Evidence map›Paper›PMID 40346193›Full record

ArticleCommunications biology2025

Tracing mitochondrial marks of neuronal aging in iPSCs-derived neurons and directly converted neurons.

Nimmy Varghese, Leonora Szabo, M Zameel Cader, Imane Lejri, Amandine Grimm, Anne Eckert

Abstract read
In one paragraph

Article in Communications biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Proanthocyanidins from Ginkgo extract EGb 761Frontiers in pharmacology · 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

6 authors.

Nimmy VargheseResearch Cluster Molecular and Cognitive Neurosciences, University of Basel, Basel, Switzerland.ORCID http://orcid.org/0000-0001-8598-0535
Leonora SzaboResearch Cluster Molecular and Cognitive Neurosciences, University of Basel, Basel, Switzerland.ORCID http://orcid.org/0000-0001-5117-3778
M Zameel CaderNuffield Department of Clinical Neuroscience, University of Oxford, Oxford, UK.ORCID http://orcid.org/0000-0002-6952-406X
Imane LejriResearch Cluster Molecular and Cognitive Neurosciences, University of Basel, Basel, Switzerland.
Amandine GrimmResearch Cluster Molecular and Cognitive Neurosciences, University of Basel, Basel, Switzerland.ORCID http://orcid.org/0000-0003-3323-1756
Anne EckertResearch Cluster Molecular and Cognitive Neurosciences, University of Basel, Basel, Switzerland. anne.eckert@unibas.ch.ORCID http://orcid.org/0000-0002-9341-3669

Funding

Novartis Stiftung für Medizinisch-Biologische Forschung (Novartis Foundation for Medical-Biological Research) 18C143Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung (Swiss National Science Foundation) 31003A-179294
6 · The paper itself

Abstract

This study aims to determine if neurons derived from induced pluripotent stem cells (iPSCsNs) and directly converted neurons (iNs) from the same source cells exhibit changes in mitochondrial properties related to aging. This research addresses the uncertainty around whether aged iPSCsNs retain aging-associated mitochondrial impairments upon transitioning through pluripotency while direct conversion maintains these impairments. We observe that both aged models exhibit characteristics of aging, such as decreased ATP, mitochondrial membrane potential, respiration, NAD

Indexed as

Cellular SenescenceInduced Pluripotent Stem CellsMitochondriaNeuronsAgingAnimalsCells, CulturedGlycolysisHumansMembrane Potential, MitochondrialMice

Identifiers

PMID40346193
PMCPMC12064796

What OpenQuestion holds

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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.