Association Between Plasma Lipoprotein-Associated Phospholipase A2 and Plaque Vulnerability in TIA Patients With Unilateral Middle Cerebral Artery Stenosis

Background: Plasma lipoprotein-associated phospholipase A2 (Lp-PLA2) has emerged as a novel biomarker for coronary atherosclerosis. However, the association between Lp-PLA2 and plaque vulnerability in atherosclerosis of cervicocerebral arteries remains poorly defined, especially for intracranial ath...

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Main Authors: Yiren Qin, Xiaoyan Qian, Xue Luo, Yuanfang Li, Dapeng Wang, Jianhua Jiang, Quanquan Zhang, Meirong Liu, Junhua Xiao, Yan Zhang, Shanshan Diao, Hongru Zhao
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-10-01
Series:Frontiers in Neurology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fneur.2020.574036/full
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spelling doaj-5ec1559d68194d548f5429d8303012712020-11-25T03:51:07ZengFrontiers Media S.A.Frontiers in Neurology1664-22952020-10-011110.3389/fneur.2020.574036574036Association Between Plasma Lipoprotein-Associated Phospholipase A2 and Plaque Vulnerability in TIA Patients With Unilateral Middle Cerebral Artery StenosisYiren Qin0Xiaoyan Qian1Xue Luo2Yuanfang Li3Dapeng Wang4Jianhua Jiang5Quanquan Zhang6Meirong Liu7Junhua Xiao8Yan Zhang9Shanshan Diao10Hongru Zhao11Department of Neurology, The First Affiliated Hospital of Soochow University, Suzhou, ChinaDepartment of Neurology, The First People's Hospital of Kunshan, Kunshan, ChinaDepartment of Neurology, Shiqian County People's Hospital, Tongren, ChinaDepartment of Neurology, Shiqian County People's Hospital, Tongren, ChinaDepartment of Neurology, The First Affiliated Hospital of Soochow University, Suzhou, ChinaDepartment of Neurology, The First Affiliated Hospital of Soochow University, Suzhou, ChinaDepartment of Neurology, The First Affiliated Hospital of Soochow University, Suzhou, ChinaDepartment of Neurology, The First Affiliated Hospital of Soochow University, Suzhou, ChinaDepartment of Gastroenterology, The First Affiliated Hospital of Soochow University, Suzhou, ChinaDepartment of Neurology, The First People's Hospital of Kunshan, Kunshan, ChinaDepartment of Neurology, The First Affiliated Hospital of Soochow University, Suzhou, ChinaDepartment of Neurology, The First Affiliated Hospital of Soochow University, Suzhou, ChinaBackground: Plasma lipoprotein-associated phospholipase A2 (Lp-PLA2) has emerged as a novel biomarker for coronary atherosclerosis. However, the association between Lp-PLA2 and plaque vulnerability in atherosclerosis of cervicocerebral arteries remains poorly defined, especially for intracranial atherosclerotic stenosis (ICAS). We aimed to investigate the association between Lp-PLA2 and plaque vulnerability in transient ischemic attack (TIA) patients with unilateral middle cerebral artery stenoses (MCAs).Methods: In this study, a total of 207 patients were enrolled from April 2017 to April 2020. Clinical data were collected, and MCA plaques were examined with high-resolution magnetic resonance imaging (HRMRI). Baseline characteristics of patients were collected during hospitalization. Statistical comparisons were performed using Pearson's chi-squared test, Mann–Whitney U test, and the Breslow–Day/Tarone's test for the determination of heterogeneity in different age strata. Multivariate binary logistic analysis was used to investigate the potential independent predictors that were highly correlated to plaque vulnerability.Results: The results showed that a high Lp-PLA2 level (>221 ng/ml) was associated with plaque vulnerability in TIA patients with unilateral MCAs. High Lp-PLA2 was independently associated with plaque vulnerability in patients ≤ 60 years old [multivariate adjusted odds ratio (OR) = 9.854; 95% CI, 2.458–39.501] but not in patients >60 years old (multivariate adjusted OR = 1.901; 95% CI, 0.640–5.650). Predictors of plaque vulnerability in different age strata were also different.Conclusion: Lp-PLA2 levels may be correlated to plaque vulnerability in TIA patients with unilateral MCAs and might be a diagnostic biomarker for plaque vulnerability in this kind of patients, especially for ones aged ≤ 60 years old.https://www.frontiersin.org/article/10.3389/fneur.2020.574036/fullLp-PLA2transient ischemic attackmiddle cerebral arteryICAsHRMRI
