Suppr超能文献

PARADIGM-HF 中普遍存在和新发的贫血及沙库巴曲缬沙坦的影响。

Prevalent and Incident Anemia in PARADIGM-HF and the Effect of Sacubitril/Valsartan.

机构信息

British Heart Foundation Cardiovascular Research Centre, University of Glasgow, Glasgow, United Kingdom.

Division of Cardiovascular Medicine, Brigham and Women's Hospital, Boston, Massachusetts, USA.

出版信息

JACC Heart Fail. 2023 Jul;11(7):749-759. doi: 10.1016/j.jchf.2022.12.012. Epub 2023 Apr 12.

Abstract

BACKGROUND

Anemia is common in patients with heart failure with reduced ejection fraction and is associated with poor clinical outcomes. Renin-angiotensin system blockers lower hemoglobin and may induce anemia.

OBJECTIVES

The authors investigated whether concomitant neprilysin inhibition might ameliorate this effect of renin-angiotensin system blockers in PARADIGM-HF (Prospective comparison of ARNI with ACEI to Determine Impact on Global Mortality and morbidity in Heart Failure).

METHODS

Anemia was defined as hemoglobin <120 g/L in women and <130 g/L in men at screening. The authors investigated the effect of randomized treatment on clinical outcomes according to anemia status, change in hemoglobin from baseline, and the incidence of anemia.

RESULTS

Of 8,239 participants with a baseline hemoglobin measurement, 1,677 (20.4%) were anemic. Patients with anemia had a more severe heart failure profile, worse kidney function, greater neurohormonal derangement, and worse clinical outcomes. Sacubitril/valsartan, compared with enalapril, decreased the risk of cardiovascular death or heart failure hospitalization similarly in patients with (HR: 0.84; 95% CI: 0.71-1.00) and without anemia (HR: 0.78 [95% CI: 0.71-0.87]; P value for interaction = 0.478). Between baseline and 12 months, hemoglobin decreased by 1.5 g/L (95% CI: 1.2-1.7 g/L) with sacubitril/valsartan compared with 2.3 g/L (95% CI: 2.0-2.6 g/L) with enalapril: mean difference 0.8 g/L (95% CI: 0.5-1.2 g/L; P < 0.001). Patients assigned to sacubitril/valsartan were less likely to develop anemia at 12 months (321 of 2,806 [11.4%]) compared with patients randomized to enalapril (440 of 2,824 [15.6%]) (OR: 0.70 [95% CI: 0.60-0.81]; P < 0.001). These findings were similar in PARAGON-HF (Prospective Comparison of ARNI with ARB Global Outcomes in HF with Preserved Ejection Fraction) (sacubitril/valsartan vs valsartan). There was biomarker evidence of increased iron utilization with sacubitril/valsartan.

CONCLUSIONS

Irrespective of anemia status, sacubitril/valsartan compared with enalapril, decreased mortality and hospitalization. Hemoglobin decreased less with sacubitril/valsartan and the incidence of new anemia was lower with sacubitril/valsartan. (Prospective comparison of ARNI with ACEI to Determine Impact on Global Mortality and morbidity in Heart Failure [PARADIGM-HF] trial; NCT01035255).

摘要

背景

贫血在射血分数降低的心力衰竭患者中很常见,与不良临床结局相关。肾素-血管紧张素系统阻滞剂可降低血红蛋白并可能导致贫血。

目的

作者研究了同时抑制脑啡肽酶是否可以改善肾素-血管紧张素系统阻滞剂在 PARADIGM-HF(血管紧张素受体脑啡肽酶抑制剂与血管紧张素转换酶抑制剂对射血分数降低心力衰竭患者全球死亡率和发病率的前瞻性比较)中的这种作用。

方法

贫血定义为女性血红蛋白<120 g/L 和男性血红蛋白<130 g/L 时的筛查。作者根据贫血状态、基线时血红蛋白的变化以及贫血的发生率,研究了随机治疗对临床结局的影响。

结果

在 8239 名有基线血红蛋白测量值的参与者中,1677 名(20.4%)患有贫血。贫血患者的心衰严重程度更高,肾功能更差,神经激素失调更严重,临床结局更差。与依那普利相比,沙库巴曲缬沙坦同样降低了有(HR:0.84;95%CI:0.71-1.00)和无贫血(HR:0.78 [95%CI:0.71-0.87])患者的心血管死亡或心力衰竭住院风险(交互 P 值=0.478)。与基线相比,沙库巴曲缬沙坦在 12 个月时使血红蛋白降低 1.5 g/L(95%CI:1.2-1.7 g/L),而依那普利使血红蛋白降低 2.3 g/L(95%CI:2.0-2.6 g/L):平均差异为 0.8 g/L(95%CI:0.5-1.2 g/L;P<0.001)。与依那普利相比,12 个月时沙库巴曲缬沙坦治疗组发生贫血的患者更少(2806 例中有 321 例[11.4%]),而依那普利组为 440 例(2824 例中有 15.6%)(OR:0.70 [95%CI:0.60-0.81];P<0.001)。PARAGON-HF(血管紧张素受体脑啡肽酶抑制剂与血管紧张素受体拮抗剂在射血分数保留的心力衰竭中的全球结局前瞻性比较)的研究结果相似(沙库巴曲缬沙坦 vs 缬沙坦)。沙库巴曲缬沙坦治疗有增加铁利用的生物标志物证据。

结论

与依那普利相比,沙库巴曲缬沙坦不论贫血状态如何,均可降低死亡率和住院率。与依那普利相比,沙库巴曲缬沙坦可使血红蛋白降低幅度较小,新发生贫血的发生率较低。(血管紧张素受体脑啡肽酶抑制剂与血管紧张素转换酶抑制剂对射血分数降低心力衰竭患者全球死亡率和发病率的前瞻性比较[PARADIGM-HF]试验;NCT01035255)。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验