Lipoprotein(a)-60 Years Later-What Do We Know?

被引:17
作者
Paslawska, Anna [1 ]
Tomasik, Przemyslaw J. [2 ]
机构
[1] Med Hosp Lab, Tuchow Hlth Ctr, Szpitalna St 1, PL-33170 Tuchow, Poland
[2] Jagiellonian Univ, Pediat Inst, Coll Med, Dept Clin Biochem, Wielicka St 265, PL-30663 Krakow, Poland
关键词
lipoprotein (a); apolipoprotein (a); cardiovascular disease; coronary heart disease; antisense oligonucleotide; PCSK9; inhibitor; ELEVATED LIPOPROTEIN(A); CARDIOVASCULAR-DISEASE; SERIES-LIPOPROTEIN; RISK;
D O I
10.3390/cells12202472
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Lipoprotein(a) (Lp(a)) molecule includes two protein components: apolipoprotein(a) and apoB100. The molecule is the main transporter of oxidized phospholipids (OxPL) in plasma. The concentration of this strongly atherogenic lipoprotein is predominantly regulated by the LPA gene expression. Lp(a) is regarded as a risk factor for several cardiovascular diseases. Numerous epidemiological, clinical and in vitro studies showed a strong association between increased Lp(a) and atherosclerotic cardiovascular disease (ASCVD), calcific aortic valve disease/aortic stenosis (CAVD/AS), stroke, heart failure or peripheral arterial disease (PAD). Although there are acknowledged contributions of Lp(a) to the mentioned diseases, clinicians struggle with many inconveniences such as a lack of well-established treatment lowering Lp(a), and common guidelines for diagnosing or assessing cardiovascular risk among both adult and pediatric patients. Lp(a) levels are different with regard to a particular race or ethnicity and might fluctuate during childhood. Furthermore, the lack of standardization of assays is an additional impediment. The review presents the recent knowledge on Lp(a) based on clinical and scientific research, but also highlights relevant aspects of future study directions that would approach more suitable and effective managing risk associated with increased Lp(a), as well as control the Lp(a) levels.
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页数:13
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