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. 2020 Aug 25;21(17):6119. doi: 10.3390/ijms21176119

Table A1.

Most valuable studies examining the role of endocan in various kidney diseases.

Condition Aims Study Group Results References
AKI Correlation between endocan levels and renal function and need for RRT in ARDS patients in ICU 96 patients with ARDS in ICU department who did not require RRT at baseline Serum creatinine and endocan together—most valuable in predicting the need for RRT (ROC AUC 0.77) [11]
AKI serum endocan levels as potential biomarkers for diagnosing AKI and its pathogenesis 39 patients diagnosed with AKI according to KDIGO definition Endocan displayed 59% of sensitivity and 76.3% of specificity in the diagnosis of AKI [12]
CKD Endocan levels in CKD and non-CKD patients; relationship between endocan levels and inflammatory and endothelial dysfunction markers in CKD; endocan as predictive marker of all-cause mortality and CVE in CKD 251 CKD pre-dialysis patients (23.1% DM; 18.7% HT; 15.9% chronic glomerulonephritis; 27.1% unknow etiology) CKD patients displayed higher plasma endocan levels than controls; plasma endocan correlated with eGFR, different markers of inflammation and vascular abnormalities (FMV and CIMT); endocan levels were associated with all-cause mortality and CVE independent of traditional risk factors [9]
DN Predictive role of endocan and endoglin as markers of DN progression 96 patients with DM2 (40 patients with normoalbuminuria, 56 patients with DN) Endocan and endoglin serum levels were higher in DM2 patients; endocan, but not endoglin levels were higher in DN compared to normoalbuminuric patients (p = 0.011 and p = 0.822, respectively) [20]
IgAN Relevance of plasma and urine endocan levels in IgAN 64 patients with IgAN diagnosed upon renal biopsy Urine and plasma endocan levels were significantly higher in IgAN group than controls; urine, but not plasma endocan correlated with CKD stage; high plasma endocan was an independent risk factor for CKD progression [30]
AR after KT Dynamic monitoring of serum endocan levels in diagnosing ARs 60 patients after KT (20 with normal renal function, 20 with biopsy-proven AR, 20 with renal allograft dysfunction from other causes) Elevated blood and tissue expression of endocan in the AR group compared to others [32]
AR after KT Endocan as marker of microvascular inflammation in KT patients 203 patients after KT Increased urine and plasma endocan levels in AMBR patients than others; higher scores of microvascular inflammation in biopsy specimens and worse renal survival in patients with increased endocan levels (urine and/or plasma); serum and urinary endocan were valuable in distinguishing between AMBR and other graft pathologies [33]

AKI—acute kidney injury; RRT—renal replacement therapy; ARDS—acute respiratory distress syndrome; ICU—intensive care unit; CKD—chronic kidney disease; CVE—cardiovascular events; DM—diabetes mellitus; HT—hypertension; eGFR -estimated glomerular filtration rate; FMV—flow-mediated vasodilation; CIMT—carotid intima media thickness; DN—diabetic nephropathy; IgAN—IgA nephropathy; AR—acute rejection; KT—kidney transplantation; AMBR—antibody-mediated acute rejection.