Evidence map›Paper›PMID 32650722›Full record

ArticleBMC gastroenterology2020

Frequently abnormal serum gamma-glutamyl transferase activity is associated with future development of fatty liver: a retrospective cohort study.

Hideki Fujii, Haruna Doi, Tetsuhisa Ko, Taito Fukuma, Toru Kadono, Kohei Asaeda, Reo Kobayashi, Takahiro Nakano, Toshifumi Doi, Yoshikazu Nakatsugawa and 9 more

Open access · goldAbstract read
In one paragraph

Article in BMC gastroenterology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.9field-weighted citation impact, top 8% 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

29 citing papers in PubMed, 60 citations in OpenAlex.

  1. Trial
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  19. Biomarkers of Hepatic Toxicity: An Overview.Current therapeutic research, clinical and experimental · 2024
    Review
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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

19 authors at 1 institution in 1 country.

Hideki FujiiDepartment of Gastroenterology, Japanese Red Cross Kyoto Daiichi Hospital, Hon-machi15-749, Higashiyama-ku, Kyoto, 605-0981, Japan. hidekifuiii710810@yahoo.co.jp.
Haruna DoiDepartment of Gastroenterology, Japanese Red Cross Kyoto Daiichi Hospital, Hon-machi15-749, Higashiyama-ku, Kyoto, 605-0981, Japan.
Tetsuhisa KoDepartment of Gastroenterology, Japanese Red Cross Kyoto Daiichi Hospital, Hon-machi15-749, Higashiyama-ku, Kyoto, 605-0981, Japan.
Taito FukumaDepartment of Gastroenterology, Japanese Red Cross Kyoto Daiichi Hospital, Hon-machi15-749, Higashiyama-ku, Kyoto, 605-0981, Japan.
Toru KadonoDepartment of Gastroenterology, Japanese Red Cross Kyoto Daiichi Hospital, Hon-machi15-749, Higashiyama-ku, Kyoto, 605-0981, Japan.
Kohei AsaedaDepartment of Gastroenterology, Japanese Red Cross Kyoto Daiichi Hospital, Hon-machi15-749, Higashiyama-ku, Kyoto, 605-0981, Japan.
Reo KobayashiDepartment of Gastroenterology, Japanese Red Cross Kyoto Daiichi Hospital, Hon-machi15-749, Higashiyama-ku, Kyoto, 605-0981, Japan.
Takahiro NakanoDepartment of Gastroenterology, Japanese Red Cross Kyoto Daiichi Hospital, Hon-machi15-749, Higashiyama-ku, Kyoto, 605-0981, Japan.
Toshifumi DoiDepartment of Gastroenterology, Japanese Red Cross Kyoto Daiichi Hospital, Hon-machi15-749, Higashiyama-ku, Kyoto, 605-0981, Japan.
Yoshikazu NakatsugawaDepartment of Gastroenterology, Japanese Red Cross Kyoto Daiichi Hospital, Hon-machi15-749, Higashiyama-ku, Kyoto, 605-0981, Japan.
Shinya YamadaDepartment of Gastroenterology, Japanese Red Cross Kyoto Daiichi Hospital, Hon-machi15-749, Higashiyama-ku, Kyoto, 605-0981, Japan.
Takeshi NishimuraDepartment of Gastroenterology, Japanese Red Cross Kyoto Daiichi Hospital, Hon-machi15-749, Higashiyama-ku, Kyoto, 605-0981, Japan.
Naoya TomatsuriDepartment of Gastroenterology, Japanese Red Cross Kyoto Daiichi Hospital, Hon-machi15-749, Higashiyama-ku, Kyoto, 605-0981, Japan.
Hideki SatoDepartment of Gastroenterology, Japanese Red Cross Kyoto Daiichi Hospital, Hon-machi15-749, Higashiyama-ku, Kyoto, 605-0981, Japan.
Yusuke OkuyamaDepartment of Gastroenterology, Japanese Red Cross Kyoto Daiichi Hospital, Hon-machi15-749, Higashiyama-ku, Kyoto, 605-0981, Japan.
Hiroyuki KimuraDepartment of Gastroenterology, Japanese Red Cross Kyoto Daiichi Hospital, Hon-machi15-749, Higashiyama-ku, Kyoto, 605-0981, Japan.
Etsuko KishimotoDepartment of Center for Health promotion, Japanese Red Cross Kyoto Daiichi Hospital, Hon-machi15-749, Higashiyama-ku, Kyoto, 605-0981, Japan.
Nami NakabeDepartment of Center for Health promotion, Japanese Red Cross Kyoto Daiichi Hospital, Hon-machi15-749, Higashiyama-ku, Kyoto, 605-0981, Japan.
Takatomo ShimaDepartment of Center for Health promotion, Japanese Red Cross Kyoto Daiichi Hospital, Hon-machi15-749, Higashiyama-ku, Kyoto, 605-0981, Japan.
Kyoto first Red Cross hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNonalcoholic fatty liver disease is characterized by excessive hepatic fat accumulation. Some individuals frequently present elevated gamma-glutamyl transferase (GGT) levels without fatty liver ultrasound images and other abnormal liver enzymes levels. However, whether these individuals are at an elevated risk for developing fatty liver is unclear. We compared fatty liver change rates and risk factors between individuals with frequently elevated GGT levels and those with normal levels.

methodsWe designed a retrospective cohort study on the basis of complete medical checkup records. One group of individuals had presented normal serum GGT levels during the observation period (Normal-GGT group, n = 2713). Another group had had abnormal elevated serum GGT levels frequently (Abnormal-GGT group, n = 264). We determined the fatty liver change incident rates before and after propensity score matching. We explored confounding factors affecting fatty changes in each group using univariate and multivariate Cox models.

resultsThe change incidence rates were 5.80/1000 and 10.02/1000 person-years in the Normal-GGT and Abnormal-GGT groups, respectively. After propensity score matching, the incidence rates were 3.08/1000 and 10.18/1000 person-years in the Normal-GGT and Abnormal-GGT groups, respectively (p = 0.026). The factors associated with fatty liver changes in the Normal-GGT group included body mass index (BMI), hemoglobin, alanine aminotransferase (ALT), albumin, triglyceride (TG), fasting blood sugar, and high-density lipoprotein levels. Those in the Abnormal-GGT group were platelet counts and TG. In our multivariable analysis, BMI, ALT, albumin, and TG levels were independent predictors of fatty changes in the Normal-GGT group, and high TG level was the only independent predictor in the Abnormal-GGT group.

conclusionsThe incidence rate of fatty liver change in the Abnormal-GGT group was higher than that in the Normal-GGT group. Consecutive elevated GGT levels increase the risk for fatty liver, and high TG levels in those individuals further independently increase the risk.

Indexed as

gamma-GlutamyltransferaseNon-alcoholic Fatty Liver DiseaseAlanine TransaminaseHumansLiver Function TestsRetrospective StudiesAlanine Transaminasegamma-Glutamyltransferasegamma-glutamyltransferase, humanFatty liverGamma-glutamyl transferaseIncidence rateTriglyceride

Identifiers

PMID32650722
PMCPMC7350574
OpenAlexW3041559542

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LicenceCC BY
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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.