Literature DB >> 21241231

The role of lipoprotein-associated phospholipase A2 (Lp-PLA₂) in cardiovascular disease.

Ignatios Ikonomidis1, Christos A Michalakeas, John Lekakis, John Parissis, Maria Anastasiou-Nana.   

Abstract

Lipoprotein-associated Phospholipase A2 (Lp-PLA(2)) is an enzyme that belongs to the A2 Phospholipase superfamily and is produced by inflammatory cells that are involved in the process of atherogenesis. Even though there is controversy in current bibliography whether Lp-PLA(2) exerts proatherogenic or anti-atherogenic properties, the weight of evidence suggests a pro-atherogenic role for this protein. Lp-PLA(2) is detected in human atherosclerotic lesions and elevated Lp-PLA(2) levels are associated with an increased risk of cardiovascular events and adverse events in patients with coronary artery disease independently of traditional risk factors and other markers of inflammation. It has been recently shown that direct pharmacological inhibition of Lp-PLA(2) activity exerts beneficiary effects on the atherosclerotic process. This finding is most interesting since it could offer a novel target for therapeutic intervention in patients suffering from cardiovascular disease. The purpose of this review article is to report on the role of Lp-PLA(2) in cardiovascular diseases and to enlighten the putative pathophysiologic mechanisms by which this protein exerts its effect on cardiovascular function. Additionally, the pharmacological interventions that influence Lp-PLA(2) activity and may offer a new approach for the treatment of atherosclerosis will be analyzed.

Entities:  

Mesh:

Substances:

Year:  2011        PMID: 21241231     DOI: 10.2174/157488711795177903

Source DB:  PubMed          Journal:  Rev Recent Clin Trials        ISSN: 1574-8871


  7 in total

1.  Leptospirosis is associated with markedly increased triglycerides and small dense low-density lipoprotein and decreased high-density lipoprotein.

Authors:  Irene F Gazi; Fotini A Apostolou; Evangelos N Liberopoulos; Theodosios D Filippatos; Constantinos C Tellis; Moses S Elisaf; Alexandros D Tselepis
Journal:  Lipids       Date:  2011-06-19       Impact factor: 1.880

2.  An effect of moderate hepatic impairment on the pharmacokinetics and safety of darapladib.

Authors:  Mindy He Magee; Shawn Shearn; Bonnie Shaddinger; Zixing Fang; Ruchira Glaser
Journal:  Br J Clin Pharmacol       Date:  2014-11       Impact factor: 4.335

3.  Systematic Review of the Association between Lipoprotein-Associated Phospholipase A2 and Atherosclerosis.

Authors:  Jing Liu; Yuling Hong; Yue Qi; Fan Zhao; Dong Zhao
Journal:  N Am J Med Sci (Boston)       Date:  2011-10

4.  Single and Multiple Dose Pharmacokinetics, Pharmacodynamics and Safety of the Novel Lipoprotein-Associated Phospholipase A2 Enzyme Inhibitor Darapladib in Healthy Chinese Subjects: An Open Label Phase-1 Clinical Trial.

Authors:  Chaoying Hu; Debra Tompson; Mindy Magee; Qian Chen; Yan Mei Liu; Wenjing Zhu; Hongxin Zhao; Annette S Gross; Yun Liu
Journal:  PLoS One       Date:  2015-10-14       Impact factor: 3.240

Review 5.  Clinical usefulness of novel serum and imaging biomarkers in risk stratification of patients with stable angina.

Authors:  George Tsaknis; Iraklis Tsangaris; Ignatios Ikonomidis; Argirios Tsantes
Journal:  Dis Markers       Date:  2014-06-19       Impact factor: 3.434

6.  Baseline elevated Lp-PLA2 is associated with increased risk for re-stenosis after stent placement.

Authors:  Dongdan Zheng; FanFang Zeng; Anping Cai; Huocheng Liao; Ling Liu; Ruofeng Qiu; Rulin Xu; Chun Xiao; Weiyi Mai
Journal:  Lipids Health Dis       Date:  2014-03-01       Impact factor: 3.876

7.  Elevated Lipoprotein-Associated Phospholipase A2 Independently Affects Age-Related Increases in Systolic Blood Pressure: A Nested Case-Control Study in a Prospective Korean Cohort.

Authors:  Hye Jin Yoo; Minjoo Kim; Sang-Hyun Lee; Jong Ho Lee
Journal:  Int J Hypertens       Date:  2020-03-31       Impact factor: 2.420

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.