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1.
J Prev Alzheimers Dis ; 10(3): 426-442, 2023.
Article in English | MEDLINE | ID: mdl-37357283

ABSTRACT

Amyloid and tau biomarkers for Alzheimer's disease are widely recognized diagnostic tools for the identification of Alzheimer's disease pathology antemortem and are recommended by the most recent clinical and research guidelines. Approved biomarkers include positron emission tomography (PET)- and fluid-based markers derived from cerebrospinal fluid and, more recently, plasma. These biomarkers are still infrequently used in clinical practice, potentially due to challenges in access to and understanding of individual assay information and methodology. We provide an overview of the diagnostic biomarkers for amyloid and tau pathology that are currently available in the US and/or EU for clinical use. Available performance data from both labels/instructions for use and the scientific literature (with focus on autopsy or PET as standard of truth) are summarized to help healthcare providers navigate the biomarker landscape. All available PET amyloid and tau biomarkers demonstrate high accuracy in identifying amyloid and tau Alzheimer's disease pathology, respectively, at autopsy. Among cerebrospinal fluid biomarkers, all showed accurate prediction of Alzheimer's disease pathology, either based on autopsy or PET findings; greater accuracy was evident for concentration ratios (Aß42/40 or P-tau181/Aß42) versus individual biomarker concentrations. Among plasma biomarkers, Aß42/40 and P-tau181 demonstrated high agreement with PET findings. Overall, we conclude that commercially available PET, cerebrospinal fluid and plasma assays accurately identify Alzheimer's disease amyloid and tau pathology. The recent development of fully automated tests for fluid-based biomarkers improves test reliability. The continued development of plasma biomarkers holds promise for the future management of patients with Alzheimer's disease.


Subject(s)
Alzheimer Disease , Humans , United States , Alzheimer Disease/diagnosis , Alzheimer Disease/cerebrospinal fluid , Amyloid beta-Peptides/cerebrospinal fluid , tau Proteins/cerebrospinal fluid , Reproducibility of Results , Amyloid , Biomarkers/cerebrospinal fluid
2.
J Prev Alzheimers Dis ; 5(1): 55-64, 2018.
Article in English | MEDLINE | ID: mdl-29405234

ABSTRACT

BACKGROUND: The GERAS II study aimed to assess societal costs and resource use associated with Alzheimer's disease (AD) for patients and their primary caregivers in Italy and Spain, stratified for different severity stages of AD at baseline. This report presents baseline results for Italy. DESIGN: GERAS II was a prospective, multicentre, observational study of routine care in AD. SETTING: Community-dwelling patients attending specialist secondary care centres (memory clinics/Alzheimer's Evaluation Units) and their primary informal caregivers were recruited into the study. PARTICIPANTS: Patients were aged ≥55 years, presented within the normal course of care, had a diagnosis of probable AD and a Mini-Mental State Examination (MMSE) score of ≤26. Patients and caregivers were stratified according to patient AD dementia severity at baseline: mild, MMSE score 21-26; moderate, MMSE score 15-20; or moderately severe/severe, MMSE score <15. MEASUREMENTS: Data collected for patients and caregivers included demographics/clinical characteristics; current medication; patient cognitive, functional and behavioural assessments; patient and caregiver health-related quality of life (HRQoL); and patient and caregiver resource use. The costs associated with the resources used were calculated. Costs were broken down into patient healthcare costs, patient social care costs and caregiver informal care costs. RESULTS: Of 198 patients enrolled from Italy, 29 (15%) had mild AD dementia, 80 (40%) had moderate AD dementia, and 89 (45%) had moderately severe/severe AD dementia. Patient and caregiver characteristics showed some differences between AD dementia severity groups; for example, a numerically higher proportion of patients with mild and moderately severe/severe AD dementia were taking memantine compared with those with moderate AD dementia. Patient functioning and behavioural and psychological symptoms worsened with increasing AD dementia severity (p<0.05 between groups for all measures). No significant difference between the disease severity groups was observed in patient HRQoL, and there was no clear pattern in resource use. However, all measures of caregiver time spent helping the patient differed significantly between groups (p<0.05) and were highest in patients with moderately severe/severe AD dementia. Mean (standard deviation) total monthly societal costs per patient (2013 values) were €1850 (1901), €1552 (1322) and €2728 (2184) for patients with mild, moderate and moderately severe/severe AD dementia, respectively (p<0.001 between groups). Caregiver informal care costs were the greatest contributor to total societal costs and amounted to €1370, €1223 and €2223 per patient per month for mild, moderate and moderately severe/severe AD dementia groups, respectively (p<0.001 between groups). CONCLUSION: Total Italian societal costs generally increased with increasing AD dementia severity. However, costs were slightly lower for moderate than for mild AD dementia, possibly reflecting the observed unusual trend of greater caregiver time and higher memantine use in patients with mild versus moderate AD dementia.


