Brahmdeep Singh Saini

Dr. Brahmdeep Singh Saini

orcid

Research Focus & Metrics

Academic Career Length

11Years (2016-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 October 2016 in The Journal of Thoracic and Cardiovascular Surgery
Verified
Journal Article
Closed access
JLJessie Mei Lim
Jessie Mei Lim
TKTheodore Kingdom
Theodore Kingdom
BSBrahmdeep Singh Saini
Brahmdeep Singh Saini
VCVann Chau
Vann Chau
MPMartin Post
Martin Post
MSMike Seed
Mike Seed

29 May 2020 in The Journal of Physiology
Verified
Journal Article
Closed access
PDF file
BSBrahmdeep Singh Saini
Brahmdeep Singh Saini
JDJack R. T. Darby
Jack R. T. Darby
SPSharon Portnoy
Sharon Portnoy
LSLiqun Sun
Liqun Sun
JAJoshua van Amerom
Joshua van Amerom
MSMike Seed
Mike Seed

21 January 2019 in Journal of Cardiovascular Magnetic Resonance
Verified
Journal Article
Open access
PDF file
ESEric M. Schrauben
Eric M. Schrauben
BSBrahmdeep Singh Saini
Brahmdeep Singh Saini
JDJack R. T. Darby
Jack R. T. Darby
JSJia Yin Soo
Jia Yin Soo
MLMitchell C Lock
Mitchell C Lock
CMChristopher K. Macgowan
Christopher K. Macgowan
To date it has not been possible to obtain a comprehensive 3D assessment of fetal hemodynamics because of the technical challenges inherent in imaging small cardiac structures, movement of the fetus during data acquisition, and the difficulty of fusing data from multiple cardiac cycles when a cardiac gating signal is absent. Here we propose the combination of volumetric velocity-sensitive cardiovascular magnetic resonance imaging (“4D flow” CMR) and a specialized animal preparation (catheters to monitor fetal heart rate, anesthesia to immobilize mother and fetus) to examine fetal sheep cardiac hemodynamics in utero. Ten pregnant Merino sheep underwent surgery to implant arterial catheters in the target fetuses. Anesthetized ewes underwent 4D flow CMR with acquisition at 3 T for fetal whole-heart coverage with 1.2–1.5 mm spatial resolution and 45–62 ms temporal resolution. Flow was measured in the heart and major vessels, and particle traces were used to visualize circulatory patterns in fetal cardiovascular shunts. Conservation of mass was used to test internal 4D flow consistency, and comparison to standard 2D phase contrast (PC) CMR was performed for validation. Streaming of blood from the ductus venosus through the foramen ovale was visualized. Flow waveforms in the major thoracic vessels and shunts displayed normal arterial and venous patterns. Combined ventricular output (CVO) was 546 mL/min per kg, and the distribution of flows (%CVO) were comparable to values obtained using other methods. Internal 4D flow consistency across 23 measurement locations was established with differences of 14.2 ± 12.1%. Compared with 2D PC CMR, 4D flow showed a strong correlation (R2 = 0.85) but underestimated flow (bias = − 21.88 mL/min per kg, p < 0.05). The combination of fetal surgical preparation and 4D flow CMR enables characterization and quantification of complex flow patterns in utero. Visualized streaming of blood through normal physiological shunts confirms the complex mechanism of substrate delivery to the fetal heart and brain. Besides offering insight into normal physiology, this technology has the potential to qualitatively characterize complex flow patterns in congenital heart disease phenotypes in a large animal model, which can support the development of new interventions to improve outcomes in this population.

2 March 2021 in Physiological Reports
Verified
Journal Article
Open access
PDF file
ACAlex J. Charest‐Pekeski
Alex J. Charest‐Pekeski
ASAyman Sheta
Ayman Sheta
LTLuiza Taniguchi
Luiza Taniguchi
MMMark J. McVey
Mark J. McVey
AFAlejandro Floh
Alejandro Floh
CHChristoph Haller
Christoph Haller
The artificial placenta (AP) as an extrauterine environment to preserve fetal physiology and to promote fetal maturation forms a promising concept to reduce morbidity and mortality in the extremely p...

1 October 2019 in The Journal of Physiology
Verified
Journal Article
Open access
PDF file
JDJack R. T. Darby
Jack R. T. Darby
BSBrahmdeep Singh Saini
Brahmdeep Singh Saini
JSJia Yin Soo
Jia Yin Soo
MLMitchell C Lock
Mitchell C Lock
SHStacey L. Holman
Stacey L. Holman
JMJanna Morrison
Janna Morrison
Key points: Substrate restriction during critical developmental windows of gestation programmes offspring for a predisposition towards cardiovascular disease in adult life. This study aimed to determine the effect of maternal resveratrol (RSV) treatment in an animal model in which chronic fetal catheterisation is possible and the timing of organ maturation reflects that of the human. Maternal RSV treatment increased uterine artery blood flow, fetal oxygenation and fetal weight. RSV was not detectable in the fetal circulation, indicating that it may not cross the sheep placenta. This study highlights RSV as a possible intervention to restore fetal substrate supply in pregnancies affected by placental insufficiency. Suboptimal in utero environments with reduced substrate supply during critical developmental windows of gestation predispose offspring to non‐communicable diseases such as cardiovascular disease (CVD). Improving fetal substrate supply in these pregnancies may ameliorate the predisposition these offspring have toward adult‐onset CVD. This study aimed to determine the effect of maternal resveratrol (RSV) supplementation on uterine artery blood flow and the direct effects of RSV on the fetal heart in a chronically catheterised sheep model of human pregnancy. Maternal RSV treatment significantly increased uterine artery blood flow as measured by phase contrast magnetic resonance imaging, mean gestational fetal and as well as fetal weight. RSV was not detectable in the fetal circulation, and mRNA and protein expression of the histone/protein deacetylase SIRT1 did not differ between treatment groups. No effect of maternal RSV supplementation on AKT/mTOR or CAMKII signalling in the fetal left ventricle was observed. Maternal RSV supplementation is capable of increasing fetal oxygenation and growth in an animal model in which cardiac development parallels that of the human.

29 March 2021 in The Journal of Physiology
Verified
Journal Article
Closed access
PDF file
BSBrahmdeep Singh Saini
Brahmdeep Singh Saini
JDJack R. T. Darby
Jack R. T. Darby
DMDavide Marini
Davide Marini
SPSharon Portnoy
Sharon Portnoy
MLMitchell C Lock
Mitchell C Lock
MSMike Seed
Mike Seed