Evidence map›Paper›PMID 32001064›Full record

ArticleKidney international2020

Serum amyloid P deposition is a sensitive and specific feature of membranous-like glomerulopathy with masked IgG kappa deposits.

Christopher P Larsen, Shree G Sharma, Tiffany N Caza, Daniel J Kenan, Aaron J Storey, Ricky D Edmondson, Christian Herzog, John M Arthur

Open access · hybridAbstract read
In one paragraph

Article in Kidney international, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

16 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
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  8. A rare cause of subnephrotic proteinuria in an adolescent: Answers.Pediatric nephrology (Berlin, Germany) · 2021
    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 2 institutions in 1 country.

Christopher P LarsenArkana Laboratories, Little Rock, Arkansas, USA. Electronic address: Chris.larsen@arkanalabs.com.
Shree G SharmaArkana Laboratories, Little Rock, Arkansas, USA.
Tiffany N CazaArkana Laboratories, Little Rock, Arkansas, USA.
Daniel J KenanArkana Laboratories, Little Rock, Arkansas, USA.
Aaron J StoreyUniversity of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
Ricky D EdmondsonUniversity of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
Christian HerzogUniversity of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
John M ArthurUniversity of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
Arkana Laboratories · USUniversity of Arkansas for Medical Sciences · US

Funding

J. NRSA TrainingTL1TR003109 · NCATS · UNIV OF ARKANSAS FOR MED SCIS · PI SEXTON, KEVIN WAYNE · 2019 to 2023
$1.5M
NCATS NIH HHS TL1 TR003109
6 · The paper itself

Abstract

Membranous-like glomerulopathy with masked IgG kappa deposits (MGMID) is a recently described pattern of glomerulonephritis with a unique histopathology. The pattern is characterized by subepithelial and/or mesangial immune deposits that are "masked", to immunoglobulin staining by routine immunofluorescence but strongly stain for IgG and kappa light chain after protease digestion. Patients with this pattern of glomerulonephritis are most commonly young females presenting with proteinuria and a vague history of autoimmune disease such as low titer antinuclear antibodies. Here we compared the mass spectrometry profile of laser capture microdissected glomeruli from nine MGMID renal biopsies with eight biopsies showing other patterns of membranous glomerulopathy. The protein most significantly increased in MGMID was serum amyloid P. Immunostaining showed serum amyloid P colocalized with IgG in the glomeruli of MGMID but not with PLA2R-associated membranous glomerulopathy. Serum amyloid P was positive in the glomeruli of all 32 MGMID biopsies but negative in biopsies of other types of membranous glomerulopathies such as those associated with PLA2R and THSD7A. There were four biopsies with glomerular serum amyloid P staining among the 173 biopsies that did not fulfill criteria for MGMID or amyloidosis. All four of these biopsies with positive serum amyloid P staining had a membranous pattern of glomerulopathy with IgG kappa deposits that only differed from MGMID by the lack of "masking". Thus, positive staining within glomerular deposits for serum amyloid P identifies a unique form of glomerulonephritis likely sharing a common pathophysiologic mechanism of disease.

Indexed as

GlomerulonephritisGlomerulonephritis, MembranousKidney DiseasesFemaleHumansImmunoglobulin GKidney GlomerulusImmunoglobulin Gglomerulonephritismasked depositsmass spectrometrymembranous-like glomerulopathysubepithelial deposits

Identifiers

PMID32001064
PMCPMC7869973
OpenAlexW2983984259

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

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.