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  1. C. 医薬保健学域; 医学類・薬学類・医薬科学類・保健学類
  2. c 10. 学術雑誌掲載論文(医・保健)
  3. 1. 査読済論文(医学・保健)

Altered gene expression in T-cell receptor signalling in peripheral blood leucocytes in acute coronary syndrome predicts secondary coronary events

http://hdl.handle.net/2297/45929
http://hdl.handle.net/2297/45929
2a09e360-d8e6-45fa-a10f-c8389f45b756
名前 / ファイル ライセンス アクション
HO-PR-TAKASHIMA-S-000400.pdf HO-PR-TAKASHIMA-S-000400.pdf (887.4 kB)
Item type 学術雑誌論文 / Journal Article(1)
公開日 2017-10-03
タイトル
タイトル Altered gene expression in T-cell receptor signalling in peripheral blood leucocytes in acute coronary syndrome predicts secondary coronary events
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ journal article
著者 Takashima, Shin-ichiro

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WEKO 24435
金沢大学研究者情報 60547165
研究者番号 60547165

Takashima, Shin-ichiro

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Usui, Soichiro

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WEKO 21777
金沢大学研究者情報 50507043
研究者番号 50507043

Usui, Soichiro

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Kurokawa, Keisuke

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WEKO 24898

Kurokawa, Keisuke

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Kitano, Teppei

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WEKO 1630
金沢大学研究者情報 90748857
研究者番号 90748857

Kitano, Teppei

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Kato, Takeshi

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WEKO 670
e-Rad 90456418
金沢大学研究者情報 90456418
研究者番号 90456418

Kato, Takeshi

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Murai, Hisayoshi

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金沢大学研究者情報 80456417
研究者番号 80456417

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Furusho, Hiroshi

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金沢大学研究者情報 70456416
研究者番号 70456416

Furusho, Hiroshi

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Oda, Hiroyuki

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Oda, Hiroyuki

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Maruyama, Michiro

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WEKO 24900

Maruyama, Michiro

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Nagata, Yoshiki

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WEKO 24901

Nagata, Yoshiki

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Usuda, Kazuo

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WEKO 24902
e-Rad 50262572

Usuda, Kazuo

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Kubota, Koji

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Kubota, Koji

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Takeshita, Yumie

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WEKO 585
金沢大学研究者情報 40507042
研究者番号 40507042

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Sakai, Yoshio

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金沢大学研究者情報 80401925
研究者番号 80401925

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Honda, Masao

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研究者番号 00272980

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Kaneko, Shuichi

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金沢大学研究者情報 60185923
研究者番号 60185923

Kaneko, Shuichi

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Takamura, Masayuki

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WEKO 594
金沢大学研究者情報 60362000
研究者番号 60362000

Takamura, Masayuki

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書誌情報 Open Heart

巻 3, 号 1, p. e000400, 発行日 2016-06-01
ISSN
収録物識別子タイプ ISSN
収録物識別子 2053-3624
DOI
関連タイプ isIdenticalTo
識別子タイプ DOI
関連識別子 10.1136/openhrt-2016-000400
出版者
出版者 BMJ Publishing Group
抄録
内容記述タイプ Abstract
内容記述 Objective: Comprehensive profiling of gene expression in peripheral blood leucocytes (PBLs) in patients with acute coronary syndrome (ACS) as a prognosticator is needed. We explored the specific profile of gene expression in PBLs in ACS for long-term risk stratification. Methods: 30 patients with ACS who underwent primary percutaneous coronary intervention (PCI) and 15 age-matched adults who participated in medical check-ups were enrolled from three centres. Peripheral blood samples were collected to extract RNA for microarray analyses. Results: During the 5-year follow-up, 36% of this cohort developed the expected non-fatal coronary events (NFEs) of target lesion revascularisation (TLR) and PCI for a de novo lesion. Class comparison analysis (p<0.005) demonstrated that 83 genes among 7785 prefiltered genes (41 upregulated vs 42 downregulated genes) were extracted to classify the patients according to the occurrence of NFE. Pathway analysis based on gene ontology revealed that the NFEs were associated with altered gene expression regarding the T-cell receptor signalling pathway in ACS. Univariate t test showed that the expression level of death-associated protein kinase1 (DAPK1), known to regulate inflammation, was the most significantly negatively regulated gene in the event group (0.61-fold, p<0.0005). Kaplan-Meier curve analysis and multivariate analysis adjusted for baseline characteristics or clinical biomarkers demonstrated that lower DAPK1 expression in PBL emerged as an independent risk factor for the NFEs (HR: 8.73; CI 1.05 to 72.8, p=0.045). Conclusions: Altered gene expression in T-cell receptor signalling in PBL in ACS could be a prognosticator for secondary coronary events. © Published by the BMJ Publishing Group Limited.
著者版フラグ
出版タイプ VoR
出版タイプResource http://purl.org/coar/version/c_970fb48d4fbd8a85
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