[GDF-15 and the risk of bleeding in patients with stable CAD receiving multicomponent antithrombotic therapy: the results of the prospective REGATA register].

Pub Date : 2024-07-30 DOI:10.26442/00403660.2024.07.202783
E N Krivosheeva, A L Komarov, E P Panchenko, M B Khakimova, E S Kropacheva, O A Pogorelova, T V Balakhonova, E V Titaeva, A B Dobrovolsky, D M Galyautdinov, E E Vlasova
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引用次数: 0

Abstract

Aim: To evaluate the prognostic value of GDF-15 in relation the development of bleeding and events in stable CAD patients, receiving combined antithrombotic therapy.

Materials and methods: The data was obtained from the prospective registry REGATA, 343 CAD patients (249 males), median age 68 [IQR 62; 75] years) were enrolled. Patients with sinus rhythm and concomitant PAD received acetylsalicylic acid in combination with rivaroxaban 2.5 mg bid (31.8%) or clopidogrel (24.8%). Other 43.4% with concomitant atrial fibrillation (AF) received direct oral anticoagulants in combination with antiplatelet therapy after elective percutaneous coronary interventions. Median follow-up was 12 months [IQR 9.0; 18.0]. The safety end point was major and clinically relevant bleedings (type 2-5) according to the BARC classification. Plasma samples for GDF-15 identification were taken at the inclusion and analyzed using ELISA assay.

Results: Frequency of BARC 2-5 bleedings was 16% (BARC 2 - 46; BARC 3 - 9; BARC 4-5 - 0), median GDF-15 level was 1185.0 pg/ml [850.0; 1680.0]. In patients with AF and concomitant MFA, the level of GDF-15 was significantly higher than in the subgroups of patients with only AF or MFA (p=0.0022). According to the quintile analysis, GDF-15 values in the top three quintiles of distribution (cut-off value >943 pg/ml) were associated with higher frequency of bleeding events: 23.2% versus 5.1%; p=0.0001. The multivariable logistic regression model demonstrated that bleeding events were independently associated with GDF-15 level>943 pg/ml (OR 2.65, 95% CI 1.11-6.30; p=0.0275), AF (OR 2.61, 95% CI 1.41-4.83; p=0.0023) and chronic kidney disease (OR 1.92, 95% CI 1.03-3.60; p=0.0401). Clinical factors determining the risk of bleeding events also determined a GDF-15 elevation.

Conclusion: Assessment of GDF-15 level may improve bleeding risk stratification in CAD patients with concomitant AF and/or PAD receiving combined antithrombotic therapy.

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[GDF-15与接受多组分抗血栓治疗的稳定型CAD患者的出血风险:前瞻性REGATA登记结果]。
目的:评估GDF-15对接受联合抗栓治疗的稳定型CAD患者出血和血栓事件发生的预后价值:数据来自前瞻性登记处 REGATA,共登记了 343 例 CAD 患者(男性 249 例,中位年龄 68 [IQR 62; 75] 岁)。窦性心律和合并 PAD 的患者接受乙酰水杨酸联合利伐沙班 2.5 毫克 bid(31.8%)或氯吡格雷(24.8%)治疗。其他43.4%的合并心房颤动(房颤)患者在择期经皮冠状动脉介入治疗后接受直接口服抗凝药联合抗血小板治疗。中位随访时间为 12 个月 [IQR 9.0; 18.0]。安全性终点是根据 BARC 分类得出的重大临床相关出血(2-5 型)。在纳入患者时采集血浆样本进行 GDF-15 鉴定,并使用 ELISA 法进行分析:结果:BARC 2-5 型出血的发生率为 16%(BARC 2 - 46;BARC 3 - 9;BARC 4-5 - 0),GDF-15水平中位数为 1185.0 pg/ml [850.0; 1680.0]。在房颤并伴有 MFA 的患者中,GDF-15 水平明显高于仅有房颤或 MFA 的亚组患者(P=0.0022)。根据五分位数分析,GDF-15 值分布的前三个五分位数(临界值大于 943 pg/ml)与较高的出血事件频率相关:23.2%对5.1%;P=0.0001。多变量逻辑回归模型显示,出血事件与 GDF-15 水平>943 pg/ml(OR 2.65,95% CI 1.11-6.30;p=0.0275)、房颤(OR 2.61,95% CI 1.41-4.83;p=0.0023)和慢性肾病(OR 1.92,95% CI 1.03-3.60;p=0.0401)独立相关。决定出血事件风险的临床因素也决定了 GDF-15 的升高:结论:GDF-15水平的评估可改善合并房颤和/或PAD的CAD患者接受联合抗栓治疗时的出血风险分层。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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