Evidence map›Paper›PMID 41954066›Full record

ArticleJournal of the American Heart Association2026

Correlates and Prognostic Value of Serial N-Terminal Pro-B-Type Natriuretic Peptide Assay in Congenitally Corrected Transposition of the Great Arteries.

Ahmed Bahnasy, Meena Bai, Sara Aboelmaaty, Mohamed Ellabbad, William R Miranda, Heidi M Connolly, Allan S Jaffe, Alexander C Egbe

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Article in Journal of the American Heart Association, 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

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Ahmed BahnasyDepartment of Cardiovascular Medicine Mayo Clinic Rochester MN USA.ORCID 0009-0004-4984-3743
Meena BaiDepartment of Cardiovascular Medicine Mayo Clinic Rochester MN USA.ORCID 0009-0007-8151-5821
Sara AboelmaatyDepartment of Cardiovascular Medicine Mayo Clinic Rochester MN USA.ORCID 0009-0006-9411-7892
Mohamed EllabbadDepartment of Cardiovascular Medicine Mayo Clinic Rochester MN USA.ORCID 0009-0005-2854-8275
William R MirandaDepartment of Cardiovascular Medicine Mayo Clinic Rochester MN USA.ORCID 0000-0001-8864-8474
Heidi M ConnollyDepartment of Cardiovascular Medicine Mayo Clinic Rochester MN USA.ORCID 0000-0003-0666-0344
Allan S JaffeDepartment of Cardiovascular Medicine Mayo Clinic Rochester MN USA.ORCID 0000-0003-1183-3959
Alexander C EgbeDepartment of Cardiovascular Medicine Mayo Clinic Rochester MN USA.ORCID 0000-0002-8810-3631

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCardiovascular biomarkers such as NT-proBNP (N-terminal pro-B-type natriuretic peptide) are used for heart failure risk stratification in patients with acquired heart disease, but there are limited data about its role in patients with congenitally corrected transposition of the great arteries. The current study aims to assess the role of serial NT-proBNP measurements for risk stratification in adults with congenitally corrected transposition of the great arteries.

methodsWe studied adults with congenitally corrected transposition of the great arteries with ≥2 NT-proBNP measurements (2003-2024). Temporal change in NT-proBNP was calculated as relative change from baseline levels.

resultsOf 152 patients (age 47±13 years, 45% men), baseline NT-proBNP was 539 (interquartile range, 193-1549) pg/mL, and relative change from baseline levels of NT-proBNP was 34% (interquartile range, -11 to 67). Of 152 patients, 45 (30%) had cardiovascular events (heart failure hospitalization [n=29], ventricular assist device [n=5], heart transplantation [n=11], and death [n=10]), yielding a 10-year incidence of 26%. Higher baseline NT-proBNP and relative change from baseline levels were associated with cardiovascular events. Serial NT-proBNP measurements had incremental prognostic value compared with baseline measurement. The correlates of higher NT-proBNP levels were atrial fibrillation, hypertension, right ventricular dilation and dysfunction, and atrioventricular valve regurgitation. Renin-angiotensin-aldosterone system antagonist was associated with lower NT-proBNP levels and lower risk of cardiovascular events.

conclusionsNT-proBNP testing is inexpensive, widely available, and noninvasive, making it well suited for longitudinal surveillance in adults with congenital heart disease. Most of the correlates for elevated NT-proBNP levels were modifiable, providing target for therapeutic interventions.

Indexed as

Congenitally Corrected Transposition of the Great ArteriesNatriuretic Peptide, BrainPeptide FragmentsTransposition of Great VesselsAdultBiomarkersFemaleHeart FailureHumansMaleMiddle AgedPredictive Value of TestsPrognosisRisk AssessmentRisk FactorsBiomarkersNatriuretic Peptide, BrainPeptide Fragmentspro-brain natriuretic peptide (1-76)heart failuremortalityprognostication

Identifiers

PMID41954066
PMCPMC13279070

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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 OpenQuestion graph.