Key result
Plasma endothelin-1 concentrations were significantly higher in cats with myocardial disease without CHF/STE (1.427 fmol/mL; P<0.05) and with CHF/STE (2.360 fmol/mL; P<0.001) versus healthy cats.
Observational (n=40)
Plasma endothelin-1 concentrations are elevated in cats with cardiomyopathy and further increased in those with congestive heart failure or systemic thromboembolism, mirroring findings in humans.
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Endothelin-1 elevation in feline cardiomyopathy is hypothesis-generating; leaves open biomarker or therapeutic translation pending prospective validation.
Plasma concentrations of endothelin-1 (ET-1), the most potent endogenous pressor substance discovered to date, are abnormally high in humans with congestive heart failure (CHF), and they correlate with the degree of functional impairment. We sought first to validate a human sandwich ELISA kit that targets that portion of the amino acid sequence that is identical in cats. The assay demonstrated linearity (R2 = .9968) and parallelism (P = .5339), recovery of spiked human ET-1 in cat plasma averaged 98.7%, and intraassay precision had a coefficient of variation <10%. We subsequently determined ET-1 immunoreactivity in healthy cats and in cats with myocardial disease with and without CHF, systemic thromboembolism (STE), or both. Plasma ET-1 immunoreactivity was measured in 12 healthy cats and in 28 cats with primary myocardial disease, including hypertrophic cardiomyopathy (HCM), dilated cardiomyopathy (DCM), or restrictive or unclassified cardiomyopathy (RCM and UCM), respectively. Plasma ET mean (95% CI) concentrations were 0.777 (0.6536-0.924) fmol/mL in the control cats, 1.427 (0.922-2.209) fmol/mL in 12 cats with cardiomyopathy (HCM = 11, RCM/UCM = 1) but without CHF or evidence of STE, and 2.360 (1.666-3.343) fmol/mL in 16 cats with cardiomyopathy (HCM = 8, RCM/UCM = 7, DCM = 1) and CHF (n = 15) or STE (n = 4). Plasma immunoreactivity of ET-1 was significantly higher in cats with myocardial disease without CHF/STE versus normal cats (P < .05) and in cats with myocardial disease with CHF/STE versus normal cats (P < .001).
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Prosek et al. (2004) conducted an observational in Cardiomyopathy (n=40). Myocardial disease with or without CHF/STE vs. Healthy cats was evaluated on Plasma ET-1 immunoreactivity concentration (p=<.001). Plasma endothelin-1 concentrations were significantly higher in cats with myocardial disease without CHF/STE (1.427 fmol/mL; P<0.05) and with CHF/STE (2.360 fmol/mL; P<0.001) versus healthy cats.
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