Evidence map›Paper›PMID 37947901›Full record

ReviewPediatric nephrology (Berlin, Germany)2024

From premature birth to premature kidney disease: does accelerated aging play a role?

Keia R Sanderson, Christel Wekon-Kemeni, Jennifer R Charlton

Abstract readReview
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 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

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

  1. Pooled it
  2. Article
  3. Article
  4. Review
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

3 authors.

Keia R SandersonDepartment of Medicine-Nephrology, University of North Carolina, Chapel Hill, NC, USA. keia_sanderson@med.unc.edu.ORCID 0000-0001-7759-4220
Christel Wekon-KemeniDepartment of Pediatrics, University of North Carolina, Chapel Hill, NC, USA.
Jennifer R CharltonDepartment of Pediatrics, Division of Nephrology, University of Virginia, Charlottesville, VA, USA.

Funding

Single-Cell Epigenomics, Transcriptomics, and Bioinformatics CoreP50DK096373 · NIDDK · UNIVERSITY OF VIRGINIA · PI Silvia Medrano · 2012 to 2026
$13.8M
Resting state MRI to map autoregulation of the kidneyR21DK134104 · NIDDK · WASHINGTON UNIVERSITY · PI BENNETT, KEVIN M · 2022 to 2023
$679k
Machine Learning Risk Prediction of Kidney Disease After Extremely Preterm BirthK23DK131289 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SANDERSON, KEIA · 2023 to 2025
$602k
Translational imaging tools to nondestructively measure nephron massR41DK129138 · NIDDK · XN BIOTECHNOLOGIES, LLC · PI BENNETT, KEVIN M · 2021 to 2021
$300k
Investigating the role of nephron mass in the progression of CKD using MRIR56DK110622 · NIDDK · WASHINGTON UNIVERSITY · PI BENNETT, KEVIN M, CHARLTON, JENNIFER R · 2021 to 2021
$100k
NIDDK NIH HHS K23 DK131289NIDDK NIH HHS K23DK131289NIDDK NIH HHS L40 DK130155NIDDK NIH HHS L40DK130155NIDDK NIH HHS P50 DK096373NIDDK NIH HHS R21 DK134104NIDDK NIH HHS R21DK134104-01NIDDK NIH HHS R41 DK129138NIDDK NIH HHS R56 DK110622
6 · The paper itself

Abstract

As the limits of fetal viability have increased over the past 30 years, there has been a growing body of evidence supporting the idea that chronic disease should be taken into greater consideration in addition to survival after preterm birth. Accumulating evidence also suggests there is early onset of biologic aging after preterm birth. Similarly, chronic kidney disease (CKD) is also associated with a phenotype of advanced biologic age which exceeds chronologic age. Yet, significant knowledge gaps remain regarding the link between premature biologic age after preterm birth and kidney disease. This review summarizes the four broad pillars of aging, the evidence of premature aging following preterm birth, and in the setting of CKD. The aim is to provide additional plausible biologic mechanisms to explore the link between preterm birth and CKD. There is a need for more research to further elucidate the biologic mechanisms of the premature aging paradigm and kidney disease after preterm birth. Given the emerging research on therapies for premature aging, this paradigm could create pathways for prevention of advanced CKD.

Indexed as

Aging, PrematurePremature BirthRenal Insufficiency, ChronicAgingFemaleHumansInfant, NewbornPregnancyRisk FactorsAcute kidney injuryChronic kidney diseaseELGANSInfantsNeonatesPremature agingVery low birth weight

Identifiers

PMID37947901
PMCPMC11082067

What OpenQuestion holds

Textmetadata
LicenceTDM
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.