Subject(s)
Alzheimer Disease/economics , Alzheimer Disease/epidemiology , Health Care Costs , Health Resources/statistics & numerical data , Aged , Aged, 80 and over , Caregivers/economics , Female , Humans , Independent Living , Italy/epidemiology , Male , Prospective Studies , Severity of Illness Index
3.
Phys Med ; 32(7): 898-904, 2016 Jul.
Article in English | MEDLINE | ID: mdl-27345259

ABSTRACT

During pelvic radiotherapy bowel loops (BL) are subject to inter-fraction changes. MVCT images have the potential to provide daily bowel segmentation. We assess the feasibility of deformable registration and contour propagation in replacing manual BL segmentation on MVCT. Four observers delineated BL on the planning kVCT and on one therapy MVCT in eight patients. Inter-observer variations in BLs contouring were quantified using DICE index. BLs were then automatically propagated onto MVCT by a commercial software for image deformation and subsequently manually corrected. The agreement between propagated BL/propagated+manually corrected BL vs manual were quantified using the DICE. Contouring times were also compared. The impact on DVH of using the deformable-registration method was assessed. The same procedures were repeated on high-resolution planning-kVCT and therapy-kVCT. MVCTs are adequate to visualize BL (average DICE: 0.815), although worse than kVCT (average DICE:0.889). When comparing propagated vs manual BL, a poor agreement was found (average DICE: 0.564/0.646 for MVCT/KVCT). After manual correction, average DICE indexes increased to 0.810/0.897. The contouring time was reduced to 15min with the semi-automatic approach from 30min with manual contouring. DVH parameters of propagated BL were significantly different from manual BL (p<0.0001); after manual correction, no significant differences were seen. MVCT are suitable for BL visualization. The use of a software to segment BL on MVCT starting from BL-kVCT contours was feasible if followed by manual correction. The method resulted in a substantial reduction of contouring time without detrimental effect on the quality of bowel segmentation and DVH estimates.


Subject(s)
Image Processing, Computer-Assisted/methods , Intestines/diagnostic imaging , Pelvis/radiation effects , Tomography, X-Ray Computed , Feasibility Studies , Humans , Male , Observer Variation , Prostatic Neoplasms/diagnostic imaging , Prostatic Neoplasms/radiotherapy , Radiotherapy Planning, Computer-Assisted , Time Factors
4.
J Nutr Health Aging ; 18(7): 677-84, 2014 Jul.
Article in English | MEDLINE | ID: mdl-25226106

ABSTRACT

OBJECTIVES: This study aimed to describe the baseline characteristics of informal carers of community-living Alzheimer's disease (AD) patients by AD severity group and to identify factors associated with two measures of caregiver burden. DESIGN AND SETTING: GERAS is a prospective observational study in France, Germany, and the UK, designed to assess costs and resource use associated with AD, for patients and their caregivers, stratified by disease severity. PARTICIPANTS: 1497 community-dwelling AD patients and their primary caregivers. MEASUREMENTS: Subjective caregiver burden assessed using the Zarit Burden Interview [ZBI] and time spent supervising patients (an objective measure of burden recorded using the Resource Utilization in Dementia instrument) during the month before the baseline visit were recorded. Separate multiple linear regression analyses using ZBI total score and caregiver supervision time as dependent variables were performed to identify patient and caregiver factors independently associated with caregiver burden. RESULTS: Increasing AD severity was associated with both subjective caregiver burden (ZBI total score) and overall caregiver time, which includes supervision time (both p<0.001, ANOVA). Better patient functioning (on instrumental activities of daily living) was independently associated with both a lower ZBI total score and less supervision time, whereas higher levels of caregiver distress due to patient behavior were associated with greater caregiver burden. Other factors independently associated with an increased ZBI total score included younger caregiver age, caregiver self-reported depression, caring for a male patient, and longer time since AD diagnosis. Caregivers living with the patient, being a male caregiver, patient living in a rural location, higher patient behavioral problem subdomain scores for apathy and psychosis, more patient emergency room visits, not receiving food delivery and receiving financial support for caregiving were all associated with greater caregiver supervision time. CONCLUSION: Our results show that subjective caregiver burden and caregiver time are influenced by different factors, reinforcing the need to consider both aspects of caregiving when trying to minimize the burden of AD. However, interventions that minimize caregiver distress and improve patient functioning may impact on both subjective and objective burden.


Subject(s)
Alzheimer Disease/economics , Caregivers/psychology , Cost of Illness , Self Report , Activities of Daily Living , Aged , Alzheimer Disease/diagnosis , Cross-Sectional Studies , Depression/epidemiology , Female , Follow-Up Studies , France , Germany , Humans , Linear Models , Longitudinal Studies , Male , Middle Aged , Multivariate Analysis , Prospective Studies , Residence Characteristics , United Kingdom
5.
Phys Med ; 30(2): 184-90, 2014 Mar.
Article in English | MEDLINE | ID: mdl-23751395

