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  Critical Parameters in Dynamic Network Modeling of Sepsis

Berner, R., Sawicki, J., Thiele, M., Löser, T., Schöll, E. (2022): Critical Parameters in Dynamic Network Modeling of Sepsis. - Frontiers in Network Physiology, 2, 904480.
https://doi.org/10.3389/fnetp.2022.904480

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 Urheber:
Berner, Rico1, Autor
Sawicki, Jakub2, Autor              
Thiele, Max1, Autor
Löser, Thomas1, Autor
Schöll, Eckehard2, Autor              
Affiliations:
1External Organizations, ou_persistent22              
2Potsdam Institute for Climate Impact Research, ou_persistent13              

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 Zusammenfassung: In this work, we propose a dynamical systems perspective on the modeling of sepsis and its organ-damaging consequences. We develop a functional two-layer network model for sepsis based upon the interaction of parenchymal cells and immune cells via cytokines, and the coevolutionary dynamics of parenchymal, immune cells, and cytokines. By means of the simple paradigmatic model of phase oscillators in a two-layer system, we analyze the emergence of organ threatening interactions between the dysregulated immune system and the parenchyma. We demonstrate that the complex cellular cooperation between parenchyma and stroma (immune layer) either in the physiological or in the pathological case can be related to dynamical patterns of the network. In this way we explain sepsis by the dysregulation of the healthy homeostatic state (frequency synchronized) leading to a pathological state (desynchronized or multifrequency cluster) in the parenchyma. We provide insight into the complex stabilizing and destabilizing interplay of parenchyma and stroma by determining critical interaction parameters. The coupled dynamics of parenchymal cells (metabolism) and nonspecific immune cells (response of the innate immune system) is represented by nodes of a duplex layer. Cytokine interaction is modeled by adaptive coupling weights between nodes representing immune cells (with fast adaptation timescale) and parenchymal cells (slow adaptation timescale), and between pairs of parenchymal and immune cells in the duplex network (fixed bidirectional coupling). The proposed model allows for a functional description of organ dysfunction in sepsis and the recurrence risk in a plausible pathophysiological context.

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Sprache(n): eng - Englisch
 Datum: 2022-06-012022-06-01
 Publikationsstatus: Final veröffentlicht
 Seiten: 16
 Ort, Verlag, Ausgabe: -
 Inhaltsverzeichnis: -
 Art der Begutachtung: Expertenbegutachtung
 Identifikatoren: DOI: 10.3389/fnetp.2022.904480
MDB-ID: No data to archive
PIKDOMAIN: RD4 - Complexity Science
Organisational keyword: RD4 - Complexity Science
Research topic keyword: Complex Networks
Research topic keyword: Nonlinear Dynamics
Model / method: Quantitative Methods
OATYPE: Gold Open Access
 Art des Abschluß: -

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Titel: Frontiers in Network Physiology
Genre der Quelle: Zeitschrift, other, oa
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Ort, Verlag, Ausgabe: -
Seiten: - Band / Heft: 2 Artikelnummer: 904480 Start- / Endseite: - Identifikator: CoNE: https://publications.pik-potsdam.de/cone/journals/resource/frontiers-network-physiology
Publisher: Frontiers