Hibiki Tanaka
Kumamoto University
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Featured researches published by Hibiki Tanaka.
PLOS ONE | 2015
Kyoko Kai; Mamoru Hashimoto; Koichiro Amano; Hibiki Tanaka; Ryuji Fukuhara; Manabu Ikeda
Background Eating is one of the most important daily activities in managing patients with dementia. Although various eating disturbance occur as dementia progresses, to our knowledge, most of the studies focused on a part of eating disturbance such as swallowing and appetite. There have been few comprehensive studies including eating habits and food preference in patients with Alzheimer’s disease (AD). The aims of this study were to investigate almost all eating disturbance and to examine the relationship of eating disturbance to dementia stage in AD. Methods A total of 220 patients with AD and 30 normal elderly (NE) subjects were recruited. Eating disturbance was assessed by a comprehensive questionnaire that had been previously validated. Potential relationships between the characteristics of eating disturbance and dementia stage as classified by the Clinical Dementia Rating (CDR) were assessed. Results Overall, 81.4% of patients with AD showed some eating and swallowing disturbance, whereas only 26.7% of the NE subjects had such a disturbance. Even in an early stage, patients with AD had many types of eating disturbance; “Appetite change” was shown in nearly half of the mild AD patients (49.5%). In the moderate stage, the scores of “change of eating habits and food preference” were highest, and in the severe stage “swallowing disturbance” became critical. Conclusion In AD, the relationship of dementia stage to eating disturbance differs according to the type of eating disturbance. The relationships between various eating disturbance and the severity of dementia should be considered.
PLOS ONE | 2016
Hiroaki Kazui; Kenji Yoshiyama; Hideki Kanemoto; Yukiko Suzuki; Shunsuke Sato; Mamoru Hashimoto; Manabu Ikeda; Hibiki Tanaka; Yutaka Hatada; Masateru Matsushita; Yoshiyuki Nishio; Etsuro Mori; Satoshi Tanimukai; Kenjiro Komori; Taku Yoshida; Hideaki Shimizu; Teruhisa Matsumoto; Takaaki Mori; Tetsuo Kashibayashi; Kazumasa Yokoyama; Tatsuo Shimomura; Yasunobu Kabeshita; Hiroyoshi Adachi; Toshihisa Tanaka
Background/Aims Behavioral and psychological symptoms of dementia (BPSDs) negatively impact the prognosis of dementia patients and increase caregiver distress. The aims of this study were to clarify the differences of trajectories of 12 kinds of BPSDs by disease severity in four major dementias and to develop charts showing the frequency, severity, and associated caregiver distress (ACD) of BPSDs using the data of a Japan multicenter study (J-BIRD). Methods We gathered Neuropsychiatric Inventory (NPI) data of patients with Alzheimer’s disease (AD; n = 1091), dementia with Lewy bodies (DLB; n = 249), vascular dementia (VaD; n = 156), and frontotemporal lobar degeneration (FTLD; n = 102) collected during a 5-year period up to July 31, 2013 in seven centers for dementia in Japan. The NPI composite scores (frequency × severity) of 12 kinds of items were analyzed using a principal component analysis (PCA) in each dementia. The factor scores of the PCA were compared in each dementia by disease severity, which was determined with Clinical Dementia Rating (CDR). Results Significant increases with higher CDR scores were observed in 1) two of the three factor scores which were loaded for all items except euphoria in AD, 2) two of the four factor scores for apathy, aberrant motor behavior (AMB), sleep disturbances, agitation, irritability, disinhibition, and euphoria in DLB, and 3) one of the four factor scores for apathy, depression, anxiety, and sleep disturbances in VaD. However, no increases were observed in any of the five factor scores in FTLD. Conclusions As dementia progresses, several BPSDs become more severe, including 1) apathy and sleep disturbances in AD, DLB, and VaD, 2) all of the BPSDs except euphoria in AD, 3) AMB, agitation, irritability, disinhibition, and euphoria in DLB, and 4) depression and anxiety in VaD. Trajectories of BPSDs in FTLD were unclear.
International Journal of Geriatric Psychiatry | 2017
Yasunobu Kabeshita; Hiroyoshi Adachi; Masateru Matsushita; Hideki Kanemoto; Shunsuke Sato; Yukiko Suzuki; Kenji Yoshiyama; Tatsuo Shimomura; Taku Yoshida; Hideaki Shimizu; Teruhisa Matsumoto; Takaaki Mori; Tetsuo Kashibayashi; Hibiki Tanaka; Yutaka Hatada; Mamoru Hashimoto; Yoshiyuki Nishio; Kenjiro Komori; Toshihisa Tanaka; Kazumasa Yokoyama; Satoshi Tanimukai; Manabu Ikeda; Masatoshi Takeda; Etsuro Mori; Takashi Kudo; Hiroaki Kazui
Sleep disturbances in Alzheimer disease (AD) may affect behavioral and psychological symptoms of dementia (BPSD). Our aim was to elucidate the associations between sleep disturbances and other BPSD at different stages of AD.
