TY - JOUR
T1 - Cholesterol and lipoprotein metabolism and atherosclerosis
T2 - Recent advances in reverse cholesterol transport
AU - Wang, Helen H.
AU - Garruti, Gabriella
AU - Liu, Min
AU - Portincasa, Piero
AU - Wang, David Q.H.
N1 - Funding Information:
This work was supported in part by research grants DK106249, DK041296 and AA103557 (to DQ-HW), DK92779, and DK95440 (to M.L.), all from the National Institutes of Health (US Public Health Service).
Publisher Copyright:
© 2017, Fundacion Clinica Medica Sur. All rights reserved.
PY - 2017/11
Y1 - 2017/11
N2 - Atherosclerosis is characterized by lipid accumulation, inflammatory response, cell death and fibrosis in the arterial wall, and is a major pathological basis for ischemic coronary heart disease (CHD), which is the leading cause of morbidity and mortality in the USA and Europe. Intervention studies with statins have shown to reduce plasma LDL cholesterol concentrations and subsequently the risk of developing CHD. However, not all the aggressive statin therapy could decrease the risk of developing CHD. Many clinical and epidemiological studies have clearly demonstrated that the HDL cholesterol is inversely associated with risk of CHD and is a critical and independent component of predicting this risk. Elucidations of HDL metabolism give rise to therapeutic targets with potential to raising plasma HDL cholesterol levels, thereby reducing the risk of developing CHD. The concept of reverse cholesterol transport is based on the hypothesis that HDL displays an cardioprotective function, which is a process involved in the removal of excess cholesterol that is accumulated in the peripheral tissues (e.g., macrophages in the aortae) by HDL, transporting it to the liver for excretion into the feces via the bile. In this review, we summarize the latest advances in the role of the lymphatic route in reverse cholesterol transport, as well as the biliary and the non-biliary pathways for removal of cholesterol from the body. These studies will greatly increase the likelihood of discovering new lipid-lowering drugs, which are more effective in the prevention and therapeutic intervention of CHD that is the major cause of human death and disability worldwide.
AB - Atherosclerosis is characterized by lipid accumulation, inflammatory response, cell death and fibrosis in the arterial wall, and is a major pathological basis for ischemic coronary heart disease (CHD), which is the leading cause of morbidity and mortality in the USA and Europe. Intervention studies with statins have shown to reduce plasma LDL cholesterol concentrations and subsequently the risk of developing CHD. However, not all the aggressive statin therapy could decrease the risk of developing CHD. Many clinical and epidemiological studies have clearly demonstrated that the HDL cholesterol is inversely associated with risk of CHD and is a critical and independent component of predicting this risk. Elucidations of HDL metabolism give rise to therapeutic targets with potential to raising plasma HDL cholesterol levels, thereby reducing the risk of developing CHD. The concept of reverse cholesterol transport is based on the hypothesis that HDL displays an cardioprotective function, which is a process involved in the removal of excess cholesterol that is accumulated in the peripheral tissues (e.g., macrophages in the aortae) by HDL, transporting it to the liver for excretion into the feces via the bile. In this review, we summarize the latest advances in the role of the lymphatic route in reverse cholesterol transport, as well as the biliary and the non-biliary pathways for removal of cholesterol from the body. These studies will greatly increase the likelihood of discovering new lipid-lowering drugs, which are more effective in the prevention and therapeutic intervention of CHD that is the major cause of human death and disability worldwide.
KW - Biliary lipid secretion
KW - Cholesterol-lowering drugs
KW - Coronary heart disease
KW - Intestinal lipid absorption
KW - Statins
KW - Stroke
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U2 - 10.5604/01.3001.0010.5495
DO - 10.5604/01.3001.0010.5495
M3 - Article
C2 - 29080338
AN - SCOPUS:85046080199
SN - 1665-2681
VL - 16
SP - s27-s42
JO - Annals of Hepatology
JF - Annals of Hepatology
ER -