Evidence map›Paper›PMID 32286426›Full record

ArticleScientific reports2020

Discovery of novel biomarkers for atherosclerotic aortic aneurysm through proteomics-based assessment of disease progression.

Hiroaki Yagi, Mitsuhiro Nishigori, Yusuke Murakami, Tsukasa Osaki, Sayaka Muto, Yutaka Iba, Kenji Minatoya, Yoshihiko Ikeda, Hatsue Ishibashi-Ueda, Takayuki Morisaki and 5 more

Erratum issuedAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Article
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  3. Single-cell Profiling Reveals Cooperative Participation ofInternational journal of medical sciences · 2026
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors.

Hiroaki Yagi *Department of Molecular Pharmacology, National Cerebral and Cardiovascular Center Research Institute, Suita, Osaka, Japan.
Mitsuhiro Nishigori *Department of Molecular Pharmacology, National Cerebral and Cardiovascular Center Research Institute, Suita, Osaka, Japan.
Yusuke Murakami *Omics Research Center, National Cerebral and Cardiovascular Center, Suita, Osaka, Japan.
Tsukasa OsakiDepartment of Molecular Pharmacology, National Cerebral and Cardiovascular Center Research Institute, Suita, Osaka, Japan.
Sayaka MutoOmics Research Center, National Cerebral and Cardiovascular Center, Suita, Osaka, Japan.
Yutaka IbaDepartment of Vascular Surgery, National Cerebral and Cardiovascular Center, Suita, Osaka, Japan.
Kenji MinatoyaDepartment of Vascular Surgery, National Cerebral and Cardiovascular Center, Suita, Osaka, Japan.
Yoshihiko IkedaDepartment of Pathology, National Cerebral and Cardiovascular Center, Suita, Osaka, Japan.
Hatsue Ishibashi-UedaDepartment of Pathology, National Cerebral and Cardiovascular Center, Suita, Osaka, Japan.
Takayuki MorisakiDepartment of Bioscience and Genetics, National Cerebral and Cardiovascular Center Research Institute, Suita, Osaka, Japan.
Hitoshi OginoDepartment of Vascular Surgery, National Cerebral and Cardiovascular Center, Suita, Osaka, Japan.
Hiroshi TanakaDepartment of Vascular Surgery, National Cerebral and Cardiovascular Center, Suita, Osaka, Japan.
Hiroaki SasakiDepartment of Vascular Surgery, National Cerebral and Cardiovascular Center, Suita, Osaka, Japan.
Hitoshi MatsudaDepartment of Vascular Surgery, National Cerebral and Cardiovascular Center, Suita, Osaka, Japan.
Naoto MinaminoDepartment of Molecular Pharmacology, National Cerebral and Cardiovascular Center Research Institute, Suita, Osaka, Japan. minamino@ncvc.go.jp.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Since aortic aneurysms (AAs) are mostly asymptomatic, but they have a high mortality rate upon rupture, their detection and progression evaluation are clinically important issues. To discover diagnostic biomarkers for AA, we performed proteome analysis of aortic media from patients with thoracic atherosclerotic AA (TAAA), comparing protein levels between the aneurysm and normal tissue areas. After hierarchical clustering analysis of the proteome analysis data, tissue samples were classified into three groups, regardless of morphological features. This classification was shown to reflect disease progression stage identified by pathological examination. This proteomics-based staging system enabled us to identify more significantly altered proteins than the morphological classification system. In subsequent data analysis, Niemann-Pick disease type C2 protein (NPC2) and insulin-like growth factor-binding protein 7 (IGFBP7) were selected as novel biomarker candidates for AA and were compared with the previously reported biomarker, thrombospondin 1 (THBS1). Blood concentrations of NPC2 and IGFBP7 were significantly increased, while THBS1 levels were decreased in TAAA and abdominal atherosclerotic AA patients. Receiver operating characteristic analysis of AA patients and healthy controls showed that NPC2 and IGFBP7 have higher specificity and sensitivity than THBS1. Thus, NPC2 and IGFBP7 are promising biomarkers for the detection and progression evaluation of AA.

Indexed as

Disease ProgressionProteomicsAdultAgedAortaAortic AneurysmAtherosclerosisBiomarkersCase-Control StudiesFemaleGene OntologyHumansMaleMiddle AgedProteomeBiomarkersProteome

Identifiers

PMID32286426
PMCPMC7156426

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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.