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对接受氯吡格雷治疗的加勒比西班牙裔患者的心血管生物标志物——对氧磷酶 1:丰度和功能。

Paraoxonase-1 as a Cardiovascular Biomarker in Caribbean Hispanic Patients Treated with Clopidogrel: Abundance and Functionality.

机构信息

Department of Pharmacology and Toxicology, School of Medicine, University of Puerto Rico, Medical Sciences Campus, San Juan, PR 00936, USA.

Research Centers in Minority Institutions (RCMI) Program, Center for Collaborative Research in Health Disparities (CCRHD), University of Puerto Rico, Medical Sciences Campus, San Juan, PR 00936, USA.

出版信息

Int J Mol Sci. 2024 Oct 3;25(19):10657. doi: 10.3390/ijms251910657.

Abstract

Clopidogrel, a prescription drug to reduce ischemic events in cardiovascular patients, has been extensively studied in mostly European individuals but not among Caribbean Hispanics. This study evaluated the low abundance and reduced activity of paraoxonase-1 (PON1) in clopidogrel-resistant patients as a predictive risk biomarker of poor responders and disease severity in this population. Thirty-six patients on clopidogrel (cases divided into poor and normal responders) were enrolled, along with 11 cardiovascular patients with no clopidogrel indications (positive control) and 13 healthy volunteers (negative control). Residual on-treatment platelet reactivity unit (PRU), PON1 abundance by Western blotting, and PON1 activity by enzymatic assays were measured. genotyping and computational haplotype phasing were performed on 512 DNA specimens for two genetic loci (rs662 and rs854560). No statistical differences in mean relative PON1 abundance were found among the groups ( > 0.05). However, a significantly lower enzymatic activity was found in poor responders (10.57 ± 6.79 µU/mL) when compared to controls (22.66 ± 8.30 µU/mL and 22.21 ± 9.66 µU/mL; = 0.004). PON1 activity among carriers of the most prevalent haplotype (AA|AA) was significantly lower than in wild types (7.90 µU/mL vs. 22.03 µU/mL; = 0.005). Our findings suggested that PON1 is a potential biomarker of cardiovascular disease severity in Caribbean Hispanics.

摘要

氯吡格雷是一种用于降低心血管病患者缺血事件的处方药,已在大多数欧洲人群中进行了广泛研究,但在加勒比西班牙裔人群中尚未进行研究。本研究评估了氯吡格雷抵抗患者中对氧磷酶 1(PON1)的低丰度和活性降低,作为该人群中不良反应者和疾病严重程度的预测风险生物标志物。共纳入 36 名服用氯吡格雷的患者(病例分为不良反应者和正常反应者),11 名无氯吡格雷适应证的心血管病患者(阳性对照)和 13 名健康志愿者(阴性对照)。测量了治疗后残余血小板反应单位(PRU)、Western 印迹法测定的 PON1 丰度和酶法测定的 PON1 活性。对 512 份 DNA 标本进行了两个遗传位点(rs662 和 rs854560)的基因分型和计算单体型相位。各组间平均相对 PON1 丰度无统计学差异( > 0.05)。然而,与对照组(22.66 ± 8.30 µU/mL 和 22.21 ± 9.66 µU/mL; = 0.004)相比,不良反应者的酶活性显著降低(10.57 ± 6.79 µU/mL)。最常见的单体型(AA|AA)携带者的 PON1 活性明显低于野生型(7.90 µU/mL 比 22.03 µU/mL; = 0.005)。我们的研究结果表明,PON1 是加勒比西班牙裔人群心血管疾病严重程度的潜在生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b7d/11477108/618b21958c6d/ijms-25-10657-g001.jpg

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