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Vol.1 No.2 June 2001 |
Dementia Poststroke
Tarja Pohjasvaara, MD, PhD (Department of Neurology, Memory Research Unit, Helsinki University Central Hospital), Risto Vataja, MD, Antero Leppävuori, MD, PhD, and Timo Erkinjuntti, MD, PhD |
The
frequency of dementia poststroke is high, and stroke considerably
increases the risk of dementia. The risk factors for dementia related to
stroke are still incompletely understood. In addition to age and low
level of education, different combinations of vascular risk factors and
stroke features have been associated with poststroke dementia. A single
explanation for poststroke dementia is not adequate; rather, multiple
factors including stroke features (dysphasia, major dominant stroke
syndrome), infarct features (type, side, site, number, and volume),
extent and type of white matter lesions (WMLs), degree and site of
atrophy, host chara- |
Quantifying
Dementia Care in Japan: A Discussion Shivani Nandi, PhD(Eisai Co., Ltd.Team Researcher, the International Research Center for Japanese Studies, Kyoto) |
The Japanese
government mandated the kaigohoken,
or Long Term Care Insurance (LTCI) in December 1997. In view of the
pressures faced by Japan as an aged society, the aim of the LTCI is to
alleviate the burden of providing care for frail older people by
ensuring good quality and readily available services to everyone over
65. The LTCI is thus a high profile, age-based entitlement programÅ|age
based for persons 65 years of age and above, and age related disability
based for ages 40 to 64. Individuals 40 years and above, including
foreigners living in Japan for more than a year, are responsible in
bearing a part of the financial responsibility by having to pay the
mandatory premium. The benefits that the insured person receives are
decided after evaluating the care requirement. Care is quantified by
being categorized into six levels of increasing requirement, starting
from support required, through five levels of increasing care. |
No Association between Presenilin 1 Intron Gene or Butyrylcholinesterase K Variantand Alzheimer’s Disease in Japanese Populations Yasuji Yamamoto, MD, PhD(Psychiatry and Neurology, Kobe University Graduate School of Medicine), Masahito Sengo, MD(Hyogo Institute for Aging Brain and Cognitive Disorders), Minoru Yasuda, MD, PhD(), and Kiyoshi Maeda, MD, PhD |
Background:
One of the purposes of this study was to examine whether apolipoprotein
E (ApoE) e4
allele as a risk factor for Alzheimer’s disease (AD) may be associated
with the higher prevalence of AD in women compared with men. Recently,
the polymorphic K variant of the butyrylcholinesterase (BChE-K) gene and
presenilin 1 (PS1) intronic polymorphism have been reported to be
associated with AD respectively. Thus we have reexamined the frequency
of BChE-K, PS1 intronic polymorphism, and the ApoE e4
allele in a large series of Japanese AD patients and controls. |
Dementia in Parkinson’s Disease: Its Incidence and a Possible Relationship with Dopa-refractory Symptoms Atsushi Takeda, MD, PhD(Department of Neurology, Tohoku University School of Medicine), Kanae Fujihara, PhD,Akio Kikuchi, MD, PhD, Teiko Kimpara, MD, PhD, and Yasuto Itoyama, MD, PhD |
Background:
The diagnostic criteria for dementia in idiopathic Parkinson’s disease
(PD) remain controversial. In PD, general intelligence is relatively
spared, although executive function is commonly impaired. |
Influence
of Apolipoprotein E3 on the Production of Paired Helical Filament in
Guamanian Parkinsonism-dementia Complex/Amyotrophic Lateral Sclerosis
and Alzheimer’s Disease
Takehide Tsuda, MD, PhD(Department of Neurology, Tohoku University School of Medicine), D.R.C. McLachlan, MD,and Yasuto Itoyama MD, PhD |
Background:
Neuropathologically, Guamanian parkinsonism-dementia complex (PDC) and
amyotrophic lateral sclerosis (ALS) are characterized by neuronal loss
and neurofibrillary tangles (NFTs). The NFTs are principally composed of
paired helical filaments (PHFs) consisting of hyperphosphorylated tau
and have been shown to be histopathologically similar to those in
Alzheimer’s disease (AD). Recent biochemical studies have suggested
that the binding of apolipoprotein E3 (ApoE3) to tau may interfere with
the hyperphosphorylation of tau, thus resulting in neuro-protective
