4.5 Article

Serum neutrophil gelatinase-associated lipocalin and resistin are associated with dengue infection in adults

Journal

BMC INFECTIOUS DISEASES
Volume 16, Issue -, Pages -

Publisher

BMC
DOI: 10.1186/s12879-016-1759-9

Keywords

Dengue; Neutrophil gelatinase-associated lipocalin (NGAL); Resistin; Serum

Funding

  1. Ministry of Science and Technology [MOST 104-2320-B-037-014-MY3, MOST 104-2314-B-037-053-MY4, MOST 103-2320-B-037-006-MY3]
  2. Kaohsiung Medical University Aim for the Top 500 Universities Grant [KMU-DT105010]
  3. Kaohsiung Medical University Aim for the Top Universities Grant [KMU-TP103A13]

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Background: Dengue is a major health problem in tropical areas, including Taiwan. Dengue virus infection affects various types of cells and results in elevation of serum inflammatory molecules. Because these molecules may be associated with dengue virus infection, the aim of this study was to identify novel molecules in febrile patients with dengue infection. In addition, we determined whether these molecules were correlated with the count of leukocytes and platelets. Methods: Febrile adults (Age >18 years old) who presented to the emergency department and were confirmed dengue virus infection were enrolled in this study. Serum from dengue patients and healthy controls was collected and serum level of sepsis-associated inflammatory molecules was measured by Luminex assay. Results: Elevated level of macrophage migration inhibitory factor, soluble vascular cell adhesion molecule-1, sFasL, resistin and interferon-gamma were detected in patients' serum. Higher levels of neutrophil gelatinase-associated lipocalin (NGAL) and resistin were detected in dengue patients with normal leukocyte count and all dengue patients, respectively. Furthermore, the serum level of NGAL, but not resistin, was correlated with cell count in dengue patients. Conclusion: Our results revealed that resistin and NGAL are novel dengue-associated molecules. These results may help elucidate the regulatory mechanisms of anti-dengue immune responses.

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