Why the study?
Diagnosis and treatment of HFpEF have seen limited progress partly due to a past lack of suitable animal models for translational studies.
This review provides a comprehensive overview of animal models that mimic metabolic disturbances in HFpEF, which are crucial for advancing translational research and understanding the disease's pathogenesis.
Animal models of metabolic HFpEF may advance mechanistic research; leaves open translation to human phenotypes.
Heart failure (HF), the terminal state of different heart diseases, imposed a significant health care burden worldwide. It is the last battlefield in dealing with cardiovascular diseases. HF with preserved ejection fraction (HFpEF) is a type of HF in which the symptoms and signs of HF are mainly ascribed to diastolic dysfunction of left ventricle, whereas systolic function is normal or near-normal. Compared to HF with reduced ejection fraction (HFrEF), the diagnosis and treatment of HFpEF have made limited progress, partly due to the lack of suitable animal models for translational studies in the past. Given metabolic disturbance and inflammatory burden contribute to HFpEF pathogenesis, recent years have witnessed emerging studies focusing on construction of animal models with HFpEF phenotype by mimicking metabolic disorders. These models prefer to recapitulate the metabolic disorders and endothelial dysfunction, leading to the more detailed understanding of the entity. In this review, we summarize the currently available animal models of HFpEF with metabolic disorders, as well as their advantages and disadvantages as tools for translational studies.
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Li et al. (2022) studied this question.
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