Evidence map›Paper›PMID 32904265›Full record

ArticleHeliyon2020

Elevated levels of autoantibodies against DNAJC2 in sera of patients with atherosclerotic diseases.

Yoichi Yoshida, Xiao-Meng Zhang, Hao Wang, Toshio Machida, Seiichiro Mine, Eiichi Kobayashi, Akihiko Adachi, Tomoo Matsutani, Ikuo Kamitsukasa, Takeshi Wada and 18 more

Open access · goldAbstract read
In one paragraph

Article in Heliyon, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

15 citing papers in PubMed, 33 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 9 institutions in 2 countries.

Yoichi YoshidaDepartment of Neurological Surgery, Graduate School of Medicine, Chiba University, Chiba 260-8670, 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.
Toshio MachidaDepartment of Neurosurgery, Chiba Cerebral and Cardiovascular Center, Ichihara, 290-0512, Chiba, Japan.
Seiichiro MineDepartment 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.
Tomoo MatsutaniDepartment of Neurological Surgery, Graduate School of Medicine, Chiba University, Chiba 260-8670, Japan.
Ikuo KamitsukasaDepartment of Neurology, Chiba Rosai Hospital, Chiba 290-0003, Japan.
Takeshi WadaDepartment of Internal Medicine, Chiba Aoba Municipal Hospital, Chiba 260-0852, Japan.
Akiyo AotsukaDepartment of Internal Medicine, Chiba Aoba Municipal Hospital, Chiba 260-0852, Japan.
Katsuro IwaseDepartment of Biochemistry and Genetics, Graduate School of Medicine, Chiba University, Chiba 260-8670, Japan.
Go TomiyoshiDepartment 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.
Natsuko ShinmenDepartment 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.
Hirotaka TakizawaPort Square Kashiwado Clinic, Kashiwado Memorial Foundation, Chiba 260-0025, Japan.
Koichi KashiwadoDepartment of Neurology, Kashiwado Hospital, Chiba 260-0854, Japan.
Hideo ShinDepartment of Neurosurgery, Higashi Funabashi Hospital, Chiba 274-0065, Japan.
Yuichi AkaogiDepartment of Neurology, Chiba Cerebral and Cardiovascular Center, Chiba 290-0512, Japan.
Junichiro ShimadaDepartment of Neurology, Chiba Cerebral and Cardiovascular Center, Chiba 290-0512, Japan.
Eiichiro NishiDepartment of Cardiovascular Medicine, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, Japan.
Mikiko OhnoDepartment of Cardiovascular Medicine, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, Japan.
Minoru TakemotoDepartment of Clinical Cell Biology and Medicine, Graduate School of Medicine, Chiba University, Chiba 260-8670, Japan.
Koutaro YokoteDepartment of Clinical Cell Biology and Medicine, Graduate School of Medicine, Chiba University, Chiba 260-8670, Japan.
Kenichiro KitamuraDepartment of Internal Medicine 3, University of Yamanashi School of Medicine, Yamamashi 409-3898, 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 · JPChiba Cerebral and Cardiovascular Center · JPChiba Aoba Municipal Hospital · JPShiga University of Medical Science · JPChibaken Saiseikai Narashino Hospital · JPFujikura (Japan) · JPFunabashi Orthopaedic Hospital · JPKishiwada City Hospital · JPUniversity of Yamanashi · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSerum antibody markers have been increasingly identified not only for cancer and autoimmune diseases but also for atherosclerosis-related diseases such as acute ischemic stroke (AIS), acute myocardial infarction (AMI), diabetes mellitus (DM), and chronic kidney disease (CKD). Biomarkers for transient ischemic attack (TIA) and non-ST segment elevation acute coronary syndrome (NSTEACS) are potentially useful for detection of early phase of atherosclerotic changes against AIS and AMI, respectively.

methodsWe utilized serological identification of antigens by recombinant cDNA expression cloning (SEREX) using a human aortic endothelial cell cDNA phage library and sera from patients with TIA or NSTEACS. Serum antibody levels were measured by amplified luminescent proximity homogeneous assay-linked immunosorbent assay (AlphaLISA) using purified recombinant antigens.

resultsScreening of sera from patients with TIA identified DnaJ heat shock protein family (Hsp40) member C2 (DNAJC2) as a candidate antigen, which was also isolated by SEREX screening using sera of patients with NSTEACS. The validation cohort revealed significantly higher DNAJC2 antibody (DNAJC2-Ab) levels in the sera of patients with TIA or AIS than those in healthy donors (HDs). Multivariate logistic regression analysis indicated that the predictive odds ratios (OR) of DNAJC2-Ab levels for TIA and AIS were 2.54 (95% confidence interval [CI]: 1.36-4.74,

conclusionSerum DNAJC2-Ab level may be useful for early detection of atherosclerotic lesions, which lead to AIS and AMI.

Indexed as

Acute ischemic strokeAcute myocardial infarctionAtherosclerosisAutoantibody biomarkerBiomarkersCardiologyCardiovascular systemClinical researchDiagnosticsDNAJC2Hematological systemNeurologyNeurosurgery

Identifiers

PMID32904265
PMCPMC7452465
OpenAlexW3072241806

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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.