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  1. COGNITION & REHABILITATION
  2. Vol.4 (2023.12)

Implementation of monoclonal antibody therapy and new rehabilitation strategies for Alzheimer disease

https://doi.org/10.69202/0002000010
https://doi.org/10.69202/0002000010
6abbebe5-cd2e-4c2b-8a3e-3ad27cd9a16f
名前 / ファイル ライセンス アクション
p59-71_Masatoshi p59-71_Masatoshi TAKEDA.pdf (975 KB)
Item type 学術雑誌論文 / Journal Article(1)
公開日 2023-12-15
タイトル
タイトル Implementation of monoclonal antibody therapy and new rehabilitation strategies for Alzheimer disease
言語 en
キーワード
主題Scheme Other
主題 Alzheimer disease
キーワード
主題Scheme Other
主題 immunotherapy
キーワード
主題Scheme Other
主題 disease-modifying therapy
キーワード
主題Scheme Other
主題 aducanumab
キーワード
主題Scheme Other
主題 lecanemab
キーワード
主題Scheme Other
主題 donanemab
キーワード
主題Scheme Other
主題 rehabilitation
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_dcae04bc
資源タイプ review article
ID登録
ID登録 10.69202/0002000010
ID登録タイプ JaLC
内容種別
内容記述タイプ Other
内容記述 Review Article
著者 Masatoshi TAKEDA

× Masatoshi TAKEDA

en Masatoshi TAKEDA

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Misa NAKAMURA

× Misa NAKAMURA

en Misa NAKAMURA

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Hirotoshi UTSUNOMIYA

× Hirotoshi UTSUNOMIYA

en Hirotoshi UTSUNOMIYA

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Tatsunori MURAKAMI

× Tatsunori MURAKAMI

en Tatsunori MURAKAMI

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Junya SAEKI

× Junya SAEKI

en Junya SAEKI

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Takanari KUBO

× Takanari KUBO

en Takanari KUBO

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Yuya NAKAGOSHI

× Yuya NAKAGOSHI

en Yuya NAKAGOSHI

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Nobuo OSHIMA

× Nobuo OSHIMA

en Nobuo OSHIMA

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Keiko SAKAI

× Keiko SAKAI

en Keiko SAKAI

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抄録
内容記述タイプ Abstract
内容記述 In June 2021, the United States Food and Drug Administration granted accelerated approval for aducanumab, the first monoclonal antibody drug to be used in clinical settings in the United States. Meanwhile, it has not received approval in Europe or in Japan owing to significant reduction of amyloid beta without evidence of slowing down the progression of cognitive decline of patients with early Alzheimer disease. In January 2023, outine approval was granted in the United States for a second antibody, lecanemab, which had sufficient evidence of clinical effect and significant deprivation of amyloid beta in the phase 3 trials. Lecanemab was pproved by the Japanese regulatory authorities in Japan in September 2023 after Eisai filed for approval in January. A framework for treatment of Alzheimer disease with antibody therapeutics is required. Although lecanemab has emonstrated efficacy, side effects including amyloid-related imaging abnormality have also been confirmed. Based on the results of clinical trials, there is ongoing discussion of the system for its use in clinical settings. ecanemab is expected to have disease-modifying effects and may inhibit the rate of cognitive decline in the early stage of Alzheimer disease, thereby prolonging the duration of mild stage period. This is also the period hen the rehabilitation is most effective, making psychosocial interventions more important than ever. Rehabilitation techniques need to be developed for patients with early Alzheimer disease receiving disease-modifying therapy. Although disease-modifying drugs inhibit the progression of symptoms in the early stages for a certain period of time, once the threshold is exceeded, cognitive function may decline more rapidly than in non-drug-treated individuals. From this perspective, the effects of disease-modifying therapy are analogous to the effect of high cognitive reserve. These considerations should be taken into account to enhance the clinical utility of rehabilitation for patients under disease-modifying therapy for Alzheimer disease.
言語 en
書誌情報 en : COGNITION & REHABILITATION

巻 4, 号 1, p. 59-71, ページ数 13, 発行日 2023-11-30
出版者
出版者 Osaka Kawasaki Rehabilitation University
言語 en
ISSN
収録物識別子タイプ PISSN
収録物識別子 2436-1097
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