Evidence mapPaperPMID 41787649Full record

ReviewInternational journal of stem cells2026

Investigating the Causal Links between the Aging Process and Alzheimer's Disease Pathogenesis.

Jaewoo Seok, Hyein Lee, Jinsoo Seo

Abstract readReview
In one paragraph

Review in International journal of stem cells, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Jaewoo SeokDepartment of Systems Biology, College of Life Science and Biotechnology, Yonsei University, Seoul, Korea.ORCID https://orcid.org/0009-0003-4280-3709
Hyein LeeDepartment of Systems Biology, College of Life Science and Biotechnology, Yonsei University, Seoul, Korea.ORCID https://orcid.org/0000-0002-1525-2599
Jinsoo SeoDepartment of Systems Biology, College of Life Science and Biotechnology, Yonsei University, Seoul, Korea.ORCID https://orcid.org/0000-0001-6432-6964

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As global societies age, the prevalence of neurodegenerative disorders, such as Alzheimer's disease, is rapidly increasing, intensifying the need to understand the mechanisms of aging and their contribution to these conditions. Consequently, the focus of aging research has shifted from the traditional concept of chronological age to a more nuanced understanding of biological age. This has spurred active investigation into robust biomarkers, including cellular senescence. However, the application of classical senescence markers to the brain presents a substantial challenge, as their validity in post-mitotic cells, such as neurons, remains unclear. In this review, we highlight the limitations of the current metrics for cellular senescence as indicators of biological aging, and propose a path forward focused on identifying and modeling cell-type-specific aging markers within the brain.

Indexed as

AgingAlzheimer diseaseBrainInduced pluripotent stem cells

Identifiers

PMID41787649
PMCPMC13218837

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.