Aim: The objective of this study was to investigate the correlation between the urinary excretion of cystatin C (CysC) and the presence of interstitial fibrosis/tubular atrophy (IF/TA) in renal transplant (RT) recipients.

Methods: This prospective study included 21 adult patients who had undergone renal biopsy and RT ≥6 months prior. According to the renal biopsy reports, the patients were divided into groups with (n=12) or without (n=9) IF/TA. Analytical parameters included the following: serum and urinary levels of CysC, creatinine (Cr) and sodium (Na), total urinary protein, urinary CysC/creatinine ratio [u(CysC/Cr)], fractional excretion of sodium (FENa) and estimated glomerular filtration rate (eGFR) based on the Chronic Kidney Disease Epidemiology Collaboration equation.

Results: The values of uCysC, u(CysC/Cr), proteinuria, and FENa were significantly higher in patients with IF/TA than in patients without IF/TA. The values of eGFR were statistically lower in patients with IF/TA (p=0.001). Values of uCysC significantly correlated with those of serum Cr, FENa, and eGFR (p<0.001). Among the patients with IF/TA, 67% presented with glomerulosclerosis (segmental/global).

Conclusion: Elevated levels of urinary CysC are associated with interstitial fibrosis and tubular atrophy in RT recipients and may become a useful tool for monitoring kidney allografts.

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.clinbiochem.2015.02.008DOI Listing

Publication Analysis

Top Keywords

patients if/ta
12
renal biopsy
8
values ucysc
8
if/ta
5
patients
5
increased urinary
4
urinary cystatin
4
cystatin level
4
level associated
4
associated interstitial
4

Similar Publications

Cardiovascular autonomic neuropathy in chronic kidney disease: a study of kidney biopsy cases.

BMC Nephrol

December 2024

Division of Nephrology and Hypertension, Department of Internal Medicine, The Jikei University School of Medicine, 3-25-8 Nishi-Shimbashi, Minato-Ku, Tokyo, 105-8461, Japan.

Background: The interplay between cardiac and kidney functions is mediated by the autonomic nervous system. Cardiovascular autonomic neuropathy (CAN) is a well-documented dysfunction of this system, with heart rate variability (HRV) serving as the principal diagnostic tool. CAN is recognized as a prognostic marker for adverse kidney outcomes in diabetic kidney disease (DKD).

View Article and Find Full Text PDF

Background: We aimed to analyze the roles of M1 and M2 macrophage infiltration in post-renal transplant antibody-mediated rejection (AMR).

Methods: A total of 102 recipients who underwent renal allotransplant from January 2020 to February 2023 were divided into an immune tolerance group (n = 56) and a rejection group (n = 46). The transplant renal biopsy specimens were harvested by ultrasound-guided puncture.

View Article and Find Full Text PDF

Background: [F] AlF-NOTA-FAPI-04 is a novel positron emission tomography (PET) ligand, which specifically targets fibroblast activation protein (FAP) expression as a FAP inhibitor (FAPI). We analysed the diagnostic value of [F] AlF-NOTA-FAPI-04 PET/CT for the non-invasive assessment of kidney interstitial inflammation and fibrosis in different renal pathologies.

Methods: Twenty-six patients (14 males and 12 females; mean age, 50.

View Article and Find Full Text PDF

Tacrolimus (TAC) has a narrow therapeutic window and patient-specific pharmacokinetic variability. In our study, we analyzed the association between TAC exposure, metabolism, and kidney graft outcomes (function, rejection, and histological lesions). TAC trough (C), coefficient of variation (TAC CV), concentration/dose ratio (C/D), and biomarkers related to kidney injury molecule-1 (KIM-1) and neutrophil gelatinase lipocalin (NGAL) were analyzed.

View Article and Find Full Text PDF
Article Synopsis
  • Rictor is identified as a key player in the process of renal vascular endothelial-mesenchymal transition (EndMT) and renal allograft interstitial fibrosis, contributing to chronic allograft dysfunction in kidney transplant patients.
  • Using cell experiments and a mouse model, the study investigates the role of Rictor/mTORC2 signaling and reveals that blocking this signaling pathway reduces EndMT and interstitial fibrosis in renal allografts.
  • The research highlights the mechanism behind these effects, specifically the role of BNIP3-mediated mitophagy in endothelial cells, suggesting potential therapeutic targets for improving kidney transplantation outcomes.
View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!