Published online Nov 16, 2022. doi: 10.12998/wjcc.v10.i32.11766
Peer-review started: August 7, 2022
First decision: September 5, 2022
Revised: September 15, 2022
Accepted: October 17, 2022
Article in press: October 17, 2022
Published online: November 16, 2022
Processing time: 93 Days and 5.5 Hours
Chronic kidney disease (CKD) has been threatening people’s lives. Without any intervention, CKD can progress to end-stage renal disease. Previously, researchers focus more on diabetic nephropathy, however there are no reports about hyperuricemic nephropathy (HN) patients. It is important to figure out the pathological difference between patients with HN in early stage and middle and late stage with CKD.
As reported, there are currently lots of classic and new biomarkers of endothelial injury and inflammation which can be tested in the blood and urine samples of CKD patients.
Through testing biomarkers, we have a clear idea of the difference in endothelial injury and inflammation between patients with HN in CKD 1-2 and CKD 3-4.
This study is a baseline data of randomized double-blinded controlled trial. During patients’ first care visit, general information and urine and plasma samples were collected. Enzyme-linked immuno
Comparison between patients with HN at CKD 1-2 and those with HN at CKD 3-4 showed that age and disease course were significant factors (P < 0.001 and P < 0.010, respectively). There were no statistical differences in sex, heart rate, body mass index, and systolic and diastolic blood pressures. The incidence of hypertension was also significant (P = 0.03). Plasma levels of heparin sulfate (P < 0.001), endocan (P = 0.034), E-selectin (P < 0.001), slCAM1 (P < 0.001), IL-1β (P = 0.006), and IL-6 (P = 0.004) and the urine levels of L-PGDS (P < 0.001), IL-1β (P = 0.003), and IL-6 (P < 0.001) were high in patients with HN at CKD 3-4 than in those with HN at CKD 1-2. The difference in plasma Ox-LDL levels was not significant (P = 0.078).
Vascular endothelial injury and inflammatory state of patients with HN in CKD 3-4 were higher than those of patients in CKD 1-2. Plasma heparin sulfate and plasma slCAM1 levels are synergistic risk factors for CKD staging in HN.
We now concluded that levels of biomarkers endothelial injury and inflammation are significantly different between patients with HN in CKD 1-2 and CKD 3-4. In the future assessment, heathy subjects, and HN patients in CKD 5 should also be involved.