Evidence map›Paper›PMID 41981774›Full record

ArticlePhysiological reports2026

Circulating elastin crosslinking desmosines are associated with arterial wall degradation in older adults with atherosclerosis.

Hana Inoue, Lisa Takahashi, Hirofumi Tomiyama, Arisa Araki, Toshitaka Nagao, Taishiro Chikamori, Toyonobu Usuki, Utako Yokoyama

Abstract read
In one paragraph

Article in Physiological reports, 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

8 authors.

Hana InoueDepartment of Physiology, Tokyo Medical University, Tokyo, Japan.ORCID 0000-0002-2278-5617
Lisa TakahashiDepartment of Physiology, Tokyo Medical University, Tokyo, Japan.
Hirofumi TomiyamaDepartment of Cardiology, Tokyo Medical University, Tokyo, Japan.
Arisa ArakiDepartment of Materials and Life Sciences, Faculty of Science and Technology, Sophia University, Tokyo, Japan.
Toshitaka NagaoDepartment of Pathology, Tokyo Medical University, Tokyo, Japan.
Taishiro ChikamoriDepartment of Cardiology, Tokyo Medical University, Tokyo, Japan.
Toyonobu UsukiDepartment of Materials and Life Sciences, Faculty of Science and Technology, Sophia University, Tokyo, Japan.
Utako YokoyamaDepartment of Physiology, Tokyo Medical University, Tokyo, Japan.ORCID 0000-0003-1803-0155

Funding

Japan Agency for Medical Research and Development (AMED) JP23ek0210183JSPS KAKENHI JP23K18320
6 · The paper itself

Abstract

Elastin, an extracellular matrix component that contributes to vascular integrity, is progressively degraded during vascular injury including atherosclerosis. We assessed circulating desmosine (DES) and isodesmosine (IDES), elastin-specific crosslinking amino acids, as indicators of arterial elastin degradation by isotope-dilution liquid chromatography-tandem mass spectrometry. Thirty-eight patients with atherosclerotic ischemic heart disease (IHD) and 30 age- and sex-matched healthy controls were enrolled. Plasma concentrations of both DES and IDES were significantly higher in IHD patients than in controls. The area under the receiver operating characteristic curve for total desmosines (DES + IDES) was 0.763. Multivariable analysis revealed that traditional risk factors for atherosclerosis were not significantly associated with plasma concentrations of desmosines. These findings suggest that circulating desmosines reflect arterial wall degeneration in atherosclerosis and are independent of traditional risk factors.

Indexed as

AtherosclerosisDesmosineElastinIsodesmosineMyocardial IschemiaAgedBiomarkersFemaleHumansMaleMiddle AgedBiomarkersDesmosineElastinIsodesmosineatherosclerosisdesmosineselastin crosslinkerischemic heart disease

Identifiers

PMID41981774
PMCPMC13079416

What OpenQuestion holds

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Registered trials

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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.