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研究者情報

マスター

アカウント（マスター）

  • 氏名

    齊藤　卓弥(サイトウ　タクヤ), サイトウ　タクヤ

所属（マスター）

  • 北海道大学病院　脳・神経・感覚器科　精神科神経科

所属（マスター）

  • 北海道大学病院　脳・神経・感覚器科　精神科神経科

独自項目

syllabus

  • 2021, 医学総論, Principles of Medicine, 博士後期課程, 医学院, 児童思春期精神疾患、神経発達障害、自殺、インターネット依存、向精神薬、機能画像、脳磁図、心理社会的治療法
  • 2021, 医学総論, Principles of Medicine, 博士後期課程, 医学院, 児童思春期精神疾患、神経発達障害、向精神薬、機能画像、脳磁図、心理社会的治療法、　新規知見

researchmap

プロフィール情報

学位

  • 医学博士（日本医科大学）

プロフィール情報

  • プロフィール

    1987年日本医科大学卒業、その後日本医科大学神経科,コーネル医科大学精神科（N.Y）、アルバート・アインシュタイン医科大学（N.Y）を経て1999年日本医科大学にて医学博士取得。
    アルバート・アインシュタイン医科大学精神科助教授、日本医科大学精神医学教室 准教授を経て2014年北海道大学大学院医学研究科 児童思春期精神医学講座 特任教授就任。現在に至る。
    精神保健指定医
    日本精神神経学会専門医・指導医
    専門:児童思春期精神医学

  • 姓

    齊藤, サイトウ

  • 名

    卓弥, タクヤ

  • ID各種

    201401081965830926

対象リソース

業績リスト

研究キーワード

  • 児童思春期精神医学   児童精神医学   自己治癒力   総合失調症   TNF-α   質的評価   統合失調症   面接分析   指標   PET   癒し   HPS   模擬患者   免疫   笑い   患者   エビデンス   分子イメージング   ドパミン   D2受容体   

研究分野

  • ライフサイエンス / 精神神経科学 / 児童思春期精神医学
  • ライフサイエンス / 精神神経科学
  • ライフサイエンス / 医療管理学、医療系社会学

経歴

  • 2014年04月 - 現在 北海道大学大学院医学研究科 児童思春期精神医学講座 特任教授
  • 2005年04月 - 2014年03月 日本医科大学 医学部 准教授

