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2.
Psychogeriatrics ; 17(5): 317-323, 2017 Sep.
Article in English | MEDLINE | ID: mdl-28130857

ABSTRACT

BACKGROUND: There are few studies addressing caregivers of bipolar disorder (BD) patients, especially patients who are older adults with an increased need for care, often given by a relative. The aim of this study was to describe which factors increase caregiver burden among caregivers of elderly BD outpatients. METHODS: Patients were older than 60 years and met the Diagnostic and Statistical Manual of Mental Disorders, fifth edition, criteria for BD. They were evaluated for current mood, cognitive and other neuropsychiatric symptoms, functionality, medical comorbidities, quality of life, years since BD diagnosis, and number of psychiatric admissions. The caregiver who spent the greatest time with each patient was evaluated with the Zarit Caregiver Burden Interview. The caregivers' global health, mood symptoms, quality of life, and tasks performed for the patient were also assessed. RESULTS: Thirty-six BD patients and their caregivers were assessed. The Zarit Caregiver Burden Interview was positively correlated with patients' neuropsychiatric symptoms (r = 0.508, P = 0.002) and functional impairment (r = 0.466, P = 0.004). The Zarit Caregiver Burden Interview was also correlated with caregivers' own depression (r = 0.576, P < 0.001), anxiety (r = 0.360, P = 0.031), quality of life (r = -0.406, P = 0.014), medical comorbidities (r = 0.387, P = 0.020), and number of tasks that they completed for the patient (r = 0.480, P = 0.003). CONCLUSIONS: In this group of elderly BD patients, caregiver burden was more associated with symptoms frequently seen in others diseases as in dementia than with depressive, manic, or anxiety symptoms, which are often used as treatment outcomes measures goals in BD. Potential treatable and modifiable factors associated with caregiver burden could be caregivers' depression, anxiety, and medical comorbidities, as well as support for caregivers in terms of services and social relationships.


Subject(s)
Anxiety/psychology , Bipolar Disorder/psychology , Caregivers/psychology , Cost of Illness , Depression/psychology , Quality of Life , Adaptation, Psychological , Aged , Aged, 80 and over , Bipolar Disorder/physiopathology , Cross-Sectional Studies , Female , Humans , Male , Middle Aged , Psychiatric Status Rating Scales
3.
Am J Geriatr Psychiatry ; 22(4): 389-97, 2014 Apr.
Article in English | MEDLINE | ID: mdl-23567429

ABSTRACT

BACKGROUND/OBJECTIVE: Cognitive impairment is a common feature of bipolar disorder (BD), with increased risk of developing dementia in late life. The aim of this study was to investigate the performance on cognitive screening tests in a sample of older adults with BD, as compared to non-BD subjects. METHODS: 186 older adults (86 with BD and 100 without BD) were included. Patients were stratified according to cognitive performance (normal cognition, mild impairment, and dementia). The comparison group comprised healthy controls; subjects with cognitive impairment but no dementia (CIND); or patients with probable or possible Alzheimer disease (AD). Sixty-five subjects were cognitively unimpaired (35 BD), 65 had CIND (25 BD), and 56 AD (26 BD). In each of these levels of cognitive function, we compared the performance of BD and non-BD subjects on the Mini-Mental State Examination (MMSE), verbal fluency test (VFT), and the Clock Drawing Test (CDT). RESULTS: Non-demented patients with BD had a slightly worse global cognitive performance as compared with healthy controls and patients with CIND, as shown by lower scores on the MMSE. Similarly, BD patients performed worse on the VFT, both in the normal cognition range and in the dementia range. Finally, demented BD patients had a significantly worse performance on the CDT as compared with patients with dementia due to AD. CONCLUSION: Older adults with BD perform significantly worse on some cognitive screening tests as compared with those without BD across different levels of cognition.


Subject(s)
Alzheimer Disease/psychology , Bipolar Disorder/psychology , Cognitive Dysfunction/psychology , Aged , Aged, 80 and over , Case-Control Studies , Cognition Disorders/psychology , Female , Humans , Male , Middle Aged , Neuropsychological Tests
4.
Neurosci Lett ; 494(1): 54-6, 2011 Apr 20.
Article in English | MEDLINE | ID: mdl-21362460

ABSTRACT

Several studies have suggested an important role for brain-derived neurotrophic factor (BDNF) in the pathophysiology and therapeutics of bipolar disorder (BPD). The mechanisms underlying the therapeutic effects of lithium in BPD seem to involve a direct regulation of neurotrophic cascades. However, no clinical study evaluated the specific effects of lithium on BDNF levels in subjects with BPD. This study aims to investigate the effects of lithium monotherapy on BDNF levels in acute mania. Ten subjects with bipolar I disorder in a manic episode were evaluated at baseline and after 28 days of lithium therapy. Changes in plasma BDNF levels and Young Mania Rating Scale (YMRS) scores were analyzed. A significant increase in plasma BDNF levels was observed after 28 days of therapy with lithium monotherapy (510.9±127.1pg/mL) compared to pre-treatment (406.3±69.5pg/mL) (p=0.03). Although it was not found a significant association between BDNF levels and clinical improvement (YMRS), 87% of responders presented an increase in BDNF levels after treatment with lithium. These preliminary data showed lithium's direct effects on BDNF levels in bipolar mania, suggesting that short-term lithium treatment may activate neurotrophic cascades. Further studies with larger samples and longer period may confirm whether this biological effect is involved in the therapeutic efficacy of lithium in BPD.


