TY - JOUR
T1 - Lipid-lowering therapies for atherosclerosis
T2 - Statins, fibrates, ezetimibe and pcsk9 monoclonal antibodies
AU - Ali, Adel Hajj
AU - Younis, Nour
AU - Abdallah, Rola
AU - Shaer, Farah
AU - Dakroub, Ali
AU - Ayoub, Mohammed Akli
AU - Iratni, Rabah
AU - Yassine, Hadi Mohamad
AU - Zibara, Kazem
AU - Orekhov, Alexander
AU - El-Yazbi, Ahmed Fawzy
AU - Eid, Ali H.
N1 - Publisher Copyright:
© 2021 Bentham Science Publishers.
PY - 2021/11
Y1 - 2021/11
N2 - Cardiovascular disease (CVD) remains the primary cause of global morbidity and mortality. CVD includes various life-threatening conditions such as myocardial infarction, stroke and peripheral arterial diseases. In this context, atherosclerosis continues to play the principal role in the pathogenesis of these conditions. Atherosclerosis emanates from a set of modifiable and non-modifiable risk factors that include age, male gender, family history, obesity, smoking, diabetes mellitus and hypertension. Recent evidence classifies atherosclerosis as a latent disease affecting all-sized arteries with a predilection for arterial branching points of decreased or absent blood supply. Atherosclerosis is not only a lipid metabolism disorder, but is also a chronic inflammatory one. This review providesa synoptic discussion of the underlying pathological mechanisms of atherosclerosis andthe currently applied therapeutic interventions. We then discuss the classical lipid-lowering therapies as well as the newly discovered therapies. For the classical therapies, we point out the importance of statins and ezetimibe in reducing plasma cholesterol levels by virtue of their effects on synthesis, reuptake and intestinal absorption of cholesterol. We also discuss the role of fibrates in modulating lipid metabolism and improving the ratio of high-density to low-density density lipoproteins. This study focuseson the more recent molecular and genetic interventions exemplified by proprotein convertase subtilisin/kexin type 9 (PCSK9) monoclonal antibodies, evinacumab, and microRNA inhibitors. Special attention is also given to clinical trials involving these therapies.
AB - Cardiovascular disease (CVD) remains the primary cause of global morbidity and mortality. CVD includes various life-threatening conditions such as myocardial infarction, stroke and peripheral arterial diseases. In this context, atherosclerosis continues to play the principal role in the pathogenesis of these conditions. Atherosclerosis emanates from a set of modifiable and non-modifiable risk factors that include age, male gender, family history, obesity, smoking, diabetes mellitus and hypertension. Recent evidence classifies atherosclerosis as a latent disease affecting all-sized arteries with a predilection for arterial branching points of decreased or absent blood supply. Atherosclerosis is not only a lipid metabolism disorder, but is also a chronic inflammatory one. This review providesa synoptic discussion of the underlying pathological mechanisms of atherosclerosis andthe currently applied therapeutic interventions. We then discuss the classical lipid-lowering therapies as well as the newly discovered therapies. For the classical therapies, we point out the importance of statins and ezetimibe in reducing plasma cholesterol levels by virtue of their effects on synthesis, reuptake and intestinal absorption of cholesterol. We also discuss the role of fibrates in modulating lipid metabolism and improving the ratio of high-density to low-density density lipoproteins. This study focuseson the more recent molecular and genetic interventions exemplified by proprotein convertase subtilisin/kexin type 9 (PCSK9) monoclonal antibodies, evinacumab, and microRNA inhibitors. Special attention is also given to clinical trials involving these therapies.
KW - Atherosclerosis
KW - Ezetimibe
KW - Fibrates
KW - MicroRNA inhibitors
KW - Monoclonal antibodies for atherosclerosis
KW - PCSK9 inhibitors
KW - Statin
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U2 - 10.2174/0929867328666210222092628
DO - 10.2174/0929867328666210222092628
M3 - Review article
C2 - 33655822
AN - SCOPUS:85118714826
SN - 0929-8673
VL - 28
SP - 7427
EP - 7445
JO - Current Medicinal Chemistry
JF - Current Medicinal Chemistry
IS - 36
ER -