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1.
Cerebellum ; 19(4): 501-509, 2020 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-32270466

RESUMEN

SCA36 is an autosomal dominant spinocerebellar ataxia (SCA) affecting many families from Costa da Morte, a northwestern region of Spain. It is caused by an intronic GGCCTG repeat expansion in NOP56. In order to characterize the cognitive and affective manifestations of this cerebellar disease, a group of 30 SCA36 mutation carriers (11 preataxic and 19 ataxic patients) were assessed with a comprehensive battery of standardized tests. Phonological verbal fluency - but not semantic fluency - was already mildly impaired in preataxic subjects. In ataxic patients, both phonological and semantic fluencies were significantly below normal. Depression, while more frequent and prominent in ataxic patients, was also often present in the preataxic stage. This is the first systematic study supporting the presence of a mild cerebellar cognitive and affective syndrome in SCA36. Routine evaluation of cognitive and emotional spheres in SCA36 patients as well as asymptomatic mutation carriers should allow early detection and timely therapeutic intervention.


Asunto(s)
Enfermedades Cerebelosas/genética , Trastornos del Conocimiento/genética , Trastornos del Humor/genética , Ataxias Espinocerebelosas/complicaciones , Adulto , Anciano , Enfermedades Cerebelosas/patología , Femenino , Humanos , Masculino , Persona de Mediana Edad , Proteínas Nucleares , Ataxias Espinocerebelosas/patología , Ataxias Espinocerebelosas/psicología
2.
J Affect Disord ; 350: 648-655, 2024 Apr 01.
Artículo en Inglés | MEDLINE | ID: mdl-38246282

RESUMEN

BACKGROUND: Obsessive compulsive disorder (OCD) is a disabling illness with a chronic course, yet data on long-term outcomes are scarce. This study aimed to examine the long-term course of OCD in patients treated with different approaches (drugs, psychotherapy, and psychosurgery) and to identify predictors of clinical outcome by machine learning. METHOD: We included outpatients with OCD treated at our referral unit. Demographic and neuropsychological data were collected at baseline using standardized instruments. Clinical data were collected at baseline, 12 weeks after starting pharmacological treatment prescribed at study inclusion, and after follow-up. RESULTS: Of the 60 outpatients included, with follow-up data available for 5-17 years (mean = 10.6 years), 40 (67.7 %) were considered non-responders to adequate treatment at the end of the study. The best machine learning model achieved a correlation of 0.63 for predicting the long-term Yale-Brown Obsessive Compulsive Scale (Y-BOCS) score by adding clinical response (to the first pharmacological treatment) to the baseline clinical and neuropsychological characteristics. LIMITATIONS: Our main limitations were the sample size, modest in the context of traditional ML studies, and the sample composition, more representative of rather severe OCD cases than of patients from the general community. CONCLUSIONS: Many patients with OCD showed persistent and disabling symptoms at the end of follow-up despite comprehensive treatment that could include medication, psychotherapy, and psychosurgery. Machine learning algorithms can predict the long-term course of OCD using clinical and cognitive information to optimize treatment options.


Asunto(s)
Trastorno Obsesivo Compulsivo , Humanos , Resultado del Tratamiento , Estudios Prospectivos , Trastorno Obsesivo Compulsivo/diagnóstico , Trastorno Obsesivo Compulsivo/terapia , Trastorno Obsesivo Compulsivo/psicología , Psicoterapia , Cognición
3.
J Affect Disord ; 333: 365-376, 2023 07 15.
Artículo en Inglés | MEDLINE | ID: mdl-37094658

