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终末期肾病患者冠状动脉疾病的争议:一项叙述性综述

The Controversies of Coronary Artery Disease in End-Stage Kidney Disease Patients: A Narrative Review.

作者信息

Hirsch Daniel, Lau Brandon, Kushwaha Virag, Yong Kenneth

机构信息

Department of Nephrology, Prince of Wales Hospital, Randwick, NSW 2031, Australia.

Prince of Wales Clinical School, University of New South Wales, Kensington, NSW 2033, Australia.

出版信息

Rev Cardiovasc Med. 2023 Jun 25;24(6):181. doi: 10.31083/j.rcm2406181. eCollection 2023 Jun.

Abstract

Cardiovascular disease (CVD) accounts for more than 50% of deaths among patients with end-stage kidney disease (ESKD). Approximately 40-50% of ESKD patients have clinically significant coronary artery disease (CAD) due to atherosclerosis which accounts for a significant proportion of CVD risk. However, other CVD pathologies including myocardial fibrosis, vascular calcification and arterial stiffening play important contributory roles. The pathophysiology of CAD in ESKD is distinct from the general population. ESKD patients is typically have diffuse multi-vessel involvement with increased calcification that involves both intimal and medial layers of the arterial wall. There is a complex interplay between an increased burden of traditional Framingham risk factors and exposure to non-traditional risk factors including chronic inflammation and dialysis . Established treatments for CAD risk factors including cholesterol lowering with statin therapy have attenuated effects and ESKD patients also have worse outcomes after revascularisation. Recent trials such as the Canakinumab Anti-Inflammatory Thrombosis Outcomes Study (CANTOS) have established that direct modulation of inflammation improves CVD outcomes in the general population, which may prove to be a potential attractive therapeutic target in ESKD patients. Multiple retrospective observational studies comparing mortality outcomes between haemodialysis (HD) and peritoneal dialysis (PD) patients have been inconclusive. Randomised trials on this issue of clinical equipoise are clearly warranted but are unlikely to be feasible. Screening for stable CAD in asymptomatic ESKD patients remains a clinical dilemma which is unique to chronic dialysis patients being assessed for kidney transplantation. This has become particularly relevant in light of the recent ISCHEMIA-CKD trial which demonstrated no difference between optimal medical therapy and revascularisation upon CVD outcomes or mortality. The optimal strategy for screening is currently being investigated in the ongoing large international multi-centre CARSK trial. Here we discuss the pathophysiology, risk modification, treatment, screening and future directions of CAD in ESKD.

摘要

心血管疾病(CVD)占终末期肾病(ESKD)患者死亡人数的50%以上。约40%-50%的ESKD患者因动脉粥样硬化患有具有临床意义的冠状动脉疾病(CAD),这在CVD风险中占很大比例。然而,其他CVD病理,包括心肌纤维化、血管钙化和动脉僵硬也起着重要作用。ESKD患者CAD的病理生理学与普通人群不同。ESKD患者通常有弥漫性多支血管受累,钙化增加,累及动脉壁的内膜和中膜层。传统的弗明汉姆风险因素负担增加与接触非传统风险因素(包括慢性炎症和透析)之间存在复杂的相互作用。针对CAD风险因素的既定治疗方法,如使用他汀类药物降低胆固醇,效果减弱,ESKD患者血管重建后的预后也更差。最近的试验,如卡那单抗抗炎血栓形成结果研究(CANTOS),已证实直接调节炎症可改善普通人群的CVD预后,这可能被证明是ESKD患者潜在的有吸引力的治疗靶点。多项比较血液透析(HD)和腹膜透析(PD)患者死亡率结果的回顾性观察研究尚无定论。显然有必要就这一临床平衡问题进行随机试验,但不太可能可行。对无症状ESKD患者进行稳定CAD筛查仍然是一个临床难题,这对于接受肾移植评估的慢性透析患者来说是独一无二的。鉴于最近的缺血性肾病(ISCHEMIA-CKD)试验表明,最佳药物治疗和血管重建在CVD预后或死亡率方面没有差异,这一点变得尤为重要。目前正在进行的大型国际多中心CARSK试验正在研究最佳筛查策略。在此,我们讨论ESKD患者CAD的病理生理学、风险修正、治疗、筛查及未来方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca15/11264163/30a976b96e8d/2153-8174-24-6-181-g1.jpg

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