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1.
J Nutr Health Aging ; 13(9): 760-7, 2009 Nov.
Article in English | MEDLINE | ID: mdl-19812865

ABSTRACT

OBJECTIVES: To determine whether in the current study the supply of a nutrient dense drink has a positive effect on mental and physical function of institutionalized elderly people. DESIGN: A 24-week, randomized, double-blind, placebo-controlled, parallel-group, intervention trial. SETTING: Homes for the elderly and nursing homes in the Netherlands. PARTICIPANTS: Institutionalized elderly people older than 60 years, with a BMI < or = 30 kg/m2, and a Mini-Mental State Examination score of at least 10 points. INTERVENTION: In addition to their usual diet the participants (n=176) received either a nutrient dense drink or a placebo drink twice a day during 24 weeks. MEASUREMENTS: The functionality measures included cognitive function, mood, physical performance and the ability to perform activities of daily living. RESULTS: In the supplement group a favorable effect of the intervention drink on body weight (1.6 kg difference in change; P = .035), calf circumference (0.9 cm difference in change; P = .048), and blood values (e.g. Hcy decreased from 16.8 to 11.2 mumol/L in the supplement group) was found. In the total group no significant effect was found on functionality outcomes. However, a subgroup of participants with BMI at baseline below 24.4 kg/m2 performed better on the cognitive subscale of Alzheimer's Disease Assessment Scale (P = .09), and its language sub score (P = .01) after 24 weeks of intervention. CONCLUSION: The results in the total group of this trial suggest that the nutritional supplement used in this study improves nutritional status. Furthermore, the results of this trial suggest that it is effective as treatment for decreasing function in a subgroup of institutionalized elderly people with low BMI.


Subject(s)
Activities of Daily Living , Cognition/drug effects , Food, Fortified , Micronutrients/pharmacology , Nutritional Status/drug effects , Aged , Aged, 80 and over , Anthropometry , Beverages , Blood Chemical Analysis , Body Mass Index , Cognition/physiology , Double-Blind Method , Female , Homes for the Aged , Humans , Male , Mental Health , Nursing Homes , Nutritional Status/physiology , Nutritive Value
2.
Eur J Clin Nutr ; 62(10): 1248-51, 2008 Oct.
Article in English | MEDLINE | ID: mdl-17609694

ABSTRACT

Mildly cobalamin-deficient elderly were supplemented with 1000 microg cobalamin (group C, n=34), 1000 microg cobalamin with 400 microg folic acid (group CF, n=31) or a placebo (n=30) for 6 months. Participants provided one single blood sample 3, 5 or 7 months after cessation of supplementation to monitor early changes in plasma concentrations of cobalamin, holotranscobalamin (holoTC) and methylmalonic acid (MMA). At the end of supplementation (groups C+CF), one participant met our criteria for mild cobalamin deficiency, as did 13, 14 and 43% of the participants assessed at respectively 3, 5 and 7 months post-supplementation. Cobalamin and holoTC declined on average with 47 and 56% relative to concentrations at the end of supplementation for the group assessed at 7 months post-supplementation. Essentially similar declines were observed for those participants assessed at 3 and 5 months post-supplementation. Mean MMA concentrations increased by 15% (P=0.07) in those participants assessed at 3 and 5 months post-supplementation, and increased by 50% (P=0.002) in those participants assessed at 7 months post-supplementation. Considering MMA as a sensitive tissue marker for cobalamin status, oral supplementation may afford adequate cobalamin status for a period of up to 5 months after cessation in the majority of participants.


