Acute Kidney Injury and Heart Failure Risk with Hypoxia-Inducible Factor-Prolyl Hydroxylase Inhibitors: A Network Meta-Analysis.

IF 4.9 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Satoru Mitsuboshi, Makoto Morizumi, Shungo Imai, Satoko Hori, Kazumasa Kotake
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Abstract

The aim of this systematic review and network meta-analysis was to clarify the risk of acute kidney injury (AKI) and acute heart failure associated with hypoxia-inducible factor-prolyl hydroxylase inhibitors (HIF-PHIs) in patients with anemia of chronic kidney disease. The certainty of evidence for each outcome was assessed using the Confidence in Network Meta-Analysis approach. The primary outcomes were AKI and acute heart failure, while the secondary outcome was any kidney injury. Thirty-five studies, performed between 2009 and 2025, were included in the network meta-analysis. HIF-PHIs were associated with a higher risk of AKI compared with erythropoiesis-stimulating agents (ESAs) (risk ratio [RR] 1.23, 95% confidence interval [CI] 1.02-1.47, moderate certainty) and placebo (RR 1.40, 95% CI 1.11-1.75, high certainty). HIF-PHIs were also associated with an increased risk of any kidney injury compared with placebo (RR 1.13, 95% CI 1.01-1.26, moderate certainty). ESAs ranked lower in terms of acute heart failure risk than both HIF-PHIs and placebo, although the differences were not statistically significant. Vadadustat (RR 0.30, 95% CI 0.12-0.74, moderate certainty) and ESAs (RR 0.40, 95% CI 0.17-0.94, high certainty) were associated with a lower risk of acute heart failure compared with placebo. In conclusion, HIF-PHIs may be associated with an increased incidence of AKI compared with placebo and ESAs. In contrast, vadadustat and ESAs might be associated with a decreased incidence of acute heart failure compared with placebo. Further robust studies should be conducted to validate these findings.

缺氧诱导因子-丙氨酸羟化酶抑制剂的急性肾损伤和心力衰竭风险:网络荟萃分析。
本系统综述和网络荟萃分析的目的是阐明慢性肾病贫血患者与缺氧诱导因子-脯氨酰羟化酶抑制剂(HIF-PHIs)相关的急性肾损伤(AKI)和急性心力衰竭的风险。每个结果的证据的确定性使用网络置信度meta分析方法进行评估。主要结局是AKI和急性心力衰竭,而次要结局是任何肾损伤。2009年至2025年间进行的35项研究被纳入网络荟萃分析。与促红细胞生成素(ESAs)(风险比[RR] 1.23, 95%可信区间[CI] 1.02-1.47,中等确定性)和安慰剂(RR 1.40, 95% CI 1.11-1.75,高确定性)相比,HIF-PHIs与AKI的风险更高。与安慰剂相比,HIF-PHIs还与任何肾损伤的风险增加相关(RR 1.13, 95% CI 1.01-1.26,中等确定性)。esa在急性心力衰竭风险方面的排名低于HIF-PHIs和安慰剂,尽管差异没有统计学意义。与安慰剂相比,Vadadustat (RR 0.30, 95% CI 0.12-0.74,中等确定性)和ESAs (RR 0.40, 95% CI 0.17-0.94,高确定性)与较低的急性心力衰竭风险相关。总之,与安慰剂和esa相比,HIF-PHIs可能与AKI发生率增加有关。相反,与安慰剂相比,vadadustat和esa可能与急性心力衰竭发生率降低有关。应该进行进一步的有力研究来验证这些发现。
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来源期刊
CiteScore
12.70
自引率
7.50%
发文量
290
审稿时长
2 months
期刊介绍: Clinical Pharmacology & Therapeutics (CPT) is the authoritative cross-disciplinary journal in experimental and clinical medicine devoted to publishing advances in the nature, action, efficacy, and evaluation of therapeutics. CPT welcomes original Articles in the emerging areas of translational, predictive and personalized medicine; new therapeutic modalities including gene and cell therapies; pharmacogenomics, proteomics and metabolomics; bioinformation and applied systems biology complementing areas of pharmacokinetics and pharmacodynamics, human investigation and clinical trials, pharmacovigilence, pharmacoepidemiology, pharmacometrics, and population pharmacology.
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