Evidence map›Paper›PMID 39417827›Full record

ArticleAmerican journal of physiology. Renal physiology2024

Maternal malnutrition in mice impairs nephrogenesis by disrupting DNA methylation of regulatory regions.

Yaniv Makayes, Eden Abergel, Athar Amleh, Dan Binyamin Varshavsky, Rimma Fok, Batia Azria, Ihab Ansari, Yehudit Bergman, Morris Nechama, Oded Volovelsky

Abstract read
In one paragraph

Article in American journal of physiology. Renal physiology, 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
–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

1 citing paper in PubMed.

  1. HMGB1 drives T-cell activation in hypertensive males and females.American journal of physiology. Renal physiology · 2025
    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.

Yaniv MakayesWohl Institute for Translational Medicine, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.ORCID 0000-0003-1802-8768
Eden AbergelWohl Institute for Translational Medicine, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.
Athar AmlehWohl Institute for Translational Medicine, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.
Dan Binyamin VarshavskyWohl Institute for Translational Medicine, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.
Rimma FokDepartment of Developmental Biology and Cancer Research, Institute for Medical Research Israel-Canada, Hebrew University Medical School, Jerusalem, Israel.
Batia AzriaDepartment of Developmental Biology and Cancer Research, Institute for Medical Research Israel-Canada, Hebrew University Medical School, Jerusalem, Israel.
Ihab AnsariDepartment of Developmental Biology and Cancer Research, Institute for Medical Research Israel-Canada, Hebrew University Medical School, Jerusalem, Israel.
Yehudit BergmanDepartment of Developmental Biology and Cancer Research, Institute for Medical Research Israel-Canada, Hebrew University Medical School, Jerusalem, Israel.
Morris NechamaWohl Institute for Translational Medicine, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.
Oded VolovelskyWohl Institute for Translational Medicine, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.ORCID 0000-0002-5378-1045

Funding

Hadassah Medical Organization (HMO) Startup GrantIsrael Science Foundation (ISF) 2030/21Israel Science Foundation (ISF) 2358/18Ministry of Science and Technology (MOST) Eshkol Award
6 · The paper itself

Abstract

Maternal caloric restriction during pregnancy significantly impacts kidney development, influencing susceptibility to chronic kidney disease in adulthood. This study explores DNA methylation changes in nephron progenitor cells resulting from caloric restriction and their implications for kidney health. Global DNA hypomethylation is observed in nephron progenitors from caloric-restricted embryos, with specific genomic regions displaying distinct methylation patterns, including hypomethylation and hypermethylation. Differentially methylated regions exhibit enhanced chromatin accessibility, indicating biological relevance. Hypomethylated regions are enriched for genes associated with developmental processes, reflecting changes in gene expression and highlighting their functional relevance in kidney development. The study also reveals that supplementing methionine, an essential amino acid, restores disrupted DNA methylation patterns, particularly in enhancer regions, emphasizing methionine's critical role in regulating nephron progenitor cell epigenetics and ensuring proper kidney development. The intricate relationship between maternal nutrition, dynamic DNA methylation, and kidney development is highlighted, emphasizing the enduring impact of early-life nutritional challenges on kidney function. This research elucidates epigenetic mechanisms as mediators for the lasting effects of maternal caloric restriction on kidney health. The study contributes valuable insights into the origins of chronic kidney diseases during early developmental stages, offering potential interventions to mitigate adverse outcomes.

Indexed as

Caloric RestrictionDNA MethylationEpigenesis, GeneticKidneyPrenatal Exposure Delayed EffectsAnimalsFemaleGene Expression Regulation, DevelopmentalMalnutritionMaternal Nutritional Physiological PhenomenaMethionineMiceMice, Inbred C57BLNephronsOrganogenesisPregnancyMethionineDNA methylationepigeneticskidney developmentmalnutritionnephron progenitor cells

Identifiers

PMID39417827
PMCPMC11687838

What OpenQuestion holds

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Registered trials

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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.