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REVIEW article

Front. Vet. Sci.

Sec. Veterinary Clinical, Anatomical, and Comparative Pathology

This article is part of the Research TopicRecent Advances in the Management of Cardiac Disease in Companion AnimalsView all 6 articles

Linking clinical and imaging diagnostic assessments of the feline hypertrophic cardiomyopathy phenotype

Provisionally accepted
Felipe  Gaia De SousaFelipe Gaia De Sousa1,2Ruthnea  Aparecida Lazaro MuzziRuthnea Aparecida Lazaro Muzzi2,3Roberto  Baracat de AraújoRoberto Baracat de Araújo1,2Rafael  Resende FaleirosRafael Resende Faleiros1Fabiana  Silva Fádel QueirozFabiana Silva Fádel Queiroz1,2Suzane  Lilian BeierSuzane Lilian Beier1,2*
  • 1Department of Veterinary Clinic and Surgery, Veterinary School, Federal University of Minas Gerais, Belo Horizonte, Brazil
  • 2VETHEART – Cardiovascular Physiology and Veterinary Cardiology Research Group, Belo Horizonte, Brazil
  • 3Universidade Federal de Lavras Departamento de Medicina Veterinaria, Lavras, Brazil

The final, formatted version of the article will be published soon.

Hypertrophic cardiomyopathy (HCM) phenotype represents the most commonly diagnosed cardiac disorder in felines, characterized by heterogeneous clinical presentations and a well-established genetic basis. This study aims to integrate clinical, laboratory, and imaging diagnostic assessments of the feline HCM phenotype, providing a comprehensive perspective on how complementary diagnostic approaches enhance disease understanding and precision. The HCM phenotype is defined by concentric hypertrophy of the left ventricular free wall and/or interventricular septum, often accompanied by secondary left atrial remodeling due to chronic pressure and volume overload. Clinical signs typically emerge with disease progression, frequently culminating in congestive heart failure (CHF) and respiratory signs; however, some cats may remain asymptomatic. Accurate diagnosis of the HCM phenotype requires an integrative approach combining thorough clinical evaluation and advanced imaging modalities to avoid misdiagnosis, which may negatively impact prognosis and quality of life. Detailed clinical history and physical examination are essential for diagnostic orientation, particularly in symptomatic patients. Routine laboratory tests support systemic assessment, although no pathognomonic biomarker has been identified to date. Cardiac biomarkers such as atrial natriuretic peptide (ANP), N-terminal pro–B-type natriuretic peptide (NT-proBNP), and cardiac troponin I (cTnI) provide complementary diagnostic information, albeit with lower sensitivity than imaging techniques. While electrocardiography may reveal conduction disturbances suggestive of HCM, transthoracic echocardiography remains the diagnostic gold standard. In addition to confirming the diagnosis, echocardiographic evaluation allows for disease staging, longitudinal monitoring, and evidence-based therapeutic decision-making. Our study reinforces the need for an integrated diagnostic framework that combines clinical examination, laboratory testing, and imaging evaluation. By promoting a multidimensional diagnostic perspective, this study contributes to refining the understanding of the feline HCM phenotype and supports the development of more precise diagnostic and therapeutic strategies, ultimately improving clinical outcomes in affected cats.

Keywords: concentric ventricular hypertrophy, congestive heart failure, cardiovascular repercussions, feline cardiomyopathies, Prognostic parameters

Received: 08 Oct 2025; Accepted: 17 Nov 2025.

Copyright: © 2025 De Sousa, Muzzi, de Araújo, Faleiros, Queiroz and Beier. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence: Suzane Lilian Beier, suzanelb@yahoo.com.br

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