Evidence map›Paper›PMID 38226339›Full record

ArticleResearch and practice in thrombosis and haemostasis2024

Activation of coagulation FXI promotes endothelial inflammation and amplifies platelet activation in a nonhuman primate model of hyperlipidemia.

Tia C L Kohs, Helen H Vu, Kelley R Jordan, Iván Parra-Izquierdo, Monica T Hinds, Joseph J Shatzel, Paul Kievit, Terry K Morgan, Samuel Tassi Yunga, Thuy T M Ngo and 8 more

Open access · goldAbstract read
In one paragraph

Article in Research and practice in thrombosis and haemostasis, 2024. 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
3.4field-weighted citation impact, top 6% 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, 16 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. 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

18 authors at 5 institutions in 1 country.

Tia C L KohsDepartment of Biomedical Engineering, Oregon Health & Science University, Portland, Oregon, USA.
Helen H VuDepartment of Biomedical Engineering, Oregon Health & Science University, Portland, Oregon, USA.
Kelley R JordanDepartment of Biomedical Engineering, Oregon Health & Science University, Portland, Oregon, USA.
Iván Parra-IzquierdoDepartment of Biomedical Engineering, Oregon Health & Science University, Portland, Oregon, USA.
Monica T HindsDepartment of Biomedical Engineering, Oregon Health & Science University, Portland, Oregon, USA.
Joseph J ShatzelDepartment of Biomedical Engineering, Oregon Health & Science University, Portland, Oregon, USA.
Paul KievitDivision of Cardiometabolic Health, Oregon National Primate Research Center, Oregon Health & Science University, Beaverton, Oregon, USA.
Terry K MorganDepartment of Pathology and Laboratory Medicine, Oregon Health & Science University, Portland, Oregon, USA.
Samuel Tassi YungaDepartment of Biomedical Engineering, Oregon Health & Science University, Portland, Oregon, USA.
Thuy T M NgoDepartment of Biomedical Engineering, Oregon Health & Science University, Portland, Oregon, USA.
Joseph E AslanDepartment of Biomedical Engineering, Oregon Health & Science University, Portland, Oregon, USA.
Michael WallischDepartment of Biomedical Engineering, Oregon Health & Science University, Portland, Oregon, USA.
Christina U LorentzDepartment of Biomedical Engineering, Oregon Health & Science University, Portland, Oregon, USA.
Erik I TuckerDepartment of Biomedical Engineering, Oregon Health & Science University, Portland, Oregon, USA.
David GailaniDepartment of Pathology, Microbiology and Immunology, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Jonathan R LindnerDivision of Cardiovascular Medicine and Robert M. Berne Cardiovascular Research Institute, University of Virginia, Charlottesville, Virginia, USA.
Cristina PuyDepartment of Biomedical Engineering, Oregon Health & Science University, Portland, Oregon, USA.
Owen J T McCartyDepartment of Biomedical Engineering, Oregon Health & Science University, Portland, Oregon, USA.
Oregon Health & Science University · USAronora (United States) · USOregon National Primate Research Center · USUniversity of Virginia · USVanderbilt University Medical Center · US

Funding

Upgrade of confocal microscopy at the Oregon National Primate Research CenterP51OD011092 · OD · OREGON HEALTH & SCIENCE UNIVERSITY · PI Bonnie J. Nagel · 2012 to 2026
$203.9M
Characterization of Coagulation Factor-platelet Interactions: Role of FXIR01HL101972 · NHLBI · OREGON HEALTH & SCIENCE UNIVERSITY · PI Owen J McCarty · 2010 to 2026
$8.5M
Targeted CEU Imaging of Atherosclerosis and AngiogenesisR01HL078610 · NHLBI · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI LINDNER, JONATHAN R · 2004 to 2022
$6.8M
Biochemistry and Pathophysiology of Factor XI and Contact ActivationR35HL140025 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI GAILANI, DAVID · 2018 to 2024
$5.5M
Augmentation of Tissue Perfusion with Ultrasound-mediated CavitationR01HL130046 · NHLBI · UNIVERSITY OF VIRGINIA · PI LINDNER, JONATHAN R · 2016 to 2023
$5.5M
Pathway Maps of Platelet Phenotype and FunctionR01HL146549 · NHLBI · OREGON HEALTH & SCIENCE UNIVERSITY · PI ASLAN, JOSEPH E · 2019 to 2023
$2.5M
Evaluating the Safety and Efficacy of Targeting the Contact Pathway to Prevent Device Associated Thrombosis.R01HL151367 · NHLBI · OREGON HEALTH & SCIENCE UNIVERSITY · PI SHATZEL, JOSEPH JAMES · 2020 to 2024
$1.5M
NHLBI NIH HHS R01 HL078610NHLBI NIH HHS R01 HL101972NHLBI NIH HHS R01 HL130046NHLBI NIH HHS R01 HL146549NHLBI NIH HHS R01 HL151367NHLBI NIH HHS R35 HL140025NIH HHS P51 OD011092
6 · The paper itself

Abstract

Background: Hyperlipidemia is associated with chronic inflammation and thromboinflammation. This is an underlying cause of several cardiovascular diseases, including atherosclerosis. In diseased blood vessels, rampant thrombin generation results in the initiation of the coagulation cascade, activation of platelets, and endothelial cell dysfunction. Coagulation factor (F) XI represents a promising therapeutic target to reduce thromboinflammation, as it is uniquely positioned at an intersection between inflammation and thrombin generation. Objectives: This study aimed to investigate the role of FXI in promoting platelet and endothelial cell activation in a model of hyperlipidemia. Methods: Nonhuman primates (NHPs) were fed a standard chow diet (lean, Results: Obese NHPs demonstrated increased sensitivity for platelet P-selectin expression and phosphatidylserine exposure in response to platelet GPVI or PAR agonists compared with lean NHPs. Obese NHPs exhibited elevated levels of C-reactive protein, cathepsin D, and myeloperoxidase compared with lean NHPs. Following pharmacological inhibition of FIX activation by FXIa, platelet priming for activation by GPVI or PAR agonists, C-reactive protein levels, and endothelial VCAM-1 levels were reduced in obese NHPs. Conclusion: FXI activation promotes the proinflammatory phenotype of hyperlipidemia by priming platelet activation and inciting endothelial cell dysfunction.

Indexed as

atherosclerosishyperlipidemiainflammationplateletsthrombin

Identifiers

PMID38226339
PMCPMC10788631
OpenAlexW4389044140

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.