Evidence map›Paper›PMID 30557999›Full record

ArticleMedicine2018

Serum cytokine profiles and Mac-2 binding protein glycosylation isomer (M2BPGi) level in patients with autoimmune hepatitis.

Kiyoshi Migita, Yoshiro Horai, Hideko Kozuru, Tomohiro Koga, Seigo Abiru, Kazumi Yamasaki, Atsumasa Komori, Yuya Fujita, Tomoyuki Asano, Shuzo Sato and 22 more

Open access · goldAbstract read
In one paragraph

Article in Medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 3 pooled it
1.2field-weighted citation impact, top 19% 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

15 citing papers in PubMed, 3 syntheses or guidelines pooled it, 20 citations in OpenAlex.

  1. Pooled it
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  3. Pooled it
  4. Trial
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  11. Recent updates on the management of autoimmune hepatitis.Clinical and molecular hepatology · 2021
    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

32 authors at 11 institutions in 1 country.

Kiyoshi MigitaDepartment of Rheumatology, Fukushima Medical University, Fukushima.
Yoshiro HoraiClinical 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.
Tomoyuki AsanoDepartment of Rheumatology, Fukushima Medical University, Fukushima.
Shuzo SatoDepartment of Rheumatology, Fukushima Medical University, Fukushima.
Eiji SuzukiDepartment of Rheumatology, Fukushima Medical University, Fukushima.
Naoki MatsuokaDepartment 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.
Noriaki NaeshiroNational Hospital Organization, Higashihiroshima Medical center, Higashihiroshima, Hiroshima.
Kaname YoshizawaNational Hospital Organization, Shinsyu-Ueda Medical Center, Ueda, Nagano.
Hajime OhtaNational Hospital Organization, Kanazawa Medical Center, Kanazawa, Ishikawa.
Hironori SakaiNational Hospital Organization, Beppu Medical Center, Beppu, Oita.
Masaaki ShimadaNational Hospital Organization, Nagoya Medical Center, Naka-ku, Nagoya, Aichi.
Hideo NishimuraNational Hospital Organization, Asahikawa Medical Center, Asahikawa, Hokkaido.
Minoru TomizawaNational Hospital Organization, Shimoshizu Hospital, Yotsukaido, Chiba.
Keisuke ArioNational Hospital Organization, Ureshino Medical Center, Ureshino, Saga.
Haruhiro YamashitaNational Hospital Organization, Okayama Medical Center, Okayama, Okayama.
Hiroshi KamitsukasaNational Hospital Organization, Tokyo National Hospital, Tokyo.
Hiroshi KohnoNational Hospital Organization, Kure Medical Center, Kure, 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.
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.
Hiroshi YastuhashiClinical Research Center, Nagasaki Medical Center, Nagasaki.
Fukushima Medical University · JPNagasaki Medical Center · JPNational Hospital Organization · JPNagasaki University · JPAsahikawa Medical University · JPBeppu Medical Center · JPHigashihiroshima Medical Center · JPKure Medical Center · JPNational Hospital Organization Takasaki Medical Center · JPTokyo National Hospital · JPUniversity of Tsukuba · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autoimmune hepatitis (AIH) is an autoimmune liver disease that is characterized by a progressive destruction of the liver parenchyma and the development of liver fibrosis. We aimed to examine the relationship between circulating cytokines/chemokines and the Mac-2 binding protein glycosylation isomer (M2BPGi) levels in Japanese patients with autoimmune hepatitis (AIH).We investigated the relationship between circulating cytokines/chemokines and M2BPGi levels in Japanese patients with AIH. Seventy-seven patients with well-documented AIH were enrolled in the National Hospital Organization (NHO)-AIH-liver-network database. We measured the serum levels of 20 cytokines in 31 selected AIH patients before and after steroid treatment using multisuspension cytokine array.Eleven cytokines and soluble adhesion molecules were increased in untreated AIH patients compared with treated AIH patients. Among these cytokines and soluble adhesion molecules, soluble intercellular adhesion molecule-1 (sICAM-1) and interferon-γ-inducible protein 10 (IP-10) were most downregulated by steroid therapy in AIH patients. We measured serum sICAM-1 and IP-10 by ELISA and found the levels were significantly higher in AIH patients (n = 77) compared with chronic viral hepatitis C patients (n = 32). Furthermore, there was a positive correlation between sICAM-1 or IP-10 and alanine aminotransferase, total bilirubin, and circulating M2BPGi levels. M2BPGi levels were increased in AIH patients with high stages of liver fibrosis. Additionally, M2BPGi levels were correlated with the histological grade of inflammation in AIH. Circulating M2BPGi levels were significantly reduced by steroid treatment in AIH patients.sICAM-1 and IP-10 are useful markers to assess immune-mediated hepatitis activity in AIH and they correlate with circulating M2BPGi. Serum M2BPGi levels increased in untreated AIH patients with active hepatitis and were decreased by steroid therapy. M2BPGi reflects autoimmune-mediated hepatic inflammation as well as liver fibrosis.

Indexed as

AgedAntigens, NeoplasmChemokinesCytokinesFemaleHepatitis, AutoimmuneHumansJapanMaleMembrane GlycoproteinsMiddle AgedResearch DesignAntigens, NeoplasmChemokinesCytokinesMembrane GlycoproteinsTAA90K protein, human

Identifiers

PMID30557999
PMCPMC6320116
OpenAlexW2904921673

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.