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Article

Advances in diagnosis and patient profiling in pulmonary arterial hypertension for precision medicine.

Therapeutic advances in respiratory disease - 1 Jan 2025

Ricchi Benedetta, Jagana Vineeta, Singh Elizabeth, Ochoa Maria T, Salamah Joudi, Bisserier Malik

Abstract excerpt

Pulmonary arterial hypertension (PAH) is a rare but fatal disease characterized by progressive vascular remodeling, which results in increased pulmonary vascular resistance and elevated pulmonary arterial pressure. These changes are detrimental to the right ventricle (RV). If not treated, it can eventually lead to maladaptive RV structural changes, right heart failure, and death. Late diagnosis at an advanced...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 40878965
DOI: 10.1177/17534666251367312
PMCID: PMC12397575

Genes

PAH

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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