TY - JOUR
T1 - The renaissance of lipoprotein(a)
T2 - Brave new world for preventive cardiology?
AU - Ellis, Katrina L.
AU - Boffa, Michael B.
AU - Sahebkar, Amirhossein
AU - Koschinsky, Marlys L.
AU - Watts, Gerald F.
PY - 2017/10/1
Y1 - 2017/10/1
N2 - Lipoprotein(a) [Lp(a)] is a highly heritable cardiovascular risk factor. Although discovered more than 50 years ago, Lp(a) has recently re-emerged as a major focus in the fields of lipidology and preventive cardiology owing to findings from genetic studies and the possibility of lowering elevated plasma concentrations with new antisense therapy. Data from genetic, epidemiological and clinical studies have provided compelling evidence establishing Lp(a) as a causal risk factor for atherosclerotic cardiovascular disease. Nevertheless, major gaps in knowledge remain and the identification of the mechanistic processes governing both Lp(a) pathobiology and metabolism are an ongoing challenge. Furthermore, the complex structure of Lp(a) presents a major obstacle to the accurate quantification of plasma concentrations, and a universally accepted and standardized approach for measuring Lp(a) is required. Significant progress has been made in the development of novel therapeutics for selectively lowering Lp(a). However, before these therapies can be widely implemented further investigations are required to assess their efficacy, safety, and cost-efficiency in the prevention of cardiovascular events. We review recent advances in molecular and biochemical aspects, epidemiology, and pathobiology of Lp(a), and provide a contemporary update on the significance of Lp(a) in clinical medicine. “Progress lies not in enhancing what is, but in advancing toward what will be.” (Khalil Gibran)
AB - Lipoprotein(a) [Lp(a)] is a highly heritable cardiovascular risk factor. Although discovered more than 50 years ago, Lp(a) has recently re-emerged as a major focus in the fields of lipidology and preventive cardiology owing to findings from genetic studies and the possibility of lowering elevated plasma concentrations with new antisense therapy. Data from genetic, epidemiological and clinical studies have provided compelling evidence establishing Lp(a) as a causal risk factor for atherosclerotic cardiovascular disease. Nevertheless, major gaps in knowledge remain and the identification of the mechanistic processes governing both Lp(a) pathobiology and metabolism are an ongoing challenge. Furthermore, the complex structure of Lp(a) presents a major obstacle to the accurate quantification of plasma concentrations, and a universally accepted and standardized approach for measuring Lp(a) is required. Significant progress has been made in the development of novel therapeutics for selectively lowering Lp(a). However, before these therapies can be widely implemented further investigations are required to assess their efficacy, safety, and cost-efficiency in the prevention of cardiovascular events. We review recent advances in molecular and biochemical aspects, epidemiology, and pathobiology of Lp(a), and provide a contemporary update on the significance of Lp(a) in clinical medicine. “Progress lies not in enhancing what is, but in advancing toward what will be.” (Khalil Gibran)
KW - Clinical medicine
KW - Epidemiology
KW - Genetics
KW - Lipoprotein(a)
KW - Metabolism
KW - Pathobiology
UR - http://www.scopus.com/inward/record.url?scp=85029604910&partnerID=8YFLogxK
U2 - 10.1016/j.plipres.2017.09.001
DO - 10.1016/j.plipres.2017.09.001
M3 - Review article
C2 - 28888913
AN - SCOPUS:85029604910
SN - 0163-7827
VL - 68
SP - 57
EP - 82
JO - Progress in Lipid Research
JF - Progress in Lipid Research
ER -