Abstract

BackgroundThe complement system has frequently been suggested to play a role in the pathophysiology of acute respiratory distress syndrome (ARDS). The current study explored the association between pulmonary depositions of a complement activation product and the clinical diagnosis of ARDS.MethodsLung tissue material from autopsied critically ill patients who died whilst on invasively mechanical ventilation was collected and stained for complement C3d. The diagnosis of ARDS was by the Berlin Definition. Lung injury scores (LIS) and driving pressures were calculated, 48 and 24 h prior to death. A pathologist who remained blinded for the clinical data scored the extent of C3d depositions, using a C3d deposition score (a minimum and maximum score of 0 and 24), and of diffuse alveolar damage (DAD). The primary analysis focused on the association between the C3d deposition score and the clinical diagnosis of ARDS. Secondary analyses focused on associations between the C3d deposition score and the presence of diffuse alveolar damage (DAD) in histopathology, and LIS and driving pressures in the last 2 days before death.ResultsOf 36 patients of whom autopsy material was available, 12 were diagnosed as having had ARDS. In all patients, C3d depositions were found in various parts of the lungs, and to a different extent. Notably, C3d deposition scores were similar for patients with ARDS and those without ARDS (4.5 [3.3–6.8] vs. 5.0 [4.0–6.0]; not significant). C3d deposition scores were also independent from the presence or absence of DAD, and correlations between C3d scores and LIS and driving pressures prior to death were poor.ConclusionPulmonary C3d depositions are found in the lungs of all deceased ICU patients, independent of the diagnosis of ARDS. The presence of complement C3d was not associated with the presence of DAD on histopathology and had a poor correlation with ventilation characteristics prior to death.

Highlights

  • The complement system has frequently been suggested to play a role in the pathophysiology of acute respiratory distress syndrome (ARDS)

  • Preclinical studies using various models of lung injury [3,4,5,6], as well as human investigations in intensive care unit (ICU) patients with ARDS, have shown complement activation in the lung [7, 8]. Though, whether this finding is unique for ARDS and whether the extent of complement activation depends on ARDS severity and ventilator settings at the moment of sampling

  • This study explored whether pulmonary C3d deposition is associated with the presence of diffuse alveolar damage (DAD) on histopathology, a characteristic finding of ARDS [9], and the lung injury score (LIS) [10] and driving pressures in the last days before death

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Summary

Introduction

The complement system has frequently been suggested to play a role in the pathophysiology of acute respiratory distress syndrome (ARDS). Preclinical studies using various models of lung injury [3,4,5,6], as well as human investigations in intensive care unit (ICU) patients with ARDS, have shown complement activation in the lung [7, 8]. It is uncertain, though, whether this finding is unique for ARDS and whether the extent of complement activation depends on ARDS severity and ventilator settings at the moment of sampling. The current study explored the presence and extent of pulmonary depositions of a complement activation product, C3d, and its association with the clinical diagnosis of ARDS. Autopsy material of critically ill patients who received invasive mechanical ventilation till death was collected, immunohistochemically stained, and analyzed

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