Evidence map›Paper›PMID 41442755›Full record

ArticleThe journals of gerontology. Series B, Psychological sciences and social sciences2025

Improving our understanding of the biology of aging: findings from the Age-It Research Program.

Fabrizio Chiti, Fiorenzo Conti, Daniela Corda, Francesco Giorgino, Andrea Graziani, Giuseppe Passarino, Marco Sandri, Fabrizio d'Adda di Fagagna

Abstract read
In one paragraph

Article in The journals of gerontology. Series B, Psychological sciences and social sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Aging well in an aging society: Italy at the forefront of global aging and the Age-It Research Program.The journals of gerontology. Series B, Psychological sciences and social sciences · 2025
    Article
  2. Positive demography: changing the perspective on population aging from the Age-It Research Program.The journals of gerontology. Series B, Psychological sciences and social sciences · 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

8 authors.

Fabrizio ChitiDepartment of Experimental and Clinical Biomedical Sciences, Section of Biochemistry, University of Florence, Florence, Italy.
Fiorenzo ContiCenter for Neurobiology of Aging, IRCCS INRCA, Ancona, Italy.
Daniela CordaInstitute of Endocrinology and Experimental Oncology (IEOS), National Research Council (CNR), Naples, Italy.
Francesco GiorginoDepartment of Precision and Regenerative Medicine and Ionian Area, Section of Internal Medicine, Endocrinology, Andrology and Metabolic Diseases, University of Bari Aldo Moro, Bari, Italy.ORCID 0000-0001-7372-2678
Andrea GrazianiDepartment of Molecular Biotechnology and Health Sciences, Molecular Biotechnology Center, University of Torino, Torino, Italy.
Giuseppe PassarinoDepartment of Biology, Ecology and Earth Science, University of Calabria, Rende, Italy.
Marco SandriDepartment of Biomedical Sciences, University of Padova, Padova, Italy.ORCID 0000-0001-8509-7558
Fabrizio d'Adda di FagagnaInstitute of Molecular Genetics (IGM), National Research Council (CNR), Pavia, Italy.

Funding

Aging Well in an Aging Society GAE 492 PNRR PE_8 Spoke 2
6 · The paper itself

Abstract

objectivesAging mechanisms at both cellular and organismal levels remain poorly understood, as do the factors influencing the variability in aging rates across organs and individuals. Our work aims to identify the key biological pathways that drive aging, determine the most relevant biomarkers of biological aging, and uncover actionable mechanisms to improve risk prediction for unsuccessful aging.

methodsTo achieve these objectives, we employ a structured approach that includes (a) investigating the molecular and cellular mechanisms underlying aging, (b) identifying and validating biomarkers associated with biological aging, and (c) assessing potential therapeutic targets that could modulate aging-related processes. These efforts are being carried out within the framework of the Age-It initiative, leveraging interdisciplinary methodologies and advanced analytical tools.

resultsOngoing studies within Age-It are generating insights into aging-related pathways and biomarkers. Preliminary findings highlight specific molecular signatures associated with biological aging and suggest potential intervention points for mitigating age-related decline. DISCUSSION: Understanding the biological underpinnings of aging will enhance our ability to predict and potentially modify aging trajectories. By identifying reliable biomarkers and actionable pathways, this research may contribute to the development of targeted interventions to promote healthy aging. The Age-It initiative represents a collaborative effort to translate these findings into practical applications for aging research and health care policy.

Indexed as

AgingAgedBiomarkersHumansBiomarkersBiomarkersCellular senescenceFrailty

Identifiers

PMID41442755
PMCPMC12736983

What OpenQuestion 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 OpenQuestion graph.