学歴

  • 1981年04月 - 1987年03月   日本医科大学

委員歴

  • 2007年04月 - 現在   日本精神神経学会   国際委員会委員

論文

  • Noa Tsujii, Takashi Okada, Masahide Usami, Hidenori Kuwabara, Junichi Fujita, Hideki Negoro, Junzo Iida, Yumi Aoki, Yoshikazu Takaesu, Takuya Saito
    Psychiatry and Clinical Neurosciences Reports 1 4 2022年12月
  • Hidenori Yamasue, Masaki Kojima, Hitoshi Kuwabara, Miho Kuroda, Kaori Matsumoto, Chieko Kanai, Naoko Inada, Keiho Owada, Keiko Ochi, Nobutaka Ono, Seico Benner, Tomoyasu Wakuda, Yosuke Kameno, Jun Inoue, Taeko Harada, Kenji Tsuchiya, Kazuo Umemura, Aya Yamauchi, Nanayo Ogawa, Itaru Kushima, Norio Ozaki, Satoshi Suyama, Takuya Saito, Yukari Uemura, Junko Hamada, Yukiko Kano, Nami Honda, Saya Kikuchi, Moe Seto, Hiroaki Tomita, Noriko Miyoshi, Megumi Matsumoto, Yuko Kawaguchi, Koji Kanai, Manabu Ikeda, Itta Nakamura, Shuichi Isomura, Yoji Hirano, Toshiaki Onitsuka, Hirotaka Kosaka, Takashi Okada
    Brain : a journal of neurology 145 2 490 - 499 2022年04月18日 
    Although intranasal oxytocin is expected to be a novel therapy for the core symptoms of autism spectrum disorder, which has currently no approved medication, the efficacy of repeated administrations was inconsistent, suggesting that the optimal dose for a single administration of oxytocin is not optimal for repeated administration. The current double-blind, placebo-controlled, multicentre, crossover trial (ClinicalTrials.gov Identifier: NCT03466671) was aimed to test the effect of TTA-121, a new formulation of intranasal oxytocin spray with an enhanced bioavailability (3.6 times higher than Syntocinon® spray, as assessed by area under the concentration-time curve in rabbit brains), which enabled us to test a wide range of multiple doses, on autism spectrum disorder core symptoms and to determine the dose-response relationship. Four-week administrations of TTA-121, at low dose once per day (3 U/day), low dose twice per day (6 U/day), high dose once per day (10 U/day), or high dose twice per day (20 U/day), and 4-week placebo were administered in a crossover manner. The primary outcome was the mean difference in the reciprocity score (range: 0-14, higher values represent worse outcomes) on the Autism Diagnostic Observation Schedule between the baseline and end point of each administration period. This trial with two administration periods and eight groups was conducted at seven university hospitals in Japan, enrolling adult males with high-functioning autism spectrum disorder. Enrolment began from June 2018 and ended December 2019. Follow-up ended March 2020. Of 109 males with high-functioning autism spectrum disorder who were randomized, 103 completed the trial. The smallest P-value, judged as the dose-response relationship, was the contrast with the peak at TTA-121 6 U/day, with inverted U-shape for both the full analysis set (P = 0.182) and per protocol set (P = 0.073). The Autism Diagnostic Observation Schedule reciprocity score, the primary outcome, was reduced in the TTA-121 6 U/day administration period compared with the placebo (full analysis set: P = 0.118, mean difference = -0.5; 95% CI: -1.1 to 0.1; per protocol set: P = 0.012, mean difference = -0.8; 95% CI: -1.3 to -0.2). The per protocol set was the analysis target population, consisting of all full analysis set participants except those who deviated from the protocol. Most dropouts from the full analysis set to the per protocol set occurred because of poor adherence to the test drug (9 of 12 in the first period and 8 of 15 in the second period). None of the secondary clinical and behavioural outcomes were significantly improved with the TTA-121 compared with the placebo in the full analysis set. A novel intranasal spray of oxytocin with enhanced bioavailability enabled us to test a wide range of multiple doses, revealing an inverted U-shape dose-response curve, with the peak at a dose that was lower than expected from previous studies. The efficacy of TTA-121 shown in the current exploratory study should be verified in a future large-scale, parallel-group trial.
  • 恐怖記憶の分子・生理学的基盤の解明とPTSDの治療開発 PTSD治療におけるmemantineの効果と意義
    金 吉晴, 堀 弘明, 伊藤 真利子, 松井 三枝, 加茂 登志子, 斎藤 卓弥, 西松 能子, 鬼頭 諭, 喜田 聡
    精神神経学雑誌 124 4付録 S - 295 (公社)日本精神神経学会 2022年04月 [査読無し]
  • Takuya Saito, Mitsuhiro Ishida, Atsushi Nishiyori, Toshimitsu Ochiai, Hideaki Katagiri, Hideo Matsumoto
    Journal of child and adolescent psychopharmacology 32 3 132 - 142 2022年04月 
    Objective: The goal of this study was to evaluate the efficacy and safety of duloxetine in children and adolescents (9-17 years of age) with major depressive disorder (MDD) in Japan. Methods: This study consists of two clinical trials. First, a 6-week, randomized double-blind placebo-controlled clinical trial (RCT) was conducted. The primary endpoint of RCT was the change in Children's Depression Rating Scale-Revised (CDRS-R) total scores from baseline. Following RCT, an open-label long-term extension trial (OLE) was conducted to investigate the longer-term safety of duloxetine for ∼1 year. Results: In RCT, CDRS-R total score changes from baseline to 6 weeks after the start of administration (primary endpoint) were -21.03 in the duloxetine group (n = 74) and -22.42 in the placebo group (n = 74). No significant difference was observed in the primary endpoint between the groups (p = 0.5587). In addition, no significant difference was observed in secondary endpoints such as CDRS-R response rates. The proportion of patients with ≥1 treatment-emergent adverse event (TEAE) in RCT was significantly higher in the duloxetine group (78.7%) than in the placebo group (62.2%), and most were mild or moderate in severity. Changes in CDRS-R total scores during OLE, in consecutive patients from the duloxetine group in RCT (n = 63), or placebo group (n = 59) in RCT, and newly enrolled patients (n = 28), were -12.1, -11.3, and -17.8, respectively. The proportion of patients with ≥1 TEAE in OLE was 90.5%, 88.1%, and 89.3% in the respective groups, and most of them were mild or moderate in severity. Conclusions: Duloxetine did not show superiority to placebo in efficacy in children and adolescents with MDD in Japan. Overall reported TEAEs were consistent with the currently available duloxetine safety profile and no new safety finding was observed in the two clinical trials.
  • Takuya Saito, Yohei Hyodo, Reiko Sakaguchi, Hiroshi Nakamura, Jun Ishigooka
    Journal of child and adolescent psychopharmacology 32 1 24 - 35 2022年02月 
    Objectives: To evaluate the long-term efficacy and safety/tolerability of oral blonanserin in adolescents with schizophrenia (Study registration number: JapicCTI-111725). Methods: This 52-week, multicenter, open-label extension study enrolled adolescent patients with schizophrenia who opted to enter in this study after the completion of the preceding placebo-controlled study. Blonanserin tablet was orally administered twice daily, after morning and evening meals, for 52 weeks using dose-titration method within a range between 4 and 24 mg/day. The primary end point was the change from baseline to the end of the study in the Positive and Negative Syndrome Scale (PANSS) total score. Safety/tolerability was assessed by the incidence and severity of adverse events. Results: Of 117 patients who completed the preceding placebo-controlled study, 109 entered this extension study and 43 (39.4%) of them discontinued the study treatment. The safety analysis set comprised 106 patients who received the study drug at least once, including 36 and 70 patients treated with placebo (DB-placebo group) and blonanserin tablet (DB-blonanserin group), respectively, in the placebo-controlled study. At the last assessment, the mean change in PANSS total score overall [mean (standard deviation)] was -24.9 (20.76) from the baseline of the placebo-controlled study, which was similar in the DB-placebo and DB-blonanserin groups. The overall incidence of adverse events was 90.6%, and most of them were mild or moderate in severity, with similar incidence of extrapyramidal symptoms (38.7%) to that in adults receiving long-term blonanserin oral tablet treatment and minimal change in weight and metabolic parameters. Conclusions: This long-term extension study showed that 52 weeks of oral blonanserin treatment improved or stabilized psychiatric symptoms in patients with adolescent schizophrenia. There were no major issues with the safety or tolerability of blonanserin administration in this study. Considering relatively less adverse effects on weight increase and metabolic parameters, blonanserin is expected to be a safe/tolerable treatment option for adolescent schizophrenia that can be used seamlessly from adolescence to adulthood.
  • Takuya Saito, Saori Sugimoto, Reiko Sakaguchi, Hiroshi Nakamura, Jun Ishigooka
    Journal of child and adolescent psychopharmacology 32 1 12 - 23 2022年02月 
    Objectives: To evaluate the short-term efficacy and safety of blonanserin in adolescents with schizophrenia. Methods: This 6-week multicenter, double-blind, randomized, placebo-controlled study investigated fixed-dose blonanserin (8 or 16 mg/day) in patients 12-18 years of age diagnosed with schizophrenia, as indicated by a Positive and Negative Syndrome Scale (PANSS) total score of 60-120 and a Clinical Global Impressions-Severity score of ≥3. The primary endpoint was change from baseline to week 6 in the PANSS total score, using a mixed model for repeated measures analysis. Safety was assessed by the incidence and severity of adverse events (AEs). Results: Among 151 randomized patients, 150 were included in the primary analysis population. Demographic and clinical characteristics were similar across groups at baseline. The rate of study discontinuation was 14.9%, 23.5%, and 28.3% in patients administered with placebo, blonanserin 8 mg/day, and blonanserin 16 mg/day, respectively. The least-squares mean change (95% confidence interval [CI]) from baseline to week 6 in PANSS total score was -10.6 (-16.10 to -5.10), -15.3 (-20.80 to -9.86), and -20.5 (-25.89 to -15.16) in patients administered placebo, 8 mg/day blonanserin, and 16 mg/day blonanserin, respectively. The 16-mg/day blonanserin group showed significantly greater reduction in the PANSS total score than the placebo group (least-squares mean difference [95% CI]: -9.9 [-17.61 to -2.25], p = 0.012, effect size: 0.538), although the 8-mg/day group showed no significant difference. The incidence of AEs such as akathisia, somnolence, and hyperprolactinemia was higher in the blonanserin groups than in the placebo group. AEs associated with blonanserin were generally mild and were consistent with its known profile in adults with schizophrenia. Conclusions: Blonanserin achieved a sufficient efficacy in adolescent patients, and the safety profile was similar to that in adults, which suggests that blonanserin may be a safe treatment option for adolescents with schizophrenia. Study registration number: Japic CTI-111724.
  • Sachiko Itoh, Keiko Yamazaki, Satoshi Suyama, Atsuko Ikeda-Araki, Chihiro Miyashita, Yu Ait Bamai, Sumitaka Kobayashi, Hideyuki Masuda, Takeshi Yamaguchi, Houman Goudarzi, Emiko Okada, Ikuko Kashino, Takuya Saito, Reiko Kishi
    Environment international 159 107026 - 107026 2022年01月15日 
    BACKGROUND: Disruption of thyroid hormone (TH) levels during pregnancy contributes to attention deficit hyperactivity disorder (ADHD). Exposure to perfluoroalkyl substances (PFAS) during gestation may affect levels of maternal and neonatal TH; however, little is known about the effect of PFAS on ADHD mediated by TH. OBJECTIVES: We investigated the impact of maternal PFAS exposure on children's ADHD symptoms with the mediating effect of TH. METHODS: In a prospective birth cohort (the Hokkaido study), we included 770 mother-child pairs recruited between 2002 and 2005 for whom both prenatal maternal and cord blood samples were available. Eleven PFAS were measured in maternal serum obtained at 28-32 weeks of gestation using ultra-performance liquid chromatography coupled with triple quadrupole tandem mass spectrometry. TH and thyroid antibody, including thyroid-stimulating hormone (TSH), free triiodothyronine (FT3), free thyroxine (FT4), thyroid peroxidase antibody (TPOAb), and thyroglobulin antibody (TgAb) were measured in maternal blood during early pregnancy (median 11 gestational weeks) and in cord blood at birth. ADHD symptoms in the children at 8 years of age were rated by their parents using the ADHD-Rating Scale (ADHD-RS). The cut-off value was set at the 80th percentile for each sex. RESULTS: Significant inverse associations were found between some PFAS in maternal serum and ADHD symptoms among first-born children. Assuming causality, we found only one significant association: maternal FT4 mediated 17.6% of the estimated effect of perfluoroundecanoic acid exposure on hyperactivity-impulsivity among first-born children. DISCUSSION: Higher PFAS levels in maternal serum during pregnancy were associated with lower risks of ADHD symptoms at 8 years of age. The association was stronger among first-born children in relation to hyperactivity-impulsivity than with regard to inattention. There was little mediating role of TH during pregnancy in the association between maternal exposure to PFAS and reduced ADHD symptoms at 8 years of age.
  • Hayato Watanabe, Atsushi Shimojo, Kazuyori Yagyu, Tsuyoshi Sonehara, Kazuyoshi Takano, Jared Boasen, Hideaki Shiraishi, Koichi Yokosawa, Takuya Saito
    PloS one 17 6 e0270090  2022年 
    Communication is one of the most important abilities in human society, which makes clarification of brain functions that underlie communication of great importance to cognitive neuroscience. To investigate the rapidly changing cortical-level brain activity underlying communication, a hyperscanning system with both high temporal and spatial resolution is extremely desirable. The modality of magnetoencephalography (MEG) would be ideal, but MEG hyperscanning systems suitable for communication studies remain rare. Here, we report the establishment of an MEG hyperscanning system that is optimized for natural, real-time, face-to-face communication between two adults in sitting positions. Two MEG systems, which are installed 500m away from each other, were directly connected with fiber optic cables. The number of intermediate devices was minimized, enabling transmission of trigger and auditory signals with almost no delay (1.95-3.90 μs and 3 ms, respectively). Additionally, video signals were transmitted at the lowest latency ever reported (60-100 ms). We furthermore verified the function of an auditory delay line to synchronize the audio with the video signals. This system is thus optimized for natural face-to-face communication, and additionally, music-based communication which requires higher temporal accuracy is also possible via audio-only transmission. Owing to the high temporal and spatial resolution of MEG, our system offers a unique advantage over existing hyperscanning modalities of EEG, fNIRS, or fMRI. It provides novel neuroscientific methodology to investigate communication and other forms of social interaction, and could potentially aid in the development of novel medications or interventions for communication disorders.
  • Nano Yoneta, Hayato Watanabe, Atsushi Shimojo, Kazuyoshi Takano, Takuya Saito, Kazuyori Yagyu, Hideaki Shiraishi, Koichi Yokosawa, Jared Boasen
    Frontiers in neuroscience 16 790057 - 790057 2022年 
    Auditory communication is an essential form of human social interaction. However, the intra-brain cortical-oscillatory drivers of auditory communication exchange remain relatively unexplored. We used improvisational music performance to simulate and capture the creativity and turn-taking dynamics of natural auditory communication. Using magnetoencephalography (MEG) hyperscanning in musicians, we targeted brain activity during periods of music communication imagery, and separately analyzed theta (5-7 Hz), alpha (8-13 Hz), and beta (15-29 Hz) source-level activity using a within-subjects, two-factor approach which considered the assigned social role of the subject (leader or follower) and whether communication responses were improvisational (yes or no). Theta activity related to improvisational communication and social role significantly interacted in the left isthmus cingulate cortex. Social role was furthermore differentiated by pronounced occipital alpha and beta amplitude increases suggestive of working memory retention engagement in Followers but not Leaders. The results offer compelling evidence for both musical and social neuroscience that the cognitive strategies, and correspondingly the memory and attention-associated oscillatory brain activities of interlocutors during communication differs according to their social role/hierarchy, thereby indicating that social role/hierarchy needs to be controlled for in social neuroscience research.
  • Kazuyori Yagyu, Ryusaku Hashimoto, Atsushi Shimojo, Michiru Iwata, Keitaro Sueda, Ayumi Seki, Hideaki Shiraishi, Takuya Saito
    Brain & development 43 9 893 - 903 2021年10月 
    BACKGROUND: Dyslexia is a neurodevelopmental disorder which occurs in childhood but continues to influence academic and occupational function in adulthood. Recently, a Japanese dyslexia questionnaire and diagnostic procedure was established for primary school children. However, there is currently no procedure for the diagnosis or screening of dyslexia in individuals at or above junior high school age; accordingly, we aimed to develop a questionnaire to screen for reading difficulties in those individuals. METHODS: A questionnaire with various candidate items was developed from two English questionnaires, one Japanese questionnaire, and newly devised items focusing on the Japanese writing system and the most appropriate 28 items were selected. In total, 462 adults and 127 junior high to high school students were enrolled. Of those, 191 participants also took part in reading tests. After the exploratory factor analysis, reliability and validity were evaluated using the above control participants and 12 adolescents with dyslexia. RESULTS: The questionnaire included three factors, i.e., silent reading sub-scale (four items), writing sub-scale (four items), and aloud reading sub-scale (three items). Five were newly devised items focusing on the Japanese writing system. Cronbach's alphas of the three factors were 0.706, 0.638, and 0.568, respectively, and the interclass correlation coefficients (2,1) were 0.743, 0.609, and 0.695, respectively. The silent reading and aloud reading sub-scales were positively correlated with word, non-word, and passage reading time. DISCUSSION: The newly developed questionnaire correlated well with actual reading performance and may be used to screen reading difficulty in Japanese individuals at or above junior high school age.
  • Hyperscanningと脳活動 脳磁図を用いたコミュニケーション脳科学
    柳生 一自, 渡辺 隼人, 高野 一義, 下條 暁司, 白石 秀明, 横澤 宏一, 齊藤 卓弥
    精神神経学雑誌 2021特別号 S490 - S490 (公社)日本精神神経学会 2021年09月
  • ハイパースキャニングによる社会脳機能計測 Dual MEGを用いたコミュニケーション脳科学の可能性
    柳生 一自, 渡辺 隼人, 高野 一義, 下條 暁司, 白石 秀明, 横澤 宏一, 齊藤 卓弥
    日本生体磁気学会誌 34 1 108 - 108 日本生体磁気学会 2021年
  • Hiroaki Hori, Mariko Itoh, Mie Matsui, Toshiko Kamo, Takuya Saito, Yoshiko Nishimatsu, Satoshi Kito, Satoshi Kida, Yoshiharu Kim
    European Journal of Psychotraumatology 12 1 1859821 - 1859821 2021年01月15日 
