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Early Postnatal Oxygen Exposure Predicts Choroidal Thinning in Neonates

PURPOSE: To evaluate whether choroidal thickness (CT) using arm-mounted optical coherence tomography (OCT) in infants screened for retinopathy of prematurity (ROP) correlates with oxygen exposure in neonates. METHODS: OCT images were obtained in infants screened for ROP in a single level IV neonatal...

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Autores principales: He, Ye, Pettenkofer, Moritz, Nittala, Muneeswar Gupta, Sadda, Srinivas R., Tsui, Irena, Chu, Alison
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Association for Research in Vision and Ophthalmology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8297422/
https://www.ncbi.nlm.nih.gov/pubmed/34269816
http://dx.doi.org/10.1167/iovs.62.9.23
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author He, Ye
Pettenkofer, Moritz
Nittala, Muneeswar Gupta
Sadda, Srinivas R.
Tsui, Irena
Chu, Alison
author_facet He, Ye
Pettenkofer, Moritz
Nittala, Muneeswar Gupta
Sadda, Srinivas R.
Tsui, Irena
Chu, Alison
author_sort He, Ye
collection PubMed
description PURPOSE: To evaluate whether choroidal thickness (CT) using arm-mounted optical coherence tomography (OCT) in infants screened for retinopathy of prematurity (ROP) correlates with oxygen exposure in neonates. METHODS: OCT images were obtained in infants screened for ROP in a single level IV neonatal intensive care unit. CT was measured at three different locations: the subfoveal center and 1.5 mm from the fovea center in each direction. Correlation and regression analyses were performed to determine the relationship between clinical factors and CT. Clinical factors included gestational age, birth weight, presence of bronchopulmonary dysplasia (BPD), and fraction of inspired oxygen (FiO(2)) at defined time points: 30 weeks postmenstrual age (PMA), 36 weeks PMA, and on day of imaging. RESULTS: Mean subfoveal, nasal, and temporal choroidal thicknesses CT (SFCT, NCT, and TCT, respectively) were 228.0 ± 51.4 µm, 179.7 ± 50.3 µm, and 186.4 ± 43.8 µm, respectively. SFCT was found to be significantly thicker than NCT and TCT (P < 0.0001 and P = 0.0002, respectively), but no significant difference was found between NCT and TCT (P = 0.547). Compared with infants without BPD, infants with BPD had thinner SFCT and NCT (P = 0.01 and P = 0.0008, respectively). Birth weight was positively correlated with SFCT (r = 0.39, P = 0.01) and NCT (r = 0.33, P = 0.045) but not TCT. Gestational age and ROP stage were not significantly associated with CT. SFCT was found to be significantly thinner with higher average FiO(2) supplementation levels at 30 weeks PMA (r = –0.51, P = 0.01) but not at 36 weeks PMA. Regression analysis revealed that FiO(2) at 30 weeks PMA was an independent predictor of SFCT in infants screened for ROP (P = 0.01). CONCLUSIONS: Early postnatal exposure (<32 weeks PMA) to higher oxygen supplementation in premature neonates statistically predicts choroidal thinning.
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spelling pubmed-82974222021-07-27 Early Postnatal Oxygen Exposure Predicts Choroidal Thinning in Neonates He, Ye Pettenkofer, Moritz Nittala, Muneeswar Gupta Sadda, Srinivas R. Tsui, Irena Chu, Alison Invest Ophthalmol Vis Sci Retina PURPOSE: To evaluate whether choroidal thickness (CT) using arm-mounted optical coherence tomography (OCT) in infants screened for retinopathy of prematurity (ROP) correlates with oxygen exposure in neonates. METHODS: OCT images were obtained in infants screened for ROP in a single level IV neonatal intensive care unit. CT was measured at three different locations: the subfoveal center and 1.5 mm from the fovea center in each direction. Correlation and regression analyses were performed to determine the relationship between clinical factors and CT. Clinical factors included gestational age, birth weight, presence of bronchopulmonary dysplasia (BPD), and fraction of inspired oxygen (FiO(2)) at defined time points: 30 weeks postmenstrual age (PMA), 36 weeks PMA, and on day of imaging. RESULTS: Mean subfoveal, nasal, and temporal choroidal thicknesses CT (SFCT, NCT, and TCT, respectively) were 228.0 ± 51.4 µm, 179.7 ± 50.3 µm, and 186.4 ± 43.8 µm, respectively. SFCT was found to be significantly thicker than NCT and TCT (P < 0.0001 and P = 0.0002, respectively), but no significant difference was found between NCT and TCT (P = 0.547). Compared with infants without BPD, infants with BPD had thinner SFCT and NCT (P = 0.01 and P = 0.0008, respectively). Birth weight was positively correlated with SFCT (r = 0.39, P = 0.01) and NCT (r = 0.33, P = 0.045) but not TCT. Gestational age and ROP stage were not significantly associated with CT. SFCT was found to be significantly thinner with higher average FiO(2) supplementation levels at 30 weeks PMA (r = –0.51, P = 0.01) but not at 36 weeks PMA. Regression analysis revealed that FiO(2) at 30 weeks PMA was an independent predictor of SFCT in infants screened for ROP (P = 0.01). CONCLUSIONS: Early postnatal exposure (<32 weeks PMA) to higher oxygen supplementation in premature neonates statistically predicts choroidal thinning. The Association for Research in Vision and Ophthalmology 2021-07-16 /pmc/articles/PMC8297422/ /pubmed/34269816 http://dx.doi.org/10.1167/iovs.62.9.23 Text en Copyright 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
spellingShingle Retina
He, Ye
Pettenkofer, Moritz
Nittala, Muneeswar Gupta
Sadda, Srinivas R.
Tsui, Irena
Chu, Alison
Early Postnatal Oxygen Exposure Predicts Choroidal Thinning in Neonates
title Early Postnatal Oxygen Exposure Predicts Choroidal Thinning in Neonates
title_full Early Postnatal Oxygen Exposure Predicts Choroidal Thinning in Neonates
title_fullStr Early Postnatal Oxygen Exposure Predicts Choroidal Thinning in Neonates
title_full_unstemmed Early Postnatal Oxygen Exposure Predicts Choroidal Thinning in Neonates
title_short Early Postnatal Oxygen Exposure Predicts Choroidal Thinning in Neonates
title_sort early postnatal oxygen exposure predicts choroidal thinning in neonates
topic Retina
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8297422/
https://www.ncbi.nlm.nih.gov/pubmed/34269816
http://dx.doi.org/10.1167/iovs.62.9.23
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