| Literature DB >> 27720550 |
Ann Hellström1, David Ley2, Ingrid Hansen-Pupp2, Boubou Hallberg3, Luca A Ramenghi4, Chatarina Löfqvist5, Lois E H Smith6, Anna-Lena Hård5.
Abstract
Retinopathy of prematurity is a potentially blinding disease, which is associated with low neonatal IGF-I serum concentrations and poor growth. In severe cases impaired retinal vessel growth is followed by pathologic neovascularization, which may lead to retinal detachment. IGF-I may promote growth even in catabolic states. Treating preterm infants with recombinant human (rh) IGF-I to concentrations normally found during gestation has been suggested to have a preventative effect on ROP. A recent phase 2 study treating infants (gestational age between 23weeks+0days and 27weeks +6days) with rhIGF-I/IGF binding protein-3 until 30 postmenstrual weeks showed no effect on ROP but a 53% reduction in severe bronchopulmonary dysplasia and 44% reduction in severe intraventricular hemorrhage. Oxygen is a major risk factor for ROP and during the phase 2 study oxygen saturation targets were increased to 90-95%, due to national guidelines, which might have affected ROP rate and severity making increased IGF-I a weaker preventative factor for ROP.Entities:
Keywords: Fetus; IGF-I; Metabolism; Postnatal growth; Preterm infant; Preterm morbidity
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Year: 2016 PMID: 27720550 PMCID: PMC5154870 DOI: 10.1016/j.ghir.2016.09.005
Source DB: PubMed Journal: Growth Horm IGF Res ISSN: 1096-6374 Impact factor: 2.372