    Background: Currently, there is a paucity of pharmacological treatment options for posttraumatic stress disorder (PTSD), and the development of a novel pharmacotherapeutic approach has become a matter of great interest. Objective: We conducted a 12-week open-label clinical trial to examine the efficacy and safety of memantine, an N-methyl-D-aspartate receptor antagonist, in the treatment of civilian PTSD. Method: Thirteen adult patients with DSM-IV PTSD, all civilian women, were enrolled. They were monitored at an ambulatory care facility every week until 4 weeks and then every 4 weeks until 12 weeks. Memantine was added to each patient's current medication, with the initial dosage of 5 mg/day and then titrated. Concomitant medications were essentially kept unchanged during the trial. The primary outcome was PTSD diagnosis and severity assessed with the Posttraumatic Diagnostic Scale (PDS). Results: Of the 13 cases, one dropped out and two were discarded due to the protocol deviation, and the analysis was done for the remaining 10. Mean PDS total scores decreased from 32.3 ± 9.7 at baseline to 12.2 ± 7.9 at endpoint, which was statistically significant with a large effect (paired t-test: p = .002, d = 1.35); intrusion, avoidance, hyperarousal symptoms were all significantly improved from baseline to endpoint. Six patients no longer fulfilled the diagnostic criteria of PTSD at endpoint. Some adverse, but not serious, effects possibly related to memantine were observed, including sleep problems, sleepiness, sedation, weight change and hypotension. Conclusions: Memantine significantly reduced PTSD symptoms in civilian female PTSD patients and the drug was well tolerated. Future randomized controlled trials are necessary to verify the efficacy and safety of memantine in the treatment of PTSD.
  • Takuya Saito, Yushiro Yamashita, Akemi Tomoda, Takashi Okada, Hideo Umeuchi, Saki Iwamori, Satoru Shinoda, Akiko Mizuno-Yasuhira, Hidetoshi Urano, Izumi Nishino, Kazuhiko Saito
    BMC psychiatry 20 1 530 - 530 2020年11月10日 
    BACKGROUND: Asverin® (tipepidine hibenzate) has been used as an antitussive for > 50 years in Japan. Studies revealed that tipepidine modulates monoamine levels, by inhibiting G-protein-activated inwardly rectifying potassium (GIRK) channels, expecting the potential therapeutic effects of tipepidine for attention-deficit/hyperactivity disorder (ADHD) in recent years. In this study, TS-141, a sustained-release tablet of tipepidine, was developed for the treatment of ADHD through a drug repositioning approach. METHODS: The sustained-release profile of TS-141 in healthy adults was investigated, and tipepidine exposure in the plasma after the TS-141 administration was compared to that of Asverin in the phase I study. Phase II study was conducted to examine the effects of TS-141 30 (once a day), 60 (once a day), 120 mg (60 mg twice a day), or placebo, that is within the exposure in the maximum dosage of Asverin, in children and adolescents with ADHD, and was designed as an 8-week treatment, randomized, parallel group, double-blind, placebo-controlled trial recruiting 6-17-year-old children and adolescents diagnosed with ADHD. A total of 216 patients were randomized according to the CYP2D6 phenotype. The primary end-point was ADHD Rating Scale IV-J changes. Furthermore, effects of CYP2D6 phenotype on the efficacy in the subgroup analysis were investigated. RESULTS: TS-141 had the sustained-release profile, and the CYP2D6 phenotype had effects on the plasma exposure of tipepidine. ADHD RS-IV-J scores in all TS-141 dosages decreased from their baseline scores; however, no significant difference was observed in ADHD RS-IV-J score changes between the placebo and TS-141-administered groups. In patients with intermediate metabolizer CYP2D6, ADHD RS-IV-J score changes in the 120 mg group tended to be larger than that in the placebo group. CONCLUSIONS: ADHD RS-IV-J changes on TS-141 may depend on the interaction between the TS-141 dose and CYP2D6 phenotype, suggesting that further clinical trials should be conducted with careful consideration of polymorphism. Drug repositioning approach of TS-141 was attempted at the same dose as that of antitussive; however, dose setting according to the indication was necessary. TRIAL REGISTRATION: Phase I study: JapicCTI-205235 (Registered 25 March 2020), Phase II study: JapicCTI-163244 (Registered 9 May 2016), https://www.clinicaltrials.jp/cti-user/trial/Show.jsp.
  • Masaki Adachi, Michio Takahashi, Tomoya Hirota, Hiroki Shinkawa, Hiroyuki Mori, Takuya Saito, Kazuhiko Nakamura
    Psychiatry and Clinical Neurosciences 74 11 628 - 629 2020年11月01日
  • 柳生 一自, 渡辺 隼人, 高野 一義, 下條 暁司, 白石 秀明, 横澤 宏一, 齊藤 卓弥
    臨床神経生理学 48 5 440 - 440 (一社)日本臨床神経生理学会 2020年10月
  • Satoshi Suyama, Kazuyori Yagyu, Atsuko Araki, Chihiro Miyashita, Sachiko Itoh, Machiko Minatoya, Keiko Yamazaki, Naomi Tamura, Akio Nakai, Takuya Saito, Reiko Kishi
    Pediatrics International 62 10 1177 - 1183 2020年10月01日 
    BACKGROUND: Motor coordination problems (MCP) in children can sometimes be diagnosed as developmental coordination disorder. Early intervention for developmental coordination disorder is necessary because it often continues into adolescence, causing mental and physical complications. Few studies have investigated the prevalence of childhood MCP in the Japanese population, examining the risk factors for MCP. We therefore investigated the prenatal factors associated with MCP in preschool-age children. METHODS: This study was based on a prospective cohort study, the Hokkaido Study on Environment and Children's Health. Mothers of 4,851 children who reached the age of 5 years within the study-period received questionnaires, including the Japanese version of the Developmental Coordination Disorder Questionnaire (DCDQ-J). We examined the risk factors associated with MCP using logistic regression analysis. RESULTS: Of 3,402 returned DCDQ-J questionnaires, 3,369 were answered completely. From the 3,369 children, we categorized having MCP by using two cut-off scores: that of the DCDQ'07 and the cut-off at the 5th percentile of a total DCDQ-J score. Comparing children with and without MCP, we found significant differences in the education level of the mothers, annual household income during pregnancy, maternal alcohol consumption and smoking during pregnancy, and sex and age of the children at the time of completing the DCDQ-J by both categorizations. Adjusted logistic regression analysis revealed that maternal smoking during the first trimester of pregnancy and male sex were significantly associated with MCP. CONCLUSIONS: Our results suggest that maternal smoking during pregnancy is the main factor associated with MCP in preschool-age children.
  • Kazuyoshi Takano, Hayato Watanabe, Kazuyori Yagyu, Atsushi Shimojo, Jared Boasen, Yui Murakami, Hideaki Shiraishi, Koichi Yokosawa, Takuya Saito
    Proceedings of the Annual International Conference of the IEEE Engineering in Medicine and Biology Society, EMBS 2020-July 2893 - 2896 2020年07月 
    Face to face communication is interactive, and involves continuous feedforward and feedback of information, thoughts, and feelings to the opposite party. To accurately assess the neural processing underlying these interactions, synchronous and simultaneous recording of the brain activity from both parties is needed, a method known as hyperscanning. Here, we investigated the neural processing underlying nonverbal face-to-face communication using a magnetoencephalographic (MEG) hyperscanning system, comprising two fiber optically connected MEGs. Eight pairs of subjects participated. Each individual in each pair viewed a combined 80 randomized 20 s trials of 40 real-time and 40 recorded (hereafter, real and simulated, respectively) videos of the opposite party's face. Non-verbal communication through actions such as gaze, eye blinks, and facial expression was intrinsically only possible during real videos. After each trial, subjects individually subjectively discriminated whether the viewed video was real or simulated. Overall subjective discrimination accuracies were slightly but significantly above chance level. Statistical analysis of brain activity revealed a significant three way interaction between theta-band rhythm amplitude, video type, and subjective discrimination response in the right frontal cortex. Additionally, when subjects responded that videos were simulated, theta activity was significantly lower for real videos compared with simulated videos (p = 0.01). This result not only demonstrates the importance of right frontal theta activity during non-verbal communication, but also indicates the existence of unconscious, semi-automated neural processing during non-verbal communication that underlies one's ability to subjectively discriminate whether or not the opposite party is real.
  • Noa Tsujii, Jakashi Okada, Masahide Usami, Hidenori Kuwabara, Junichi Fujita, Hideki Negoro, Michiyo Kavwamura, Junzo Lida, Fand Takuya Saito
    Journal of Clinical Psychiatry 81 3 E1 - E11 2020年06月 
    OBJECTIVE: This study aimed to compare the effect of continuing and discontinuing medications on quality of life of patients with attention-deficit/hyperactivity disorder (ADHD). DATA SOURCES: PubMed, Cochrane Library, and Embase databases were searched using generic terms for ADHD, discontinuing, continuing, pharmacotherapy, and randomized controlled trials without date or language restrictions. STUDY SELECTION: Of the 3,672 screened studies, 9 met the predefined inclusion criteria on patients with ADHD; 5 of these 9 studies reporting on 1,463 patients (children and adolescents, n = 894; adults, n = 569) measured quality of life and were included in this meta-analysis. Only randomized, double-blind, placebo-controlled withdrawal trials of ADHD medications were included. DATA EXTRACTION: Data were independently extracted according to the Cochrane Handbook for Systematic Reviews of Interventions. Analyses were based on random-effects models. RESULTS: Compared with continuing medications, discontinuing them significantly worsened quality of life score in patients with ADHD (standardized mean difference [SMD] = 0.19; 95% CI, 0.08 to 0.30]). Moreover, discontinuing medications worsened this score in children and adolescents with ADHD (SMD = 0.21; 95% CI, 0.06 to 0.36) but not in adults with ADHD (SMD = 0.02; 95% CI, -0.46 to 0.50). CONCLUSIONS: Discontinuing medications was associated with a small but statistically significant decrease in quality of life among children and adolescents with ADHD but not in adults with ADHD. Quality of life can be applied in pharmacologic interventions regarding continuing and discontinuing medication because this concept is related to individuals' appraisal of their situation. Quality of life is an important factor for planning individualized ADHD medication treatment.
  • Takuya Saito, Elin H. Reines, Ioana Florea, Mads K. Dalsgaard
    Journal of Child and Adolescent Psychopharmacology 29 10 753 - 763 2019年12月 
    Objectives: In Japan, there are currently no approved antidepressant treatments for pediatric patients with depression. This study aimed to estimate the prevalence of depression among adolescents under medical care in Japan, the pharmacological treatments used, and the perceived unmet needs among the medical specialties treating depression in the pediatric population. Methods: The study was conducted in November 2014 as an internet survey among physicians in clinical practice. It included a sample of 731 physicians with the potential to treat adolescent patients with depression and 161 physicians who had treated at least one adolescent with depression with pharmacotherapy in the previous 12 months. Of the sample of 161 treating physicians, 60 were internal medicine specialists, 73 were psychiatrists, and 28 were certified specialists from the Japanese Society of Child and Adolescent Psychiatry, Japanese Society of Psychosomatic Medicine Pediatrics, or Japanese Society of Pediatric Psychiatry and Neurology. The participants completed questionnaires concerning their patient population with depression, drug-treated population, and drugs prescribed. Results: Estimates of prevalence data indicated that there were ∼550,000 adolescent patients with depression in Japan (10% of the patient population with depression) under medical care of different medical specialties; ∼64% of these patients were receiving pharmacotherapy. Pharmacotherapy for adolescents with depression was prescribed mainly by psychiatrists (62% of prescriptions for these patients). The most common first-choice agent was sertraline (23% of respondents) followed by anxiolytics (17%) and fluvoxamine (13%), while antipsychotics were the preferred choice for 7%. Conclusion: The study indicates a high prevalence of depression among adolescents in Japan. These patients are seen by different medical specialties; the use of pharmacotherapy is relatively common and comprises various drug classes, including antidepressants, anxiolytics, and antipsychotics. This study shows that there is a medical need for approved treatments for adolescents with depression in Japan.
  • 北海道胆振東部地震における子どもの心のケア 北海道子どものこころのケアチームの活動報告
    杉山 紗詠子, 才野 均, 宮内 まや, 田原 恵, 氏家 武, 傳田 健三, 田中 康雄, 上田 敏彦, 末田 慶太朗, 立野 佳子, 緑川 由紀, 木下 弘基, 中野 育子, 鹿野 智子, 館農 勝, 南波 江太郎, 花香 真宣, 佐藤 祐基, 齊藤 卓弥, 黒川 新二
    日本児童青年精神医学会総会抄録集 60回 O15 - 2 (一社)日本児童青年精神医学会 2019年12月
  • リアルタイムコミュニケーションを計測するためのdual MEGシステムの構成
    渡辺 隼人, 下條 暁司, 柳生 一自, 曽根原 剛志, 白石 秀明, 横澤 宏一, 齊藤 卓弥
    日本生体磁気学会誌 32 1 158 - 159 日本生体磁気学会 2019年 [査読無し][通常論文]
  • Yasuyuki Okumura, Masahide Usami, Takashi Okada, Takuya Saito, Hideki Negoro, Noa Tsujii, Junichi Fujita, Junzo Iida
    Journal of Child and Adolescent Psychopharmacology 28 7 454 - 462 2018年09月 
    OBJECTIVE: We aimed to evaluate glucose and prolactin monitoring in children and adolescents initiating antipsychotic therapy using a nationwide claims database. METHODS: A retrospective 15-month cohort study was conducted using the National Database of Health Insurance Claim Information and Specified Medical Checkups in Japan. Patients aged ≤18 years, who were newly prescribed antipsychotics between April 2014 and March 2015, were followed up for 450 days. Outcomes were the use of glucose and prolactin testing through 15 months after drug initiation (index date) with consideration of persistence with antipsychotic therapy. The incidence proportion of patients monitored was assessed within the following four time windows: baseline (between 30 days before the index date and the index date), at 1-3 months (between 1 and 90 days after the index date), at 4-9 months (between 91 and 270 days after the index date), and at 10-15 months (between 271 and 450 days after the index date). RESULTS: Of 43,608 new users in 6620 medical institutions, the percentage of persistent antipsychotic users was 46.4% at 90 days, 29.7% at 270 days, and 23.8% at 450 days after the index date. The proportion of patients who received monitoring within the baseline period was 13.5% (95% confidence interval [CI], 13.2-13.8) for glucose and 0.6% (95% CI, 0.5-0.6) for prolactin, respectively. The proportion of patients who received glucose monitoring at all time windows decreased to 0.9%. The proportion of patients who received prolactin monitoring by the second time window decreased to 0.1%. CONCLUSIONS: Our study shows that monitoring for glucose and prolactin is infrequent in children and adolescents initiating antipsychotic therapy. Strategies for physicians, patients, and guardians are needed to overcome the barriers in glucose and prolactin monitoring.
  • 渡辺 隼人, 柳生 一自, 下條 暁司, 曽根原 剛志, 品田 大成, 前田 珠希, 白石 秀明, 横澤 宏一, 齊藤 卓弥
    日本生体磁気学会誌 31 1 98 - 99 日本生体磁気学会 2018年06月 [査読無し][通常論文]
  • 成人期ADHD症状評価スケールHASCAP(ハスカップ)について
    館農 勝, 中野 育子, 白木 淳子, 館農 幸恵, 金澤 潤一郎, 白石 将毅, 河西 千秋, 氏家 武, 齊藤 卓弥
    精神神経学雑誌 2018特別号 S375 - S375 (公社)日本精神神経学会 2018年06月 [査読有り][通常論文]
  • 市川 宏伸, 齊藤 万比古, 齊藤 卓弥, 仮屋 暢聡, 小平 雅基, 太田 晴久, 岸田 郁子, 三上 克央, 太田 豊作, 姜 昌勲, 小坂 浩隆, 堀内 史枝, 奥津 大樹, 藤原 正和, 岩波 明
    精神医学 = Clinical psychiatry 60 4 399 - 409 医学書院 2018年04月 [査読有り][通常論文]
  • Masaru Tateno, Takahiko Inagaki, Takuya Saito, Anthony P S Guerrero, Norbert Skokauskas
    Psychiatry investigation 14 5 525 - 531 2017年09月 
    Japan has been facing a serious shortfall of child and adolescent psychiatric workforce relative to increasing service needs. Likely because of a combination of limited workforce supply and limited trust or perception of effectiveness, mental health services are under-utilized by the educational and child welfare systems. Child and adolescent psychiatry (CAP) has not been a formally established specialty in Japan. The lack of basic structure in the specialty most likely contributes to a lack of training facilities, limited exposure to and interest in the specialty, and hence an inadequate workforce. To date, there exists no standardized training program for CAP in Japan and each training hospital determines its own teaching curriculum and training content. Clinical experience in CAP varies greatly among hospitals. To solve current problems in child and adolescent psychiatry in Japan, we advocate for the development and establishment of a more standardized child and adolescent psychiatry training system that is akin to what exists in the US and that teaches and evaluates according to specific competencies. Through standardizing care and education and ultimately improving workforce, the quality of mental health services can be raised. The tragic and costly consequences of unidentified and untreated mental illness in youth can be avoided by taking timely evidence based actions in partnership with others.
  • 柳生 一自, 齊藤 卓弥
    精神科 31 2 131 - 134 (有)科学評論社 2017年08月
  • 柳生 一自, 齋藤 卓弥
    最新精神医学 21 6 407 - 412 (株)世論時報社 2016年11月
  • Noa Tsujii, Takuya Saito, Yuji Izumoto, Masahide Usami, Takashi Okada, Hideki Negoro, Junzo Iida
    Journal of child and adolescent psychopharmacology 26 7 642 - 5 2016年09月 
    OBJECTIVE: In child and adolescent psychiatry, the off-label prescribing of psychotropic medications is common. The purpose of this study was to examine the experiences of Japanese child and adolescent psychiatrists with off-label prescribing to children and/or adolescents (hereafter referred to as "children") and to identify the factors associated with these experiences. METHODS: A prospective questionnaire was sent to 1628 psychiatrists belonging to the Japanese Society for Child and Adolescent Psychiatry. Stepwise logistic regression analyses were used to determine whether demographic characteristics or categories of psychotropic medications were able to independently predict patient refusals of off-label prescribing. RESULTS: The final sample included 447 psychiatrists, and 93% of the respondents (416/447) had experiences with off-label prescribing to children. In addition, 39.7% of the respondents (165/416) experienced patient refusal of off-label prescribing when they informed the children and/or parents of the prescribing. The most commonly prescribed off-label psychotropic medications were antipsychotics (82.0%). Patient refusal was significantly more frequent when the respondents informed parents (p=0.02) and children (p<0.01) about off-label prescribing than when they did not. A stepwise logistic regression analysis revealed that informing parents (odds ratio [OR], 2.73; 95% confidence interval [CI], 1.09-6.82) or children (OR, 1.70; 95% CI, 1.12-2.58) about off-label prescribing and antidepressant use (OR, 2.98; 95% CI, 1.25-7.10) increased the odds of patient refusal of off-label prescribing; however, prescribers' years in practice decreased the odds (OR, 0.98; 95% CI, 0.96-1). CONCLUSIONS: Off-label prescribing of psychotropic medications is common among child and adolescent psychiatrists in Japan. Furthermore, the psychiatrists' experiences with patient refusal of off-label prescribing were significantly associated with informing the parents/patients about off-label prescribing, particularly with regard to use of antidepressants. Further studies are required to support the development of decision making among clinicians.
  • 成重 竜一郎, 川島 義高, 澤谷 篤, 齊藤 卓弥, 大久保 善朗
    児童青年精神医学とその近接領域 56 2 179 - 189 日本児童青年精神医学会 2015年 [査読有り][通常論文]
  • Conners' Adult ADHD Rating Scale(CAARS)日本語版の開発 CAARS自己報告式の信頼性と妥当性の検討
    大西 将史, 染木 史緒, 石井 礼花, 市川 宏伸, 内山 敏, 金澤 潤一郎, 神尾 陽子, 川久保 友紀, 齊藤 万比古, 斉藤 卓弥, 杉山 登志郎, 武田 俊信, 竹林 淳和, 田中 康雄, 根來 秀樹, 松本 英夫, 渡部 京太, 辻井 正次, 森 則夫, 中村 和彦
    日本児童青年精神医学会総会抄録集 54回 400 - 400 (一社)日本児童青年精神医学会 2013年10月
  • 自殺未遂者の心理社会的特性と自殺企図手段との関係性に関する検討
    成重 竜一郎, 大高 靖史, 齊藤 卓弥, 大久保 善朗
    精神神経学雑誌 2013特別 S - 681 (公社)日本精神神経学会 2013年05月
  • 高橋秀俊, 豊永公司, 高橋雄一, 荒井宏, 船曳康子, 宮川真一, 廣常秀人, 本田教一, 齊藤卓弥, 築島健, 吉田佳郎
    総合病院精神医学 24 4 349 - 360 (一社)日本総合病院精神医学会 2012年10月15日 [査読無し][通常論文]
     
