Evidence map›Paper›PMID 23820815›Full record

ReviewNature reviews. Nephrology2013

Treatment of idiopathic membranous nephropathy.

Julia M Hofstra, Fernando C Fervenza, Jack F M Wetzels

Registry-linked trialAbstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Nephrology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03549663 (Random, Open, Control and Monocentric Clinical Research on Tacrolimus Monotherapy for Idiopathic Membranous Nephropathy), which is not on this map. Cited by 60 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed, 2 pooled it
7.1field-weighted citation impact, top 2% 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.

NCT03549663 naunknown statusnot on this mapstarted 2018, after this paper: background citation

Random, Open, Control and Monocentric Clinical Research on Tacrolimus Monotherapy for Idiopathic Membranous Nephropathy (IMN)

TypeinterventionalSponsorXinhua Hospital, Shanghai Jiao Tong University School of MedicineRan2018 to 2021Enrolled108ConditionsIdiopathic Membranous NephropathyArmsTacrolimus, Prednisone
3 · Its place in the literature

Who cites it

60 citing papers in PubMed, 2 syntheses or guidelines pooled it, 120 citations in OpenAlex.

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  5. Rituximab for Severe Membranous Nephropathy: A 6-Month Trial with Extended Follow-Up.Journal of the American Society of Nephrology : JASN · 2017
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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

3 authors at 2 institutions in 2 countries.

Julia M HofstraDepartment of Nephrology, Radboud University Nijmegen Medical Center, PO Box 9101, 6500 HB, Nijmegen, The Netherlands. j.hofstra@nier.umcn.nl
Fernando C Fervenza
Jack F M Wetzels
Radboud University Nijmegen · NLMayo Clinic · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immunosuppressive treatment of patients with idiopathic membranous nephropathy (iMN) is heavily debated. The controversy is mainly related to the toxicity of the therapy and the variable natural course of the disease-spontaneous remission occurs in 40-50% of patients. The 2012 Kidney Disease: Improving Global Outcomes (KDIGO) Clinical Practice Guideline for Glomerulonephritis provides guidance for the treatment of iMN. The guideline suggests that immunosuppressive therapy should be restricted to patients with nephrotic syndrome and persistent proteinuria, deteriorating renal function or severe symptoms. Alkylating agents are the preferred therapy because of their proven efficacy in preventing end-stage renal disease. Calcineurin inhibitors can be used as an alternative although efficacy data on hard renal end points are limited. In this Review, we summarize the KDIGO guideline and address remaining areas of uncertainty. Better risk prediction is needed to identify patients who will benefit from immunosuppressive therapy, and the optimal timing and duration of this therapy is unknown because most of the randomized controlled trials were performed in low-risk or medium-risk patients. Alternative therapies, directed at B cells, are under study. The discovery of anti-M type phospholipase A2 receptor-antibodies is a major breakthrough and we envisage that in the near future, antibody-driven therapy will enable more individualized treatment of patients with iMN.

Indexed as

Adrenocorticotropic HormoneAlgorithmsAlkylating AgentsAntibodiesAntibodies, Monoclonal, Murine-DerivedAnticoagulantsAntimetabolitesCalcineurin InhibitorsGlomerulonephritis, MembranousGlucocorticoidsHumansHydroxymethylglutaryl-CoA Reductase InhibitorsImmunologic FactorsImmunosuppressive AgentsPractice Guidelines as TopicPrognosisAdrenocorticotropic HormoneAlkylating AgentsAntibodiesAntibodies, Monoclonal, Murine-DerivedAnticoagulantsAntimetabolitesCalcineurin InhibitorsGlucocorticoidsHydroxymethylglutaryl-CoA Reductase InhibitorsImmunologic FactorsImmunosuppressive AgentsPLA2R1 protein, humanReceptors, Phospholipase A2Rituximab

Identifiers

PMID23820815
OpenAlexW2115928661

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.