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1.
Neurosci Biobehav Rev ; 137: 104648, 2022 06.
Artículo en Inglés | MEDLINE | ID: mdl-35367224

RESUMEN

BACKGROUND: Brain co-morbidities in DMD are well-documented, less is known about the cognitive, behavioral and psychosocial functioning of patients with BMD. METHODS: The systematic review was carried out on two databases (Pubmed and Scopus) according to the PRISMA guidelines. We included all research articles specific to BMD written after 1995. RESULTS: Studies examining neuropsychological and neurobehavioral functioning in BMD are few and have several methods limitations. BMD population is characterized by high rates of cognitive impairment, with specific involvement of different cognitive areas. Unlike DMD, verbal skills are better preserved. Neurodevelopmental and emotional/behavioral disorders have great importance in BMD, due to their high prevalence. Lack of Dp140 or Dp71 can cause intellectual disability, these isoforms are probably responsible for the other brain-related comorbidities as well. DISCUSSION: The results suggest that cognitive and neuropsychiatric comorbid symptoms may affect a significant proportion of BMD patients therefore it is important to mental health and neuropsychological screening. Finding tools for an adequate assessment is a priority in order to include brain outcome measures in clinical trials.


Asunto(s)
Distrofia Muscular de Duchenne , Encéfalo/metabolismo , Cognición , Distrofina/metabolismo , Humanos , Distrofia Muscular de Duchenne/complicaciones , Distrofia Muscular de Duchenne/epidemiología , Isoformas de Proteínas
2.
Biomolecules ; 11(8)2021 08 20.
Artículo en Inglés | MEDLINE | ID: mdl-34439911

RESUMEN

The urgent need for new therapies for some devastating neuromuscular diseases (NMDs), such as Duchenne muscular dystrophy or amyotrophic lateral sclerosis, has led to an intense search for new potential biomarkers. Biomarkers can be classified based on their clinical value into different categories: diagnostic biomarkers confirm the presence of a specific disease, prognostic biomarkers provide information about disease course, and therapeutic biomarkers are designed to predict or measure treatment response. Circulating biomarkers, as opposed to instrumental/invasive ones (e.g., muscle MRI or nerve ultrasound, muscle or nerve biopsy), are generally easier to access and less "time-consuming". In addition to well-known creatine kinase, other promising molecules seem to be candidate biomarkers to improve the diagnosis, prognosis and prediction of therapeutic response, such as antibodies, neurofilaments, and microRNAs. However, there are some criticalities that can complicate their application: variability during the day, stability, and reliable performance metrics (e.g., accuracy, precision and reproducibility) across laboratories. In the present review, we discuss the application of biochemical biomarkers (both validated and emerging) in the most common NMDs with a focus on their diagnostic, prognostic/predictive and therapeutic application, and finally, we address the critical issues in the introduction of new biomarkers.


Asunto(s)
Esclerosis Amiotrófica Lateral/sangre , Biomarcadores/sangre , Creatina Quinasa/metabolismo , Distrofia Muscular de Duchenne/sangre , Animales , Anticuerpos/química , Progresión de la Enfermedad , Humanos , Filamentos Intermedios/química , Filamentos Intermedios/metabolismo , Ratones , MicroARNs/metabolismo , Modelos Biológicos , Enfermedad de la Neurona Motora/metabolismo , Enfermedades Neuromusculares , Reproducibilidad de los Resultados
3.
Neurol Sci ; 41(9): 2561-2567, 2020 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-32246354

RESUMEN

Previous studies demonstrated the benefits of motor exercise and physical activity in neuromuscular disorders. However, very few papers assessed the effects of sport practise. The aim of this multicentre study was to assess the impact of sport activity on self-esteem and emotional regulation in a cohort of athletes with neuromuscular disorders. The 38 patients with Duchenne, Becker or other types of muscular dystrophy or spinal muscular atrophy practising sport (aged 13-49 years) and 39 age-, gender-, disability- and disease-matched patients not practising sport were enrolled. Testing procedures to assess self-esteem, anxiety and depression disorder, personality trait and quality of life (QoL) were used. Patients practising sport had a significantly higher self-esteem, lower level of depression, greater social own identity and adherence and QoL. Frequency of sport activity may represent a complementary therapy in neuromuscular disorders to improve mental and social well-being.


Asunto(s)
Enfermedades Neuromusculares , Deportes , Adolescente , Adulto , Atletas , Humanos , Persona de Mediana Edad , Enfermedades Neuromusculares/terapia , Calidad de Vida , Autoimagen , Adulto Joven
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