Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 8 de 8
Filtrar
1.
J Neurol Sci ; 418: 117109, 2020 Nov 15.
Artículo en Inglés | MEDLINE | ID: mdl-32927370

RESUMEN

BACKGROUND: The role of subthreshold depression (subD) in Parkinson's Disease (PD) is not clear. The present study aimed to compare the quality of life (QoL) in PD patients with subD vs patients with no depressive disorder (nonD). Factors related to subD were identified. MATERIAL AND METHODS: PD patients and controls recruited from the COPPADIS cohort were included. SubD was defined as Judd criteria. The 39-item Parkinson's disease Questionnaire (PDQ-39) and the EUROHIS-QOL 8-item index (EUROHIS-QOL8) were used to assess QoL. RESULTS: The frequency of depressive symptoms was higher in PD patients (n = 694) than in controls (n = 207) (p < 0.0001): major depression, 16.1% vs 7.8%; minor depression, 16.7% vs 7.3%; subD, 17.4% vs 5.8%. Both health-related QoL (PDQ-39; 18.1 ±â€¯12.8 vs 11.6 ±â€¯10; p < 0.0001) and global QoL (EUROHIS-QOL8; 3.7 ±â€¯0.5 vs 4 ±â€¯0.5; p < 0.0001) were significantly worse in subD (n = 120) than nonD (n = 348) PD patients. Non-motor Symptoms Scale (NMSS) total score was higher in subD patients (45.9 ±â€¯32 vs 29.1 ±â€¯25.8;p < 0.0001). Non-motor symptoms burden (NMSS;OR = 1.019;95%CI 1.011-1.028; p < 0.0001), neuropsychiatric symptoms (NPI; OR = 1.091; 95%CI 1.045-1.139; p < 0.0001), impulse control behaviors (QUIP-RS; OR = 1.035; 95%CI 1.007-1063; p = 0.013), quality of sleep (PDSS; OR = 0.991; 95%CI 0.983-0.999; p = 0.042), and fatigue (VAFS-physical; OR = 1.185; 95%CI 1.086-1.293; p < 0.0001; VAFS-mental; OR = 1.164; 95%CI 1.058-1.280; p = 0.0001) were related to subD after adjustment to age, disease duration, daily equivalent levodopa dose, motor status (UPDRS-III), and living alone. CONCLUSIONS: SubD is a frequent problem in patients with PD and is more prevalent in these patients than in controls. QoL is worse and non-motor symptoms burden is greater in subD PD patients.


Asunto(s)
Enfermedad de Parkinson , Calidad de Vida , Depresión/epidemiología , Depresión/etiología , Fatiga/epidemiología , Fatiga/etiología , Humanos , Enfermedad de Parkinson/complicaciones , Enfermedad de Parkinson/epidemiología , Encuestas y Cuestionarios
2.
Parkinsons Dis ; 2020: 7537924, 2020.
Artículo en Inglés | MEDLINE | ID: mdl-32269748

RESUMEN

OBJECTIVE: 5- (5 times oral levodopa tablet taken/day) 2- (2 hours of OFF time/day) 1- (1 hour/day of troublesome dyskinesia) criteria have been proposed by a Delphi expert consensus panel for diagnosing advanced Parkinson's disease (PD). The aim of the present study is to compare quality of life (QoL) in PD patients with "5-2-1 positive criteria" vs QoL in PD patients without "5-2-1 positive criteria" (defined as meeting ≥1 of the criteria). METHODS: This is a cross-sectional, observational, monocenter study. Three different instruments were used to assess QoL: the 39-Item Parkinson's Disease Quality of Life Questionnaire Summary Index Score (PDQ-39SI); a subjective rating of perceived QoL (PQ-10); and the EUROHIS-QOL 8-Item Index (EUROHIS-QOL8). RESULTS: From a cohort of 102 PD patients (65.4 ± 8.2 years old, 53.9% males; disease duration 4.7 ± 4.5 years), 20 (19.6%) presented positive 5-2-1 criteria: 6.9% for 5, 17.6% for 2, and 4.9% for 1. 37.5% (12/32) and 25% (5/20) of patients with motor complications and dyskinesia, respectively, presented 5-2-1 negative criteria. Both health-related (PDQ-39SI, 25.6 ± 14 vs 12.1 ± 9.2; p < 0.0001) and global QoL (PQ-10, 6.1 ± 2 vs 7.1 ± 1.3; p=0.007; EUROHIS-QOL8, 3.5 ± 0.5 vs 3.7 ± 0.4; p=0.034) were worse in patients with 5-2-1 positive criteria. Moreover, nonmotor symptoms burden (Non-Motor Symptoms Scale total score, 64.8 ± 44.8 vs 39.4 ± 35.1; p < 0.0001) and autonomy for activities of daily living (ADLS scale, 73.5 ± 13.1 vs 89.2 ± 9.3; p < 0.0001) were worse in patients with 5-2-1 positive criteria. Patient's principal caregiver's strain (Caregiver Stain Index, 4.3 ± 3 vs 1.5 ± 1.6; p < 0.0001), burden (Zarit Caregiver Burden Inventory, 28.4 ± 12.5 vs 10.9 ± 9.8; p < 0.0001), and mood (Beck Depression Inventory II, 12.2 ± 7.2 vs 6.2 ± 6.1; p < 0.0001) were worse in patients with 5-2-1 positive criteria as well. CONCLUSIONS: QoL is worse in patients meeting ≥1 of the 5-2-1 criteria. This group of patients and their caregivers are more affected as a whole. These criteria could be useful for identifying patients in which it is necessary to optimize Parkinson's treatment.