RESUMEN

BACKGROUND: The study of Obsessive-Compulsive Disorder (OCD) genomics has primarily been tackled by Genome-wide association studies (GWAS), which have encountered troubles in identifying replicable single nucleotide polymorphisms (SNPs). Endophenotypes have emerged as a promising avenue of study in trying to elucidate the genomic bases of complex traits such as OCD. METHODS: We analyzed the association of SNPs across the whole genome with the construction of visuospatial information and executive performance through four neurocognitive variables assessed by the Rey-Osterrieth Complex Figure Test (ROCFT) in a sample of 133 OCD probands. Analyses were performed at SNP- and gene-level. RESULTS: No SNP reached genome-wide significance, although there was one SNP almost reaching significant association with copy organization (rs60360940; P = 9.98E-08). Suggestive signals were found for the four variables at both SNP- (P < 1E-05) and gene-levels (P < 1E-04). Most of the suggestive signals pointed to genes and genomic regions previously associated with neurological function and neuropsychological traits. LIMITATIONS: Our main limitations were the sample size, which was limited to identify associated signals at a genome-wide level, and the composition of the sample, more representative of rather severe OCD cases than a population-based OCD sample with a broad severity spectrum. CONCLUSIONS: Our results suggest that studying neurocognitive variables in GWAS would be more informative on the genetic basis of OCD than the classical case/control GWAS, facilitating the genetic characterization of OCD and its different clinical profiles, the development of individualized treatment approaches, and the improvement of prognosis and treatment response.


Asunto(s)
Estudio de Asociación del Genoma Completo , Trastorno Obsesivo Compulsivo , Humanos , Trastorno Obsesivo Compulsivo/genética , Trastorno Obsesivo Compulsivo/psicología , Polimorfismo de Nucleótido Simple/genética , Endofenotipos , Genómica
4.
J Affect Disord ; 317: 52-58, 2022 11 15.
Artículo en Inglés | MEDLINE | ID: mdl-36029870

RESUMEN

BACKGROUND: Obsessive Compulsive Disorder (OCD) is characterized by the presence of executive dysfunctions. As organizational strategies may play an important role as a possible endophenotype of the disorder, we decided to investigate non-verbal memory and organizational abilities in OCD. We also investigated how organization and non-verbal memory differ between responder and non-responder patients to pharmacological treatment, to test whether cognitive functions can predict the response to pharmacological treatment. METHODS: In Study 1, executive and clinical functioning measures were applied to 162 OCD and 95 controls. In Study 2, clinical, intelligence and executive functioning measures were applied to 72 OCD responders and 63 OCD non-responder patients. RESULTS: OCD patients and controls from Study 1 differed in copy organization (p < 0.01) and delayed recall (p = 0.048). In Study 2, the OCD responders displayed better copy organization (p = 0.013) and lower depressive, anxious and OCD symptoms (p < 0.01 in the three cases). Scores in the following instruments were found to predict the response to pharmacological treatment: HDRS, Y-BOCS, Raven progressive matrices, and Direct digit subtest from the Wechsler's scale (p < 0.01 in all four cases). LIMITATIONS: In Study 1, the imbalance of the sample can be considered a limitation, whilst in Study 2, some of the levels of pharmacological resistance were not represented. CONCLUSIONS: In this study, non-verbal memory and organization was affected in OCD. Responder patients also displayed better executive functioning and fluid intelligence. Organizational ability is a predictor of pharmacological response to SSRI monotherapy in a predictive model controlling for anxious symptoms.


Asunto(s)
Disfunción Cognitiva , Trastorno Obsesivo Compulsivo , Cognición , Disfunción Cognitiva/diagnóstico , Disfunción Cognitiva/tratamiento farmacológico , Función Ejecutiva , Humanos , Pruebas Neuropsicológicas , Trastorno Obsesivo Compulsivo/psicología
5.
Sci Rep ; 11(1): 319, 2021 01 11.
Artículo en Inglés | MEDLINE | ID: mdl-33431980

