替卡格雷与氯吡格雷对高尿酸血症急性冠状动脉综合征患者全因死亡率和心血管死亡率的影响

IF 2.9 3区 医学 Q2 PHARMACOLOGY & PHARMACY Clinical Drug Investigation Pub Date : 2024-03-01 Epub Date: 2024-02-07 DOI:10.1007/s40261-024-01342-6
Shanshan Nie, Yuhang Zhao, Zeying Feng, Chan Zou, Fangfang Ding, Liying Gong, Hongwei Lu, Yu Cao, Guoping Yang
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引用次数: 0

摘要

背景和目的:高尿酸血症与急性冠状动脉综合征(ACS)患者死亡率之间的关系存在很大争议。此外,双重抗血小板疗法(DAPT)的策略尚未在伴有高尿酸血症的 ACS 患者中进行评估。本研究旨在评估高尿酸血症对 ACS 预后的影响,并探讨与氯吡格雷相比,替卡格雷对高尿酸血症患者的疗效:研究共纳入4319例患者,分为高尿酸血症组(HUA,n = 1060)和正常尿酸血症组(NUA,n = 3259)。采用逆概率治疗加权(IPTW)调整后的Cox回归分析评估了替卡格雷与氯吡格雷对全因死亡率和心血管死亡率的影响:与NUA患者相比,高尿酸血症明显增加了7天[调整后危险比(HR):4.292,95%置信区间(CI)1.727-10.67];P = 0.002]、14天(调整后HR:2.871,95% CI 1.326-6.219;P = 0.0074)、30 天(调整后 HR:2.168,95% CI 1.056-4.453;P = 0.035)、3 个月(调整后 HR:2.018,95% CI 1.152-3.533;P = 0.0144)和 1 年(调整后 HR:1.702,95% CI 1.137-2.548;P = 0.009)。在同时患有高尿酸血症的患者中,替卡格雷和氯吡格雷在1年全因死亡率方面无明显差异[7.0%对5.5%,调整HR:1.114(95% CI 0.609-2.037),P = 0.725]:结论:高尿酸血症与接受PCI治疗的ACS患者全因死亡和心血管死亡风险增加密切相关。随访1年后,在高尿酸血症患者的全因死亡和心血管死亡方面,替卡格雷和氯吡格雷之间没有显著差异。
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Effect of Ticagrelor versus Clopidogrel on All-Cause and Cardiovascular Mortality in Acute Coronary Syndrome Patients with Hyperuricemia.

Background and objective: The relationship between hyperuricemia and mortality in patients with acute coronary syndrome (ACS) is considerably controversial. Additionally, the strategy of dual antiplatelet therapy (DAPT) has not been evaluated in patients with ACS with hyperuricemia. This study aims to evaluate the impact of hyperuricemia on the prognosis of ACS and explore the efficacy of ticagrelor compared with clopidogrel in patients with hyperuricemia.

Methods: The study enrolled 4319 patients divided into hyperuricemia (HUA, n = 1060) and normouricemia (NUA, n = 3259) groups. The inverse probability of treatment weighting (IPTW)-adjusted Cox regression analysis was used to evaluate the impact of ticagrelor versus clopidogrel on all-cause and cardiovascular mortality.

Results: Hyperuricemia significantly increased the risk of all-cause death compared with patients with NUA at 7 days [adjusted hazard ratio (HR): 4.292, 95% confidence interval (CI) 1.727-10.67]; P = 0.002), 14 days (adjusted HR: 2.871, 95% CI 1.326-6.219; P = 0.0074), 30 days (adjusted HR: 2.168, 95% CI 1.056-4.453; P = 0.035), 3 months (adjusted HR: 2.018, 95% CI 1.152-3.533; P = 0.0144) and 1 year (adjusted HR: 1.702, 95% CI 1.137-2.548; P = 0.009). No significant difference was found between ticagrelor and clopidogrel in 1-year all-cause mortality [7.0% versus 5.5%, adjusted HR: 1.114 (95% CI 0.609-2.037), P = 0.725] among patients with concomitant hyperuricemia.

Conclusion: Hyperuricemia was independently related to an increased risk of all-cause and cardiovascular death in patients with ACS undergoing PCI. At 1-year follow-up, there were no significant differences between ticagrelor and clopidogrel concerning all-cause and cardiovascular death in patients with hyperuricemia.

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来源期刊
CiteScore
5.90
自引率
3.10%
发文量
108
审稿时长
6-12 weeks
期刊介绍: Clinical Drug Investigation provides rapid publication of original research covering all phases of clinical drug development and therapeutic use of drugs. The Journal includes: -Clinical trials, outcomes research, clinical pharmacoeconomic studies and pharmacoepidemiology studies with a strong link to optimum prescribing practice for a drug or group of drugs. -Clinical pharmacodynamic and clinical pharmacokinetic studies with a strong link to clinical practice. -Pharmacodynamic and pharmacokinetic studies in healthy volunteers in which significant implications for clinical prescribing are discussed. -Studies focusing on the application of drug delivery technology in healthcare. -Short communications and case study reports that meet the above criteria will also be considered. Additional digital features (including animated abstracts, video abstracts, slide decks, audio slides, instructional videos, infographics, podcasts and animations) can be published with articles; these are designed to increase the visibility, readership and educational value of the journal’s content. In addition, articles published in Clinical Drug Investigation may be accompanied by plain language summaries to assist readers who have some knowledge, but non in-depth expertise in, the area to understand important medical advances.
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