collection DOAJ
language English
format Article
sources DOAJ
author Yiren Qin
Xiaoyan Qian
Xue Luo
Yuanfang Li
Dapeng Wang
Jianhua Jiang
Quanquan Zhang
Meirong Liu
Junhua Xiao
Yan Zhang
Shanshan Diao
Hongru Zhao
spellingShingle Yiren Qin
Xiaoyan Qian
Xue Luo
Yuanfang Li
Dapeng Wang
Jianhua Jiang
Quanquan Zhang
Meirong Liu
Junhua Xiao
Yan Zhang
Shanshan Diao
Hongru Zhao
Association Between Plasma Lipoprotein-Associated Phospholipase A2 and Plaque Vulnerability in TIA Patients With Unilateral Middle Cerebral Artery Stenosis
Frontiers in Neurology
Lp-PLA2
transient ischemic attack
middle cerebral artery
ICAs
HRMRI
author_facet Yiren Qin
Xiaoyan Qian
Xue Luo
Yuanfang Li
Dapeng Wang
Jianhua Jiang
Quanquan Zhang
Meirong Liu
Junhua Xiao
Yan Zhang
Shanshan Diao
Hongru Zhao
author_sort Yiren Qin
title Association Between Plasma Lipoprotein-Associated Phospholipase A2 and Plaque Vulnerability in TIA Patients With Unilateral Middle Cerebral Artery Stenosis
title_short Association Between Plasma Lipoprotein-Associated Phospholipase A2 and Plaque Vulnerability in TIA Patients With Unilateral Middle Cerebral Artery Stenosis
title_full Association Between Plasma Lipoprotein-Associated Phospholipase A2 and Plaque Vulnerability in TIA Patients With Unilateral Middle Cerebral Artery Stenosis
title_fullStr Association Between Plasma Lipoprotein-Associated Phospholipase A2 and Plaque Vulnerability in TIA Patients With Unilateral Middle Cerebral Artery Stenosis
title_full_unstemmed Association Between Plasma Lipoprotein-Associated Phospholipase A2 and Plaque Vulnerability in TIA Patients With Unilateral Middle Cerebral Artery Stenosis
title_sort association between plasma lipoprotein-associated phospholipase a2 and plaque vulnerability in tia patients with unilateral middle cerebral artery stenosis
publisher Frontiers Media S.A.
series Frontiers in Neurology
issn 1664-2295
publishDate 2020-10-01
description Background: Plasma lipoprotein-associated phospholipase A2 (Lp-PLA2) has emerged as a novel biomarker for coronary atherosclerosis. However, the association between Lp-PLA2 and plaque vulnerability in atherosclerosis of cervicocerebral arteries remains poorly defined, especially for intracranial atherosclerotic stenosis (ICAS). We aimed to investigate the association between Lp-PLA2 and plaque vulnerability in transient ischemic attack (TIA) patients with unilateral middle cerebral artery stenoses (MCAs).Methods: In this study, a total of 207 patients were enrolled from April 2017 to April 2020. Clinical data were collected, and MCA plaques were examined with high-resolution magnetic resonance imaging (HRMRI). Baseline characteristics of patients were collected during hospitalization. Statistical comparisons were performed using Pearson's chi-squared test, Mann–Whitney U test, and the Breslow–Day/Tarone's test for the determination of heterogeneity in different age strata. Multivariate binary logistic analysis was used to investigate the potential independent predictors that were highly correlated to plaque vulnerability.Results: The results showed that a high Lp-PLA2 level (>221 ng/ml) was associated with plaque vulnerability in TIA patients with unilateral MCAs. High Lp-PLA2 was independently associated with plaque vulnerability in patients ≤ 60 years old [multivariate adjusted odds ratio (OR) = 9.854; 95% CI, 2.458–39.501] but not in patients >60 years old (multivariate adjusted OR = 1.901; 95% CI, 0.640–5.650). Predictors of plaque vulnerability in different age strata were also different.Conclusion: Lp-PLA2 levels may be correlated to plaque vulnerability in TIA patients with unilateral MCAs and might be a diagnostic biomarker for plaque vulnerability in this kind of patients, especially for ones aged ≤ 60 years old.
topic Lp-PLA2
transient ischemic attack
middle cerebral artery
ICAs
HRMRI
url https://www.frontiersin.org/article/10.3389/fneur.2020.574036/full
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