Subject(s)
Antimanic Agents/therapeutic use , Bipolar Disorder/blood , Bipolar Disorder/drug therapy , Brain-Derived Neurotrophic Factor/blood , Lithium/therapeutic use , Adult , Female , Humans , Male , Treatment Outcome
5.
Clinics (Sao Paulo) ; 64(10): 967-73, 2009.
Article in English | MEDLINE | ID: mdl-19841703

ABSTRACT

OBJECTIVE: To determine the accuracy of the Mini-Mental State Examination combined with the Verbal Fluency Test and Clock Drawing Test for the identification of patients with mild cognitive impairment and Alzheimer's disease (AD). METHOD: These tests were used to evaluate cognitive function in 247 older adults. Subjects were divided into three groups according to their cognitive state: mild cognitive impairment (n=83), AD (n=81), cognitively unimpaired controls (n=83), based on clinical and neuropsychological data. The diagnostic accuracy of each test for discriminating between these diagnostic groups (mild cognitive impairment or AD vs. controls) was examined with the aid of Receiver Operating Characteristic (ROC) curves. Additionally, we evaluated the benefit of the combination of tests on diagnostic accuracy. RESULTS: Although they were accurate enough for the identification of Alzheimer's disease, neither test alone proved adequate for the correct separation of patients with mild cognitive impairment from healthy subjects. Combining these tests did not improve diagnostic accuracy, as compared to the Mini-Mental State Examination alone, in the identification of patients with mild cognitive impairment or Alzheimer's disease. CONCLUSIONS: The present data do not warrant the combined use of the Mini-Mental State Examination, the Verbal Fluency Test and the Clock Drawing Test as a sufficient diagnostic schedule in screening for mild cognitive impairment. The present data do not support the notion that the combination of test scores is better that the use of Mini-Mental State Examination scores alone in the screening for Alzheimer's disease.


Subject(s)
Alzheimer Disease/diagnosis , Cognition Disorders/diagnosis , Neuropsychological Tests/standards , Aged , Epidemiologic Methods , Female , Humans , Male , Mental Status Schedule/standards
6.
Clinics ; 64(10): 967-973, 2009. tab
Article in English | LILACS | ID: lil-529539

ABSTRACT

OBJECTIVE: To determine the accuracy of the Mini-Mental State Examination combined with the Verbal Fluency Test and Clock Drawing Test for the identification of patients with mild cognitive impairment and Alzheimer's disease (AD). METHOD: These tests were used to evaluate cognitive function in 247 older adults. Subjects were divided into three groups according to their cognitive state: mild cognitive impairment (n=83), AD (n=81), cognitively unimpaired controls (n=83), based on clinical and neuropsychological data. The diagnostic accuracy of each test for discriminating between these diagnostic groups (mild cognitive impairment or AD vs. controls) was examined with the aid of Receiver Operating Characteristic (ROC) curves. Additionally, we evaluated the benefit of the combination of tests on diagnostic accuracy. RESULTS: Although they were accurate enough for the identification of Alzheimer's disease, neither test alone proved adequate for the correct separation of patients with mild cognitive impairment from healthy subjects. Combining these tests did not improve diagnostic accuracy, as compared to the Mini-Mental State Examination alone, in the identification of patients with mild cognitive impairment or Alzheimer's disease. CONCLUSIONS: The present data do not warrant the combined use of the Mini-Mental State Examination, the Verbal Fluency Test and the Clock Drawing Test as a sufficient diagnostic schedule in screening for mild cognitive impairment. The present data do not support the notion that the combination of test scores is better that the use of Mini-Mental State Examination scores alone in the screening for Alzheimer's disease.


Subject(s)
Aged , Female , Humans , Male , Alzheimer Disease/diagnosis , Cognition Disorders/diagnosis , Neuropsychological Tests/standards , Epidemiologic Methods , Mental Status Schedule/standards
7.
Parasitol Res ; 96(6): 418-21, 2005 Aug.
Article in English | MEDLINE | ID: mdl-15940524

ABSTRACT

Although there is indirect evidence to suggest that glycogen is present in G. lamblia, to date it has not been purified and identified from this organism. In this study, a high molecular weight carbohydrate was purified and characterized and its physiological role as an energetic reserve was established. The monosaccharide constituents of the carbohydrate reserve were identified as glucose by two independent methods: thin layer chromatography and an enzymatic assay. The degree of branching of the molecule was evaluated by comparing its absorbance spectrum in the presence of lugol with spectra of standard solutions of glycogen and starch under the same conditions. The results strongly suggest that glycogen is present in G. lamblia and acts as an energy reserve in trophozoites of this organism.


Subject(s)
Energy Metabolism/physiology , Giardia lamblia/cytology , Glycogen/metabolism , Animals , Chromatography, Thin Layer , Giardia lamblia/chemistry , Giardia lamblia/metabolism , Glycogen/chemistry
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