Literature DB >> 35422513

Protective association of HLA-DPB1*04:01:01 with acute encephalopathy with biphasic seizures and late reduced diffusion identified by HLA imputation.

Mariko Kasai1,2, Yosuke Omae3, Seik-Soon Khor3, Akiko Shibata4,5, Ai Hoshino4, Masashi Mizuguchi4,6, Katsushi Tokunaga3.   

Abstract

Acute encephalopathy with biphasic seizures and late reduced diffusion (AESD) is a severe syndrome of acute encephalopathy that affects infants and young children. AESD is a polygenic disorder preceded by common viral infections with high fever. We conducted an association study of human leukocyte antigen (HLA) regions with AESD using HLA imputation. SNP genotyping was performed on 254 Japanese patients with AESD and 799 healthy controls. We conducted 3-field HLA imputation for 14 HLA genes based on Japanese-specific references using data from our previous genome-wide association study. After quality control, 208 patients and 737 controls were included in the analysis of HLA alleles. We then compared the carrier frequencies of HLA alleles and haplotypes between the patients and controls. HLA-DPB1*04:01:01 showed a significant association with AESD, exerting a protective effect against the disease (p = 0.0053, pcorrected = 0.042, odds ratio = 0.43, 95% confidence interval = 0.21-0.80). The allele frequency of HLA-DPB1*04:01:01 was lower in East Asians than in Caucasians, which may partially account for the higher incidence of AESD in the Japanese population. The present results demonstrate the importance of fine-mapping of the HLA region to investigate disease susceptibilities and elucidate the pathogenesis of AESD.
© 2022. The Author(s), under exclusive licence to Springer Nature Limited.

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Year:  2022        PMID: 35422513     DOI: 10.1038/s41435-022-00170-y

Source DB:  PubMed          Journal:  Genes Immun        ISSN: 1466-4879            Impact factor:   2.676


  37 in total

1.  Carnitine palmitoyl transferase II polymorphism is associated with multiple syndromes of acute encephalopathy with various infectious diseases.

Authors:  Mayu Shinohara; Makiko Saitoh; Jun-ichi Takanashi; Hideo Yamanouchi; Masaya Kubota; Tomohide Goto; Masahiro Kikuchi; Takashi Shiihara; Gaku Yamanaka; Masashi Mizuguchi
Journal:  Brain Dev       Date:  2010-10-12       Impact factor: 1.961

2.  Missense mutations in sodium channel SCN1A and SCN2A predispose children to encephalopathy with severe febrile seizures.

Authors:  Makiko Saitoh; Atsushi Ishii; Yukiko Ihara; Ai Hoshino; Hiroshi Terashima; Masaya Kubota; Kenjiro Kikuchi; Gaku Yamanaka; Kaoru Amemiya; Shinichi Hirose; Masashi Mizuguchi
Journal:  Epilepsy Res       Date:  2015-08-06       Impact factor: 3.045

3.  Diffusion MRI abnormalities after prolonged febrile seizures with encephalopathy.

Authors:  J Takanashi; H Oba; A J Barkovich; H Tada; Y Tanabe; H Yamanouchi; S Fujimoto; M Kato; M Kawatani; A Sudo; H Ozawa; T Okanishi; M Ishitobi; Y Maegaki; Y Koyasu
Journal:  Neurology       Date:  2006-05-09       Impact factor: 9.910

4.  Case-control association study of rare nonsynonymous variants of SCN1A and KCNQ2 in acute encephalopathy with biphasic seizures and late reduced diffusion.

Authors:  Akiko Shibata; Mariko Kasai; Hiroshi Terashima; Ai Hoshino; Taku Miyagawa; Kenjiro Kikuchi; Atsushi Ishii; Hiroshi Matsumoto; Masaya Kubota; Shinichi Hirose; Akira Oka; Masashi Mizuguchi
Journal:  J Neurol Sci       Date:  2020-04-02       Impact factor: 3.181

5.  Epidemiology of acute encephalopathy in Japan, with emphasis on the association of viruses and syndromes.

Authors:  Ai Hoshino; Makiko Saitoh; Akira Oka; Akihisa Okumura; Masaya Kubota; Yoshiaki Saito; Jun-Ichi Takanashi; Shinichi Hirose; Takanori Yamagata; Hideo Yamanouchi; Masashi Mizuguchi
Journal:  Brain Dev       Date:  2011-09-15       Impact factor: 1.961

6.  Thermolabile polymorphism of carnitine palmitoyltransferase 2: A genetic risk factor of overall acute encephalopathy.

Authors:  Akiko Shibata; Mariko Kasai; Ai Hoshino; Taku Miyagawa; Hiroshi Matsumoto; Gaku Yamanaka; Kenjiro Kikuchi; Ichiro Kuki; Akira Kumakura; Shinya Hara; Takashi Shiihara; Sawako Yamazaki; Masayasu Ohta; Takanori Yamagata; Jun-Ichi Takanashi; Masaya Kubota; Akira Oka; Masashi Mizuguchi
Journal:  Brain Dev       Date:  2019-07-24       Impact factor: 1.961

7.  ADORA2A polymorphism predisposes children to encephalopathy with febrile status epilepticus.

Authors:  Mayu Shinohara; Makiko Saitoh; Daisuke Nishizawa; Kazutaka Ikeda; Shinichi Hirose; Jun-ichi Takanashi; Junko Takita; Kenjiro Kikuchi; Masaya Kubota; Gaku Yamanaka; Takashi Shiihara; Akira Kumakura; Masahiro Kikuchi; Mitsuo Toyoshima; Tomohide Goto; Hideo Yamanouchi; Masashi Mizuguchi
Journal:  Neurology       Date:  2013-03-27       Impact factor: 9.910

8.  Clinical spectrum and prognostic factors of acute necrotizing encephalopathy in children.

Authors:  Hye-Eun Seo; Su-Kyeong Hwang; Byung Ho Choe; Min-Hyun Cho; Sung-Pa Park; Soonhak Kwon
Journal:  J Korean Med Sci       Date:  2010-02-17       Impact factor: 2.153

9.  Specific HLA genotypes confer susceptibility to acute necrotizing encephalopathy.

Authors:  A Hoshino; M Saitoh; T Miyagawa; M Kubota; J-I Takanashi; A Miyamoto; K Tokunaga; A Oka; M Mizuguchi
Journal:  Genes Immun       Date:  2016-07-28       Impact factor: 2.676

10.  GWAS identifies candidate susceptibility loci and microRNA biomarkers for acute encephalopathy with biphasic seizures and late reduced diffusion.

Authors:  Mariko Kasai; Yosuke Omae; Yosuke Kawai; Akiko Shibata; Ai Hoshino; Masashi Mizuguchi; Katsushi Tokunaga
Journal:  Sci Rep       Date:  2022-01-25       Impact factor: 4.379

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