Translating advances from the basic biology of aging into clinical application
Open accessAbstract
Recently, lifespan and healthspan have been extended in experimental animals using interventions that are potentially translatable into humans. A great deal of thought and work is needed beyond the usual steps in drug development to advance these findings into clinical application. Realistic pre-clinical and clinical trial paradigms need to be devised. Focusing on subjects with symptoms of age-related diseases or frailty or who are at imminent risk of developing these problems, measuring effects on short-term, clinically relevant outcomes, as opposed to long-term outcomes such as healthspan or lifespan, and developing biomarkers and outcome measures acceptable to regulatory agencies will be important. Research funding is a major roadblock, as is lack of investigators with combined expertise in the basic biology of aging, clinical geriatrics, and conducting investigational new drug clinical trials. Options are reviewed for developing a path from the bench to the bedside for interventions that target fundamental aging processes.
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The geroscience hypothesis predicts that targeting fundamental ageing mechanisms, such as cellular senescence, could have a large impact on increasing health span and decreasing chronic disease burden.
“The geroscience hypothesis leverages the fact that ageing is the major risk factor for most chronic diseases, including diabetes, and predicts that targeting fundamental ageing mechanisms, such as cellular senescence, could have a large impact on increasing health span and decreasing chronic disease burden.”
From Cellular senescence: at the nexus between ageing and diabetes (2019) · cites this paper as [5]
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References 55 · Cited by 128
Research works printed but not linked: 1
- Committee on the Future Health Care Workforce for Older Americans, I.o.M. Retooling for an Aging America: Building the Health Care Workforce Washington, DC The National Academies Press 2008 25009893
- Authors
- Kirkland, J. L.
- Affiliations
- Mayo Clinic (US)
- Corresponding author
- Kirkland, James L.
- ORCID
- Kirkland, James L.
- Venue
- Experimental Gerontology
- Publisher
- Elsevier BV
- Published
- 2013-01
- Volume
- 48
- Issue
- 1
- Pages
- 1-5
- ISSN
- 0531-5565 (ISSN-L)
- PMC
- PMC3543864
- OpenAlex
- W2010790248
- Cited by
- 128
- References
- 55
- Citations by year
- 2026: 1 · 2025: 4 · 2024: 6 · 2023: 11 · 2022: 8 · 2021: 12 · 2020: 16 · 2019: 13 · 2018: 10 · 2017: 7 · 2016: 10 · 2015: 11 · 2014: 11 · 2013: 8
- FWCI
- 0.97
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Experimental Gerontology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- NIH (AG13925, AG41122)
- Noaber, Ellison, and Glenn Foundations
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Aging › Genetics, Aging, and Longevity in Model Organisms
- Health Sciences › Medicine › Physiology › Telomeres, Telomerase, and Senescence
- Health Sciences › Medicine › Geriatrics and Gerontology › Sirtuins and Resveratrol in Medicine
- Keywords
- aging, age-related diseases, frailty, healthspan extension, lifespan extension, anti-aging interventions, translational research, clinical trials, biomarkers, outcome measures, regulatory approval, research funding, drug development, clinical geriatrics
- MeSH terms
- Aging, Animals, Diffusion of Innovation, Geriatrics, Humans, Longevity, Models, Animal
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