研究等業績 - その他 - 今西 彩
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Miyagawa T.
npj Genomic Medicine ( npj Genomic Medicine ) 7 ( 1 ) 2022年12月
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Kawakita Y.
BMC Psychiatry ( BMC Psychiatry ) 22 ( 1 ) 2022年12月
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Imanishi A.
Sleep and Biological Rhythms ( Sleep and Biological Rhythms ) 20 ( 4 ) 585 - 594 2022年10月
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Uemura S.I.
Neuropsychopharmacology Reports ( Neuropsychopharmacology Reports ) 42 ( 3 ) 288 - 298 2022年09月
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Genome-wide association study of idiopathic hypersomnia in a Japanese population
Tanida K.
Sleep and Biological Rhythms ( Sleep and Biological Rhythms ) 20 ( 1 ) 137 - 148 2022年01月
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Imanishi A.
Psychiatry and Clinical Neurosciences ( Psychiatry and Clinical Neurosciences ) 75 ( 10 ) 320 - 322 2021年10月
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Induction of narcolepsy-like symptoms by orexin receptor antagonists in mice
Kaushik M.K.
Sleep ( Sleep ) 44 ( 8 ) 2021年08月
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Yoshizawa K.
Neuropsychiatric Disease and Treatment ( Neuropsychiatric Disease and Treatment ) 17 2955 - 2963 2021年
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中枢性過眠症と神経発達症の関連とそれらの治療(神経発達症の増加はH1N1インフルエンザに起因?)
神林 崇, 今西 彩, 富永 杜絵, 石戸 秀明, 入鹿山 容子, 韓 庫銀, 木村 昌由美, 近藤 英明
神経治療学 ( 日本神経治療学会 ) 38 ( 4 ) 503 - 507 2021年
<p>Even though we are currently in the midst of pandemic from coronavirus infection, the new influenza (H1N1) epidemic in 2009–2010 was unforgettable. Concurrently with the H1N1, narcolepsy surged in post–affected children in China. In Northern Europe, narcolepsy surged in children after H1N1 vaccination. Although there were many cases of H1N1 in Japan, there was no change in the incidence of narcolepsy because anti–influenza drugs prevented the disease from becoming more severe and the vaccine did not contain an adjuvant. It has recently become clear that the Spanish flu that prevailed about 100 years ago was also H1N1. Economo's encephalitis lethargica, which was prevalent at the same time, is thought to be autoimmune encephalitis rather than H1N1–induced influenza encephalitis. It has been reported that Economo's encephalitis caused damage to the hypothalamus, including the orexin system, resulting in lethargic symptoms.</p><p>Since the 2010s, the number of patients with neurodevelopmental disorders (ADHD, ASD) has been increasing among the patients who complain of hypersomnolence. Consideration of the course of symptoms revealed that the patient was originally below the threshold of the diagnostic criteria for neurodevelopmental disease, that hypersomnolence occurred from around adolescence, and that the case also met the criteria for neurodevelopmental disease. Although hypersomnolence was not noticeable in early childhood and inattention was the main symptom, the diagnostic criteria were not met. Hypersomnolence, on the other hand, increased from around adolescence, was added, and attention deficit was exacerbated. Therefore, it is considered that there are many cases that satisfy both the diagnosis of ADHD and central hypersomnia. ADHD characteristics such as attention deficit, hyperactivity, and poor impulsivity may be observed in children who have recovered from Economo's encephalitis and are called post–encephalitis behavioral disorders. The pathophysiology of Economo's encephalitis is presumed to be a disorder of the hypothalamus, including the orexin system, but it is possible that the disorder remained even after recovery.</p><p>We believe that impaired attention, and restlessness caused by the hypersomnolence in neurodevelopmental disorders can be explained by dysfunctions of the orexin system and its arousal system. H1N1 morbidity may trigger neurodevelopmental disorders accompanied by hypersomnolence.</p>
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神林 崇, 今西 彩, 石戸 秀明, 大森 佑貴, 富永 杜絵, 小野 太輔, 西野 精治, 近藤 英明
神経治療学 ( 日本神経治療学会 ) 37 ( 6 ) S139 - S139 2020年
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Ono H.
Sleep and Biological Rhythms ( Sleep and Biological Rhythms ) 17 ( 1 ) 123 - 140 2019年01月
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A variant at 9q34.11 is associated with HLA-DQB1*06:02 negative essential hypersomnia
Miyagawa T.
Journal of Human Genetics ( Journal of Human Genetics ) 63 ( 12 ) 1259 - 1267 2018年12月
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Continuous intrathecal orexin delivery inhibits cataplexy in a murine model of narcolepsy
Kaushik M.K.
Proceedings of the National Academy of Sciences of the United States of America ( Proceedings of the National Academy of Sciences of the United States of America ) 115 ( 23 ) 6046 - 6051 2018年06月
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Omori Y.
