药物干预对亚洲和白人患者射血分数降低心衰的比较疗效:一项随机对照试验的meta分析。

IF 3 4区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS
Wenxi Huang, Huilin Tang, Yujia Li, Wei-Han Chen, Shao-Hsuan Chang, Jiang Bian, Mustafa M Ahmed, Stephen E Kimmel, Jingchuan Guo
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引用次数: 0

摘要

心衰(HF)在美国和世界范围内造成了重大的公共卫生负担,与其他种族和族裔群体相比,亚洲人群的发病率更高,年龄更小。目的:本研究旨在评价不同HF药物干预对亚洲和白人HF伴射血分数降低(HFrEF)患者的治疗效果。方法:我们对成人HFrEF患者的随机对照试验(rct)进行了两两荟萃分析。我们检索了Embase、PubMed和Cochrane Central Register of Controlled Trials数据库,检索时间从创立到2022年2月9日。我们确定了调查HF药物疗效的随机对照试验,包括血管紧张素转换酶抑制剂、血管紧张素受体-neprilysin抑制剂(sacubitril/缬沙坦)、β受体阻滞剂、超极化激活的环核苷酸门控通道阻滞剂、钠-葡萄糖共转运蛋白2 (SGLT2)抑制剂、肾素抑制剂、加压素V2受体阻滞剂和口服可溶性鸟苷酸环化酶刺激剂。主要终点是HF住院、心血管死亡和全因死亡率的复合终点。结果:我们纳入了11项随机对照试验,涉及32,654名来自亚洲和白人人群的参与者。在亚洲患者中,SGLT2抑制剂(风险比[RR] 0.61;95%可信区间[CI] 0.49-0.75)在降低HF住院综合终点方面最有效,其次是超极化激活的环核苷酸门控通道阻滞剂(RR 0.62;95% ci 0.42-0.89)。在白人患者中,受体阻滞剂(RR 0.68;95% CI 0.59-0.78)在降低不良结局风险方面最有效,其次是SGLT2抑制剂(RR 0.72;95% ci 0.53-0.97)。总体而言,在所有HFrEF患者中,SGLT2抑制剂是降低不良结局风险的最有效治疗方法(RR 0.72;95% CI 0.53-0.97),亚洲患者的治疗效果优于白人患者(P_interaction = 0.014)。结论:本研究的结果表明,SGLT2抑制剂治疗在降低亚洲和白人HFrEF患者不良临床结局的风险方面都是有效的,在亚洲人群中效果更明显。这些结果强调了在心衰管理中考虑种族和民族差异的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparative Efficacy of Pharmacological Interventions for Heart Failure with Reduced Ejection Fraction Between Asian and White Patients: A Meta-analysis of Randomized Controlled Trials.

Introduction: Heart failure (HF) poses a significant public health burden in the USA and worldwide, with a higher incidence and disproportionate presentation at a younger age in Asian populations than in other racial and ethnic groups.

Objective: This study aimed to evaluate the treatment efficacy of different HF pharmacological interventions in Asian versus white patients with HF with reduced ejection fraction (HFrEF).

Methods: We conducted a pairwise meta-analysis of randomized controlled trials (RCTs) in adults with HFrEF. We searched the Embase, PubMed, and Cochrane Central Register of Controlled Trials databases from inception to February 9, 2022. We identified RCTs investigating the efficacy of HF drugs, including angiotensin-converting enzyme inhibitors, an angiotensin receptor-neprilysin inhibitor (sacubitril/valsartan), beta-blockers, hyperpolarization-activated cyclic nucleotide-gated channel blockers, sodium-glucose cotransporter 2 (SGLT2) inhibitors, renin inhibitors, vasopressin V2 receptor blockers, and oral soluble guanylate cyclase stimulators. The primary outcome was a composite endpoint of hospitalization of HF, cardiovascular death, and all-cause mortality.

Results: We included 11 RCTs involving 32,654 participants from Asian and white populations. In Asian patients, SGLT2 inhibitors (risk ratio [RR] 0.61; 95% confidence interval [CI] 0.49-0.75) were the most effective in reducing the composite endpoint of hospitalization of HF, followed by hyperpolarization-activated cyclic nucleotide-gated channel blockers (RR 0.62; 95% CI 0.42-0.89). In white patients, beta-blockers (RR 0.68; 95% CI 0.59-0.78) were the most effective in lowering the risk of adverse outcomes, followed by SGLT2 inhibitors (RR 0.72; 95% CI 0.53-0.97). Overall, SGLT2 inhibitors were the most effective treatment in reducing the risk of adverse outcomes among all patients with HFrEF (RR 0.72; 95% CI 0.53-0.97), with a better treatment effect in Asian patients than in their white counterparts (P_interaction = 0.014).

Conclusions: The findings from this study suggest that treatment with SGLT2 inhibitors is effective in lowering the risk of adverse clinical outcomes in patients with HFrEF for both Asian and white populations, with a more pronounced effect in Asian populations. These results highlight the importance of considering racial and ethnic differences in the management of HF.

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来源期刊
CiteScore
6.70
自引率
3.30%
发文量
38
审稿时长
>12 weeks
期刊介绍: Promoting rational therapy within the discipline of cardiology, the American Journal of Cardiovascular Drugs covers all aspects of the treatment of cardiovascular disorders, particularly the place in therapy of newer and established agents. Via a program of reviews and original clinical research articles, the journal addresses major issues relating to treatment of these disorders, including the pharmacology, efficacy and adverse effects of the major classes of drugs; information on newly developed drugs and drug classes; the therapeutic implications of latest research into the aetiology of cardiovascular disorders; and the practical management of specific clinical situations. The American Journal of Cardiovascular Drugs offers a range of additional enhanced features designed to increase the visibility, readership and educational value of the journal’s content. Each article is accompanied by a Key Points summary, giving a time-efficient overview of the content to a wide readership. Articles may be accompanied by plain language summaries to assist patients, caregivers and others in understanding important medical advances. The journal also provides the option to include various other types of enhanced features including slide sets, videos and animations. All enhanced features are peer reviewed to the same high standard as the article itself. Peer review is conducted using Editorial Manager®, supported by a database of international experts. This database is shared with other Adis journals.
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