Evidence map›Paper›PMID 36525302›Full record

ArticleJournal of clinical laboratory analysis2023

Serum calprotectin can indicate current and future severity of COVID-19.

Hajar Shokri-Afra, Mona Moradi, Hadis Musavi, Hemen Moradi-Sardareh, Bahman Moradi Poodeh, Arash Kazemi Veisari, Ziaeddin Oladi, Mahboobe Ebrahimi

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical laboratory analysis, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 21% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 1 synthesis or guideline pooled it, 8 citations in OpenAlex.

  1. Pooled it
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  5. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 5 institutions in 2 countries.

Hajar Shokri-AfraGut and Liver Research Center, Non-communicable Diseases Institute, Mazandaran University of Medical Sciences, Sari, Iran.ORCID https://orcid.org/0000-0001-9558-7104
Mona MoradiPediatric Infectious Diseases Research Center, Communicable Diseases Institute, Mazandaran University of Medical Sciences, Sari, Iran.
Hadis MusaviDepartment of Clinical Biochemistry, School of Medicine, Babol University of Medical Sciences, Babol, Iran.
Hemen Moradi-SardarehDepartment of Research and Technology, Asadabad School of Medical Science, Asadabad, Iran.
Bahman Moradi PoodehDepartment of Laboratory Sciences, Lahijan Branch, Islamic Azad University, Lahijan, Iran.
Arash Kazemi VeisariGut and Liver Research Center, Non-communicable Diseases Institute, Mazandaran University of Medical Sciences, Sari, Iran.
Ziaeddin OladiDepartment of Internal Medicine, School of Medicine, Ghaem Shahr Razi Hospital, Mazandaran University of Medical Sciences, Sari, Iran.ORCID https://orcid.org/0000-0002-1509-2273
Mahboobe EbrahimiGut and Liver Research Center, Non-communicable Diseases Institute, Mazandaran University of Medical Sciences, Sari, Iran.
Mazandaran University of Medical Sciences · IRBabol University of Medical Sciences · IRHamedan University of Medical Sciences · IRIslamic Azad University, Lahijan Branch · IRRazi Hospital · IR

Funding

Mazandaran University of Medical Sciences 7899
6 · The paper itself

Abstract

backgroundPredictive and prognostic biomarkers to guide 2019 novel coronavirus disease (COVID-19) are critically evolving. Dysregulated immune responses are the pivotal cause of severity mainly mediated by neutrophil activation. Thus, we evaluated the association of calprotectin, neutrophil secretory protein, and other mediators of inflammation with the severity and outcomes of COVID-19.

methodsThis two-center prospective study focused on PCR-proven COVID-19 patients (n = 76) with different clinical presentations and SARS-CoV-2 negative control subjects (n = 24). Serum calprotectin (SC) was compared with IL-6 and other laboratory parameters.

resultsMedian levels of SC were significantly higher in COVID-19 patients in comparison to the control group (3760 vs. 2100 ng/ml, p < 0.0001). Elevated SC was significantly respective of disease severity (3760 ng/ml in mild up to 5700 ng/ml in severe cases, p < 0.0001). Moreover, the significant positive and negative correlations of SC with disease severity and oxygenation status indicated disease progression and respiratory worsening, respectively. It was found that SC was high in severe patients during hospitalization and significantly declined to normal after recovery. The logistic analysis identified the independent predictive power of SC for respiratory status or clinical severity. Indeed, SC behaved as a better discriminator for both outcomes, as it exhibited the largest area under the curve (receiver operating curve analysis), with the highest specificity and sensitivity when the predictive value of inflammatory biomarkers was compared.

conclusionCalprotectin can be used as a reliable prognostic tool to predict the poor clinical outcomes of COVID-19 patients.

Indexed as

COVID-19BiomarkersHumansLeukocyte L1 Antigen ComplexProspective StudiesSARS-CoV-2Severity of Illness IndexBiomarkersLeukocyte L1 Antigen ComplexcalprotectinCOVID-19IL-6inflammatory biomarkersoutcome

Identifiers

PMID36525302
PMCPMC9833977
OpenAlexW4311667138

What OpenQuestion holds

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Registered trials

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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.