使用微神经电图评估 SGLT2 抑制剂对无尿血液透析患者的交感神经溶解作用:机制概念验证试验研究方案》。

IF 2.3 4区 医学 Q2 PERIPHERAL VASCULAR DISEASE Kidney & blood pressure research Pub Date : 2024-01-01 Epub Date: 2024-09-28 DOI:10.1159/000541568
Aaron Yee Shuen See, Evgenija Blazeska, Awf Abdulrahman Shaban, Mark Thomas, Sayeh Heidari Nejad, Antonella Soarez Dornelles, Anu Joyson, Sally Burrows, Markus Schlaich, Srivathsan Thiruvengadam
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引用次数: 0

摘要

简介:葡萄糖钠共转运体 2 抑制剂(SGLT2i)已被证明能有效保护心肾功能,降低心力衰竭(HF)和慢性肾病(CKD)等疾病的死亡率。虽然已经确定了几种机制,但最近的研究揭示了这种药物能够减弱交感神经系统(SNS)的活动。然而,对于这究竟是由于药物的肾外效应,还是仅仅由于其肾保护作用,还存在争议。不过,最近的试验强调,尽管肾功能下降,SGLT2i 仍能持续发挥疗效。因此,研究 SGLT2i 独立于肾脏而减弱 SNS 的能力可能会使人们对其作用机制有更深入的了解。迄今为止,关于 SGLT2i 对透析患者肾脏外影响的研究还很有限,因为 SGLT2i 对肾脏的糖尿作用可以忽略不计。因此,本研究旨在调查 SGLT2i 对无尿血液透析患者 SNS 的影响:我们制定了一项机理研究方案,以调查 SGLT2i 对 SNS 的肾外影响。该研究将是一项由研究者主导的开放标签前瞻性研究,涉及 20 名残余尿量(RUO)≤250 毫升/天的成年(年龄≥18 岁)血液透析患者。参与者将每天服用 25 毫克的恩格列净,持续 6 周。用药前后将通过微神经电图测量基线SNS活性,以评估中枢SNS流出量。此外,还将检测 SNS 应激反应、心率变异性和内皮功能等次要结果与基线相比的变化。我们假设,使用恩格列净将导致无尿血液透析患者的交感神经驱动减少:这将是首个评估 SGLT2i 对血液透析患者交感神经系统影响的研究。这项研究旨在加深我们对 SGLT2i 引起的交感神经系统减弱在肾功能明显减退情况下的潜在作用的了解。该研究已获得珀斯皇家医院人类研究伦理委员会(Royal Perth Hospital Human Research Ethics Committee)的伦理批准。澳大利亚新西兰临床试验注册中心 (ANZCTR) ID:ACTRN12623001237673。
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Assessing the Sympatholytic Effects of SGLT2 Inhibitors in Anuric Haemodialysis Patients Using Microneurography: Study Protocol for a Mechanistic Proof-of-Concept Trial.

Introduction: Sodium-glucose co-transporter 2 inhibitors (SGLT2is) have been shown to provide effective cardiorenal protection, reducing mortality in conditions such as heart failure and chronic kidney disease. While several mechanisms have been identified, recent research has shed light on the drug's ability to attenuate sympathetic nervous system (SNS) activity. Controversy exists on whether this is due to the extra-renal effects of the drug, or simply due to its renoprotective effects. However, recent trials have highlighted the persistent efficacy of SGLT2i despite declining renal function. Therefore, investigating the ability of SGLT2i to attenuate the SNS independently of the kidney could lead to more insight into its mechanism of action. So far, there has been limited research done on investigating the extra-renal effects of SGLT2i in human subjects on dialysis where the glycosuric renal effects of SGLT2i are negligible. This current study therefore aims to investigate the effects of SGLT2i on the SNS in anuric haemodialysis patients.

Methods: We developed a protocol for a mechanistic study to investigate the extra-renal effects of SGLT2i on the SNS. The study will be an investigator-led, open-label, prospective study involving 20 adult (aged ≥18 years) haemodialysis patients with a residual urine output of ≤250 mL/day. Participants will be administered empagliflozin 25 mg/day for 6 weeks. Baseline SNS activity will be measured before and after administration by microneurography to assess central SNS outflow. Secondary outcomes such as changes from baseline in SNS stressor response, heart rate variability, and endothelial function will also be examined. We hypothesize that the use of empagliflozin will result in reduced sympathetic drive in anuric haemodialysis patients.

Discussion: This will be the first study evaluating the effects of SGLT2i on the SNS in haemodialysis subjects. This study aims to enhance our understanding of the potential role of SGLT2i-induced SNS reduction in the setting of markedly reduced renal function. The study has received ethics approval from the Royal Perth Hospital Human Research Ethics Committee (RGS0000003840) (Australian New Zealand Clinical Trials Registry [ANZCTR] ID: ACTRN12623001237673).

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来源期刊
Kidney & blood pressure research
Kidney & blood pressure research 医学-泌尿学与肾脏学
CiteScore
4.80
自引率
3.60%
发文量
61
审稿时长
6-12 weeks
期刊介绍: This journal comprises both clinical and basic studies at the interface of nephrology, hypertension and cardiovascular research. The topics to be covered include the structural organization and biochemistry of the normal and diseased kidney, the molecular biology of transporters, the physiology and pathophysiology of glomerular filtration and tubular transport, endothelial and vascular smooth muscle cell function and blood pressure control, as well as water, electrolyte and mineral metabolism. Also discussed are the (patho)physiology and (patho) biochemistry of renal hormones, the molecular biology, genetics and clinical course of renal disease and hypertension, the renal elimination, action and clinical use of drugs, as well as dialysis and transplantation. Featuring peer-reviewed original papers, editorials translating basic science into patient-oriented research and disease, in depth reviews, and regular special topic sections, ''Kidney & Blood Pressure Research'' is an important source of information for researchers in nephrology and cardiovascular medicine.
期刊最新文献
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