ABSTRACT

The purpose of this study is to evaluate the use of MapCHECK2 in a patient-specific quality assurance (QA) procedure for Rapid Arc (RA) radiotherapy and to obtain reference values of gamma index (γ) for different irradiation geometries. Dose distributions of 386 patients, optimized with Eclipse treatment planning system for RA on Varian Clinac 2300IX were exported and measured with MapCHECK2 detector array inserted in a MapPHAN dedicated phantom. Gamma index analysis was used to evaluate differences between calculated and delivered doses; collected data were analysed on the basis of complexity of plans and type of disease. Angular dependence and dose drift of detectors were estimated. The overall mean passing rate (percentage of points with γ < 1) was equal to 97.0% ± 3.1%; plan-specific evaluation of %γ < 1 showed significant differences among different treatment protocols (pancreas 98.6% ± 1.5%, prostate 96.6% ± 2.8% and rectum 92.8% ± 5.7%). MapCHECK2 demonstrated a strong angular dependence over a restricted range of angles (90° ± 5° and 270° ± 5°); this condition affected the result of pre-treatment QA only for plans with intense lateral fluence. The drift of diode array response due to the accumulated dose was found to be comparable with the manufacturer's declaration (0.5% per 1000 Gy). MapCHECK2 proved to be a useful and accurate tool in the process of patient-specific QA for RA treatment. Excluding the irradiation geometries with a high contribution of lateral fluence, the mean percentage of cases with γ-index > 95% equal to 90.3% was obtained instead of 81.7% including all plans.


Subject(s)
Quality Assurance, Health Care , Radiotherapy Planning, Computer-Assisted/methods , Radiotherapy, Intensity-Modulated/methods , Humans , Neoplasms/radiotherapy , Phantoms, Imaging , Radiotherapy Dosage , Radiotherapy Planning, Computer-Assisted/instrumentation , Reproducibility of Results , Software , Time Factors
6.
Neurosci Biobehav Rev ; 33(4): 601-10, 2009 Apr.
Article in English | MEDLINE | ID: mdl-17904221

ABSTRACT

UNLABELLED: Childhood neglect and poor child-parent relationships have been reported to increase substance use disorders susceptibility. Stressful environmental factors, including emotional neglect, could affect individual personality traits and mental health, possibly inducing stable changes in hypothalamic-pituitary-adrenal (HPA) axis and brain mono-amine function, in turn involved in addictive behavior vulnerability. Therefore, we decided to investigate homovanillic (HVA) and prolactin (PRL) plasma levels, as expression of possible changes in dopamine function, ACTH and cortisol plasma levels, as measures of HPA axis function, and concomitant psychiatric symptoms profile in abstinent cocaine addicts, in relationship to their childhood history of neglect and poor parental care perception. METHODS: Fifty abstinent cocaine dependent patients, and 44 normal controls, matched for age and sex, were submitted to a detailed psychiatric assessment (DSM IV criteria). All patients and controls completed the Symptoms Check List-90 (SCL-90) and the Buss Durkee Hostility Inventory (BDHI), to evaluate psychiatric symptoms frequency and aggressiveness levels. The Childhood Experience of Care and Abuse-Questionnaire (CECA-Q) and Parental Bonding Instrument (PBI) have been used to retrospectively investigate parent-child relationships. Blood samples were collected to determine HVA, PRL, ACTH and cortisol basal plasma levels. RESULTS: Cocaine addicted individuals in general showed significantly lower HVA, and higher PRL, ACTH and cortisol basal levels respect to controls. In particular, neuroendocrine changes characterized cocaine addicts with childhood history of neglect and low perception of parental care. Obsessive-compulsive, depression and aggressiveness symptoms have been found related to poor parenting, inversely associated to HVA levels and directly associated to PRL, ACTH and cortisol levels. CONCLUSIONS: These findings suggest the possibility that childhood experience of neglect and poor parent-child attachment may partially contribute to a complex neurobiological derangement including HPA axis and dopamine system dysfunctions, playing a crucial role in addictive and affective disorders susceptibility.


Subject(s)
Child Abuse , Cocaine-Related Disorders/psychology , Mental Disorders , Parenting/psychology , Adolescent , Adrenocorticotropic Hormone/blood , Adult , Child , Child, Preschool , Chromatography, High Pressure Liquid/methods , Electrochemistry , Female , Homovanillic Acid/blood , Humans , Hydrocortisone/blood , Male , Mental Disorders/blood , Mental Disorders/physiopathology , Mental Disorders/psychology , Personality , Prolactin/blood , Regression Analysis , Retrospective Studies , Surveys and Questionnaires , Young Adult
7.
Pharmacopsychiatry ; 41(1): 17-23, 2008 Jan.
Article in English | MEDLINE | ID: mdl-18203047

ABSTRACT

INTRODUCTION: The aim of this study was to evaluate the efficacy of a psychoeducational program (PEP) for weight control in patients who had experienced an increase of body weight during treatment with olanzapine. METHODS: Eligible patients were randomised to the PEP (Group 1) or to no intervention (Group 2) and continued on olanzapine. After 12 weeks, the PEP was also started in Group 2 and continued in Group 1, up to week 24. Body weight was measured every month. Other measures included quality of life, and change in plasma glucose and lipids levels. RESULTS: Patients in Group 1 (n=15) had a mean weight loss of 3.6 kg at week 12 and 4.5 kg at week 24 (p<0.01 at both times, p<0.01 between groups at week 12), while those in Group 2 (n=18) had no changes at week 12 and a significant weight loss at week 24 (-3.6 kg from week 12, p<0.01). Changes of BMI paralleled those of body weight. Quality of life (Q-LES-Q-SF categorisation) and functioning (GAF) significantly improved in the total population at endpoint (p<0.01). No significant changes were observed in fasting glucose and lipid profile, while insulin levels significantly decreased from baseline to endpoint in both groups (p<0.05). HOMA index and hepatic insulin sensitivity improved, too. DISCUSSION: Patients with increased BMI during treatment with olanzapine experienced significant weight and BMI loss following a structured psychoeducational program.


