Cotyledon‐Specific Flow Evaluation of Rhesus Macaque Placental Injury Using Ferumoxytol Dynamic Contrast‐Enhanced MRI

Author:

Chen Ruiming1ORCID,Seiter Daniel1,Keding Logan T.23,Vazquez Jessica24,Antony Kathleen M.3,Simmons Heather A.24,Basu Puja2,Mejia Andres F.2,Johnson Kevin M.156,Stanic Aleksandar K.3,Liu Ruo‐Yu1,Shah Dinesh M.3,Golos Thaddeus G.234,Wieben Oliver15

Affiliation:

1. Medical Physics University of Wisconsin‐Madison Madison Wisconsin USA

2. Wisconsin National Primate Research Center University of Wisconsin‐Madison Madison Wisconsin USA

3. Obstetrics and Gynecology University of Wisconsin‐Madison Madison Wisconsin USA

4. Comparative Biosciences University of Wisconsin‐Madison Madison Wisconsin USA

5. Radiology University of Wisconsin‐Madison Madison Wisconsin USA

6. Biomedical Engineering University of Wisconsin‐Madison Madison Wisconsin USA

Abstract

BackgroundRecently, dynamic contrast‐enhanced (DCE) MRI with ferumoxytol as contrast agent has recently been introduced for the noninvasive assessment of placental structure and function throughout. However, it has not been demonstrated under pathological conditions.PurposeTo measure cotyledon‐specific rhesus macaque maternal placental blood flow using ferumoxytol DCE MRI in a novel animal model for local placental injury.Study TypeProspective animal model.SubjectsPlacental injections of Tisseel (three with 0.5 mL and two with 1.5 mL), monocyte chemoattractant protein 1 (three with 100 μg), and three with saline as controls were performed in a total of 11 rhesus macaque pregnancies at approximate gestational day (GD 101). DCE MRI scans were performed prior (GD 100) and after (GD 115 and GD 145) the injection (term = GD 165).Field Strength/Sequence3 T, T1‐weighted spoiled gradient echo sequence (product sequence, DISCO).AssessmentSource images were inspected for motion artefacts from the mother or fetus. Placenta segmentation and DCE processing were performed for the dynamic image series to measure cotyledon specific volume, flow, and normalized flow. Overall placental histopathology was conducted for controls, Tisseel, and MCP‐1 animals and regions of tissue infarctions and necrosis were documented. Visual inspections for potential necrotic tissue were conducted for the two Tisseelx3 animals.Statistical TestsWilcoxon rank sum test, significance level P < 0.05.ResultsNo motion artefacts were observed. For the group treated with 1.5 mL of Tisseel, significantly lower cotyledon volume, flow, and normalized flow per cotyledon were observed for the third gestational time point of imaging (day ~145), with mean normalized flow of 0.53 minute−1. Preliminary histopathological analysis shows areas of tissue necrosis from a selected cotyledon in one Tisseel‐treated (single dose) animal and both Tisseelx3 (triple dose) animals.Data ConclusionThis study demonstrates the feasibility of cotyledon‐specific functional analysis at multiple gestational time points and injury detection in a placental rhesus macaque model through ferumoxytol‐enhanced DCE MRI.Level of EvidenceNATechnical EfficacyStage 2

Funder

National Institutes of Health

Eunice Kennedy Shriver National Institute of Child Health and Human Development

Publisher

Wiley

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