Evidence map›Paper›PMID 33232305›Full record

ArticleJCI insight2021

Shear stress associated with cardiopulmonary bypass induces expression of inflammatory cytokines and necroptosis in monocytes.

Lan N Tu, Lance Hsieh, Masaki Kajimoto, Kevin Charette, Nataliya Kibiryeva, Adriana Forero, Sarah Hampson, Jennifer A Marshall, James O'Brien, Marta Scatena and 8 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in JCI insight, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07393243 (Does Clear Priming of the Cardiopulmonary Bypass Circuit Reduce Bypass Associated Inflammation in Ventricular Septal Defect Patients?), which is not on this map. Cited by 27 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 14% 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.

NCT07393243 nanot yet recruitingnot on this mapstarted 2026, after this paper: background citation

Does Clear Priming of the Cardiopulmonary Bypass Circuit Reduce Bypass Associated Inflammation in Ventricular Septal Defect Patients?

TypeinterventionalSponsorSeattle Children's HospitalRan2026 to 2030Enrolled60ConditionsVentricular Septal DefectArmsClear priming of the bypass pump
3 · Its place in the literature

Who cites it

27 citing papers in PubMed, 1 synthesis or guideline pooled it, 42 citations in OpenAlex.

  1. Pooled it
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  7. Recruitment of CCR5Genes and immunity · 2026
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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

18 authors at 4 institutions in 1 country.

Lan N TuDepartment of Pediatrics, Cardiology, University of Washington, Seattle, Washington, USA.
Lance HsiehDepartment of Pediatrics, Cardiology, University of Washington, Seattle, Washington, USA.
Masaki KajimotoDepartment of Pediatrics, Cardiology, University of Washington, Seattle, Washington, USA.
Kevin CharetteCenter for Integrative Brain Research, Seattle Children's Research Institute, Seattle, Washington, USA.
Nataliya KibiryevaWard Family Heart Center, Children's Mercy Hospital, Kansas City, Missouri, USA.
Adriana ForeroDepartment of Immunology and.
Sarah HampsonDepartment of Pediatrics, Cardiology, University of Washington, Seattle, Washington, USA.
Jennifer A MarshallWard Family Heart Center, Children's Mercy Hospital, Kansas City, Missouri, USA.
James O'BrienWard Family Heart Center, Children's Mercy Hospital, Kansas City, Missouri, USA.
Marta ScatenaDepartment of Bioengineering, University of Washington, Seattle, Washington, USA.
Michael A PortmanDepartment of Pediatrics, Cardiology, University of Washington, Seattle, Washington, USA.
Ram SavanDepartment of Immunology and.
Chris BennerDepartment of Medicine, UCSD, La Jolla, California, USA.
Alberto AlisedaDepartment of Mechanical Engineering, University of Washington, Seattle, Washington, USA.
Muhammad NuriCenter for Integrative Brain Research, Seattle Children's Research Institute, Seattle, Washington, USA.
Douglas BittelWard Family Heart Center, Children's Mercy Hospital, Kansas City, Missouri, USA.
Peter PastuszkoDepartment of Cardiovascular Surgery, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Vishal NigamDepartment of Pediatrics, Cardiology, University of Washington, Seattle, Washington, USA.
University of Washington · USChildren's Mercy Hospital · USIcahn School of Medicine at Mount Sinai · USUniversity of California San Diego · US

Funding

A Multiscale Modeling Approach to Hypoplastic Left Heart SyndromeR01HL128630 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI DEL ALAMO, JUAN CARLOS, NIGAM, VISHAL · 2016 to 2019
$1.5M
NHLBI NIH HHS R01 HL128630
6 · The paper itself

Abstract

Cardiopulmonary bypass (CPB) is required during most cardiac surgeries. CBP drives systemic inflammation and multiorgan dysfunction that is especially severe in neonatal patients. Limited understanding of molecular mechanisms underlying CPB-associated inflammation presents a significant barrier to improve clinical outcomes. To better understand these clinical issues, we performed mRNA sequencing on total circulating leukocytes from neonatal patients undergoing CPB. Our data identify myeloid cells, particularly monocytes, as the major cell type driving transcriptional responses to CPB. Furthermore, IL-8 and TNF-α were inflammatory cytokines robustly upregulated in leukocytes from both patients and piglets exposed to CPB. To delineate the molecular mechanism, we exposed THP-1 human monocytic cells to CPB-like conditions, including artificial surfaces, high shear stress, and cooling/rewarming. Shear stress was found to drive cytokine upregulation via calcium-dependent signaling pathways. We also observed that a subpopulation of THP-1 cells died via TNF-α-mediated necroptosis, which we hypothesize contributes to post-CPB inflammation. Our study identifies a shear stress-modulated molecular mechanism that drives systemic inflammation in pediatric CPB patients. These are also the first data to our knowledge to demonstrate that shear stress causes necroptosis. Finally, we observe that calcium and TNF-α signaling are potentially novel targets to ameliorate post-CPB inflammation.

Indexed as

AnimalsAnimals, NewbornCalcium SignalingCardiopulmonary BypassCytokinesFemaleHeart Defects, CongenitalHumansInfantInfant, NewbornInflammation MediatorsInterleukin-8MaleModels, AnimalMonocytesNecroptosisCytokinesInflammation MediatorsInterleukin-8Tumor Necrosis Factor-alphaCalcium signalingCardiologyCytokinesInflammationSurgery

Identifiers

PMID33232305
PMCPMC7821587
OpenAlexW3106800765

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.