Role of Uremic Toxins, Oxidative Stress, and Renal Fibrosis in Chronic Kidney Disease

被引:7
作者
Frak, Weronika [1 ]
Dabek, Bartlomiej [1 ]
Balcerczyk-Lis, Marta [1 ]
Motor, Jakub [1 ]
Radzioch, Ewa [1 ]
Mlynarska, Ewelina [1 ]
Rysz, Jacek [2 ]
Franczyk, Beata [1 ]
机构
[1] Med Univ Lodz, Dept Nephrocardiol, ul Zeromskiego 113, PL-90549 Lodz, Poland
[2] Med Univ Lodz, Dept Nephrol Hypertens & Family Med, ul Zeromskiego 113, PL-90549 Lodz, Poland
关键词
chronic kidney disease; uremic toxins; oxidative stress; renal fibrosis; treatment; CARDIOVASCULAR OUTCOMES; NEPRILYSIN INHIBITION; MECHANISMS; HOMOCYSTEINE; CANAKINUMAB; RISK; THERAPEUTICS; INFLAMMATION; FINERENONE; ENALAPRIL;
D O I
10.3390/antiox13060687
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Affecting millions of people worldwide, chronic kidney disease is a serious medical problem. It results in a decrease in glomerular filtration rate below 60 mL/min/1.73 m, albuminuria, abnormalities in urine sediment and pathologies detected by imaging studies lasting a minimum of 3 months. Patients with CKD develop uremia, and as a result of the accumulation of uremic toxins in the body, patients can be expected to suffer from a number of medical consequences such as progression of CKD with renal fibrosis, development of atherosclerosis or increased incidence of cardiovascular events. Another key element in the pathogenesis of CKD is oxidative stress, resulting from an imbalance between the production of antioxidants and the production of reactive oxygen species. Oxidative stress contributes to damage to cellular proteins, lipids and DNA and increases inflammation, perpetuating kidney dysfunction. Additionally, renal fibrogenesis involving the accumulation of fibrous tissue in the kidneys occurs. In our review, we also included examples of forms of therapy for CKD. To improve the condition of CKD patients, pharmacotherapy can be used, as described in our review. Among the drugs that improve the prognosis of patients with CKD, we can include: GLP-1 analogues, SGLT2 inhibitors, Finerenone monoclonal antibody-Canakinumab and Sacubitril/Valsartan.
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页数:19
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