A Computational, Tissue-Realistic Model of Pressure Ulcer Formation in Individuals with Spinal Cord Injury.

People with spinal cord injury (SCI) are predisposed to pressure ulcers (PU). PU remain a significant burden in cost of care and quality of life despite improved mechanistic understanding and advanced interventions. An agent-based model (ABM) of ischemia/reperfusion-induced inflammation and PU (the...

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Main Authors: Cordelia Ziraldo, Alexey Solovyev, Ana Allegretti, Shilpa Krishnan, M Kristi Henzel, Gwendolyn A Sowa, David Brienza, Gary An, Qi Mi, Yoram Vodovotz
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-06-01
Series:PLoS Computational Biology
Online Access:http://europepmc.org/articles/PMC4482429?pdf=render
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author Cordelia Ziraldo
Alexey Solovyev
Ana Allegretti
Shilpa Krishnan
M Kristi Henzel
Gwendolyn A Sowa
David Brienza
Gary An
Qi Mi
Yoram Vodovotz
author_facet Cordelia Ziraldo
Alexey Solovyev
Ana Allegretti
Shilpa Krishnan
M Kristi Henzel
Gwendolyn A Sowa
David Brienza
Gary An
Qi Mi
Yoram Vodovotz
author_sort Cordelia Ziraldo
collection DOAJ
description People with spinal cord injury (SCI) are predisposed to pressure ulcers (PU). PU remain a significant burden in cost of care and quality of life despite improved mechanistic understanding and advanced interventions. An agent-based model (ABM) of ischemia/reperfusion-induced inflammation and PU (the PUABM) was created, calibrated to serial images of post-SCI PU, and used to investigate potential treatments in silico. Tissue-level features of the PUABM recapitulated visual patterns of ulcer formation in individuals with SCI. These morphological features, along with simulated cell counts and mediator concentrations, suggested that the influence of inflammatory dynamics caused simulations to be committed to "better" vs. "worse" outcomes by 4 days of simulated time and prior to ulcer formation. Sensitivity analysis of model parameters suggested that increasing oxygen availability would reduce PU incidence. Using the PUABM, in silico trials of anti-inflammatory treatments such as corticosteroids and a neutralizing antibody targeted at Damage-Associated Molecular Pattern molecules (DAMPs) suggested that, at best, early application at a sufficiently high dose could attenuate local inflammation and reduce pressure-associated tissue damage, but could not reduce PU incidence. The PUABM thus shows promise as an adjunct for mechanistic understanding, diagnosis, and design of therapies in the setting of PU.
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spelling doaj.art-66c3864b9b14470a9db7f411bc12a8002022-12-21T18:31:31ZengPublic Library of Science (PLoS)PLoS Computational Biology1553-734X1553-73582015-06-01116e100430910.1371/journal.pcbi.1004309A Computational, Tissue-Realistic Model of Pressure Ulcer Formation in Individuals with Spinal Cord Injury.Cordelia ZiraldoAlexey SolovyevAna AllegrettiShilpa KrishnanM Kristi HenzelGwendolyn A SowaDavid BrienzaGary AnQi MiYoram VodovotzPeople with spinal cord injury (SCI) are predisposed to pressure ulcers (PU). PU remain a significant burden in cost of care and quality of life despite improved mechanistic understanding and advanced interventions. An agent-based model (ABM) of ischemia/reperfusion-induced inflammation and PU (the PUABM) was created, calibrated to serial images of post-SCI PU, and used to investigate potential treatments in silico. Tissue-level features of the PUABM recapitulated visual patterns of ulcer formation in individuals with SCI. These morphological features, along with simulated cell counts and mediator concentrations, suggested that the influence of inflammatory dynamics caused simulations to be committed to "better" vs. "worse" outcomes by 4 days of simulated time and prior to ulcer formation. Sensitivity analysis of model parameters suggested that increasing oxygen availability would reduce PU incidence. Using the PUABM, in silico trials of anti-inflammatory treatments such as corticosteroids and a neutralizing antibody targeted at Damage-Associated Molecular Pattern molecules (DAMPs) suggested that, at best, early application at a sufficiently high dose could attenuate local inflammation and reduce pressure-associated tissue damage, but could not reduce PU incidence. The PUABM thus shows promise as an adjunct for mechanistic understanding, diagnosis, and design of therapies in the setting of PU.http://europepmc.org/articles/PMC4482429?pdf=render
spellingShingle Cordelia Ziraldo
Alexey Solovyev
Ana Allegretti
Shilpa Krishnan
M Kristi Henzel
Gwendolyn A Sowa
David Brienza
Gary An
Qi Mi
Yoram Vodovotz
A Computational, Tissue-Realistic Model of Pressure Ulcer Formation in Individuals with Spinal Cord Injury.
PLoS Computational Biology
title A Computational, Tissue-Realistic Model of Pressure Ulcer Formation in Individuals with Spinal Cord Injury.
title_full A Computational, Tissue-Realistic Model of Pressure Ulcer Formation in Individuals with Spinal Cord Injury.
title_fullStr A Computational, Tissue-Realistic Model of Pressure Ulcer Formation in Individuals with Spinal Cord Injury.
title_full_unstemmed A Computational, Tissue-Realistic Model of Pressure Ulcer Formation in Individuals with Spinal Cord Injury.
title_short A Computational, Tissue-Realistic Model of Pressure Ulcer Formation in Individuals with Spinal Cord Injury.
title_sort computational tissue realistic model of pressure ulcer formation in individuals with spinal cord injury
url http://europepmc.org/articles/PMC4482429?pdf=render
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