Mechanical Ventilation Clinical Trial
Official title:
Involvement of Fibrocytes in Repair Processes During Acute Respiratory Distress Syndrome (Validation Study-2)
Fibrocyte is a monocyte sub-population involved in fibroproliferation/repair processes and associated with outcome in different diseases. In previous study, we have demonstrated the presence of alveolar fibrocytes during Acute expiratory Distress Syndrome (ARDS) and their association with patient outcome. The purpose of this multicentric observational prospective study is to describe the percentage of alveolar fibrocytes in ICU patients with ARDS (survivors vs. non survivors) and to confirm their association with 28-day mortality.
Background: The acute respiratory distress syndrome (ARDS) remains common (15% of ventilated
patients in the ICU), severe (30% of mortality) and have no specific treatment. Impaired
epithelial repair with fibroproliferation is observed in non resolutive form of ARDS.
Fibrocytes are cells that both express markers of hematopoietic cells (CD34+, CD45+) and
fibroblasts (collagen-1). Fibrocytes may be recruited directly from the pool of circulating
blood monocytes but also derive from monocytes in situ in absence of serum amyloid P (SAP or
pentraxin-2). In murine models of lung injury, it has been shown that fibrocytes were
recruited in the lung and contribute to the local fibrogenesis. Our team is the first to
have demonstrated during ARDS in human the presence of fibrocytes among the alveolar cells
obtained by bronchoalveolar lavage (BAL) (Quesnel et al, Eur Resp J, 2010). In a second
single-center work enrolling 122 patients, we have shown that a percentage of alveolar
fibrocytes > 6% was associated with an increased risk of death (HR = 6.2 [2.8 to 13.6], p
<0.0001). However, this result remains to be confirmed in a second cohort because it was not
the main objective of the first study and because of the variable lead time of BAL sampling
in this cohort of patients with ARDS (Quesnel et al, CCM, 2012). Furthermore, the
correlation of the percentage of blood fibrocytes (Fsg%) with the percentage of alveolar
fibrocytes (Fal%) remains unknown and their kinetics remain to be studied during ARDS
evolution.
Hypothesis and Objective: We hypothesize that percentage of alveolar fibrocytes is a
prognostic marker during ARDS. Our main goal is to confirm in a validation cohort that the %
of alveolar fibrocytes measured in BAL fluid during the first 48 hours of ARDS evolution is
associated with 28-day mortality.
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