RESUMEN

De novo mutations (DNMs), including germinal and postzygotic mutations (PZMs), are a strong source of causality for Autism Spectrum Disorder (ASD). However, the biological processes involved behind them remain unexplored. Our aim was to detect DNMs (germinal and PZMs) in a Spanish ASD cohort (360 trios) and to explore their role across different biological hierarchies (gene, biological pathway, cell and brain areas) using bioinformatic approaches. For the majority of the analysis, a combined ASD cohort (N = 2171 trios) was created using previously published data by the Autism Sequencing Consortium (ASC). New plausible candidate genes for ASD such as FMR1 and NFIA were found. In addition, genes harboring PZMs were significantly enriched for miR-137 targets in comparison with germinal DNMs that were enriched in GO terms related to synaptic transmission. The expression pattern of genes with PZMs was restricted to early mid-fetal cortex. In contrast, the analysis of genes with germinal DNMs revealed a spatio-temporal window from early to mid-fetal development stages, with expression in the amygdala, cerebellum, cortex and striatum. These results provide evidence of the pathogenic role of PZMs and suggest the existence of distinct mechanisms between PZMs and germinal DNMs that are influencing ASD risk.


Asunto(s)
Trastorno del Espectro Autista/genética , Mutación , Estudios de Cohortes , Exoma/genética , Predisposición Genética a la Enfermedad/genética , Humanos , MicroARNs/genética
6.
Eur Psychiatry ; 64(1): e45, 2021 06 08.
Artículo en Inglés | MEDLINE | ID: mdl-34100343

RESUMEN

BACKGROUND: Although the consequences of the COVID-19 pandemic on emotional health are evident, little is known about its impact on patients with obsessive-compulsive disorder (OCD). METHODS: One hundred and twenty-seven patients with OCD who attended a specialist OCD Clinic in Barcelona, Spain, were assessed by phone from April 27 to May 25, 2020, during the early phase of the pandemic, using the Yale-Brown Obsessive-Compulsive Scale (Y-BOCS) and a structured interview that collected clinical and sociodemographic information. Results were compared with those for 237 healthy controls from the same geographic area who completed an online survey. RESULTS: Although 65.3% of the patients with OCD described a worsening of their symptoms, only 31.4% had Y-BOCS scores that increased >25%. The risk of getting infected by SARS-CoV2 was reported as a new obsession by 44.8%, but this only became the main obsessive concern in approximately 10% of the patients. Suicide-related thoughts were more frequent among the OCD cohort than among healthy controls. The presence of prepandemic depression, higher Y-BOCS scores, contamination/washing symptoms, and lower perceived social support all predicted a significantly increased risk of OCD worsening. CONCLUSIONS: Most patients with OCD appear to be capable of coping with the emotional stress of the COVID-19 outbreak and its consequences during the initial phase of the pandemic. Nevertheless, the current crisis constitutes a risk factor for a significant worsening of symptoms and suicidal ideation. Action is needed to ensure effective and individualized follow-up care for patients with OCD in the COVID-19 era.


Asunto(s)
COVID-19/psicología , Trastorno Obsesivo Compulsivo/psicología , Pandemias , Adaptación Psicológica , Adulto , COVID-19/epidemiología , Estudios de Casos y Controles , Femenino , Humanos , Estudios Longitudinales , Masculino , Persona de Mediana Edad , Trastorno Obsesivo Compulsivo/terapia , Distrés Psicológico , España/epidemiología , Ideación Suicida , Encuestas y Cuestionarios
7.
Farm Hosp ; 28(6): 440-4, 2004.
Artículo en Español | MEDLINE | ID: mdl-15628947

RESUMEN

Hospital pharmacists, according to the Ley del Medicamento 25/1990 of 20th December, should ensure appropriate drug preservation within the Pharmacy Department and in hospital stocks. The storage and preservation of thermolabile drugs according to manufacturer recommendations guarantees stability and optimal use conditions until the expiration date. Cold chain disruption may significantly affect the activity and toxicity of these drugs. Pharmacists should make quick decisions in case of cold chain-related events, hence the relevance of up-to-date information on stability under temperatures differing from those recommended. A review of the information available on the stability of drugs commonly used in the hospital setting that require a fridge for storage has been carried out.


