Analysis of profibrogenic microRNAs (miRNAs) expression in urine and serum of chronic kidney disease (CKD) stage 1-4 patients and their relationship with proteinuria and kidney function

被引:19
作者
Donderski, Rafal [1 ,2 ]
Szczepanek, Joanna [3 ]
Naruszewicz, Natalia [4 ]
Naruszewicz, Renata [5 ]
Tretyn, Andrzej [6 ]
Skoczylas-Makowska, Natalia [7 ]
Tyloch, Janusz [8 ]
Odrowaz-Sypniewska, Grazyna [9 ]
Manitius, Jacek [1 ]
机构
[1] Bydgoszcz Nicolaus Copernicus Univ, Univ Hosp, Dept Nephrol Hypertens & Internal Med, Torun, Poland
[2] Sklodowskiej Curie 9, PL-85094 Bydgoszcz, Poland
[3] Nicolaus Copernicus Univ, Ctr Modern Interdisciplinary Technol, Torun, Poland
[4] Nicolaus Copernicus Univ, Dept Plant Physiol & Biotechnol, Torun, Poland
[5] Davita Poland, Hemodialysis Unit, Naklo, Poland
[6] Nicolaus Copernicus Univ, Inst Gen & Mol Biol, Dept Biotechnol, Torun, Poland
[7] Nicolaus Copernicus Univ, Univ Hosp Bydgoszcz, Dept Clin Pathol, Torun, Poland
[8] Nicolaus Copernicus Univ, Univ Hosp Bydgoszcz, Dept Urol, Torun, Poland
[9] Nicolaus Copernicus Univ, Univ Hosp Bydgoszcz, Dept Clin Lab Med, Torun, Poland
关键词
Chronic kidney disease (CKD); microRNAs expression; Tubulointerstitial compartment damage; Kidney fibrosis; BIOMARKERS; MIR-21;
D O I
10.1007/s11255-021-02928-1
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Purpose Besides conventional kidney diseases diagnostics, micro RNAs (miRNAs) assessment in urine and serum is considered to be a promising non-invasive method of diagnostics of renal parenchymal diseases and valuable therapeutic target also. The purpose of the study was to investigate the role of several miRNAs as a markers of kidney damage. Methods Assessment of 45 chronic kidney disease (CKD) patients stage 1-4 and 17 healthy control. Sample of urine and blood was taken from each participant for molecular analysis using Real Time PCR method to identify such micro-RNAs as: hsa-miR-155-5p, hsa-miR-214-3p, hsa-miR-200a-5p, hsa-miR-29a-5p, hsa-miR-21-5p, hsa-miR-93-5p, and hsa-miR-196a-5p. Basic biochemical test was done. Analysis was performed in CKD patients group and subgroup with chronic glomerulonephritis (CGN) confirmed by kidney biopsy. Moreover, analysis was performed in subgroup with different estimated glomerular filtration rate (eGFR) (according to CKD-EPI equation: eGFR < 60 ml/min, eGFR > 60 ml/min) and different daily protein excretion (DPE): (DPE < 3.5 g; DPE > 3.5 g). Results Increased relative expression of hsa-miR-29-5p, hsa-miR-21-5p, and hsa-miR-196a-5p and decreased expression of hsa-miR-155-5p, hsa-miR-214-5p, hsa-miR-200a-5p, and hsa-miR-93-5p was demonstrated in urine of analyzed CKD patients. In subpopulation of chronic glomerulonephritis (CGN) patients, there was higher level of expression in urine of hsa-miR-155-5p, hsa-miR 214-3p, hsa-miR-93-5p, and hsa-miR-196a-5p in CGN with DPE < 3.5 g. CGN patients with eGFR < 60 ml/min showed higher expression level of miRNAs such as hsa-miR-214-3p, hsa-miR-29-5p, hsa-miR-93-5p, and hsa-miR-196-5p in urine. There was increase in hsa-miR 155-5p, hsa-miR-214-3p, and hsa-miR-200a-5p serum expression level in CKD population and reduction of hsa-miR-29a-5p, hsa-miR-21-5p, and hsa-miR-93-5p expression. Increased level of expression of hsa-miR-155-5p; hsa-miR-214-3p, hsa-miR-200a-5p, and hsa-miR-29-5p was found in CGN patients with eGFR > 60 ml/min. Conclusion Increased relative expression of profibrogenic miRNAs in urine or serum of CKD patients with eGFR > 60 ml/min and DPE < 3.5 g may indicate higher degree of fibrosis at early CKD stages.
引用
收藏
页码:937 / 947
页数:11
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