Evidence map›Paper›PMID 34620968›Full record

ArticleScientific reports2021

sFlt-1 and CA 15.3 are indicators of endothelial damage and pulmonary fibrosis in SARS-CoV-2 infection.

Marilena Greco, Salvatore Suppressa, Roberta Assunta Lazzari, Fernando Sicuro, Carmelo Catanese, Giambattista Lobreglio

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.2field-weighted citation impact, top 18% 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

11 citing papers in PubMed, 20 citations in OpenAlex.

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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

6 authors at 1 institution in 1 country.

Marilena GrecoClinical Pathology and Microbiology, Vito Fazzi General Hospital ASL-Lecce, 73100 Piazza Muratore, Lecce, Italy. grecomarilena@gmail.com.ORCID 0000-0002-6829-897X
Salvatore SuppressaClinical Pathology and Microbiology, Vito Fazzi General Hospital ASL-Lecce, 73100 Piazza Muratore, Lecce, Italy.
Roberta Assunta LazzariClinical Pathology and Microbiology, Vito Fazzi General Hospital ASL-Lecce, 73100 Piazza Muratore, Lecce, Italy.
Fernando SicuroClinical Pathology and Microbiology, Vito Fazzi General Hospital ASL-Lecce, 73100 Piazza Muratore, Lecce, Italy.
Carmelo CataneseIntensive Care Unit, Vito Fazzi General Hospital ASL-Lecce, Lecce, Italy.
Giambattista LobreglioClinical Pathology and Microbiology, Vito Fazzi General Hospital ASL-Lecce, 73100 Piazza Muratore, Lecce, Italy.
Ospedale Vito Fazzi · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

COVID-19 pandemic led to a worldwide increase of hospitalizations for interstitial pneumonia with thrombosis complications, endothelial injury and multiorgan disease. Common CT findings include lung bilateral infiltrates, bilateral ground-glass opacities and/or consolidation whilst no current laboratory parameter consents rapidly evaluation of COVID-19 risk and disease severity. In the present work we investigated the association of sFLT-1 and CA 15.3 with endothelial damage and pulmonary fibrosis. Serum sFlt-1 has been associated with endothelial injury and sepsis severity, CA 15.3 seems an alternative marker for KL-6 for fibrotic lung diseases and pulmonary interstitial damage. We analysed 262 SARS-CoV-2 patients with differing levels of clinical severity; we found an association of serum sFlt-1 (ROC AUC 0.902, decision threshold > 90.3 pg/mL, p < 0.001 Sens. 83.9% and Spec. 86.7%) with presence, extent and severity of the disease. Moreover, CA 15.3 appeared significantly increased in COVID-19 severe lung fibrosis (ICU vs NON-ICU patients 42.6 ± 3.3 vs 25.7 ± 1.5 U/mL, p < 0.0001) and was associated with lung damage severity grade (ROC AUC 0.958, decision threshold > 24.8 U/mL, p < 0.0001, Sens. 88.4% and Spec. 91.8%). In conclusion, serum levels of sFlt-1 and CA 15.3 appeared useful tools for categorizing COVID-19 clinical stage and may represent a valid aid for clinicians to better personalise treatment.

Indexed as

AgedBiomarkersCOVID-19FemaleHumansLung Diseases, InterstitialMaleMiddle AgedMucin-1Pulmonary FibrosisSARS-CoV-2Vascular Endothelial Growth Factor Receptor-1BiomarkersFLT1 protein, humanMucin-1Vascular Endothelial Growth Factor Receptor-1

Identifiers

PMID34620968
PMCPMC8497540
OpenAlexW3204525761

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Registered trials

None linked

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.