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Foreman, B.

Publications and source records attributed to Foreman, B..

3 recordsLinked to original sources

Physics-Informed Digital Twin Can Predict Cerebral Blood Flow and Cerebral Vascular Regulation Mechanisms in Neurocritical Care Patients

1Cerebral blood flow is vital for brain function and is acutely controlled through a set of physiological mechanisms known as cerebral vascular regulation (CVR)[1-3]. It remains challenging to directly measure the dynamics and function of individual CVR mechanisms[4], limiting our ability to understand and optimize brain perfusion, particularly for neurologically injured patients. Digital twins offer an ideal tool for overcoming this gap because they enable estimation, tracking, and forecasting of unmeasured physiological states[5, 6]. Here, we introduce CereBRLSIM (Cerebral Blood Regulation Latent State Inference and Modeling), a digital twin that integrates physiological knowledge and patient data to infer CVR function and predict cerebral dynamics. Using both in vivo experiments and simulated data, CereBRLSIM predicted cerebral hemodynamics with high accuracy and estimated the dynamics of myogenic, endothelial, and metabolic mechanisms underlying CVR. When personalized to neurocritical care patient data, CereBRLSIM differentiated cerebral hemodynamic phenotypes, predicted patient outcomes, and forecasted blood flow with significantly higher accuracy than machine learning models. This work provides a novel, interpretable, and clinically compatible approach for quantifying CVR function and forecasting cerebral blood flow, enabling new opportunities in precision diagnostics and foundational understanding of cerebral hemodynamics.

bioengineering↗

Depth-Sensitive Assessment of Cerebral Blood Flow and Low-Frequency Oscillations After Traumatic Brain Injury in Mice Using Time-Gated Diffuse Correlation Spectroscopy

Traumatic brain injury (TBI) can lead to long-lasting impairments in cerebral perfusion, making early detection of microvascular changes critical for guiding clinical interventions. In this study, we employed time-gated diffuse correlation spectroscopy (TG-DCS) at 1064 nm to non-invasively quantify depth-resolved cerebral blood flow (CBF) and low-frequency oscillations (LFOs) in a mouse model of closed-head injury. By analyzing early (superficial) and late (deeper) photon arrival times, we identified a significant drop in CBF shortly after injury, with a partial recovery observed at 2 hours post-trauma. Power spectral analysis of the blood flow index revealed significant alterations in LFO bands, particularly in slow-5 (0.01-0.027 Hz) and slow-3 (0.073-0.198 Hz) ranges, with p < 0.05 at both early and late gates. These changes were more pronounced than BFI alterations alone, indicating that LFOs may serve as sensitive biomarkers of neurovascular disruption. Our findings demonstrate the feasibility of TG-DCS for depth-specific monitoring of cerebral hemodynamics and oscillatory dynamics after TBI and suggest its potential utility in translational neurotrauma research.

bioengineering↗

An optimized messenger RNA vaccine candidate protects non-human primates from Zika virus infection

Zika virus (ZIKV), an arbovirus transmitted by mosquitoes, was identified as a cause of congenital disease during a major outbreak in the Americas in 2016. Vaccine design strategies relied on limited available isolate sequence information due to the rapid response necessary. The first-generation ZIKV mRNA vaccine, mRNA-1325, was initially generated and, as additional strain sequences became available, a second mRNA vaccine, mRNA-1893, was developed. Herein, we compared the immune responses following mRNA-1325 and mRNA-1893 vaccination and reported that mRNA-1893 generated comparable neutralizing antibody titers to mRNA-1325 at 1/20th of the dose and provided complete protection from ZIKV challenge in non-human primates. In depth characterization of these vaccines indicated that the observed immunologic differences could be attributed to a single amino acid residue difference that compromised mRNA-1325 virus-like particle formation.

immunology↗