Evidence map›Paper›PMID 34975853›Full record

ArticleFrontiers in immunology2021

Investigation of the Molecular Mechanism of Coagulopathy in Severe and Critical Patients With COVID-19.

Daniel Elieh Ali Komi, Yaghoub Rahimi, Rahim Asghari, Reza Jafari, Javad Rasouli, Mehdi Mohebalizadeh, Ata Abbasi, Rahim Nejadrahim, Farzin Rezazadeh, Vahid Shafiei-Irannejad

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
0.6field-weighted citation impact, top 29% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 13 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
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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

10 authors at 2 institutions in 1 country.

Daniel Elieh Ali KomiCellular and Molecular Research Center, Cellular and Molecular Medicine Institute, Urmia University of Medical Sciences, Urmia, Iran.
Yaghoub RahimiCellular and Molecular Research Center, Cellular and Molecular Medicine Institute, Urmia University of Medical Sciences, Urmia, Iran.
Rahim AsghariHematology, Immune Cell Therapy, and Stem Cells Transplantation Research Center, Clinical Research Institute, Urmia University of Medical Sciences, Urmia, Iran.
Reza JafariHematology, Immune Cell Therapy, and Stem Cells Transplantation Research Center, Clinical Research Institute, Urmia University of Medical Sciences, Urmia, Iran.
Javad RasouliDepartment of Epidemiology and Biostatistics, Faculty of Medicine, Urmia University of Medical Sciences, Urmia, Iran.
Mehdi MohebalizadehStudent Research Committee, Urmia University of Medical Sciences, Urmia, Iran.
Ata AbbasiDepartment of Pathology, Faculty of Medicine, Urmia University of Medical Sciences, Urmia, Iran.
Rahim NejadrahimDepartment of Infectious Diseases, Faculty of Medicine, Urmia University of Medical Sciences, Urmia, Iran.
Farzin RezazadehDepartment of Emergency Medicine, Faculty of Medicine, Urmia University of Medical Sciences, Urmia, Iran.
Vahid Shafiei-IrannejadCellular and Molecular Research Center, Cellular and Molecular Medicine Institute, Urmia University of Medical Sciences, Urmia, Iran.
Urmia University · IRUrmia University of Medical Sciences

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Coagulopathy is a frequently reported finding in the pathology of coronavirus disease 2019 (COVID-19); however, the molecular mechanism, the involved coagulation factors, and the role of regulatory proteins in homeostasis are not fully investigated. We explored the dynamic changes of nine coagulation tests in patients and controls to propose a molecular mechanism for COVID-19-associated coagulopathy. Coagulation tests including prothrombin time (PT), partial thromboplastin time (PTT), fibrinogen (FIB), lupus anticoagulant (LAC), proteins C and S, antithrombin III (ATIII), D-dimer, and fibrin degradation products (FDPs) were performed on plasma collected from 105 individuals (35 critical patients, 35 severe patients, and 35 healthy controls). There was a statically significant difference when the results of the critical (CRT) and/or severe (SVR) group for the following tests were compared to the control (CRL) group: PT

Indexed as

Blood CoagulationAdultAgedBlood Coagulation DisordersBlood Coagulation FactorsBlood Coagulation TestsCOVID-19FemaleFibrinFibrin Fibrinogen Degradation ProductsHomeostasisHumansMaleMiddle AgedPartial Thromboplastin TimePrognosisBlood Coagulation FactorsFibrinFibrin Fibrinogen Degradation Productsfibrin fragment DProtein Cantithrombin III (ATIII)coagulopathyCOVID-19D-dimer (DD)fibrinogenprotein C (PC)protein S

Identifiers

PMID34975853
PMCPMC8716500
OpenAlexW4200585840

What OpenQuestion holds

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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.