Psychogeriatrics | 2015
Hibiki Tanaka; Mamoru Hashimoto; Ryuji Fukuhara; Tomohisa Ishikawa; Yusuke Yatabe; Keiichiro Kaneda; Seiji Yuuki; Kazuki Honda; Shiho Matsuzaki; Atsuko Tsuyuguchi; Yutaka Hatada; Manabu Ikeda
The features of behavioural and psychological symptoms of dementia (BPSD) are influenced by dementia stage. In early‐onset Alzheimers disease (EOAD), the association between BPSD and dementia stage remains unclear because of the difficulty of recruiting subjects with a wide range of disease severity. We used a combination of community‐based and hospital‐based approaches to investigate the relationship between dementia severity and BPSD in EOAD patients.
Psychogeriatrics | 2017
Asuka Koyama; Masateru Matsushita; Mamoru Hashimoto; Noboru Fujise; Tomohisa Ishikawa; Hibiki Tanaka; Yutaka Hatada; Yusuke Miyagawa; Maki Hotta; Manabu Ikeda
Caregiver burden in dementia is an important issue, but few studies have examined the mental health of younger and older family caregivers by comparing them with age‐ and gender‐matched community residents. We aimed to compare the mental health of dementia caregivers with that of community residents and to clarify factors related to mental health problems in younger and older caregivers.
International Psychogeriatrics | 2014
Ryuji Fukuhara; Amitabha Ghosh; Jong-Ling Fuh; Jacqueline Dominguez; Paulus Anam Ong; Aparna Dutt; Yi Chien Liu; Hibiki Tanaka; Manabu Ikeda
BACKGROUND Previous studies in western countries have shown that about 30%-50% of patients with frontotemporal lobar degeneration (FTLD) have a positive family history, whereas the few epidemiological studies on FTLD done in Asia reported much lower frequencies. It is not clear the reason why the frequencies of FTLD with positive family history were lower in Asia. Furthermore, these findings were not from studies focused on family history. Therefore, it is necessary to conduct further studies on the family history of FTLD in Asia. This international multi-center research aims to investigate the family histories in patients with FTLD and related neurodegenerative diseases such as progressive supranuclear palsy (PSP), corticobasal syndrome (CBS), and motor neuron diseases in a larger Asian cohort. METHODS Participants were collected from five countries: India, Indonesia, Japan, Taiwan, and Philippines. All patients were diagnosed with behavioral variant frontotemporal dementia (bvFTD), semantic dementia (SD), progressive non-fluent aphasia (PA), frontotemporal dementia with motor neuron disease (FTD/MND), PSP, and corticobasal degeneration (CBD) according to international consensus criteria. Family histories of FTLD and related neurodegenerative diseases were investigated in each patient. RESULTS Ninety-one patients were included in this study. Forty-two patients were diagnosed to have bvFTD, two patients had FTD/MND, 22 had SD, 15 had PA, one had PA/CBS, five had CBS and four patients had PSP. Family history of any FTLD spectrum disorder was reported in 9.5% in bvFTD patients but in none of the SD or PA. CONCLUSION In contrast to patients of the western countries, few Asian FTLD patients have positive family histories of dementia.
International Psychogeriatrics | 2013
Kazuki Honda; Mamoru Hashimoto; Yusuke Yatabe; Keiichiro Kaneda; Seiji Yuki; Yusuke Ogawa; Shiho Matsuzaki; Atsuko Tsuyuguchi; Hibiki Tanaka; Hiroko Kashiwagi; Noriko Hasegawa; Tomohisa Ishikawa; Manabu Ikeda
BACKGROUND Dementia with Lewy bodies (DLB) is the second most common type of neurodegenerative dementia. It is frequently difficult to differentiate DLB from Alzheimers disease (AD) and other types of dementia. This study examined the usefulness of monitoring sleep talking for the diagnosis of DLB. METHODS A total of 317 patients with dementia were selected from a consecutive series at the Dementia Clinic of Kumamoto University Hospital. Diagnostic categories consisted of probable DLB (n = 55), probable AD (n = 191), frontotemporal lobar degeneration (FTLD) (n = 16), vascular dementia (VaD) (n = 18), and other/unspecified dementia (n = 37). We evaluated sleep talking in all dementia patients and normal elderly subjects (n = 32) using an originally designed sleep talking questionnaire. RESULTS Sleep talking occurred most frequently in the DLB group (61.8%), followed by the VaD group (33.3%), other/unspecified dementia group (27.0%), AD group (18.8%), FTLD group (12.5%), and normal elderly subjects group (6.3%). The prevalence of sleep talking in the DLB group was significantly higher than in other groups, except in the VaD group. The sleep talking yielded high specificity (81.2%) and some sensitivity (61.8%) for the differential diagnosis of DLB from AD. Furthermore, loud sleep talking may improve the specificity (96.9%). For the differentiation of DLB from all other dementia types, the specificity of sleep talking and loud sleep talking was also high (79.4% and 95.8% respectively). CONCLUSIONS Assessing sleep talking, especially the volume of sleep talking, may be useful in the clinical discrimination of DLB from not only AD but also from all other types of dementia.
