Evidence map›Paper›PMID 30151729›Full record

ReviewGeroScience2018

A framework for selection of blood-based biomarkers for geroscience-guided clinical trials: report from the TAME Biomarkers Workgroup.

Jamie N Justice, Luigi Ferrucci, Anne B Newman, Vanita R Aroda, Judy L Bahnson, Jasmin Divers, Mark A Espeland, Santica Marcovina, Michael N Pollak, Stephen B Kritchevsky and 2 more

2 registry-linked trialsOpen access · bronzeAbstract readReview
In one paragraph

Review in GeroScience, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 214 papers, 6 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
214citing papers in PubMed, 6 pooled it
22.9field-weighted citation impact, top 1% 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.

NCT04241159 early_phase1withdrawnnot on this mapstarted 2020, after this paper: background citation

A Small-Scale Study to Explore the Safety and Feasibility of Allogeneic Young Plasma Infusion in Older Adults Experiencing Disability Across the Spectrum of Frailty Syndrome

TypeinterventionalSponsorWake Forest University Health SciencesRan2020 to 2020Enrolled0ConditionsFrailty Syndrome, Heart FailureArmsAllogeneic Young Plasma
NCT05732935 nacompletednot on this mapstarted 2023, after this paper: background citation

Fasting to Provide Energy Needed to Help Adults in Need of Cognitive Enhancement (FASTING ENHANCE)

TypeinterventionalSponsorUniversity of FloridaRan2023 to 2026Enrolled45ConditionsOverweight and Obesity, Time Restricted Feeding, Alzheimer DiseaseArmsTime Restricted Eating intervention, Successful Aging Comparison Group (LEARN)
3 · Its place in the literature

Who cites it

214 citing papers in PubMed, 6 syntheses or guidelines pooled it, 314 citations in OpenAlex.

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154 more citing papers are in PubMed but not listed here.

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

12 authors at 8 institutions in 2 countries.

Jamie N JusticeInternal Medicine Section on Gerontology and Geriatrics, and the Sticht Center for Healthy Aging and Alzheimer's Prevention, Wake Forest School of Medicine, 1 Medical Center Blvd, Winston-Salem, NC, 27157, USA. jnjustic@wakehealth.edu.ORCID 0000-0003-2953-4404
Luigi FerrucciNational Institute on Aging, National Institutes of Health, Baltimore, MD, 21224, USA.
Anne B NewmanDepartment of Epidemiology, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA, 15260, USA.
Vanita R ArodaDepartment of Medicine, Division of Diabetes, Endocrinology, and Hypertension Brigham and Women's Hospital, Harvard Medical School, Boston, MA, 02115, USA.
Judy L BahnsonDepartment of Biostatistical Sciences, Wake Forest School of Medicine, Winston-Salem, NC, 27157, USA.
Jasmin DiversDepartment of Biostatistical Sciences, Wake Forest School of Medicine, Winston-Salem, NC, 27157, USA.
Mark A EspelandDepartment of Biostatistical Sciences, Wake Forest School of Medicine, Winston-Salem, NC, 27157, USA.
Santica MarcovinaDivision of Metabolism, Endocrinology, and Nutrition, University of Washington, Seattle, WA, 98109, USA.
Michael N PollakDepartment of Oncology, Jewish General Hospital, McGill University, Montreal, Quebec, H3T1E2, Canada.
Stephen B KritchevskyInternal Medicine Section on Gerontology and Geriatrics, and the Sticht Center for Healthy Aging and Alzheimer's Prevention, Wake Forest School of Medicine, 1 Medical Center Blvd, Winston-Salem, NC, 27157, USA.
Nir BarzilaiDepartment of Medicine, Institute for Aging Research, Albert Einstein College of Medicine, Bronx, NY, 10461, USA.
George A KuchelUConn Center on Aging, University of Connecticut School of Medicine, Farmington, CT, 06030, USA.
Wake Forest University · USAlbert Einstein College of Medicine · USBrigham and Women's Hospital · USJewish General Hospital · CANational Institutes of Health · USUConn Health · USUniversity of Pittsburgh · USUniversity of Washington · US

Funding

Wake Forest Claude D. Pepper OAIC - RenewalP30AG021332 · NIA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI LEON LENCHIK · 2002 to 2026
$36.4M
VARIABILITY, STABILITY & SMOOTHNESS OF WALKINGP30AG024827 · NIA · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI JENNIFER S BRACH · 2004 to 2026
$28.6M
Wake Forest Alzheimer's Disease Core CenterP30AG049638 · NIA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI WILLIAMSON, JEFF DOUGLAS · 2016 to 2020
$12.2M
Einstein's Nathan Shock Center of Excellence in Basic Biology of AgingP30AG038072 · NIA · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI VIJG, JAN · 2010 to 2024
$10.8M
Exceptional Survival: Trajectories to Functional Aging (CHS All Stars)R01AG023629 · NIA · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI NEWMAN, ANNE B. · 2004 to 2016
$9.5M
High-resolution single cell profiling of vaccine responsiveness in the elderlyR01AI142086 · NIAID · JACKSON LABORATORY · PI UCAR, DUYGU · 2019 to 2023
$2.9M
Genomics and Epigenomics of the Elderly Response to Pneumococcal VaccinesR01AG052608 · NIA · JACKSON LABORATORY · PI BANCHEREAU, JACQUES F · 2016 to 2019
$2.5M
Identification and Interpretation of Chromatin Changes Associated with the Aging of Human Immune CellsR35GM124922 · NIGMS · JACKSON LABORATORY · PI UCAR, DUYGU · 2017 to 2021
$2.3M
Immune Response to High-Dose vs. Standard Dose Influenza VaccineR01AG048023 · NIA · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI KUCHEL, GEORGE A, MCELHANEY, JANET E. · 2014 to 2018
$2.1M
Senescent Cell Burden in Human Aging and Obesity: Functional Consequences and Reduction by Caloric RestrictionK01AG059837 · NIA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI JUSTICE, JAMIE NICOLE · 2018 to 2022
$519k
NIAID NIH HHS R01 AI142086NIA NIH HHS AG048023NIA NIH HHS AG052608NIA NIH HHS Intramural Research ProgramNIA NIH HHS K01 AG059837NIA NIH HHS K01 AG059837-01NIA NIH HHS L30 AG057113NIA NIH HHS P30 AG021332NIA NIH HHS P30 AG024827NIA NIH HHS P30 AG038072NIA NIH HHS P30 AG049638NIA NIH HHS R01 AG023629NIA NIH HHS R01 AG048023NIA NIH HHS R01 AG052608NIGMS NIH HHS GM124922NIGMS NIH HHS R35 GM124922
6 · The paper itself

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.

Indexed as

Biomedical ResearchAgingBiomarkersHumansHypoglycemic AgentsMetforminRandomized Controlled Trials as TopicReproducibility of ResultsBiomarkersHypoglycemic AgentsMetforminAgingBiomarkersEpidemiologyInflammationMetforminMortalityRandomized controlled trial

Identifiers

PMID30151729
PMCPMC6294728
OpenAlexW2889170508

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.