Related Experiment Video
Updated: Oct 4, 2025

Monitoring Dynamic Growth of Retinal Vessels in Oxygen-Induced Retinopathy Mouse Model
Published on: April 2, 2021
Association of Cardiovascular Disease with Retinopathy of Prematurity
Faizah Bhatti1,2, Yinxi Yu3, Gui-Shuang Ying3
1Neonatal Perinatal Medicine, Department of Pediatrics, University of Oklahoma Health, Sciences Center, Oklahoma City, Oklahoma, USA.
Insights
Cardiovascular diseases (CVDs) in premature infants may increase the risk of retinopathy of prematurity (ROP). Specifically, increased pulmonary blood flow (PBF) is linked to ROP, and pulmonary hypertension (PPHN) to severe ROP.
Area of Science:
- Neonatology
- Ophthalmology
- Pediatric Cardiology
Background:
- Retinopathy of prematurity (ROP) is a significant cause of visual impairment in premature infants.
- Cardiovascular diseases (CVDs) are common in premature infants and may influence ROP development.
Purpose of the Study:
- To investigate the association between the presence and types of cardiovascular diseases (CVDs) and the development of retinopathy of prematurity (ROP) in premature infants.
- To identify specific CVDs that may pose a higher risk for ROP development.
Main Methods:
- Secondary analysis of data from the multi-center Postnatal Growth and ROP Validation Study (GROP-2).
- CVDs were categorized by pulmonary blood flow (PBF), systemic blood flow (SBF), pulmonary hypertension (PPHN), or dysrhythmia.
- Multivariable logistic regression models were used to calculate adjusted odds ratios (aOR) and 95% confidence intervals (95% CI), controlling for birth weight (BW), gestational age (GA), and supplemental oxygen use.
Main Results:
- Among 3980 infants, 13.3% had CVD and 40.4% developed ROP.
- The presence of CVD was not significantly associated with an increased risk of any ROP or severe ROP in multivariable analyses.
- Trends suggested that CVD with increased PBF was associated with a higher risk of ROP (aOR=1.32), and PPHN with a higher risk of severe ROP (aOR=2.04).
- These associations became significant when adjusting only for BW and GA.
Conclusions:
- Cardiovascular disease with increased pulmonary blood flow may increase the risk of retinopathy of prematurity.
- Pulmonary hypertension is likely associated with an increased risk of severe retinopathy of prematurity.
Purpose:
To determine the associations of presence and types of cardiovascular diseases (CVDs) with development of retinopathy of prematurity (ROP) in premature infants undergoing ROP examinations.
Study Design:
We performed secondary analyses of data from the multi-center Postnatal Growth and ROP Validation Study (GROP-2). CVD was categorized based on pulmonary blood flow (PBF), systemic blood flow (SBF), pulmonary hypertension (PPHN), or dysrhythmia. Adjusted odds ratios (aOR) and 95% confidence intervals (95% CI) were calculated from multivariable logistic regression models that included any ROP or severe ROP as outcome variable and any CVD or type of CVD as independent variable, with adjustment of covariates including birth weight (BW), gestational age (GA), and days on supplemental oxygen in the first month of postnatal life.
Result:
Among 3980 infants, 528 (13.3%) had CVD (304 had increased PBF, 101 had decreased PBF, and 49 had PPHN), 1643 (40.4%) developed ROP, and 503 (12.6%) developed severe ROP. In multivariable analyses, presence of CVD was not significantly associated with increased risk of any ROP (aOR = 1.15, 95% CI: 0.90-1.46, p = .26) or severe ROP (aOR = 0.98, 95% CI: 0.72-1.34, p = .92). However, there were trends associating CVD resulting in increased PBF with a higher risk of ROP (aOR = 1.32, 95% CI: 0.97-1.80, p = .08) and PPHN with a higher risk of severe ROP (aOR = 2.04, 95% CI: 0.96-4.35, p = .07). When adjusting only for BW and GA, these associations were significant (aOR = 1.47, 95% CI: 1.09-1.99, and aOR = 2.35, 95% CI: 1.19-4.65, respectively).
Conclusion:
CVD with increased PBF likely increases the risk of ROP. PPHN likely increases the risk of severe ROP.
Related Concept Videos
Photoreceptors and Visual Pathways
The Retina

