. 2007;10(2):159-63. doi: 10.1007/s11102-007-0027-9. Pituitary. 2007. PMID: 17410471 Review.
-
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).J Endocrinol Invest. 2006 Sep;29(8):732-7. doi: 10.1007/BF03344184. J Endocrinol Invest. 2006. PMID: 17033263 Review.
-
A pharmacogenomic approach to the treatment of children with GH deficiency or Turner syndrome.Eur J Endocrinol. 2013 Jul 29;169(3):277-89. doi: 10.1530/EJE-13-0069. Print 2013 Sep. Eur J Endocrinol. 2013. PMID: 23761422 Free PMC article. Clinical Trial.
-
Optimising management in Turner syndrome: from infancy to adult transfer.Arch Dis Child. 2006 Jun;91(6):513-20. doi: 10.1136/adc.2003.035907. Arch Dis Child. 2006. PMID: 16714725 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Miscellaneous