Evidence map›Paper›PMID 31705303›Full record

ArticleCEN case reports2020

Membranous nephropathy associated with thrombospondin type-1 domain-containing 7A (THSD7A) in an adult woman with eosinophilia.

Sayuri Shirai, Shin'ichi Akiyama, Atsuko Kamijo-Ikemori, Tomo Suzuki, Daisuke Ichikawa, Junki Koike, Kenjiro Kimura, Yugo Shibagaki

Open access · hybridAbstract readCase Reports
In one paragraph

Article in CEN case reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 36% of its field
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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
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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 at 3 institutions in 1 country.

Sayuri ShiraiDivision of Nephrology and Hypertension, Department of Internal Medicine, St. Marianna University School of Medicine Yokohama City Seibu Hospital, 1197-1 Yasashi-cho, Asahi-ku, Yokohama, 241-0811, Japan. sirababu@marianna-u.ac.jp.ORCID 0000-0002-0965-4997
Shin'ichi AkiyamaDivision of Nephrology, Department of Internal Medicine, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya, 466-8550, Japan.
Atsuko Kamijo-IkemoriDepartment of Anatomy, St. Marianna University School of Medicine, 2-16-1 Sugao, Miyamae-ku, Kawasaki, 216-8511, Japan.
Tomo SuzukiDepartment of Nephrology, Kameda Medical Center, 929 Higashicho, Kamogawa, 296-8602, Japan.
Daisuke IchikawaDivision of Nephrology and Hypertension, Department of Internal Medicine, St. Marianna University School of Medicine, 2-16-1 Sugao, Miyamae-ku, Kawasaki, 216-8511, Japan.
Junki KoikeDepartment of Diagnostic Pathology, St. Marianna University School of Medicine, 2-16-1 Sugao, Miyamae-ku, Kawasaki, 216-8511, Japan.
Kenjiro KimuraDivision of Nephrology, Department of Internal Medicine, Tokyo Takanawa Hospital, 3-10-11 Takanawa, Minato-ku, Tokyo, 108-8606, Japan.
Yugo ShibagakiDivision of Nephrology and Hypertension, Department of Internal Medicine, St. Marianna University School of Medicine, 2-16-1 Sugao, Miyamae-ku, Kawasaki, 216-8511, Japan.
St. Marianna University School of Medicine · JPKameda Medical Center · JPNagoya University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A 30-year-old woman on steroid therapy for eosinophilia presented with nephrotic syndrome during steroid tapering. She was diagnosed with membranous nephropathy (MN) stage II-III (positive for IgG1 and IgG4) by renal biopsy. There was no evidence of secondary MN. Her urinary protein level was controlled to 0.5 g/day or less, and her eosinophil count in white blood cell differential was stabilized at less than 10% without increasing the steroid dosage. The renal specimen did not show any enhanced granular expression of PLA2R along the glomerular basement membrane, and PLA2R was not detected in the patient's serum. On retrospective analysis, enhanced granular staining for thrombospondin type-1 domain-containing 7A (THSD7A) in the glomeruli was detected in the biopsy, and anti-THSD7A IgG was detected in the serum using a commercial indirect immunofluorescence test (IFT). Based on these, the case was considered as THSD7A-associated MN with comorbid eosinophilia. The causal relationship between THSD7A-related MN and eosinophilia was unclear. However, a few cases of THSD7A-associated MN with eosinophilia have been reported, and further clarification on the relationship between THSD7A-related MN and eosinophilia is warranted.

Indexed as

Adrenal Cortex HormonesAdultAutoantibodiesBiopsyEosinophiliaFemaleFluorescent Antibody Technique, IndirectGlomerular Basement MembraneGlomerulonephritis, MembranousHumansImmunoglobulin GKidneyKidney GlomerulusNephrotic SyndromeReceptors, Phospholipase A2Retrospective StudiesAdrenal Cortex HormonesAutoantibodiesImmunoglobulin GPLA2R1 protein, humanReceptors, Phospholipase A2ThrombospondinsTHSD7A protein, humanEosinophiliaMembranous nephropathyPLA2RTHSD7A

Identifiers

PMID31705303
PMCPMC6990191
OpenAlexW2983975139

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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 OpenQuestion graph.