Evidence map›Paper›PMID 35437902›Full record

ArticleJournal of diabetes investigation2022

Combined evaluation of Fibrosis-4 index and fatty liver for stratifying the risk for diabetes mellitus.

Yasuhiko Todo, Teruki Miyake, Shinya Furukawa, Bunzo Matsuura, Toru Ishihara, Masumi Miyazaki, Akihito Shiomi, Hironobu Nakaguchi, Sayaka Kanzaki, Yasunori Yamamoto and 10 more

Open access · goldAbstract read
In one paragraph

Article in Journal of diabetes investigation, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 38% 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

4 citing papers in PubMed, 3 citations in OpenAlex.

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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

20 authors at 4 institutions in 1 country.

Yasuhiko TodoDepartment of Diabetes and Endocrinology, Uwajima City Hospital, Uwajima, Japan.
Teruki MiyakeDepartment of Gastroenterology and Metabology, Ehime University Graduate School of Medicine, Toon, Japan.ORCID https://orcid.org/0000-0002-9905-5356
Shinya FurukawaHealth Services Center, Ehime University, Bunkyo, Matsuyama, Japan.
Bunzo MatsuuraDepartment of Lifestyle-Related Medicine and Endocrinology, Ehime University Graduate School of Medicine, Toon, Japan.
Toru IshiharaDepartment of Gastroenterology and Metabology, Ehime University Graduate School of Medicine, Toon, Japan.
Masumi MiyazakiDepartment of Gastroenterology and Metabology, Ehime University Graduate School of Medicine, Toon, Japan.
Akihito ShiomiDepartment of Diabetes and Endocrinology, Uwajima City Hospital, Uwajima, Japan.
Hironobu NakaguchiHealth Services Center, Ehime University, Bunkyo, Matsuyama, Japan.
Sayaka KanzakiDepartment of Gastroenterology and Metabology, Ehime University Graduate School of Medicine, Toon, Japan.
Yasunori YamamotoDepartment of Gastroenterology and Metabology, Ehime University Graduate School of Medicine, Toon, Japan.
Yohei KoizumiDepartment of Gastroenterology and Metabology, Ehime University Graduate School of Medicine, Toon, Japan.
Osamu YoshidaDepartment of Gastroenterology and Metabology, Ehime University Graduate School of Medicine, Toon, Japan.
Yoshio TokumotoDepartment of Gastroenterology and Metabology, Ehime University Graduate School of Medicine, Toon, Japan.
Masashi HirookaDepartment of Gastroenterology and Metabology, Ehime University Graduate School of Medicine, Toon, Japan.
Eiji TakeshitaDepartment of Gastroenterology and Metabology, Ehime University Graduate School of Medicine, Toon, Japan.
Teru KumagiPostgraduate Medical Education Center, Ehime University Graduate School of Medicine, Toon, Japan.
Yoshio IkedaDepartment of Gastroenterology and Metabology, Ehime University Graduate School of Medicine, Toon, Japan.
Masanori AbeDepartment of Gastroenterology and Metabology, Ehime University Graduate School of Medicine, Toon, Japan.
Takeru IwataEhime General Health Care Association, Matsuyama, Japan.
Yoichi HiasaDepartment of Gastroenterology and Metabology, Ehime University Graduate School of Medicine, Toon, Japan.ORCID https://orcid.org/0000-0003-4117-339X
Ehime University · JPMatsuyama University · JPUwajima City Hospital · JPEhime Medical Center · JP

Funding

Japan Society for the Promotion of Science JP19K11743JSPS JP19K11743
6 · The paper itself

Abstract

AIMS/

introductionTo investigate whether the Fibrosis-4 index can help stratify the risk of diabetes mellitus in patients with fatty liver disease. MATERIALS AND

methodsBased on fatty liver disease and Fibrosis-4 index (cut-off value 1.3), we retrospectively divided 9,449 individuals, who underwent at least two annual health checkups, into four groups stratified by sex: normal; high Fibrosis-4 index without fatty liver disease; low Fibrosis-4 index with fatty liver disease; and high Fibrosis-4 index with fatty liver disease.

resultsOnset rates for diabetes mellitus in the normal, high Fibrosis-4 index without fatty liver disease, low Fibrosis-4 index with fatty liver disease and high Fibrosis-4 index with fatty liver disease groups were 1.6%, 4.3%, 6.8% and 10.2%, respectively, in men, and 0.6%, 0.9%, 5.3% and 7.0%, respectively, in women. Compared with the normal group, the high Fibrosis-4 index without fatty liver disease, low Fibrosis-4 index with fatty liver disease and high Fibrosis-4 index with fatty liver disease groups were at a significant risk for diabetes mellitus onset in both male and female participants. Furthermore, in both sexes, high Fibrosis-4 index with fatty liver disease remained a significant risk factor on multivariate analysis (high fibrosis-4 index with fatty liver disease group: adjusted hazard ratio 4.03, 95% confidence interval 2.19-7.42 [men] and adjusted hazard ratio 6.40, 95% confidence interval 1.77-23.14 [women]).

conclusionsIndividuals with fatty liver disease and high Fibrosis-4 index had a higher risk of diabetes mellitus onset. Therefore, Fibrosis-4 index can help stratify the risk of diabetes mellitus in patients with fatty liver disease and identify patients requiring intervention.

Indexed as

Diabetes MellitusDiabetes Mellitus, Type 2Non-alcoholic Fatty Liver DiseaseFemaleFibrosisHumansMaleRetrospective StudiesRisk FactorsDiabetes mellitusFibrosisNon-alcoholic fatty liver disease

Identifiers

PMID35437902
PMCPMC9434594
OpenAlexW4224233789

What OpenQuestion holds

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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.