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Nutritional status, genetic susceptibility, and insulin resistance--important precedents to atherosclerosis
Fiona C McGillicuddy1, Helen M Roche
1UCD Conway Institute, School of Public Health & Population Science, University College Dublin, Dublin, Ireland.
Insights
Atherosclerosis, a progressive condition leading to coronary artery disease (CAD), is influenced by both nutrition and genetics. Lifestyle interventions like diet modification and weight loss can mitigate risks and improve metabolic health.
Area of Science:
- Cardiovascular Science
- Metabolic Health
- Nutritional Science
Background:
- Atherosclerosis, manifesting as coronary artery disease (CAD), is a leading cause of mortality.
- Key CAD risk factors include hypercholesterolemia, hypertension, obesity, smoking, and genetics.
- Rising obesity rates highlight the need to understand links between overnutrition and cardiovascular risk.
Purpose of the Study:
- To debate the relative impact of nutrition versus genetics in driving CAD.
- To investigate how overnutrition affects adipose tissue biology, insulin resistance (IR), and cardiovascular implications.
- To discuss lifestyle interventions for improving IR and metabolic dyslipidemia in obesity.
Main Methods:
- Review of current literature on atherosclerosis, nutrition, genetics, and metabolic health.
- Analysis of the interplay between overnutrition, adipose tissue dysfunction, and cardiovascular risk.
- Examination of the efficacy of lifestyle interventions, including diet and weight loss.
Main Results:
- Overnutrition contributes to adipose tissue dysfunction and insulin resistance, impacting cardiovascular health.
- Lifestyle interventions such as diet modification and weight loss can improve insulin resistance and metabolic dyslipidemia.
- Genetic susceptibility interacts with nutritional status, influencing diet-related risk and intervention response.
Conclusions:
- Lifestyle interventions can delay or negate the need for chronic pharmacotherapy in individuals at risk for CAD.
- A personalized nutrition approach may be more effective in managing diet-related cardiovascular risk.
- Understanding the interplay of nutrition and genetics is crucial for personalized cardiovascular disease prevention.
Abstract:
Atherosclerosis is a progressive disease that starts early in life and is manifested clinically as coronary artery disease (CAD), cerebrovascular disease, or peripheral artery disease. CAD remains the leading cause of morbidity and mortality in Western society despite the great advances made in understanding its underlying pathophysiology. The key risk factors associated with CAD include hypercholesterolemia, hypertension, poor diet, obesity, age, male gender, smoking, and physical inactivity. Genetics also play an important role that may interact with environmental factors, including diet, nutritional status, and physiological parameters. Furthermore, certain chronic inflammatory conditions also predispose to the development of CAD. The spiraling increase in obesity rates worldwide has made it more pertinent than ever before to understand the metabolic perturbations that link over nutrition to enhanced cardiovascular risk. Great breakthroughs have been made at the pharmacological level to manage CAD; statins and aspirin have revolutionized treatment of CAD and prolonged lifespan. Nonetheless, lifestyle intervention prior to clinical presentation of CAD symptoms would negate/delay the need for chronic pharmacotherapy in at-risk individuals which in turn would relieve healthcare systems of a costly burden. Throughout this review, we debate the relative impact of nutrition versus genetics in driving CAD. We will investigate how overnutrition affects adipose tissue biology and drives IR and will discuss the subsequent implications for the cardiovascular system. Furthermore, we will discuss how lifestyle interventions including diet modification and weight loss can improve both IR and metabolic dyslipidemia that is associated with obesity. We will conclude by delving into the concept that nutritional status interacts with genetic susceptibility, such that perhaps a more personalized nutrition approach may be more effective in determining diet-related risk as well as response to nutritional interventions.
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