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Author Spotlight: Exploring the Relationship Between Lipotoxicity and HFpEF
Published on: February 23, 2024
The Cardiohepatic Axis in Metabolic Disease: Liver to Heart
Andrew Hakeem1, Jop van Berlo2, Xavier S Revelo3
1Department of Integrative Biology and Physiology, University of Minnesota Medical School, Minneapolis, Minnesota, USA.
Insights
Metabolic dysfunction-associated steatotic liver disease (MASLD) drives heart disease through liver-secreted factors and systemic inflammation. Targeting this liver-heart axis offers integrated strategies for better cardiometabolic health outcomes.
Area of Science:
- Cardiology
- Hepatology
- Metabolic Disease Research
Background:
- Cardiometabolic diseases frequently coexist due to complex cardio-hepatic interactions.
- Metabolic dysfunction-associated steatotic liver disease (MASLD) is increasingly recognized for its contribution to cardiovascular complications.
Purpose of the Study:
- To explore the mechanisms of organ crosstalk in cardiometabolic disease, focusing on the liver-to-heart axis.
- To elucidate how MASLD influences cardiac metabolism, inflammation, and remodeling through hepatic secretory factors.
Main Methods:
- Review of emerging evidence on organ crosstalk in cardiometabolic disease.
- Analysis of molecular mechanisms linking MASLD to cardiovascular pathology.
- Discussion of shared systemic inflammation pathways, including bone marrow reprogramming and clonal hematopoiesis of indeterminate potential.
Main Results:
- MASLD, especially its inflammatory forms, releases hepatic factors that impact cardiac function.
- Secreted hepatic factors are key mediators of communication between the liver and heart.
- Bone marrow reprogramming and clonal hematopoiesis contribute to systemic inflammation regulating the heart-liver axis.
Conclusions:
- The liver-to-heart axis is a critical pathway in cardiometabolic disease pathogenesis.
- Integrated therapeutic strategies targeting both liver and cardiovascular health are essential.
- Understanding shared inflammatory mechanisms can improve patient outcomes in cardiometabolic conditions.
Abstract:
Heart and liver metabolic diseases often coexist because of local and systemic disorders that affect both organs via cardio-hepatic interactions. Here, we discuss the emerging evidence of organ crosstalk during cardiometabolic disease with an emphasis on the liver-to-heart axis. We highlight potential mechanisms by which metabolic dysfunction-associated steatotic liver disease contributes to cardiovascular complications. Metabolic dysfunction-associated steatotic liver disease, particularly its inflammatory entity, leads to the production of liver-derived secretory factors that regulate cardiac metabolism, inflammation, and remodeling. Thus, secreted hepatic factors represent an important mechanism of communication between the liver and heart during cardiometabolic disease. In addition to the direct crosstalk between organs, we argue that bone marrow reprogramming and clonal hematopoiesis of indeterminate potential are shared mechanisms of systemic inflammation that regulate the heart-liver axis during cardiometabolic disease. Thus, integrated cardiometabolic strategies hold a significant potential to bridge the gap between liver and cardiovascular health to improve patient outcomes.
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