Evidence map›Paper›PMID 31464928›Full record

ArticleMedicine2019

Galectin-9 in autoimmune hepatitis: Correlation between serum levels of galectin-9 and M2BPGi in patients with autoimmune hepatitis.

Naoki Matsuoka, Hideko Kozuru, Tomohiro Koga, Seigo Abiru, Kazumi Yamasaki, Atsumasa Komori, Yuya Fujita, Junpei Tenmoku, Tomoyuki Asano, Shuzo Sato and 18 more

Open access · goldAbstract read
In one paragraph

Article in Medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

8 citing papers in PubMed, 19 citations in OpenAlex.

  1. Elevated Serum Soluble Tim-3 in Primary Biliary Cholangitis: Lack of Correlation with Cytokines, Chemokines, and Clinical Parameters.The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology · 2025
    Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. The roles of galectins in hepatic diseases.Journal of molecular histology · 2020
    Review
  8. 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

28 authors at 9 institutions in 1 country.

Naoki MatsuokaClinical Research Center, Nagasaki Medical Center, Nagasaki.
Hideko KozuruClinical Research Center, Nagasaki Medical Center, Nagasaki.
Tomohiro KogaDepartment of Immunology and Rheumatology, Unit of Translational Medicine, Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki.
Seigo AbiruClinical Research Center, Nagasaki Medical Center, Nagasaki.
Kazumi YamasakiClinical Research Center, Nagasaki Medical Center, Nagasaki.
Atsumasa KomoriClinical Research Center, Nagasaki Medical Center, Nagasaki.
Yuya FujitaDepartment of Rheumatology, Fukushima Medical University, Fukushima.
Junpei TenmokuDepartment of Rheumatology, Fukushima Medical University, Fukushima.
Tomoyuki AsanoDepartment of Rheumatology, Fukushima Medical University, Fukushima.
Shuzo SatoDepartment of Rheumatology, Fukushima Medical University, Fukushima.
Eiji SuzukiDepartment of Rheumatology, Fukushima Medical University, Fukushima.
Makiko FuruyaDepartment of Rheumatology, Fukushima Medical University, Fukushima.
Hiroko KobayashiDepartment of Rheumatology, Fukushima Medical University, Fukushima.
Hiroshi WatanabeDepartment of Rheumatology, Fukushima Medical University, Fukushima.
Atsushi NaganumaNational Hospital Organization, Takasaki Medical Center, Takasaki.
Kaname YoshizawaNational Hospital Organization, Shinsyu-Ueda Medical Center, Ueda, Nagano.
Masaaki ShimadaNational Hospital Organization, Nagoya Medical Center, Nagoya, Aichi.
Keisuke ArioNational Hospital Organization, Ureshino Medical Center, Ureshino, Saga.
Haruhiro YamashitaNational Hospital Organization, Okayama Medical Center, Okayama.
Hiroshi KohnoNational Hospital Organization, Kure Medical Center, Kure.
Toshihiko KaneyoshiNational Hospital Organization, Fukuyama Medical Center, Fukuyama, Hiroshima.
Minoru NakamuraDepartment of Hepatology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki.
Hiroshi FurukawaMolecular and Genetic Epidemiology Laboratory, Faculty of Medicine, University of Tsukuba, Tsukuba.
Atsushi TakahashiDepartment of Gastroenterology, Fukushima Medical University, Fukushima, Japan.
Atsushi KawakamiDepartment of Immunology and Rheumatology, Unit of Translational Medicine, Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki.
Hiromasa OhiraDepartment of Gastroenterology, Fukushima Medical University, Fukushima, Japan.
Hiroshi YatsuhashiClinical Research Center, Nagasaki Medical Center, Nagasaki.
Kiyoshi MigitaClinical Research Center, Nagasaki Medical Center, Nagasaki.
Fukushima Medical University · JPNagasaki Medical Center · JPNagasaki University · JPNational Hospital Organization · JPFukuyama Cardiovascular Hospital · JPNagoya Medical Center · JPNational Hospital Organization Takasaki Medical Center · JPOkayama Medical Center · JPUniversity of Tsukuba · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autoimmune hepatitis (AIH) is a disorder of unknown etiology in which immune-mediated liver damage progresses to cirrhosis or hepatocellular carcinoma (HCC). The mainstay therapy for AIH is steroids and other immunosuppressive treatments. Currently, there are no validated markers for monitoring immune-mediated hepatic inflammation. Galectin-9 has recently been identified as a potential biomarker in patients with chronic liver disease. The objective of this study was to determine whether Galectin-9 and other serum proteins are associated with active disease in AIH patients.We enrolled 77 Japanese patients with well-documented AIH who were identified from the National Hospital Organization-AIH-liver-network database, as well as 32 patients with chronic hepatitis C (CHC), 27 patients with SLE, and 17 healthy control subjects. Serum levels of galectin-9, and markers of liver injury were measured and compared between groups.Serum levels of galectin-9 were significantly higher in AIH patients than in CHC patients (13.8 ± 4.9 ng/mL vs 8.9 ± 3.0 ng/mL, P < .001) or healthy controls (13.8 ± 4.9 ng/mL vs 5.0 ± 1.3 ng/mL, P < .001). In AIH group, serum galectin-9 levels weakly correlated with alanine aminotransferase levels or total bilirubin (TB) and strongly correlated with C-X-C motif chemokine 10 (CXCL10) and Mac-2 binding protein glycosylation isomer (M2BPGi) levels, but did not correlate with the histological grade of liver fibrosis. Steroid treatment of AIH patients significantly reduced serum galectin-9 levels (14.1 ± 4.9 ng/mL vs 8.3 ± 3.8 ng/mL, P < .001). SLE patients exhibited higher galectin-9 levels, whereas the galectin-9 levels did not correlate with liver function tests such as alanine aminotransferase levels.Serum galectin-9 correlated with disease status in AIH patients and could thus be useful biomarkers to detect hepatic autoimmunity. Because circulating galectin-9 reflects autoimmune-mediated inflammation, it may have additional utility as a biomarker for other autoimmune disorders.

Indexed as

AdultAntigens, NeoplasmBiomarkersBiomarkers, TumorCarrier ProteinsCase-Control StudiesExtracellular Matrix ProteinsFemaleGalectinsGlycoproteinsHepatitis, AutoimmuneHepatitis C, ChronicHumansJapanMaleMembrane GlycoproteinsAntigens, NeoplasmBiomarkersBiomarkers, TumorCarrier ProteinsExtracellular Matrix ProteinsGalectinsGlycoproteinsLGALS3BP protein, humanLGALS9 protein, humanMembrane GlycoproteinsSteroidsTAA90K protein, human

Identifiers

PMID31464928
PMCPMC6736219
OpenAlexW2970702830

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.