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1.
J Prev Alzheimers Dis ; 1(2): 99-109, 2014.
Article in English | MEDLINE | ID: mdl-25530953

ABSTRACT

INTRODUCTION: The PGSA (Placebo Group Simulation Approach) aims at avoiding problems of sample representativeness and ethical issues typical of placebo-controlled secondary prevention trials with MCI patients. The PGSA uses mathematical modeling to forecast the distribution of quantified outcomes of MCI patient groups based on their own baseline data established at the outset of clinical trials. These forecasted distributions are then compared with the distribution of actual outcomes observed on candidate treatments, thus substituting for a concomitant placebo group. Here we investigate whether a PGSA algorithm that was developed from the MCI population of ADNI 1*, can reliably simulate the distribution of composite neuropsychological outcomes from a larger, independently selected MCI subject sample. METHODS: Data available from the National Alzheimer's Coordinating Center (NACC) were used. We included 1523 patients with single or multiple domain amnestic mild cognitive impairment (aMCI) and at least two follow-ups after baseline. In order to strengthen the analysis and to verify whether there was a drift over time in the neuropsychological outcomes, the NACC subject sample was split into 3 subsamples of similar size. The previously described PGSA algorithm for the trajectory of a composite neuropsychological test battery (NTB) score was adapted to the test battery used in NACC. Nine demographic, clinical, biological and neuropsychological candidate predictors were included in a mixed model; this model and its error terms were used to simulate trajectories of the adapted NTB. RESULTS: The distributions of empirically observed and simulated data after 1, 2 and 3 years were very similar, with some over-estimation of decline in all 3 subgroups. The by far most important predictor of the NTB trajectories is the baseline NTB score. Other significant predictors are the MMSE baseline score and the interactions of time with ApoE4 and FAQ (functional abilities). These are essentially the same predictors as determined for the original NTB score. CONCLUSION: An algorithm comprising a small number of baseline variables, notably cognitive performance at baseline, forecasts the group trajectory of cognitive decline in subsequent years with high accuracy. The current analysis of 3 independent subgroups of aMCI patients from the NACC database supports the validity of the PGSA longitudinal algorithm for a NTB. Use of the PGSA in long-term secondary AD prevention trials deserves consideration.

2.
Clin Neurophysiol ; 124(11): 2146-52, 2013 Nov.
Article in English | MEDLINE | ID: mdl-23786792

ABSTRACT

OBJECTIVE: To establish a model for better identification of patients in very early stages of Alzheimer's disease, AD (including patients with amnestic MCI) using high-resolution EEG and genetic data. METHODS: A total of 26 patients in early stages of probable AD and 12 patients with amnestic MCI were included. Both groups were similar in age and education. All patients had a comprehensive neuropsychological examination and a high resolution EEG. Relative band power characteristics were calculated in source space (LORETA inverse solution for spectral data) and compared between groups. A logistic regression model was calculated including relative band-power at the most significant location, ApoE status, age, education and gender. RESULTS: Differences in the delta band at 34 temporo-posterior source locations (p<.01) between AD and MCI groups were detected after correction for multiple comparisons. Classification slightly increased when ApoE status was added (p=.06 maximum likelihood test). Adjustment of analyses for the confounding factors age, gender and education did not alter results. CONCLUSIONS: Quantitative EEG (qEEG) separates between patients with amnestic MCI and patients in early stages of probable AD. Adding information about Apo ε4 allele frequency slightly enhances diagnostic accuracy. SIGNIFICANCE: qEEG may help identifying patients who are candidates for possible benefit from future disease modifying treatments.