Subject(s)
Antipsychotic Agents/adverse effects , Benzodiazepines/adverse effects , Cognitive Behavioral Therapy/methods , Obesity/chemically induced , Obesity/therapy , Weight Gain/drug effects , Adolescent , Adult , Aged , Analysis of Variance , Evaluation Studies as Topic , Female , Humans , Male , Mental Disorders/complications , Mental Disorders/drug therapy , Middle Aged , Olanzapine , Psychiatric Status Rating Scales/statistics & numerical data , Time Factors
8.
J Neural Transm (Vienna) ; 114(12): 1637-47, 2007.
Article in English | MEDLINE | ID: mdl-17690947

ABSTRACT

BACKGROUND: Attention deficit hyperactivity disorder (ADHD) seems to be a risk condition for substance use disorders, possibly in relationship to common neurobiological changes, underlying both addictive and externalising behaviour susceptibility. Although this vulnerability has been primarily attributed to gene variants, previous studies suggest that also adverse childhood experiences may influence neurotransmission, affecting in particular brain dopamine (DA) system and possibly concurring to the development of behavioural disorders. Therefore, we decided to investigate ADHD symptoms and plasma concentrations of the DA metabolite homovanillic acid (HVA) in abstinent addicted patients, in comparison with healthy control subjects, evaluating whether ADHD scores were related with HVA levels, as expression of DA turnover, and whether HVA values, in turn, were associated with childhood emotional neglect. METHODS: Eighty-two abstinent drug dependent patients, and 44 normal controls, matched for age and sex, completed the Wender Utah Rating Scale (WURS), measuring ADHD symptoms, and the Childhood Experience of Care and Abuse Questionnaire (CECA-Q). Blood samples were collected to determine HVA plasma levels. RESULTS: Addicted individuals showed significantly higher ADHD scores and lower HVA levels respect to control subjects. ADHD scores at WURS in addicted patients negatively correlated with plasma HVA values. In turn, plasma HVA levels were inversely associated with childhood neglect measures, reaching statistical significance with "mother-antipathy" and "mother neglect" scores. CONCLUSIONS: These findings suggest the possibility that childhood experience of neglect and poor mother-child attachment may have an effect on central dopamine function as an adult, in turn contributing to both ADHD and substance abuse neurobiological vulnerability.


Subject(s)
Attention Deficit Disorder with Hyperactivity/blood , Attention Deficit Disorder with Hyperactivity/epidemiology , Child Abuse , Homovanillic Acid/blood , Substance-Related Disorders/blood , Substance-Related Disorders/epidemiology , Adult , Antisocial Personality Disorder/epidemiology , Anxiety/complications , Attention Deficit Disorder with Hyperactivity/psychology , Child , Child Abuse/psychology , Comorbidity , Depressive Disorder, Major/epidemiology , Female , Humans , Male , Substance-Related Disorders/psychology
9.
G Chir ; 27(5): 214-6, 2006 May.
Article in English | MEDLINE | ID: mdl-16857110

ABSTRACT

A potentially serious complication of laparoscopic cholecystectomy is the inadvertent dissemination of unsuspected gallbladder carcinoma. There are increasing reports of seeding of tumor at the trocar sites following laparoscopic cholecystectomy in patients with unexpected or inapparent gallbladder carcinoma. Although the mechanism of the abdominal wall recurrence is still unclear, laparoscopic handling of the tumor, perforation of the gallbladder, and extraction of the specimen without an endobag may be risk factors for the spreading of malignant cells. The Authors report the case of late development of umbilical metastasis after laparoscopic cholecystectomy; the presence of an incisional hernia and the finding of a stone in subcutaneous tissue demonstrate the diffusion of tumor cells into subcutaneous tissue during the extraction of gallbladder. The patient underwent an excision of the metastases. She is disease free two years after surgical treatment.


Subject(s)
Abdominal Neoplasms/secondary , Abdominal Wall , Adenocarcinoma/secondary , Cholecystectomy, Laparoscopic/adverse effects , Gallbladder Neoplasms , Hernia, Abdominal/etiology , Neoplasm Seeding , Abdominal Neoplasms/surgery , Abdominal Wall/surgery , Adenocarcinoma/surgery , Aged , Disease-Free Survival , Female , Follow-Up Studies , Gallbladder Neoplasms/surgery , Hernia, Abdominal/diagnostic imaging , Humans , Surgical Mesh , Time Factors , Tomography, X-Ray Computed
10.
Acta Neurol Scand ; 112(2): 65-71, 2005 Aug.
Article in English | MEDLINE | ID: mdl-16008529

