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Peer-reviewed veterinary case report

Heart disease and death rates in New Zealand non-purebred cats

By Seo, J et al.·Published in New Zealand veterinary journal·2025·wharau Ora - School of Veterinary Science·View original on PubMed

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Original publication title: Prevalence of cardiomyopathy and cardiac mortality in a colony of non-purebred cats in New Zealand.

Species:
cat

Plain-English summary

A group of non-purebred cats in New Zealand was studied to see how common heart disease, specifically hypertrophic cardiomyopathy (HCM), is among them. Out of 132 cats, 24 had heart disease, with 20 diagnosed with HCM. Over a ten-year period, only a small number of cats (7 out of 132) died from heart-related issues, suggesting that many cats with HCM may not show symptoms or progress to severe disease. This highlights the importance for pet owners and veterinarians to be aware of heart health in cats, even if they seem healthy.

People also search for: cat heart disease symptoms · hypertrophic cardiomyopathy in cats · how to check cat heart health

Abstract

AIMS: To evaluate the prevalence of subclinical cardiomyopathy and cardiac mortality in a research colony of non-purebred cats, established as a model of the wider cat population in New Zealand. METHODS: All apparently healthy, compliant, non-pregnant, non-neonatal cats in the colony at the Centre for Feline Nutrition (Massey University, Palmerston North, NZ) underwent physical examination and echocardiography using a 4.4-6.2-MHz probe by a board-certified veterinary cardiologist. Cardiac phenotype was classified following current guidelines. Hypertrophic cardiomyopathy (HCM) phenotype was defined as an end-diastolic left ventricular wall thickness ≥ 6 mm. Colony mortality data from February 2012 to February 2022 was reviewed to determine cardiac mortality. RESULTS: Cats (n = 132; 65 females and 67 males) included in the study had a median age of 4.1 (IQR 3.0-8.0) years. Thirty-two (24%) cats had a heart murmur, and three (2%) cats had an arrhythmia. Echocardiography revealed heart disease in 24 (18.2%) cats, including 23 with an HCM phenotype and one with a restrictive cardiomyopathy phenotype. Of the cats with the HCM phenotype, 3/23 had systemic hypertension or hyperthyroidism or both, and these cats were excluded from the final diagnosis of HCM (20/132; 15.2 (95% CI = 9.5-22.4)%).Between 2012 and 2022, 168 colony cats died, with 132 undergoing post-mortem examination. Heart disease was considered the cause of death in 7/132 (5.3%; 95% CI = 2.2-10.6%) cats; five had HCM, one a congenital heart defect, and one myocarditis. The overall prevalence of death related to HCM in the colony during this period was 3.8% (95% CI = 1.2-8.6%). Three cats with HCM and the cat with a congenital heart defect died unexpectedly without prior clinical signs, while congestive heart failure was observed prior to death in two cats with HCM and the cat with myocarditis. Additionally, 30/132 (22.7%) cats had cardiac abnormalities but died for non-cardiac reasons. CONCLUSIONS: Subclinical cardiomyopathy, specifically HCM, was common in cats in the colony. Given that the colony originated as a convenience selection of non-purebred cats in New Zealand, the true prevalence of HCM in the wider New Zealand population is likely to fall within the 95% CI (9.5-22%). The proportion of deaths of colony cats due to HCM was lower (3.8%) supporting the conclusion that subclinical cardiomyopathy may not progress to clinical disease causing death. CLINICAL RELEVANCE: Veterinarians should be aware of the high prevalence of subclinical HCM when treating cats. ABBREVIATIONS: CAM: Systolic anterior motion of the chordae tendineae; CFN: Centre for Feline Nutrition; HCM: Hypertrophic cardiomyopathy; LA/Ao: Left atrial to aortic ratio; LV FS: Left ventricular fractional shortening; LVIDd: Left ventricular internal diameters in end-diastole; LVIDs: Left ventricular internal diameter in end-systole; LVWT: Max Maximum left ventricular wall thickness; SAM: Systolic anterior motion of the mitral valve; 2D: Two-dimensional.

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Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/39343434/