effects. Methods: In order to clarify the influence of ApoE3 on the production of PHFs in various pathological conditions, the e3 allele frequency in patients with Guamanian PDC and ALS, as well as AD, was examined. Results: The results obtained in this study showed no significant differences between these affected groups and each of the controls in terms of the frequency of the ApoE3 allele. Conclusion: Although ApoE3 has been implicated in the production of PHFs, the present study suggests that ApoE3 may not have a strong inhibitory effect on the production of NFTs in these affected patients. |
Effect
of Presenilin 1 Missense Mutation and Aluminum on Early Neuronal
Development of the Mouse Brain
Eriko Fukusho, MA(Department of Clinical Neuroscience, Psychiatry, Osaka University Graduate School of Medicine), Yu Nakamura, MD, PhD, Yujiro Kashiwagi, MD, PhD, Takashi Kudo, MD, PhD, Toshihisa Tanaka, MD, PhD, Naohiko Matsumoto, MD, Tomoyuki Kida, MD, Yuka Nakano, MD, PhD, Kazuhiro Shinosaki, MD, PhD, and Masatoshi Takeda, MD, PhD |
Background:
The pathology of Alzheimer’s disease (AD) has not been fully
elucidated. Presenilin 1 (PS1) mutation is one of the major genetic
factors of AD, while aluminum is a candidate for the environmental risk
factor. Methods: First, we investigated the influence of PS1 mutation on the neuronal development in ‘knock-in’ mice of PS1 I213T mutation. Next, the effect of prenatal exposure to aluminum on the neuronal development of the knock-in mice was examined. Results: In the newborns with the mutated PS1 allele, a tendency of delayed neurological development was seen and an abnormal distribution of neurofilaments was found, implying that the PS1 mutation might alter early neuronal development. Intraperitoneal administration of aluminum-maltol resulted in the increase of aluminum in brain tissues of newborns, and in abnormal distribution of neurofilaments. Furthermore, the PS1 mutation promoted a change in neurofilament distribution induced by exposure to aluminum. Conclusion: Thus, PS1 mutation and aluminum are suggested to affect early neuronal development, as reflected in some aspects of the pathology of AD. |
Interrater Reliability of the Todai-shiki Observational Rating Scale (TORS) for Group Psychotherapy of Elderly Patients with Dementia Osamu Matsuda, PhD(Department of Psychology, Faculty of Education, Tokyo Gakugei University), Yukiko Kurokawa, PhD, Masahiko Saito, MD, Kaori Maruyama, MA, and Noriko Miyamoto, BA |
Background:
Various types of psychosocial approaches have been developed in the
field of dementia patient care. One of these approaches, reminiscence
groups, is often applied in the care setting. We developed the
Todai-shiki Observational Rating Scale (TORS) to assess the
effectiveness of reminiscence groups, and we examined its interrater
reliability in this preliminary study. Methods: The subjects of the study were nine elderly patients with mild to moderate dementia. The TORS consists of 20 items covering four aspects of the patients’ clinical picture: verbal communication, nonverbal communication, attention and interest, and emotion. The intraclass correlation coefficient (ICC) for each item was calculated. The mean ICCs for each item over five sessions were used as a reliable index. Results: The mean ICCs ranged from 0.53 to 1.00, and averaged 0.83. Conclusion: This preliminary study suggested that the TORS might be a useful tool to evaluate the effects of group psychotherapy for patients with dementia. |
Pathology
in Senile Patients with Abnormal Body Sensation
Tohru Takahashi, MD(Department of Psychiatry, Shinshu University School of Medicine), Tsunemi Tamaru, MD, Junko Imai, MD, Shinsuke Washizuka, MD, Hiroshi Ozawa, MD, Yuzuru Harada, MD, PhD, Akihito Morishima, MD, and Naoji Amano, MD, PhD |
Background:
Senile people tend to develop abnormal body sensations such as
delusion of parasitosis. To discuss the pathology of senile abnormal
body sensation, we studied patients
with abnormal body sensation, cenesthopathy, and delusion of parasitosis