Asunto(s)
Almacenaje de Medicamentos/normas , Preservación Biológica/normas , Estabilidad de Medicamentos , Humanos , Preparaciones Farmacéuticas/normas , Farmacología Clínica/normas , Servicio de Farmacia en Hospital , Refrigeración , Temperatura
9.
Rev Neurol ; 50 Suppl 2: S41-9, 2010 Feb 08.
Artículo en Español | MEDLINE | ID: mdl-20205141

RESUMEN

INTRODUCTION: Parkinson's disease (PD) is associated with mood and behavioral symptoms contributing to morbidity and reduced quality of life of the patients. Most characteristic are depression, anxiety and impulse control disorder. DEVELOPMENT: Identification and treatment of neuropsychiatric symptoms is necessary for an appropriate management of PD. Affective symptoms may be the initial manifestation of PD, are highly prevalent and pathogenically complex. Impulse control disorders are usually not a spontaneous complaint, so asking about these symptoms may be the only way to detect and treat a serious socio-familial problem. Pharmacological treatment of these manifestations is difficult to balance with an adequate control of motor symptoms. Psychological support from early stages and throughout the evolution of PD is fundamental. CONCLUSIONS: Neurologist and other healthcare professionals treating PD patients need to be aware of behavioral and emotional manifestations of the disease. This will lead to an appropriate patient management and better adaptation of the familial and social situation.


Asunto(s)
Síntomas Afectivos/etiología , Trastornos Disruptivos, del Control de Impulso y de la Conducta/etiología , Trastornos Disruptivos, del Control de Impulso y de la Conducta/fisiopatología , Trastornos del Humor/etiología , Trastornos del Humor/fisiopatología , Enfermedad de Parkinson/complicaciones , Enfermedad de Parkinson/fisiopatología , Síntomas Afectivos/tratamiento farmacológico , Síntomas Afectivos/fisiopatología , Antiparkinsonianos/uso terapéutico , Ansiedad/tratamiento farmacológico , Ansiedad/etiología , Ansiedad/fisiopatología , Depresión/tratamiento farmacológico , Depresión/etiología , Depresión/fisiopatología , Trastornos Disruptivos, del Control de Impulso y de la Conducta/tratamiento farmacológico , Emociones/fisiología , Humanos , Trastornos del Humor/tratamiento farmacológico , Enfermedad de Parkinson/tratamiento farmacológico , Calidad de Vida
10.
Actas Esp Psiquiatr ; 32(5): 259-63, 2004.
Artículo en Español | MEDLINE | ID: mdl-15529209

RESUMEN

INTRODUCTION: The present study assesses the role of attributions and self-esteem in depressive states. In depression, attributions can become central biased coping mechanisms that guide individual behavior. METHODS: Self-esteem and attribution bias was assessed in 40 depressed and 80 normal controls. RESULTS: Results of this investigation show that depressed patients made more internal attributions to negative events, and more external attributions for positive events than their normal counterparts, confirming an exaggerated attributional bias. CONCLUSIONS: The results suggest that depressed patients tend to blame themselves for their mistakes. Depressed patients made more stable and global attributions for negative events than for positive events, as opposed to what happens with the normal controls, making us believe that this bias will be maintained in time, and will eventually generalize to other life areas. This kind of study seems useful to develop efficient treatment programs and evaluation tools of depression.


Asunto(s)
Depresión/psicología , Autoimagen , Adulto , Cognición , Femenino , Humanos , Masculino , Persona de Mediana Edad , Encuestas y Cuestionarios
11.
Actas Esp Psiquiatr ; 30(6): 343-9, 2002.
Artículo en Español | MEDLINE | ID: mdl-12487944

RESUMEN

OBJECTIVE: This present work assesses the prevalence of anorexia nervosa, its partial syndromes, bulimia nervosa and binge eating in a university sample of Galician students (Spain). METHOD: The sample is made up of 298 women and 157 men. The scales used were: Eating Disorders Inventory (EDI) and a Questionnaire on eating behavior. RESULTS: Women had higher scores in drive for thinness, bulimia, interoceptive awareness, body dissatisfaction and ineffectiveness than men; furthermore the women had lower scores in BMI. We find a very high prevalence, a total of 6.4% of cases of eating disorders. CONCLUSIONS: The high values of probable eating disorders make it especially necessary to carry out primary and secondary prevention programs in university students populations.


