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Published on: April 2, 2021
Retinopathy of prematurity and serum level of insulin-like growth factor-1
1Department of Children's Diseases, Clinical Center of Montenegro, Podgorica, Montenegro. drbanjac@t-com.me
Insights
Serum insulin-like growth factor-1 (IGF-1) levels were similar in preterm infants with and without retinopathy of prematurity (ROP) at 33 weeks. This suggests IGF-1 levels may normalize by ROP phase 2.
Area of Science:
- Neonatology
- Pediatric Ophthalmology
Background:
- Retinopathy of prematurity (ROP) is a significant cause of visual impairment in premature infants.
- Low serum insulin-like growth factor-1 (IGF-1) levels have been linked to ROP severity in phase 1.
- ROP phase 2 commences around postmenstrual week 33.
Purpose of the Study:
- To measure and compare serum IGF-1 levels at postmenstrual age of 33 weeks in preterm infants with and without ROP.
- To investigate potential changes in IGF-1 levels during ROP phase 2.
Main Methods:
- Prospective cohort study of 74 premature infants (gestational age ≤ 33 weeks).
- Serum IGF-1 levels measured at postmenstrual age of 33 weeks.
- Infants were monitored for ROP development.
Main Results:
- The incidence of ROP in the cohort was 50.7%.
- Infants with ROP had significantly lower birth weight and gestational age.
- No significant difference in serum IGF-1 levels was found between infants with and without ROP at 33 weeks.
Conclusions:
- Serum IGF-1 levels do not significantly differ between preterm infants with and without ROP at the onset of ROP phase 2 (33 weeks).
- Further research with repeated IGF-1 measurements is needed to confirm potential normalization in ROP phase 2.
Abstract:
The aim of our study was to measure and compare serum insulin-like growth factor-1 (IGF-1) levels at postmenstrual age of 33 weeks between preterm infants with and without retinopathy of prematurity (ROP). ROP occurs in two phases. Low serum levels of IGF-1 during ROP phase 1 have been found to correlate with the severity of ROP. ROP phase 2 begins around postmenstrual week 33. We conducted a prospective cohort study to measure serum IGF-1 levels in premature infants at postmenstrual age of 33 weeks. The study included all premature infants (N = 74), gestational age < or = 33 weeks, hospitalized at Department of Neonatology, Clinical Center of Montenegro, from April 2008 to July 2009. The incidence of ROP in the study cohort was 50.7%. Infants with ROP had a significantly lower birth weight and significantly shorter gestational age. The mean level of IGF-1 at postmenstrual age of 33 weeks was 23.7 mcg/L. Study results showed that there was no significant difference in serum IGF-1 level between newborns with and without ROP at postmenstrual age of 33 weeks (in newborns with ROP, it was the beginning of ROP phase 2). A large controlled study with repeated measurement of IGF-1 level in the neonatal period is needed to confirm that restoration of IGF-I level occurs in ROP phase 2, i.e. that the low level of IGF-1 is only a feature of ROP phase 1.
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