Subject(s)
Alzheimer Disease/classification , Alzheimer Disease/genetics , Apolipoproteins E/genetics , Cognitive Dysfunction/diagnosis , Cognitive Dysfunction/genetics , Electroencephalography/methods , Aged , Alzheimer Disease/diagnosis , Brain Mapping , Diagnosis, Differential , Female , Genotype , Humans , Logistic Models , Male , Models, Neurological
3.
Rev Med Suisse ; 9(382): 838-47, 2013 Apr 17.
Article in French | MEDLINE | ID: mdl-23667974

ABSTRACT

The 2012 Swiss consensus paper on diagnosis and management of patients suffering from dementia resulted from the work of an expert panel who met on March 23d to 25th in Luzem. Based on a literature review, panel members wrote a first draft that was subsequently circulated among multiple dementia experts in Switzerland. After adaptation and revisions according to comments, all consulted dementia specialists and panel members fully endorse the consensus content. The conference was financed by the Swiss Alzheimer Forum.


Subject(s)
Dementia/diagnosis , Dementia/therapy , Consensus , Humans , Switzerland
5.
Praxis (Bern 1994) ; 101(7): 451-64, 2012 Mar 28.
Article in German | MEDLINE | ID: mdl-22454307

ABSTRACT

Memory Clinics provide evidence based diagnosis and treatment of dementia. Whenever a diagnosis of dementia is made, it is important to inform the patients about the possible impact of dementia on driving. Patients and their next of kin require competent advice whenever this difficult question is addressed and the mobility desire and the risks related to driving need to be carefully weight up. The time of diagnosis does not necessarily equate to the time when a person with dementia becomes an unsafe driver. The cause and severity of dementia, comorbidities and the current medication need to be carefully taken into account for this decision. On behalf of the association of the Swiss Memory Clinics, a group of experts has developed recommendations to assess fitness to drive in cognitively impaired older adults.


Subject(s)
Accidents, Traffic/prevention & control , Automobile Driving/legislation & jurisprudence , Automobile Driving/psychology , Dementia/psychology , Accidents, Traffic/legislation & jurisprudence , Aged , Algorithms , Dementia/diagnosis , Disability Evaluation , Humans , Mass Screening , Mental Disorders/diagnosis , Mental Disorders/psychology , Patient Education as Topic , Physician-Patient Relations , Presbyopia/diagnosis , Presbyopia/psychology , Psychotropic Drugs/adverse effects , Psychotropic Drugs/therapeutic use , Risk Assessment , Switzerland
6.
Int J Clin Pract ; 64(9): 1198-209, 2010 Aug.
Article in English | MEDLINE | ID: mdl-20529136

ABSTRACT

The prevalence of dementia is reaching epidemic proportions globally, but there remain a number of issues that prevent people with dementia, their families and caregivers, from taking control of their condition. In 2008, Alzheimer's Disease International (ADI) launched a Global Alzheimer's Disease Charter, which comprises six principles that underscore the urgency for a more ambitious approach to diagnosis, treatment and care. This review highlights some of the most important aspects and challenges of dementia diagnosis and treatment. These issues are reviewed in light of the six principles of the recent ADI Charter: promoting dementia awareness and understanding; respecting human rights; recognizing the key role of families and caregivers; providing access to health and social care; stressing the importance of optimal diagnosis and treatment; and preventing dementia through improvements in public health. The authors continue to hope that, one day, a cure for Alzheimer's disease will be found. Meanwhile, healthcare professionals need to unite in rising to the challenge of managing all cases of dementia, using the tools available to us now to work toward improved patient care.


Subject(s)
Alzheimer Disease/rehabilitation , Alzheimer Disease/diagnosis , Alzheimer Disease/prevention & control , Caregivers , Family Health , Health Promotion , Health Services Accessibility , Humans , Life Style , Magnetic Resonance Imaging , Neuroprotective Agents/therapeutic use , Patient Rights , Practice Guidelines as Topic , Role , Social Support
7.
Mult Scler ; 14(8): 1106-12, 2008 Sep.
Article in English | MEDLINE | ID: mdl-18632780

