Key result
Adipose tissue hypertrophy, dyslipidemia, and systemic inflammation play a synergistic causal role in the development and instability of atherosclerotic plaques.
Understanding the synergistic inflammatory mechanisms in atherosclerosis highlights potential molecular targets, such as pattern recognition receptors, for reducing cardiovascular risk.
May guide targeted anti-inflammatory strategies in atherosclerosis; leaves open prospective validation in clinical trials.
Recent experimental and clinical evidence has suggested a synergistic causal role among adipose tissue hypertrophy, dyslipidemia, and systemic inflammation in the development and instability of the atherosclerotic plaque. Here, we summarize some of the most recent findings regarding the role of whi te adipose tissue hypertrophy in the development of dyslipidemia and chronic low-grade systemic inflammation. We also review the contribution of dyslipidemia in releasing free-fatty acids, cholesterol, and oxidized low-density lipoproteins as metabolic ligands able to trigger inflammatory signal pathways in macrophages via pattern recognition receptor (PRR) activation. Finally, we discuss the possible mechanisms through which dyslipidemia-related metabolic ligands and chronic low-grade systemic inflammation are capable of inducing macrophage activation, which in turn is involved in mediating instability and rupture of the atherosclerotic plaque. A better understanding of the inflammatory mechanisms contributing to atherosclerosis may help to identify potential molecular targets to decrease the cardiovascular risk in patients by using anti-inflammatory therapies and PRR blockers.
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Torres-Castro et al. (2018) conducted a review in Atherosclerosis. Adipose tissue hypertrophy, dyslipidemia, and systemic inflammation was evaluated. Adipose tissue hypertrophy, dyslipidemia, and systemic inflammation play a synergistic causal role in the development and instability of atherosclerotic plaques.
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