Annals of the American Thoracic Society · 2025
Endothelial Glycocalyx Degradation in Sepsis: Analysis of the Crystalloid Liberal or Vasopressors Early Resuscitation in Sepsis (CLOVERS) Trial, a Multicenter, Phase 3, Randomized Trial.
СтатьяРандомизированное исследованиеМногоцентровое исследованиеКлиническое исследование III фазыНазвание и аннотация: Перевод в очереди
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Oshima Kaori, Di Gravio Chiara, Yan Bailu, McMurtry Sarah A, Burke Ryan, Levoir Lisa M, Kravitz Max S, Stephenson Daniel, Issaian Aaron, Hansen Kirk C, D'Alessandro Angelo, Douglas Ivor S, Self Wesley H, Lindsell Christopher J, Schildcrout Jonathan S, Schmidt Eric P, Shapiro Nathan I
Аннотация
Rationale: Prior evidence suggests that endothelial glycocalyx degradation contributes to sepsis pathogenesis and is potentially worsened by intravenous fluid resuscitation. Objectives: To assess 1) the association of endothelial glycocalyx degradation with sepsis mortality, 2) the impact of a randomly assigned liberal versus restrictive intravenous fluid resuscitation strategy on endothelial glycocalyx degradation, and 3) whether there is a differential treatment effect for mortality based on baseline endothelial glycocalyx degradation. Methods: We used an enriched sampling strategy to define a cohort of 574 patients enrolled in the CLOVERS (Crystalloid Liberal or Vasopressors Early Resuscitation in Sepsis) trial, which compared liberal versus restrictive intravenous fluid resuscitation strategies. We used mass spectrometry to quantify plasma heparan sulfate as the primary measure of endothelial glycocalyx degradation. Plasma syndecan-1, quantified by enzyme-linked immunoassay, served as a clinically feasible complementary index of endothelial glycocalyx degradation. The primary outcome was 90-day all-cause mortality. Results: There was an association between baseline heparan sulfate level and mortality, with increasing mortality by baseline heparan sulfate tertile: lower tertile, 9.9% (95% confidence interval, 7.0-12.7%); middle tertile, 20.4% (15.6-25.0%); and upper tertile, 44.2% (35.6-51.6%) (P < 0.001; log-rank test), with an adjusted hazard ratio for interquartile range change in heparan sulfate of 3.12 (95% confidence interval, 2.18-4.46). We observed no effect of assigned fluid resuscitation strategy on endothelial glycocalyx degradation 24 hours after randomization. We observed no evidence of differential treatment effect of fluid resuscitation strategy based on baseline plasma heparan sulfate for 90-day mortality. Similar findings were observed using plasma syndecan-1 as an index of endothelial glycocalyx degradation. Conclusions: Endothelial glycocalyx degradation is a strong predictor of mortality in sepsis. Fluid resuscitation strategy had no impact on endothelial glycocalyx degradation, and there was no evidence for a differential effect of resuscitation strategy by baseline levels of endothelial glycocalyx degradation. Clinical trial registered with www.clinicaltrials.gov (NCT03434028).