Your browser doesn't support javascript.
loading
Elevated lipoprotein(a) levels: A crucial determinant of cardiovascular disease risk and target for emerging therapies.
Afzal, Zeeshan; Cao, Huili; Chaudhary, Mueed; Chigurupati, Himaja Dutt; Neppala, Sivaram; Alruwaili, Waleed; Awad, Maan; Sandesara, Darshan; Siddique, Muzammil; Farman, Ali; Zafrullah, Fnu; Gonuguntla, Karthik; Sattar, Yasar.
Afiliação
  • Afzal Z; Department of Medicine, Shanxi Medical University, China.
  • Cao H; Department of Cardiology, Second Hospital of Shanxi Medical University, China.
  • Chaudhary M; Department of Medicine, Wah Medical College, Pakistan.
  • Chigurupati HD; Department of Internal Medicine, New York Medical College at Saint Michael's Medical Center, NJ, USA.
  • Neppala S; Department of Medicine, University of Texas Health Science Center, San Antonio, TX, USA.
  • Alruwaili W; Department of Internal Medicine, West Virginia University, Morgantown, WV, USA.
  • Awad M; Department of Internal Medicine, West Virginia University, Morgantown, WV, USA.
  • Sandesara D; Department of Cardiology, Apex Heart Institute, Ahmedabad, India.
  • Siddique M; University Hospital of North Midland Trust NHS, UK.
  • Farman A; Department of Medicine, Corewell Health Dearborn Hospital, Dearborn, MI, USA.
  • Zafrullah F; Department of Cardiology, Ascension Borgess Hospital, MI, USA.
  • Gonuguntla K; Department of Cardiology, West Virginia University, Morgantown, WV, USA.
  • Sattar Y; Department of Cardiology, West Virginia University, Morgantown, WV, USA. Electronic address: mdyasarsattar@gmail.com.
Curr Probl Cardiol ; 49(8): 102586, 2024 Aug.
Article em En | MEDLINE | ID: mdl-38653440
ABSTRACT
Cardiovascular disease (CVD) remains a significant global health challenge despite advancements in prevention and treatment. Elevated Lipoprotein(a) [Lp(a)] levels have emerged as a crucial risk factor for CVD and aortic stenosis, affecting approximately 20 of the global population. Research over the last decade has established Lp(a) as an independent genetic contributor to CVD and aortic stenosis, beginning with Kare Berg's discovery in 1963. This has led to extensive exploration of its molecular structure and pathogenic roles. Despite the unknown physiological function of Lp(a), studies have shed light on its metabolism, genetics, and involvement in atherosclerosis, inflammation, and thrombosis. Epidemiological evidence highlights the link between high Lp(a) levels and increased cardiovascular morbidity and mortality. Newly emerging therapies, including pelacarsen, zerlasiran, olpasiran, muvalaplin, and lepodisiran, show promise in significantly lowering Lp(a) levels, potentially transforming the management of cardiovascular disease. However, further research is essential to assess these novel therapies' long-term efficacy and safety, heralding a new era in cardiovascular disease prevention and treatment and providing hope for at-risk patients.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Cardiovasculares / Lipoproteína(a) Limite: Humans Idioma: En Revista: Curr Probl Cardiol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Cardiovasculares / Lipoproteína(a) Limite: Humans Idioma: En Revista: Curr Probl Cardiol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China