Neuropsychiatric Disease and Treatment ( Neuropsychiatric Disease and Treatment ) 14 1281 - 1286 2018年05月
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Omori Y.
Neuropsychiatric Disease and Treatment ( Neuropsychiatric Disease and Treatment ) 14 451 - 457 2018年02月
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夜間睡眠の延長と睡眠相後退症候群に対するaripiprazoleの有効性の検討
神林 崇, 清水 徹男, 大森 佑貴, 今西 彩, 高木 学, 佐川 洋平, 筒井 幸, 竹島 正浩, 小野 太輔, 塩見 利明
神経治療学 ( 日本神経治療学会 ) 34 ( 4 ) 406 - 410 2018年
<p>Delayed sleep phase disorder (DSPD) comprises a persistent or recurrent pattern of sleep disturbances, sleep disruption that leads to insomnia and/or excessive daytime sleepiness, and impaired functioning in social, occupational, or other spheres. Three techniques are typically used to treat DSPD : chronotherapy, phototherapy, and exogenous melatonin administration. Antipsychotics have not been reported in the treatment of DSPD, aripiprazole (APZ), which is a second generation antipsychotic, manifests a novel mechanism of action by serving as a partial agonist of D2 receptors. Depression is reported to be the most common psychopathology associated with DSPD, and APZ is reported to be effective in major depressive disorder as adjunctive therapy. Therefore, we speculated that APZ might be effective to treat DSPD, and we observed how APZ works for the treatment of DSPD.</p><p>Methods : 18 subjects (including 7 women) who are 14–48–year–old (the average is 31.6) were included. The patients were prescribed 0.75–4.5mg APZ at once a day.</p><p>Results : We prescribed 1.5–3.0mg/day of APZ, all subject reduced total sleep time (9.6 +/− 2.3h → 7.8 +/− 2.0h, p=0.03), many cases got up earlier (9.1 +/− 1.9h → 6.7 +/− 1.4h, p=0.005) in the morning and advanced their sleep phase within one week. The sleep onset was not significantly changed (23.5 +/− 2.0h → 22.9 +/− 1.9h, n.s.).</p><p>Conclusion : Low dose of APZ would reduce nocturnal sleep time in the subjects who had prolonged sleep time and DSPD symptoms. The mechanism of action would be dopaminergic up regulation due to dopamine D3 agonistic activity. Since it is difficult for physicians to treat prolonged sleep time and DSPD symptoms, this medication would become a new therapeutic tool for these patients.</p>
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夜間睡眠の延長と睡眠相後退症候群に対するaripiprazoleの有効性の検討
神林 崇, 大森 佑貴, 今西 彩, 高木 学, 佐川 洋平, 筒井 幸, 竹島 正浩, 小野 太輔, 塩見 利明, 清水 徹男
神経治療学 ( 日本神経治療学会 ) 34 ( 4 ) 406 - 410 2018年
<p>Delayed sleep phase disorder (DSPD) comprises a persistent or recurrent pattern of sleep disturbances, sleep disruption that leads to insomnia and/or excessive daytime sleepiness, and impaired functioning in social, occupational, or other spheres. Three techniques are typically used to treat DSPD : chronotherapy, phototherapy, and exogenous melatonin administration. Antipsychotics have not been reported in the treatment of DSPD, aripiprazole (APZ), which is a second generation antipsychotic, manifests a novel mechanism of action by serving as a partial agonist of D2 receptors. Depression is reported to be the most common psychopathology associated with DSPD, and APZ is reported to be effective in major depressive disorder as adjunctive therapy. Therefore, we speculated that APZ might be effective to treat DSPD, and we observed how APZ works for the treatment of DSPD.</p><p>Methods : 18 subjects (including 7 women) who are 14–48–year–old (the average is 31.6) were included. The patients were prescribed 0.75–4.5mg APZ at once a day.</p><p>Results : We prescribed 1.5–3.0mg/day of APZ, all subject reduced total sleep time (9.6 +/− 2.3h → 7.8 +/− 2.0h, p=0.03), many cases got up earlier (9.1 +/− 1.9h → 6.7 +/− 1.4h, p=0.005) in the morning and advanced their sleep phase within one week. The sleep onset was not significantly changed (23.5 +/− 2.0h → 22.9 +/− 1.9h, n.s.).</p><p>Conclusion : Low dose of APZ would reduce nocturnal sleep time in the subjects who had prolonged sleep time and DSPD symptoms. The mechanism of action would be dopaminergic up regulation due to dopamine D3 agonistic activity. Since it is difficult for physicians to treat prolonged sleep time and DSPD symptoms, this medication would become a new therapeutic tool for these patients.</p>
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Suda H.
Sleep and Biological Rhythms ( Sleep and Biological Rhythms ) 15 ( 4 ) 311 - 316 2017年10月
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Takahashi J.
Sleep and Biological Rhythms ( Sleep and Biological Rhythms ) 15 ( 3 ) 235 - 241 2017年07月