ABSTRACT

OBJECTIVE: A door-to-door two-phase study was designed in order to estimate the prevalence of cognitive deficit amongst the residents of a district in Tuscany (central Italy). Identification of cases with mild cognitive impairment (MCI) was given high priority, because this condition has been suggested as a term for the boundary area between normal aging and dementia. METHODS: Of the 1600 subjects who completed the screening phase, 354 scored under the cut-off point of the Mini Mental State Examination and Clinical Dementia Rating and were investigated by means of a standardized diagnostic protocol. RESULTS: The prevalence of MCI and age-related cognitive decline was 4.9 and 9.3%, respectively; low levels of education significantly increased the risk of these conditions. The prevalence of dementia over age 65 was 6.2%, with a significant risk association with age. In our population, Alzheimer's disease was the most frequent type of dementia (prevalence rate 4.2%) and increased risk depending on age, sex and education has been found. CONCLUSIONS: Our findings are somewhat similar to previous studies. Further epidemiological and longitudinal studies are warranted to identify which diagnostic category is more predictive for dementia.


Subject(s)
Cognition Disorders/epidemiology , Dementia/epidemiology , Age Factors , Aged , Alzheimer Disease/diagnosis , Alzheimer Disease/epidemiology , Alzheimer Disease/psychology , Cognition Disorders/diagnosis , Cognition Disorders/psychology , Comorbidity , Cross-Sectional Studies , Dementia/diagnosis , Dementia/psychology , Dementia, Vascular/diagnosis , Dementia, Vascular/epidemiology , Dementia, Vascular/psychology , Disease Progression , Educational Status , Female , Humans , Italy/epidemiology , Male , Mass Screening , Neuropsychological Tests , Prevalence , Sex Factors
11.
Parkinsonism Relat Disord ; 10(8): 481-5, 2004 Dec.
Article in English | MEDLINE | ID: mdl-15542008

ABSTRACT

To date the aetiology of Parkinson's disease (PD) is unknown although both genetic susceptibility and environmental factors appear to play an important role in the development of the disease. Recent data have also indicated that chronic exposure to a common pesticide can reproduce the neurochemical, behavioral and neuropathological features of PD. The epidemiological studies previously carried on the prevalence of PD in population exposed to environmental factors have produced controversial results, probably because of different trial design and different analysis methods. A case-control retrospective study was conducted in a well-defined geographic area in Tuscany-Italy with the aim to identify environmental factors possibly related to PD. No significant difference between PD patients and control subjects was observed in time spent in rural or industrial residence, in well water drinking and in the exposure to herbicides and pesticides. A significant difference between patients with PD and controls was reported for cigarette smoking, controls resulting more likely cigarette smokers in comparison with PD patients. The present findings support the view of a protective effect of cigarette smoking and do not show any significant association between environmental factors and the risk of development of PD.


Subject(s)
Environment , Parkinson Disease/epidemiology , Aged , Antiparkinson Agents/therapeutic use , Case-Control Studies , Environmental Exposure , Female , Humans , Italy/epidemiology , Male , Middle Aged , Parkinson Disease/diagnosis , Pesticides , Risk Factors , Rural Population , Smoking/epidemiology , Water Supply
12.
Eur J Neurol ; 11(5): 315-20, 2004 May.
Article in English | MEDLINE | ID: mdl-15142224

ABSTRACT

Behavioural disturbances are frequently observed in Parkinson's disease (PD), including mood and anxiety disorders. The existence of a comorbidity between such psychiatric disorders in PD patients has been suggested only in a few studies. To assess the prevalence of mood and anxiety disturbances, and the rate of comorbidity of such disorders in PD. Secondary aim was to correlate the prevalence of psychiatric disorders in PD with age, sex, laterality of motor symptomatology, clinical features, severity of disease, age of onset and PD duration, and anti-parkinsonian therapy. Ninety consecutive PD outpatients, and 90 age- and sex-matched controls were included. All PD patients enrolled were non-fluctuating (21 de novo, 69 treated with levodopa or dopamine agonists). PD patients and controls with Mini Mental State Examination score <23 were excluded. Psychiatric diagnosis was performed by semistructured interview according with DSM-IV criteria and the severity of depressive and anxious symptoms was rated with clinical rating scales. Major depression was found in 21.1% PD patients vs. 3.3% controls (P < 0.01, chi-square analysis), dystimia in 18.8% PD patients vs. 4.4% controls (P < 0.05), panic disorders in 30% PD patients vs. 5.5% controls (P < 0.01). No difference in the prevalence of other anxiety disorders was observed between the two groups. The comorbidity of mood and anxiety disorders was found in 19.3% PD patients vs. 8.6% controls (P < 0.01). No correlation was reported between the prevalence of behavioural disturbances and any of the demographic, clinical or pharmacological data taken into account. Our findings might suggest the existence of a wide spectrum of psychiatric disorders in PD ranging from pure depressive disorders, comorbid depressive and anxiety disorders, and pure anxiety disorders, presumably linked to the same neurobiological substrate.


