Evidence map›Paper›PMID 37982669›Full record

SynthesisThe journals of gerontology. Series A, Biological sciences and medical sciences2024

Proteomic Analysis of the Senescence-Associated Secretory Phenotype: GDF-15, IGFBP-2, and Cystatin-C Are Associated With Multiple Aging Traits.

Daniel S Evans, Danielle Young, Toshiko Tanaka, Nathan Basisty, Stefania Bandinelli, Luigi Ferrucci, Judith Campisi, Birgit Schilling

Open access · hybridAbstract readMeta-Analysis
In one paragraph

Synthesis in The journals of gerontology. Series A, Biological sciences and medical sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed, 1 pooled it
13.2field-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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

50 citing papers in PubMed, 1 synthesis or guideline pooled it, 53 citations in OpenAlex.

  1. Pooled it
  2. Review
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  7. Article
  8. Functional, molecular, and digital measurements of biological age.The Journal of clinical investigation · 2026
    Review
  9. Multicellular senescence programs in the aged heart.Journal of molecular and cellular cardiology plus · 2026
    Review
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  11. Article
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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

8 authors at 4 institutions in 2 countries.

Daniel S EvansCalifornia Pacific Medical Center Research Institute, San Francisco, California, USA.ORCID 0000-0003-4185-7687
Danielle YoungCalifornia Pacific Medical Center Research Institute, San Francisco, California, USA.
Toshiko TanakaLongitudinal Studies Section, Translational Gerontology Branch, NIA, NIH, Baltimore, Maryland, USA.ORCID 0000-0002-4161-3829
Nathan BasistyLongitudinal Studies Section, Translational Gerontology Branch, NIA, NIH, Baltimore, Maryland, USA.ORCID 0000-0001-6173-1139
Stefania BandinelliGeriatric Unit, Azienda Sanitaria Firenze (ASF), Florence, Tuscany, Italy.
Luigi FerrucciLongitudinal Studies Section, Translational Gerontology Branch, NIA, NIH, Baltimore, Maryland, USA.ORCID 0000-0002-6273-1613
Judith CampisiBuck Institute for Research on Aging, Novato, California, USA.
Birgit SchillingBuck Institute for Research on Aging, Novato, California, USA.
National Institute on Aging · USBuck Institute for Research on Aging · USUniversity of California, San Francisco · USAzienda Sanitaria di Firenze · IT

Funding

The Baltimore Longitudinal Study Of AgingZIAAG000015 · NIA · NATIONAL INSTITUTE ON AGING · PI SIMONSICK, ELEANOR MARIE · 2009 to 2025
$116.9M
Senescent cell mapping, identification and validation for human somatic and reproductive tissuesU54AG075932 · NIA · BUCK INSTITUTE FOR RESEARCH ON AGING · PI Simon Melov, Birgit Schilling · 2021 to 2026
$12.5M
Quantitative Proteomics to Develop Robust Senescence-Related Biomarkers for AgingU01AG060906 · NIA · BUCK INSTITUTE FOR RESEARCH ON AGING · PI SCHILLING, BIRGIT · 2018 to 2022
$4.0M
The InChianti StudyZIAAG001050 · NIA · NATIONAL INSTITUTE ON AGING · PI FERRUCCI, LUIGI · 2009 to 2025
$2.1M
Development of Sensitive and Specific Proteomic Biomarkers of Aging, Health, Frailty, and Morbidity in Human CohortsZIAAG000345 · NIA · NATIONAL INSTITUTE ON AGING · PI BASISTY, NATHAN · 2021 to 2025
$689k
TripleTOF 5600 High Resolution Mass SpectrometerS10OD016281 · OD · BUCK INSTITUTE FOR RESEARCH ON AGING · PI GIBSON, BRADFORD WAYNE · 2013 to 2013
$597k
NIA NIH HHS U01 AG060906NIA NIH HHS U54 AG075932NIH HHS S10 OD016281NIH HHS U01 AG060906
6 · The paper itself

Abstract

Cellular senescence, a hallmark of aging, results in a senescence-associated secretory phenotype (SASP) with an increased production of proinflammatory cytokines, growth factors, and proteases. Evidence from nonhuman models demonstrates that SASP contributes to tissue dysfunction and pathological effects of aging. However, there are relatively few human studies on the relationship between SASP and aging-related health outcomes. Proteins from the SASP Atlas were measured in plasma using aptamer-based proteomics (SomaLogic). Regression models were used to identify SASP protein associations with aging-related traits representing multiple aspects of physiology in 1 201 participants from 2 human cohort studies (BLSA/GESTALT and InCHIANTI). Traits examined were fasting glucose, C-reactive protein, interleukin-6, alkaline phosphatase, blood urea nitrogen, albumin, red blood cell distribution width, waist circumference, systolic and diastolic blood pressure, gait speed, and grip strength. Study results were combined with a fixed-effect inverse-variance weighted meta-analysis. In the meta-analysis, 28 of 77 SASP proteins were significantly associated with age. Of the 28 age-associated SASP proteins, 18 were significantly associated with 1 or more clinical traits, and 7 SASP proteins were significantly associated with 3 or more traits. Growth/differentiation factor 15, Insulin-like growth factor-binding protein 2, and Cystatin-C showed significant associations with inflammatory markers and measures of physical function (grip strength or gait speed). These results support the relevance of SASP proteins to human aging, identify specific traits that are potentially affected by SASP, and prioritize specific SASP proteins for their utility as biomarkers of human aging.

Indexed as

CystatinsSenescence-Associated Secretory PhenotypeAgingCellular SenescenceGrowth Differentiation Factor 15HumansInsulin-Like Growth Factor Binding Protein 2PhenotypeProteomicsCystatinsGrowth Differentiation Factor 15Insulin-Like Growth Factor Binding Protein 2Aging biomarkersCellular senescenceGait speedGrip strengthProteomics

Identifiers

PMID37982669
PMCPMC10876076
OpenAlexW4388823394

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.