Abstract
BackgroundImpaired gastric emptying is common in critically ill patients. Intestinal dysmotility, a major cause of feed intolerance, may foster infectious complications due to mucosal barrier disruption. However, little is known about gut-directed immune activation, intestinal barrier function and its association with impaired gastric emptying in critically ill patients at ICU admission.MethodsWe conducted a prospective observational study at two tertiary care medical ICUs. Fifty consecutive patients needing invasive mechanical ventilation were recruited within 24 h of ICU admission, prior to any nutritional support. The acute physiology and chronic health evaluation (APACHE) II score, the sequential organ failure assessment (SOFA) score and the multiple organ dysfunction score (MODS) were used to assess illness severity and multiple organ dysfunction. Gastric emptying was assessed by paracetamol absorption test. Peripheral blood mononuclear cells were freshly isolated and cultured for 24 h, and TNF-α, IL-1β and IL-10 measured in cell culture supernatants and in serum by ELISA. The intestinal epithelial barrier was assessed, quantifying serum concentrations of intestinal fatty acid binding protein (I-FABP), ileal bile-acid binding protein (I-BABP) and zonulin-1 by ELISA. Small bowel homing T lymphocytes (CD4+ α4β7 + CCR9+) were analyzed by flow cytometry. The Mann-Whitney test and Spearman correlation were used in statistical evaluation.ResultsCD4 + α4β7 + CCR9+ T lymphocytes were inversely correlated with gastric emptying. Patients with delayed gastric emptying at ICU admission (n = 35) had significantly higher serum and PBMC-induced TNF-α and IL-1β and increased intestinal barrier disruption reflected by higher I-FABP, I-BABP and zonulin-1. Patients who died in the ICU had significantly impaired gastric empting at admission compared to ICU survivors. No differences were observed in APACHE II, SOFA or MODS in patients with delayed gastric emptying compared to patients with normal gastric emptying.ConclusionsExaggerated CD4 + α4β7 + CCR9+ T lymphocyte homing with increased pro-inflammatory cytokine release and intestinal epithelial barrier disruption are associated with delayed gastric emptying. This is not simply due to differences in overall severity of illness at ICU admission and may represent a pathophysiological mechanism of gut-directed immune activation leading to impaired barrier function in the critically ill.
Highlights
Impaired gastric emptying is common in critically ill patients
While we have previously identified association between CD4 + α4β7 + CCR9+ T lymphocytes and gastric emptying [6], we hypothesized that CD4 + α4β7 + CCR9+ T lymphocytes are associated with enhanced proinflammatory cytokine secretion, intestinal barrier disruption and delayed gastric emptying in the critically ill
Increased intestinal permeability predicts the development of multiple organ failure and early enteral nutrition is a key factor for preservation of gut barrier function reducing the risk of organ failure [11]
Summary
Impaired gastric emptying is common in critically ill patients. Little is known about gut-directed immune activation, intestinal barrier function and its association with impaired gastric emptying in critically ill patients at ICU admission. Enteral nutrition via the gastrointestinal tract is accepted to improve health outcomes in critically ill patients [1]. The advantages of enteral nutrition include a decrease in infectious complications and mucosal barrier protection against bacterial translocation [2, 3]. The intestine participates in the inflammatory response locally with cytokine production and leukocyte recruitment. To perform their immunological functions, T lymphocytes must exit the blood and enter into different tissues in the body. Co-expression of α4β7 and CCR9 delineates a subset of T lymphocytes preferentially migrating to the lamina propria of the small intestine [5]
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