ABSTRACT

BACKGROUND: Families with a parent suffering from multiple sclerosis (MS) must cope with the unpredictable course of the disease. Most studies analyzing factors that influence coping abilities in families with a member affected with MS used questionnaires to assess this ability. METHODS: On the contrary, the present study used a semi-structured psychiatric interview and used the resulting information to calculate a general measure of coping ability (coping index [CI]). We administered this interview to 44 MS patients, their partners and offspring and conducted a neuropsychological and physical evaluation of the patients to determine the impact of physical disability, cognitive dysfunction, and depression on the process of coping by the patient, the healthy partner, and children. RESULTS: The CI of patients was best predicted by measures of their depressive symptoms, divided attention, and estimated verbal intelligence. None of the patient variables predicted the CI of healthy partners or their offspring. We found an association between the CI of the healthy partner and the children. CONCLUSIONS: These findings suggest that MS patients' emotional and neuropsychological functions are associated with their ability to cope with the disease. These should be carefully assessed at the beginning of treatment so that those factors known to negatively influence patient coping are targeted in the treatment plan if necessary. Comprehensive care of a patient with MS should include support of coping abilities of the family members.


Subject(s)
Adaptation, Psychological , Disabled Persons/psychology , Multiple Sclerosis/psychology , Parents/psychology , Adult , Child , Cognition Disorders/epidemiology , Cognition Disorders/psychology , Depression/epidemiology , Depression/psychology , Disabled Persons/statistics & numerical data , Female , Humans , Interviews as Topic , Male , Parent-Child Relations , Predictive Value of Tests
8.
Dtsch Med Wochenschr ; 133(9): 431-6, 2008 Feb.
Article in German | MEDLINE | ID: mdl-18288630

ABSTRACT

Half the patients with mild cognitive impairment (MCI) will develop dementia over a four-year period. The scientific literature was searched and analysed for predictors of rapid decline (MCI-plus) in patients with MCI. The most important predictors of fast cognitive deterioration were found to be: old age, previous rapid decline, severity and multiplicity of cognitive deficits, somatic co-morbidity, vascular and Alzheimer-type changes in the brain, Alzheimer-type cerebrospinal fluid findings and apolipoprotein E4 polymorphism. Many patients with MCI suffer from anxiety, depression or apathy and subtle, but subjectively significant, difficulties in the activities of daily living. It is concluded that MCI-plus offers a window for medical and psychological prophylaxis and rehabilitation.


Subject(s)
Cognition Disorders/diagnosis , Dementia/prevention & control , Age Factors , Apolipoprotein E4/genetics , Brain/pathology , Cerebrospinal Fluid/chemistry , Cognition Disorders/rehabilitation , Comorbidity , Dementia/etiology , Humans , Polymorphism, Genetic , Predictive Value of Tests , Prognosis , Severity of Illness Index , Time Factors
9.
Stat Med ; 27(10): 1777-90, 2008 May 10.
Article in English | MEDLINE | ID: mdl-17968872

ABSTRACT

Diagnostic tests yield measurements on very different types of scales. Quantitative scales may consist of non-negative integers, either unbounded or bounded, with a fixed number of different values, or they may consist of continuous or percentage values. Remembering a different threshold value for each diagnostic variable would be cumbersome, in particular if covariates have to be taken into account. As a convenient way to overcome such problems we propose to compute z-scores for all measurements. They will be adjusted for covariates so that any individual can be judged on any test result on one single scale with an appropriate standard normal quantile as threshold. Two issues need to be addressed: Selection of covariates in the regression model which delivers the adjustment and normality of the residuals. The first will be treated by cross-validation and the latter by applying an appropriate transformation. We apply this methodology to neuropsychological tests and adjust for age, length of education and sex. Normality of residuals is needed on the diagnostically relevant side only. This allows to use parametric transformations, which can be easily implemented, e.g. in database systems. Since we have measurements at baseline and at follow-up we also analyze change values in a similar manner. For ease of interpretation, we transform the resulting z-scores back to the original scale.


