Evidence map›Paper›PMID 35083232›Full record

ArticleFrontiers in medicine2021

A Thrombomodulin Promoter Gene Polymorphism, rs2239562, Influences Both Susceptibility to and Outcome of Sepsis.

Eizo Watanabe, Osamu Takasu, Youichi Teratake, Teruo Sakamoto, Toshiaki Ikeda, Joji Kotani, Nobuya Kitamura, Masaaki Ohmori, Ayako Teratani, Goichi Honda and 4 more

Open access · goldAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Frontiers in medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 44% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Dysregulated haemostasis in thrombo-inflammatory disease.Clinical science (London, England : 1979) · 2022
    Review
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

14 authors at 9 institutions in 2 countries.

Eizo WatanabeDepartment of Emergency and Critical Care Medicine, Chiba University Graduate School of Medicine, Chiba, Japan.
Osamu TakasuDepartment of Emergency and Critical Care Medicine, Kurume University School of Medicine, Kurume, Japan.
Youichi TeratakeBiomedical Research Center, Chiba University, Chiba, Japan.
Teruo SakamotoDepartment of Emergency and Critical Care Medicine, Kurume University School of Medicine, Kurume, Japan.
Toshiaki IkedaDivision of Critical Care and Emergency Medicine, Tokyo Medical University Hachioji Medical Center, Hachioji, Japan.
Joji KotaniDepartment of Emergency, Disaster and Critical Care Medicine, Hyogo College of Medicine, Nishinomiya, Japan.
Nobuya KitamuraDepartment of Emergency and Critical Care Medicine, Kimitsu Chuo Hospital, Kisarazu, Japan.
Masaaki OhmoriDepartment of Emergency and Critical Care Medicine, Chiba University Graduate School of Medicine, Chiba, Japan.
Ayako TerataniDepartment of Emergency and Critical Care Medicine, Chiba University Graduate School of Medicine, Chiba, Japan.
Goichi HondaMedical Affairs Department, Asahi Kasei Pharma Corporation, Tokyo, Japan.
Masahiko HatanoBiomedical Research Center, Chiba University, Chiba, Japan.
Benjamin MayerInstitute for Epidemiology and Medical Biometry, Ulm Universtiy, Ulm, Germany.
E Marion SchneiderDivision of Experimental Anesthesiology, University Hospital Ulm, Ulm, Germany.
Shigeto OdaDepartment of Emergency and Critical Care Medicine, Chiba University Graduate School of Medicine, Chiba, Japan.
Chiba University · JPChiba University Hospital · JPKurume University · JPAsahi Kasei (Japan) · JPHyogo Medical University · JPKisarazu Hospital · JPTokyo Medical University Hachioji Medical Center · JPUniversity Hospital Ulm · DEZimmer Biomet (Germany) · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

disseminated intravascular coagulationgenetic predisposition to diseasegenetic testingmulticenter studiessingle nucleotide polymorphisms

Identifiers

PMID35083232
PMCPMC8785550
OpenAlexW4205105836

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.