3.
Eur J Neurol ; 27(7): 1210-1223, 2020 07.
Artículo en Inglés | MEDLINE | ID: mdl-32181979

RESUMEN

BACKGROUND AND PURPOSE: The objective of this study was to analyze the relationship between motor complications and non-motor symptom (NMS) burden in a population of patients with Parkinson's disease (PD) and also in a subgroup of patients with early PD. METHODS: Patients with PD from the COPPADIS cohort were included in this cross-sectional study. NMS burden was defined according to the Non-Motor Symptoms Scale (NMSS) total score. Unified Parkinson's Disease Rating Scale (UPDRS) part IV was used to establish motor complication types and their severity. Patients with ≤5 years of symptoms from onset were included as patients with early PD. RESULTS: Of 690 patients with PD (62.6 ± 8.9 years old, 60.1% males), 33.9% and 18.1% presented motor fluctuations and dyskinesia, respectively. The NMS total score was higher in patients with motor fluctuations (59.2 ± 43.1 vs. 38.3 ± 33.1; P < 0.0001) and dyskinesia (63.5 ± 40.7 vs. 41.4 ± 36.3; P < 0.0001). In a multiple linear regression model and after adjustment for age, sex, disease duration, Hoehn & Yahr stage, UPDRS-III score and levodopa equivalent daily dose, UPDRS-IV score was significantly related to a higher NMSS total score (ß = 0.27; 95% confidence intervals, 2.81-5.61; P < 0.0001), as it was in a logistic regression model on dichotomous NMSS total score (≤40, mild or moderate vs. >40, severe or very severe) (odds ratio, 1.31; 95% confidence intervals, 1.17-1.47; P < 0.0001). In the subgroup of patients with early PD (n = 396; mean disease duration 2.7 ± 1.5 years), motor fluctuations were frequent (18.1%) and similar results were obtained. CONCLUSIONS: Motor complications were frequent and were associated with a greater NMS burden in patients with PD even during the first 5 years of disease duration.


Asunto(s)
Enfermedad de Parkinson , Anciano , Estudios Transversales , Femenino , Humanos , Levodopa/uso terapéutico , Masculino , Persona de Mediana Edad , Enfermedad de Parkinson/complicaciones , Enfermedad de Parkinson/epidemiología , Índice de Severidad de la Enfermedad
4.
J Neural Transm (Vienna) ; 126(12): 1599-1608, 2019 12.
Artículo en Inglés | MEDLINE | ID: mdl-31673927

