2022
DOI: 10.14336/ad.2021.0929
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The Functional Role of Lipoproteins in Atherosclerosis: Novel Directions for Diagnosis and Targeting Therapy

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Cited by 30 publications
(15 citation statements)
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“…In the present study, we demonstrated that Rb1 administration attenuates arterial endothelial damage, lipid metabolism disruption and inhibits systemic inflammation in a rat model of AS. Disorders of lipid metabolism and endothelial damage are the main pathologic changes in the early stages of AS [ [32] , [33] , [34] ]. Dyslipidemia can induce vascular endothelial injury and regulation of macrophage phenotype, thus accelerating the formation of AS plaques [ 35 ].…”
Section: Discussionmentioning
confidence: 99%
“…In the present study, we demonstrated that Rb1 administration attenuates arterial endothelial damage, lipid metabolism disruption and inhibits systemic inflammation in a rat model of AS. Disorders of lipid metabolism and endothelial damage are the main pathologic changes in the early stages of AS [ [32] , [33] , [34] ]. Dyslipidemia can induce vascular endothelial injury and regulation of macrophage phenotype, thus accelerating the formation of AS plaques [ 35 ].…”
Section: Discussionmentioning
confidence: 99%
“…It was found that the ApoB-100 peptide P210 vaccine significantly attenuated aortic atherosclerosis in a humanized mouse model ( 47 ). The decrease of dose-dependent in apolipoproteins, such as Lp(a), and LDL-C, were observed after the administration of mipomersen in clinical trials ( 13 ). If ApoB proves to be a risk factor for CKD, mipomersen may be an alternative strategy for alleviating such metabolic risk-associated impairment in kidney function.…”
Section: Discussionmentioning
confidence: 99%
“…At present, lipid-lowering therapy by reducing the production of ApoB is mainly used in patients with atherosclerosis ( 10 , 11 ). For example, mipomersen is the first Food and Drug Administration approved antisense ApoB synthesis inhibitor for patients who tolerate statin therapy and are at high CVD risk ( 12 , 13 ). In the study of clinical trials, dose-dependent reductions were produced by mipomersen in different types of ApoB-containing lipoproteins, including lipoprotein (a) [Lp(a)] and low-density lipoprotein-cholesterol (LDL-C) ( 14 ).…”
Section: Introductionmentioning
confidence: 99%
“…As shown in Figure 3, we can observe that, independently of the increase in body weight, a triggering risk factor in the development of atherosclerosis is dyslipidemia, which can be of environmental, genetic, or combined origin, initially producing an infiltration of macrophages in the subendothelium, which accumulates until reaching the early lesion; in the intermediate lesion, there is already an intra and extracellular accumulation, which gives rise to the development of the extracellular lipid nucleus or atheroma [61]. In the late stages, a fibrotic layer is produced and calcified, leading to complicated lesions, causing plaque rupture, thrombosis, and blockage of blood flow.…”
Section: Dyslipidemia As a Lox-1 Inducermentioning
confidence: 99%