Evidence map›Paper›PMID 28951873›Full record

ReviewBioMed research international2017

Multiple Targets for Novel Therapy of FSGS Associated with Circulating Permeability Factor.

Virginia J Savin, Mukut Sharma, Jianping Zhou, David Genochi, Ram Sharma, Tarak Srivastava, Amna Ilahe, Pooja Budhiraja, Aditi Gupta, Ellen T McCarthy

Open access · hybridAbstract readReview
In one paragraph

Review in BioMed research international, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

14 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
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  4. CRLF1 and CLCF1 in Development, Health and Disease.International journal of molecular sciences · 2022
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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

10 authors at 3 institutions in 1 country.

Virginia J SavinRenal Research Laboratory, Research and Development, MBRF and Kansas City VA Medical Center, Kansas City, MO, USA.ORCID 0000-0002-9454-5217
Mukut SharmaRenal Research Laboratory, Research and Development, MBRF and Kansas City VA Medical Center, Kansas City, MO, USA.
Jianping ZhouRenal Research Laboratory, Research and Development, MBRF and Kansas City VA Medical Center, Kansas City, MO, USA.
David GenochiRenal Research Laboratory, Research and Development, MBRF and Kansas City VA Medical Center, Kansas City, MO, USA.
Ram SharmaRenal Research Laboratory, Research and Development, MBRF and Kansas City VA Medical Center, Kansas City, MO, USA.ORCID 0000-0002-7485-1356
Tarak SrivastavaRenal Research Laboratory, Research and Development, MBRF and Kansas City VA Medical Center, Kansas City, MO, USA.ORCID 0000-0002-8654-0627
Amna IlaheKidney Institute, University of Kansas Medical Center, Kansas City, KS, USA.
Pooja BudhirajaKidney Institute, University of Kansas Medical Center, Kansas City, KS, USA.
Aditi GuptaKidney Institute, University of Kansas Medical Center, Kansas City, KS, USA.
Ellen T McCarthyKidney Institute, University of Kansas Medical Center, Kansas City, KS, USA.
University of Kansas Medical Center · USKansas City VA Medical Center · USChildren's Mercy Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A plasma component is responsible for altered glomerular permeability in patients with focal segmental glomerulosclerosis. Evidence includes recurrence after renal transplantation, remission after plasmapheresis, proteinuria in infants of affected mothers, transfer of proteinuria to experimental animals, and impaired glomerular permeability after exposure to patient plasma. Therapy may include decreasing synthesis of the injurious agent, removing or blocking its interaction with cells, or blocking signaling or enhancing cell defenses to restore the permeability barrier and prevent progression. Agents that may prevent the synthesis of the permeability factor include cytotoxic agents or aggressive chemotherapy. Extracorporeal therapies include plasmapheresis, immunoadsorption with protein A or anti-immunoglobulin, or lipopheresis. Oral or intravenous galactose also decreases

Indexed as

AnimalsCalcineurin InhibitorsCytokinesGlomerulosclerosis, Focal SegmentalHumansJanus Kinase 2Kidney GlomerulusPermeabilityReceptors, CytokineCalcineurin Inhibitorscardiotrophin-like cytokineCytokinesJanus Kinase 2Receptors, Cytokine

Identifiers

PMID28951873
PMCPMC5603123
OpenAlexW2744767605

What OpenQuestion holds

Textmetadata
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.