Publications by authors named "Christopher Macgowan"

Programming effects of maternal undernutrition on fetal metabolic and cardiovascular systems are well elucidated, yet a detailed characterization of maternal haemodynamics is not available. This study used comprehensive cardiovascular magnetic resonance (CMR) imaging to quantify maternal haemodynamics after 29 days (111-140 days) of late-gestation undernutrition (LGUN) in pregnant sheep. Control ewes received 100% of metabolizable energy requirements (MERs, n = 15), whereas LGUN ewes were globally nutrient restricted to 50% MER (n = 18), with a subset of fetuses undergoing continuous glucose infusion (LGUN + G, n = 6/18).

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A novel method for creating "golden" 3D center-out radial MRI sampling trajectories was developed and analyzed. This method, called ELECTRO (ELECTRic potential energy Optimized), uses repulsive forces to minimize electric potential energy. An objective function [Formula: see text], the electric potential energies of all subsets of consecutive readouts in a 3D radial trajectory, and its reduced form were minimized using a multi-stage optimization strategy.

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Placental function plays a crucial role in fetal development, as it serves as the primary interface for delivery of nutrients and oxygen from the mother to fetus. Magnetic resonance imaging (MRI) has significantly improved our ability to visualize and understand the placenta's complex structure and function. This review provides an up-to-date examination of the most common and novel placental MRI techniques.

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Background: Cardiac MRI feature tracking (FT) allows objective assessment of segmental left ventricular (LV) function following a myocardial infarction (MI), but its utilization in sheep, where interventions can be tested, is lacking.

Purpose: To apply and validate FT in a sheep model of MI and describe post-MI LV remodeling.

Study Type: Animal model, longitudinal.

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Introduction: The fetal haemodynamic response to acute episodes of hypoxaemia are well characterised. However, how these responses change when the hypoxaemia becomes more chronic in nature such as that associated with fetal growth restriction (FGR), is less well understood. Herein, we utilised a combination of clinically relevant MRI techniques to comprehensively characterize and differentiate the haemodynamic responses occurring during acute and chronic periods of fetal hypoxaemia.

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Increasing placental perfusion (PP) could improve outcomes of growth-restricted fetuses. One way of increasing PP may be by using phosphodiesterase (PDE)-5 inhibitors, which induce vasodilatation of vascular beds. We used a combination of clinically relevant magnetic resonance imaging (MRI) techniques to characterize the impact that tadalafil infusion has on maternal, placental and fetal circulations.

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Background: Fetuses with cyanotic congenital heart disease (CHD) exhibit profound fetal circulatory disturbances that may affect early outcomes.

Objectives: This study sought to investigate the relationship between fetal hemodynamics and early survival and neurodevelopmental (ND) outcomes in patients with cyanotic CHD.

Methods: In this longitudinal observational study, fetuses with cyanotic CHD underwent late gestational fetal cardiovascular magnetic resonance (CMR) to measure vessel blood flow and oxygen content.

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Background: Non-Cartesian magnetic resonance imaging trajectories at golden angle increments have the advantage of allowing motion correction and gating using intermediate real-time reconstructions. However, when the acquired data are cardiac binned for cine imaging, trajectories can cluster together at certain heart rates (HR) causing image artifacts. Here, we demonstrate an approach to reduce clustering by inserting additional angular increments within the trajectory, and optimizing them while still allowing for intermediate reconstructions.

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Article Synopsis
  • Recent studies have found microplastics in human blood and placenta, but their health effects are not fully understood.
  • In experiments with pregnant mice, exposure to polystyrene microplastics led to fetal growth restriction, prompting further research on polyethylene, a common type of microplastic.
  • The study showed that while polyethylene exposure did not affect fetal growth, it significantly increased blood flow in the umbilical artery, indicating potential risks to placental function and adverse pregnancy outcomes.
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  • Babies with fetal growth restriction (FGR) face increased risk of cardiometabolic diseases, as FGR negatively impacts heart growth, metabolism, and function due to reduced nutrient supply during development.
  • Using a sheep model, researchers found that key proteins and genes involved in fatty acid transport and metabolism in the heart were significantly reduced in FGR fetuses, indicating impaired cardiac metabolic function.
  • Despite the diminished metabolic capacity and lower mitochondrial numbers in the hearts of FGR fetuses, these changes did not correlate with heart output, suggesting that altered metabolism may lead to poor cardiac health later in life for affected individuals.
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  • The study investigates how exposure to polystyrene nanoplastics in pregnant mice affects fetal brain metabolism, particularly during gestation and lactation.
  • Pregnant mice were given drinking water containing nanoplastics and researchers found significant decreases in important metabolites like GABA, creatine, and glucose in the fetal brain.
  • The findings suggest that maternal nanoplastic exposure disrupts normal brain development in fetuses, highlighting potential risks for human pregnancies and the need for further research.
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Late gestational supine positioning reduces maternal cardiac output due to inferior vena caval (IVC) compression, despite increased collateral venous return. However, little is known about the impact of maternal position on oxygen (O ) delivery and consumption of the gravid uterus, fetus, placenta and lower limbs. We studied the effects of maternal positioning on these parameters in 20 healthy pregnant subjects at 36 ± 2 weeks using magnetic resonance imaging (MRI); a follow-up MRI was performed 6-months postpartum (n = 16/20).

