Evidence map›Paper›PMID 30382162›Full record

ArticleScientific reports2018

Differential Assessment of Factor Xa Activity and Global Blood Coagulability Utilizing Novel Dielectric Coagulometry.

Satomi Hamada, Yuki Hasegawa, Ai Oono, Anna Suzuki, Naomi Takahashi, Takuro Nishimura, Takatoshi Koyama, Michio Hagihara, Shuji Tohda, Tetsushi Furukawa and 2 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. 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 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 42% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 2 institutions in 1 country.

Satomi HamadaDepartment of Biofunctional Informatics, Tokyo Medical and Dental University (TMDU), Tokyo, Japan.
Yuki HasegawaDepartment of Biofunctional Informatics, Tokyo Medical and Dental University (TMDU), Tokyo, Japan.
Ai OonoDepartment of Biofunctional Informatics, Tokyo Medical and Dental University (TMDU), Tokyo, Japan.
Anna SuzukiDepartment of Biofunctional Informatics, Tokyo Medical and Dental University (TMDU), Tokyo, Japan.
Naomi TakahashiDepartment of Biofunctional Informatics, Tokyo Medical and Dental University (TMDU), Tokyo, Japan.
Takuro NishimuraHeart Rhythm Centre, Tokyo Medical and Dental University (TMDU), Tokyo, Japan.
Takatoshi KoyamaDepartment of Laboratory Molecular Genetics of Haematology, Tokyo Medical and Dental University (TMDU), Tokyo, Japan.
Michio HagiharaDepartment of Clinical Laboratory, Medical Hospital, Tokyo Medical and Dental University (TMDU), Tokyo, Japan.
Shuji TohdaDepartment of Clinical Laboratory, Medical Hospital, Tokyo Medical and Dental University (TMDU), Tokyo, Japan.
Tetsushi FurukawaDepartment of Bio-informational Pharmacology, Medical Research Institute, Tokyo Medical and Dental University (TMDU), Tokyo, Japan.
Kenzo HiraoDepartment of Cardiovascular Medicine, Tokyo Medical and Dental University (TMDU), Tokyo, Japan.
Tetsuo SasanoDepartment of Biofunctional Informatics, Tokyo Medical and Dental University (TMDU), Tokyo, Japan. sasano.bi@tmd.ac.jp.ORCID http://orcid.org/0000-0003-3582-6104
Tokyo Medical and Dental University · JPTokyo Medical and Dental University Hospital · JP

Funding

Japan Society for the Promotion of Science (JSPS) 16K09494
6 · The paper itself

Abstract

An easy-to-use assessment for activated factor X (FXa) is lacking despite its pivotal role in the coagulation. Dielectric blood coagulometry (DBCM) was recently invented as a novel assessment tool for determining the whole blood coagulability by measuring the temporal change in the permittivity of blood. We previously reported that it could evaluate the global blood coagulability. This study aimed to apply the DBCM for assessing FXa activity and its inhibition by anticoagulants. We performed the DBCM analysis along with measurement of the FXa activity by a fluorometric assay in samples from healthy subjects, and identified a new index named maximum acceleration time (MAT) that had a correlation to the FXa activity. Next the DBCM analysis was performed using blood samples mixed with anticoagulants (unfractionated heparin, dalteparin, and edoxaban). Blood samples with three anticoagulants had different profiles of the temporal change in the permittivity, reflecting their different selectivity for FXa. We compared the MAT with the anti-FXa activity assay, and found that the prolongation of MAT was similarly correlated with the anti-FXa activity regardless of the type of anticoagulants. In conclusion, the DBCM has the possibility for evaluating the innate FXa activity and effect of anticoagulants focusing on their FXa inhibition.

Indexed as

Electric ImpedanceAdultAnticoagulantsBlood CoagulationBlood Coagulation TestsFactor XaFactor Xa InhibitorsFemaleHumansMaleAnticoagulantsFactor XaFactor Xa Inhibitors

Identifiers

PMID30382162
PMCPMC6208345
OpenAlexW2898600127

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.