Testing the Geroscience Hypothesis
Sara Espinoza

TL;DR
This paper explores how targeting aging mechanisms can delay age-related diseases and improve healthy lifespan.
Contribution
It presents recent translational studies and clinical trials testing the geroscience hypothesis with gerotherapeutics.
Findings
Rapamycin and novel agents are being studied in preclinical models for healthspan extension.
Clinical trials are underway to evaluate the effectiveness of gerotherapeutics in humans.
The geroscience hypothesis is being tested through translational research on aging mechanisms.
Abstract
Aging is the most significant risk factor for many chronic diseases and geriatric syndromes. The geroscience hypothesis posits that by targeting underlying cellular and molecular mechanisms of aging, it is possible to delay age-related diseases and thereby extend healthy years of life spent free of multimorbidity, disability, and frailty (healthspan). Towards this end, and informed by scientific discoveries in the biology of aging field, translational studies are ongoing to test the geroscience hypothesis by examining potential gerotherapeutics to extend healthspan. This session focuses on recent research to test the geroscience hypothesis, including studies of rapamycin and novel agents in preclinical models and human studies, including clinical trials.
Genes, proteins, chemicals, diseases, species, mutations and cell lines named across the full text — each resolved to its canonical identifier and authoritative record.
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Taxonomy
TopicsGenetics, Aging, and Longevity in Model Organisms · Telomeres, Telomerase, and Senescence · Frailty in Older Adults