Subject(s)
Biometry/methods , Data Interpretation, Statistical , Diagnostic Tests, Routine/methods , Analysis of Variance , Humans , Neuropsychological Tests , Reference Values , Regression Analysis , Reproducibility of Results
10.
J Geriatr Psychiatry Neurol ; 18(1): 39-44, 2005 Mar.
Article in English | MEDLINE | ID: mdl-15681627

ABSTRACT

CERAD-NAB (Consortium to Establish a Registry for Alzheimer's Disease-Neuropsychological Assessment Battery) data were compared between 51 patients with frontotemporal dementia, 13 with semantic dementia, and 69 with Alzheimer's disease. There were statistically significant differences between the 3 groups. Compared with patients with Alzheimer's disease, patients with frontotemporal dementia were more impaired on Animal Fluency but not on any other CERAD-NAB subtest. Patients with semantic dementia performed worse in Animal Fluency and Boston Naming Test compared with frontotemporal dementia and Alzheimer's disease. Multiple logistic regression analysis revealed that in the differentiation between frontotemporal dementia and Alzheimer's disease, the combination of Animal Fluency and Boston Naming Test correctly classified 90.5% of patients. In segregating semantic dementia and Alzheimer's disease, the combination of Boston Naming Test and Mini Mental State Examination resulted in a correct classification of 96.3%. These findings demonstrate that the Mini Mental State Examination and the language subtests of the CERAD-NAB are valuable clinical instruments for the differential diagnosis between early frontotemporal dementia, semantic dementia, and Alzheimer's disease.


Subject(s)
Alzheimer Disease/diagnosis , Dementia/diagnosis , Mental Status Schedule , Aged , Alzheimer Disease/psychology , Dementia/psychology , Diagnosis, Differential , Female , Humans , Language , Male , Middle Aged , Neuropsychological Tests , Semantics , Severity of Illness Index
11.
Int J Obes Relat Metab Disord ; 28(9): 1163-7, 2004 Sep.
Article in English | MEDLINE | ID: mdl-15224124

ABSTRACT

OBJECTIVE: To investigate whether under- or overweight and weight change is associated with cognitive performance of elderly citizens. DESIGN: Explorative analysis out of the Basel Study cohort. SUBJECTS: In all, 531 healthy subjects (445 men/86 women) were assessed with the Consortium to Establish a Registry for Alzheimer's Disease-Neuropsychological Assessment Battery (CERAD-NAB) in 2000 (age: 69.4+/-7.8 y) and weight measurements obtained in 1990 (body mass index (BMI): 25.2+/-3.1 kg/m(2)) and in 2000 (BMI: 25.6+/-3.4 kg/m(2)). METHODS: The predictive power of the annual change in BMI with cognitive performance was investigated by a binary logistic regression analysis (backward) using sex, age, BMI 1990, BMI 2000, diastolic blood pressure, diabetes status, and optimal health status as additional predictors. RESULTS: In the last step, the following variables remained in the model: annual change in BMI (quadratic term; P<0.01); ApoE genotype (P<0.05); and optimal health status (P<0.01). CONCLUSION: The association between the extent of weight change and poorer cognitive performance could be either a consequence of cognitive impairment or an early symptom of neurodegenerative decline.


Subject(s)
Body Weight , Cognition Disorders/physiopathology , Aged , Apolipoproteins E/genetics , Body Mass Index , Cognition Disorders/genetics , Female , Follow-Up Studies , Genetic Predisposition to Disease , Genotype , Humans , Logistic Models , Male , Middle Aged , Neuropsychological Tests , Weight Gain , Weight Loss
13.
Stud Health Technol Inform ; 77: 195-9, 2000.
Article in English | MEDLINE | ID: mdl-11187541

