Verduzco Hector Alvarado, Shirazian Shayan
Department of Medicine, Division of Nephrology, Columbia University College of Physicians and Surgeons, New York, New York, USA.
Kidney Int Rep. 2020 May 8;5(9):1387-1402. doi: 10.1016/j.ekir.2020.04.027. eCollection 2020 Sep.
Chronic kidney disease-associated pruritus (CKD-aP) is a common, troubling and in some cases debilitating problem for patients with CKD and end-stage renal disease. Despite a prevalence rate of approximately 20% in CKD and 40% in end-stage renal disease, and a clear association with poorer psychosocial and medical outcomes, this condition is often underreported by patients and overlooked by health care providers. This is likely due, in part, to uncertainty regarding its pathogenesis and treatment. Most commonly, CKD-aP is attributed to toxin build-up, peripheral neuropathy, immune system dysregulation, or opioid dysregulation. Prior treatment studies of CKD-aP have targeted these potential etiologies but have been limited by noncontrolled design, small sample size, and non-uniform definitions of CKD-aP. Recently, several large, randomized controlled trials targeting opioid dysregulation have yielded promising results. These trials have spurred new hope for understanding and treating this condition.
慢性肾脏病相关性瘙痒(CKD-aP)是慢性肾脏病(CKD)和终末期肾病患者常见、令人困扰且在某些情况下会导致身体衰弱的问题。尽管在CKD中的患病率约为20%,在终末期肾病中的患病率为40%,并且与较差的心理社会和医疗结局有明确关联,但这种情况常常未被患者充分报告,也被医疗保健提供者忽视。这可能部分归因于其发病机制和治疗方面的不确定性。最常见的是,CKD-aP归因于毒素蓄积、周围神经病变、免疫系统失调或阿片类物质失调。先前对CKD-aP的治疗研究针对这些潜在病因,但受到非对照设计、样本量小以及CKD-aP定义不统一的限制。最近,几项针对阿片类物质失调的大型随机对照试验取得了有希望的结果。这些试验为理解和治疗这种疾病带来了新的希望。