grant

Elucidating perifoveal vascular development in infants

Organization DUKE UNIVERSITYLocation DURHAM, UNITED STATESPosted 30 Sept 2022Deadline 31 Aug 2027
NIHUS FederalResearch GrantFY20250-11 years old21+ years old3-D3-D analysis3-Dimensional3-dimensional analysis3D3D analysisAdultAdult HumanAgeAnastomosisAnastomosis - actionAngiogramAngiographyAnimal ModelAnimal Models and Related StudiesBiomedical EngineeringBlindnessBlood VesselsBlood capillariesCausalityChildChild YouthChildhoodChildren (0-21)Chronologic Fetal MaturityComplexConeDataDevelopmentDevicesDiminished VisionDiseaseDisorderDoppler OCTDysfunctionEarly DiagnosisEtiologyExhibitsFetal AgeFoveaFunctional disorderFundusGestationGestational AgeGoalsHistoryHumanImageImaging ProceduresImaging TechnicsImaging TechniquesImpairmentIndividualInfantInfant DevelopmentKnowledgeLocationLow VisionMethodsModern ManNeurological disabilityOCT TomographyOCT angiographyOCTAOphthalmologistOptical Coherence TomographyPartial SightPathologyPatternPhotoreceptor CellPhotoreceptorsPhotosensitive CellPhysiopathologyPigmentationPigmentation physiologic functionPregnancyPremature BirthPremature InfantPrematurely deliveringPreterm BirthPrevalenceProcessRecording of previous eventsReduced VisionResearchRetinaRetinal Blood VesselsRetinal VesselsRetinopathy of PrematurityRetrolental FibroplasiaSamplingSightSourceSpeedSubnormal VisionSystemThree-dimensional analysisTranslationsVascular DiseasesVascular DisorderVascularizationVisionVisual AcuityVisual ReceptorVisual disabilityVisual impairmentVisualizationVisually disabledWorkadulthoodagesanalyzing longitudinalangiographic imagingbio-engineeredbio-engineersbioengineeringbiological engineeringblood vessel disordercapillarycausationdensitydevelopmentaldisease causationdisorder of macula luteadisorder of macula of retinaearly detectionfovea centralishistoriesimagingimaging systemimprovedin vivoinfants born prematureinfants born prematurelyinsightkidslater in lifelater lifelongitudinal analysismacula abnormalitymacula lutea abnormalitymacular diseasemacular disordermacular edemamaculopathymodel of animalmultidisciplinaryoptical Doppler tomographyoptical coherence Doppler tomographyoptical coherence tomography angiographypathophysiologypediatricpigmentationsprematurepremature babypremature childbirthpremature deliverypremature infant humanpremature retinopathyprematuritypreterm babypreterm deliverypreterm infantpreterm infant humanretina blood vessel structureretinal vascular networkretinal vascular structureretinal vasculaturethree dimensionaltranslationvascularvascular dysfunctionvasculopathyvision disabilityvision impairmentvision lossvisual functionvisual lossvisually impairedyoungster
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Full Description

PROJECT SUMMARY
One out of every ten infants is born preterm. Preterm birth can cause retinopathy of prematurity (ROP), a

leading cause of childhood blindness. Even in the absence of ROP or neurological disability, children born

preterm exhibit subtle impairments in visual acuity and visual function, though the etiology of this suboptimal

vision in preterm infants remains unclear. The fovea, an indentation in the central retina, is the most critical

region determining visual acuity. The fovea is surrounded by anastomosis of three layers of capillaries, forming

the foveal avascular zone. It is well-established that children and adults with history of prematurity have a small

or absent foveal avascular zone, retained foveal inner retinal layers, and decreased photoreceptor function,

and that these abnormalities are more severe in individuals with history of treated ROP. The development of

human perifoveal vasculature, however, is difficult to study due to the absence of fovea in most easily

accessible animal models and the rarity of human histopathological samples during late gestation.

Our multidisciplinary team with complementary expertise will work together to use advanced bedside handheld

optical coherence tomography (OCT) angiography imaging to fill the gap in our knowledge of perifoveal

vascular development in infants. We propose to elucidate the human perifoveal vascular development through

the following specific aims: 1) optimize bedside handheld infant OCT angiography to visualize perifoveal

vascular development; 2) determine if perifoveal vascular development is delayed in preterm infants compared

to term infants, further delayed in ROP, and associates with poor outer retinal maturation; and 3) determine the

association of macular edema and decreased perifoveal deep vascular complex formation and outer retinal

maturation in preterm infants. This research will expand our knowledge of human foveal development and

inform the pathophysiology of diseases of macular and retinal vascular development.

Grant Number: 5R01EY034134-04
NIH Institute/Center: NIH

Principal Investigator: Xi Chen

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