4.7 Article

Soluble Urokinase-Type Plasminogen Activator Receptor as a Prognostic Marker of Ugandan Children at Risk of Severe and Fatal Malaria

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CLINICAL INFECTIOUS DISEASES
卷 76, 期 3, 页码 E1079-E1086

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OXFORD UNIV PRESS INC
DOI: 10.1093/cid/ciac457

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soluble urokinase-type plasminogen activator receptor; severe malaria; prognostic marker; risk-stratification; mortality outcome

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This study identified soluble urokinase-type plasminogen activator receptor (suPAR) as a prognostic marker of severe and fatal malaria in Ugandan children. Measuring suPAR at presentation can identify children at risk of severe and fatal malaria, and adding suPAR to clinical scores could improve the recognition and triage of children at risk of death.
Current malaria diagnostic tests do not reliably identify children at risk of severe malaria and death. We identified soluble urokinase-type plasminogen activator receptor (suPAR) as a prognostic marker of severe and fatal malaria in Ugandan children. Background Current malaria diagnostic tests do not reliably identify children at risk of severe and fatal infection. Host immune and endothelial activation contribute to malaria pathogenesis. Soluble urokinase-type plasminogen activator receptor (suPAR) is a marker of these pathways. We hypothesized that measuring suPAR at presentation could risk-stratify children with malaria. Methods Plasma suPAR levels were determined in consecutive febrile children with malaria at presentation to hospital in Jinja, Uganda. We evaluated the accuracy of suPAR in predicting in-hospital mortality, and whether suPAR could improve a validated clinical scoring system (Lambarene Organ Dysfunction Score [LODS]). Results Of the 1226 children with malaria, 39 (3.2%) died. suPAR concentrations at presentation were significantly higher in children who went on to die than in those who survived (P < .0001). suPAR levels were associated with disease severity (LODS: 0 vs 1, P = .001; 1 vs 2, P < .001; 2 vs 3, 0 vs 2, 1 vs 3, and 0 vs 3, P < .0001). suPAR concentrations were excellent predictors of in-hospital mortality (area under the receiver operating characteristic curve [AUROC], 0.92 [95% confidence interval {CI}, .91-.94]). The prognostic accuracy of LODS (AUROC, 0.93 [95% CI, .91-.94]) was improved when suPAR was added (AUROC, 0.97 [95% CI, .96-.98]; P < .0001). Conclusions Measuring suPAR at presentation can identify children at risk of severe and fatal malaria. Adding suPAR to clinical scores could improve the recognition and triage of children at risk of death. suPAR can be detected with a point-of-care test and can now be evaluated in prospective trials.

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