Determining mechanisms of cerebral blood flow and metabolism derangements in pediatric cerebral malaria (flow)

Ended Project Grant Awarded Last action

Award ID
R56NS132781
Recipient
Awarding agency
Obligated
$465,437

Award facts

Completion date
Originally
Place of performance
Ohio, USA

Award details come from USAspending.gov.

Description

Abstract
Cerebral malaria (CM), even with effective anti-malarial drugs, results in >450,000 deaths annually, with pediatric case fatality rates ranging from 15-30%. This equates to >1300 dead children on any given day. Long-term neurologic sequelae are identified in 30-50% of survivors. The neuropathogenesis of CM is unclear and under-investigated, but an improved understanding is necessary to develop efficacious therapies that improve outcomes. We have, in two different populations of african children with CM, identified five distinct patterns of abnormal transcranial doppler ultrasound (TCD) cerebral blood flow velocities and waveforms, each with differing risks of neurologic morbidity or mortality. In a small cohort of children with CM, we have also determined that multiple different types of disrupted flow- metabolism coupling and cerebral metabolic dysfunction (luxury perfusion, misery perfusion, ischemia, mitochondrial dysfunction) occurred in 85% of patients with CM. We hypothesize that in children with CM, due to parasite and/or host factors, altered bioavailability of various vasoactive peptides results in altered cerebrovascular tone/cerebral blood flow, flow metabolism uncoupling, and cerebral metabolic dysfunction, with different combinations of abnormalities inherently associated with differing kinds and risk of neurologic injury. This project will establish altered cerebral blood flow (CBF) and metabolism as mechanistic contributors to neurologic injury in CM for the first time. Using non-targeted metabolomics, we will also determine putative peptides contributing to the different categories of abnormal CBF and metabolism. These peptides may then act as biomarkers of underlying mechanisms of injury or as therapeutic targets. Using the large amounts of data that will be captured in the proposed work, machine learning/cluster analysis will, also for the first time, determine endotypes of CM. This work is innovative in that we will establish new mechanisms of neurologic injury in CM, identify associated vasoactive peptides, and develop a novel framework that is a necessary step towards the delivery of precision medicine in CM. Additionally, the work is innovative in that we will further develop and validate a portable, non-invasive approach to measure CBF, cerebral metabolic rate of oxygen consumption, and oxygen extraction fraction, an approach that may have widespread implications for patient neuromonitoring during any acute neurocritical illness across all settings.

Transactions

Action Obligated Date
Amendment -$5,540
Original award $470,977

Subawards

Subrecipient Amount Awarded
Subrecipient not on record Specifically the site will: 1. Identify patients that meet all inclusion and exclusion criteria and enroll in the study when parents agree to give informed… $60,481
Lodja District Referral Hospital Specifically the site will: 1. Identify patients that meet all inclusion and exclusion criteria and enroll in the study when parents agree to give informed… $54,459
Chipata Central Hospital 1. Identify patients that meet all inclusion and exclusion criteria and enroll in the study when parents agree to give informed consent 2. Capture all data… $32,076
University Of Malawi College Of Medicine Specifically the site will: 1. Identify patients that meet all inclusion and exclusion criteria and enroll in the study when parents agree to give informed… $43,740

Quick answers

Who received award R56NS132781?

R56NS132781 was awarded to Research Institute At Nationwide Children's Hospital by National Institute of Neurological Disorders and Stroke (National Institutes of Health) on May 15, 2024.

How much is award R56NS132781 worth?

$465,437 has been obligated on R56NS132781.

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