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Published on: December 5, 2015
Uteroplacental Responses to Physiological Challenges Throughout Pregnancy Using MRI
Esra Abaci Turk1,2, Neel Dey3,4,5, Tiantian Lei1
1Fetal-Neonatal Neuroimaging & Developmental Science Center, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Journal of Magnetic Resonance Imaging : JMRI
|August 12, 2026
Summary
Uterine contractions decrease placental oxygenation and volume, with effects intensifying with gestational age. Maternal hyperoxia increases placental oxygenation uniformly, differing from contraction-induced changes.
Area of Science:
- Obstetrics and Gynecology
- Radiology
- Fetal Medicine
Background:
- Placental MRI reveals T2* changes during contractions and hyperoxia.
- The relationship between contraction-induced placental oxygenation/deformation and uterine changes, versus hyperoxia effects, is unclear.
Purpose of the Study:
- To quantify placental T2* and deformation during non-labor contractions and maternal hyperoxia.
- To test if contractions cause distinct mechanical placental responses compared to hyperoxia.
Main Methods:
- Retrospective analysis of 49 MRI datasets from 46 pregnancies (24-39 weeks gestation).
- Dynamic multi-echo gradient-echo echo-planar imaging at 3T.
- Quantified placental T2* and deformation during normoxia (with/without contractions) and hyperoxia, with regional analysis of cotyledons.
Main Results:
- Contractions decreased placental T2* by 4.64 ms; hyperoxia increased it by 11.36 ms.
- Contraction effects on placental deformation and T2* reduction intensified with gestational age and duration.
- Contractions reduced placental T2* heterogeneity between cotyledons and surrounding tissue, while hyperoxia did not.
Conclusions:
- Spontaneous contractions decrease placental volume and oxygenation, intensifying with gestation and duration.
- Maternal hyperoxia increases placental oxygenation more uniformly and to a greater extent than contractions.
- Contraction-induced placental changes are mechanically mediated and distinct from hyperoxia responses.

