Evidence map›Paper›PMID 27085376›Full record

ReviewAmerican journal of kidney diseases : the official journal of the National Kidney Foundation2016

Membranous Nephropathy: A Journey From Bench to Bedside.

Jean M Francis, Laurence H Beck, David J Salant

Open access · greenAbstract readReview
In one paragraph

Review in American journal of kidney diseases : the official journal of the National Kidney Foundation, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed, 2 pooled it
13.5field-weighted citation impact, top 1% 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

66 citing papers in PubMed, 2 syntheses or guidelines pooled it, 147 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Review
  5. Membranous Nephropathy: Antigenic Landscape and a Novel Pathogenetic Model.International journal of molecular sciences · 2026
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  19. Stroke associated with primary membranous nephropathy in a young adult: Case reportBiomedica : revista del Instituto Nacional de Salud · 2024
    Article
  20. Article

6 more citing papers are in PubMed but not listed here.

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

3 authors at 1 institution in 1 country.

Jean M FrancisDepartment of Medicine, Boston University Medical Center, Boston, MA.
Laurence H BeckDepartment of Medicine, Boston University Medical Center, Boston, MA.
David J SalantDepartment of Medicine, Boston University Medical Center, Boston, MA. Electronic address: djsalant@bu.edu.
Boston University · US

Funding

RESEARCH TRAINING IN NEPHROLOGYT32DK007053 · NIDDK · BOSTON UNIVERSITY MEDICAL CAMPUS · PI RIFKIN, IAN R · 1986 to 2019
$3.9M
Role of PLA2R and anti-PLA2R in idiopathic membranous nephropathyR01DK090029 · NIDDK · BOSTON MEDICAL CENTER · PI SALANT, DAVID J · 2011 to 2015
$1.9M
Redefining membranous nephropathy by autoantibody-specific subclassificationR01DK097053 · NIDDK · BOSTON MEDICAL CENTER · PI BECK, LAURENCE H · 2013 to 2017
$1.7M
NIDDK NIH HHS R01 DK090029NIDDK NIH HHS R01 DK097053NIDDK NIH HHS T32 DK007053
6 · The paper itself

Abstract

Lessons from an animal model that faithfully resembles human membranous nephropathy (MN) have informed our understanding of the pathogenesis of this organ-specific autoimmune disease and common cause of nephrotic syndrome. After it was established that the subepithelial immune deposits that characterize experimental MN form in situ when circulating antibodies bind to an intrinsic podocyte antigen, it was merely a matter of time before the human antigen was identified. The M-type phospholipase A2 receptor 1 (PLA2R) represents the major target antigen in primary MN, and thrombospondin type 1 domain-containing 7A (THSD7A) was more recently identified as a minor antigen. Serologic tests for anti-PLA2R and kidney biopsy specimen staining for PLA2R show >90% specificity and 70% to 80% sensitivity for the diagnosis of primary MN in most populations. The assays distinguish most cases of primary MN from MN associated with other systemic diseases, and sequential anti-PLA2R titers are useful to monitor treatment response. A positive pretransplantation test result for anti-PLA2R is also helpful for predicting the risk for posttransplantation recurrence. Identification of target epitopes within PLA2R and the genetic association of primary MN with class II major histocompatibility and PLA2R1 variants are 2 additional examples of our evolving understanding of this disease.

Indexed as

Glomerulonephritis, MembranousAutoantibodiesBiomedical ResearchHumansKidneyPrognosisReceptors, Phospholipase A2RecurrenceAutoantibodiesPLA2R1 protein, humanReceptors, Phospholipase A2class II major histocompatibilityepitopegenetic polymorphismsMembranous nephropathy (MN)M-type phospholipase A(2) receptor 1 (PLA(2)R)nephrotic syndromeorgan-specific autoimmunityPLA2R1post-transplant recurrent diseasethrombospondin type 1 domain-containing 7A (THSD7A)

Identifiers

PMID27085376
PMCPMC4921260
OpenAlexW2338867472

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.