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  1. 20 医学系研究科・医学部
  2. 20A 学術誌論文
  3. 20A1 雑誌掲載論文

Effects of NR1I2 and ABCB1 Genetic Polymorphisms on Everolimus Pharmacokinetics in Japanese Renal Transplant Patients

http://hdl.handle.net/10295/00006225
http://hdl.handle.net/10295/00006225
3cf120a3-4ab1-4017-ad16-f29c0255977b
名前 / ファイル ライセンス アクション
iA_2022_82.pdf iA_2022_82.pdf (521.8 kB)
Item type 学術雑誌論文 / Journal Article(1)
公開日 2023-02-23
タイトル
タイトル Effects of NR1I2 and ABCB1 Genetic Polymorphisms on Everolimus Pharmacokinetics in Japanese Renal Transplant Patients
言語 en
言語
言語 eng
主題
主題Scheme Other
主題 everolimus
主題
主題Scheme Other
主題 polymorphism
主題
主題Scheme Other
主題 pregnane X-receptor
主題
主題Scheme Other
主題 P-glycoprotein
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
アクセス権
アクセス権 open access
アクセス権URI http://purl.org/coar/access_right/c_abf2
作成者 Yagishita, Hironobu

× Yagishita, Hironobu

en Yagishita, Hironobu

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Kagaya, Hideaki

× Kagaya, Hideaki

en Kagaya, Hideaki

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Saito, Mitsuru

× Saito, Mitsuru

en Saito, Mitsuru

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Numakura, Kazuyuki

× Numakura, Kazuyuki

en Numakura, Kazuyuki

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Yamamoto, Ryohei

× Yamamoto, Ryohei

en Yamamoto, Ryohei

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Sagehashi, Ryuichiro

× Sagehashi, Ryuichiro

en Sagehashi, Ryuichiro

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Habuchi, Tomonori

× Habuchi, Tomonori

en Habuchi, Tomonori

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Satoh, Shigeru

× Satoh, Shigeru

en Satoh, Shigeru

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Miura, Masatomo

× Miura, Masatomo

en Miura, Masatomo

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内容記述
内容記述タイプ Abstract
内容記述 The purpose of this study was to evaluate the effects of NR1I2 (7635G>A and 8055C>T) and ABCB1 (1236C>T, 2677G>T/A, and 3435C>T) genetic polymorphisms on everolimus pharmacokinetics in 98 Japanese renal transplant patients. On day 15 after everolimus administration, blood samples were collected just prior to and 1, 2, 3, 4, 6, 9, and 12 h after administration. The dose-adjusted area under the blood concentration-time curve (AUC(0-12)) of everolimus was significantly lower in patients with the NR1I2 8055C/C genotype than in those with other genotypes (p = 0.022) and was significantly higher in male patients than female patients (p = 0.045). Significant correlations between the dose-adjusted AUC(0-12) of everolimus and age (p = 0.001), aspartate transaminase (p = 0.001), and alanine transaminase (p = 0.005) were found. In multivariate analysis, aging (p = 0.008) and higher alanine transaminase levels (p = 0.032) were independently predictive of a higher dose-adjusted everolimus AUC(0-12). Aging and hepatic dysfunction in patients may need to be considered when evaluating dose reductions in everolimus. In renal transplant patients, management using everolimus blood concentrations after administration may be more important than analysis of NR1I2 8055C>T polymorphism before administration.
言語 en
出版タイプ
出版タイプ VoR
出版タイプResource http://purl.org/coar/version/c_970fb48d4fbd8a85
書誌情報 en : INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES

巻 23, 号 19, 発行日 2022
収録物識別子
収録物識別子タイプ ISSN
収録物識別子 1422-0067
出版者
出版者 MDPI
関連情報
関連タイプ isIdenticalTo
識別子タイプ DOI
関連識別子 https://doi.org/10.3390/ijms231911742
権利情報
権利情報 © 2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access
article distributed under the terms and conditions of the Creative Commons Attribution
(CC BY) license (http://creativecommons.org/licenses/by/4.0/).
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