Evidence map›Paper›PMID 38191808›Full record

ReviewPediatric radiology2024

Computed tomographic findings in TBX4 mutation: a common cause of severe pulmonary artery hypertension in children.

Helio V Neves da Silva, Jason P Weinman, Erin K Englund, Robin R Deterding, Dunbar D Ivy, Lorna P Browne

Abstract readReview
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In one paragraph

Review in Pediatric radiology, 2024. 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
2.1field-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.

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, 5 citations in OpenAlex.

  1. Article
  2. Review
  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

6 authors at 2 institutions in 1 country.

Helio V Neves da SilvaDepartment of Radiology, Children's Hospital Colorado, Aurora, CO, USA. heliondsilva@gmail.com.ORCID 0000-0002-8572-9946
Jason P WeinmanDepartment of Radiology, Children's Hospital Colorado, Aurora, CO, USA.
Erin K EnglundDepartment of Radiology, Children's Hospital Colorado, Aurora, CO, USA.
Robin R DeterdingUniversity of Colorado School of Medicine, Anschutz Medical Campus, Aurora, CO, USA.
Dunbar D IvyUniversity of Colorado School of Medicine, Anschutz Medical Campus, Aurora, CO, USA.
Lorna P BrowneDepartment of Radiology, Children's Hospital Colorado, Aurora, CO, USA.
Children's Hospital Colorado · USAlameda Health System · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMutations in the T-Box 4 (TBX4) gene are a lesser-known cause of heritable pulmonary arterial hypertension (PAH). Patients with heritable PAH typically have worse outcomes when compared with patients with idiopathic PAH, yet little is known about the phenotypical presentation of this mutation.

objectiveThis article reviews the pattern of chest CT findings in pediatric patients with PAH and TBX4 mutations and compares their radiographic presentation with those of age-matched patients with PAH but without TBX4 mutations. MATERIALS AND

methodsA retrospective chart review of the pulmonary arterial hypertension database was performed. Pediatric patients with PAH-confirmed TBX4 mutations and an available high CT were included. Fifteen (9 females) patients met the inclusion criteria. Fourteen (8 females) age-matched controls with diagnosed PAH but without TBX4 mutations were also evaluated. The median age at diagnosis was 7.4 years (range: 0.1-16.4 years). Demographic information and clinical outcomes were collected. CTs of the chest were reviewed for multiple airway, parenchymal, and structural abnormalities (16 imaging findings in total). Chi-square tests were used to compare the prevalence of each imaging finding in the TBX4 cohort compared to the control group.

resultsPatients with TBX-4 mutations had increased presence of peripheral or subpleural irregularity (73% vs 0%, P < 0.01), cystic lucencies (67% vs 7%, P < 0.01), and linear or reticular opacity (53% vs 0%, P < 0.01) compared to the control group. Ground glass opacities, bronchiectasis, and centrilobular nodules were not significantly different between the two patient groups (P > 0.05).

conclusionTBX4 mutations have distinct imaging phenotypes in pediatric patients with PAH. Compared to patients without this mutation, patients with TBX-4 genes typically present with peripheral or subpleural irregularity, cystic lucencies, and linear or reticular opacity.

Indexed as

Hypertension, PulmonaryPulmonary Arterial HypertensionAdolescentChildChild, PreschoolFamilial Primary Pulmonary HypertensionFemaleHumansInfantMutationPulmonary ArteryRetrospective StudiesT-Box Domain ProteinsTomography, X-Ray ComputedT-Box Domain ProteinsTBX4 protein, humanChest CTHeritable PAHPediatric PAHPulmonary arterial hypertensionTBX4

Identifiers

PMID38191808
OpenAlexW4390686905

What OpenQuestion holds

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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.