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A New Insight on Atherosclerosis Mechanism and Lipid-Lowering Drugs.

作者信息

Li Penghui, Jiang Wei

机构信息

Binhai New Area Hospital of TCM, 300000 Tianjin, China.

First Teaching Hospital of Tianjin University of Traditional Chinese Medicine, 300000 Tianjin, China.

出版信息

Rev Cardiovasc Med. 2025 Mar 5;26(3):25321. doi: 10.31083/RCM25321. eCollection 2025 Mar.


DOI:10.31083/RCM25321
PMID:40160588
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11951287/
Abstract

Atherosclerosis (AS) is a chronic vascular disease primarily affecting large and medium-sized arteries, involving complex pathological mechanisms such as inflammatory responses, lipid metabolism disorders and vascular plaque formation. In recent years, several emerging research hotspots have appeared in the field of atherosclerosis, including gut microbiota, pyroptosis, ferroptosis, autophagy, cuproptosis, exosomes and non-coding RNA. Traditional lipid-lowering drugs play a crucial role in the treatment of AS but are not able to significantly reverse the pathological changes. This article aims to summarize the latest research progress in the pathogenesis of AS and the diagnosis and treatment of the disease by comprehensively analyzing relevant literature mainly from the past five years. Additionally, the mechanisms of action and research advances of statins, cholesterol absorption inhibitors, fibrates and novel lipid-lowering drugs are reviewed to provide new insights into the diagnosis and treatment of AS.

摘要

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A New Insight on Atherosclerosis Mechanism and Lipid-Lowering Drugs.

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[2]
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[3]
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[8]
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[10]
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本文引用的文献

[1]
Copper's dual role: unravelling the link between copper homeostasis, cuproptosis, and cardiovascular diseases.

Hypertens Res. 2024-5

[2]
Copper homeostasis and cuproptosis in atherosclerosis: metabolism, mechanisms and potential therapeutic strategies.

Cell Death Discov. 2024-1-13

[3]
Epitranscriptomic Modification of MicroRNA Increases Atherosclerosis Susceptibility.

Circulation. 2023-11-28

[4]
Inflammatory Cell-Derived MYDGF Attenuates Endothelial LDL Transcytosis to Protect Against Atherogenesis.

Arterioscler Thromb Vasc Biol. 2023-11

[5]
Different stimuli induce endothelial dysfunction and promote atherosclerosis through the Piezo1/YAP signaling axis.

Arch Biochem Biophys. 2023-10-1

[6]
Adrenomedullin, transcriptionally regulated by vitamin D receptors, alleviates atherosclerosis in mice through suppressing AMPK-mediated endothelial ferroptosis.

Environ Toxicol. 2024-1

[7]
Phosphatidylethanolamine alleviates OX-LDL-induced macrophage inflammation by upregulating autophagy and inhibiting NLRP1 inflammasome activation.

Free Radic Biol Med. 2023-11-1

[8]
IQGAP1 promotes mitochondrial damage and activation of the mtDNA sensor cGAS-STING pathway to induce endothelial cell pyroptosis leading to atherosclerosis.

Int Immunopharmacol. 2023-10

[9]
NPRC deletion mitigated atherosclerosis by inhibiting oxidative stress, inflammation and apoptosis in ApoE knockout mice.

Signal Transduct Target Ther. 2023-8-9

[10]
Apigenin inhibits macrophage pyroptosis through regulation of oxidative stress and the NF-κB pathway and ameliorates atherosclerosis.

Phytother Res. 2023-11

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