Evidence map›Paper›PMID 41452713›Full record

ArticleAging and disease2025

Aging as a Networked Process: Systems, Signals, and Interventions Across the Lifespan.

Zaid Nathani, Zaid Qaddura, Kunlin Jin

Abstract readEditorialComment
In one paragraph

Article in Aging and disease, 2025. 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

5 · Who and what money

Authors and funding

3 authors.

Zaid NathaniTexas College of Osteopathic Medicine, University of North Texas Health Science Center, Fort Worth, Texas 76107, USA.
Zaid QadduraTexas College of Osteopathic Medicine, University of North Texas Health Science Center, Fort Worth, Texas 76107, USA.
Kunlin JinDepartment of Pharmacology and Neuroscience, University of North Texas Health Science Center, Fort Worth, Texas 76107, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As global populations age, chronic disease burden rises across multiple organ systems. This special issue treats aging as a multi-system process shaped by biology, environment, and behavior. Across 30 original studies and reviews, the collection centers on shared mechanisms of decline, including mitochondrial dysfunction, circadian disruption, hypoxia, inter-organ signaling, and cellular senescence. The articles track how these processes change across tissues and across time. Multiple contributions link systemic changes to tissue-level dysfunction. Vascular, immune, and metabolic shifts appear repeatedly as upstream drivers. The issue also emphasizes local context. Tissue microenvironments shape how the same systemic stressor produces different outcomes, which helps explain heterogeneity in aging trajectories. Several papers move toward translation. They propose biomarkers and diagnostic strategies aimed at earlier detection, risk stratification, and longitudinal monitoring. The strongest translational value comes when authors connect a proposed tool to a defined endpoint and a defined use case, rather than broad "precision" framing. Overall, the issue argues for tighter alignment between mechanism and measurable outcomes. The collection also highlights critical areas where further validation and integration are needed to support clinical translation.

Indexed as

AgingLongevityHumansSignal Transduction

Identifiers

PMID41452713
PMCPMC12727073

What Socratic holds

Textmetadata
LicenceCC BY
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.