Lekawanvijit Suree, Krum Henry
Department of Pathology, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand.
Department of Epidemiology and Preventive Medicine, Centre of Cardiovascular Research and Education in Therapeutics, Monash University, Melbourne, Australia.
J Ren Nutr. 2015 Mar;25(2):149-54. doi: 10.1053/j.jrn.2014.10.009. Epub 2014 Dec 31.
Renal impairment is a strong independent risk factor associated with poor prognosis in cardiovascular disease patients. Renal dysfunction is likely contributed by progressive renal structural damage. Accurate detection of kidney injury in a timely manner as well as increased knowledge of the pathophysiology and mechanisms underlying this injury is of great importance in developing therapeutic interventions for combating renal complications at an early stage. Regarding the role of uremic solutes in the pathophysiology of cardiorenal syndrome, a number of further studies are warranted. There may be uremic solutes discovered from proteomics not yet chemically identified or tested for biological activity. Beyond Protein-bound uremic toxins, uremic solutes in other classes (according to the European Uraemic Toxin Work Group classification) may have adverse cardiorenal effects. Although most small water-soluble solutes and middle molecules can be satisfactorily removed by either conventional or newly developed dialysis strategies, targeting uremic toxins with cardiorenal toxicity at predialysis stage of chronic kidney disease may retard or prevent incident dialysis as well as the initiation/progression of cardiorenal syndrome.
肾功能损害是心血管疾病患者预后不良的一个强有力的独立危险因素。肾功能障碍可能是由进行性肾结构损伤所致。及时准确地检测肾损伤以及增加对这种损伤的病理生理学和机制的了解,对于开发早期对抗肾脏并发症的治疗干预措施至关重要。关于尿毒症溶质在心肾综合征病理生理学中的作用,有必要进行更多的研究。可能存在从蛋白质组学中发现但尚未进行化学鉴定或生物活性测试的尿毒症溶质。除了与蛋白质结合的尿毒症毒素外,其他类别(根据欧洲尿毒症毒素工作组的分类)的尿毒症溶质可能对心肾有不良影响。尽管大多数小的水溶性溶质和中分子可以通过传统的或新开发的透析策略得到满意的清除,但在慢性肾脏病的透析前阶段针对具有心肾毒性的尿毒症毒素进行干预,可能会延缓或预防透析的发生以及心肾综合征的启动/进展。