Evidence map›Paper›PMID 36748664›Full record

Trial reportClinical and translational science2023

Association between psychomotor function and ALDH2 genotype after consuming barley shochu: A randomized crossover trial.

Keiko Matsuura, Satoshi Kushio, Hiromitsu Imai, Hideo Kudo, Hirokazu Wakuda, Naoyuki Otani, Masae Kuranari, Ai Sekiguchi, Tetsuji Ohyama, Naoto Uemura

Open access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Clinical and translational science, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Trial
  2. Article
  3. 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

10 authors at 4 institutions in 2 countries.

Keiko MatsuuraDepartment of Biomedicine, Faculty of Medicine, Oita University, Oita, Japan.ORCID 0000-0002-8006-5669
Satoshi KushioSanwa Research and Development Laboratory, Sanwa Shurui Co., Oita, Japan.
Hiromitsu ImaiDepartment of Medical Ethics, Faculty of Medicine, Oita University, Oita, Japan.ORCID 0000-0001-7805-1180
Hideo KudoDepartment of Clinical Pharmacology and Therapeutics, Faculty of Medicine, Oita University, Oita, Japan.
Hirokazu WakudaClinical Pharmacology Center, Oita University Hospital, Oita, Japan.
Naoyuki OtaniDepartment of Clinical Pharmacology and Therapeutics, Faculty of Medicine, Oita University, Oita, Japan.
Masae KuranariGeneral Clinical Research Center, Oita University Hospital, Oita, Japan.
Ai SekiguchiDepartment of Clinical Pharmacology and Therapeutics, Faculty of Medicine, Oita University, Oita, Japan.
Tetsuji OhyamaBiostatistics Center, Kurume University, Kurume, Japan.
Naoto UemuraClinical Pharmacology Center, Oita University Hospital, Oita, Japan.
Oita University · JPOita University Hospital · JPDaiichi Sankyo (Germany) · DEKurume University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sustained exposure to acetaldehyde, the major metabolite of ethanol, may influence psychomotor performance even after the breath ethanol level significantly drops several hours following ethanol consumption. We examined the relationship between psychomotor function and changes in exhaled ethanol and acetaldehyde concentrations after consuming a low dose (0.33 g/kg) of barley shochu, a traditional Japanese distilled alcohol beverage, at the point when the exhaled ethanol concentrations dropped below 78,000 parts per billion (0.15 mg/L), the standard threshold for driving under the influence of alcohol in Japan. We assessed how the genetic polymorphisms of rs671 G/G homozygous (*1/*1) and G/A heterozygous (*1/*2) of ALDH2 influenced the kinetics of ethanol and acetaldehyde in exhaled air and psychomotor dynamics using the Digit Symbol Substitution Test (DSST), Critical Flicker Fusion Test (CFFT), and visual analogue scale (VAS) up to 12 h after shochu or water intake. There was no significant difference in DSST and CFFT scores depending on genotype; however, the time required for the DSST to attain the level prior to drinking was longer in the ALDH2 *1/*2 group than in the *1/*1 group. In the VAS test, facial flushing and mood elevation tended to be higher in the *1/*2 group after shochu consumption. VAS scores for mood elevation and facial flushing correlated with acetaldehyde concentration in exhaled breath. These results indicate that DSST recovery tends to be slower and mood elevation higher in the ALDH2 *1/*2 group even when exposed to a low dose of alcohol.

Indexed as

Aldehyde DehydrogenaseHordeumAcetaldehydeAlcohol DrinkingAldehyde Dehydrogenase, MitochondrialCross-Over StudiesEthanolFlushingGenotypeHumansPsychomotor PerformanceAcetaldehydeAldehyde DehydrogenaseAldehyde Dehydrogenase, MitochondrialALDH2 protein, humanEthanol

Identifiers

PMID36748664
PMCPMC10087066
OpenAlexW4319334207

What OpenQuestion holds

Textmetadata
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.