Effect of vitamin D on antiplatelet drug responsiveness in elderly patients with ischemic stroke

Liang Chen, Jing Zhang, Xiao-Jie Shi, Zhizhong Liu, Yanyan Sun
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Abstract

Objective To investigate the effect of vitamin D on platelet reactivity after combined treatment with aspirin and clopidogrel in elderly patients with ischemic stroke. Methods A total of 190 elderly patients with ischemic stroke treated with aspirin and clopidogrel in Beijing Bo′ai Hospital from June 2017 to August 2018 were enrolled in this study.Venous blood was collected for platelet aggregation rate, 25-hydroxyvitamin D[25(OH)D] and clinical biochemical indexes during 1~2 weeks.According to 25 (OH) D quartile, the patients were further divided into Q1(≤7.18 μg/L) group (n=50), Q2: (>7.18-≤9.39 μg/L) group (n=50), Q3: (>9.39-≤13.74 μg/L) group (50), Q4: (>13.74 μg/L) (n=40). In order to evaluate the effect of calcitriol on platelet aggregation, platelet rich plasma (PRP) in healthy group (15 cases) and clopidogrel resistance group (15 cases) were treated with calcitriol (10 nmol/L) and saline (37 ℃ pretreatment for 5 minutes), respectively, and to compare the difference of maximum platelet aggregation rate induced by ADP between the two treatments. Results There were significant differences in ADP-induced maximum platelet aggregation rate (MPAR) ((49.36±23.34)%, (48.80±20.90)%, (37.02±18.24)%, (36.02±14.46)%, F=3.426, P=0.018) and clopidogrel resistance (CR)/ clopidogrel sensitive (CS) ratio (30/20, 24/26, 15/35, 10/30, χ2=15.119, P=0.002) among the vitamin D quartiles (increasing). Moreover, the MPAR and CR showed a decreasing trend with the increase of vitamin D concentration.Logistic regression analysis showed that serum 25(OH)D level was an independent inhibited factor for clopidogrel resistance in elderly patients with ischemic stroke (Q4 vs Q1, OR=0.699, 95%CI 0.582~0.838, P<0.001; Q3 vs Q1, OR=0.848, 95%CI 0.755-0.953, P=0.006). In vitro, compared with physiological saline, the aggregation rates of platelet in healthy group and CR group decreased after calcitriol pretreatment, and the difference was statistically significant(healthy group: (69.8±12.7)% vs (58.6±11.5)%, t=12.13, P<0.001; CR group: (65.5±8.3)% vs (56.3±7.6)%, t=11.48, P<0.001). Conclusion Vitamin D reduces the high residual platelet reactivity after antiplatelet therapy.Further study is needed to determine whether vitamin D supplementation may improve the efficacy of clopidogrel. Key words: Ischemic stroke; Antiplatelet therapy; Vitamin D; Drug resistance
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维生素D对老年缺血性脑卒中患者抗血小板药物反应性的影响
目的探讨维生素D对老年缺血性脑卒中患者阿司匹林与氯吡格雷联合治疗后血小板反应性的影响。方法选取2017年6月至2018年8月在北京博爱医院接受阿司匹林和氯吡格雷联合治疗的老年缺血性脑卒中患者190例。1~2周采集静脉血检测血小板聚集率、25-羟基维生素D[25(OH)D]及临床生化指标。根据25 (OH) D四分位数进一步分为Q1(≤7.18 μg/L)组(n=50)、Q2(>7.18-≤9.39 μg/L)组(n=50)、Q3(>9.39-≤13.74 μg/L)组(50)、Q4 (>13.74 μg/L)组(n=40)。为评价骨化三醇对血小板聚集的影响,将健康组(15例)和氯吡格雷耐药组(15例)的富血小板血浆(PRP)分别给予骨化三醇(10 nmol/L)和生理盐水(37℃预处理5分钟)处理,比较两种处理对ADP诱导血小板最大聚集率的差异。结果adp诱导的血小板最大聚集率(MPAR)分别为(49.36±23.34)%、(48.80±20.90)%、(37.02±18.24)%、(36.02±14.46)%,F=3.426, P=0.018)和氯吡格雷耐药/氯吡格雷敏感比(30/ 20,24 / 26,15 / 35,10 /30,χ2=15.119, P=0.002)在维生素D四分位数间差异有统计学意义(增高)。随着维生素D浓度的增加,MPAR和CR呈下降趋势。Logistic回归分析显示,血清25(OH)D水平是老年缺血性卒中患者氯吡格雷耐药的独立抑制因素(Q4 vs Q1, OR=0.699, 95%CI 0.582~0.838, P<0.001;Q3 vs Q1, OR=0.848, 95%CI 0.755-0.953, P=0.006)。在体外,与生理盐水相比,骨化三醇预处理后健康组和CR组血小板聚集率降低,差异有统计学意义(健康组:(69.8±12.7)% vs(58.6±11.5)%,t=12.13, P<0.001;CR组:(65.5±8.3)% vs(56.3±7.6)%,t = 11.48, P < 0.001)。结论维生素D可降低抗血小板治疗后残余血小板高反应性。补充维生素D是否可以提高氯吡格雷的疗效还需要进一步的研究。关键词:缺血性脑卒中;抗血小板治疗;维生素D;耐药性
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来源期刊
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期刊介绍: Clinical Medicine of China is an academic journal organized by the Chinese Medical Association (CMA), which mainly publishes original research papers, reviews and commentaries in the field. Clinical Medicine of China is a source journal of Peking University (2000 and 2004 editions), a core journal of Chinese science and technology, an academic journal of RCCSE China Core (Extended Edition), and has been published in Chemical Abstracts of the United States (CA), Abstracts Journal of Russia (AJ), Chinese Core Journals (Selection) Database, Chinese Science and Technology Materials Directory, Wanfang Database, China Academic Journal Database, JST Japan Science and Technology Agency Database (Japanese) (2018) and other databases.
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