4.6 Review

Guidelines on models of diabetic heart disease

Journal

Publisher

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/ajpheart.00058.2022

Keywords

cardiac function; diabetic cardiomyopathy; obesity; type 1 diabetes; type 2 diabetes

Funding

  1. British Heart Foundation Intermediate Basic Science Fellow Grant [FS/17/58/33072]
  2. National Institutes of Health (NIH) [R01 HL132989, R01 HL144788, R01 HL136438, P20 GM104357, P01 HL051971, P20 GM104320, R01 HL155766, R01 HL133011]
  3. New Zealand Marsden Fund [19-UOA-268]
  4. Health Research Council of New Zealand [19/190]
  5. Canadian Institutes of Health Research (CIHR) Project [PJT-156136]
  6. Heart and Stroke Foundation of Canada
  7. Dutch Heart Foundation Dekker Senior Scientist Grant [2019T041]
  8. FRQS Junior 1 Research Scholar [281577]
  9. CIHR Project [PJT159648]
  10. Tier 2 Canada Research Chair (Pharmacotherapy of Energy Metabolism in Obesity)

Ask authors/readers for more resources

Diabetes is a significant risk factor for cardiovascular diseases, and various models have been used to study its mechanisms and impacts. This review aims to provide information on the accuracy of different models in reproducing cardiovascular disease in diabetic individuals, highlighting their advantages, disadvantages, practical challenges, and technical considerations.
Diabetes is a major risk factor for cardiovascular diseases, including diabetic cardiomyopathy, atherosclerosis, myocardial infarction, and heart failure. As cardiovascular disease represents the number one cause of death in people with diabetes, there has been a major emphasis on understanding the mechanisms by which diabetes promotes cardiovascular disease, and how antidiabetic therapies impact diabetic heart disease. With a wide array of models to study diabetes (both type 1 and type 2), the field has made major progress in answering these questions. However, each model has its own inherent limitations. Therefore, the purpose of this guidelines document is to provide the field with information on which aspects of cardiovascular disease in the human diabetic population are most accurately reproduced by the available models. This review aims to emphasize the advantages and disadvantages of each model, and to highlight the practical challenges and technical considerations involved. We will review the preclinical animal models of diabetes (based on their method of induction), appraise models of diabetes-related atherosclerosis and heart failure, and discuss in vitro models of diabetic heart disease. These guidelines will allow researchers to select the appropriate model of diabetic heart disease, depending on the specific research question being addressed.

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