Department of Physiology, University of Arizona Health Sciences Center, Tucson, Arizona, USA.
J Vasc Res. 2023;60(3):125-136. doi: 10.1159/000531647. Epub 2023 Aug 3.
Polycystic kidney disease (PKD) is one of the most common hereditary kidney diseases, which is characterized by progressive cyst growth and secondary hypertension. In addition to cystogenesis and renal abnormalities, patients with PKD can develop vascular abnormalities and cardiovascular complications. Progressive cyst growth substantially alters renal structure and culminates into end-stage renal disease. There remains no cure beyond renal transplantation, and treatment options remain largely limited to chronic renal replacement therapy. In addition to end-stage renal disease, patients with PKD also present with hypertension and cardiovascular disease, yet the timing and interactions between the cardiovascular and renal effects of PKD progression are understudied. Here, we review the vascular dysfunction found in clinical and preclinical models of PKD, including the clinical manifestations and relationship to hypertension, stroke, and related cardiovascular diseases. Finally, our discussion also highlights the critical questions and emerging areas in vascular research in PKD.
多囊肾病 (PKD) 是最常见的遗传性肾脏疾病之一,其特征是进行性囊肿生长和继发性高血压。除了囊肿形成和肾脏异常外,PKD 患者还会出现血管异常和心血管并发症。进行性囊肿生长会极大地改变肾脏结构,并最终导致终末期肾病。除了肾移植外,目前尚无治愈方法,治疗选择仍然主要限于慢性肾脏替代治疗。除了终末期肾病外,PKD 患者还会出现高血压和心血管疾病,但 PKD 进展对心血管和肾脏的影响的时机和相互作用仍研究不足。在这里,我们回顾了临床和临床前 PKD 模型中发现的血管功能障碍,包括临床表现以及与高血压、中风和相关心血管疾病的关系。最后,我们的讨论还强调了 PKD 血管研究中的关键问题和新兴领域。