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Background: The aim of this study is to investigate the clinicopathologic characteristics, treatment and prognosis of crescentic glomerulonephritis (Crescentic GN) in patients with normal renal function at diagnosis, and compare to those with impaired renal function.
Methods: We conducted a retrospective review of patients with renal biopsy proven Crescentic GN at our center and divided them into normal eGFR group (eGFR≥60 ml/min/1.73 m) and low eGFR group (eGFR <60 ml/min/1.73 m). Clinical and renal pathological findings at diagnosis and renal outcomes were compared between the two groups using t-test, Wilcoxon rank sum test or Kruskal-Wallis H test.
Results: From Jan 2010 to Dec 2021, 90 Crescentic GN patients with normal eGFR were included, in which clinicopathological diagnoses were LN (lupus nephritis) (60 cases, 66.77 %), IgAN (IgA nephropathy) (9 cases, 10 %), HSPN (Henoch-Schnlein purpura nephritis) (14 cases, 15.6 %) and AAV (ANCA-associated GN) (7 cases, 7.8 %). Compared with the low eGFR group (n = 300), the following characteristics were observed in the normal eGFR group: younger age (p < 0.001), female predominance (p < 0.001), longer time from onset to biopsy (p < 0.001), lower hypertension rate (p < 0.001), lower rate of oliguria (p < 0.001), and anemia (p < 0.001), lower levels of C3 (p < 0.001), C4 (p < 0.001) and Urine RBC (p < 0.001), higher titers of ANA (p < 0.001) and ds-DNA (p = 0.002), lower positive rate of ANCA (<0.001) and GBM (p = 0.02), less extra-renal involvement (p < 0.05), lower proportions of crescents (56.3(51.8-62.7) % vs 66.7 (56.3-81.3) %, p < 0.001) and glomerular sclerosis (p < 0.001), less severe tubulointerstitial lesion (p < 0.001) and interstitial inflammation (p < 0.001), higher degree of immune complex deposition of IgA, IgM, C3, C4 and C1q by Immunofluorescence. Normal eGFR group received lower frequency of intravenous methylprednisolone pulse therapy (71.2 % vs 89 %, p = 0.044) and dialysis treatment (0 % vs 53.7 %, p < 0.001). The 5- and 10-year cumulative renal survival rates from ESRD were 90.7 % vs 45.5 % and 58.3 % vs 43.7 %, respectively in normal and low eGFR group.
Conclusion: Crescentic GN may present with normal renal function, which has poor renal outcomes and may benefit from intensive immunosuppressive treatment. This often occurs in patients with abnormal immunological indicators and systemic autoimmune disease. Shorter time from onset to biopsy may help better management and improve long-term outcomes in these cases. Renal biopsy remains the diagnostic gold standard when urinary abnormalities are present in nephritis.
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http://dx.doi.org/10.1016/j.amjms.2025.04.011 | DOI Listing |
Arthritis Rheumatol
July 2025
Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts.
Objective: Interleukin-17-producing CD4 Th17 cells contribute to the pathogenesis of autoimmune diseases, including crescentic glomerulonephritis. Although ADAM9 has been reported to contribute to organ inflammation, the mechanism remains poorly understood. The goal of the current study was to investigate how ADAM9 alters T cell metabolism to promote the generation of Th17 cell differentiation.
View Article and Find Full Text PDFBMC Nephrol
August 2025
Centre de Recherche des Cordeliers, INSERM U1138, Université Paris Cité, 15 rue de l'Ecole de Médecine, Paris, 75006, France.
Objective And Design: The kynurenine (KYN) pathway is activated in acute kidney disease, including crescentic glomerulonephritis (CGN), an immune-mediated life-threatening syndrome characterized by rapid loss of renal function. The non-invasive measurement of KP metabolites may have clinical diagnostic or prognostic value, but has never been systematically studied using sensitive analytical tools.
Methods: We have recently developed and validated a sensitive and rapid liquid chromatography-tandem mass spectrometry (LC-MS/MS) method to measure a comprehensive panel of tryptophan (TRP) catabolic intermediates in blood and urine.
Diagnostics (Basel)
August 2025
School of Medicine, Aristotle University of Thessaloniki (AUTH), 54124 Thessaloniki, Greece.
IgA nephropathy (IgAN) is the most prevalent primary glomerulonephritis worldwide, with a heterogeneous clinical course that may progress to end-stage kidney disease (ESKD) in approximately 20% of patients. Despite recent advances, including the U.S.
View Article and Find Full Text PDFMedicina (Kaunas)
August 2025
Department of Nephrology, The Children's Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health, Hangzhou 310052, China.
: This study aimed to explore the risk factors of histopathological crescent formation in pediatric IgA vasculitis nephritis (IgAVN). : Enrolled patients with biopsy-proven IgAVN from Zhejiang University's hospital were split into two groups: 377 with no crescents on histopathology (Group 1) and 364 with crescentic nephritis (Group 2). Collected data included clinical features, lab indicators, histopathological grading, and factors causing glomerular sclerosis.
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.
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