ABSTRACT

The diagnosis of early stage dementia is a highly complex process involving not only a somatic examination but also a neuropsychological assessment of the patient's cognitive capability. The American 'Consortium to Establish a Registry for Alzheimer's Disease' (CERAD) has proposed a set of tests in English which has been translated into German. This paper presents the statistical methodology applied to determine normal ranges adjusted for demographic variables for the German CERAD neuropsychological assessment battery (CERAD-NAB). The study population consists of participants of the Basel Study on the Elderly (Project BASEL) which aims at identifying preclinical markers of Alzheimer's disease. The normative sample has been defined by carefully excluding potentially relevant medical history and concomitant diseases and consists of 617 participants which are between 53 and 92 years old. Test results should be adjusted for gender, age, and years of education. For this purpose, a set of linear models including these predictors and subsets of their interactions and squares was evaluated for all 11 test scores derived from the CERAD-NAB battery. Model selection was based on the PRESS (predicted residual sum of squares) statistic. Although a strict application of this criterion selected 6 different models, a slight compromise allowed to fit all test scores by two models. In several tests of the CERAD-NAB many participants achieve maximal scores. Residuals of such test scores are heavily skewed. An arcsine transformation has been tuned to the data, so that residuals are close to a normal distribution, at least for residuals in the lower quartile which is relevant in diagnosing cognitive impairment. Test results are finally presented as z-scores which can be easily compared to a standard normal distribution. The evaluation of the CERAD-NAB is implemented on the Internet and in an Excel application.


Subject(s)
Alzheimer Disease/diagnosis , Diagnosis, Computer-Assisted/statistics & numerical data , Neuropsychological Tests/statistics & numerical data , Aged , Aged, 80 and over , Female , Humans , Male , Middle Aged , Reference Values , Registries/statistics & numerical data , Reproducibility of Results , Switzerland
14.
Arch Gerontol Geriatr ; 30(1): 17-24, 2000.
Article in English | MEDLINE | ID: mdl-15374045

ABSTRACT

Large numbers of elderly patients, suspected of having dementia, need medical evaluation, often in early phases of their illness. A complete outpatient assessment clearly could be advantageous. Thirty-five centers from 15 European countries, known to their scientific gerontological and geriatric societies to have experience in outpatient care for elderly patients with dementia, participated in an effort to develop a consensus statement for the assessment needs of these patients. The comparison of the centers showed that a wide variety of approaches was currently in practice. Differences appeared to be mainly based on local facilities and organization. A consensus for diagnostic outpatient assessment was easily reached. Diagnosis should be based on DSM-IV criteria, which requires a standardized assessment (including neuropsychological, functional and technical evaluation) and should be multidisciplinary. An assessment of dementia of elderly outpatients appears to be very feasible - a consensus approach with minimum diagnostic requirements is presented.

15.
Pathologe ; 20(3): 159-68, 1999 May.
Article in German | MEDLINE | ID: mdl-10412175

ABSTRACT

Argyrophilic grain disease (AgD) constitutes one cause of late onset dementia and is histologically characterized by the presence of abundant argyrophilic grains and coiled bodies. Both abnormalities are found mainly in limbic structures, among them the sector CA1 of the hippocampus, the entorhinal cortex, and the amygdala. Using appropriate silver staining techniques, they are easily detectable and can easily be distinguished from neurofibrillary lesions of Alzheimer's disease (i.e., tangles and threads). Although the histopathology of AgD is well characterized, the nosological status is still unclear because most cases of AgD are associated with Alzheimer-type changes. For some authors, therefore, AgD is considered a variant of Alzheimer's disease rather than a distinct disease entity. The present review is aimed at presenting argyrophilic grain disease to a larger readership than just neuropathologists who are interested in neurodegenerative disorders. In this review we summarize morphological, immunohistochemical, clinico-pathological and genetic data obtained in more than 90 subjects with AgD. The main conclusions of this review are that AgD represents one of the most frequent, dementing disorders of old age and that it has to be clearly distinguished from Alzheimer's disease.


