Evidence map›Paper›PMID 25704355›Full record

ReviewAdvances in chronic kidney disease2015

Novel therapies for FSGS: preclinical and clinical studies.

Laura Malaga-Dieguez, Diana Bouhassira, Debbie Gipson, Howard Trachtman

Registry-linked trialOpen access · bronzeAbstract readReview
In one paragraph

Review in Advances in chronic kidney disease, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03939741 (Evaluation of Therapeutic Potential of Stromal Vascular Fraction), which is not on this map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
4.5field-weighted citation impact, top 5% 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.

NCT03939741 phase1 / phase2unknown statusnot on this mapstarted 2019, after this paper: background citation

Evaluation of Therapeutic Potential of Stromal Vascular Fraction (Autologous Adipose Derived Mesenchymal Stem Cell) Based Treatment for Chronic Kidney Disease

TypeinterventionalSponsorBangladesh Laser & Cell Surgery Institute & HospitalRan2019 to 2025Enrolled31ConditionsChronic Kidney DiseasesArmsSVF Containg Autologous Non Expanded ADSC
3 · Its place in the literature

Who cites it

18 citing papers in PubMed, 37 citations in OpenAlex.

  1. Review
  2. Article
  3. Quantification of Glomerular Structural Lesions: Associations With Clinical Outcomes and Transcriptomic Profiles in Nephrotic Syndrome.American journal of kidney diseases : the official journal of the National Kidney Foundation · 2022
    Observational
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Review
  12. Noninvasive diagnosis of chronic kidney diseases using urinary proteome analysis.Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association · 2017
    Article
  13. Review
  14. Optimal management of primary focal segmental glomerulosclerosis in adults.International journal of nephrology and renovascular disease · 2017
    Review
  15. Review
  16. Article
  17. Review
  18. 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

4 authors at 1 institution in 1 country.

Laura Malaga-DieguezDivision of Nephrology, Department of Pediatrics, CS Mott Children's Hospital; and NYU Langone Medical Center, New York, NY.
Diana BouhassiraDivision of Nephrology, Department of Pediatrics, CS Mott Children's Hospital; and NYU Langone Medical Center, New York, NY.
Debbie GipsonDivision of Nephrology, Department of Pediatrics, CS Mott Children's Hospital; and NYU Langone Medical Center, New York, NY.
Howard TrachtmanDivision of Nephrology, Department of Pediatrics, CS Mott Children's Hospital; and NYU Langone Medical Center, New York, NY. Electronic address: howard.trachtman@nyumc.org.
NYU Langone Health · US

Funding

Novel Therapies for Resistant FSGSR33DK070341 · NIDDK · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI TRACHTMAN, HOWARD · 2008 to 2011
$1.5M
Novel Therapies for Resistant FSGSR21DK070341 · NIDDK · FEINSTEIN INSTITUTE FOR MEDICAL RESEARCH · PI TRACHTMAN, HOWARD · 2005 to 2006
$435k
NIDDK NIH HHS DK70341NIDDK NIH HHS R21 DK070341NIDDK NIH HHS R33 DK070341
6 · The paper itself

Abstract

Focal segmental glomerulosclerosis (FSGS) is a rare but important cause of end-stage kidney disease in children and adults. Current therapy, consisting of corticosteroids and calcineurin inhibitors, fails to achieve a sustained remission in most patients. Therefore, there is a pressing need to develop new treatments for this glomerulopathy. Traditional approaches have focused on agents that modulate the immune system. In this review, we summarize preclinical and clinical data with newer agents that may ameliorate FSGS. We focus on drugs that inhibit immune injury or inflammation, such as abatacept, rituximab, adalimumab, and stem cells. The potential of agents that block the glomerular action of circulating permeability factors such as soluble urokinase receptor is reviewed. Finally, because fibrosis represents the final common pathway of glomerular damage in FSGS, the experience with a wide range of antifibrotic agents is presented. Despite extensive research on the podocyte dysfunction in the pathogenesis of FSGS, there are few agents that directly target podocyte structure or viability. We conclude that FSGS is a heterogeneous disorder and that intensified translational research is vital to improve our understanding of distinct subtypes that have a defined prognosis and predictable response to targeted therapeutic interventions.

Indexed as

Glomerulosclerosis, Focal SegmentalKidney Failure, ChronicAdultAntibodies, Monoclonal, HumanizedChildDisease ProgressionFibrosisHumansImmunomodulationPodocytesTherapies, InvestigationalAntibodies, Monoclonal, HumanizedCirculating factorsFibrosisFSGSImmune modulatorsInflammation

Identifiers

PMID25704355
PMCPMC7409581
OpenAlexW1965482229

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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.