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缺氧诱导因子脯氨酰羟化酶抑制剂在伴有肾性贫血的心力衰竭患者中的作用。

Impact of HIF prolyl hydroxylase inhibitors in heart failure patients with renal anemia.

机构信息

Department of Cardiovascular Medicine, Tosei General Hospital, Seto, Japan.

Department of Advanced Cardiovascular Therapeutics, Nagoya University Graduate School of Medicine, 65 Tsurumai, Showa, Nagoya, 466-8550, Japan.

出版信息

BMC Res Notes. 2024 Mar 1;17(1):60. doi: 10.1186/s13104-024-06726-7.

Abstract

OBJECTIVE

Hypoxia-inducible factor prolyl hydroxylase (HIF-PH) inhibitors are a new class of anti-anemia agents. We retrospectively evaluated the safety and efficacy of HIF-PH inhibitors in patients with heart failure (HF) complicated by anemia associated with chronic kidney disase. HIF-PH inhibitor treatment was initiated in 32 patients with chronic HF complicated by renal anemia and were followed up for 3 months.

RESULTS

Hematocrit and hemoglobin levels markedly improved 3 months after HIF-PH inhibitor treatment. However, levels of NT-proBNP, which is an indicator of HF, did not decrease considerably. Based on the rate of change in NT-proBNP, we divided the patients into "responder" and "non-responder" groups. The results showed that considerably more patients had a ferritin level of less than 100 ng/mL in the non-responder group at baseline. There were substantially more patients with TSAT of less than 20% in the non-responder group at 1 month after HIF-PH inhibitor treatment. The cut-off values to maximize the predictive power of ferritin level at baseline and TSAT value at 1 month after treatment were 41.8 ng/ml and 20.75. HIF-PH inhibitor treatment can be expected to be effective for improving both anemia and HF if ferritin≥41.8 ng/ml at baseline or TSAT≥20.75 at 1 month after treatment.

摘要

目的

缺氧诱导因子脯氨酰羟化酶(HIF-PH)抑制剂是一类新型的抗贫血药物。我们回顾性评估了 HIF-PH 抑制剂在伴有慢性肾脏病贫血的心力衰竭(HF)患者中的安全性和疗效。在 32 例伴有慢性 HF 和肾性贫血的患者中开始使用 HIF-PH 抑制剂治疗,并随访 3 个月。

结果

HIF-PH 抑制剂治疗 3 个月后,红细胞比容和血红蛋白水平显著改善。然而,HF 的指标 NT-proBNP 水平并没有明显降低。根据 NT-proBNP 的变化率,我们将患者分为“应答者”和“非应答者”两组。结果显示,基线时非应答组的铁蛋白水平<100ng/ml 的患者明显更多。在 HIF-PH 抑制剂治疗 1 个月后,非应答组的转铁蛋白饱和度(TSAT)<20%的患者明显更多。铁蛋白水平在基线时和治疗后 1 个月时的截断值分别为 41.8ng/ml 和 20.75,以最大限度地提高预测效力。如果基线时铁蛋白≥41.8ng/ml 或治疗后 1 个月时 TSAT≥20.75,则 HIF-PH 抑制剂治疗有望有效改善贫血和 HF。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/37c1/10905796/64cd6052abd7/13104_2024_6726_Fig1_HTML.jpg

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