Subject(s)
Alzheimer Disease/pathology , Brain/pathology , Dementia/pathology , Diagnosis, Differential , Humans , Neurodegenerative Diseases/pathology , Plaque, Amyloid/pathology
16.
Acta Neuropathol ; 96(3): 225-7, 1998 Sep.
Article in English | MEDLINE | ID: mdl-9754953

ABSTRACT

Apolipoprotein E (ApoE) genotypes were analyzed in 35 subjects with argyrophilic grain diseases (AgD). Neuropathologically, all cases were characterized by abundant argyrophilic grains in the hippocampus and in the entorhinal or parahippocampal cortex. We found an ApoE epsilon4 allele frequency of 0.007 in AgD patients, which is significantly different from the epsilon4 allele frequencies reported in age-matched Alzheimer's disease (AD) patients (0.24), but not from age-matched controls (0.09). We conclude that the ApoE epsilon4 allele does not constitute a risk factor for the development of AgD. Our results further suggest that AgD is a progressive disorder differentiated from AD by morphological and genetic criteria.


Subject(s)
Alleles , Apolipoproteins E/genetics , Gene Frequency , Neurodegenerative Diseases/genetics , Aged , Aged, 80 and over , Alzheimer Disease/genetics , Apolipoprotein E2 , Brain/pathology , Brain Chemistry , Cerebellum/chemistry , DNA/analysis , Dementia/etiology , Dementia/genetics , Diagnosis, Differential , Female , Genotype , Humans , Kidney/chemistry , Liver/chemistry , Male , Polymerase Chain Reaction , Risk Factors
17.
Ann Med Interne (Paris) ; 149(4): 221-7, 1998 Jun.
Article in English | MEDLINE | ID: mdl-11499407

ABSTRACT

Currently, eleven Memory Clinics (MC) in Switzerland offer their services to patients, caregivers and family doctors. Their primary goal is the early diagnosis and management of dementia in elderly outpatients. Special emphasis is put on the detection of reversible causes of dementing disorders. Diagnoses and medical, pharmacological, neuropsychological and social treatment recommendations are established in a multidisciplinary consensus conference and communicated back to the referring physicians. The psychosocial therapies and supportive activities include counseling, memory training for patients, neuropsychological rehabilitation, caregiver groups, relaxation and biofeedback training, day care centers, Alzheimer's Tanzcafé, and special vacations for dementia patients. These activities vary from MC to MC according to the availability of resources. Research activities are an integral part of all MCs and range from the attempt to identify preclinical markers of Alzheimer's disease to studies of neuropathological correlates of cognitive disturbances. Moreover, patients are encouraged to participate in studies investigating new medications. MCs play an important role in the education and training of health care professionals and in raising awareness and support in the general population.


Subject(s)
Alzheimer Disease/rehabilitation , Hospitals, Special/trends , Patient Care Team , Aged , Aged, 80 and over , Alzheimer Disease/diagnosis , Alzheimer Disease/epidemiology , Alzheimer Disease/etiology , Combined Modality Therapy , Female , Forecasting , Health Services Needs and Demand/trends , Humans , Male , Patient Care Team/trends , Population Dynamics , Switzerland
18.
Acta Neuropathol ; 94(4): 353-8, 1997 Oct.
Article in English | MEDLINE | ID: mdl-9341936

