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Endothelial and inflammatory pathophysiology in dengue shock: New insights from a prospective cohort study in Vietnam.
McBride, Angela; Duyen, Huynh Thi Le; Vuong, Nguyen Lam; Tho, Phan Vinh; Tai, Luong Thi Hue; Phong, Nguyen Thanh; Ngoc, Nguyen Thanh; Yen, Lam Minh; Nhat, Phung Tran Huy; Vi, Tran Thuy; Llewelyn, Martin J; Thwaites, Louise; Hao, Nguyen Van; Yacoub, Sophie.
Affiliation
  • McBride A; Oxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.
  • Duyen HTL; Brighton and Sussex Medical School, Brighton, United Kingdom.
  • Vuong NL; Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom.
  • Tho PV; Oxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.
  • Tai LTH; Oxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.
  • Phong NT; University of Medicine and Pharmacy, Ho Chi Minh City, Vietnam.
  • Ngoc NT; Hospital for Tropical Disease, Ho Chi Minh City, Vietnam.
  • Yen LM; Hospital for Tropical Disease, Ho Chi Minh City, Vietnam.
  • Nhat PTH; Hospital for Tropical Disease, Ho Chi Minh City, Vietnam.
  • Vi TT; Oxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.
  • Llewelyn MJ; Oxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.
  • Thwaites L; Oxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.
  • Hao NV; Oxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.
  • Yacoub S; Brighton and Sussex Medical School, Brighton, United Kingdom.
PLoS Negl Trop Dis ; 18(3): e0012071, 2024 Mar.
Article in En | MEDLINE | ID: mdl-38536887
ABSTRACT
Dengue shock (DS) is the most severe complication of dengue infection; endothelial hyperpermeability leads to profound plasma leakage, hypovolaemia and extravascular fluid accumulation. At present, the only treatment is supportive with intravenous fluid, but targeted endothelial stabilising therapies and host immune modulators are needed. With the aim of prioritising potential therapeutics, we conducted a prospective observational study of adults (≥16 years) with DS in Vietnam from 2019-2022, comparing the pathophysiology underlying circulatory failure with patients with septic shock (SS), and investigating the association of biomarkers with clinical severity (SOFA score, ICU admission, mortality) and pulmonary vascular leak (daily lung ultrasound for interstitial and pleural fluid). Plasma was collected at enrolment, 48 hours later and hospital discharge. We measured biomarkers of inflammation (IL-6, ferritin), endothelial activation (Ang-1, Ang-2, sTie-2, VCAM-1) and endothelial glycocalyx breakdown (hyaluronan, heparan sulfate, endocan, syndecan-1). We enrolled 135 patients with DS (median age 26, median SOFA score 7, 34 required ICU admission, 5 deaths), together with 37 patients with SS and 25 healthy controls. Within the DS group, IL-6 and ferritin were associated with admission SOFA score (IL-6 ßeta0.70, p<0.001 & ferritin ßeta0.45, p<0.001), ICU admission (IL-6 OR 2.6, p<0.001 & ferritin OR 1.55, p<0.001) and mortality (IL-6 OR 4.49, p = 0.005 & ferritin OR 13.8, p = 0.02); both biomarkers discriminated survivors and non-survivors at 48 hours and all patients who died from DS had pre-mortem ferritin ≥100,000ng/ml. IL-6 most strongly correlated with severity of pulmonary vascular leakage (R = 0.41, p<0.001). Ang-2 correlated with pulmonary vascular leak (R = 0.33, p<0.001) and associated with SOFA score (ß 0.81, p<0.001) and mortality (OR 8.06, p = 0.002). Ang-1 was associated with ICU admission (OR 1.6, p = 0.005) and mortality (OR 3.62, p = 0.006). All 4 glycocalyx biomarkers were positively associated with SOFA score, but only syndecan-1 was associated with ICU admission (OR 2.02, p<0.001) and mortality (OR 6.51, p<0.001). This study highlights the central role of hyperinflammation in determining outcomes from DS; the data suggest that anti-IL-1 and anti-IL-6 immune modulators and Tie2 agonists may be considered as candidates for therapeutic trials in severe dengue.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Shock, Septic / Sepsis / Severe Dengue Limits: Adult / Humans Country/Region as subject: Asia Language: En Journal: PLoS Negl Trop Dis Journal subject: MEDICINA TROPICAL Year: 2024 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Shock, Septic / Sepsis / Severe Dengue Limits: Adult / Humans Country/Region as subject: Asia Language: En Journal: PLoS Negl Trop Dis Journal subject: MEDICINA TROPICAL Year: 2024 Document type: Article Affiliation country: Country of publication: