Evidence map›Paper›PMID 42675453›Full record

ArticleNephrology (Carlton, Vic.)2026

Successful Control of Late-Onset Nephrotic Syndrome in FN1-Associated Fibronectin Glomerulopathy: A 17-Year Clinical Course.

Nobuhiro Kanazawa, Masayuki Iyoda, Kazuki Abe, Taihei Suzuki, Yoko Shirai, Kenichiro Miura, Kazuho Honda, Hirokazu Honda

Abstract readCase Reports
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.

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

8 authors.

Nobuhiro KanazawaDepartment of Nephrology, Showa Medical University Graduate School of Medicine, Shinagawa, Japan.ORCID https://orcid.org/0000-0001-6111-8027
Masayuki IyodaDepartment of Nephrology, Showa Medical University Graduate School of Medicine, Shinagawa, Japan.ORCID https://orcid.org/0000-0002-1153-3000
Kazuki AbeDepartment of Nephrology, Showa Medical University Graduate School of Medicine, Shinagawa, Japan.
Taihei SuzukiDepartment of Nephrology, Showa Medical University Graduate School of Medicine, Shinagawa, Japan.ORCID https://orcid.org/0000-0002-9531-7814
Yoko ShiraiDepartment of Pediatric Nephrology, Tokyo Women's Medical University, Shinjuku, Japan.ORCID https://orcid.org/0000-0003-3734-4766
Kenichiro MiuraDepartment of Pediatric Nephrology, Tokyo Women's Medical University, Shinjuku, Japan.ORCID https://orcid.org/0000-0002-9483-8482
Kazuho HondaDepartment of Diagnostic Pathology, Showa Medical University Graduate School of Medicine, Shinagawa, Japan.ORCID https://orcid.org/0000-0003-4179-8832
Hirokazu HondaDepartment of Nephrology, Showa Medical University Graduate School of Medicine, Shinagawa, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fibronectin glomerulopathy (FNG) is a rare renal disorder characterized by excessive glomerular fibronectin deposition, often associated with variants in the fibronectin 1 (FN1) gene. Clinically, FNG presents with proteinuria, hematuria, and hypertension, and may progress to end-stage kidney disease. However, its long-term clinical course and optimal management remain incompletely defined. We report a sporadic case of FNG in a 26-year-old woman carrying an FN1 variant, c.2918A > G (NM_212482.4). Seventeen years after initial detection of proteinuria, she developed nephrotic syndrome with generalized edema. Supportive therapy, including renin-angiotensin system inhibitors and diuretics, was insufficient, and prednisolone and cyclosporine A were initiated for management of nephrotic syndrome. The patient subsequently achieved partial remission, with urinary protein decreasing to < 1 g/gCr and no major adverse events. During tapering of immunosuppression, a sodium-glucose cotransporter 2 (SGLT2) inhibitor was added as adjunct therapy. This case suggests a potential role for immunosuppressive therapy in management of late-onset nephrotic syndrome associated with FNG, with SGLT2 inhibition potentially contributing to maintenance of remission.

Indexed as

CyclosporineFibronectinsImmunosuppressive AgentsNephrotic SyndromeAdultFemaleGenetic Predisposition to DiseaseGlomerulonephritis, MembranoproliferativeHumansMutationPrednisoloneRemission InductionTime FactorsTreatment OutcomeCyclosporineFibronectinsFN1 protein, humanImmunosuppressive AgentsPrednisolonecyclosporine Afibronectin glomerulopathyFN1 mutationnephrotic syndromeprednisoloneSGLT2 inhibitor

Identifiers

PMID42675453
PMCPMC13529923

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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.