    日本総合病院精神医学会の学会員を対象に、総合病院における児童青年期精神科診療の実態について調査を行った。平成24年7月学会誌にアンケート用紙を同封した。更に、学会のメーリングリストでアンケート用紙のファイルを添付した。140名から回答を得た。同一施設内複数回答は3施設(各施設2名ずつ)のみと少数であった。約半数が精神科病床を有しており、精神科病床を有する施設は大学病院や精神科病院に多かった。半数が一般病院、1/4が大学病院に勤務しており、合計で8割近くが総合病院に勤務していた。所属施設の精神科医師の人数は、最頻値は、常勤・非常勤を合わせると3名で、常勤に限ると1名となり、少数の精神科医で対応していた。回答者の所属施設の8割で児童青年期精神科外来を実施していた。うち、8割以上の施設が精神科で実施していた。入院診療については、成人と共用の施設で実施、実施していない施設が各4割以上あった。児童青年期精神医療に関する研修は4割が受けたことがなかった。
  • 成重 竜一郎, 川島 義高, 大高 靖史, 齊藤 卓弥, 大久保 善朗
    臨床精神医学 41 9 1255 - 1261 アークメディア 2012年09月 [査読有り][通常論文]
  • 川島 義高, 伊藤 敬雄, 成重 竜一郎, 大高 靖史, 齊藤 卓弥, 大久保 善朗
    臨床精神医学 39 11 1397 - 1404 アークメディア 2010年11月 [査読無し][招待有り]
  • 川島 義高, 伊藤 敬雄, 中井 有希, 齊藤 卓弥, 大久保 善朗
    臨床精神医学 38 9 1279 - 1286 アークメディア 2009年09月 [査読有り][通常論文]
  • RD Strous, KA Nolan, R Lapidus, L Diaz, T Saito, HM Lachman
    AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS 120B 1 29 - 34 2003年07月 [査読有り][通常論文]
     
