Evidence map›Paper›PMID 41540732›Full record

ArticleGeriatrics & gerontology international2026

Longitudinal Association Between the Carotid Intima-Media Thickness and Sarcopenia in an Older Japanese Population: The SONIC Study.

Ken Terashima, Hiroshi Akasaka, Yuri Onishi, Taku Fujimoto, Shino Yoshida, Ryoichi Ohara, Tomohiro Minami, Yukiko Yasunobe, Masaaki Isaka, Kayo Godai and 13 more

Abstract read
In one paragraph

Article in Geriatrics & gerontology international, 2026. 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

23 authors.

Ken TerashimaDepartment of Geriatric and General Medicine, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.ORCID https://orcid.org/0009-0001-8574-1494
Hiroshi AkasakaDepartment of Geriatric and General Medicine, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.
Yuri OnishiDepartment of Geriatric and General Medicine, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.ORCID https://orcid.org/0009-0009-0898-6496
Taku FujimotoDepartment of Geriatric and General Medicine, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.ORCID https://orcid.org/0009-0008-2503-3921
Shino YoshidaDepartment of Geriatric and General Medicine, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.
Ryoichi OharaDepartment of Geriatric and General Medicine, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.
Tomohiro MinamiDepartment of Geriatric and General Medicine, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.
Yukiko YasunobeDepartment of Geriatric and General Medicine, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.
Masaaki IsakaDepartment of Geriatric and General Medicine, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.ORCID https://orcid.org/0000-0003-0390-3400
Kayo GodaiDivision of Health Sciences, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.
Yuya AkagiDivision of Health Sciences, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.
Michiko KidoDivision of Health Sciences, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.
Mai KabayamaDivision of Health Sciences, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.ORCID https://orcid.org/0000-0003-1394-1152
Saori YasumotoGraduate School of Human Sciences, Osaka University, Suita, Osaka, Japan.
Madoka OgawaGraduate School of Human Sciences, Osaka University, Suita, Osaka, Japan.
Takeshi NakagawaGraduate School of Human Sciences, Osaka University, Suita, Osaka, Japan.
Yukie MasuiTokyo Metropolitan Institute for Geriatrics and Gerontology, Itabashi, Tokyo, Japan.ORCID https://orcid.org/0000-0001-6197-6697
Takumi HirataTokyo Metropolitan Institute for Geriatrics and Gerontology, Itabashi, Tokyo, Japan.
Kazunori IkebeDepartment of Prosthodontics, Gerodontology and Oral Rehabilitation, Osaka University Graduate School of Dentistry, Suita, Osaka, Japan.
Yasumichi AraiCenter for Supercentenarian Medical Research, Keio University School of Medicine, Shinjuku, Tokyo, Japan.
Yasuyuki GondoGraduate School of Human Sciences, Osaka University, Suita, Osaka, Japan.
Kei KamideDivision of Health Sciences, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.ORCID https://orcid.org/0000-0003-1720-2218
Koichi YamamotoDepartment of Geriatric and General Medicine, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.

Funding

Japan Society for the Promotion of Science JP20K07803
6 · The paper itself

Abstract

aimSarcopenia increases the risk of long-term care, disease development, and mortality in older adults. It is also a risk factor for cardiovascular disease and vice versa. Using cross-sectional and longitudinal cohort study designs, we investigated the association between the carotid intima-media thickness (CIMT) and sarcopenia in older adults.

methodsData were extracted from the Septuagenarians, Octogenarians, Nonagenarians Investigation with Centenarians (SONIC) study. Using data from Wave 3 of the SONIC participants, we examined the association between CIMT and sarcopenia using cross-sectional analysis and the association between CIMT at baseline and sarcopenia status 3 years later (Wave 4) in a longitudinal study. Sarcopenia was diagnosed according to the Asian Working Group for Sarcopenia (AWGS) 2019 guidelines.

resultsThe cross-sectional study included 735 participants (347 males, mean age: 76.0 ± 0.9 years); the longitudinal study included 498 participants (247 males, mean age: 75.9 ± 0.9 years). In the cross-sectional study, 130 (17.7%) participants had sarcopenia; multiple logistic regression analysis revealed an odds ratio (OR) of 1.55 (95% confidence interval [CI]: 1.15-2.07) for sarcopenia for every 1 mm increase in the maximum CIMT. In the longitudinal study, 100 participants (20.1%) had sarcopenia at Wave 4. Multiple logistic regression analysis revealed an OR of 1.63 for sarcopenia (95% CI: 1.13-2.36) for each 1 mm increase from the baseline maximum CIMT.

conclusionCIMT was associated with sarcopenia. These results help clarify the pathophysiology of sarcopenia and the possible use of the CIMT as a marker to identify individuals at high risk of sarcopenia.

Indexed as

Carotid Intima-Media ThicknessSarcopeniaAgedAged, 80 and overCross-Sectional StudiesEast Asian PeopleFemaleHumansJapanLongitudinal StudiesMaleRisk Factorscardiovascular diseasecarotid intima‐media thicknesslongitudinal studyolder peoplesarcopenia

Identifiers

PMID41540732
PMCPMC12809006

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.