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Elevated Lipoprotein-Associated Phospholipase A2 Is Associated With Intracranial Atherosclerosis

BACKGROUND: Lipoprotein-associated phospholipase A2 (Lp-PLA2) is an inflammatory factor in the pathogenesis of atherosclerotic plaque and is associated with an increased risk of ischemic stroke. Whether Lp-PLA2 is associated with stenosis subtypes in acute ischemic stroke (AIS) has not been investig...

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Autores principales: Wang, Yuan, Liu, Gang, Song, Haiqing, Cao, Catherine, Ji, Xunming, Cao, Guodong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9226299/
https://www.ncbi.nlm.nih.gov/pubmed/35756924
http://dx.doi.org/10.3389/fneur.2022.858302
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author Wang, Yuan
Liu, Gang
Song, Haiqing
Cao, Catherine
Ji, Xunming
Cao, Guodong
author_facet Wang, Yuan
Liu, Gang
Song, Haiqing
Cao, Catherine
Ji, Xunming
Cao, Guodong
author_sort Wang, Yuan
collection PubMed
description BACKGROUND: Lipoprotein-associated phospholipase A2 (Lp-PLA2) is an inflammatory factor in the pathogenesis of atherosclerotic plaque and is associated with an increased risk of ischemic stroke. Whether Lp-PLA2 is associated with stenosis subtypes in acute ischemic stroke (AIS) has not been investigated. METHODS: A total of 126 eligible AIS patients were divided into four groups: (1) no cerebral artery stenosis (NCS); (2) intracranial artery stenosis (ICAS); (3) extracranial artery stenosis (ECAS); and (4) combined intracranial and extracranial artery stenosis (IECS). Associations between serum Lp-PLA2 levels and the stenosis subtypes were assessed. RESULTS: The ICAS group had a lower frequency of dyslipidemia as compared to the NCS group and the IECS group (35.3% vs. 70% vs. 71.8%, respectively, p = 0.001) and was more likely to be symptomatic than the ECAS group (76.5% vs. 43.8%, respectively, p = 0.014). Lp-PLA2 levels in the ICAS group were 112.2 ± 66.8 μg/L which are, higher than those in the NCS, ECAS, and IECS groups (81.7 ± 38.5, 106.1 ± 57.8, 89.3 ± 52.2 μg/L, respectively, p = 0.025). In the third and fourth quartiles of Lp-PLA2 levels, stenosis had occurred more frequently in the ICAS group than in the other three groups (third Q: 50.0% vs. 3.1% vs. 28.1% vs. 18.8%, p = 0.002; fourth Q: 48.4% vs. 16.1% vs. 25.8% vs. 9.7%, p = 0.014). Lp-PLA2 levels were higher in patients with more or severe stenosis in the ICAS group. CONCLUSIONS: Elevated Lp-PLA2 levels were differentially associated with increased risk in AIS patients with ICAS compared to those with ECAS or no stenosis. Lp-PLA2 may be a promising biomarker and potential therapeutic target for ICAS.
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spelling pubmed-92262992022-06-25 Elevated Lipoprotein-Associated Phospholipase A2 Is Associated With Intracranial Atherosclerosis Wang, Yuan Liu, Gang Song, Haiqing Cao, Catherine Ji, Xunming Cao, Guodong Front Neurol Neurology BACKGROUND: Lipoprotein-associated phospholipase A2 (Lp-PLA2) is an inflammatory factor in the pathogenesis of atherosclerotic plaque and is associated with an increased risk of ischemic stroke. Whether Lp-PLA2 is associated with stenosis subtypes in acute ischemic stroke (AIS) has not been investigated. METHODS: A total of 126 eligible AIS patients were divided into four groups: (1) no cerebral artery stenosis (NCS); (2) intracranial artery stenosis (ICAS); (3) extracranial artery stenosis (ECAS); and (4) combined intracranial and extracranial artery stenosis (IECS). Associations between serum Lp-PLA2 levels and the stenosis subtypes were assessed. RESULTS: The ICAS group had a lower frequency of dyslipidemia as compared to the NCS group and the IECS group (35.3% vs. 70% vs. 71.8%, respectively, p = 0.001) and was more likely to be symptomatic than the ECAS group (76.5% vs. 43.8%, respectively, p = 0.014). Lp-PLA2 levels in the ICAS group were 112.2 ± 66.8 μg/L which are, higher than those in the NCS, ECAS, and IECS groups (81.7 ± 38.5, 106.1 ± 57.8, 89.3 ± 52.2 μg/L, respectively, p = 0.025). In the third and fourth quartiles of Lp-PLA2 levels, stenosis had occurred more frequently in the ICAS group than in the other three groups (third Q: 50.0% vs. 3.1% vs. 28.1% vs. 18.8%, p = 0.002; fourth Q: 48.4% vs. 16.1% vs. 25.8% vs. 9.7%, p = 0.014). Lp-PLA2 levels were higher in patients with more or severe stenosis in the ICAS group. CONCLUSIONS: Elevated Lp-PLA2 levels were differentially associated with increased risk in AIS patients with ICAS compared to those with ECAS or no stenosis. Lp-PLA2 may be a promising biomarker and potential therapeutic target for ICAS. Frontiers Media S.A. 2022-06-10 /pmc/articles/PMC9226299/ /pubmed/35756924 http://dx.doi.org/10.3389/fneur.2022.858302 Text en Copyright © 2022 Wang, Liu, Song, Cao, Ji and Cao. 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 Neurology
Wang, Yuan
Liu, Gang
Song, Haiqing
Cao, Catherine
Ji, Xunming
Cao, Guodong
Elevated Lipoprotein-Associated Phospholipase A2 Is Associated With Intracranial Atherosclerosis
title Elevated Lipoprotein-Associated Phospholipase A2 Is Associated With Intracranial Atherosclerosis
title_full Elevated Lipoprotein-Associated Phospholipase A2 Is Associated With Intracranial Atherosclerosis
title_fullStr Elevated Lipoprotein-Associated Phospholipase A2 Is Associated With Intracranial Atherosclerosis
title_full_unstemmed Elevated Lipoprotein-Associated Phospholipase A2 Is Associated With Intracranial Atherosclerosis
title_short Elevated Lipoprotein-Associated Phospholipase A2 Is Associated With Intracranial Atherosclerosis
title_sort elevated lipoprotein-associated phospholipase a2 is associated with intracranial atherosclerosis
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9226299/
https://www.ncbi.nlm.nih.gov/pubmed/35756924
http://dx.doi.org/10.3389/fneur.2022.858302
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