Evidence map›Paper›PMID 42349469›Full record

ArticlePathology international2026

Glomerular Capillary Microaneurysms in Membranoproliferative Glomerulonephritis: A Clinicopathological Study Highlighting the Involvement of IgG3.

Akiko Mii, Tomohiro Kaneko, Momoko Arai, Takehisa Yamada, Mayuko Takeuchi, Tetsuya Kashiwagi, Naomi Kuwahara, Arimi Ishikawa, Ryuji Ohashi, Yukinao Sakai and 2 more

Abstract read
In one paragraph

Article in Pathology international, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Akiko MiiDepartment of Endocrinology, Metabolism and Nephrology, Nippon Medical School, Tokyo, Japan.
Tomohiro KanekoDepartment of Endocrinology, Metabolism and Nephrology, Nippon Medical School, Tokyo, Japan.
Momoko AraiDepartment of Endocrinology, Metabolism and Nephrology, Nippon Medical School, Tokyo, Japan.
Takehisa YamadaDepartment of Endocrinology, Metabolism and Nephrology, Nippon Medical School, Tokyo, Japan.
Mayuko TakeuchiDepartment of Endocrinology, Metabolism and Nephrology, Nippon Medical School, Tokyo, Japan.
Tetsuya KashiwagiDepartment of Endocrinology, Metabolism and Nephrology, Nippon Medical School, Tokyo, Japan.
Naomi KuwaharaDepartment of Analytic Human Pathology, Nippon Medical School, Tokyo, Japan.
Arimi IshikawaDepartment of Analytic Human Pathology, Nippon Medical School, Tokyo, Japan.
Ryuji OhashiDepartment of Integrated Diagnostic Pathology, Nippon Medical School, Bunkyō, Japan.
Yukinao SakaiDepartment of Endocrinology, Metabolism and Nephrology, Nippon Medical School, Tokyo, Japan.ORCID https://orcid.org/0000-0002-8558-0571
Masato IwabuDepartment of Endocrinology, Metabolism and Nephrology, Nippon Medical School, Tokyo, Japan.
Akira ShimizuDepartment of Analytic Human Pathology, Nippon Medical School, Tokyo, Japan.ORCID https://orcid.org/0000-0002-4364-9251

Funding

Japan Society for the Promotion of Science 20K08620Japan Society for the Promotion of Science 23K07710Ministry of Education, Culture, Sports, Science and Technology
6 · The paper itself

Abstract

Glomerular capillary microaneurysm (GCM) is a pathological lesion defined by aneurysmal dilatation of glomerular capillaries resulting from mesangiolysis with severe endothelial damage and is commonly observed in diabetic nephropathy and thrombotic microangiopathy. However, its clinicopathological significance in membranoproliferative glomerulonephritis (MPGN)-pattern glomerular diseases remains unclear. We retrospectively reviewed 50 renal biopsy cases diagnosed as MPGN or MPGN-like glomerulopathy and identified 12 GCM-positive cases for clinicopathological analysis, including Pathologische Anatomie Leiden Endothelium (PAL-E) staining and CD34 immunohistochemistry to assess endothelial injury. Among GCM-positive cases, proliferative glomerulonephritis with monoclonal immunoglobulin G deposits (PGNMID) was significantly enriched; however, exclusive glomerular IgG3 positivity was consistently observed across other diagnostic categories, irrespective of light-chain restriction. Electron microscopy revealed continuous, irregularly shaped, fine granular subendothelial electron-dense materials with endothelial denudation. PAL-E staining was positive in all evaluable cases, with ultrastructurally identified diaphragmed endothelial fenestrae. Furthermore, CD34 staining demonstrated loss of continuous lining in GCM lesions, suggesting severe endothelial injury. Clinically, all patients presented with nephrotic-range proteinuria, and more than half progressed to end-stage kidney disease or died within 3 years. These findings indicate that GCM-positive MPGN-pattern glomerular diseases represent an aggressive subset associated with IgG3-dominant deposition and severe endothelial injury, with important diagnostic implications.

Indexed as

Glomerulonephritis, MembranoproliferativeImmunoglobulin GKidney GlomerulusMicroaneurysmAdolescentAdultAgedCapillariesFemaleHumansImmunohistochemistryMaleMiddle AgedRetrospective StudiesImmunoglobulin Gendothelial injuryglomerular capillary microaneurysmsIgG3membranoproliferative glomerulonephritis

Identifiers

PMID42349469
PMCPMC13301001

What Socratic holds

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Registered trials

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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 Socratic graph.