Subject(s)
Folic Acid/blood , Nutritional Status , Vitamin B 12 Deficiency/blood , Vitamin B 12 Deficiency/epidemiology , Vitamin B 12/blood , Vitamin B Complex/blood , Aged, 80 and over , Biological Availability , Biomarkers/blood , Dietary Supplements , Female , Folic Acid/pharmacology , Follow-Up Studies , Humans , Male , Methylmalonic Acid/blood , Randomized Controlled Trials as Topic , Time Factors , Treatment Outcome , Vitamin B 12/administration & dosage , Vitamin B 12/pharmacokinetics , Vitamin B 12 Deficiency/drug therapy , Vitamin B Complex/administration & dosage , Vitamin B Complex/pharmacokinetics
3.
Eur J Nutr ; 45(2): 70-8, 2006 Mar.
Article in English | MEDLINE | ID: mdl-16052295

ABSTRACT

BACKGROUND: Several cross-sectional, case-control and prospective studies revealed a relation between homocysteine and cognitive function or dementia. These studies included either patient populations or healthy, community- dwelling elderly people. AIM OF THE STUDY: In this study we tested the hypothesis that homocysteine was inversely associated with cognitive function in a population of institutionalised elderly (aged >/= 60 y; n = 157). METHODS: For testing this hypothesis baseline data of a recently conducted intervention study in institutionalised elderly (median age 83 years) were used. Cognitive function was evaluated by the cognitive subscale of the Alzheimer's disease Assessment Scale (ADAS-cog). The association between fasting plasma homocysteine level and cognitive function was investigated by multiple linear regression analysis. RESULTS: In the crude model homocysteine concentration was not significantly related to ADAS-cog score (beta = 0.061; p = 0.45). Age was found to be related to ADAS-cog score (beta = 0.161; p < 0.05). Adjusting for age did however not result in a relation between homocysteine and cognitive function. CONCLUSIONS: In our study no association was found between homocysteine and cognitive function in a population of very old institutionalised subjects.


Subject(s)
Cognition/physiology , Geriatric Assessment/methods , Homocysteine/blood , Psychiatric Status Rating Scales , Age Factors , Aged , Aged, 80 and over , Alzheimer Disease/blood , Alzheimer Disease/diagnosis , Biomarkers/blood , Cognition/drug effects , Cross-Sectional Studies , Female , Homes for the Aged , Homocysteine/pharmacology , Humans , Linear Models , Male
4.
Neth J Med ; 63(4): 149-50, 2005 Apr.
Article in English | MEDLINE | ID: mdl-15869044

ABSTRACT

The authors report an 85-year-old patient admitted because of cognitive impairment. During examination hypertension and hypokalaemia were found. After some time it was discovered that the patient was eating too much liquorice. The case demonstrates that liquorice intoxication should be considered as a cause of hypertension in old age. Furthermore the case demonstrates that missing an intoxication is a pitfall for medical history taking of patients with cognitive impairment.


Subject(s)
Glycyrrhetinic Acid/toxicity , Glycyrrhiza/toxicity , Hypertension/chemically induced , Aged , Aged, 80 and over , Candy , Chronic Disease , Feeding Behavior , Female , Glycyrrhiza/chemistry , Humans , Hypokalemia/chemically induced , Memory Disorders/complications , Pseudohypoaldosteronism/chemically induced
5.
Ned Tijdschr Geneeskd ; 147(1): 32-5, 2003 Jan 04.
Article in Dutch | MEDLINE | ID: mdl-12564296

ABSTRACT

In two patients, men aged 80 and 75 years with cognitive deterioration, hallucinations and parkinsonism, the clinical diagnosis 'dementia with Lewy bodies' was established. Treatment with an atypical antipsychotic, risperidone and olanzapine respectively, resulted in an exacerbation of the parkinsonism. Rivastigmine evidently improved the psychosis, the anxiety and the cognitive, mood and behaviour disorders. Titrated treatment with levodopa improved the mobility without an increase of the psychosis. The treatment of dementia with Lewy bodies is complex. Levodopa can lead to an increase in visual hallucinations. Antipsychotics often cause serious side effects, such as increasing parkinsonism, sedation and cognitive deterioration. Cholinesterase inhibitors such as rivastigmine could possibly provide an alternative treatment for the neuropsychiatric symptoms.


