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Common therapeutic targets in cardiometabolic disease
Gabrielle Fredman1, Lale Ozcan1, Ira Tabas2
1Department of Medicine, Department of Pathology and Cell Biology, and Department of Physiology, Columbia University, New York, NY 10032-3725, USA.
Abstract:
The interactions between cardiovascular disease (CVD) and insulin resistance syndromes suggest the possibility of joint targets for cardiometabolic research. The best drugs would go beyond minimizing adverse effects and have protective actions against both metabolic disease and CVD. In this perspective, we will outline a few examples in which a deep mechanistic understanding of the many cellular pathways that contribute to type 2 diabetes and CVD, regardless of cell type, have resulted in common upstream pathogenic pathways that can be therapeutically targeted.
Insights
Cardiovascular disease and insulin resistance share common pathways. Targeting these shared mechanisms offers a promising strategy for developing drugs that protect against both metabolic disease and cardiovascular disease.
Area of Science:
- Cardiology
- Metabolic Research
- Pathogenesis
Background:
- Cardiovascular disease (CVD) and insulin resistance syndromes are increasingly recognized as interconnected health issues.
- Existing treatments often focus on individual conditions, necessitating a broader approach.
Purpose of the Study:
- To explore the potential for joint therapeutic targets in cardiometabolic research.
- To identify common upstream pathogenic pathways linking type 2 diabetes and CVD.
Main Methods:
- Review of mechanistic understanding of cellular pathways in type 2 diabetes and CVD.
- Analysis of shared pathogenic mechanisms across different cell types.
Main Results:
- Interactions between CVD and insulin resistance syndromes highlight shared biological pathways.
- Common upstream pathogenic pathways amenable to therapeutic targeting have been identified.
Conclusions:
- Developing drugs with protective actions against both metabolic disease and CVD is a key goal.
- A deep mechanistic understanding can lead to novel therapeutic strategies for cardiometabolic diseases.
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