Mapping the network biology of metabolic response to stress in posttraumatic stress disorder and obesity

The co-occurrence of stress-induced posttraumatic stress disorder (PTSD) and obesity is common, particularly among military personnel but the link between these conditions is unclear. Individuals with comorbid PTSD and obesity manifest other physical and psychological problems, which significantly d...

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Main Authors: Thomas P. Chacko, J. Tory Toole, Spencer Richman, Garry L. Spink, Matthew J. Reinhard, Ryan C. Brewster, Michelle E. Costanzo, Gordon Broderick
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-07-01
Series:Frontiers in Psychology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fpsyg.2022.941019/full
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author Thomas P. Chacko
Thomas P. Chacko
J. Tory Toole
J. Tory Toole
Spencer Richman
Garry L. Spink
Matthew J. Reinhard
Ryan C. Brewster
Michelle E. Costanzo
Gordon Broderick
author_facet Thomas P. Chacko
Thomas P. Chacko
J. Tory Toole
J. Tory Toole
Spencer Richman
Garry L. Spink
Matthew J. Reinhard
Ryan C. Brewster
Michelle E. Costanzo
Gordon Broderick
author_sort Thomas P. Chacko
collection DOAJ
description The co-occurrence of stress-induced posttraumatic stress disorder (PTSD) and obesity is common, particularly among military personnel but the link between these conditions is unclear. Individuals with comorbid PTSD and obesity manifest other physical and psychological problems, which significantly diminish their quality of life. Current understanding of the pathways connecting stress to PTSD and obesity is focused largely on behavioral mediators alone with little consideration of the biological regulatory mechanisms that underlie their co-occurrence. In this work, we leverage prior knowledge to systematically highlight such bio-behavioral mechanisms and inform on the design of confirmatory pilot studies. We use natural language processing (NLP) to extract documented regulatory interactions involved in the metabolic response to stress and its impact on obesity and PTSD from over 8 million peer-reviewed papers. The resulting network describes the propagation of stress to PTSD and obesity through 34 metabolic mediators using 302 documented regulatory interactions supported by over 10,000 citations. Stress jointly affected both conditions through 21 distinct pathways involving only two intermediate metabolic mediators out of a total of 76 available paths through this network. Moreover, oxytocin (OXT), Neuropeptide-Y (NPY), and cortisol supported an almost direct propagation of stress to PTSD and obesity with different net effects. Although stress upregulated both NPY and cortisol, the downstream effects of both markers are reported to relieve PTSD severity but exacerbate obesity. The stress-mediated release of oxytocin, however, was found to concurrently downregulate the severity of both conditions. These findings highlight how a network-informed approach that leverages prior knowledge might be used effectively in identifying key mediators like OXT though experimental verification of signal transmission dynamics through each path will be needed to determine the actual likelihood and extent of each marker’s participation.
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spelling doaj.art-6d5bd1a6605f4b1e94efc490f5f01dbc2022-12-22T03:41:10ZengFrontiers Media S.A.Frontiers in Psychology1664-10782022-07-011310.3389/fpsyg.2022.941019941019Mapping the network biology of metabolic response to stress in posttraumatic stress disorder and obesityThomas P. Chacko0Thomas P. Chacko1J. Tory Toole2J. Tory Toole3Spencer Richman4Garry L. Spink5Matthew J. Reinhard6Ryan C. Brewster7Michelle E. Costanzo8Gordon Broderick9Center for Clinical Systems Biology, Rochester General Hospital, Rochester, NY, United StatesInstitute of Health Sciences and Technology, Rochester Institute of Technology, Rochester, NY, United StatesCenter for Clinical Systems Biology, Rochester General Hospital, Rochester, NY, United StatesInstitute of Health Sciences and Technology, Rochester Institute of Technology, Rochester, NY, United StatesCenter for Clinical Systems Biology, Rochester General Hospital, Rochester, NY, United StatesRochester Regional Behavioral Health, Rochester, NY, United StatesWar Related Illness and Injury Study Center, United States Department of Veterans Affairs, Washington, DC, United StatesWar Related Illness and Injury Study Center, United States Department of Veterans Affairs, Washington, DC, United StatesWar Related Illness and Injury Study Center, United States Department of Veterans Affairs, Washington, DC, United StatesCenter for Clinical Systems Biology, Rochester General Hospital, Rochester, NY, United StatesThe co-occurrence of stress-induced posttraumatic stress disorder (PTSD) and obesity is common, particularly among military personnel but the link between these conditions is unclear. Individuals with comorbid PTSD and obesity manifest other physical and psychological problems, which significantly diminish their quality of life. Current understanding of the pathways connecting stress to PTSD and obesity is focused largely on behavioral mediators alone with little consideration of the biological regulatory mechanisms that underlie their co-occurrence. In this work, we leverage prior knowledge to systematically highlight such bio-behavioral mechanisms and inform on the design of confirmatory pilot studies. We use natural language processing (NLP) to extract documented regulatory interactions involved in the metabolic response to stress and its impact on obesity and PTSD from over 8 million peer-reviewed papers. The resulting network describes the propagation of stress to PTSD and obesity through 34 metabolic mediators using 302 documented regulatory interactions supported by over 10,000 citations. Stress jointly affected both conditions through 21 distinct pathways involving only two intermediate metabolic mediators out of a total of 76 available paths through this network. Moreover, oxytocin (OXT), Neuropeptide-Y (NPY), and cortisol supported an almost direct propagation of stress to PTSD and obesity with different net effects. Although stress upregulated both NPY and cortisol, the downstream effects of both markers are reported to relieve PTSD severity but exacerbate obesity. The stress-mediated release of oxytocin, however, was found to concurrently downregulate the severity of both conditions. These findings highlight how a network-informed approach that leverages prior knowledge might be used effectively in identifying key mediators like OXT though experimental verification of signal transmission dynamics through each path will be needed to determine the actual likelihood and extent of each marker’s participation.https://www.frontiersin.org/articles/10.3389/fpsyg.2022.941019/fullpsychoneuroimmunologymetabolismposttraumatic stress disorderobesitycomputational modelregulatory logic
spellingShingle Thomas P. Chacko
Thomas P. Chacko
J. Tory Toole
J. Tory Toole
Spencer Richman
Garry L. Spink
Matthew J. Reinhard
Ryan C. Brewster
Michelle E. Costanzo
Gordon Broderick
Mapping the network biology of metabolic response to stress in posttraumatic stress disorder and obesity
Frontiers in Psychology
psychoneuroimmunology
metabolism
posttraumatic stress disorder
obesity
computational model
regulatory logic
title Mapping the network biology of metabolic response to stress in posttraumatic stress disorder and obesity
title_full Mapping the network biology of metabolic response to stress in posttraumatic stress disorder and obesity
title_fullStr Mapping the network biology of metabolic response to stress in posttraumatic stress disorder and obesity
title_full_unstemmed Mapping the network biology of metabolic response to stress in posttraumatic stress disorder and obesity
title_short Mapping the network biology of metabolic response to stress in posttraumatic stress disorder and obesity
title_sort mapping the network biology of metabolic response to stress in posttraumatic stress disorder and obesity
topic psychoneuroimmunology
metabolism
posttraumatic stress disorder
obesity
computational model
regulatory logic
url https://www.frontiersin.org/articles/10.3389/fpsyg.2022.941019/full
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