急性和呼吸机诱发肺损伤的无标度模型:受地震学启发的网络理论方法。

Frontiers in network physiology Pub Date : 2024-05-01 eCollection Date: 2024-01-01 DOI:10.3389/fnetp.2024.1392701
Drew C Gottman, Bradford J Smith
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引用次数: 0

摘要

简介急性呼吸窘迫综合征(ARDS)是一项重大的临床挑战,呼吸机诱发的肺损伤(VILI)是挽救生命的机械通气所引起的严重并发症。方法:用 Ilastik 对最初健康的小鼠和接受第二次呼吸机诱发肺损伤的肺灌洗损伤小鼠的组织切片进行分割,以确定肺损伤区域。采用无标度网络方法评估损伤区域之间的相关性,将损伤区域表示为网络中的 "节点","边 "量化节点之间的相关程度。进行了模拟时间序列分析,以模拟损伤事件的时间序列:结果:自动分割识别出的不同肺部区域与人工评分结果一致,"损伤 "像素的灵敏度为 78%,特异度为 85%。损伤"、"空气 "和 "其他 "像素的总体准确率为 81%。损伤区域的大小呈幂律分布,表明肺损伤的分布存在 "越丰富越严重 "的现象。网络分析揭示了损伤相关性的无规模分布,突出了损伤中心,可作为治疗干预的焦点。模拟时间序列分析进一步支持了初始损伤后二次损伤事件的概念,其模式与地震学研究中观察到的余震模式相似:结论:损伤区域的大小分布凸显了急性肺损伤和呼吸机诱发肺损伤在空间上的异质性。网络理论的应用表明,损伤 "中心 "的出现符合 "富者愈富 "的动态。模拟时间序列分析表明,肺部损伤事件的发展可能遵循类似于地震学中余震发展的时空模式,为损伤分布和传播机制提供了新的见解。这两种现象都表明,针对这些损伤 "枢纽 "的干预措施有可能在 ARDS 的治疗中减少 VILI 的影响。
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A scale-free model of acute and ventilator-induced lung injury: a network theory approach inspired by seismology.

Introduction: Acute respiratory distress syndrome (ARDS) presents a significant clinical challenge, with ventilator-induced lung injury (VILI) being a critical complication arising from life-saving mechanical ventilation. Understanding the spatial and temporal dynamics of VILI can inform therapeutic strategies to mitigate lung damage and improve outcomes.

Methods: Histological sections from initially healthy mice and pulmonary lavage-injured mice subjected to a second hit of VILI were segmented with Ilastik to define regions of lung injury. A scale-free network approach was applied to assess the correlation between injury regions, with regions of injury represented as 'nodes' in the network and 'edges' quantifying the degree of correlation between nodes. A simulated time series analysis was conducted to emulate the temporal sequence of injury events.

Results: Automated segmentation identified different lung regions in good agreement with manual scoring, achieving a sensitivity of 78% and a specificity of 85% across 'injury' pixels. Overall accuracy across 'injury', 'air', and 'other' pixels was 81%. The size of injured regions followed a power-law distribution, suggesting a 'rich-get-richer' phenomenon in the distribution of lung injury. Network analysis revealed a scale-free distribution of injury correlations, highlighting hubs of injury that could serve as focal points for therapeutic intervention. Simulated time series analysis further supported the concept of secondary injury events following an initial insult, with patterns resembling those observed in seismological studies of aftershocks.

Conclusion: The size distribution of injured regions underscores the spatially heterogeneous nature of acute and ventilator-induced lung injury. The application of network theory demonstrates the emergence of injury 'hubs' that are consistent with a 'rich-get-richer' dynamic. Simulated time series analysis demonstrates that the progression of injury events in the lung could follow spatiotemporal patterns similar to the progression of aftershocks in seismology, providing new insights into the mechanisms of injury distribution and propagation. Both phenomena suggest a potential for interventions targeting these injury 'hubs' to reduce the impact of VILI in ARDS management.

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