Textor Stephen C, Lerman Lilach O
Division of Nephrology and Hypertension, Mayo Clinic, Rochester, Minnesota
Division of Nephrology and Hypertension, Mayo Clinic, Rochester, Minnesota.
J Am Soc Nephrol. 2015 Sep;26(9):2074-80. doi: 10.1681/ASN.2014121274. Epub 2015 Apr 13.
Results of recent clinical trials and experimental studies indicate that whereas atherosclerotic renovascular disease can accelerate both systemic hypertension and tissue injury in the poststenotic kidney, restoring vessel patency alone is insufficient to recover kidney function for most subjects. Kidney injury in atherosclerotic renovascular disease reflects complex interactions among vascular rarefication, oxidative stress injury, and recruitment of inflammatory cellular elements that ultimately produce fibrosis. Classic paradigms for simply restoring blood flow are shifting to implementation of therapy targeting mitochondria and cell-based functions to allow regeneration of vascular, glomerular, and tubular structures sufficient to recover, or at least stabilize, renal function. These developments offer exciting possibilities of repair and regeneration of kidney tissue that may limit progressive CKD in atherosclerotic renovascular disease and may apply to other conditions in which inflammatory injury is a major common pathway.
近期临床试验和实验研究结果表明,虽然动脉粥样硬化性肾血管疾病可加速全身性高血压以及狭窄后肾脏的组织损伤,但对大多数受试者而言,仅恢复血管通畅不足以恢复肾功能。动脉粥样硬化性肾血管疾病中的肾损伤反映了血管稀疏、氧化应激损伤以及炎症细胞成分募集之间的复杂相互作用,这些最终会导致纤维化。单纯恢复血流的传统模式正在转向针对线粒体和基于细胞的功能实施治疗,以实现血管、肾小球和肾小管结构的再生,从而足以恢复或至少稳定肾功能。这些进展为肾组织的修复和再生提供了令人兴奋的可能性,这可能会限制动脉粥样硬化性肾血管疾病中慢性肾脏病的进展,并且可能适用于炎症损伤是主要共同途径的其他病症。