Evidence map›Paper›PMID 32766674›Full record

ArticleThe journals of gerontology. Series A, Biological sciences and medical sciences2021

Association Between Elevated suPAR, a New Biomarker of Inflammation, and Accelerated Aging.

Line Jee Hartmann Rasmussen, Avshalom Caspi, Antony Ambler, Andrea Danese, Maxwell Elliott, Jesper Eugen-Olsen, Ahmad R Hariri, HonaLee Harrington, Renate Houts, Richie Poulton and 4 more

Registry-linked trialOpen access · hybridAbstract read
In one paragraph

Article in The journals of gerontology. Series A, Biological sciences and medical sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05368337 (Feasibility and Usability of Intrinsic Capacity Monitoring With Eforto and Its Predictive Value for Health Outcomes in Older Community-dwelling Persons), which is not on this map. Cited by 42 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed, 1 pooled it
5.4field-weighted citation impact, top 3% 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.

NCT05368337 unknown statusnot on this mapstarted 2022, after this paper: background citation

Feasibility and Usability of Intrinsic Capacity Monitoring With Eforto and Its Predictive Value for Health Outcomes in Older Community-dwelling Persons

TypeobservationalSponsorVrije Universiteit BrusselRan2022 to 2023Enrolled160ConditionsFrailty
3 · Its place in the literature

Who cites it

42 citing papers in PubMed, 1 synthesis or guideline pooled it, 58 citations in OpenAlex.

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  14. uPAR Immuno-PET in Pancreatic Cancer, Aging, and Chemotherapy-Induced Senescence.Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2024
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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

14 authors at 4 institutions in 4 countries.

Line Jee Hartmann RasmussenDepartment of Psychology and Neuroscience, Duke University, Durham, North Carolina.
Avshalom CaspiDepartment of Psychology and Neuroscience, Duke University, Durham, North Carolina.
Antony AmblerDepartment of Psychology, University of Otago, Dunedin, New Zealand.
Andrea DaneseDepartment of Child and Adolescent Psychiatry, Institute of Psychiatry, Psychology, and Neuroscience, King's College London, UK.
Maxwell ElliottDepartment of Psychology and Neuroscience, Duke University, Durham, North Carolina.
Jesper Eugen-OlsenDepartment of Clinical Research, Copenhagen University Hospital Amager and Hvidovre, Hvidovre, Denmark.
Ahmad R HaririDepartment of Psychology and Neuroscience, Duke University, Durham, North Carolina.
HonaLee HarringtonDepartment of Psychology and Neuroscience, Duke University, Durham, North Carolina.
Renate HoutsDepartment of Psychology and Neuroscience, Duke University, Durham, North Carolina.
Richie PoultonDepartment of Psychology, University of Otago, Dunedin, New Zealand.
Sandhya RamrakhaDepartment of Psychology, University of Otago, Dunedin, New Zealand.
Karen SugdenDepartment of Psychology and Neuroscience, Duke University, Durham, North Carolina.
Benjamin WilliamsDepartment of Psychology and Neuroscience, Duke University, Durham, North Carolina.
Terrie E MoffittDepartment of Psychology and Neuroscience, Duke University, Durham, North Carolina.
Duke University · USUniversity of Otago · NZHvidovre Hospital · DKNational Health Service · GB

Funding

Resource Core 3 - Metabolomics CoreP30AG028716 · NIA · DUKE UNIVERSITY · PI Sarah B. Peskoe · 2006 to 2026
$24.6M
Quantifying Individual Differences in Midlife Structural Brain Integrity Associated with Later AD/ADRD RiskR01AG049789 · NIA · DUKE UNIVERSITY · PI AHMAD R. HARIRI, TERRIE E MOFFITT · 2015 to 2026
$10.6M
Is mental disorder a preventable cause of age-related disease? The Dunedin Study.R01AG032282 · NIA · DUKE UNIVERSITY · PI CASPI, AVSHALOM, MOFFITT, TERRIE E · 2009 to 2025
$9.5M
Validating a 3rd-generation methylation measure of accelerated aging: DunedinPoAm4xR01AG073207 · NIA · DUKE UNIVERSITY · PI CASPI, AVSHALOM, MOFFITT, TERRIE E · 2022 to 2025
$2.9M
Medical Research Council MR/P005918NIA NIH HHS P30 AG028716NIA NIH HHS R01 AG032282NIA NIH HHS R01 AG049789NIA NIH HHS R01 AG073207
6 · The paper itself

Abstract

backgroundTo understand and measure the association between chronic inflammation, aging, and age-related diseases, broadly applicable standard biomarkers of systemic chronic inflammation are needed. We tested whether elevated blood levels of the emerging chronic inflammation marker soluble urokinase plasminogen activator receptor (suPAR) were associated with accelerated aging, lower functional capacity, and cognitive decline.

methodsWe used data from the Dunedin Study, a population-representative 1972-1973 New Zealand birth cohort (n = 1037) that has observed participants to age 45 years. Plasma suPAR levels were analyzed at ages 38 and 45 years. We performed regression analyses adjusted for sex, smoking, C-reactive protein, and current health conditions.

resultsOf 997 still-living participants, 875 (88%) had plasma suPAR measured at age 45. Elevated suPAR was associated with accelerated pace of biological aging across multiple organ systems, older facial appearance, and with structural signs of older brain age. Moreover, participants with higher suPAR levels had greater decline in physical function and cognitive function from childhood to adulthood compared to those with lower suPAR levels. Finally, improvements in health habits between ages 38 and 45 (smoking cessation or increased physical activity) were associated with less steep increases in suPAR levels over those years.

conclusionsOur findings provide initial support for the utility of suPAR in studying the role of chronic inflammation in accelerated aging and functional decline.

Indexed as

AdultAgingBiomarkersCognitionCohort StudiesFemaleHumansInflammationInflammation MediatorsLongitudinal StudiesMaleMiddle AgedNew ZealandPhysical Functional PerformanceReceptors, Urokinase Plasminogen ActivatorSolubilityBiomarkersInflammation MediatorsPLAUR protein, humanReceptors, Urokinase Plasminogen ActivatorGait speedImmunosenescenceInflammagingMRIPace of aging

Identifiers

PMID32766674
PMCPMC7812430
OpenAlexW3043607727

What OpenQuestion holds

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LicenceCC BY
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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.