A framework for selection of blood-based biomarkers for geroscience-guided clinical trials: report from the TAME Biomarkers Workgroup
- PMID: 30151729
- PMCID: PMC6294728
- DOI: 10.1007/s11357-018-0042-y
A framework for selection of blood-based biomarkers for geroscience-guided clinical trials: report from the TAME Biomarkers Workgroup
Abstract
Recent advances indicate that biological aging is a potentially modifiable driver of late-life function and chronic disease and have led to the development of geroscience-guided therapeutic trials such as TAME (Targeting Aging with MEtformin). TAME is a proposed randomized clinical trial using metformin to affect molecular aging pathways to slow the incidence of age-related multi-morbidity and functional decline. In trials focusing on clinical end-points (e.g., disease diagnosis or death), biomarkers help show that the intervention is affecting the underlying aging biology before sufficient clinical events have accumulated to test the study hypothesis. Since there is no standard set of biomarkers of aging for clinical trials, an expert panel was convened and comprehensive literature reviews conducted to identify 258 initial candidate biomarkers of aging and age-related disease. Next selection criteria were derived and applied to refine this set emphasizing: (1) measurement reliability and feasibility; (2) relevance to aging; (3) robust and consistent ability to predict all-cause mortality, clinical and functional outcomes; and (4) responsiveness to intervention. Application of these selection criteria to the current literature resulted in a short list of blood-based biomarkers proposed for TAME: IL-6, TNFα-receptor I or II, CRP, GDF15, insulin, IGF1, cystatin C, NT-proBNP, and hemoglobin A1c. The present report provides a conceptual framework for the selection of blood-based biomarkers for use in geroscience-guided clinical trials. This work also revealed the scarcity of well-vetted biomarkers for human studies that reflect underlying biologic aging hallmarks, and the need to leverage proposed trials for future biomarker discovery and validation.
Keywords: Aging; Biomarkers; Epidemiology; Inflammation; Metformin; Mortality; Randomized controlled trial.
Conflict of interest statement
JNJ, NB, JB, JD, MAE, LF, SBK, SM, ABN, MP, and GAK report no conflicts of interest to this work. VRA was the MedStar Health Research Institute’s principal clinical trial investigator for studies involving Elcelyx (delayed release metformin).
Figures


References
-
- (IOM) (2010) Evaluation of biomarkers and surrogate endpoints in chronic disease. 2101 CONSTITUTION AVE, WASHINGTON, DC 20418 USA - PubMed
-
- Administration FaD (2018) Early Alzheimer’s disease: developing drugs for treatment guidance for industry. Rockville, MD
Publication types
MeSH terms
Substances
Grants and funding
- P30 AG024827/AG/NIA NIH HHS/United States
- Intramural Research Program/AG/NIA NIH HHS/United States
- AG052608/AG/NIA NIH HHS/United States
- R01 AG023629/AG/NIA NIH HHS/United States
- AG048023/AG/NIA NIH HHS/United States
- P30 AG021332/AG/NIA NIH HHS/United States
- K01 AG059837-01/AG/NIA NIH HHS/United States
- R35 GM124922/GM/NIGMS NIH HHS/United States
- L30 AG057113/AG/NIA NIH HHS/United States
- K01 AG059837/AG/NIA NIH HHS/United States
- R01 AG052608/AG/NIA NIH HHS/United States
- P30 AG049638/AG/NIA NIH HHS/United States
- P30 AG038072/AG/NIA NIH HHS/United States
- GM124922/GM/NIGMS NIH HHS/United States
- R01 AG048023/AG/NIA NIH HHS/United States
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Research Materials
Miscellaneous