RESUMEN

C-reactive protein (CRP) is a biomarker of systemic inflammation that has been linked to accelerated decline in walking speed in older adults. The aim of the present study was to compare the CRP levels of PD patients with vs patients without freezing of gait (FOG). Patients and controls participating in the COPPADIS-2015 study that performed blood extraction for determining molecular serum biomarkers were included. Patients with FOG were identified as those with a score of 1 or greater on item-3 of the Freezing of Gait Questionnaire (FOG-Q). Immunoassay was used for determining ultrasensitive CRP (US-CRP) level (mg/dL). In the PD group (n = 225; 61.8 ± 9.5 years old, 61.8% males), 32% of the patients presented FOG but none in the control group (n = 65; 60.3 ± 6.1 years old, 56.9% males) (p < 0.0001). Differences in US-CRP level were significant in patients with FOG vs patients without FOG and vs controls (0.31 ± 0.52 vs 0.16 ± 0.21 vs 0.21 ± 0.22; p = 0.04). Significant differences were also observed between patients with vs without FOG (p = 0.001) but not between patients and controls (p = 0.163). US-CRP level was related to FOG (OR = 4.369; 95% CI 1.105-17.275; p = 0.036) along with H&Y (OR = 2.974; 95% CI 1.113-7.943; p = 0.030) and non-motor symptoms burden (NMSS total score; OR = 1.017; 95% CI 1.005-1.029; p = 0.006) after adjusting for age, gender, disease duration, equivalent daily levodopa dose, number of non-antiparkinsonian drugs per day, motor fluctuations, cognition, motor phenotype, and chronic use of anti-inflammatory drugs. The present study suggests that serum US-CRP level is related to FOG in PD patients. Inflammation could be linked to FOG development.


Asunto(s)
Biomarcadores/sangre , Proteína C-Reactiva/análisis , Trastornos Neurológicos de la Marcha/sangre , Enfermedad de Parkinson/sangre , Anciano , Femenino , Trastornos Neurológicos de la Marcha/etiología , Humanos , Masculino , Persona de Mediana Edad , Enfermedad de Parkinson/complicaciones
5.
Rev. neurol. (Ed. impr.) ; 54(supl.4): s13-s22, 3 oct., 2012. ilus, tab
Artículo en Español | IBECS | ID: ibc-150514

RESUMEN

Introducción. El estudio del sistema motor y de sus trastornos ha sido un tema importante para la neurofisiología, siendo uno de sus objetivos intentar comprender los mecanismos fisiopatológicos que subyacen a las disfunciones del mismo. Desarrollo: Se revisa lo más relevante acerca de: (1) Técnicas neurofisiológicas utilizadas en el diagnóstico de la EP y otros parkinsonismos; (2) Utilidad de la estimulación magnética transcraneal (EMT); (3) Estudios neurofisiológicos de los trastornos del sueño en la EP; (4) Aspectos neurofisiológicos de la estimulación cerebral profunda (ECP). Conclusiones: Las pruebas neurofisiológicas puede ayudar en el diagnóstico diferencial del parkinsonismo además de profundizar en la fisiopatología de los síntomas y signos parkinsonianos. Diferentes técnicas pueden emplearse en el estudio de los trastornos del sueño en la EP. La EMT resulta útil tanto desde el punto de vista diagnóstico como probablemente también terapéutico en la EP. Actualmente, los registros con microelectrodos constituyen la forma más precisa de poder identificar la diana seleccionada en la cirugía de la EP (AU)


Introduction. The study of motor system and its diseases has been an interesting topic for neurophysiology, being one of the objectives of this to know the physiopathology mechanisms. Development. We review the most relevant about: (1) Neurophysiological techniques used in the diagnosis of Parkinson's disease (PD) and other parkinsonisms; (2) Utility of transcranial magnetic stimulation (TMS); (3) Neurophysiological techniques used in the diagnosis of sleep disorders in PD patients; (4) Neurophysiological aspects of deep brain stimulation (DBS). Conclusions. Different neurophysiological techniques can be used for differential diagnosis of PD and others parkinsonisms besides to investigate in the physiopathology mechanisms. We can use different techniques for study sleep disorders in PD patients. TMS results to be utility for diagnosis and probably such as therapy in PD patients. Actually, microelectrode recording could be the best method for target identification in DBS surgery (AU)


Asunto(s)
Humanos , Masculino , Femenino , Enfermedad de Parkinson/genética , Trastornos del Sueño-Vigilia/psicología , Estimulación Magnética Transcraneal/métodos , Ganglios Basales/patología , Médula Espinal/fisiopatología , Hipocinesia/psicología , Trastorno del Dedo en Gatillo/metabolismo , Enfermedades Respiratorias/diagnóstico , Enfermedad de Parkinson/complicaciones , Trastornos del Sueño-Vigilia/metabolismo , Estimulación Magnética Transcraneal/instrumentación , Ganglios Basales/metabolismo , Médula Espinal/anomalías , Hipocinesia/terapia , Trastorno del Dedo en Gatillo/terapia , Enfermedades Respiratorias/complicaciones
6.
Rev Neurol ; 50 Suppl 2: S65-74, 2010 Feb 08.
Artículo en Español | MEDLINE | ID: mdl-20205145

