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Hydra, a Computer-Based Platform for Aiding Clinicians in Cardiovascular Analysis and Diagnosis
Published on: September 26, 2018
Cardiovascular disease and modifiable cardiometabolic risk factors
1Harvard Medical School Cardiovascular Division, Brigham and Women's Hospital Boston, Massachusetts 02115, USA. cpcannon@partners.org
Insights
Cardiovascular disease (CVD) remains a leading cause of death globally. New pharmacologic therapies show promise in managing multiple CVD risk factors simultaneously, potentially improving patient outcomes.
Area of Science:
- Cardiology
- Metabolic Diseases
- Pharmacology
Background:
- Cardiovascular disease (CVD) is the primary cause of mortality in the US and globally.
- Modifiable risk factors for CVD include tobacco use, inactivity, hypertension, high LDL cholesterol, and metabolic syndrome.
- Despite progress, many patients struggle with adequate CVD risk factor control, and rising obesity and type 2 diabetes mellitus (DM) threaten gains.
Purpose of the Study:
- To review the current landscape of cardiovascular disease (CVD) risk factors and management strategies.
- To explore emerging pharmacologic therapies for CVD risk factor reduction.
- To highlight the potential of new agents in addressing multiple CVD risk factors concurrently.
Main Methods:
- Review of existing literature on CVD risk factors and prevalence.
- Analysis of current and emerging pharmacologic treatments for hypertension, dyslipidemia, obesity, and type 2 DM.
- Discussion of novel drug classes targeting metabolic pathways relevant to CVD.
Main Results:
- Obesity and type 2 DM are increasing CVD risk, undermining previous mortality reductions.
- Lifestyle interventions for weight loss show limited long-term adherence.
- Emerging pharmacologic agents (e.g., endocannabinoid receptor antagonists, PPAR agonists, GLP-1 modulators) offer potential for multi-factor risk reduction.
Conclusions:
- New pharmacologic therapies may offer a consolidated approach to managing multiple CVD risk factors.
- These agents have the potential to improve cardiovascular outcomes by addressing underlying metabolic dysregulation.
- Further evaluation of these novel strategies is crucial for long-term CVD risk reduction.
Abstract:
Cardiovascular disease (CVD) is the leading cause of death in the United States and many parts of the world. Potentially modifiable risk factors for CVD include tobacco use, physical inactivity, hypertension, elevated low-density lipoprotein cholesterol, and a cluster of interrelated metabolic risk factors. Over the last several decades, efforts to prevent or treat CVD risk factors have resulted in significantly lower rates of CVD-related mortality. However, many patients never achieve adequate control of CVD risk factors even when these factors have been identified. In addition, the growing prevalence of obesity and type 2 diabetes mellitus (DM) threatens to undermine the improvements in CVD that have been achieved. In the United States, approximately two thirds of adults are overweight or obese, and even modest excess body weight is associated with a significantly increased risk of CVD-related mortality. Lifestyle interventions to promote weight loss reduce the risk of CVD-related illness but are difficult for patients to sustain over long periods of time. The increased incidence of obesity has also contributed to significant increases in the prevalence of other important CVD risk factors, including hypertension, dyslipidemia, insulin resistance, and type 2 DM. Pharmacologic therapies are currently available to address individual CVD risk factors, and others are being evaluated, including endocannabinoid receptor antagonists, inhibitors of peroxisome proliferator-activated receptor subtypes alpha and gamma, and several agents that modulate the activity of glucagon-like peptide-1. The new agents have the potential to significantly improve several CVD risk factors with a single medication and may provide clinicians with several new strategies to reduce the long-term risk of CVD.
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