Asunto(s)
Trastornos de Alimentación y de la Ingestión de Alimentos/epidemiología , Adolescente , Adulto , Femenino , Humanos , Masculino , Prevalencia , España/epidemiología , Universidades
12.
Neurología (Barc., Ed. impr.) ; 26(3): 129-136, abr. 2011.
Artículo en Español | IBECS (España) | ID: ibc-98227

RESUMEN

Introducción: La expansión de los estudios genéticos está transformando la práctica de la Neurología y enfrenta a los servicios clínicos con nuevos retos, como la articulación del asesoramiento genético. La amplitud de los conocimientos tanto clínicos como moleculares precisos, así como la necesidad de una evaluación psicológica y apoyo familiar, especialmente en los análisis predictivos y planificación reproductiva, hacen necesario un enfoque multidisciplinar. Desarrollo: Las características principales de las enfermedades neurodegenerativas de base genética son el elevado nivel de especialización requerido —por tratarse de enfermedades poco comunes y de difícil diagnóstico— junto con su carácter generalmente progresivo, la ausencia de tratamientos eficaces, la problemática generada por la posibilidad de estudios predictivos y la interpretación de los resultados genéticos. El objetivo del asesoramiento genético es proporcionar la información suficiente y objetiva para que cada individuo pueda tomar sus propias decisiones sobre el estudio genético. Debe incluir la evaluación de aspectos psicológicos y de comunicación familiar. El programa PICOGEN del Hospital Clinic de Barcelona para el análisis y asesoramiento genético en demencias es un buen ejemplo de una estrategia integrada capaz de abordar esta nueva situación asistencial en Neurología. Lamentablemente, este programa es una excepción en España y los pacientes con enfermedades neurogenéticas y sus familias no tienen garantizada habitualmente una asistencia adecuada.Conclusiones: El asesoramiento genético es un acto clínico per se, que precisa de un espacio, tiempo y recursos suficientes. Implica una participación multidisciplinar, atención a los aspectos psicológicos y familiares y no se puede llevar a cabo correctamente en el seno de una consulta rutinaria estándar de Neurología (AU)


Introduction: The generalization of genetic studies is transforming the practice of Neurology and confronts the clinical departments with new challenges, such as the organization of genetic counseling. The requirement of specialized knowledge, both clinical and molecular, as well as the need for psychological evaluation and family support, especially for predictive testing and reproductive planning, makes a multidisciplinary approach mandatory.Development: The main characteristics of genetic neurodegenerative diseases are the high level of required specialization — since these disorders are often rare and of difficult diagnosis— together with a generally progressive course, unavailability of effective treatment, the issues generated by predictive testing and the interpretation of genetic testing. The aim of geneticcounseling is to provide sufficient and objective information for each individual to make their own decision on genetic testing. It must touch upon psychological aspects and family communication.The PICOGEN program from the Clinic Hospital in Barcelona for genetic testing and counseling of dementias is a good example of integrated strategy capable of managing this new clinical scenario in neurology. Unfortunately, this program is an exception in Spain and the patients with neurogenetic disorders and their families usually do not have guaranteed access to an appropriate care. Conclusions: Genetic counseling is a unique clinical activity that requires provision of enough time, space and resources to be developed. It implies multidisciplinary participation, due attention to psychological and family issues, and cannot be carried out adequately in a routine Neurology clinic. Legislation is needed to promote a correct articulation of genetic counselingin our country with guarantee of quality and equity (AU)


