Evidence map›Paper›PMID 40761632›Full record

ArticleUpsala journal of medical sciences2025

ARDS severity in COVID-19: a case-control study of laboratory biomarkers and IL-10 SNP analysis.

Shukur Wasman Smail, Niaz Albarzinji, Karim Jalal Karim, Rebaz Hamza Salih, Christer Janson

Abstract read
In one paragraph

Article in Upsala journal of medical sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. 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

5 authors.

Shukur Wasman SmailDepartment of Biology, College of Science, Salahaddin University-Erbil, Erbil, Iraq.ORCID https://orcid.org/0000-0001-8188-2540
Niaz AlbarzinjiCollege of Medicine, Hawler Medical University, Erbil, Iraq.
Karim Jalal KarimDepartment of Medical Laboratory Science, Faculty of Science and Health, Koya University, Erbil, Iraq.
Rebaz Hamza SalihDepartment of Respiratory Medicine, PAR Private Hospital, Erbil, Iraq.
Christer JansonDepartment of Medical Science, Respiratory Medicine, and Allergology, Uppsala University and University Hospital, Uppsala, Sweden.ORCID https://orcid.org/0000-0001-5093-6980

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Acute respiratory distress syndrome (ARDS), which is often observed in severe cases of coronavirus disease 2019 (COVID-19), is known to be a major contributor to higher mortality rates. This study assesses how hematological parameters, inflammatory biomarkers, cytokines, and the -1,082 A/G polymorphism are associated with ARDS severity in COVID-19 patients. Methods: Following exclusions, a 6-month prospective case-control study included 82 healthy controls (HCs) and 158 COVID-19 patients with varying severities of ARDS (mild: 73, moderate: 53, and severe: 32). Blood samples were collected at admission, and laboratory biomarkers were assessed using various methods. Statistical analyses included one-way analysis of variance with Tukey's test for group comparisons, Pearson correlation, and receiver operating characteristic curve for analyzing independent associations with COVID-19 severity. Multiple linear regression and chi-square tests were used to evaluate quantitative outcomes and categorical associations, respectively. Results: Severe ARDS patients exhibited higher C-reactive protein (CRP) levels compared to HCs. Compared to HCs, patients with moderate and severe ARDS had higher neutrophil to lymphocyte ratio (NLR), neutrophil counts, tumor necrosis factor-alpha, and interleukin-10 (IL-10), as well as lower lymphocyte counts and reduced partial pressure of oxygen/fraction of inspired oxygen (PaO Conclusion: Hematological indices (neutrophil count and NLR), CRP, and serum IL-10 hold promise in monitoring ARDS severity in COVID-19 patients. In addition, COVID-19 patients with GG and AG genotypes and the G allele of the IL-10 gene's-1,082 A/G polymorphism experience less severe ARDS. This highlights the potential protective role of IL-10 genetic variation in modulating the severity of inflammatory responses during severe acute respiratory syndrome-coronavirus-2 infection and may serve as a useful genetic marker for risk stratification in clinical settings.

Indexed as

COVID-19Interleukin-10Polymorphism, Single NucleotideRespiratory Distress SyndromeAdultAgedBiomarkersCase-Control StudiesC-Reactive ProteinFemaleHumansMaleMiddle AgedProspective StudiesSARS-CoV-2Severity of Illness IndexBiomarkersC-Reactive ProteinIL10 protein, humanInterleukin-10Acute respiratory distress syndromeCOVID-19cytokineshematological parameterspolymorphism

Identifiers

PMID40761632
PMCPMC12320925

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.