Evidence map›Paper›PMID 39589759›Full record

ArticleAmerican journal of physiology. Heart and circulatory physiology2025

MicroRNA in pediatric pulmonary hypertension microRNA profiling to inform disease classification, severity, and treatment response in pediatric pulmonary hypertension.

Michael A Smith, Sam Chiacchia, Jason Boehme, Sanjeev A Datar, Emily Morell, Roberta L Keller, Amy Romer, Elizabeth Colglazier, Claire Parker, Jasmine Becerra and 1 more

Abstract read
In one paragraph

Article in American journal of physiology. Heart and circulatory physiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. 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

11 authors.

Michael A SmithDivision of Pediatric Critical Care, Department of Pediatrics, University of California, San Francisco, California, United States.ORCID 0000-0002-7899-7248
Sam ChiacchiaDepartment of Emergency Medicine, Stanford University, Palo Alto, California, United States.
Jason BoehmeDivision of Pediatric Critical Care, Department of Pediatrics, University of California, San Francisco, California, United States.ORCID 0000-0003-4908-9934
Sanjeev A DatarDivision of Pediatric Critical Care, Department of Pediatrics, University of California, San Francisco, California, United States.ORCID 0009-0003-6986-2821
Emily MorellDivision of Pediatric Critical Care, Department of Pediatrics, University of California, San Francisco, California, United States.ORCID 0000-0002-5608-0367
Roberta L KellerDivision of Pediatric Pulmonary Hypertension, Department of Pediatrics, University of California, San Francisco, California, United States.
Amy RomerDivision of Pediatric Critical Care, Department of Pediatrics, Children's Hospital of Philadelphia, Pennsylvania, United States.
Elizabeth ColglazierDivision of Pediatric Pulmonary Hypertension, Department of Pediatrics, University of California, San Francisco, California, United States.
Claire ParkerDivision of Pediatric Pulmonary Hypertension, Department of Pediatrics, University of California, San Francisco, California, United States.ORCID 0000-0002-8431-7130
Jasmine BecerraDivision of Pediatric Pulmonary Hypertension, Department of Pediatrics, University of California, San Francisco, California, United States.
Jeffrey R FinemanDivision of Pediatric Critical Care, Department of Pediatrics, University of California, San Francisco, California, United States.

Funding

TGF-ß-SOX18-Collagen metabolism in pulmonary vascular disease associated with CHDP01HL146369 · NHLBI · UNIVERSITY OF ARIZONA · PI Ting Wang · 2020 to 2026
$18.7M
Altered Lymphatic Function and Development in Congenital Heart DiseaseR01HL133034 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Sanjeev A. Datar · 2016 to 2026
$6.4M
Multidisciplinary Research Training in Pediatric Pulmonary Vascular DiseaseT32HL160508 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Steven Herbert Abman, Eric Douglas Austin · 2022 to 2026
$1.7M
Pulmonary vascular glutamine metabolism at the intersection of hemodynamic forces and smooth muscle proliferation in congenital heart diseaseK08HL148512 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BOEHME, JASON · 2020 to 2024
$874k
HHS | National Institutes of Health (NIH) K08HL148512HHS | National Institutes of Health (NIH) P01HL146369HHS | National Institutes of Health (NIH) R01HL133034HHS | National Institutes of Health (NIH) T32HL160508-01A1NHLBI NIH HHS K08 HL148512NHLBI NIH HHS P01 HL146369NHLBI NIH HHS R01 HL133034NHLBI NIH HHS T32 HL160508
6 · The paper itself

Abstract

Pediatric pulmonary hypertension is a heterogeneous disease associated with significant morbidity and mortality. MicroRNAs have been implicated as both pathologic drivers of disease and potential therapeutic targets in pediatric pulmonary hypertension. We sought to characterize the circulating microRNA profiles of a diverse array of pediatric patients with pulmonary hypertension using high-throughput sequencing technology. Peripheral blood samples were drawn from patients recruited at the time of a clinically indicated cardiac catheterization, and microRNA sequencing followed by differential expression and target/pathway enrichment analyses were performed. Among 63 pediatric patients with pulmonary hypertension, we identified specific microRNA signatures that uniquely classified patients by disease subtype, correlated with indicators of disease severity including invasive hemodynamic metrics, and changed over the course of treatment for pulmonary hypertension. These microRNA profiles include a number of specific microRNA molecules known to function in signaling pathways critical to pulmonary vascular biology and disease, including transforming growth factor-β (TGF-β), VEGF, PI3K/Akt, cGMP-PKG, and HIF-1 signaling. Circulating levels of miR-122-5p, miR-124-3p, miR-204-5p, and miR-9-5p decreased over the course of treatment in a subset of patients who had multiple samples drawn during the study period. Our findings support the further investigation of specific microRNAs as mechanistic mediators, biomarkers, and therapeutic targets in pulmonary hypertension.

Indexed as

Gene Expression ProfilingHypertension, PulmonarySeverity of Illness IndexAdolescentAntihypertensive AgentsBiomarkersChildChild, PreschoolCirculating MicroRNAFemaleHumansInfantMaleMicroRNAsSignal TransductionTreatment OutcomeAntihypertensive AgentsBiomarkersCirculating MicroRNAMicroRNAsmicroRNApediatricspulmonary hypertension

Identifiers

PMID39589759
PMCPMC12077658

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.