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Background: Urine sediment examination is an important preliminary investigation for the nephrologist and helps him decide whether the patient has a proliferative or non-proliferative glomerular pathology. Recently, there is an increasing trend of using easier, non-specific dipstick method for urine examination leading to a decline in the importance of urine sediment examination. Here, we attempt to define guidelines for bio-chemical and microscopic parameters in order to develop a uniform and clinically relevant reporting system for urine sediment examination.
Methods: Urine samples were reported as inactive or active sediment. A tiered system of reporting urine sediments was developed including inactive sediment, Inactive sediment with moderate/significant proteinuria, glomerular hematuria, and active sediment, active sediment with significant proteinuria / features of proliferative activity. The urine sediment was compared to kidney biopsies of these patients which were grouped into non proliferative and proliferative glomerulopathy.
Results: 795 paired samples of urine sediment and kidney biopsies were examined and compared. Patients of non-proliferative glomerulopathy (Minimal change disease, Focal segmental glomerulosclerosis, amyloid and membranous nephropathy) showed features of Inactive sediment. Patients with proliferative glomerulopathy (focal proliferative glomerulonephritis [GN], Diffuse proliferative GN, Membranoproliferative GN, Mesangio-proliferative GN and crescentic GN) predominantly showed active sediment, with increase in percentage of dysmorphic red blood cells and formed elements. The sensitivity of this urine reporting system was 82.0%, specificity 74.4% with p value <0.001.
Conclusions: This system of reporting urine sediment is a sensitive and efficient method of predicting the severity of underlying kidney disease and need for performing renal biopsy.
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http://dx.doi.org/10.34067/KID.0000000941 | DOI Listing |
Int J Mol Sci
August 2025
Research Centre for Medical Genetics, Moskvorechie 1, Moscow 115478, Russia.
Genome instability in induced pluripotent stem cells (IPSC) poses a significant challenge for their use in research and medicine. Cataloging and precisely describing all the identified aberrations that arise during cell reprogramming, expansion, and differentiation is essential for improving approaches to instability prevention and ensuring genetic quality control. We report the karyotypic analysis of 65 cell lines derived from skin fibroblasts, urinal sediment, and peripheral blood mononuclear cells of 33 individuals, 82% of whom suffer from monogenic genetic disorders not associated with genetic instability.
View Article and Find Full Text PDFKidney360
August 2025
Dept of Paediatrics, Lady Hardinge Medical College and assoc. Kalawati Saran Children's Hospital, New Delhi, India.
Background: Urine sediment examination is an important preliminary investigation for the nephrologist and helps him decide whether the patient has a proliferative or non-proliferative glomerular pathology. Recently, there is an increasing trend of using easier, non-specific dipstick method for urine examination leading to a decline in the importance of urine sediment examination. Here, we attempt to define guidelines for bio-chemical and microscopic parameters in order to develop a uniform and clinically relevant reporting system for urine sediment examination.
View Article and Find Full Text PDFMitochondrion
August 2025
Institute for Maternal and Child Health IRCCS Burlo Garofolo, 34137 Trieste, Italy; University of Padova Department of Neuroscience, Veneto Institute of Molecular Medicine, Via Orus 2, Padova 35128, Italy. Electronic address:
The diagnosis of disorders associated with mitochondrial DNA (mtDNA) variants presents substantial complexity due to their genetic and clinical heterogeneity, which is largely influenced by mtDNA heteroplasmy. However, the level of heteroplasmy alone is often not sufficient to predict the clinical phenotype including its severity and progression. This study concerns the characterization of the m.
View Article and Find Full Text PDFJ Appl Lab Med
August 2025
Department of Medical Biology, CHR Haute Senne, Soignies, Belgium.
Background: Urine sediment analysis is a cornerstone of diagnostic testing. This study evaluates FUS-3000 Plus, an automated urine sediment analyzer using advanced imaging and artificial intelligence, to assess its technical performance and diagnostic accuracy for routine clinical use.
Methods: The study analyzed 98 urine samples for chemical parameters (pH, protein, blood, leukocyte esterase, and nitrite) and 76 samples for particle analysis (red blood cells [RBCs], white blood cells, epithelial cells, crystals, bacteria) by both FUS-3000 Plus and sediMAX™, the current laboratory analyzer in use.
Z Rheumatol
August 2025
Research Department, Reha Rheinfelden, Salinenstr. 98, 4310, Rheinfelden, Schweiz.
A 46-year-old female patient had been suffering from multiple symptoms such as arthralgia, myalgia, general fatigue, exhaustion, concentration problems, forgetfulness, difficulty falling asleep and sleeping through the night and depression since the age of 27 years old. Rheumatological preliminary findings revealed rheumatoid arthritis with a lack of response to basic treatment as well as secondary fibromyalgia. Supplementary metabolic examinations were carried out in the case of laboratory tests for hypouricemia, which showed massively increased xanthine levels in the urine.
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