Evidence map›Paper›PMID 27672219›Full record

ArticleClinical journal of the American Society of Nephrology : CJASN2016

Glomerular Diseases: Registries and Clinical Trials.

Marva M Moxey-Mims, Michael F Flessner, Lawrence Holzman, Frederick Kaskel, John R Sedor, William E Smoyer, Aliza M Thompson, Lynne Yao

Abstract read
In one paragraph

Article in Clinical journal of the American Society of Nephrology : CJASN, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

10 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Review
  4. Biomimetic models of the glomerulus.Nature reviews. Nephrology · 2022
    Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. 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

8 authors.

Marva M Moxey-MimsDue to the number of contributing authors, the affiliations are provided in the Supplemental Material .
Michael F Flessner
Lawrence Holzman
Frederick Kaskel
John R Sedor
William E Smoyer
Aliza M Thompson
Lynne Yao

Funding

Slit Diaphragm and Actin DynamicsR01DK080751 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI HOLZMAN, LAWRENCE B. · 2008 to 2017
$3.6M
NIDDK NIH HHS R01 DK080751
6 · The paper itself

Abstract

Nephrology has conducted few high-quality clinical trials, and the trials that have been conducted have not resulted in the approval of new treatments for primary or inflammatory glomerular diseases. There are overarching process issues that affect the conduct of all clinical trials, but there are also some specialty-specific issues. Within nephrology, primary glomerular diseases are rare, making adequate recruitment for meaningful trials difficult. Nephrologists need better ways, beyond histopathology, to phenotype patients with glomerular diseases and stratify the risk for progression to ESRD. Rigorous trial design is needed for the testing of new therapies, where most patients with glomerular diseases are offered the opportunity to enroll in a clinical trial if standard therapies have failed or are lacking. Training programs to develop a core group of kidney specialists with expertise in the design and implementation of clinical trials are also needed. Registries of patients with glomerular disease and observational studies can aid in the ability to determine realistic estimates of disease prevalence and inform trial design through a better understanding of the natural history of disease. Some proposed changes to the Common Rule, the federal regulations governing the ethical conduct of research involving humans, and the emerging use of electronic health records may facilitate the efficiency of initiating multicenter clinical trials. Collaborations among academia, government scientific and regulatory agencies, industry, foundations, and patient advocacy groups can accelerate therapeutic development for these complex diseases.

Indexed as

NephrologyRegistriesBiomarkersEndpoint DeterminationGlomerulonephritis, MembranousGlomerulosclerosis, Focal SegmentalHumansKidney DiseasesNational Institute of Diabetes and Digestive and Kidney Diseases (U.S.)Nephrosis, LipoidPediatricsPublic-Private Sector PartnershipsRandomized Controlled Trials as TopicResearch DesignUnited StatesBiomarkersChronicclinical trialCooperative BehaviorElectronic Health RecordsFoundationsglomerular diseaseGovernmentHumanskidneyKidney FailureKidney GlomerulusnephrologyPatient AdvocacyPhenotypePrevalenceregistriesRegistriesResearchScienceSpecialization

Identifiers

PMID27672219
PMCPMC5142054

What OpenQuestion holds

Textmetadata
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.