    We have previously reported that increased aggressive behavior in schizophrenic patients may be associated with a polymorphism at codon 158 of the catechol O-methyltransferase (COMT) gene that encodes a low enzyme activity variant. The finding has been replicated by one group, but not others. The discordant findings could be due to statistical errors or methodological issues in the assessment of aggressive/violent behavior. Consequently, additional studies are needed. Patients with schizophrenia (SZ) were assessed for violent behavior using the Lifetime History of Aggression (LHA) scale, an 11-item. questionnaire that includes Aggression, Self-Directed Aggression, and Consequences/Antisocial Behavior subscales. DNA was genotyped for the COMT 158 polymorphism, as well as a functional polymorphism in the monoamine oxidase A (MAOA) gene promoter. Similar to our previously reported findings, a statistically significant association was found between aggressive behavior in SZ and the COMT 158 polymorphism; mean LHA scores were higher in subjects homozygous for 158Met, the low enzyme activity COMT variant (F(2,105) = 5.616, P = 0.005). Analysis of the major LHA subscales revealed that the association with 158Met was due to high scores on the Aggression, and Self-Directed Aggression subscales, but not the Consequences/Antisocial Behavior subscale. No significant association was detected for the AMOA gene alone. Our findings provide further support that COMT is a modifying gene that plays a role in determining interindividual variability in the proclivity for outward and self-directed aggressive behavior found in some schizophrenic patients. (C) 2003 Wiley-Liss, Inc.
  • KA Nolan, J Volavka, HM Lachman, T Saito
    PSYCHIATRIC GENETICS 10 3 109 - 115 2000年09月 [査読有り][通常論文]
     
