Evidence map›Paper›PMID 40682081›Full record

ArticleMalaria journal2025

Preliminary assessment of serum endocan as a biomarker of disease severity in Plasmodium falciparum and Plasmodium vivax malaria.

Kwannan Nantavisai, Srisombat Puttikamonkul, Parnpen Viriyavejakul

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In one paragraph

Article in Malaria journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Kwannan NantavisaiDepartment of Microbiology, Faculty of Medicine, Srinakharinwirot University, 114 Sukhumvit 23, Bangkok, 10110, Thailand. Kwannan@g.swu.ac.th.
Srisombat PuttikamonkulDepartment of Microbiology, Faculty of Medicine, Srinakharinwirot University, 114 Sukhumvit 23, Bangkok, 10110, Thailand.
Parnpen ViriyavejakulDepartment of Tropical Pathology, Faculty of Tropical Medicine, Mahidol University, 420/6 Rajvithi Road, Bangkok, 10400, Thailand.

Funding

Faculty of Medicine, Srinakharinwirot University, Thailand. 262/2558
6 · The paper itself

Abstract

backgroundEndocan, a component of endothelial glycocalyx, is a recognized biomarker of endothelial dysfunction in various inflammatory and infectious diseases. Malaria, characterized by marked endothelial activation and microvascular pathology, may involve endocan, but its role remains unclear. This study aimed to assess serum endocan levels in various clinical presentations of malaria and evaluate its correlation with laboratory parameters of disease severity.

methodsLeftover serum samples from 99 participants were categorized into four groups: healthy controls (n = 20), Plasmodium vivax malaria (n = 36), uncomplicated Plasmodium falciparum malaria (n = 30), and severe P. falciparum malaria (n = 13). Serum endocan concentrations were measured via enzyme-linked immunosorbent assay on day 0 (pre-treatment) and day 7 (post-treatment). Correlation analyses examined associations between endocan levels and laboratory parameters, including parasite density, white blood cell count, haemoglobin, and platelet count.

resultsAll malaria groups showed significantly higher serum endocan levels compared to healthy controls (p < 0.0001). Levels were highest in severe P. falciparum (median 4.67 [IQR 2.85-7.93] ng/ml), followed by uncomplicated P. falciparum (median 3.27 [IQR 2.24-4.33] ng/ml), and P. vivax malaria (median 1.85 [IQR 1.44-3.23] ng/ml). Endocan correlated positively with parasite density in P. vivax (r

conclusionSerum endocan is elevated in malaria in a severity-dependent manner-highest in severe P. falciparum malaria-and correlates with circulating parasite density and thrombocytopenia, highlighting its potential as a biomarker of endothelial injury in malaria.

Indexed as

Malaria, FalciparumMalaria, VivaxNeoplasm ProteinsProteoglycansAdolescentAdultAgedBiomarkersFemaleHumansMaleMiddle AgedPlasmodium falciparumPlasmodium vivaxSeverity of Illness IndexYoung AdultBiomarkersESM1 protein, humanNeoplasm ProteinsProteoglycansBiomarkerDisease severityEndocanEndothelial dysfunctionMalariaPlasmodium falciparumPlasmodium vivax

Identifiers

PMID40682081
PMCPMC12273299

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.