Evidence map›Paper›PMID 37178770›Full record

ArticleJournal of thrombosis and haemostasis : JTH2023

Role of circulating mitochondria in venous thrombosis in glioblastoma.

Ricardo Gonzalez-Delgado, Nina M Muñoz, Wendolyn Carlos-Alcalde, Min Soon Cho, Hani Lee, Jeff Jin, Victoria Serpas, Olga Gorlova, Rahul A Sheth, Vahid Afshar-Kharghan

Open access · bronzeAbstract read
In one paragraph

Article in Journal of thrombosis and haemostasis : JTH, 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
1.4field-weighted citation impact, top 19% 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, 9 citations in OpenAlex.

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

10 authors at 2 institutions in 1 country.

Ricardo Gonzalez-DelgadoSection of Benign Hematology, the University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Nina M MuñozDepartment of Interventional Radiology, the University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Wendolyn Carlos-AlcaldeSection of Benign Hematology, the University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Min Soon ChoSection of Benign Hematology, the University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Hani LeeSection of Benign Hematology, the University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Jeff JinInformation Services, Enterprise Development & Integration, the University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Victoria SerpasDepartment of GI Medical Oncology, the University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Olga GorlovaSection of Epidemiology and Population Science, Department of Medicine, Baylor College of Medicine, Houston, Texas, USA.
Rahul A ShethDepartment of Interventional Radiology, the University of Texas MD Anderson Cancer Center, Houston, Texas, USA. Electronic address: rasheth@mdanderson.org.
Vahid Afshar-KharghanSection of Benign Hematology, the University of Texas MD Anderson Cancer Center, Houston, Texas, USA. Electronic address: vakharghan@mdanderson.org.
The University of Texas MD Anderson Cancer Center · USBaylor College of Medicine · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
U.T. M. D. Anderson Cancer Center SPORE in Ovarian CancerP50CA217685 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI SOOD, ANIL K · 2017 to 2021
$7.9M
Platelets promote growth of ovarian cancerR01CA177909 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI AFSHAR-KHARGHAN, VAHID, SOOD, ANIL K · 2013 to 2023
$4.1M
Genetics of Graft-versus-Host DiseaseR01CA231141 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI AFSHAR-KHARGHAN, VAHID, GORLOVA, OLGA · 2018 to 2022
$1.6M
NCI NIH HHS P30 CA016672NCI NIH HHS P50 CA217685NCI NIH HHS R01 CA177909NCI NIH HHS R01 CA231141
6 · The paper itself

Abstract

backgroundMany patients with glioblastoma multiforme (GBM) develop deep venous thrombosis or pulmonary emboli. Cell-free circulating mitochondria increase after brain injury and are associated with coagulopathy.

objectivesThis study evaluated whether mitochondria play a role in the GBM-induced hypercoagulable state.

methodsWe examined the correlation between cell-free circulating mitochondria and venous thrombosis in patients with GBM and the impact of mitochondria on venous thrombosis in mice with inferior vena cava stenosis.

resultsUsing plasma samples of 82 patients with GBM, we found that patients with GBM had a higher number of mitochondria in their plasma (GBM with venous thromboembolism [VTE],: 2.8 × 10

conclusionWe concluded that mitochondria might play a role in the GBM-induced hypercoagulable state. We propose that quantifying circulating mitochondria or anticardiolipin antibody concentrations in patients with GBM might identify patients at increased risk of VTE.

Indexed as

GlioblastomaVenous ThromboembolismVenous ThrombosisAnimalsConstriction, PathologicMiceRisk Factorsanticardiolipin antibodyglioblastomamitochondrianeutrophilsvenous thrombosis

Identifiers

PMID37178770
PMCPMC11603921
OpenAlexW4376126919

What OpenQuestion holds

Textmetadata
LicenceTDM
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.