    Serotonergic pathways have been implicated in impulsive and aggressive behavior. Polymorphisms in the regulatory region of the serotonin transporter (5-HTT), in intron 7 of the tryptophan hydroxylase (TPH) gene and in the MAOA gene were previously reported to be associated with mood and anxiety disorders, impulsivity and aggression. In this study, we analyzed these polymorphisms in men and women with schizophrenia or schizoaffective disorder (n = 84) who met our criteria for violence (history of two or more assaults on others) or nonviolence (no history of either assaultive or threatening behavior). In males, a modest association between TPH genotype and history of violence (chi-square test = 6.703, degrees of freedom = 2, P = 0.035) was not statistically significant after correction for multiple comparisons (corrected P = 0.21). The TPH L allele was more frequent in violent males (chi-square = 5.323, degrees of freedom = 1, P = 0.021) but this difference also failed to withstand correction (corrected P = 0.126). No significant associations were found for either the 5-HTT or MAOA polymorphisms in males or females. These results tend to support previous reports by New et nl. (1996; 1998) of an association between the TPH L allele and impulsive aggression in males with personality disorder, but larger studies are needed. Psychiatr Genet 10:109-115 (C) 2000 Lippincott Williams & Wilkins.
  • T Hallikainen, T Saito, HM Lachman, J Volavka, T Pohjalainen, OP Ryynanen, J Kauhanen, E Syvalahti, J Hietala, J Tiihonen
    MOLECULAR PSYCHIATRY 4 4 385 - 388 1999年07月 [査読有り][通常論文]
     
    A common 44-base pair insertion/deletion polymorphism in the promoter region of the human serotonin transporter (5-HTT) gene has been observed to be associated with affective illness and anxiety-related traits, This biallelic functional polymorphism, designated long (L) and short (S), affects 5-HTT gene expression since the S promoter is less active than the L promoter. Since there is strong evidence of a disturbance in brain serotonergic transmission among antisocial, impulsive, and violent type 2 alcoholic subjects, we decided to test the hypothesis that the frequency of the S allele, which is associated with reduced 5-HTT gene expression, is higher among habitually violent type 2 alcoholics when compared with race and gender-matched healthy controls and non-violent late-onset (type 1) alcoholics, The 5-HTT promoter genotype was determined by a PCR-based method in 114 late onset (type 1) non-violent alcoholics, 51 impulsive violent recidivistic offenders with early onset alcoholism (type 2), and 54 healthy controls, All index subjects and controls were white Caucasian males of Finnish origin. The S allele frequency was higher among type 2 alcoholics compared with type 1 alcoholics chi(2)=4.86, P=0.028 and healthy controls chi(2) = 8.24, P = 0.004, The odds ratio for SS genotype vs LL genotype was 3.90, 95% CI 1.37-11.11, P=0.011 when type 2 alcoholics were compared with healthy controls. The results suggest that the 5-HTT 'S' promoter polymorphism is associated with an increased risk for early onset alcoholism associated with antisocial personality disorder and impulsive, habitually violent behavior.

