Evidence map›Paper›PMID 37325957›Full record

ArticleThe journals of gerontology. Series A, Biological sciences and medical sciences2023

Drugs Targeting Mechanisms of Aging to Delay Age-Related Disease and Promote Healthspan: Proceedings of a National Institute on Aging Workshop.

Sara E Espinoza, Sundeep Khosla, Joseph A Baur, Rafael de Cabo, Nicolas Musi

Open access · hybridAbstract read
In one paragraph

Article in The journals of gerontology. Series A, Biological sciences and medical sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
4.7field-weighted citation impact, top 4% of its field
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

14 citing papers in PubMed, 27 citations in OpenAlex.

  1. Review
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  5. Exercise attenuates the hallmarks of aging: Novel perspectives.Journal of sport and health science · 2025
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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

5 authors at 5 institutions in 1 country.

Sara E EspinozaSam and Ann Barshop Institute for Longevity and Aging Studies, University of Texas Health Science Center at San Antonio.
Sundeep KhoslaDivision of Endocrinology and Kogod Center on Aging, Mayo Clinic, Rochester, Minnesota, USA.ORCID 0000-0002-2936-4372
Joseph A BaurDepartment of Physiology and Institute for Diabetes, Obesity, and Metabolism, Perelman School of Medicine, University of Pennsylvania, Philadelphia, USA.ORCID 0000-0001-8262-6549
Rafael de CaboTranslational Gerontology Branch, Experimental Gerontology Section, National Institute on Aging, National Institutes of Health, Baltimore, Maryland, USA.ORCID 0000-0003-2830-5693
Nicolas MusiDepartment of Medicine, Division of Endocrinology, Diabetes and Metabolism, Cedars Sinai Medical Center, Los Angeles, California, USA.
Cedars-Sinai Medical Center · USMayo Clinic · USNational Institutes of Health · USThe University of Texas Health Science Center at San Antonio · USUniversity of Pennsylvania · US

Funding

TRANSGENIC COREP30AG013319 · NIA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI JAMES FLOYD NELSON · 1995 to 2026
$30.6M
Molecular Transducers of Physical Activity Consortium Adult Clinical CenterU01AR071130 · NIAMS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI MUSI, NICOLAS, RASMUSSEN, BLAKE B · 2017 to 2024
$17.7M
San Antonio OAIC - Research Education Component (REC)P30AG044271 · NIA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Adam Salmon · 2015 to 2026
$14.1M
The KAPP-Sen Tissue Mapping Center CollaborativeU54AG075941 · NIA · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI GAROVIC, VESNA D, KUCHEL, GEORGE A · 2021 to 2025
$13.8M
TRAINING GRANT ON THE BIOLOGY OF AGINGT32AG021890 · NIA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Erzsebet Kokovay, JAMES FLOYD NELSON · 2003 to 2026
$11.4M
Targeting NAD Metabolism to Improve Glucose Homeostasis in Obesity and AgingR01DK098656 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI Joseph A. Baur · 2013 to 2026
$6.1M
Single nuclei RNA-sequencing to map adipose cellular populations and senescent cells in older subjectsR01AG075684 · NIA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Nicolas Musi · 2022 to 2026
$3.4M
Metformin for Preventing Frailty in High Risk Older AdultsR01AG052697 · NIA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI ESPINOZA, SARA ELYSE, MUSI, NICOLAS · 2017 to 2022
$2.7M
Understanding the roles of cardiac NAD pools and therapeutic effects of precursor supplements in heart failureR01HL165792 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI BAUR, JOSEPH A. · 2022 to 2025
$2.7M
Does Metformin Modulate the Pillars of Aging in Older Adults?R01AG069690 · NIA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI ESPINOZA, SARA ELYSE, MUSI, NICOLAS · 2020 to 2024
$1.9M
Geroscience Education and Training (GET) NetworkR25AG073119 · NIA · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI ESPINOZA, SARA ELYSE, KUCHEL, GEORGE A · 2021 to 2023
$925k
Targeting cellular senescence with senolytics to improve skeletal health in older humansR21AG065868 · NIA · MAYO CLINIC ROCHESTER · PI FARR, JOSHUA NICHOLAS, KHOSLA, SUNDEEP · 2020 to 2021
$419k
NHLBI NIH HHS R01 HL165792NIAMS NIH HHS U01 AR071130NIA NIH HHS P30 AG013319NIA NIH HHS P30 AG044271NIA NIH HHS R01 AG069690NIA NIH HHS R01 AG075684NIA NIH HHS R21 AG065868NIA NIH HHS R25 AG073119NIA NIH HHS T32 AG021890NIA NIH HHS U54 AG075941NIDDK NIH HHS R01 DK098656NIH HHS R01 AG052697
6 · The paper itself

Abstract

The geroscience hypothesis posits that by targeting key hallmarks of aging we may simultaneously prevent or delay several age-related diseases and thereby increase healthspan, or life span spent free of significant disease and disability. Studies are underway to examine several possible pharmacological interventions for this purpose. As part of a National Institute on Aging workshop on the development of function-promoting therapies, scientific content experts provided literature reviews and state-of-the-field assessments for the studies of senolytics, nicotinamide adenine dinucleotide (NAD+) boosters, and metformin. Cellular senescence increases with age, and preclinical studies demonstrate that the use of senolytic drugs improves healthspan in rodents. Human studies using senolytics are in progress. NAD+ and its phosphorylated form, NADP+, play vital roles in metabolism and cellular signaling. Increasing NAD+ by supplementation with precursors including nicotinamide riboside and nicotinamide mononucleotide appears to extend healthspan in model organisms, but human studies are limited and results are mixed. Metformin is a biguanide widely used for glucose lowering, which is believed to have pleiotropic effects targeting several hallmarks of aging. Preclinical studies suggest it improves life span and healthspan, and observational studies suggest benefits for the prevention of several age-related diseases. Clinical trials are underway to examine metformin for healthspan and frailty prevention. Preclinical and emerging clinical studies suggest there is potential to improve healthspan through the use of pharmacologic agents reviewed. However, much further research is needed to demonstrate benefits and general safety for wider use, the appropriate target populations, and longer-term outcomes.

Indexed as

MetforminNADAgingHumansNational Institute on Aging (U.S.)SenotherapeuticsUnited StatesMetforminNADSenotherapeuticsAgingCellular senescenceGeroscienceHealthspanMetforminNicotinamide riboside

Identifiers

PMID37325957
PMCPMC10272987
OpenAlexW4380869416

What OpenQuestion holds

Textmetadata
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.