Evidence map›Paper›PMID 32945427›Full record

ArticleInternational journal of molecular medicine2020

Association between serum anti‑ASXL2 antibody levels and acute ischemic stroke, acute myocardial infarction, diabetes mellitus, chronic kidney disease and digestive organ cancer, and their possible association with atherosclerosis and hypertension.

Shu-Yang Li, Yoichi Yoshida, Eiichi Kobayashi, Akihiko Adachi, Seiichiro Hirono, Tomoo Matsutani, Seiichiro Mine, Toshio Machida, Mikiko Ohno, Eiichiro Nishi and 18 more

Open access · hybridAbstract read
In one paragraph

Article in International journal of molecular medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.3field-weighted citation impact, top 20% of its field
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

12 citing papers in PubMed, 24 citations in OpenAlex.

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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

28 authors at 7 institutions in 1 country.

Shu-Yang LiDepartment of Neurological Surgery, Graduate School of Medicine, Chiba University, Chiba 260‑8670, Japan.
Yoichi YoshidaDepartment of Neurological Surgery, Graduate School of Medicine, Chiba University, Chiba 260‑8670, Japan.
Eiichi KobayashiDepartment of Neurological Surgery, Graduate School of Medicine, Chiba University, Chiba 260‑8670, Japan.
Akihiko AdachiDepartment of Neurological Surgery, Graduate School of Medicine, Chiba University, Chiba 260‑8670, Japan.
Seiichiro HironoDepartment of Neurological Surgery, Graduate School of Medicine, Chiba University, Chiba 260‑8670, Japan.
Tomoo MatsutaniDepartment of Neurological Surgery, Graduate School of Medicine, Chiba University, Chiba 260‑8670, Japan.
Seiichiro MineDepartment of Neurological Surgery, Graduate School of Medicine, Chiba University, Chiba 260‑8670, Japan.
Toshio MachidaDepartment of Neurological Surgery, Chiba Cerebral and Cardiovascular Center, Chiba 290‑0512, Japan.
Mikiko OhnoDepartment of Cardiovascular Medicine, Graduate School of Medicine, Kyoto University, Kyoto 606‑8507, Japan.
Eiichiro NishiDepartment of Cardiovascular Medicine, Graduate School of Medicine, Kyoto University, Kyoto 606‑8507, Japan.
Yoshiro MaezawaDepartment of Endocrinology, Hematology and Gerontology, Graduate School of Medicine, Chiba University, Chiba 260‑8670, Japan.
Minoru TakemotoDepartment of Endocrinology, Hematology and Gerontology, Graduate School of Medicine, Chiba University, Chiba 260‑8670, Japan.
Koutaro YokoteDepartment of Endocrinology, Hematology and Gerontology, Graduate School of Medicine, Chiba University, Chiba 260‑8670, Japan.
Kenichiro KitamuraDepartment of Internal Medicine 3, University of Yamanashi School of Medicine, Yamanashi 409‑3898, Japan.
Makoto SumazakiDepartment of Gastroenterological Surgery and Clinical Oncology, Toho University Graduate School of Medicine, Tokyo 143‑8541, Japan.
Masaaki ItoDepartment of Gastroenterological Surgery and Clinical Oncology, Toho University Graduate School of Medicine, Tokyo 143‑8541, Japan.
Hideaki ShimadaDepartment of Gastroenterological Surgery and Clinical Oncology, Toho University Graduate School of Medicine, Tokyo 143‑8541, Japan.
Hirotaka TakizawaPort Square Kashiwado Clinic, Kashiwado Memorial Foundation, Chiba 260‑0025, Japan.
Koichi KashiwadoDepartment of Neurology, Kashiwado Hospital, Chiba 260‑8656, Japan.
Go TomiyoshiDepartment of Biochemistry and Genetics, Graduate School of Medicine, Chiba University, Chiba 260‑8670, Japan.
Natsuko ShinmenDepartment of Biochemistry and Genetics, Graduate School of Medicine, Chiba University, Chiba 260‑8670, Japan.
Rika NakamuraDepartment of Biochemistry and Genetics, Graduate School of Medicine, Chiba University, Chiba 260‑8670, Japan.
Hideyuki KurodaMedical Project Division, Research Development Center, Fujikura Kasei Co., Saitama 340‑0203, Japan.
Xiao-Meng ZhangDepartment of Biochemistry and Genetics, Graduate School of Medicine, Chiba University, Chiba 260‑8670, Japan.
Hao WangDepartment of Biochemistry and Genetics, Graduate School of Medicine, Chiba University, Chiba 260‑8670, Japan.
Kenichiro GotoDepartment of Biochemistry and Genetics, Graduate School of Medicine, Chiba University, Chiba 260‑8670, Japan.
Yasuo IwadateDepartment of Neurological Surgery, Graduate School of Medicine, Chiba University, Chiba 260‑8670, Japan.
Takaki HiwasaDepartment of Neurological Surgery, Graduate School of Medicine, Chiba University, Chiba 260‑8670, Japan.
Chiba University · JPToho University · JPKyoto University · JPChiba Cerebral and Cardiovascular Center · JPFujikura (Japan) · JPKishiwada City Hospital · JPUniversity of Yamanashi · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of the present study was to identify novel antibody markers for the early diagnosis of atherosclerosis in order to improve the prognosis of patients at risk for acute ischemic stroke (AIS) and acute myocardial infarction (AMI). A first screening involved the serological identification of antigens by recombinant cDNA expression cloning and identified additional sex combs‑like 2 (ASXL2) as a target antigen recognized by serum IgG antibodies in the sera of patients with atherosclerosis. Antigens, including the recombinant glutathione S‑transferase‑fused ASXL2 protein and its synthetic peptide were then prepared to examine serum antibody levels. Amplified luminescence proximity homogeneous assay‑linked immunosorbent assay, which incorporates glutathione‑donor beads and anti‑human‑IgG‑acceptor beads, revealed significantly higher serum antibody levels against the ASXL2 protein and its peptide in the patients with AIS, diabetes mellitus, AMI, chronic kidney disease, esophageal squamous cell carcinoma, or colorectal carcinoma compared with those in healthy donors. The ASXL2 antibody levels were well associated with hypertension complication, but not with sex, body mass index, habitual smoking, or alcohol intake. These results suggest that the serum ASXL2 antibody marker can discriminate between hypertension‑induced atherosclerotic AIS and AMI, as well as a number of digestive organ cancers.

Indexed as

AgedAntibodiesBiomarkersBrain IschemiaCardiovascular DiseasesDiabetes MellitusDigestive System NeoplasmsFemaleHumansIschemic StrokeMaleMiddle AgedRenal Insufficiency, ChronicRepressor ProteinsAntibodiesASXL2 protein, humanBiomarkersRepressor Proteins

Identifiers

PMID32945427
PMCPMC7447314
OpenAlexW3045861247

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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.