Evidence map›Paper›PMID 26576418›Full record

ReviewBioMed research international2015

Antiphospholipase A2 Receptor Autoantibodies: A Step Forward in the Management of Primary Membranous Nephropathy.

Bogdan Obrisca, Gener Ismail, Roxana Jurubita, Catalin Baston, Andreea Andronesi, Gabriel Mircescu

Open access · hybridAbstract readReview
In one paragraph

Review in BioMed research international, 2015. 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
1.4field-weighted citation impact, top 20% 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, 31 citations in OpenAlex.

  1. Review
  2. Article
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  11. Review
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  14. Viral-Associated GN: Hepatitis B and Other Viral Infections.Clinical journal of the American Society of Nephrology : CJASN · 2017
    Review
  15. Observational
  16. Article
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

6 authors at 2 institutions in 1 country.

Bogdan Obrisca"Carol Davila" University of Medicine and Pharmacy, Dionisie Lupu Street No. 37, District 1, 022328 Bucharest, Romania.
Gener Ismail"Carol Davila" University of Medicine and Pharmacy, Dionisie Lupu Street No. 37, District 1, 022328 Bucharest, Romania ; Center of Internal Medicine-Nephrology, Fundeni Clinical Institute, 258 Fundeni Street, District 2, 022328 Bucharest, Romania.
Roxana Jurubita"Carol Davila" University of Medicine and Pharmacy, Dionisie Lupu Street No. 37, District 1, 022328 Bucharest, Romania ; Center of Internal Medicine-Nephrology, Fundeni Clinical Institute, 258 Fundeni Street, District 2, 022328 Bucharest, Romania.
Catalin Baston"Carol Davila" University of Medicine and Pharmacy, Dionisie Lupu Street No. 37, District 1, 022328 Bucharest, Romania ; Center for Uronephrology and Renal Transplantation, Fundeni Clinical Institute, 258 Fundeni Street, District 2, 022328 Bucharest, Romania.
Andreea Andronesi"Carol Davila" University of Medicine and Pharmacy, Dionisie Lupu Street No. 37, District 1, 022328 Bucharest, Romania ; Center of Internal Medicine-Nephrology, Fundeni Clinical Institute, 258 Fundeni Street, District 2, 022328 Bucharest, Romania.
Gabriel Mircescu"Carol Davila" University of Medicine and Pharmacy, Dionisie Lupu Street No. 37, District 1, 022328 Bucharest, Romania ; "Dr. Carol Davila" Teaching Hospital of Nephrology, Calea Grivitei Street No. 4, District 1, 010731 Bucharest, Romania.
Carol Davila University of Medicine and Pharmacy · ROInstitutul Clinic Fundeni · RO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Since the identification of PLA2R (M-type phospholipase A2 receptor) as the first human antigenic target in primary membranous nephropathy (MN), perpetual progress has been made in understanding the pathogenesis of this disease. Accumulating clinical data support a pathogenic role for the anti-PLA2R antibodies (PLA2R ABs), but confirmation in an animal model is still lacking. However, PLA2R ABs were related to disease activity and outcome, as well as to response therapy. Accordingly, PLA2R ABs assay seems to be promising tool not only to diagnose MN but also to predict the course of the disease and could open the way to personalize therapy. Nevertheless, validation of a universal assay with high precision and definition of cut-off levels, followed by larger studies with a prolonged follow-up period, are needed to confirm these prospects.

Indexed as

AnimalsAntibodies, MonoclonalAutoantibodiesEvidence-Based MedicineGlomerulonephritis, MembranousHumansMolecular Targeted TherapyReceptors, Phospholipase A2Antibodies, MonoclonalAutoantibodiesReceptors, Phospholipase A2

Identifiers

PMID26576418
PMCPMC4630372
OpenAlexW2102768836

What OpenQuestion holds

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LicenceCC BY
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.