Evidence map›Paper›PMID 40846767›Full record

ArticleScientific reports2025

High red blood cell distribution width associated with incident frailty in patients with cardiometabolic diseases: A longitudinal study.

Kazuhito Oba, Yoshiaki Tamura, Joji Ishikawa, Yuji Murao, Fumino Yorikawa, Remi Kodera, Ayumi Toba, Kenji Toyoshima, Yuko Chiba, Ai Iizuka and 3 more

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Article
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

13 authors.

Kazuhito ObaDepartment of Diabetes, Metabolism, and Endocrinology, Tokyo Metropolitan Institute for Geriatrics and Gerontology, 35-2 Sakae-Cho, Itabashi-Ku, Tokyo, 173-0015, Japan. kazuhito_oba@tmghig.jp.
Yoshiaki TamuraDepartment of Diabetes, Metabolism, and Endocrinology, Tokyo Metropolitan Institute for Geriatrics and Gerontology, 35-2 Sakae-Cho, Itabashi-Ku, Tokyo, 173-0015, Japan.
Joji IshikawaCenter for Comprehensive Care and Research for Prefrailty, Tokyo Metropolitan Institute for Geriatrics and Gerontology, Tokyo, Japan.
Yuji MuraoCenter for Comprehensive Care and Research for Prefrailty, Tokyo Metropolitan Institute for Geriatrics and Gerontology, Tokyo, Japan.
Fumino YorikawaCenter for Comprehensive Care and Research for Prefrailty, Tokyo Metropolitan Institute for Geriatrics and Gerontology, Tokyo, Japan.
Remi KoderaDepartment of Diabetes, Metabolism, and Endocrinology, Tokyo Metropolitan Institute for Geriatrics and Gerontology, 35-2 Sakae-Cho, Itabashi-Ku, Tokyo, 173-0015, Japan.
Ayumi TobaCenter for Comprehensive Care and Research for Prefrailty, Tokyo Metropolitan Institute for Geriatrics and Gerontology, Tokyo, Japan.
Kenji ToyoshimaDepartment of Diabetes, Metabolism, and Endocrinology, Tokyo Metropolitan Institute for Geriatrics and Gerontology, 35-2 Sakae-Cho, Itabashi-Ku, Tokyo, 173-0015, Japan.
Yuko ChibaDepartment of Diabetes, Metabolism, and Endocrinology, Tokyo Metropolitan Institute for Geriatrics and Gerontology, 35-2 Sakae-Cho, Itabashi-Ku, Tokyo, 173-0015, Japan.
Ai IizukaCenter for Comprehensive Care and Research for Prefrailty, Tokyo Metropolitan Institute for Geriatrics and Gerontology, Tokyo, Japan.
Takumi HirataHuman Care Research Team, Tokyo Metropolitan Institute for Geriatrics and Gerontology, Tokyo, 173-0015, Japan.
Yoshinori FujiwaraCenter for Comprehensive Care and Research for Prefrailty, Tokyo Metropolitan Institute for Geriatrics and Gerontology, Tokyo, Japan.
Atsushi ArakiDepartment of Diabetes, Metabolism, and Endocrinology, Tokyo Metropolitan Institute for Geriatrics and Gerontology, 35-2 Sakae-Cho, Itabashi-Ku, Tokyo, 173-0015, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Frailty is an important health issue in older adults that leads to disability and increased mortality. Red blood cell distribution width (RDW), a measure of variability in red blood cell volume, is associated with inflammation, anemia, and cardiovascular diseases. This study examined whether high RDW (≥ 13.5%) predicts incident frailty over three years in 469 older adults with cardiometabolic disease but without baseline frailty, as defined by the modified Cardiovascular Health Study (mCHS) criteria or the Kihon Checklist (KCL). RDW was measured through a complete blood cell count. Multivariate Cox regression estimated hazard ratios (HRs) and 95% confidence intervals (CIs) for high RDW and incident frailty, adjusting for age, sex, body mass index, eGFR, HbA1c, and basely ne mCHS or KCL score, with low RDW as the reference. During the follow-up period, 29.5% and 24.6% of the patients developed frailty, as defined by the mCHS and KCL, respectively. High RDW was significantly associated with incident mCHS- and KCL-defined frailty, with adjusted HRs of 1.62 (95% CI: 1.10-2.37) and 1.49 (95% CI: 1.02-2.34), respectively. Thus, elevated RDW levels (≥ 13.5%) were found to be an independent predictor of the incidence of two distinct types of frailty in older adults with cardiometabolic diseases.

Indexed as

Cardiovascular DiseasesErythrocyte IndicesErythrocytesFrailtyAgedAged, 80 and overFemaleHumansIncidenceLongitudinal StudiesMaleFrailtyLongitudinal studyRed blood cell distribution width (RDW)

Identifiers

PMID40846767
PMCPMC12373841

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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.