Evidence map›Paper›PMID 31624517›Full record

ArticleJournal of arrhythmia2019

Genetic variants of alcohol-metabolizing enzymes in Brugada syndrome: Insights into syncope after drinking alcohol.

Qi Wu, Hideki Hayashi, Daiki Hira, Keiko Sonoda, Satoshi Ueshima, Seiko Ohno, Takeru Makiyama, Tomohiro Terada, Toshiya Katsura, Katsuyuki Miura and 1 more

Open access · goldAbstract read
In one paragraph

Article in Journal of arrhythmia, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.0field-weighted citation impact, top 22% 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

5 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Brugada Syndrome: Oligogenic or Mendelian Disease?International journal of molecular sciences · 2020
    Review
  5. Article
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 4 institutions in 1 country.

Qi WuDepartment of Cardiovascular Medicine Shiga University of Medical Science Ohtsu Japan.ORCID https://orcid.org/0000-0001-9212-4139
Hideki HayashiDepartment of Cardiovascular Medicine Shiga University of Medical Science Ohtsu Japan.
Daiki HiraDepartment of Pharmacy Shiga University of Medical Science Hospital Ohtsu Japan.
Keiko SonodaDepartment of Cardiovascular Medicine Shiga University of Medical Science Ohtsu Japan.
Satoshi UeshimaCollege of Pharmaceutical Sciences Ritsumeikan University Kusatsu Japan.
Seiko OhnoDepartment of Cardiovascular Medicine Shiga University of Medical Science Ohtsu Japan.ORCID https://orcid.org/0000-0003-1209-8896
Takeru MakiyamaDepartment of Cardiovascular and Medicine Kyoto University Graduate School of Medicine Kyoto Japan.
Tomohiro TeradaDepartment of Pharmacy Shiga University of Medical Science Hospital Ohtsu Japan.
Toshiya KatsuraCollege of Pharmaceutical Sciences Ritsumeikan University Kusatsu Japan.
Katsuyuki MiuraCenter for Epidemiologic Research in Asia Shiga University of Medical Science Ohtsu Japan.
Minoru HorieDepartment of Cardiovascular Medicine Shiga University of Medical Science Ohtsu Japan.ORCID https://orcid.org/0000-0002-9029-2339
Shiga University of Medical Science · JPRitsumeikan University · JPKyoto University · JPShiga University of Medical Science Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPatients with Brugada syndrome (BrS) are known to have arrhythmic events after alcohol drinking and are recommended to avoid its excessive intake. Mechanisms underlying the alcohol-induced cardiac events are however unknown. This study aimed to test the hypothesis whether activity of alcohol-metabolizing enzymes determines fatal arrhythmic events after drinking alcohol.

methodsA total of 198 Japanese patients with BrS were enrolled in this study. These patients were classified into symptomatic (n = 90) and asymptomatic (n = 108) groups. The former was divided into an alcohol-related group (syncope after alcohol drinking, n = 16) and an alcohol-unrelated group (n = 74). Polymerase chain reaction was performed to determine genetic variants of genes encoding alcohol dehydrogenase 1B (

resultsThe genotype distribution for

conclusionsArrhythmic events after alcohol drinking was associated with enhanced activity of alcohol-metabolizing enzyme

Indexed as

alcoholalcohol‐metabolizing enzymesBrugada syndromepolymorphismsyncope

Identifiers

PMID31624517
PMCPMC6787161
OpenAlexW2969437328

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.