Advances in the Early Diagnosis and Management of Renal Diseases

A special issue of Journal of Clinical Medicine (ISSN 2077-0383).

Deadline for manuscript submissions: 31 May 2024 | Viewed by 1184

Special Issue Editors


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Guest Editor
Department of Nephrology and Transplantation Medicine - University Clinical Hospital Jan Mikulicz Radecki, Borowska 213, 50-556, Wrocław, Poland
Interests: kidney stones; arterial hypertension; renal hypertension; urination disorders; cysts nephropathy; glomerulonephritis; proteinuria, hematuria; diabetic kidney disease; polycystic kidney disease; urinary tract infections; cystitis; pyelonephritis; chronic kidney disease; transplant kidney; renal failure; edema; acidosis; metabolic disorders; hyperparathyroidism; nephrocalcinosis; abnormal GFR
Special Issues, Collections and Topics in MDPI journals

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Guest Editor
Department of Pediatric Nephrology, Wroclaw Medical University, Wybrzeże L. Pasteura 1, 50-367 Wrocław, Poland
Interests: acute kidney injury; biomarkers in nephrology; CAKUT; obstructive uropathy; vesico-ureteral reflux; hemolytic uremic syndrome; idiopathic/congenital/infantile nephrotic syndrome; primary glomerulopathies; chronic kidney disease; hemodialysis; peritoneal dialysis; transition medicine; hypertension
Special Issues, Collections and Topics in MDPI journals

Special Issue Information

Dear Colleagues,

The last decade has seen a number of advances in the diagnostics and management of glomerulopathies, interstitial and hypertensive nephropathy, kidney stone disease, vasculitis, and diabetic kidney disease.

Since the progressive loss of functioning renal tissue may result from a number of different disturbances (congenital hypoplasia or obstructive uropathy with or without associated infections, other anomalies, polycystic kidneys, chronic pyelonephritis, glomerulonephritis, etc.), an exact diagnosis is essential to establish the appropriate therapy.

With a few exceptions, invasive diagnostics—namely, a kidney biopsy—are currently required for the precise diagnosis of many chronic kidney diseases. In order to effectively develop personalized medicine for renal diseases, we urgently need to develop highly accurate biomarkers for use in the clinic since the current biomarkers of kidney damage (creatinine and/or urine albumin excretion) apply to later stages of the disease. A promising, non-invasive approach is urinary proteome analysis, which has the potential to identify various types of renal disease. Renal failure, a consequence of renal disease progression, is among the most deadly and economically costly diseases faced by patients and modern society. Despite this, there are relatively few new therapies in development for the treatment of renal disease. Multiple factors have contributed to the diminishing interest in pharmaceutical investment in the field of renal disease. Many costly phase 3 trials have failed to provide improved renal outcomes, and the awareness of renal diseases remains poor among patients, physicians, and payers. Nevertheless, several therapeutics remain in development for the treatment of CKD, including mineralocorticoid receptor antagonists, sodium/glucose cotransporter 2 inhibitors, anti-inflammatory drugs, and drugs that mitigate oxidative injury.

The success of the future management of renal disease will depend not only on an improved understanding of disease pathogenesis but also on increasing awareness of this disease among the public and the greater medical community, as well as quick diagnostics and appropriate treatment.

Prof. Dr. Mariusz A. Kusztal
Prof. Dr. Kinga Musiał
Guest Editors

Manuscript Submission Information

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Keywords

  • chronic kidney disease
  • glomerulonephritis
  • biomarkers
  • kidney biopsy
  • treatment

Published Papers (1 paper)

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Research

12 pages, 1310 KiB  
Article
Systemic Immune Inflammation Index as a Key Predictor of Dialysis in Pediatric Chronic Kidney Disease with the Use of Random Forest Classifier
by Anna Kawalec, Jakub Stojanowski, Paulina Mazurkiewicz, Anna Choma, Magdalena Gaik, Mateusz Pluta, Michał Szymański, Aleksandra Bruciak, Tomasz Gołębiowski and Kinga Musiał
J. Clin. Med. 2023, 12(21), 6911; https://doi.org/10.3390/jcm12216911 - 03 Nov 2023
Cited by 2 | Viewed by 948
Abstract
Background: Low-grade inflammation is a significant component of chronic kidney disease (CKD). Systemic immune inflammation index (SII), a newly defined ratio combining neutrophil, lymphocyte, and platelet counts, has not yet been evaluated in the pediatric CKD population nor in the context of CKD [...] Read more.
Background: Low-grade inflammation is a significant component of chronic kidney disease (CKD). Systemic immune inflammation index (SII), a newly defined ratio combining neutrophil, lymphocyte, and platelet counts, has not yet been evaluated in the pediatric CKD population nor in the context of CKD progression or dialysis. Thus, this study aimed to analyze the complete blood cell count (CBC)-driven parameters, including SII, in children with CKD and to assess their potential usefulness in the prediction of the need for chronic dialysis. Methods: A single-center, retrospective study was conducted on 27 predialysis children with CKD stages 4–5 and 39 children on chronic dialysis. The data were analyzed with the artificial intelligence tools. Results: The Random Forest Classifier (RFC) model with the input variables of neutrophil count, mean platelet volume (MPV), and SII turned out to be the best predictor of the progression of pediatric CKD into end-stage kidney disease (ESKD) requiring dialysis. Out of these variables, SII showed the largest share in the prediction of the need for renal replacement therapy. Conclusions: Chronic inflammation plays a pivotal role in the progression of CKD into ESKD. Among CBC-driven ratios, SII seems to be the most useful predictor of the need for chronic dialysis in CKD children. Full article
(This article belongs to the Special Issue Advances in the Early Diagnosis and Management of Renal Diseases)
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