Evidence map›Paper›PMID 36516179›Full record

ArticlePloS one2022

Age-dependent sex difference of non-alcoholic fatty liver disease in TSOD and db/db mice.

Erdenetsogt Dungubat, Hiroyuki Kusano, Ichiro Mori, Hirosuke Tawara, Mitsuko Sutoh, Naoki Ohkura, Masakatsu Takanashi, Masahiko Kuroda, Naoki Harada, Emiko Udo and 4 more

Abstract read
In one paragraph

Article in PloS one, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
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

9 citing papers in PubMed.

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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

14 authors.

Erdenetsogt DungubatDepartment of Pathology, School of Medicine, International University of Health and Welfare, Narita, Japan.ORCID 0000-0003-4216-6829
Hiroyuki KusanoDepartment of Pathology, School of Medicine, International University of Health and Welfare, Narita, Japan.
Ichiro MoriDepartment of Pathology, School of Medicine, International University of Health and Welfare, Narita, Japan.
Hirosuke TawaraInstitute for Animal Reproduction, Kasumigaura, Japan.
Mitsuko SutohInstitute for Animal Reproduction, Kasumigaura, Japan.
Naoki OhkuraFaculty of Pharma Sciences, Laboratory of Host Defence, Teikyo University, Tokyo, Japan.
Masakatsu TakanashiDepartment of Molecular Pathology, Tokyo Medical University, Tokyo, Japan.
Masahiko KurodaDepartment of Molecular Pathology, Tokyo Medical University, Tokyo, Japan.
Naoki HaradaDepartment of Applied Biological Chemistry, Graduate School of Agriculture, Osaka Metropolitan University, Osaka, Japan.ORCID 0000-0003-3846-388X
Emiko UdoClinical Genomics Center, Nagasaki University Hospital, Nagasaki, Japan.
Masakazu SoudaClinical Genomics Center, Nagasaki University Hospital, Nagasaki, Japan.
Bungo FurusatoClinical Genomics Center, Nagasaki University Hospital, Nagasaki, Japan.
Toshio FukusatoGeneral Medical Education and Research Center, Teikyo University, Tokyo, Japan.
Yoshihisa TakahashiDepartment of Pathology, School of Medicine, International University of Health and Welfare, Narita, Japan.ORCID 0000-0002-9610-2137

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

According to previous clinical studies, the prevalence of non-alcoholic fatty liver disease (NAFLD) is higher in men than women only during the reproductive age. Animal models of NAFLD that reflect sex differences in humans have not been established. In this study, we examined sex differences in the hepatic lesions of Tsumura Suzuki obese diabetes (TSOD) and db/db mice, which are representative genetic models of NAFLD. Male and female TSOD and db/db mice were fed with a normal diet and tap water ad libitum. Six male and female mice of each strain were sacrificed at the ages of 3 and 9 months, respectively, and serum biochemical, pathological, and molecular analyses were performed. Serum aspartate aminotransferase (AST) levels were significantly higher in male than female mice of both strains at the age of 3 months; however, at 9 months, significant sex differences were not observed. Similarly, alanine aminotransferase (ALT) levels were significantly higher in male mice than in female TSOD mice at the age of 3 months; however, at 9 months, significant sex differences were not observed. Image analysis of histological slides revealed that the frequency of the steatotic area was significantly higher in male than female db/db mice at the age of 3 months; however, significant sex differences were not observed at 9 months. The frequency of Sirius red-positive fibrotic area was significantly higher in male than female mice in both strains at the age of 3 months; however, significant sex differences were not observed at 9 months. Serum AST and ALT levels and hepatic steatosis and fibrosis in TSOD and db/db mice showed age-dependent sex differences consistent with those observed in human NAFLD. These mice may be suitable for studying sex differences of the disease.

Indexed as

Diabetes MellitusNon-alcoholic Fatty Liver DiseaseAlanine TransaminaseAnimalsDisease Models, AnimalFemaleHumansInfantLiverMaleMiceMice, Inbred StrainsMice, ObeseObesitySex CharacteristicsAlanine Transaminase

Identifiers

PMID36516179
PMCPMC9750023

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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.