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Background: Cardiovascular disease (CVD) is excessively prevalent and premature in bipolar disorder (BD), even after controlling for traditional cardiovascular risk factors. The increased risk of CVD in BD may be subserved by microvascular dysfunction. We examined coronary microvascular function in relation to youth BD.

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Dramatic advances in the management of congenital heart disease (CHD) have improved survival to adulthood from less than 10% in the 1960s to over 90% in the current era, such that adult CHD (ACHD) patients now outnumber their pediatric counterparts. ACHD patients demonstrate domain-specific neurocognitive deficits associated with reduced quality of life that include deficits in educational attainment and social interaction. Our hypothesis is that ACHD patients exhibit vascular brain injury and structural/physiological brain alterations that are predictive of specific neurocognitive deficits modified by behavioral and environmental enrichment proxies of cognitive reserve (e.

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Maternal exposure to microplastics and nanoplastics has been shown to result in fetal growth restriction in mice. In this study, we investigated the placental and fetal hemodynamic responses to plastics exposure in mice using high-frequency ultrasound. Healthy, pregnant CD-1 dams were given either 106 ng/L of 5 μm polystyrene microplastics or 106 ng/L of 50 nm polystyrene nanoplastics in drinking water throughout gestation and were compared with controls.

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  • Babies born growth-restricted face higher risks for poor health outcomes both in the short and long term, and current treatments aren't effective in mitigating these risks.
  • Maternal treatment with resveratrol (RSV) may improve fetal conditions by increasing blood flow and oxygenation, but there are concerns that high polyphenol diets could negatively affect fetal blood circulation.
  • MRI studies showed that acute RSV exposure did not change fetal blood pressure, heart rate, or oxygen delivery, supporting its potential safety as a treatment for fetal growth restriction.
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  • The growing use of plastics has led to increased microplastic pollution, which may negatively affect pregnancy and fetal development, as seen in studies with pregnant mice.
  • Research focused on how maternal exposure to microplastics alters placental metabolism, revealing significant reductions in important metabolites like lysine and glucose.
  • Findings indicate that microplastic exposure disrupts metabolic pathways in the placenta, underscoring the need to limit plastic exposure during pregnancy to protect fetal health.
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  • Newborns exposed to sildenafil citrate (SC) in the womb show higher rates of persistent pulmonary hypertension, but the exact mechanism is unclear.
  • The study used MRI techniques to investigate how SC affects blood flow and oxygen delivery in fetal sheep.
  • Findings revealed increased pulmonary blood flow and oxygen delivery with SC, alongside reduced right to left heart shunting, suggesting that SC may contribute to poor pulmonary outcomes after birth.
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Magnetic resonance imaging (MRI) assessment of fetal blood oxygen saturation (SO ) can transform the clinical management of high-risk pregnancies affected by fetal growth restriction (FGR). Here, a novel MRI method assesses the feasibility of identifying normally grown and FGR fetuses in sheep and is then applied to humans. MRI scans are performed in pregnant ewes at 110 and 140 days (term = 150d) gestation and in pregnant women at 28  ± 2 weeks to measure feto-placental SO .

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Fetal cardiac MRI is challenging due to fetal and maternal movements as well as the need for a reliable cardiac gating signal and high spatiotemporal resolution. Ongoing research and recent technical developments to address these challenges show the potential of MRI as an adjunct to ultrasound for the assessment of the fetal heart and great vessels. MRI measurements of blood flow have enabled the assessment of normal fetal circulation as well as conditions with disrupted circulations, such as congenital heart disease, along with associated organ underdevelopment and hemodynamic instability.

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Fetal development relies on a complex circulatory network. Accurate assessment of flow distribution is important for understanding pathologies and potential therapies. In this paper, we demonstrate a method for volumetric imaging of fetal flow with magnetic resonance imaging (MRI).

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Background: Evaluation of structural lung abnormalities with magnetic resonance imaging (MRI) has previously been shown to be predictive of clinical neonatal outcomes in preterm birth. MRI during free-breathing with phase-resolved functional lung (PREFUL) may allow for complimentary functional information without exogenous contrast.

Purpose: To investigate the feasibility of structural and functional pulmonary MRI in a cohort of neonates and infants with no cardiorespiratory disease.

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Objectives: To evaluate the impact of fetal haemodynamics on surgical and neurodevelopmental outcomes in severe Ebstein anomaly and tricuspid valve dysplasia.

Methods: Thirty-four fetuses with Ebstein anomaly/tricuspid valve dysplasia were referred from 2013 to 2019 for fetal echocardiography and clinical management. Nineteen fetuses with Ebstein anomaly/tricuspid valve dysplasia and 30 controls underwent cardiovascular magnetic resonance to quantify the fetal blood flow and to calculate cerebral oxygen delivery (cDO2) and consumption (cVO2).

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Purpose: Ten percent of pregnancies are affected by intrauterine growth restriction (IUGR), and evidence suggests that affected neonates have reduced activity of hepatic cytochrome P450 (CYP) drug metabolising enzymes. Given that almost all pregnant individuals take medications and additional medications are often required during an IUGR pregnancy, we aimed to determine the impact of IUGR on hepatic CYP activity in sheep fetuses and pregnant ewes.

Methods: Specific probes were used to determine the impact of IUGR on the activity of several CYP isoenzymes (CYP1A2, CYP2C19, CYP2D6 and CYP3A) in sheep fetuses and pregnant ewes.

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