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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)

Risedronate prevents persistent bone loss in prostate cancer patients treated with androgen deprivation therapy: Results of a 2-year follow-up study

http://hdl.handle.net/2297/29565
http://hdl.handle.net/2297/29565
83a42afa-05dc-4c05-8e48-26db894e816e
名前 / ファイル ライセンス アクション
ME-PR-IZUMI-K-238.pdf ME-PR-IZUMI-K-238.pdf (308.0 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 Risedronate prevents persistent bone loss in prostate cancer patients treated with androgen deprivation therapy: Results of a 2-year follow-up study
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 Izumi, Kouji

× Izumi, Kouji

WEKO 362
金沢大学研究者情報 80646787
研究者番号 80646787

Izumi, Kouji

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Mizokami, Atsushi

× Mizokami, Atsushi

WEKO 97
e-Rad 50248580
金沢大学研究者情報 50248580
研究者番号 50248580

Mizokami, Atsushi

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Sugimoto, Kazuhiro

× Sugimoto, Kazuhiro

WEKO 22565

Sugimoto, Kazuhiro

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Narimoto, Kazutaka

× Narimoto, Kazutaka

WEKO 22566
e-Rad 50645207

Narimoto, Kazutaka

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Kitagawa, Yasuhide

× Kitagawa, Yasuhide

WEKO 361
研究者番号 00452102

Kitagawa, Yasuhide

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Koh, Eitetsu

× Koh, Eitetsu

WEKO 20455
e-Rad 90283134
研究者番号 90283134

Koh, Eitetsu

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Namiki, Mikio

× Namiki, Mikio

WEKO 20454
e-Rad 70155985
研究者番号 70155985

Namiki, Mikio

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書誌情報 Prostate Cancer and Prostatic Diseases

巻 14, 号 3, p. 238-242, 発行日 2011-09-01
ISSN
収録物識別子タイプ ISSN
収録物識別子 1365-7852
NCID
収録物識別子タイプ NCID
収録物識別子 AA11470216
DOI
関連タイプ isVersionOf
識別子タイプ DOI
関連識別子 10.1038/pcan.2011.10
出版者
出版者 Nature Publishing Group
抄録
内容記述タイプ Abstract
内容記述 Androgen deprivation therapy (ADT) for prostate cancer (PCa) causes bone loss. Although we reported previously that risedronate significantly recovers bone mineral density (BMD) for up to 12 months, there have been no reports with longer follow-up periods to date. This study extended our earlier series extending the follow-up period to 24 months. Eligible patients had histologically confirmed PCa without lumbar spine metastasis and underwent ADT. Lumbar spine BMD, urinary deoxypyridinoline (uDPD) and serum bone alkaline phosphatase were measured at 6, 12 and 24 months. Among the total of 96 patients, we analyzed 26 and 18 patients in risedronate administration and control groups, respectively. BMD relative to the young adult mean ratio, uDPD and serum bone alkaline phosphatase of the risedronate administration group recovered significantly after 24 months compared with the control group (P0.0001, P0.0001, and P0.0001, respectively). Transient blurred vision, malaise and vertigo were observed in 1 patient each among the 46 patients treated with risedronate within 28 days after first administration. Oral administration of risedronate is safe and effective for the recovery of ADT-induced bone loss in PCa patients even at 24 months after commencement of treatment. © 2011 Macmillan Publishers Limited All rights reserved.
著者版フラグ
出版タイプ AM
出版タイプResource http://purl.org/coar/version/c_ab4af688f83e57aa
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