MISC

所属学協会

  • 日本総合病院精神医学会   日本精神科診断学会   日本医学英語教育学会   関東子ども精神保健学会   日本サイコセラピー学会   日本医学教育学会   日本ADHD学会   日本うつ病学会   日本児童青年期精神医学会   Society for Neuroscience   American Psychological Association   The Royal College of Psychiatrists   World Federation of ADHD   Society of Biological Psychiatry   American Academy of Child and Adolescent Psychiatry   American Psychiatric association   日本精神神経学会   

共同研究・競争的資金等の研究課題

  • 日本学術振興会：科学研究費助成事業 基盤研究(A)
    研究期間 : 2022年04月 -2026年03月 
    代表者 : 岸 玲子, 宮下 ちひろ, 小林 澄貴, 伊藤 佐智子, 山崎 圭子, アイツバマイ ゆふ, 山口 健史, 田村 菜穂美, 齊藤 卓弥
  • 日本学術振興会：科学研究費助成事業 基盤研究(B)
    研究期間 : 2022年04月 -2026年03月 
    代表者 : 足立 匡基, 高橋 芳雄, 和久田 学, 廣田 智也, 西村 倫子, 門田 麗, 森 裕幸, 三上 美咲, 齊藤 卓弥
  • 日本学術振興会：科学研究費助成事業 基盤研究(C)
    研究期間 : 2021年04月 -2026年03月 
    代表者 : 柳生 一自, 齊藤 卓弥, 横澤 宏一, 白石 秀明
     
    私たちは北海道大学にある2台の脳磁計（Magnetoencephalography: MEG）を光ファイバーで接続し、映像・音声での仮想的対面を可能とするDual-MEGシステムを構築した。さらによりリアルな対面を行えるようカメラとプロジェクタの視差をなくすハーフミラーを用い正面からの視線合致を可能とした。このDual-MEGシステムを用いて、実対面（相手の映像と実際に対面している状況）、擬対面（録画された相手の映像と対面している状況）とを用いて、被験者に判断させる課題を行った。結果、本人は擬対面だと答えている（実対面には気付いていない）にも関わらず、右下前頭部におけるθ波の活動が、映像が実対面では脱同期、擬対面では過同期をすることを明らかにした。すなわち意識レベルでは相手の存在に気づいていない（非意識）にも関わらず、「相手の存在」を脳内で表象化する機構が同部位に存在することを示した。さらに考察をすすめこの二条件の違いは、他者との無意識の交互作用にあること、そのやりとりはfacial mimicry（表情模倣）にあることを推論した。こうした点は進化学的見地、発達学的見地からも合理的であると考えられ、トップダウンの認知とは別の、ボトムアップによって他者が象徴化される機構を示しているのかもしれない。こうした中前頭回を中心としたこの非意識下における他者存在の象徴化については統計学的な検討を深めた上で、研究成果については現在論文化を進めている。さらに2021年度は、研究対象として健常者同士によるコミュニケーションモジュールの同定、解析方法としては単一被験者の脳活動におけるモジュール同定を目的とした周波数解析と事象関連同期・脱同期の解析を進めた。熟練した脳磁図計測および解析方法を行える研究協力者が必要であり、育成を進めている。
  • 日本学術振興会：科学研究費助成事業 基盤研究(B)
    研究期間 : 2020年04月 -2024年03月 
    代表者 : 横澤 宏一, 小野 弓絵, 齊藤 卓弥, 柳生 一自, 豊巻 敦人
     
    コミュニケーションは特に人類において発達した社会的行動の基礎をなす。本研究の第１の目的は、その神経基盤を明らかにすることである。このため、ミリ秒レベルの時間分解能と数ミリメートル程度の空間分解能を併せ持つ脳磁計を２台、光ファイバーで連結したDual MEGを用い、コミュニケーション中の脳活動の同時記録（ハイパースキャニング）を実施してきた。音響・映像機器により２人の実験参加者は仮想的に対面でき、自然なコミュニケーションが可能である。 コミュニケーションには言語コミュニケーションと非言語コミュニケーションがある。実際のコミュニケーションは、これらが複合し絶え間なく入れ替わる極めて複雑なプロセスである。そこで本研究は、非言語コミュニケーションと言語コミュニケーションを個別に実験、解析したのち、統合するというプロセスで推進中である。 これまでは主に非言語コミュニケーションに着目した研究を実施してきた。相手と実時間で対面している場合（実対面映像）と、少し前に録画した映像（録画映像）と対面している場合の脳活動を比較した。その結果、実験参加者は実対面映像と録画対面映像をほとんど区別できないが、実対面している場合に特異な活動が右前頭脳領域に生じることを見出した。つまり、人の意識に上らない脳活動が非言語コミュニケーションを成立させている可能性があることがわかった。一方で、この課題のようにコミュニケーションが明示的ではない場合、コミュニケーションの成立を定義するのが難しいことが明らかになってきた。コミュニケーションが成立した瞬間をとらえないと脳の機能領野間の相関・因果関係を解析することが難しい。以上が初年度の成果と、新たに明らかになった課題である。
  • 日本学術振興会：科学研究費助成事業 基盤研究(A)
    研究期間 : 2019年04月 -2023年03月 
    代表者 : 岸 玲子, 池田 敦子, 小林 澄貴, 齊藤 卓弥, 湊屋 街子, 山崎 圭子, 中島 そのみ, 宮下 ちひろ, 白石 秀明, アイツバマイ ゆふ, 三浦 りゅう
     
    本研究は、出生コーホート研究で保存された母体血・臍帯血および学童期から思春期に採取した児の尿を用いて、胎児期および生後の環境化学物質曝露が児のアレルギー、神経行動発達、第二次性徴等のアウトカムへ及ぼす影響についてリスク評価を行うことを目的とした。 令和3年度は、出生コーホートの参加者について11歳で第二次性徴に関する調査票1182件、12歳で小学校の学校健診記録から転記する身長体重調査票1236件、15歳で中学校の身長体重調査票1440件、17歳調査1787件を発送した。回収数は11歳812件（回収率68.7.％）、12歳771件（回収率62.4％）、15歳815件（回収率56.5％）、17歳855件（47.8％）であった。生後のアウトカム評価として、これまでの質問票調査によるアレルギー、神経行動発達、第二次性徴の評価を行った。脳波調査では、有機フッ素化合物（PFAS）の胎児期曝露が児の認知機能に関連する可能性を検討した。妊娠初期母体血清中のフタル酸7代謝物と第二次性徴発来のタイミングおよび、成長や肥満などの体格との解析を実施した。
  • 日本学術振興会：科学研究費助成事業 基盤研究(C)
    研究期間 : 2016年04月 -2020年03月 
    代表者 : 柳生 一自, 橋本 竜作, 関 あゆみ, 齊藤 卓弥, 須山 聡, 白石 秀明
     
    臨床上、表現される読字障害は、純粋な読字障害だけでなく、基盤となる脳機能の異常や合併する疾患によって様々な中間表現型が存在する。本研究は読字障害の脳機能、中間表現型、臨床表現型の病態生理の解明を目指した。 脳機能研究では脳磁図を用いて、両側下前頭葉、左上側頭葉に読字障害児の脳活動に特徴的変化が現れることが明らかとなった。臨床表現型の研究では、中学生以降に適用可能な読み困難に関する自記式質問紙の開発を行った。読字障害の診断スクリーニングに高い感度・特異度が示された。中間表現型研究としては特異的言語障害及び発達性協調運動症についての質問紙を作成し有用性を示した。
  • 日本学術振興会：科学研究費助成事業 基盤研究(A)
    研究期間 : 2016年04月 -2019年03月 
    代表者 : 岸 玲子, 荒木 敦子, 宮下 ちひろ, 中島 そのみ, 花岡 知之, 山崎 圭子, 小林 澄貴, 湊屋 街子, 有賀 正, 齊藤 卓弥, 鈴川 晶夫, 梶原 淳睦, 佐田 文宏, 西條 泰明, 吉岡 英治
     
