Evidence map›Paper›PMID 41525388›Full record

Observational studyKidney & blood pressure research2026

Clinical Profile and Outcome of C3-Dominant Glomerulonephritis: Retrospective Study.

Vishrut Khullar, Attur Ravindra Prabhu, Shankar Prasad Nagaraju, Dharshan Rangaswamy, Indu Ramachandra Rao, Srinivas Vinayak Shenoy, Mohan V Bhojaraja, Gaurvi Piplani, Mahesha Vankalakunti

Abstract readObservational Study
In one paragraph

Observational study in Kidney & blood pressure research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Vishrut KhullarDepartment of Nephrology, Kasturba Medical College, Manipal Academy of Higher Education, Manipal, India.
Attur Ravindra PrabhuDepartment of Nephrology, Kasturba Medical College, Manipal Academy of Higher Education, Manipal, India, ravindra.prabhu@manipal.edu.
Shankar Prasad NagarajuDepartment of Nephrology, Kasturba Medical College, Manipal Academy of Higher Education, Manipal, India.
Dharshan RangaswamyDepartment of Nephrology, Kasturba Medical College, Manipal Academy of Higher Education, Manipal, India.
Indu Ramachandra RaoDepartment of Nephrology, Kasturba Medical College, Manipal Academy of Higher Education, Manipal, India.
Srinivas Vinayak ShenoyDepartment of Nephrology, Kasturba Medical College, Manipal Academy of Higher Education, Manipal, India.
Mohan V BhojarajaDepartment of Nephrology, Kasturba Medical College, Manipal Academy of Higher Education, Manipal, India.
Gaurvi PiplaniDepartment of Pathology, Kasturba Medical College, Manipal Academy of Higher Education, Manipal, India.
Mahesha VankalakuntiDepartment of Pathology and Laboratory Medicine, Manipal Hospitals, Bengaluru, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundComplement 3 (C3)-dominant glomerulonephritis (GN) are rare diseases resulting from alternative complement pathway dysregulation; they include C3 glomerulopathy (C3G), paraprotein-associated GN, and C3-dominant infection-related GN (IRGN). To our knowledge, long-term follow-up studies of clinical profile and outcomes of this rare disorder are sparse. We studied kidney histopathology baseline findings, outcomes, treatment, and its complications of C3-dominant GN in our setting.

objectivesWe studied the clinical, pathological profiles, and outcomes of patients with C3-dominant GN.

methodsThis study was a single centre, retrospective, case record based observational study at a tertiary care hospital in Southern India. Consecutive patients of C3-dominant GN on kidney biopsy from 2013 to 2023 were included. Demography, laboratory and histopathological data, treatment and outcomes were studied.

resultsOf 2,175 kidney biopsies, 141 (6.48%) showed C3-dominant GN; 74 (52.5%) C3G, 67 (47.5%) IRGN. Median age was 43 years (IQR 29-59.5), males 90 (63.8%). Preceding skin/throat infections were seen in 32/141 (22.7%). At presentation, median serum creatinine was 1.7 mg/dL (IQR: 1.2-3.6), eGFR <60 mL/min/1.73 m2 in 91/141 (64.5%), 111/141 (78.7%) had low serum C3 levels. Nephrotic proteinuria was seen in 65/141 (46%), Crescents in 45 (31.9%). Remission was partial in 38/141 (27%), complete in 45/141 (31.9%) and 31/141 (22%) progressed to end-stage kidney disease (ESKD). On immunosuppression, commonest infection was pneumonia in 15/70 (21.4%) and 27/141 (19.1%) died at an average follow-up of 25.7 months. Diabetes mellitus, percentage sclerosis, and presence of crescents predicted development of CKD stage 5.

conclusionOver 10 years, C3-dominant GN represented 6.48% of kidney biopsies. Nephrotic proteinuria and kidney failure are common at presentation with 58% achieving some remission, 22% going on to ESKD and mortality of 19%.

Indexed as

Complement C3GlomerulonephritisAdultFemaleHumansKidneyMaleMiddle AgedRetrospective StudiesTreatment OutcomeComplement C3C3-dominant glomerulonephritisC3 glomerulonephritisC3 glomerulopathyComplement 3Infection-related glomerulonephritis

Identifiers

PMID41525388
PMCPMC12912761

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.