Atherosclerosis: Recent Trials, New Targets and Future Directions
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Mortality from cardiovascular diseases (CVD) represents the primary cause of death worldwide. Prevention or treatment of atherosclerosis and its clinical sequelae is a central goal in the management of patients with established vascular disease or those at high-risk for vascular events. This paper provides a review of the contemporary pharmacological armamentarium targeting atherosclerosis and also highlights strategies to support future clinical trial design. Powering future trials targeting LDL-cholesterol to its absolute reduction and including patients with a higher LDL-C despite optimal medical therapy (or unable to tolerate statins) will increase the odds of meaningful results. Mendelian randomization studies may identify new causal risk factors for CVD that would help in the selection of the patients most likely to benefit from a specific new compound. Furthermore, imaging techniques integrating a morphological and functional assessment such as IVUS, OCT, PET/CT and PET/MRI may represent in a near future robust "soft" endpoints to support successful translation of early research into meaningful phase III clinical outcome trials.
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Wu Y, Li B, Yu X, Liu Y, Chui R, Sun K Cancer Innov. 2024; 3(3):e114.
PMID: 38947757 PMC: 11212282. DOI: 10.1002/cai2.114.
Alalawi S, Albalawi F, Ramji D Int J Mol Sci. 2023; 24(10).
PMID: 37239823 PMC: 10218101. DOI: 10.3390/ijms24108476.
Chan Y, Ramji D Methods Mol Biol. 2022; 2419:3-19.
PMID: 35237955 DOI: 10.1007/978-1-0716-1924-7_1.
Moss J, Williams J, Al-Ahmadi W, OMorain V, Chan Y, Hughes T Food Funct. 2021; 12(8):3657-3671.
PMID: 33900312 PMC: 8359826. DOI: 10.1039/d0fo02867c.
Dihomo-γ-linolenic acid inhibits several key cellular processes associated with atherosclerosis.
Gallagher H, Williams J, Ferekidis N, Ismail A, Chan Y, Michael D Biochim Biophys Acta Mol Basis Dis. 2019; 1865(9):2538-2550.
PMID: 31202985 PMC: 6620504. DOI: 10.1016/j.bbadis.2019.06.011.