    胎児期および生後の環境化学物質曝露が児の神経行動発達や第二次性徴等へ及ぼす影響を単一および複合曝露によるリスク評価を行い、環境-遺伝交互作用も検討した。児の尿中MEHP濃度は2012-2017年の間で有意な減少を認めた。胎児期フタル酸エステル類およびBPA曝露は、MECPP が5歳の児の問題行動のリスク増加を示し、MnBP, MiBP, MEHPが女児のみで第二次性徴開始月齢の早発を認めた。環境化学物質の複合曝露による性ホルモン値の有意な変動が認められ, MEHPとPFOSの寄与が大きかった。児のエストロゲン受容体1型のXbaI遺伝子型において右手の2D:4D比の低下が見られた。
  • 日本学術振興会：科学研究費助成事業 挑戦的萌芽研究
    研究期間 : 2016年04月 -2018年03月 
    代表者 : 岸 玲子, 荒木 敦子, 齊藤 卓弥, 三浦 りゅう, 山崎 圭子, アイツバマイ ゆふ, 小林 澄貴
     
    本研究は、胎児期の環境化学物質曝露が注意欠陥/多動性障害（ADHD）発症に至る機序の1つとして、DNAメチル化変化に注目し、臍帯血 DNAの45万ヶ所メチル化部位（CpG部位）の網羅的解析を行った。有機フッ素化合物、フタル酸エステル類、ビスフェノールAの胎児期曝露について、多重比較補正後も統計学的に有意に関連するメチル変化部位を特定した。 ６歳のADHD-RS調査票で見いだされたADHD疑い群（n=245）とコントロール群（n=317）の臍帯血DNAを用いて、網羅的解析で明らかとなった曝露に起因するCpG部位を次世代シークエンサーにより解析し、メチル変化とADHDとの関連を検討している。
  • 日本学術振興会：科学研究費助成事業 基盤研究(C)
    研究期間 : 2015年04月 -2018年03月 
    代表者 : 齊藤 卓弥, 松本 俊彦, 角間 辰之
     
    本研究では対象は、６歳から１８歳の札幌市の小中学高校生に対してに対して本人および保護者から得た上で、1年目の希死念慮が2年目にどのように変化したかを2年連続して回答した小中高校生118名を対象に評価した。同時に、希死念慮と、抑うつ尺度、BCL(子ども行動チェックリスト)、Birleson：自己記入式抑うつ評価尺度（DSRS-C）、FTTを実施し、児童思春期における自殺行動に関連する、心理、コミュニケーション能力、発達障害の影響について探索的研究を行った。に自殺念慮の変化ならびにそれに関する要因を解析した。
  • 日本学術振興会：科学研究費助成事業 基盤研究(C)
    研究期間 : 2008年 -2010年 
    代表者 : 齊藤 卓弥, 大久保 善朗, 舘野 周
     
    児童・思春期にある子ども(以下子ども)の約5から8%にうつ病がみられ、年齢が高くなるにつれて頻度が増加すると報告されている。一方で、子どものうつ病に関する適切なバイオマーカーが存在せず、子どものうつ病の診断・治療のためにバイオマーカーが強く求められているとしい。特に、脳の機能的あるいは構造上の変化とうつ病の症候や生化学的な因子との関連を研究は重要である。DSM-IV-TRに基づき大うつ病と診断された患者8名と、性別および年齢で合致する非うつ病群7名を対象にしてMRIによる脳の構造的な比較を行った。またうつ病群に関してはCBCL(子ども行動チェックリスト)、Birleson自己記入式抑うつ評価尺度(DSRS-C)、PedQLを用いて症状の重症度、日常機能および生命の質(QoL)と脳の構造的な変化との相関を求めた。また、子どものうつ症は、候学的に、従来の報告で示されていたように外在化症状あるいは攻撃的行動として表出されることが多く、自殺に関連する行動も多く、QoLの低下および日常機能の低下も著しく、適切な介入がこの研究からも求められることが明らかになった。この研究により、子どものうつ病の生物学的な理解を深め、また子どものうつ病の症候学的な特徴および子どものうつ病の日常機能への影響が明らかになったことにより、子どものうつ病の診断・治療の重要性、特に子どものうつ病群に自殺行動が多くみられたことから今後ライフスタイルを通しての自殺予防が重要であることも明らかになった。
  • 日本学術振興会：科学研究費助成事業 基盤研究(B)
    研究期間 : 2007年 -2010年 
    代表者 : 大久保 善朗, 齊藤 卓弥, 舘野 周, 一宮 哲哉, 肥田 道彦, 須原 哲也
     
    PET による分子イメージング技術を用いて、ドパミン系を中心に統合失調症患者の神経伝達異常の解明を目指した。新規ドパミンPETリガンドの研究では、ドパミンD2アゴニストリガンドである[^<11>C]MNPAによって、D2アゴニスト結合の測定できることを確かめた。統合失調症患者のドパミン神経伝達に関する臨床研究では、[^<11>C]NNC112と[^<11>C]SCH23390の二種類のPETリガンドを用いて、統合失調症患者群においてドパミンD1受容体結合能が低下していることを確認した。また、L-[β-^<11>C]DOPA を用いてドパミン合成能の異常を調べ、統合失調症患者群では、左尾上核においてドパミン合成脳が亢進していること、視床と右側頭葉のドパミン合成脳は症状の重症度と相関することを明らかにした。さらに、[^<11>C]PE2Iを用いて統合失調症群では、健常対照群と比較し視床ドパミントランスポーター結合能が上昇していること、視床ドパミントランスポーターの上昇は精神症状の重症度と相関していることを明らかにした。以上の結果から、統合失調症では、シナプス前機能が亢進してドパミン神経伝達が過剰になっている病態が示唆された。
  • 日本学術振興会：科学研究費助成事業 挑戦的萌芽研究
    研究期間 : 2007年 -2009年 
    代表者 : 高柳 和江, 齊藤 卓弥, 伊藤 要子
     
    心からの感動の笑いを学んだ職員によるケアで患者さんの治癒力が高まるエビデンスをだすことを目的として、病院職員に研修を行った。【対象】参加者は病院内の各部署からの41名(医師6,看護師20,薬剤部2,検査部2,放射線部2,臨床工学部1,PT1,栄養部1,福祉相談部1,事務部5)。【方法】自然の形で笑いを引き出す2日間の研修を4回行った。カリキュラムは,笑いの理論学習,自然な形で笑いを引き出す手法の実践,実習、体感トレーニングで構成された。この笑医セラピスト41名が,新たに院内から募った2チーム(計80名)に対して2日間の研修実習を行った。参加度,理解度を取り,POMS (Profile of mode score),心のパワーアップ(PU)スケール(高柳作成)を用いた。これは,満足度,余裕度、患者に対する意識の変化,自己効力感の変化をみるものである。また、一人の脳卒中後うつ患者にコア笑医セラピストによる笑医療法を行い、この患者の行動変容をFIM評価で検証した。【結果】研修前後で参加度、理解度はそれぞれ有意に改善した。POMSは,緊張・不安,抑うつ・落ち込み、怒り・敵意は大きく低下し,疲労と混乱は減少した。活気は大きく高まった(P<0.05)。心のPUスケールで活力が出る,安全だ,頭の回転が良くなる,効率が良い,幸せだ,などという結果が出た。また、身体的にも不眠が改善,持病の頑固な肩こりが治癒,腰痛の軽減などの声があった。実症例においても,脳卒中後のうつの70歳男性患者に,笑医セラピスト研修生が第62-70病日の間に3回面会し動機づけしたところ,うつ状態が改善し,ADLが自立,17日後にはFIM評価125/126になり退院し、その2カ月後に医師として職場復帰した本研究は、土浦協同病院(院長藤原秀臣)の全面的協力を得ており、土浦協同病院倫理委員会で本研究が認められた。

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