and investigated their age and gender. Methods: The subjects were a mix of patients reported in Japan and our patients. They were classified into two groups; Group 1 were those with a condition considered to be a somatoform disorder and Group 2 were those with a delusion of parasitosis and chronic tactile hallucinosis. Results: Group 1 consisted of 29 patients aged 46.4±9.6 years; the male:female ratio was 1:4.8. Group 2 consisted of 51 patients aged 65.8±9.4 years; the male:female ratio was 1:1.125. Conclusion: Based on the age tendency characteristics, Group 1 was called the involutional group and Group 2 the senile group. The age and gender distribution in the involutional group (Group 1) may be related mainly to climacteric disorders and suggested some influences of climacteric changes on the appearance of abnormal body sensation. On the other hand, the pathology in the senile group (Group 2) appeared to be associated with senile organic changes in addition to climacteric changes and sensory changes of skin and mucosal area during the involutional period. |
Severe
Sequelae of Group B Streptococcal (Streptococcus Agalactiae) Meningitis
in an 82-year-old Man
Kazuo Fujihara, MD (Department of Neurology, Hiroshima Red Cross and Atomic Bomb Survivors’ Hospital;Department of Neurology, Tohoku University School of Medicine), Yasuhiro Fujioka, MD, Michiya Ohta, MD,and Yasuto Itoyama, MD, PhD |
Group B streptococcal (GBS) meningitis is rare in adults, and only 2 cases have been reported in Japan. Here we report GBS meningitis in an 82-year-old man. The patient with a history of colon cancer developed a high fever and severe headache, and was taken to our hospital several hours later. On admission he was semi-comatose, light and corneal reflexes were normal, his neck was only mildly stiff. He was then on a respirator due to status epilepticus. Cerebrospinal fluid examination demonstrated marked pleocytoisis (46,250/m l, mostly polymorphonuclear cells) and GBS. With intensive care and antibiotic therapy, he regained consciousness 10 days later. However, he suffered severe dementia, hearing loss, limb muscle atrophy, and urinary retention in the chronic stage of the disease. Although survivors of adult GBS meningitis are reported to be free of severe neurologic sequelae, factors such as being the oldest patient among the reported cases, the premorbid malignancy and the marked inflammation were considered to be related to the severe neurologic sequelae in the present case. |
A Case of Traumatic
Brain Injury Developing Frontal Lobe Syndrome after a Long Incubation
Period
Junya Nagasawa, MD (Department of Psychiatry,Shinshu University School of Medicine), Naoji Amano, MD, PhD, Miho Takahashi, and Tomoki Kaneko, MD |
A 55-year-old man, who was a heavy drinker for about 30 years, had experienced a heavy blow on the right posterior temporal region on account of a traffic accident at the age of 16. He recovered without any sequelae. However, he began to make mistakes and had trouble with his job about 40 years after the accident. His symptoms and neuropsychological examination suggested frontal lobe syndrome. Cranial magnetic resonance imaging (MRI) showed that the frontal and temporal lobes seemed to be predominantly atrophic and that there was great enlargement of the lateral and third ventricles, and a post-contusion lesion in the left frontal lobe. Brain single photon emission computer tornography (SPECT) demonstrated diffuse cerebral hypoperfusion. Cranial MRI suggested that the contusion was proportionate to contre coup injury resulting from the accident. We supposed that the extensive brain damage induced edema and ischemia soon after the accident. Consequently, the circulatory disturbance might have caused cerebral atrophy and enlargement of the ventricles. Since he was relatively young at the time of the accident, the plasticity of his brain compensated for the injury intensively, and obvious symptoms suggesting frontal lobe syndrome were latent for about 40 years after the accident. Continuous drinking may have induced recent dysfunction of the compensated brain. However, such severe atrophy and focal damaged lesion could not be solely accounted for by heavy alcohol consumption. On the other hand, organic changes due to aging and brain circulatory insufficiency caused by hypertension or hyperlipidemia may also disclose the cerebral dysfunction. His cranial MRI and SPECT seemed not to be consistent with frontotemporal dementia. Furthermore, we considered that his case was also different from Alzheimer’s disease and normal pressure hydrocephalus. However, it is necessary to follow up neuro-imaging. Conclusively, he developed frontal lobe syndrome based on traumatic brain injury and induced by continuous drinking, aging, and brain circulatory insufficiency. |
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