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2
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Front Physiol. 2022 Aug 30;13:931931. doi: 10.3389/fphys.2022.931931. eCollection 2022.
3
Stress and cardiovascular risk burden after the pandemic: current status and future prospects.疫情后压力与心血管风险负担:现状与未来展望。
Expert Rev Cardiovasc Ther. 2022 Jul;20(7):507-513. doi: 10.1080/14779072.2022.2092097. Epub 2022 Jun 23.
4
PON1 (Paraoxonase 1) Q192R Gene Polymorphism in Ischemic Stroke among North Indian Population.北印度人群缺血性卒中中对氧磷酶1(PON1)Q192R基因多态性
Ann Indian Acad Neurol. 2022 Jan-Feb;25(1):100-105. doi: 10.4103/aian.aian_571_21. Epub 2021 Oct 22.
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Paraoxonase and arylesterase activity of serum PON-1 enzyme in psoriatic patients: a systematic review and meta-analysis.银屑病患者血清对氧磷酶-1(PON-1)酶的对氧磷酶和芳基酯酶活性:一项系统评价和荟萃分析
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伴有和不伴有冠状动脉疾病的急性缺血性中风患者中血脂异常、氧化应激与临床结局的相互作用

The Interplay of Dyslipidemia, Oxidative Stress, and Clinical Outcomes in Acute Ischemic Stroke Patients with and without Coronary Artery Disease.

作者信息

Kollar Branislav, Siarnik Pavel, Konarikova Katarina, Oravec Stanislav, Klobucka Stanislava, Klobucnikova Katarina, Poddany Michal, Radikova Zofia, Janubova Maria, Turcani Peter, Gajdosova Livia, Zitnanova Ingrid

机构信息

1st Department of Neurology, Faculty of Medicine, Comenius University, 813 69 Bratislava, Slovakia.

Institute of Medical Chemistry, Biochemistry and Clinical Biochemistry, Faculty of Medicine, Comenius University, 813 72 Bratislava, Slovakia.

出版信息

Biomedicines. 2024 Feb 1;12(2):332. doi: 10.3390/biomedicines12020332.

DOI:10.3390/biomedicines12020332
PMID:38397934
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10886910/
Abstract

We assessed lipid and lipoprotein profiles, along with oxidative stress (OS) parameters, in patients within the crucial 24 h period following an acute ischemic stroke (AIS), comparing those with and without coronary artery disease (CAD). We aimed to correlate these measures with clinical condition scales (NIHSS, mRS) post-AIS. This study included 27 AIS patients without CAD (AIS group) and 37 AIS patients with CAD (CAD-AIS group). Using polyacrylamide gel electrophoresis (Lipoprint system), we determined plasma LDL and HDL subfractions. Spectrophotometric methods were used to assess plasma antioxidant capacity, lipoperoxides, homocysteine (HC) levels, paraoxonase1, and catalase activities. We also measured urine isoprostanes and the activities of antioxidant enzymes (SOD, GPx) with commercial kits. CAD-AIS patients had notably higher HC levels, while there were no significant differences in lipoprotein subfractions and OS parameters between both groups. In the AIS group, mRS scores showed negative correlations with catalase, GPx activities, and total cholesterol. In the CAD-AIS group, atherogenic lipoproteins (IDLC, LDL2, LDL3-7) exhibited a significant positive correlation with mRS. This study underscores the role of dyslipidemia and OS in the development of AIS and CAD. It emphasizes the complex connections between specific biomarkers and post-stroke clinical outcomes. Our results suggest a significant impact of CAD treatment on lipid profile but not on homocysteine levels. The traditional narrative associating high cholesterol as the ultimate risk factor for cardiovascular diseases needs to be challenged, at least with respect to neurological outcomes. These insights may guide more targeted therapeutic approaches.

摘要

我们评估了急性缺血性卒中(AIS)后关键的24小时内患者的脂质和脂蛋白谱以及氧化应激(OS)参数,并比较了有无冠状动脉疾病(CAD)的患者。我们旨在将这些指标与AIS后的临床状况量表(NIHSS、mRS)相关联。本研究纳入了27例无CAD的AIS患者(AIS组)和37例有CAD的AIS患者(CAD-AIS组)。使用聚丙烯酰胺凝胶电泳(Lipoprint系统),我们测定了血浆低密度脂蛋白(LDL)和高密度脂蛋白(HDL)亚组分。采用分光光度法评估血浆抗氧化能力、脂过氧化物、同型半胱氨酸(HC)水平、对氧磷酶1和过氧化氢酶活性。我们还使用商业试剂盒测量了尿异前列腺素和抗氧化酶(超氧化物歧化酶、谷胱甘肽过氧化物酶)的活性。CAD-AIS患者的HC水平显著更高,而两组之间的脂蛋白亚组分和OS参数没有显著差异。在AIS组中,mRS评分与过氧化氢酶、谷胱甘肽过氧化物酶活性和总胆固醇呈负相关。在CAD-AIS组中,致动脉粥样硬化脂蛋白(中间密度脂蛋白、LDL2、LDL3-7)与mRS呈显著正相关。本研究强调了血脂异常和OS在AIS和CAD发生发展中的作用。它强调了特定生物标志物与卒中后临床结局之间的复杂联系。我们的结果表明CAD治疗对脂质谱有显著影响,但对同型半胱氨酸水平没有影响。将高胆固醇视为心血管疾病最终危险因素的传统观点需要受到挑战,至少在神经学结局方面是这样。这些见解可能会指导更有针对性的治疗方法。