TY - JOUR
T1 - Pharmacological management of behavioral disturbances in patients with Alzheimer’s disease
AU - Nagata, Tomoyuki
AU - Shinagawa, Shunichiro
AU - Nakajima, Shinichiro
AU - Noda, Yoshihiro
AU - Mimura, Masaru
N1 - Funding Information:
S Shinagawa has received a Grant-in-Aid for Young Scientists (KAKENHI), a research grant from the Japanese Agency for Medical Research and Development (AMED). S Shinagawa also receives research grants from the Mitsui Life Social Welfare Foundation, Eisai, and Pfizer. Y Noda has received a Grant-in-Aid for Young Scientists (KAKENHI), a research grant from the Japanese Agency for Medical Research and Development (AMED) and an investigator-initiated clinical study grant from Teijin Pharma Limited. Dr. Noda also receives research grants from the Japanese Health Foundation, the Meiji Yasuda Mental Health Foundation, the Mitsui Life Social Welfare Foundation, the Takeda Science Foundation, the SENSHIN Medical Research Foundation, the Health Science Center Foundation, the Mochida Memorial Foundation for Medical and Pharmaceutical Research, and the Daiichi Sankyo Scholarship Donation Program. Furthermore, he has received research support from Otsuka Pharmaceutical, Shionogi, and Meiji Seika Pharma. He also receives equipment-in-kind support for an investigator-initiated study from Magventure Inc, Inter Reha Co., Ltd., Rogue Resolutions Ltd., and Miyuki Giken Co., Ltd. M Mimura has also received grants or speaker’s honoraria from Asahi Kasei Pharma, Astellas Pharmaceutical, Daiichi Sankyo, Dainippon-Sumitomo Pharma, Eisai, Eli Lilly and Company, GlaxoSmithKline, Janssen Pharmaceuticals, Meiji-Seika Pharma, Mochida Pharmaceutical, Merck Sharp and Dohme, Novartis Pharma, Otsuka Pharmaceutical, Pfizer, Shionogi, Takeda, Tanabe Mitsubishi Pharma, and Yoshitomi-Yakuhin within the past 3 years. Finally, S Nakajima has received research support from the Japanese Society for the Promotion of Science, the Japanese Research Foundation for Clinical Pharmacology, the Naito Foundation, the Takeda Science Foundation, Daiichi Sankyo, and manuscript fees or speaker’s honoraria from Dainippon Sumitomo Pharma, Eisai, and Yoshitomi Yakuhin within the past three years. The authors have no other relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript apart from those disclosed.
Publisher Copyright:
© 2020, © 2020 Informa UK Limited, trading as Taylor & Francis Group.
PY - 2020/6/12
Y1 - 2020/6/12
N2 - Neuropsychiatric symptoms (NPS) inevitably occur during the course of Alzheimer’s disease (AD) including psychosis, aggression, and depression. The effectiveness of pharmacological treatments for NPS has been limited because of their lack of efficacy, discontinuation due to undesirable adverse events, or poor adherence. In recent consensus guidelines, non-pharmacological treatments for NPS have been prioritized as first-line management strategies. Pharmacological treatments for severe NPS should be administrated as a second-line approach, and have been suggested to be started at a lower dosage followed by titration to a minimum effective dosage and for a limited time period. However, recent studies have shown that some patients receiving pharmacological treatments do not exhibit treatment efficacy in comparison with placebo. The concurrence of several sub-symptoms in NPS makes it difficult to target one symptom exclusively. Therefore, the current review focuses on a strategy for such refractory NPS in patients with AD. Recent randomized controlled trials have shown that the severity of NPS gradually reduces in a time-dependent manner regardless of active treatments. Therefore, clinicians should consider potential causes of NPS sub-symptoms from multifactorial aspects and select alternative treatments (e.g. neuromodulation or relocation into specialized care units) during the long-term disease course.
AB - Neuropsychiatric symptoms (NPS) inevitably occur during the course of Alzheimer’s disease (AD) including psychosis, aggression, and depression. The effectiveness of pharmacological treatments for NPS has been limited because of their lack of efficacy, discontinuation due to undesirable adverse events, or poor adherence. In recent consensus guidelines, non-pharmacological treatments for NPS have been prioritized as first-line management strategies. Pharmacological treatments for severe NPS should be administrated as a second-line approach, and have been suggested to be started at a lower dosage followed by titration to a minimum effective dosage and for a limited time period. However, recent studies have shown that some patients receiving pharmacological treatments do not exhibit treatment efficacy in comparison with placebo. The concurrence of several sub-symptoms in NPS makes it difficult to target one symptom exclusively. Therefore, the current review focuses on a strategy for such refractory NPS in patients with AD. Recent randomized controlled trials have shown that the severity of NPS gradually reduces in a time-dependent manner regardless of active treatments. Therefore, clinicians should consider potential causes of NPS sub-symptoms from multifactorial aspects and select alternative treatments (e.g. neuromodulation or relocation into specialized care units) during the long-term disease course.
KW - Neuropsychiatric symptoms
KW - alzheimer’s disease
KW - efficacy
KW - pharmacological treatment
KW - randomized controlled trial
KW - tolerance
UR - http://www.scopus.com/inward/record.url?scp=85083575224&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85083575224&partnerID=8YFLogxK
U2 - 10.1080/14656566.2020.1745186
DO - 10.1080/14656566.2020.1745186
M3 - Review article
C2 - 32281891
AN - SCOPUS:85083575224
SN - 1465-6566
VL - 21
SP - 1093
EP - 1102
JO - Expert Opinion on Pharmacotherapy
JF - Expert Opinion on Pharmacotherapy
IS - 9
ER -