Study of the Involvement of Fatty Acids in Retinopathy of Prematurity: Relationship Between Retinopathy of Prematurity and the Rate of Expression of Transplacental Fatty Acid Receptors.

Status: Recruiting
Location: See location...
Intervention Type: Biological, Other
Study Type: Observational
SUMMARY

The development of the retinal vascular network is completed during the third trimester of pregnancy and and the first 15 days of life of the newborn. This late maturation can be problematic in cases of preterm births and result in immature retinal vascularization, known as retinopathy of prematurity (ROP). Among the various factors influencing retinal vascular development, the tissue content of omega-3 polyunsaturated fatty acids (PUFAs) appears to be a crucial element. In a previous project, OMEGA-ROP, we showed a difference in the blood bioavailability of omega-3 PUFAs in infants born at less than 28 weeks of amenorrhea who develop ROP compared to healthy newborns with no retinopathy. This study also showed that mothers experienced variations in the blood levels of omega-3 PUFAs that were contrary to the types of variations observed in their children. This suggests a sequestration of omega-3 PUFAs in the mothers of children who will develop ROP. This new project aims to better understand the underlying molecular mechanisms by studying the expression levels of placental fatty acid receptors in relation to the development of ROP in newborns.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
View:

• Mothers giving birth to premature babies less than 29 weeks of amenorrhea (WA), after obtaining their non-opposition.

• Mothers giving birth at term between 39 and 41WA+6 days, after obtaining their non-opposition.

• ≥18 years

• Mothers not under legal protection

Locations
Other Locations
France
Chu Dijon Bourogne
RECRUITING
Dijon
Contact Information
Primary
Catherine CREUZOT-GARCHER
catherine.creuzot-garcher@chu-dijon.fr
03.80.29.51.73
Time Frame
Start Date: 2021-04-20
Estimated Completion Date: 2027-02
Participants
Target number of participants: 135
Treatments
Women giving birth prematurely
Delivery before 29 WA
Women giving birth at term
Childbirth between 39WA and 31WA+6 days
Related Therapeutic Areas
Sponsors
Leads: Centre Hospitalier Universitaire Dijon

This content was sourced from clinicaltrials.gov