Asunto(s)
Humanos , Asesoramiento Genético/métodos , Enfermedades Neurodegenerativas/genética , Genética de Población/tendencias , Enfermedades Raras/genética , Marcadores Genéticos , Predisposición Genética a la Enfermedad
14.
Actas esp. psiquiatr ; 32(5): 259-263, sept.-oct. 2004. tab
Artículo en Español | IBECS (España) | ID: ibc-112492

RESUMEN

Introducción. En la presente investigación se ha analizado el papel de desempeñan la variable atribucional y la autoestima en estados depresivos. El estudio atribucional es de capital importancia en la dinámica de la personalidad, ya que las atribuciones causales son mecanismos sesgados de afrontamiento que guían la conducta del sujeto. Métodos. Para llevar a cabo esta investigación se ha evaluado la autoestima y los sesgos atribucionales en una muestra de 40 pacientes depresivos y se ha comparado con 80 sujetos control normales. Resultados. Los resultados de esta investigación muestran que los pacientes depresivos realizaron atribuciones más internas para los eventos negativos que el grupo control normal y atribuciones más externas que los normales para los sucesos positivos, presentando un exagerado sesgo atribucional. Conclusiones. Estos datos nos sugieren que los pacientes depresivos tienden a culparse a sí mismos de sus fallos. Los pacientes depresivos realizaron atribuciones más estables y globales para los hechos negativos que para los positivos en comparación con los sujetos normales, considerando que dicha situación negativa se mantendrá en el tiempo y se globalizará a otras áreas de su vida. Este tipo de estudios resultan de utilidad para el desarrollo de programas eficaces de tratamiento y de instrumentos de evaluación de la depresión (AU)


Introduction. The present study assesses the role of attribution and self esteem in depressive states. In depression, attributions can become central biased coping mechanism that guide individual behavior. Methods. Self-esteem and attribution bias was assessed in 40 depressed and 80 normal controls. Results. Results of this investigation show that depressed patients made more internal attributions to negative events and more external attributions for positive events than their normal counterparts, confirming an exaggerated attributional bias. Conclusions. The results suggest that depressed patients tend to blame themselves for their mistakes. Depressed patients made more stable and global attributions for negative events than for positive events, as opposed to what happens with the normal controls, making us believe that this bias will be maintained in time, and will eventually generalize to other life areas. This kind of study seems useful to develop efficient treatment programs and evaluation tools of depression (AU)


Asunto(s)
Humanos , Depresión/complicaciones , Depresión/diagnóstico , Autoimagen
15.
Actas esp. psiquiatr ; 30(6): 343-349, nov. 2002.
Artículo en Es | IBECS (España) | ID: ibc-16915

RESUMEN

Introducción. El presente estudio evalúa la prevalencia de la anorexia nerviosa, sus síndromes parciales, bulimia nerviosa y trastorno por atracón en una muestra de estudiantes universitarias de Galicia (España).Metodología. Un total de 298 chicas y 157 chicos forman nuestra muestra. En el estudio empleamos el Eating Disorders Inventory (EDI) y un cuestionario sobre el comportamiento alimentario para detectar los sujetos con riesgo de padecer trastornos alimentarios. Resultados. El análisis de las medias indicó que las chicas mostraron puntuaciones más altas en impulso para adelgazar, bulimia, conciencia interoceptiva, insatisfacción corporal e ineficacia que los chicos; además, las chicas tienen un índice de masa corporal más bajo. Encontramos una prevalencia muy alta, un total de 6,4 per cent de casos de trastornos de la conducta alimentaria. Conclusiones. Los elevados valores de probables trastornos de la conducta alimentaria hace especialmente necesario llevar a cabo programas de prevención primaria y secundaria en poblaciones universitarias (AU)


Asunto(s)
Adolescente , Adulto , Masculino , Femenino , Humanos , España , Universidades , Prevalencia , Trastornos de Alimentación y de la Ingestión de Alimentos
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