A minimally invasive swine model of chronic kidney disease-associated heart failure

Chronic kidney disease (CKD) is on the rise, and over 50% of patients die from cardiac causes. Patients develop heart failure due to unelucidated reno-cardiac interactions, termed type 4 cardiorenal syndrome (CRS4). The aim of this study is to establish and characterize a reliable model of CRS4 in swine with marked cardiac diastolic dysfunction. Yorkshire pigs (19.9 ± 1.7 kg, 4 females and 5 males) underwent staged renal artery embolization using autologous clot. Echocardiogram, aortic pressure (AoP), renal angiogram, and blood samples were assessed monthly. At 4 mo, animals were euthanized after measuring glomerular filtration rate (GFR) and left ventricular (LV) pressure-volume parameters. Heart and kidneys were collected for postmortem analyses. Size-matched swine (<i>n</i> = 5; 43.7 ± 9.8 kg) served as controls. After three dose-titrated renal embolization, serum creatinine (SCr) and AoP increased by wk 10. At 4 mo, SCr (2.03 ± 0.45 vs. 1.34 ± 0.17 mg/dL, <i>P</i> = 0.013) and AoP (158 ± 16 vs. 121 ± 8 mmHg, <i>P</i> = 0.001) were higher, and GFR was lower (12 ± 3 vs. 131 ± 7 mL/min, <i>P</i> < 0.001) than size-matched controls. Although the LV ejection fraction was similar, the slope of the end-diastolic pressure-volume relationship was steeper in pigs after renal embolization (0.36 ± 0.09 vs. 0.17 ± 0.06, <i>P</i> = 0.003), indicating increased LV stiffness. LV mass index (2.73 ± 0.19 vs. 2.50 ± 0.13 g/kg, <i>P</i> = 0.043) and wall-thickness (11.4 ± 0.8 vs. 8.9 ± 1.2 mm, <i>P</i> = 0.003) increased. These were accompanied by histologically increased fibrosis, cardiomyocyte hypertrophy, and vascular rarefaction. Repeat titrated renal embolization resulted in a model that exhibits advanced CKD and cardiac abnormalities consistent with CRS4.<b>NEW & NOTEWORTHY</b> Cardiac pathological changes consistent with heart failure with preserved ejection fraction can be induced in a large animal model by serial and titrated renal embolization of kidneys with autologous clot, leading to severe renal dysfunction and impaired cardiac diastolic function.

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Journal
American Journal of Physiology-Heart and Circulatory Physiology
Published
2024-12-24
DOI
https://doi.org/10.1152/ajpheart.00449.2024
Citations
3
Primary Topic
Cardiovascular Function and Risk Factors
Type
article
Field-Weighted Citation Impact
1.21

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article

A minimally invasive swine model of chronic kidney disease-associated heart failure

Susmita Sahoo, Genya Sunagawa, Kelly P. Yamada, Renata Mazurek et al.
3 citations
American Journal of Physiology-Heart and Circulatory Physiology
Cardiovascular Function and Risk Factors
1.21
article

A minimally invasive swine model of chronic kidney disease-associated heart failure

Susmita Sahoo, Genya Sunagawa, Kelly P. Yamada, Renata Mazurek, Kiyotake Ishikawa, Daniel Singleton, Tadao Aikawa, Tomoki Sakata, Kenji Watanabe, Spyros A. Mavropoulos, Taro Kariya, Samta Veera, Kyra Leonard
article en
3 citations

Abstract

Chronic kidney disease (CKD) is on the rise, and over 50% of patients die from cardiac causes. Patients develop heart failure due to unelucidated reno-cardiac interactions, termed type 4 cardiorenal syndrome (CRS4). The aim of this study is to establish and characterize a reliable model of CRS4 in swine with marked cardiac diastolic dysfunction. Yorkshire pigs (19.9 ± 1.7 kg, 4 females and 5 males) underwent staged renal artery embolization using autologous clot. Echocardiogram, aortic pressure (AoP), renal angiogram, and blood samples were assessed monthly. At 4 mo, animals were euthanized after measuring glomerular filtration rate (GFR) and left ventricular (LV) pressure-volume parameters. Heart and kidneys were collected for postmortem analyses. Size-matched swine (<i>n</i> = 5; 43.7 ± 9.8 kg) served as controls. After three dose-titrated renal embolization, serum creatinine (SCr) and AoP increased by wk 10. At 4 mo, SCr (2.03 ± 0.45 vs. 1.34 ± 0.17 mg/dL, <i>P</i> = 0.013) and AoP (158 ± 16 vs. 121 ± 8 mmHg, <i>P</i> = 0.001) were higher, and GFR was lower (12 ± 3 vs. 131 ± 7 mL/min, <i>P</i> < 0.001) than size-matched controls. Although the LV ejection fraction was similar, the slope of the end-diastolic pressure-volume relationship was steeper in pigs after renal embolization (0.36 ± 0.09 vs. 0.17 ± 0.06, <i>P</i> = 0.003), indicating increased LV stiffness. LV mass index (2.73 ± 0.19 vs. 2.50 ± 0.13 g/kg, <i>P</i> = 0.043) and wall-thickness (11.4 ± 0.8 vs. 8.9 ± 1.2 mm, <i>P</i> = 0.003) increased. These were accompanied by histologically increased fibrosis, cardiomyocyte hypertrophy, and vascular rarefaction. Repeat titrated renal embolization resulted in a model that exhibits advanced CKD and cardiac abnormalities consistent with CRS4.<b>NEW & NOTEWORTHY</b> Cardiac pathological changes consistent with heart failure with preserved ejection fraction can be induced in a large animal model by serial and titrated renal embolization of kidneys with autologous clot, leading to severe renal dysfunction and impaired cardiac diastolic function.

American Journal of Physiology-Heart and Circulatory PhysiologyVol. 328(2)
Cardiovascular Institute Hospital (JP), Icahn School of Medicine at Mount Sinai (US)
Thomas Jefferson University, National Institutes of Health, National Heart, Lung, and Blood Institute
Good health and well-being
Openalex Percentile: Top 17%
Cardiovascular Function and Risk Factors
1.21
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