RESUMEN

INTRODUCTION: In addition to the motor disturbances experienced by the patients suffering from Parkinson's disease (PD), several non-motor symptoms also affect the PD patients: neurobehavior symptoms (dementia, depression, anxiety, psychosis), autonomic (postural hypotension, urinary symptoms, gastro intestinal symptoms, diaphoresis), sleep disorders (insomnia, somnolence, REM sleep behavior disorder, apnea), sensitive-motor (fatigue, diplopia, restless legs syndrome), and sensory symptoms. DEVELOPMENT: We review the most relevant about sensory symptoms in PD: visual dysfunction, olfactory dysfunction, taste, hearing loss, and pain and other sensitive associate symptoms. CONCLUSIONS: Pain is frequently observed in patients with PD, being its prevalence high and probably infra diagnosed. Its identification and classification is very important for a correct treatment. Hyposmia is a common symptom in PD and could be a predictor of future PD. Visual dysfunction and hearing dysfunction among others must be considered in patients with PD.


Asunto(s)
Dolor/etiología , Dolor/fisiopatología , Enfermedad de Parkinson/complicaciones , Enfermedad de Parkinson/fisiopatología , Trastornos de la Sensación/etiología , Trastornos de la Sensación/fisiopatología , Diagnóstico Diferencial , Humanos , Dolor/tratamiento farmacológico , Dolor/epidemiología , Enfermedad de Parkinson/tratamiento farmacológico , Enfermedad de Parkinson/epidemiología , Trastornos de la Sensación/tratamiento farmacológico , Trastornos de la Sensación/epidemiología
7.
Rev Neurol ; 48 Suppl 1: S33-6, 2009 Jan 23.
Artículo en Español | MEDLINE | ID: mdl-19222013

RESUMEN

INTRODUCTION: Restless legs syndrome (RLS) is a movement disorder with a neurological origin that manifests in the form of sensory-motor symptoms which are located mainly in the lower limbs. DEVELOPMENT: We review the epidemiological, pathophysiological, clinical and therapeutic characteristics of this disease, with special emphasis on the diagnostic criteria. CONCLUSIONS: Diagnosis of RLS is mainly clinical and is based on the criteria established by the National Institutes of Health consensus development conference in 2002. There are specific criteria for special groups (the elderly with cognitive impairment and children) in which it is not possible to determine whether RLS exists or not using the usual diagnostic criteria.


Asunto(s)
Síndrome de las Piernas Inquietas/diagnóstico , Síndrome de las Piernas Inquietas/fisiopatología , Ensayos Clínicos como Asunto , Dopaminérgicos/uso terapéutico , Humanos , Síndrome de las Piernas Inquietas/epidemiología , Síndrome de las Piernas Inquietas/terapia
8.
Rev. neurol. (Ed. impr.) ; 48(supl.1): 33-36, 23 feb., 2009.
Artículo en Español | IBECS | ID: ibc-94959

RESUMEN

Resumen. Introducción. El síndrome de piernas inquietas (SPI) es un trastorno del movimiento de origen neurológico, que se manifiesta por clínica sensitivomotora localizada principalmente en las extremidades inferiores. Desarrollo. Se revisan las características epidemiológicas, fisiopatológicas clínicas y terapéuticas de esta enfermedad, y se hace un especial énfasis en los criterios diagnósticos. Conclusiones. El diagnóstico del SPI es eminentemente clínico y se basa en los criterios de la conferencia de consenso de los National Institutes of Health de 2002. Existen criterios específicos para grupos especiales (ancianos con deterioro cognitivo y niños) en los cuales no es posible determinar si existe SPI mediante los criterios diagnósticos habituales (AU)


Summary. Introduction. Restless legs syndrome (RLS) is a movement disorder with a neurological origin that manifests in the form of sensory-motor symptoms which are located mainly in the lower limbs. Development. We review the epidemiological, pathophysiological, clinical and therapeutic characteristics of this disease, with special emphasis on the diagnostic criteria. Conclusions. Diagnosis of RLS is mainly clinical and is based on the criteria established by the National Institutes of Health consensus development conference in 2002. There are specific criteria for special groups (the elderly with cognitive impairment and children) in which it is not possible to determine whether RLS exists or not using the usual diagnostic criteria (AU)


Asunto(s)
Humanos , Síndrome de las Piernas Inquietas/diagnóstico , Agonistas de Dopamina/uso terapéutico , Síndrome de las Piernas Inquietas/tratamiento farmacológico , Examen Neurológico/métodos
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA