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Sex difference in circulating PCSK9 and its clinical implications.
Jia, Fang; Fei, Si-Fan; Tong, De-Bing; Xue, Cong; Li, Jian-Jun.
Affiliation
  • Jia F; Department of Cardiology, The Third Affiliated Hospital of Soochow University, Changzhou, China.
  • Fei SF; Department of Cardiology, The Third Affiliated Hospital of Soochow University, Changzhou, China.
  • Tong DB; Department of Cardiology, The Third Affiliated Hospital of Soochow University, Changzhou, China.
  • Xue C; Department of Cardiology, The Third Affiliated Hospital of Soochow University, Changzhou, China.
  • Li JJ; Cardio-Metabolic Center, Fu Wai Hospital, Chinese Academy of Medical Sciences, Peking Union Medical College, Beijing, China.
Front Pharmacol ; 13: 953845, 2022.
Article in En | MEDLINE | ID: mdl-36160427
ABSTRACT
Proprotein convertase subtilisin kexin type 9 (PCSK9) is a proprotein convertase that increases plasma low-density lipoprotein cholesterol (LDL-C) levels by triggering the degradation of LDL receptors (LDLRs). Beyond the regulation of circulating LDL-C, PCSK9 also has direct atherosclerotic effects on the vascular wall and is associated with coronary plaque inflammation. Interestingly, emerging data show that women have higher circulating PCSK9 concentrations than men, suggesting that the potential roles of PCSK9 may have different impacts according to sex. In this review, we summarize the studies concerning sex difference in circulating levels of PCSK9. In addition, we report on the sex differences in the relations of elevated circulating PCSK9 levels to the severity and prognosis of coronary artery disease, the incidence of type 2 diabetes mellitus, and neurological damage after cardiac arrest and liver injury, as well as inflammatory biomarkers and high-density lipoprotein cholesterol (HDL-C). Moreover, sex difference in the clinical efficacy of PCSK9 inhibitors application are reviewed. Finally, the underlying mechanisms of sex difference in circulating PCSK9 concentrations and the clinical implications are also discussed.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Front Pharmacol Year: 2022 Document type: Article Affiliation country: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Front Pharmacol Year: 2022 Document type: Article Affiliation country: China