Subject(s)
Anxiety Disorders/epidemiology , Depressive Disorder/epidemiology , Parkinson Disease/psychology , Aged , Aged, 80 and over , Anxiety Disorders/etiology , Case-Control Studies , Comorbidity , Depressive Disorder/etiology , Female , Humans , Male , Mental Status Schedule , Middle Aged , Parkinson Disease/complications , Prevalence
13.
Neurology ; 60(12): 1995-7, 2003 Jun 24.
Article in English | MEDLINE | ID: mdl-12821751

ABSTRACT

The acute antidyskinetic effects of IV amantadine in HD were evaluated. A 2-hour IV infusion of amantadine or placebo was administered to nine patients with HD on two different days in a double-blind, randomized crossover fashion. All patients subsequently received oral amantadine unblinded for a 1-year period. A reduction of dyskinesia scores was reported during both IV and oral amantadine treatment (p < 0.05). No significant changes were observed in neuropsychological tests or psychiatric rating scales.


Subject(s)
Amantadine/therapeutic use , Excitatory Amino Acid Antagonists/therapeutic use , Huntington Disease/drug therapy , Administration, Oral , Aged , Amantadine/administration & dosage , Cross-Over Studies , Drug Administration Schedule , Excitatory Amino Acid Antagonists/administration & dosage , Female , Glutamic Acid/metabolism , Humans , Huntington Disease/physiopathology , Huntington Disease/psychology , Infusions, Intravenous , Male , Middle Aged , Motor Activity/drug effects , Neuropsychological Tests , Severity of Illness Index , Treatment Outcome
14.
Acta Neurol Scand ; 105(1): 32-9, 2002 Jan.
Article in English | MEDLINE | ID: mdl-11903106

ABSTRACT

The idiopathic cerebellar ataxias (IDCA) comprise a wide spectrum of neurodegenerative diseases with heterogeneous neuropathology, characterized by the negativity of search for any known genetic mutation. On the basis of both their clinical presentation and their magnetic resonance imaging pattern, patients with IDCA can be subdivided into patients with a purely cerebellar syndrome and atrophy of the cerebellum (IDCA-C) and patients with additional noncerebellar symptoms and atrophy of both cerebellum and brainstem (IDCA-P). The aim of the present study was to evaluate the disaggregated contribution of brainstem and cerebellum in the control of eye movements, by means of an extensive battery of quantitative tests covering most oculomotor subfunctions related to lesions of the cerebellum and the brainstem. The smooth-pursuit movement analysis showed a decrease in gain and magnitude in both subgroups of IDCA with respect to normal controls, without any significant differences in the prevalence pattern between the two subgroups; the mean values of these parameters, however, were significantly lower in IDCA-P than in IDCA-C subjects in both gain (P < 0.01) and magnitude (P < 0.001). No statistically significant difference was observed between the two subgroups in the analysis of saccadic movements or in the other parameters investigated. The distinction between IDCA-P and IDCA-C subgroups has clinical implications, as a poorer prognosis is related to brainstem involvement, which may occur late in the course of the disease. Thus, the possibility to detect the brainstem involvement, also in association with cerebellar impairment, by a relatively simple eye-movement analysis, potentially useful mainly in follow-up investigations, needs to be evaluated further.


Subject(s)
Brain Stem/physiopathology , Cerebellar Ataxia/diagnosis , Cerebellar Ataxia/physiopathology , Cerebellum/physiopathology , Models, Neurological , Ocular Motility Disorders/diagnosis , Ocular Motility Disorders/physiopathology , Adult , Aged , Brain Stem/pathology , Cerebellar Ataxia/pathology , Cerebellum/pathology , Diagnosis, Differential , Electronystagmography , Female , Humans , Magnetic Resonance Imaging , Male , Middle Aged , Ocular Motility Disorders/pathology , Oculomotor Nerve/pathology , Oculomotor Nerve/physiopathology
15.
Neurol Sci ; 23 Suppl 2: S83-4, 2002 Sep.
Article in English | MEDLINE | ID: mdl-12548355

ABSTRACT

Huntington's disease (HD) is characterized by chorea, cognitive and behavioral changes. Amantadine, a non-competitive NMDA receptor antagonist, has shown an antidyskinetic effect on levodopa-induced dyskinesias, which are known to have strict pathogenetic analogies with choreic hyperkinesias. The antidyskinetic efficacy of amantadine and its effects on cognitive and behavioural symptoms were evaluated. Eight HD patients received oral amantadine (100 mg tid) unblinded for a 1-year period. A significant reduction of dyskinesias was reported ( p<0.01). No changes were observed in neuropsychologic and psychiatric assessments after 6 and 12 months of therapy. These data may have relevance to the treatment of HD with amantadine.


Subject(s)
Amantadine/pharmacology , Dyskinesia, Drug-Induced/drug therapy , Excitatory Amino Acid Antagonists/pharmacology , Huntington Disease/drug therapy , Aged , Dyskinesia, Drug-Induced/metabolism , Female , Humans , Huntington Disease/metabolism , Hyperkinesis/chemically induced , Levodopa/adverse effects , Male , Receptors, N-Methyl-D-Aspartate/metabolism , Time Factors
16.
Clin Neuropharmacol ; 24(4): 221-7, 2001.
Article in English | MEDLINE | ID: mdl-11479393

ABSTRACT

Selective serotonin reuptake inhibitors (SSRIs) have been reported to be useful in the treatment of depression in patients with Parkinson's disease (PD). However, a few reports have suggested that SSRIs may worsen parkinsonian motor symptomatology and extrapyramidal side effects have been reported in depressed patients treated with SSRIs. So far, no prospective trial comparing the effects of different SSRIs in depressed patients with PD has been performed. The aim of the present study was to assess the effects of four SSRIs (citalopram, fluoxetine, fluvoxamine, and sertraline) on motor performance and their efficacy on depression in a group of patients with PD. Sixty-two consecutive nondemented, nonfluctuating, depressed patients with PD were included in four treatment groups (15 patiens received citalopram, 16 fluoxetine, 16 fluvoxamine, and 15 sertraline). The evaluation of extrapyramidal and depressive symptomatology was performed with use of the Unified Parkinson's Disease Rating Scale (UPDRS), Beck Depression Inventory, and Hamilton Depression Rating Scale at baseline and after 1, 3, and 6 months. Fifty-two patients completed the study. UPDRS scores were not significantly modified by the add-on therapy with each of the SSRIs studied. A significant improvement in depressive symptoms from baseline to the end of the trial was obtained with all SSRIs (Beck and Hamilton scores improving; p < 0.05 according to an analysis of variance). Our findings suggest that SSRIs do not significantly worsen extrapyramidal symptomatology and may ameliorate depression in patients with PD.


Subject(s)
Depression/drug therapy , Parkinson Disease/drug therapy , Psychomotor Performance/drug effects , Selective Serotonin Reuptake Inhibitors/pharmacology , Selective Serotonin Reuptake Inhibitors/therapeutic use , Aged , Analysis of Variance , Citalopram/pharmacology , Citalopram/therapeutic use , Depression/complications , Depression/psychology , Female , Fluoxetine/pharmacology , Fluoxetine/therapeutic use , Fluvoxamine/pharmacology , Fluvoxamine/therapeutic use , Humans , Male , Middle Aged , Parkinson Disease/complications , Parkinson Disease/psychology , Prospective Studies , Psychiatric Status Rating Scales/statistics & numerical data , Sertraline/pharmacology , Sertraline/therapeutic use
17.
Prostate ; 47(4): 231-8, 2001 Jun 01.
Article in English | MEDLINE | ID: mdl-11398170

ABSTRACT

BACKGROUND: Terazosin and tamsulosin are drugs currently used in the treatment of benign prostatic hypertrophy (BPH). The potency of these two alpha(1) receptor antagonists and that of prazosin to inhibit contractions induced by noradrenaline and the binding of [(3)H]-prazosin in human prostate and four different human arterial and venous vessels (saphenous and umbilical veins, renal and mesenteric arteries) was studied. METHODS: By bioassay and binding studies, we examined the receptor affinities of different alpha(1) receptor antagonists in different human tissues. RESULTS: pKb of terazosin, tamsulosin, and prazosin obtained in the prostatic tissues (8.15, 9.64, and 8.59, respectively) were not different from those obtained in the umbilical veins (8.07, 9.56, and 8.30, respectively), in the mesenteric artery (8.27, 10.29, and 9.01, respectively), renal artery (8.35, 10.13, and 8.76, respectively) and saphenous vein (7.8, 10.3, and 9.32, respectively). IC(50) (nM) of prazosin, terazosin, and tamsulosin obtained from binding studies in membrane preparations from prostate tissue were similar to those from umbilical veins, saphenous vein, and renal artery. CONCLUSIONS: All of the evaluated drugs showed similar selectivity for prostatic vs. vascular tissues. Thus, different clinical profiles of the present drugs should not result from their differential affinity for prostatic versus vascular alpha(1)-adrenoceptors.


Subject(s)
Adrenergic alpha-1 Receptor Antagonists , Adrenergic alpha-Antagonists/pharmacology , Muscle, Smooth, Vascular/drug effects , Prostate/drug effects , Adrenergic alpha-Antagonists/metabolism , Dose-Response Relationship, Drug , Female , Humans , Kinetics , Male , Mesenteric Arteries/drug effects , Muscle Contraction/drug effects , Muscle, Smooth, Vascular/metabolism , Muscle, Smooth, Vascular/physiology , Norepinephrine/physiology , Prazosin/analogs & derivatives , Prazosin/metabolism , Prazosin/pharmacology , Prostate/metabolism , Prostate/physiology , Receptors, Adrenergic, alpha-1/metabolism , Receptors, Adrenergic, alpha-1/physiology , Renal Artery/drug effects , Saphenous Vein/drug effects , Sulfonamides/metabolism , Sulfonamides/pharmacology , Tamsulosin , Umbilical Veins/drug effects
18.
Neurology ; 55(8): 1216-8, 2000 Oct 24.
Article in English | MEDLINE | ID: mdl-11071504

ABSTRACT

Selective serotonin reuptake inhibitors have been used in the treatment of depression in patients with PD. Conflicting data as to whether selective serotonin reuptake inhibitors worsen parkinsonian motor symptomatology have been reported. In this study, the additional 6 months therapy with paroxetine 20 mg/d in a group of depressed patients with PD did not modify parkinsonian motor function (Unified Parkinson's Disease Rating Scale scores); however, in one patient, fully reversible worsening of tremor was observed. Depression, as evaluated by Beck Depression Inventory and Hamilton Depression Rating Scale, improved from baseline to final visit (p < 0.05 by analysis of variance).