Subject(s)
Carbamates/therapeutic use , Cholinesterase Inhibitors/therapeutic use , Lewy Body Disease/drug therapy , Neuroprotective Agents/therapeutic use , Phenylcarbamates , Pirenzepine/analogs & derivatives , Aged , Aged, 80 and over , Antiparkinson Agents/therapeutic use , Antipsychotic Agents/adverse effects , Antipsychotic Agents/therapeutic use , Benzodiazepines , Drug Therapy, Combination , Humans , Levodopa/therapeutic use , Lewy Body Disease/psychology , Male , Olanzapine , Pirenzepine/adverse effects , Pirenzepine/therapeutic use , Risperidone/adverse effects , Risperidone/therapeutic use , Rivastigmine , Treatment Outcome
6.
Aging Ment Health ; 7(1): 34-8, 2003 Jan.
Article in English | MEDLINE | ID: mdl-12554313

ABSTRACT

This study assessed the information provided in a memory clinic and the patient and caregiver factors that influenced the provision of information. The study was part of a larger cross-sectional study of the diagnosis of dementia and satisfaction with information given. The participants were 51 elderly patients suspected of having dementia and living at home together with their caregivers. The main outcome measures were the checklist of information communicated to the patients and caregivers, patients' behavioural problems, patients' instrumental activities of daily living (IADL) problems, and caregivers' sense of competence. The results indicate that basic information about the diagnosis was given to 86% of patients and 88% of caregivers. Specific information about patients' behaviour and professional care was more often given when patients had more cognitive, behavioural, or IADL problems and caregivers had a lower sense of competence. Providing the majority of patients with information is feasible. These results contribute to an explanation of previous findings indicating that caregivers of patients with cognitive problems not related to dementia were less satisfied with the information they received. Adequate information should not only include issues considered relevant by clinicians but should also be tailored to the information needs of patients and caregivers.


Subject(s)
Caregivers , Cognition , Dementia/diagnosis , Information Dissemination , Aged , Aged, 80 and over , Cross-Sectional Studies , Dementia/psychology , Female , Humans , Male , Mental Disorders/etiology , Mental Health Services/supply & distribution , Middle Aged , Neuropsychological Tests , Surveys and Questionnaires
7.
J Fam Pract ; 51(8): 693-9, 2002 Aug.
Article in English | MEDLINE | ID: mdl-12184965

ABSTRACT

OBJECTIVES: To explore and quantify the relative contribution of guideline recommendations and other determinants in the family physicianamprsquos diagnostic work-up of patients suspected of dementia. STUDY DESIGN: We prospectively studied 64 family physicians in an Eastern district in the Netherlands who diagnosed dementia according to the national Dutch guidelines in primary care. Their diagnoses were compared with the reference standard embodied by the memory clinic team of the University Medical Center Nijmegen. POPULATION: The physicians evaluated 107 patients older than 55 years suspected of having dementia. OUTCOMES MEASURED: Predictive values of various clinical and demographic parameters were measured in both univariate and multivariate logistic regression analyses. RESULTS: Activities of daily living (ADL) dependency (odds ratio [OR] = 5.3, P =.03), years since symptoms first started (OR = 1.84, P =.03), and the presence of somatic comorbidity (OR = 0.48, P =.02) independently contributed to the prediction of the presence or absence of dementia. The area under the receiver-operating characteristic (ROC) curve for these 3 variables together was 0.79. The ROC area of the family physiciansamprsquo diagnosis to determine the final diagnosis was 0.74. The number of recommendations applied did not additionally contribute to the assessment of the final diagnosis. CONCLUSIONS: The diagnostic accuracy of the family physician was reasonable. For family physicians, ADL dependency is a better predictor of dementia than cognitive impairment. Family physicians should be aware of diagnostic difficulties in patients with somatic comorbidity. We were unable to confirm the diagnostic value of many of the recommendations of dementia guidelines.


Subject(s)
Dementia/diagnosis , Practice Guidelines as Topic , Activities of Daily Living , Decision Making , Family Practice , Humans , Logistic Models , Middle Aged , Netherlands , Practice Patterns, Physicians' , ROC Curve
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