PLOS ONE | 2016
Asuka Koyama; Mamoru Hashimoto; Hibiki Tanaka; Noboru Fujise; Masateru Matsushita; Yusuke Miyagawa; Yutaka Hatada; Ryuji Fukuhara; Noriko Hasegawa; Shuji Todani; Kengo Matsukuma; Michiyo Kawano; Manabu Ikeda
Malnutrition among dementia patients is an important issue. However, the biochemical markers of malnutrition have not been well studied in this population. The purpose of this study was to compare biochemical blood markers among patients with Alzheimer’s disease (AD), dementia with Lewy bodies (DLB), and frontotemporal lobar degeneration (FTLD). A total of 339 dementia outpatients and their family caregivers participated in this study. Low serum albumin was 7.2 times more prevalent among patients with DLB and 10.1 times more prevalent among those with FTLD than among those with AD, with adjustment for age. Low hemoglobin was 9.1 times more common in female DLB patients than in female AD patients, with adjustment for age. The levels of biochemical markers were not significantly correlated with cognitive function. Family caregivers of patients with low total protein, low albumin, or low hemoglobin were asked if the patients had loss of weight or appetite; 96.4% reported no loss of weight or appetite. In conclusion, nutritional status was worse in patients with DLB and FTLD than in those with AD. A multidimensional approach, including blood testing, is needed to assess malnutrition in patients with dementia.
Annals of General Psychiatry | 2017
Tomoko Kajiya; Hiroko Sugawara; Yusuke Kajio; Satoru Morieda; Hibiki Tanaka; Tadashi Jono; Noboru Fujise; Mamoru Hashimoto
BackgroundMajor depressive episodes with psychotic features are more common in bipolar disorder than in major depressive disorder; however, there is little information on the optimal treatment for bipolar depression with psychotic features.Case presentationThe patient was a 69-year-old man. At the age of 66, he was admitted to the hospital for the treatment of bipolar depression with psychotic features. He was treated with a combination therapy of antipsychotics and antidepressants during long-term hospitalization. At the age of 69, he relapsed and was admitted to the hospital again. He was initially treated with olanzapine and lithium for the treatment of bipolar depression with psychotic features. He partially responded to the combination therapy, and psychomotor retardation and delusion of guilt disappeared; however, he developed psychomotor agitation and delusion of persecution, which was a mood-incongruent psychotic feature. Finally, he fully recovered with an additional dosage of lamotrigine, and had no experience of relapse after discontinuation of olanzapine.ConclusionsThis case report implicates the utility of lamotrigine for bipolar depression with psychotic features, and further studies are needed to establish the optimal treatment.
Dementia and geriatric cognitive disorders extra | 2018
Asuka Koyama; Mamoru Hashimoto; Ryuji Fukuhara; Naoko Ichimi; Akihiro Takasaki; Masateru Matsushita; Tomohisa Ishikawa; Hibiki Tanaka; Yusuke Miyagawa; Manabu Ikeda
Background: Caregiver burden is a serious concern for family caregivers of dementia patients, but its nature is unclear in patients with semantic dementia (SD). This study aimed to clarify caregiver burden for right- (R > L) and left-sided (L > R) predominant SD versus behavioral-variant frontotemporal dementia (bvFTD) patients. Methods: Using the Japanese version of the Zarit Burden Interview (ZBI) and the Neuropsychiatric Inventory, we examined caregiver burden and behavioral and psychological symptoms of dementia (BPSD) in 43 first-visit outpatient/family caregiver dyads (bvFTD, 20 dyads; SD [L > R], 13 dyads; SD [R > L], 10 dyads). Results: We found a significant difference in ZBI score between the 3 diagnostic groups. Post hoc tests revealed a significantly higher ZBI score in the bvFTD than in the SD (L > R) group. The ZBI scores in the SD (L > R) and SD (R > L) groups were not significantly different, although the effect size was large. Caregiver burden was significantly correlated with BPSD scores in all groups and was correlated with activities of daily living and instrumental activities of daily living decline in the bvFTD and SD (R > L) groups. Conclusion: Caregiver burden was highest in the bvFTD group, comparatively high in the SD (R > L) group, and lowest in the SD (L > R) group. Adequate support and intervention for caregivers should be tailored to differences in caregiver burden between these patient groups.