Subject(s)
Depressive Disorder/drug therapy , Parkinson Disease/drug therapy , Paroxetine/therapeutic use , Psychomotor Performance/drug effects , Aged , Analysis of Variance , Female , Humans , Male , Middle Aged
19.
Eur J Pharmacol ; 386(1): 25-31, 1999 Dec 10.
Article in English | MEDLINE | ID: mdl-10611460

ABSTRACT

FR 172357, a new non-peptide antagonist of the kinin B(2) receptor was tested in three isolated vessels, the human umbilical vein, the rabbit jugular vein, and the pig coronary artery, to evaluate its antagonistic activities against bradykinin. FR 172357 displaced to the right the concentration-response curves of bradykinin. The displacements were parallel to the controls without reduction of the maximum effect in the human umbilical vein and in the rabbit jugular vein, but not in the pig coronary artery. Schild plots confirmed that FR 172357 acts as a competitive antagonist in the human umbilical vein (pA(2) 8.65) and in the rabbit jugular vein (pA(2) 9. 07), and as a non-competitive antagonist in the pig coronary artery (pK(B) 10.14). FR 172357 is selective for the kinin B(2) receptor since it does not influence the effects of Lys-des-Arg(9)-bradykinin in the human umbilical vein, in the rabbit aorta, and in the pig renal vein. It is specific because it does not affect the contractions induced by angiotensin II, noradrenaline, 5-hydroxytryptamine, or endothelin-1 in the human umbilical vein. It, however, interacts with the tachykinin NK(1) receptor of the rabbit jugular vein and pig coronary artery. Compared to other bradykinin B(2) receptor antagonists, FR 172357 emerges as a very potent compound, which may represent a choice for experimental (and clinical?) applications.


Subject(s)
Bradykinin Receptor Antagonists , Muscle, Smooth, Vascular/drug effects , Pyridines/pharmacology , Animals , Aorta, Thoracic/drug effects , Aorta, Thoracic/metabolism , Bradykinin/analogs & derivatives , Bradykinin/pharmacology , Coronary Vessels/drug effects , Female , Humans , In Vitro Techniques , Jugular Veins/drug effects , Pregnancy , Rabbits , Receptor, Bradykinin B2 , Swine , Umbilical Veins/drug effects , Umbilical Veins/metabolism
20.
Clin Neuropharmacol ; 22(1): 24-9, 1999.
Article in English | MEDLINE | ID: mdl-10047930

ABSTRACT

Tolcapone, a central and peripheral catechol O-methyltransferase (COMT) inhibitor, reduces the conversion of L-Dopa into 3-O-methyl-Dopa (3-OMD), thus leading to more stable and sustained L-Dopa plasma levels. This study was designed to evaluate the effects of acute and 6-week tolcapone administration on L-Dopa pharmacokinetics and pharmacodynamics in Parkinson's disease (PD) patients with predictable motor fluctuations. Tapping test, walking time, and tremor, as well as L-Dopa and 3-OMD plasma levels, were assessed before and for 5 hours after the administration of a single L-Dopa dose, alone or in combination with 200 mg tolcapone, in seven patients with PD. This clinical and pharmacokinetic study was repeated after 6 weeks of tolcapone therapy (200 mg three times daily). It was observed that tolcapone, after both acute and chronic administration, prolonged the motor improvement induced by L-Dopa. As a result, at week 6 of tolcapone therapy, the daily hours spent "off" were significantly decreased. Tolcapone significantly increased the area under the curve of L-Dopa plasma levels by slowing down the elimination of L-Dopa from plasma, whereas the maximal concentration of L-Dopa was not modified. 3-OMD levels decreased significantly after acute tolcapone administration, and after 6 weeks of tolcapone therapy, they were approximately one sixth of pre-tolcapone values. The data confirm that tolcapone decreases L-Dopa clearance and prolongs motor response in PD patients with motor fluctuations, and that this effect is maintained after 6 weeks of tolcapone therapy.


Subject(s)
Antiparkinson Agents/pharmacokinetics , Benzophenones/therapeutic use , Enzyme Inhibitors/therapeutic use , Levodopa/pharmacokinetics , Parkinson Disease/metabolism , Antiparkinson Agents/blood , Antiparkinson Agents/metabolism , Antiparkinson Agents/pharmacology , Benzophenones/pharmacology , Drug Interactions , Enzyme Inhibitors/pharmacology , Female , Humans , Levodopa/blood , Levodopa/metabolism , Levodopa/pharmacology , Male , Middle Aged , Motor Activity/drug effects , Nitrophenols , Parkinson Disease/blood , Parkinson Disease/drug therapy , Tolcapone , Tyrosine/analogs & derivatives , Tyrosine/blood , Tyrosine/pharmacokinetics
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