Evidence map›Paper›PMID 36817288›Full record

ArticleGlomerular diseases2022

Gluten-Free Diet in Childhood Difficult-to-Treat Nephrotic Syndrome: A Pilot Feasibility Study.

Tarak Srivastava, Katherine M Dell, Kevin V Lemley, Debbie S Gipson, Frederick J Kaskel, Kevin Edward Meyers, Christian Faul, Ayelet Goldhaber, LauraJane Pehrson, Howard Trachtman

Open access · goldAbstract read
In one paragraph

Article in Glomerular diseases, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 45% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. 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

10 authors at 8 institutions in 1 country.

Tarak SrivastavaChildren's Mercy Hospital, Kansas City, Missouri, USA.
Katherine M DellCleveland Clinic-Children's, Case Western Reserve University, Cleveland, Ohio, USA.
Kevin V LemleyChildren's Hospital Los Angeles, Los Angeles, California, USA.
Debbie S GipsonC S Mott Hospital, Ann Arbor, Michigan, USA.
Frederick J KaskelChilden's Hospital at Montefiore, Bronx, New York, USA.
Kevin Edward MeyersChildren's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
Christian FaulUniversty of Alabama-Birmingham, Birmingham, Alabama, USA.
Ayelet GoldhaberHassenfeld Children's Hospital, NYU Grossman School of Medicine, New York, New York, USA.
LauraJane PehrsonHassenfeld Children's Hospital, NYU Grossman School of Medicine, New York, New York, USA.
Howard TrachtmanHassenfeld Children's Hospital, NYU Grossman School of Medicine, New York, New York, USA.
New York University · USChildren's Hospital at Montefiore · USChildren's Hospital of Los Angeles · USChildren's Hospital of Philadelphia · USChildren's Mercy Hospital · USCleveland Clinic · USC. S. Mott Children's Hospital · USUniversity of Alabama at Birmingham · US

Funding

Hyperphosphatemia Contributes to Systemic Inflammation and Anemia in Chronic Kidney DiseaseR01DK125459 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI FAUL, CHRISTIAN · 2020 to 2023
$1.5M
NIDDK NIH HHS R01 DK125459
6 · The paper itself

Abstract

Introduction: Minimal change disease in childhood can follow a frequently relapsing or steroid-dependent course in up to 40% of cases. Second-line immunosuppressive medications that are used to manage these patients are associated with significant adverse effects. There is a need for safer alternative treatments for difficult-to-treat nephrotic syndrome. Therefore, we conducted an open-label feasibility study to assess the safety and efficacy of a gluten-free diet as treatment for pediatric patients with difficult-to-treat nephrotic syndrome. As a second aim, we sought to determine if the plasma zonulin concentration can identify those who are more likely to respond to this intervention. Methods: Seventeen patients were placed on a gluten-free diet for 6 months. A positive response was defined as a 50% reduction in the relapse rate compared to the preceding 6 months or the ability to discontinue 1 immunosuppressive drug. Results: Five (29%) participants had a positive response to the dietary intervention. The gluten-free diet was well tolerated with no clinical or laboratory adverse events. Plasma zonulin concentration was elevated in patients who failed to benefit from the gluten-free diet. Discussion/Conclusion: A gluten-free diet may be a useful adjunctive intervention for patients with difficult-to-treat nephrotic syndrome that can be implemented prior to resorting to second-line immunosuppressive therapy. Development of the plasma zonulin level as a biomarker to predict efficacy would facilitate rational use of a gluten-free diet in the management of nephrotic syndrome.

Indexed as

ChildhoodDifficult-to-treat diseaseGlomerular diseaseGluten-free dietNephrotic syndromePilot studyProteinuriaZonulin

Identifiers

PMID36817288
PMCPMC9936750
OpenAlexW4283322090

What Socratic holds

Textmetadata
LicenceCC BY-NC
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 Socratic graph.