Evidence map›Paper›PMID 34185390›Full record

ArticleInternational journal of laboratory hematology2021

Thrombin generation abnormalities in commonly encountered platelet function disorders.

Tanmya Sharma, Justin G Brunet, Subia Tasneem, Stephanie A Smith, James H Morrissey, Catherine P M Hayward

Open access · hybridAbstract read
In one paragraph

Article in International journal of laboratory hematology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.9field-weighted citation impact, top 25% 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, 8 citations in OpenAlex.

  1. Review
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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 3 institutions in 2 countries.

Tanmya SharmaDepartment of Pathology and Molecular Medicine, McMaster University, Hamilton, ON, Canada.
Justin G BrunetDepartment of Pathology and Molecular Medicine, McMaster University, Hamilton, ON, Canada.
Subia TasneemDepartment of Pathology and Molecular Medicine, McMaster University, Hamilton, ON, Canada.ORCID https://orcid.org/0000-0002-8859-4119
Stephanie A SmithUniversity of Michigan Medical School, Ann Arbor, MI, USA.ORCID https://orcid.org/0000-0003-4895-6215
James H MorrisseyUniversity of Michigan Medical School, Ann Arbor, MI, USA.ORCID https://orcid.org/0000-0002-1570-1569
Catherine P M HaywardDepartment of Pathology and Molecular Medicine, McMaster University, Hamilton, ON, Canada.ORCID https://orcid.org/0000-0002-2843-0817
McMaster University · CAUniversity of Michigan · USHamilton Regional Laboratory Medicine Program · CA

Funding

Mechanisms in Blood ClottingR35HL135823 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MORRISSEY, JAMES H. · 2017 to 2023
$4.8M
Canadian Hemophilia SocietyNHLBI NIH HHS R35 HL135823NIH Clinical Center NIH grant R35 HL135823
6 · The paper itself

Abstract

introductionStudies of thrombin generation (TG) with platelet-rich plasma (PRP) and platelet-poor plasma (PPP) have provided insights on bleeding disorders. We studied TG for a cohort with commonly encountered platelet function disorders (PFD).

methodsParticipants included 40 controls and 31 with PFD due to: nonsyndromic dense granule (DG) deficiency (PFD-DGD, n = 9), RUNX1 haploinsufficiency (n = 6) and aggregation defects from other, uncharacterized causes (n = 16). TG was tested with PRP and PPP samples. As DG store ADP and polyphosphate that enhance platelet-dependent TG, PFD-DGD PRP TG was tested for correction with ADP, polyphosphate and combined additives. Tissue factor pathway inhibitor (TFPI), platelet factor V (FV), and platelet TFPI and ANO6 transcript levels were also evaluated. Findings were tested for associations with TG endpoints and bleeding.

resultsPFD samples had impaired PRP TG, but also impaired PPP TG, with strong associations between their PRP and PPP TG endpoints (P ≤ .005). PFD-DGD PRP TG endpoints showed associations to PPP TG endpoints but not to DG counts, and were improved, but not fully corrected, by adding polyphosphate and agonists. PFD participants had increased plasma TFPI and reduced platelet TFPI (P ≤ .02) but normal levels of platelet FV, and platelet TFPI and ANO6 transcripts levels. PFD plasma TFPI levels showed significant association to several PPP TG endpoints (P ≤ .04). Several PFD PRP TG endpoints showed significant associations to bleeding symptoms, including wound healing problems and prolonged bleeding from minor cuts (P ≤ .04).

conclusionTG is impaired in commonly encountered PFD, with their PRP TG findings showing interesting associations to symptoms.

Indexed as

BiomarkersBlood CoagulationDisease SusceptibilityBlood Coagulation TestsBlood Platelet DisordersDisease ManagementHumansPhenotypePlatelet-Rich PlasmaPrognosisThrombinBiomarkersThrombinbleedingblood platelet disorderscoagulationplatelet storage pool deficiencythrombin generation

Identifiers

PMID34185390
PMCPMC8599625
OpenAlexW3176504490

What OpenQuestion holds

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LicenceCC BY
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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.