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Association of microvascular function and endothelial biomarkers with clinical outcome in dengue: an observational study

Authors :
Tran Thi Toan
Bridget Wills
Phung Khanh Lam
Ngo Ha
Nguyen Van Kinh
Nguyen Than Ha Quyen
Le Hoang Mai Vu
Sophie Yacoub
Juthathip Mongkolspaya
Huynh Thi Le Duyen
Cameron P. Simmons
Thi Lien Le
Annette Fox
Marcel Wolbers
Gavin R. Screaton
Heiman F. L. Wertheim
Nguyen T. B. Van
Wellcome Trust
Source :
The Journal of Infectious Diseases, 214, 5, pp. 697-706, The Journal of Infectious Diseases, The Journal of Infectious Diseases, 214, 697-706
Publication Year :
2016
Publisher :
Oxford University Press, 2016.

Abstract

Background. The hallmark of severe dengue is increased microvascular permeability, but alterations in the microcirculation and their evolution over the course of dengue are unknown. Methods. We conducted a prospective observational study to evaluate the sublingual microcirculation using side-stream dark-field imaging in patients presenting early (Results. A total of 165 patients were enrolled. No difference was found between the microcirculatory parameters comparing dengue with other febrile illnesses. The proportion of perfused vessels (PPV) and the mean flow index (MFI) were lower in patients with dengue with plasma than those without leakage (PPV, 88.1% vs 90.6% [P = .01]; MFI, 2.1 vs 2.4 [P = .007]), most markedly during the critical phase. PPV and MFI were correlated with the endothelial activation markers vascular cell adhesion molecule 1 (P < .001 for both) and angiopoietin 2 (P < .001 for both), negatively correlated. Conclusions. Modest microcirculatory alterations occur in dengue, are associated with plasma leakage, and are correlate with molecules of endothelial activation, angiopoietin 2 and vascular cell adhesion molecule 1.

Details

Language :
English
ISSN :
00221899
Database :
OpenAIRE
Journal :
The Journal of Infectious Diseases, 214, 5, pp. 697-706, The Journal of Infectious Diseases, The Journal of Infectious Diseases, 214, 697-706
Accession number :
edsair.doi.dedup.....0e08c742f80f4d7ddade550bb2294dbb