Evidence map›Paper›PMID 42847324›Full record

ArticleNephrology (Carlton, Vic.)2026

Distinct Complement Activation Profiles Between NELL1- and PLA2R-Associated Membranous Nephropathy: A Clinicopathological and Proteomic Study.

Taihei Suzuki, Kang Dedong, Kunio Kawanishi, Masataka Ueda, Yuki Kajio, Kazuki Kobayashi, Nobuhiro Kanazawa, Mayumi Takahashi-Kobayashi, Joichi Usui, Masaki Baba and 3 more

Abstract readComparative Study
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In one paragraph

Article in Nephrology (Carlton, Vic.), 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.

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4 · The record

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5 · Who and what money

Authors and funding

13 authors.

Taihei SuzukiDepartment of Nephrology, Showa Medical University Graduate School of Medicine, Tokyo, Japan.ORCID https://orcid.org/0000-0002-9531-7814
Kang DedongDepartment of Anatomy, Showa Medical University Graduate School of Medicine, Tokyo, Japan.ORCID https://orcid.org/0000-0002-2474-8609
Kunio KawanishiDepartment of Anatomy, Showa Medical University Graduate School of Medicine, Tokyo, Japan.ORCID https://orcid.org/0000-0003-3502-3467
Masataka UedaDepartment of Nephrology, Showa Medical University Graduate School of Medicine, Tokyo, Japan.ORCID https://orcid.org/0009-0003-7739-6648
Yuki KajioDepartment of Nephrology, Showa Medical University Graduate School of Medicine, Tokyo, Japan.
Kazuki KobayashiDepartment of Nephrology, Showa Medical University Graduate School of Medicine, Tokyo, Japan.
Nobuhiro KanazawaDepartment of Nephrology, Showa Medical University Graduate School of Medicine, Tokyo, Japan.ORCID https://orcid.org/0000-0001-6111-8027
Mayumi Takahashi-KobayashiDepartment of Nephrology, Institute of Medicine, University of Tsukuba, Ibaraki, Japan.ORCID https://orcid.org/0000-0001-8581-0464
Joichi UsuiDepartment of Nephrology, Institute of Medicine, University of Tsukuba, Ibaraki, Japan.
Masaki BabaDepartment of Anatomy, Showa Medical University Graduate School of Medicine, Tokyo, Japan.ORCID https://orcid.org/0009-0002-9566-184X
Hirokazu HondaDepartment of Nephrology, Showa Medical University Graduate School of Medicine, Tokyo, Japan.
Kazuho HondaDepartment of Diagnostic Pathology, Showa Medical University Graduate School of Medicine, Tokyo, Japan.ORCID https://orcid.org/0000-0003-4179-8832
Masayuki IyodaDepartment of Nephrology, Showa Medical University Graduate School of Medicine, Tokyo, Japan.ORCID https://orcid.org/0000-0002-1153-3000

Funding

Japan Society for the Promotion of Science (JSPS) 23K06451Japan Society for the Promotion of Science (JSPS) 26K11171
6 · The paper itself

Abstract

aimPrimary membranous nephropathy (MN) is classified into antigen-defined subtypes, most commonly M-type phospholipase A2 receptor (PLA2R)-associated MN and neural epidermal growth factor-like 1 (NELL1)-associated MN. Whether complement activation differs between these subtypes remains unclear. This study compared their clinicopathological features and complement-related protein expression.

methodsWe retrospectively compared PLA2R-associated MN (n = 17) and NELL1-associated MN (n = 9), including five additional NELL1-associated MN cases from an external institution. Glomerular C3 and C4d deposition were assessed by immunostaining, with quantitative C4d analysis using digital pathology. Complement-related proteins were additionally evaluated by laser microdissection-assisted data-dependent acquisition mass spectrometry in cases with available proteomic data.

resultsPatients with NELL1-associated MN were older and showed greater interstitial fibrosis and tubular atrophy than those with PLA2R-associated MN. Glomerular IgG4 and C3 deposition were significantly lower in NELL1-associated MN. Quantitative analysis demonstrated lower glomerular C4d deposition in NELL1-associated MN at both the glomerulus and patient levels, whereas C4d intensity was not significantly correlated with serum anti-PLA2R antibody titres. In the proteomic analysis, C3, C5 and complement factor H were numerically more abundant in PLA2R-associated MN than in NELL1-associated MN, although these differences were not statistically significant.

conclusionNELL1-associated MN and PLA2R-associated MN differ not only in clinical and histological features but also in glomerular complement deposition. Reduced C3 and C4d deposition in NELL1-associated MN suggests less prominent glomerular complement activation than in PLA2R-associated MN, supporting biological heterogeneity among antigen-defined MN subtypes.

Indexed as

Calcium-Binding ProteinsComplement ActivationGlomerulonephritis, MembranousKidney GlomerulusNerve Tissue ProteinsProteomicsReceptors, Phospholipase A2AdultAgedComplement C3Complement C4bFemaleHumansMaleMiddle AgedPeptide FragmentsC3 protein, humanCalcium-Binding ProteinsComplement C3Complement C4bcomplement C4dNELL1 protein, humanNerve Tissue ProteinsPeptide FragmentsPLA2R1 protein, humanReceptors, Phospholipase A2complement system proteinshuman NELL1 proteinmembranous glomerulonephritisnephrotic syndromephospholipase A2 receptors

Identifiers

PMID42847324

What Socratic holds

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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.