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Sex difference in circulating PCSK9 and its clinical implications
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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9490038/ https://www.ncbi.nlm.nih.gov/pubmed/36160427 http://dx.doi.org/10.3389/fphar.2022.953845 |
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author | Jia, Fang Fei, Si-Fan Tong, De-Bing Xue, Cong Li, Jian-Jun |
author_facet | Jia, Fang Fei, Si-Fan Tong, De-Bing Xue, Cong Li, Jian-Jun |
author_sort | Jia, Fang |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-9490038 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-94900382022-09-22 Sex difference in circulating PCSK9 and its clinical implications Jia, Fang Fei, Si-Fan Tong, De-Bing Xue, Cong Li, Jian-Jun Front Pharmacol Pharmacology 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. Frontiers Media S.A. 2022-09-07 /pmc/articles/PMC9490038/ /pubmed/36160427 http://dx.doi.org/10.3389/fphar.2022.953845 Text en Copyright © 2022 Jia, Fei, Tong, Xue and Li. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Pharmacology Jia, Fang Fei, Si-Fan Tong, De-Bing Xue, Cong Li, Jian-Jun Sex difference in circulating PCSK9 and its clinical implications |
title | Sex difference in circulating PCSK9 and its clinical implications |
title_full | Sex difference in circulating PCSK9 and its clinical implications |
title_fullStr | Sex difference in circulating PCSK9 and its clinical implications |
title_full_unstemmed | Sex difference in circulating PCSK9 and its clinical implications |
title_short | Sex difference in circulating PCSK9 and its clinical implications |
title_sort | sex difference in circulating pcsk9 and its clinical implications |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9490038/ https://www.ncbi.nlm.nih.gov/pubmed/36160427 http://dx.doi.org/10.3389/fphar.2022.953845 |
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