Evidence map›Paper›PMID 42836726›Full record

ArticlePediatric pulmonology2026

Variant Class-Specific Phenotypes and Outcomes in Pediatric TBX4-Associated Pulmonary Hypertension.

Cara Morgan, Alistair Calder, Matina Prapa, Thivya Sekar, Andrew Constantine, Tomas Woodgate, Annabelle Barnes, Eimear McGovern, Paul Aurora, Rossa Brugha and 3 more

Abstract read
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Article in Pediatric pulmonology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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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

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4 · The record

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5 · Who and what money

Authors and funding

13 authors.

Cara MorganUK National Paediatric Pulmonary Hypertension Service, Great Ormond Street Hospital for Children, London, UK.ORCID https://orcid.org/0009-0007-7038-6286
Alistair CalderDepartment of Radiology, Great Ormond Street Hospital for Children, London, UK.
Matina PrapaSt George's University Hospitals NHS Foundation Trust, SW Thames Centre for Genomic Medicine, London, UK.
Thivya SekarDepartment of Histopathology, Great Ormond Street Hospital for Children, London, UK.
Andrew ConstantineDepartment of Cardiology, Adult Congenital Heart Disease Unit, Queen Elizabeth Hospital Birmingham, Birmingham, UK.ORCID https://orcid.org/0000-0001-7899-463X
Tomas WoodgateUK National Paediatric Pulmonary Hypertension Service, Great Ormond Street Hospital for Children, London, UK.ORCID https://orcid.org/0009-0000-2928-4367
Annabelle BarnesUK National Paediatric Pulmonary Hypertension Service, Great Ormond Street Hospital for Children, London, UK.
Eimear McGovernDepartment of Paediatric Cardiology, Children's Health Ireland at Crumlin, Dublin, Ireland.
Paul AuroraDepartment of Paediatric Respiratory Medicine, Great Ormond Street Hospital for Children, London, UK.
Rossa BrughaDepartment of Paediatric Respiratory Medicine, Great Ormond Street Hospital for Children, London, UK.
Sadia QuyamUK National Paediatric Pulmonary Hypertension Service, Great Ormond Street Hospital for Children, London, UK.ORCID https://orcid.org/0009-0004-9902-5706
Andrew BushNational Heart and Lung Institute and Imperial Centre for Paediatrics and Child Health, Imperial College, London, UK.
Shahin MoledinaUK National Paediatric Pulmonary Hypertension Service, Great Ormond Street Hospital for Children, London, UK.ORCID https://orcid.org/0000-0003-0262-2340

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimTo describe the variant class associations with phenotype, natural history, treatment response, and outcomes in children with TBX4-associated pulmonary hypertension (TBX4-PH).

methodsRetrospective cohort analysis of children < 18 years referred to the National Paediatric Pulmonary Hypertension Service between 2001 and 2025.

resultsTwenty-one children were identified carrying either a copy number variant (CNV group = 10) encompassing TBX4 or a single nucleotide variant (SNV group = 11). Distinct phenotypic differences were observed between variant classes. Children in the CNV group were referred at a younger age (p = 0.03), more frequently had prolonged oxygen dependence from birth (p < 0.01), more severe lung disease (p < 0.01) and cyanosis (p = 0.04), congenital heart disease (p = 0.03), neurodevelopmental disorders (p < 0.01), and deafness (p = 0.01). Children in the SNV group were less likely to have any lung disease (p = 0.03). Histopathology from five children (CNV = 3, SNV = 2) demonstrated predominantly lung growth abnormalities with variable pulmonary vascular remodeling. Twenty of 21 (95%) children received long-term pulmonary vasodilator therapy, and 9 (43%) received concurrent calcium-channel blockers. Treatment-naïve children (n = 12) demonstrated stable/improved functional class with therapy initiation. Median follow-up was 7.1 years (range 0.7-17.2). Transplant- or Potts shunt-free survival at 1 and 5 years was 100% and 94.4% respectively and was worse in the CNV group (Log-rank p < 0.05).

conclusionsIn this large pediatric TBX4-PH cohort, children carrying CNVs had greater multisystem involvement and poorer outcomes than those carrying SNVs, highlighting the importance of the underlying genetic finding for risk stratification and tailored management strategies.

Indexed as

Hypertension, PulmonaryT-Box Domain ProteinsAdolescentChildChild, PreschoolDNA Copy Number VariationsFemaleHumansInfantMalePhenotypePolymorphism, Single NucleotideRetrospective StudiesT-Box Domain ProteinsTBX4 protein, humancase serieschildreninterstitial lung diseaselung developmental diseasepulmonary arterial hypertensionsmall‐patellar syndrome

Identifiers

PMID42836726
PMCPMC13640964

What Socratic holds

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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.