ABSTRACT

In a previous study we reported on a late onset dementia which occurred in only half of the patients with argyrophilic grain disease (AgD) investigated. To find a correlation between the distribution of argyrophilic grains (ArG) and the occurrence of a late onset dementia, we examined the limbic area in 35 subjects who had ArG as the main neuropathological finding. A retrospective clinical analysis was performed by collecting information from hospital charts supplemented by standardized interviews based on DSM IV criteria for dementia. Sections from the rostral and caudal hippocampal regions, including the entorhinal/transentorhinal and parahippocampal cortex on both sides, were strained by the Gallays method. Nineteen subjects were diagnosed as demented according to these criteria; 16 were considered to have been cognitively normal. High numbers of ArG were observed in the anterior part of the CA1 subfield in all cases. However, the posterior half of CA1 was involved significantly more often and more severely in demented than in non-demented individuals (P < 0.01). Moreover, the distribution of ArG in the entorhinal/transentorhinal and parahippocampal cortex was more widespread in the group of demented patients (P < 0.05). These results show that the intellectual status of patients with AgD was related to the extension of ArG in the limbic area. We suggest that AgD is a progressive neurodegenerative disorder with early subclincial lesions in the anterior part of the hippocampal formation. To provide a more accurate clinicopathological correlation, the rostrocaudal extension of ArG in the limbic area should be evaluated in AgD cases.


Subject(s)
Dementia/pathology , Hippocampus/pathology , Neurodegenerative Diseases/pathology , Aged , Aged, 80 and over , Female , Histocytochemistry , Humans , Male , Retrospective Studies , Silver Staining
19.
Praxis (Bern 1994) ; 86(35): 1340-2, 1997 Aug 27.
Article in German | MEDLINE | ID: mdl-9381025

ABSTRACT

Neuropsychological assessment of dementia should be obtained using a two-step procedure: 1) a family physician performs a mental screening; 2) specialists determine the diagnosis after a thorough differential diagnostic process. This second step includes the quantitative neuropsychological assessment of the patients' cognitive functions which has the following purposes: a) to contribute to the differential diagnostic process; b) to aid in diagnosing patients at the earliest stage of dementia; c) to document disease progression and therapy outcomes; and, d) to identify relatively intact areas of cognition to serve as a basis for cognitive therapy. A Swiss consensus to utilize the Consortium to Establish a Registry for Alzheimer's disease (CERAD) Neuropsychological Battery as a minimal standard assessment instrument is introduced.


Subject(s)
Alzheimer Disease/diagnosis , Dementia/diagnosis , Activities of Daily Living/classification , Aged , Alzheimer Disease/classification , Alzheimer Disease/therapy , Cognitive Behavioral Therapy , Combined Modality Therapy , Dementia/classification , Dementia/therapy , Female , Follow-Up Studies , Humans , Male , Neuropsychological Tests
20.
Acta Neurol Scand ; 95(2): 81-4, 1997 Feb.
Article in English | MEDLINE | ID: mdl-9059725

ABSTRACT

OBJECTIVES: To establish the comparative efficacy to differentiate between Swiss patients with dementia of the Alzheimer type (DAT) and elderly normal control subjects (NC) on two different verbal fluency tasks: category fluency and letter fluency. MATERIAL AND METHODS: Fifty Swiss German DAT patients in the early stages of the disease and 50 matched normal control subjects were compared on letter and category fluency tasks. RESULTS: DAT patients exhibited an overproportional impairment on category fluency as compared with letter fluency. Receiver operating characteristic curves (ROC) showed that category fluency correctly classified a significantly higher number of DAT patients and NC subjects (84%) than letter fluency (70%). CONCLUSION: As similar findings have been described for English-speaking DAT patients, we conclude that deficiencies in category fluency are a general phenomenon, reflecting impaired structures of semantic knowledge occurring early in the course of Alzheimer's disease.


Subject(s)
Alzheimer Disease/physiopathology , Language Disorders/physiopathology , Memory Disorders/physiopathology , Aged , Aged, 80 and over , Alzheimer Disease/complications , Analysis of Variance , Case-Control Studies , Chi-Square Distribution , Concept Formation/physiology , Female , Humans , Language Disorders/etiology , Male , Memory Disorders/etiology , Mental Recall/physiology , Middle Aged , Neuropsychological Tests , Phonetics , ROC Curve , Semantics , Sensitivity and Specificity , Switzerland , Verbal Behavior/physiology
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