From the Division of Nephrology and Hypertension (A.S., S.M.S.H., A.E., C.M.F., L.O.L., S.C.T.) and Department of Radiology (J.F.G., H.B., M.A.M., S.M.), Mayo Clinic, Rochester, MN.
Circ Cardiovasc Interv. 2017 Sep;10(9). doi: 10.1161/CIRCINTERVENTIONS.117.005487.
Atherosclerotic renal artery stenosis reduces renal blood flow (RBF) and amplifies stenotic kidney hypoxia. Revascularization with percutaneous transluminal renal angioplasty (PTRA) and stenting often fails to recover renal function, possibly because of ischemia/reperfusion injury developing after PTRA. Elamipretide is a mitochondrial-targeted peptide that binds to cardiolipin and stabilizes mitochondrial function. We tested the hypothesis that elamipretide plus PTRA would improve renal function, oxygenation, and RBF in patients with atherosclerotic renal artery stenosis undergoing PTRA.
Inpatient studies were performed in patients with severe atherosclerotic renal artery stenosis scheduled for PTRA. Patients were treated before and during PTRA with elamipretide (0.05 mg/kg per hour intravenous infusion, n=6) or placebo (n=8). Stenotic kidney cortical/medullary perfusion and RBF were measured using contrast-enhanced multidetector CT, and renal oxygenation by 3-T blood oxygen level-dependent magnetic resonance imaging before and 3 months after PTRA. Age and basal glomerular filtration rate did not differ between groups. Blood oxygen level-dependent imaging demonstrated increased fractional hypoxia 24 hours after angiography and stenting in placebo (+47%) versus elamipretide (-6%). These were reverted to baseline 3 months later. Stenotic kidney RBF rose (202±29-262±115 mL/min; =0.04) 3 months after PTRA in the elamipretide-treated group only. Over 3 months, systolic blood pressure decreased, and estimated glomerular filtration rate increased (=0.003) more in the elamipretide group than in the placebo group (=0.11).
Adjunctive elamipretide during PTRA was associated with attenuated postprocedural hypoxia, increased RBF, and improved kidney function in this pilot trial. These data support a role for targeted mitochondrial protection to minimize procedure-associated ischemic injury and to improve outcomes of revascularization for human atherosclerotic renal artery stenosis.
URL: https://www.clinicaltrials.gov. Unique identifier: NCT01755858.
动脉粥样硬化性肾动脉狭窄会减少肾血流量(RBF)并放大狭窄肾脏缺氧。经皮腔内肾血管成形术(PTRA)和支架置入术再血管化常常无法恢复肾功能,这可能是因为 PTRA 后发生缺血/再灌注损伤。Elamipretide 是一种靶向线粒体的肽,与心磷脂结合并稳定线粒体功能。我们测试了这样一个假设,即在接受 PTRA 的动脉粥样硬化性肾动脉狭窄患者中,Elamipretide 加 PTRA 治疗会改善肾功能、氧合和 RBF。
在计划接受 PTRA 的严重动脉粥样硬化性肾动脉狭窄患者中进行住院研究。在 PTRA 之前和期间,患者分别接受 Elamipretide(0.05mg/kg/小时静脉输注,n=6)或安慰剂(n=8)治疗。使用对比增强多排 CT 测量狭窄肾皮质/髓质灌注和 RBF,并用 3T 血氧水平依赖磁共振成像测量肾氧合,分别在 PTRA 前和 PTRA 后 3 个月进行。两组的年龄和基础肾小球滤过率无差异。血氧水平依赖成像显示,在血管造影和支架置入后 24 小时,安慰剂组(+47%)比 Elamipretide 组(-6%)的局部缺氧分数增加。这些在 3 个月后恢复到基线。仅在 Elamipretide 治疗组,PTRA 后 3 个月狭窄肾 RBF 升高(202±29-262±115mL/min;=0.04)。在 3 个月期间,Elamipretide 组的收缩压下降,估算肾小球滤过率增加(=0.003),安慰剂组的收缩压下降,估算肾小球滤过率增加(=0.11)。
在 PTRA 期间辅助 Elamipretide 治疗与减轻术后缺氧、增加 RBF 和改善肾功能有关。这些数据支持靶向线粒体保护的作用,以最大限度地减少与手术相关的缺血性损伤,并改善人类动脉粥样硬化性肾动脉狭窄的血运重建结果。