Evidence map›Paper›PMID 38233720›Full record

ReviewPediatric nephrology (Berlin, Germany)2024

Pediatric contributions and lessons learned from the NEPTUNE cohort study.

Zubin J Modi, Yan Zhai, Jennifer Yee, Hailey Desmond, Wei Hao, Matthew G Sampson, Christine B Sethna, Chia-Shi Wang, Debbie S Gipson, Howard Trachtman and 2 more

Abstract readReview
PubMed Publisher
In one paragraph

Review in Pediatric nephrology (Berlin, Germany), 2024. 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 42% 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, 1 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

12 authors at 5 institutions in 1 country.

Zubin J ModiDivision of Pediatric Nephrology, Department of Pediatrics, University of Michigan, Ann Arbor, MI, USA.
Yan ZhaiDivision of Pediatric Nephrology, Department of Pediatrics, University of Michigan, Ann Arbor, MI, USA.
Jennifer YeeDivision of Pediatric Nephrology, Department of Pediatrics, University of Michigan, Ann Arbor, MI, USA.
Hailey DesmondDivision of Pediatric Nephrology, Department of Pediatrics, University of Michigan, Ann Arbor, MI, USA.
Wei HaoDepartment of Biostatistics, University of Michigan, Ann Arbor, MI, USA.
Matthew G SampsonDivision of Pediatric Nephrology, Boston Children's Hospital, Boston, MA, USA.
Christine B SethnaCohen Children's Medical Center, New Hyde Park, NY, USA.
Chia-Shi WangEmory University School of Medicine and Children's Healthcare of Atlanta, Atlanta, GA, USA.
Debbie S GipsonDivision of Pediatric Nephrology, Department of Pediatrics, University of Michigan, Ann Arbor, MI, USA.
Howard TrachtmanDivision of Pediatric Nephrology, Department of Pediatrics, University of Michigan, Ann Arbor, MI, USA. howardtrachtman21@gmail.com.ORCID 0009-0006-7778-292X
Matthias KretzlerDepartment of Internal Medicine, Division of Nephrology, University of Michigan, Ann Arbor, MI, USA.
NEPTUNE investigators
University of Michigan · USBrigham and Women's Hospital · USBroad Institute · USCohen Children's Medical Center · USEmory University · US

Funding

The Impact of COVID-19 on People Living with Rare Diseases and Their FamiliesU2CTR002818 · NCATS · CINCINNATI CHILDRENS HOSP MED CTR · PI Maurizio Macaluso, Michael Wagner · 2019 to 2026
$51.2M
Training Program in Clinical & Translationa Research in Human Glomerular DiseaseU54DK083912 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KRETZLER, MATTHIAS · 2009 to 2023
$20.3M
Integrating large scale genomics and functional studies to accelerate FSGS/NS discoveryRC2DK122397 · NIDDK · BETH ISRAEL DEACONESS MEDICAL CENTER · PI HILDEBRANDT, FRIEDHELM, POLLAK, MARTIN R. · 2020 to 2024
$7.4M
Whole Genome Sequencing for Nephrotic Syndrome DiscoveryR01DK119380 · NIDDK · BOSTON CHILDREN'S HOSPITAL · PI Dongwon Lee, MATTHEW Gordon SAMPSON · 2019 to 2026
$3.7M
Kids: Nocturnal Investigation into Glomerular Disease, Hypertension, and Transcriptomics (kNIGHT)R01HL162912 · NHLBI · FEINSTEIN INSTITUTE FOR MEDICAL RESEARCH · PI Christine B Sethna · 2023 to 2026
$2.9M
NCATS NIH HHS U2CTR002818NHLBI NIH HHS R01 HL162912NIDDK NIH HHS U54DK083912NIH HHS 2U54DK083912NIH HHS R01DK119380NIH HHS RC2DK122397
6 · The paper itself

Abstract

Primary glomerular diseases are rare entities. This has hampered efforts to better understand the underlying pathobiology and to develop novel safe and effective therapies. NEPTUNE is a rare disease network that is focused on patients of all ages with minimal change disease, focal segmental glomerulosclerosis, and membranous nephropathy. It is a longitudinal cohort study that collects detailed demographic, clinical, histopathologic, genomic, transcriptomic, and metabolomic data. The goal is to develop a molecular classification for these disorders that supersedes the traditional pathological features-based schema. Pediatric patients are important contributors to this ongoing project. In this review, we provide a snapshot of the children and adolescents enrolled in NEPTUNE and summarize some key observations that have been made based on the data accumulated during the study. In addition, we describe the development of NEPTUNE Match, a program that aims to leverage the multi-scalar information gathered for each individual patient to provide guidance about potential clinical trial participation based on the molecular characterization and non-invasive biomarker profile. This represents the first organized effort to apply principles of precision medicine to the treatment of patients with primary glomerular disease. NEPTUNE has proven to be an invaluable asset in the study of glomerular diseases in patients of all ages including children and adolescents.

Indexed as

Glomerulosclerosis, Focal SegmentalAdolescentChildChild, PreschoolCohort StudiesFemaleGlomerulonephritis, MembranousHumansLongitudinal StudiesMaleNephrosis, LipoidPrecision MedicineRare DiseasesBiomarkerGlomerular diseaseKidney biopsyNephrotic syndromePediatricsPrecision medicine

Identifiers

PMID38233720
OpenAlexW4390980336

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.