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Background: Visual scoring of tubular damage has limitations in capturing the full spectrum of structural changes and prognostic potential. Here, we investigated if computationally quantified tubular features can enhance prognostication and reveal spatial relationships with interstitial fibrosis.
Methods: Deep-learning and image-analysis approaches were employed on 254/266 Periodic acid Schiff-stained whole slide image (WSI) kidney biopsies from participants in the NEPTUNE/CureGN prospective observational cohort studies (135/153 with focal segmental glomerulosclerosis (FSGS) and 119/113 with minimal change disease (MCD)) to segment cortex, tubular lumen (TL), epithelium (TE), nuclei (TN), and basement membrane (TBM). One hundred four pathomic features were extracted from these segmented tubular substructures and aggregated at the patient level using summary statistics. In the NEPTUNE dataset, tubular features were quantified at the WSI level and in manually segmented regions of mature interstitial fibrosis and tubular atrophy (IFTA), pre-IFTA, and non-IFTA. Minimum Redundancy Maximum Relevance was then used to select features most associated with disease progression and proteinuria remission. Ridge-penalized Cox models evaluated their predictive discrimination compared to clinical/demographic data and visual-assessment. Models were evaluated in the CureGN dataset.
Results: Nine features were predictive of disease progression and/or proteinuria remission. Models with tubular features had high prognostic accuracy in both NEPTUNE and CureGN, and higher prognostic accuracy for both outcomes compared to conventional parameters alone in NEPTUNE. TBM thickness/area and TE flattening and/or reduced cell size progressively increased from non- to pre- and mature IFTA.
Conclusions: Previously underrecognized computationally derived and quantifiable tubular characteristics may contribute to improving prognostic accuracy and risk stratification in patients with FSGS/MCD. Future studies are needed to test their generalizability across different diseases and populations before they can be deployed in clinical practice.
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http://dx.doi.org/10.1016/j.kint.2025.04.026 | DOI Listing |
Pediatr Nephrol
September 2025
Division of Nephrology, Department of Pediatrics, All India Institute of Medical Sciences, Ansari Nagar, New Delhi, 110029, India.
Background: Kidney involvement in pediatric sarcoidosis is rare and often underrecognized, leading to diagnostic delays and treatment challenges. We report six patients with renal sarcoidosis to highlight their diverse presentations and outcomes and challenges in management.
Methods: Medical records of patients diagnosed with renal sarcoidosis during 2020-24 were reviewed.
Indian J Endocrinol Metab
August 2025
Department of Endocrinology and Metabolism, All India Institute of Medical Sciences, New Delhi, India.
Introduction: Tumour-induced osteomalacia (TIO) is rare. At our referral centre, we see a substantial number of TIO. Therefore, we planned to study their profile and treatment outcomes to provide insight in management.
View Article and Find Full Text PDFZhong Nan Da Xue Xue Bao Yi Xue Ban
May 2025
Department of Nephropathy and Rheumatology, Third Xiangya Hospital, Central South University, Changsha 410013.
Dent disease is a rare X-linked recessive inherited renal tubular disorder characterized by low molecular weight proteinuria (LMWP), hypercalciuria, nephrocalcinosis, and other clinical features, and can lead to progressive renal failure. It is primarily caused by mutations in the gene. This article reports the case of a 10-year-old male patient of Chinese descent who was incidentally found to have asymptomatic proteinuria during a routine health examination.
View Article and Find Full Text PDFMod Pathol
September 2025
Department of Medicine, University of Padua, Italy; Veneto Institute of Oncology, IOV-IRCCS, Padua, Italy. Electronic address:
A subset of gastric cancers (GCs) is linked to Epstein-Barr virus (EBV) infection. This study aims to characterize the histopathological and molecular features of EBV-associated GCs (EBVaGCs), focusing on predictive biomarkers and genomic and transcriptomic analysis. A total of 35 primary EBVaGCs were considered.
View Article and Find Full Text PDFExp Cell Res
September 2025
Organ Transplant Center, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong 510080, China; Guangdong Provincial Key Laboratory of Organ Donation and Transplant Immunology, Guangzhou, Guangdong 510080, China. Electronic address:
Background: Chronic rejection is a major cause of long-term kidney allograft failure, characterized by persistent inflammation and progressive fibrosis. Macrophages are central mediators of this process, but their phenotypic heterogeneity and regulatory mechanisms in chronic rejection remain incompletely understood.
Methods: We performed single-cell transcriptomic analysis on renal allograft biopsies from patients with different types of rejection and on a time-course rat model of chronic rejection.