Evidence map›Paper›PMID 42364072›Full record

ArticleGeroScience2026

Plasma proteins associated with disability and mortality risks in Japanese community-dwelling octogenarians.

Yusuke Osawa, Takashi Sasaki, Julián Candia, Yukiko Abe, Glenn Wong, Stefania Bandinelli, Luigi Ferrucci, Yasumichi Arai

Abstract read
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In one paragraph

Article in GeroScience, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Yusuke OsawaGraduate School of Health Management, Keio University, Kanagawa, Japan. yosawa@keio.jp.ORCID http://orcid.org/0000-0002-7706-5166
Takashi SasakiCenter for Supercentenarian Medical Research, Keio University School of Medicine, Tokyo, Japan.
Julián CandiaTranslational Gerontology Branch, National Institute On Aging, Baltimore, MD, USA.
Yukiko AbeCenter for Supercentenarian Medical Research, Keio University School of Medicine, Tokyo, Japan.
Glenn WongDepartment of Biological Sciences, National University of Singapore, Singapore, Singapore.
Stefania BandinelliASL Azienda Sanitaria Locale Toscana Centro, Florence, Italy.
Luigi FerrucciTranslational Gerontology Branch, National Institute On Aging, Baltimore, MD, USA.
Yasumichi AraiGraduate School of Health Management, Keio University, Kanagawa, Japan. yasumich@keio.jp.ORCID http://orcid.org/0000-0003-1746-965X

Funding

Foundation for the National Institutes of Health R01HL111271Foundation for the National Institutes of Health R21HL112662Japan Agency for Medical Research and Development 17jm0210051h0001Japan Agency for Medical Research and Development 23ae0121041h0003Japan Agency for Medical Research and Development 23zf0127007h0002Japan Science and Technology Corporation JP15667051Japan Society for the Promotion of Science London 21K10505Japan Society for the Promotion of Science London 23H03337Japan Society for the Promotion of Science London 24K02711Keio Global Research Institute Pre-Start-up Grant T04EZ00011NIA NIH HHS 263 MD 821336NIA NIH HHS 263 MD 9164NIA NIH HHS 263MD9164NIA NIH HHS N01-AG-5-0002NIA NIH HHS N.1-AG-1-1NIA NIH HHS N.1-AG-1-2111the Italian Ministry of Health ICS110.1/RF97.71
6 · The paper itself

Abstract

Japan has one of the world's longest life expectancies, yet biomarkers associated with disability and mortality in very old adults remain uncertain. The goal of this study was to identify plasma proteins associated with incident disability and mortality in community-dwelling octogenarians. Two prospective cohorts were analyzed: the Kawasaki Aging Well-being Project (KAWP; 2017-2018; 4.5-year follow-up) as discovery and Invecchiare in Chianti (InCHIANTI; 1998-2000; 15-year follow-up) for external replication. The discovery sample comprised 230 disability-free adults aged 85-89 years (50.4% women). Twenty-nine plasma proteins were assayed using Luminex xMAP. Associations with incident disability and mortality were estimated with elastic net-regularized Cox models and tested in multivariable Cox models in the full KAWP cohort and in InCHIANTI. Higher beta-2-microglobulin and cystatin C levels were associated with an increased risk of disability (hazard ratio [HR] 1.35, 95% confidence interval [CI] 1.11-1.64; HR 1.42, 95% CI 1.14-1.76). For mortality, epidermal growth factor was inversely associated (HR 0.51, 95% CI 0.27-0.96), while interferon gamma-induced protein 10 was positively associated (HR 1.23, 95% CI 1.06-1.44). Associations with disability were broadly replicated in the full KAWP cohort and among InCHIANTI participants aged ≥ 80 years, whereas mortality-related findings were not replicated. In conclusion, beta-2-microglobulin and cystatin C may serve as biomarkers of future disability. These patterns implicate kidney dysfunction and inflammation as drivers of health decline in very old adults and support early risk stratification to guide preventive interventions.

Indexed as

DisabilityLong-Term CareMortalityOctogenariansPlasma protein

Identifiers

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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.