Evidence map›Paper›PMID 30759165›Full record

ArticlePloS one2019

Elevated levels of autoantibodies against EXD2 and PHAX in the sera of patients with chronic thromboembolic pulmonary hypertension.

Akira Naito, Takaki Hiwasa, Nobuhiro Tanabe, Takayuki Jujo Sanada, Toshihiko Sugiura, Ayako Shigeta, Jiro Terada, Hirotaka Takizawa, Koichi Kashiwado, Seiichiro Sakao and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

4 citing papers in PubMed, 12 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

11 authors at 1 institution in 1 country.

Akira NaitoDepartment of Respirology, Graduate School of Medicine, Chiba University, Chiba, Japan.ORCID 0000-0002-6487-4845
Takaki HiwasaDepartment of Biochemistry and Genetics, Graduate School of Medicine, Chiba University, Chiba, Japan.
Nobuhiro TanabeDepartment of Respirology, Graduate School of Medicine, Chiba University, Chiba, Japan.
Takayuki Jujo SanadaDepartment of Respirology, Graduate School of Medicine, Chiba University, Chiba, Japan.
Toshihiko SugiuraDepartment of Respirology, Graduate School of Medicine, Chiba University, Chiba, Japan.
Ayako ShigetaDepartment of Respirology, Graduate School of Medicine, Chiba University, Chiba, Japan.
Jiro TeradaDepartment of Respirology, Graduate School of Medicine, Chiba University, Chiba, Japan.
Hirotaka TakizawaPort Square Kashiwado Clinic, Kashiwado Memorial Foundation, Chiba, Japan.
Koichi KashiwadoDepartment of Neurology, Kashiwado Hospital, Kashiwado Memorial Foundation, Chiba, Japan.
Seiichiro SakaoDepartment of Respirology, Graduate School of Medicine, Chiba University, Chiba, Japan.
Koichiro TatsumiDepartment of Respirology, Graduate School of Medicine, Chiba University, Chiba, Japan.
Chiba University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

While circulating autoantibodies have been detected in patients with several cardiovascular diseases, such studies have not been performed for chronic thromboembolic pulmonary hypertension (CTEPH) and pulmonary arterial hypertension (PAH). Here we investigated the production of certain auto-antibodies in CTEPH patients. Initial screening was performed in 5 CTEPH patients and 5 healthy donors (HDs) using a ProtoArray Human Protein Microarray v5.1 containing 9,375 human proteins, and we selected 34 antigens recognized by IgG antibodies more strongly in the sera of CTEPH patients than in the sera of HDs. In subsequent second/third analyses, we validated the auto-antibody level using amplified luminescent proximity homogeneous assay-linked immunosorbent assay (AlphaLISA) in 96 CTEPH patients and 96 HDs as follows: At the second screening, we used 63 crude peptides derived from those selected 34 antigens and found that the serum levels of autoantibodies for 4 peptides seemed higher in CTEPH patients than in HDs. In third analysis, we used the purified peptides of those selected in second screening and found that serum antibodies against peptides derived from exonuclease 3'-5' domain-containing 2 (EXD2) and phosphorylated adaptor for RNA export (PHAX) were significantly higher in CTEPH patients than in HDs. The serum antibody levels to these antigens were also elevated in PAH patients. The titers against EXD2 peptide decreased after surgical treatment in CTEPH patients. These autoantibodies may be useful as biomarkers of CTEPH and PAH, and further investigations may provide novel insight into the etiology.

Indexed as

AdultAgedAutoantibodiesFemaleHumansHypertension, PulmonaryMaleMiddle AgedPeptidesPulmonary EmbolismSleep Apnea SyndromesAutoantibodiesPeptides

Identifiers

PMID30759165
PMCPMC6373903
OpenAlexW2911457815

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.