Evidence map›Paper›PMID 26489422›Full record

ArticleBMC gastroenterology2015

Evaluation of the role of HLA-DR antigens in Japanese type 1 autoimmune hepatitis.

Yohei Furumoto, Toru Asano, Tomonori Sugita, Hiroshi Abe, Yoshimichi Chuganji, Kazuhiko Fujiki, Akihiko Sakata, Yoshio Aizawa

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in BMC gastroenterology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

17 citing papers in PubMed, 29 citations in OpenAlex.

  1. [Role of HLA genetic variants in autoimmune diseases].Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2026
    Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. HLA, gut microbiome and hepatic autoimmunity.Frontiers in immunology · 2022
    Review
  7. Article
  8. Pathogenesis of Autoimmune Hepatitis-Cellular and Molecular Mechanisms.International journal of molecular sciences · 2021
    Review
  9. Review
  10. Review
  11. Article
  12. Article
  13. Autoimmune Hepatitis in the Asia-Pacific Area.Journal of clinical and translational hepatology · 2018
    Review
  14. Review
  15. Article
  16. Article
  17. Autoimmune hepatitis: current challenges and future prospects.Clinical and experimental gastroenterology · 2017
    Review
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

8 authors at 3 institutions in 1 country.

Yohei FurumotoDepartment of Internal Medicine, Tokyo Metropolitan Bokutoh Hospital, 4-23-15 Kotobashi, Sumida, Tokyo, Japan. youhei_furumoto@tmhp.jp.
Toru AsanoDepartment of Internal Medicine, Tokyo Metropolitan Bokutoh Hospital, 4-23-15 Kotobashi, Sumida, Tokyo, Japan. asanomd985393@aol.com.
Tomonori SugitaDepartment of Gastroenterology and Hepatology, the Jikei University School of Medicine Katsushika Medical Center, Tokyo, Japan. tonexpress@hotmail.com.
Hiroshi AbeDepartment of Gastroenterology and Hepatology, the Jikei University School of Medicine Katsushika Medical Center, Tokyo, Japan. hiroshiabe43222@gmail.com.
Yoshimichi ChuganjiDepartment of Internal Medicine, Tokyo Metropolitan Bokutoh Hospital, 4-23-15 Kotobashi, Sumida, Tokyo, Japan. yoshimichi_chuuganji@tmhp.jp.
Kazuhiko FujikiDepartment of Internal Medicine, Tokyo Metropolitan Bokutoh Hospital, 4-23-15 Kotobashi, Sumida, Tokyo, Japan. kazu-7426@jcom.home.ne.jp.
Akihiko SakataDepartment of Pathology, the Jikei University School of Medicine Katsushika Medical Center, Tokyo, Japan. sakata-a@jikei.ac.jp.
Yoshio AizawaDepartment of Gastroenterology and Hepatology, the Jikei University School of Medicine Katsushika Medical Center, Tokyo, Japan. aichanyoshi@yahoo.co.jp.
Tokyo Metropolitan Bokutoh Hospital · JPJikei University School of Medicine · JPKatsushika Medical Center · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe role of HLA-DR antigens in the clinicopathological features of autoimmune hepatitis (AIH) is not clearly understood. We examined the implications of HLA-DR antigens in Japanese AIH, including the effect of HLA-DR4 on the age and pattern of AIH onset, clinicopathological features, and treatment efficacy.

methodsA total of 132 AIH patients consecutively diagnosed and treated in 2000-2014 at 2 major hepatology centers of eastern Tokyo district were the subjects of this study. The frequency of HLA-DR phenotypes was compared with that in the healthy Japanese population. AIH patients were divided into HLA-DR4-positive or HLA-DR4-negative groups and further sub-classified into elderly and young-to-middle-aged groups, and differences in clinical and histological features were examined. Clinical features associated with the response to immunosuppressive therapy were also determined.

resultsThe frequency of the HLA-DR4 phenotype was significantly higher in AIH than in control subjects (59.7 % vs. 41.8 %, P < 0.001), and the relative risk was 2.14 (95 % CI; 1.51-3.04). HLA-DR4-positive AIH patients were younger than HLA-DR4-negative patients (P = 0.034). Serum IgG and IgM levels were higher (P < 0.001 and P = 0.007, respectively) in HLA-DR4-positive patients. These differences were more prominent in elderly AIH patients. However, there was no difference in IgG and IgM levels between HLA-DR4-positive and HLA-DR4-negative patients of the young-to-middle-aged group. There were no differences in the histological features. In patients with refractory to immunosuppressive therapy, higher total bilirubin, longer prothrombin time, lower serum albumin, and lower platelet count were found. Imaging revealed splenomegaly to be more frequent in refractory patients than in non-refractory patients (60.0 % vs. 30.8 %, P = 0.038). HLA-DR phenotype distribution was similar regardless of response to immunosuppressive therapy.

conclusionsHLA-DR4 was the only DR antigen significantly associated with Japanese AIH. The clinical features of HLA-DR4-positive AIH differed between elderly patients and young-to-middle-aged patients. Treatment response depended on the severity of liver dysfunction but not on HLA-DR antigens.

Indexed as

Gene FrequencyAdolescentAdultAgedAged, 80 and overAge FactorsBilirubinBiomarkersChildFemaleHealthy VolunteersHepatitis, AutoimmuneHLA-DR4 AntigenHumansImmunoglobulin GImmunoglobulin MBilirubinBiomarkersHLA-DR4 AntigenImmunoglobulin GImmunoglobulin MImmunosuppressive Agents

Identifiers

PMID26489422
PMCPMC4618735
OpenAlexW1864000862

What OpenQuestion holds

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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.