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Retinopathy of prematurity screening at ≥30 weeks: urinary NTpro-BNP performance
J E Berrington1,2, P Clarke3, N D Embleton1,4
1Newcastle Neonatal Service, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.
Urinary NTproBNP levels do not predict retinopathy of prematurity (ROP) in more mature infants. This finding suggests ROP pathophysiology may differ in these infants, impacting screening strategies.
Area of Science:
- Neonatal ophthalmology
- Biomarker research
- Perinatal medicine
Background:
- Urinary N-terminal B-type natriuretic peptide (NTproBNP) is linked to retinopathy of prematurity (ROP) in premature infants (<30 weeks gestation).
- ROP incidence is low in more mature infants meeting screening criteria.
- Predictive biomarkers for ROP in this subgroup are needed.
Purpose of the Study:
- To investigate if urinary NTproBNP levels can predict ROP development in infants born at or after 30 weeks gestation.
- To determine the utility of urinary NTproBNP as a screening tool for ROP in a specific cohort of preterm infants.
Main Methods:
- Prospective observational study of 151 UK infants (≥30 + 0 and <32 weeks gestation and/or <1501 g).
- Urinary NTproBNP levels measured on day of life 14 and day 28.
- Correlation of NTproBNP levels with ROP development.
Main Results:
- No significant difference in urinary NTproBNP concentrations on DOL 14 (median 144 vs 128 mcg/mL, p=0.86) or DOL 28 (median 117 vs 94 mcg/mL, p=0.64) between infants with and without ROP.
- The previously observed association between urinary NTproBNP and ROP in younger infants was not replicated.
Conclusions:
- Urinary NTproBNP is not a reliable predictor of ROP in preterm infants born at or after 30 weeks gestation.
- The findings suggest urinary NTproBNP may not aid in optimizing ophthalmoscopic screening for ROP in this population.
- A potential difference in ROP pathophysiology between preterm infants <30 weeks and those ≥30 weeks is indicated.
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