Challenges in developing Geroscience trials
- PMID: 37598227
- PMCID: PMC10439920
- DOI: 10.1038/s41467-023-39786-7
Challenges in developing Geroscience trials
Abstract
Geroscience is becoming a major hope for preventing age-related diseases and loss of function by targeting biological mechanisms of aging. This unprecedented paradigm shift requires optimizing the design of future clinical studies related to aging in humans. Researchers will face a number of challenges, including ideal populations to study, which lifestyle and Gerotherapeutic interventions to test initially, selecting key primary and secondary outcomes of such clinical trials, and which age-related biomarkers are most valuable for both selecting interventions and predicting or monitoring clinical responses ("Gerodiagnostics"). This article reports the main results of a Task Force of experts in Geroscience.
© 2023. Springer Nature Limited.
Conflict of interest statement
The views expressed in the manuscript the personal views of the authors and may not be understood as being made on behalf of organizations with which the authors are affiliated. Y.R. reports support from CHU Toulouse, University Paul Sabatier, INSERM CERPOP1295 (Employee), to be a shareholder of SARQOL SPRL, a spin-off of the University of Liege, consultancy fees from Longeveron, Biophytis, and honoraria for lectures for Pfizer. N.B. reported grants from the National Institutes of Health (P01AG021654) (N.B.), the Nathan Shock Center of Excellence for the basic Biology of Aging (P30AG038072) (N.B.), the Einstein-Paul Glenn Foundation for Medical Research Center for the Biology of Human Aging (N.B.), and taking part to advisory boards of Longevity Biotceh Association and Health Longevity Medical Society. A.O. reports support from Longeveron (Employee) and grants from National Institute on Aging (NIA)/National Institutes of Health (NIH) and Alzheimer’s Association. WE reports grants from the National Institutes of Health (1R01AG059416, R01CA246695, 5R01AG055443-02, 1R01AG065265, UCB 20210962, UCB 20210962, R01 AG074956-01, 1U01CA271277-01, 1R37CA258761-01A1) and consulting fees from BioAge Labs. B.V. reports support from CHU Toulouse, University Paul Sabatier and INSERM CERPOP1295 (employee), grant from Pfizer, Pierre Fabre. J.K. reports grants from US NIH paid to Mayo Clinic (grant R01AG 072301, P01AG 062413, R37AG 13925, R33AG 61456, R01AG 64165, R01AG 55529, R01DK 120292, R01DK 119167, R01HL 141819, R01AG 68048, UH3AG 56933 U54AG 075941, UG3CA 268103, R25AG 073119, R01AG 61414) and the Alzheimer’s Association (PTC REG-20-651687), consulting fees from Oklahoma Medical Research Foundation Scientific Advisory Board, and Henry Ford Health System, support for attending meetings (travel expense reimbursement) from AFAR, FASEB meeting, American Thoracic Society 2022 International Conference, Association for Research in Vision and Ophthalmology, Oriel College (Oxford University), 12th International Conference on Frailty and Sarcopenia Research (Boston), University of California (San Diego), Harvard University, 2nd Euro Geroscience Conference (Toulouse), University of North Carolina, University of Kansas Medical Center, Steadman Clinic (Vail), Gerontological Society of American, Longevity Medicine Society, patents (planned, issued, or pending/rights held by Mayo Clinic), and leadership at the American Federation for Aging Research board. Other authors (F.S., L.F., R.d.C., J.M., D.A., P.d.S.B., and J.R.) report no conflicts of interest.
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