OmegaROP-2 prospective study: Expression of placental fatty acid receptors in preterm newborns with retinopathy of prematurity

Author:

Carré Chloé1,Acar Niyazi2,Daruich Alejandra3,Grégoire Stéphane2,Martine Lucy2,Buteau Bénédicte2,Aho Serge4,Eid Petra1,Arnould Louis1,Bron Alain1,Driessen Marine5,Kermorvant Elsa6,Simon Emmanuel7,Creuzot-Garcher Catherine1,Gabrielle Pierre-Henry1

Affiliation:

1. Department of Ophthalmology, Dijon University Hospital

2. Eye and Nutrition Research Group, Centre des Sciences du Goût et de l’Alimentation, AgroSup Dijon, CNRS, INRAE, Université Bourgogne Franche-Comté

3. Department of Ophthalmology, Necker Hospital

4. Department of Epidemiology & Biostatistics, Dijon University Hospital

5. Department of Gynecology, Necker Hospital

6. Department of Neonatology, Necker Hospital

7. Department of Gynecology, Dijon University Hospital

Abstract

Abstract Background Incomplete vascularization of the retina in preterm infants carries a risk of retinopathy of prematurity (ROP). Progress in neonatal resuscitation in developing countries has led to the survival of an increasing number of premature infants, resulting in an increased rate of ROP and consequently in visual disability. Strategies to reduce ROP involve optimizing oxygen saturation, nutrition, and normalizing factors such as insulin-like growth factor 1 and n-3 long-chain polyunsaturated fatty acids (LC-PUFA). Our previous study, OmegaROP, showed that there is an accumulation or retention of docosahexaenoic acid (DHA) in mothers of infants developing ROP, suggesting abnormalities in the LC-PUFA placental transfer via fatty acid transporting proteins. The present study aims to better understand the LC-PUFA transport dysfunction in the fetoplacental unit during pregnancy and to find a novel target for the prevention of ROP development. Methods The study protocol is designed to evaluate the correlation between the expression level of placental fatty acid receptors and ROP occurrence. This ongoing study will include 100 patients: patients giving birth before 29 weeks of gestational age (GA) and patients with full-term pregnancies. Recruitment is planned for over 46 months. Maternal and cord blood samples as well as placental tissue samples will be taken following delivery. ROP screening will be performed using wide-field camera imaging according to the International Classification of ROP consensus statement. Discussion The results of this study will have a tangible impact on public health. Indeed, if we show a correlation between the expression level of placental omega-3 receptors and the occurrence of ROP, it would be an essential step in discovering novel pathophysiological mechanisms involved in this retinopathy. Trial registration: 2020-A03253-36

Publisher

Research Square Platform LLC

Reference48 articles.

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2. Fierson WM. Screening examination of premature infants for retinopathy of prematurity.Pediatrics. 2018;142.

3. An update on progress and the changing epidemiology of causes of childhood blindness worldwide;Kong L;J aapos,2012

4. Retinopathy of prematurity;Asano MK;Dis Mon,2014

5. Epidemiology of blindness in children;Solebo AL;Arch Dis Child,2017

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