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1.
J Food Sci ; 82(10): 2448-2455, 2017 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-28850673

RESUMEN

Micronutrient fortification can improve nutrient intake of older adults in long-term care. However, previous studies indicate that micronutrient fortification can alter food sensory attributes and, potentially, consumer liking. Others have found no effect of fortification on liking. This research investigates the effect of micronutrient powder addition on the sensory properties of selected foods commonly served in long-term care. A micronutrient powder containing 9 vitamins and 3 minerals was added to tomato soup and oatmeal at different levels. Using projective mapping, changes in sensory properties were observed with powder addition. Descriptive analysis, used to quantify these changes, showed that both the tomato soup and oatmeal had reduced flavor as the amount of added micronutrient powder increased. Oatmeal also showed changes in texture with fortification. Consumer liking scores for tomato soup showed that micronutrient addition affected liking when 100% of a daily dose was added into the soup. Addition of 50% of the daily dose did not affect liking. Oatmeal liking did not differ between fortified and unfortified samples. PRACTICAL APPLICATION: Results from this research can be used to decide whether a micronutrient powder of selected vitamins and minerals can be added to foods served to older adults in long-term care. Although sensory properties of the foods will be altered, fortification of both tomato soup and oatmeal with the developed powder is possible without reducing consumer liking to the point where it is disliked.


Asunto(s)
Aditivos Alimentarios/metabolismo , Preferencias Alimentarias , Micronutrientes/metabolismo , Anciano , Anciano de 80 o más Años , Femenino , Aromatizantes/análisis , Aromatizantes/metabolismo , Aditivos Alimentarios/análisis , Alimentos Fortificados/análisis , Humanos , Masculino , Micronutrientes/análisis , Persona de Mediana Edad , Minerales/análisis , Minerales/metabolismo , Polvos/análisis , Gusto , Oligoelementos/análisis , Oligoelementos/metabolismo , Vitaminas/análisis , Vitaminas/metabolismo
2.
Folia Phoniatr Logop ; 65(6): 312-7, 2013.
Artículo en Inglés | MEDLINE | ID: mdl-25033761

RESUMEN

BACKGROUND: There is no appropriately validated scale with which to rate the problem of residue after swallowing. The Boston Residue and Clearance Scale (BRACS) was developed to meet this need. Initial reliability and validity were assessed. METHODS: BRACS is an 11-point ordinal residue rating scale scoring three aspects of residue during a fiberoptic endoscopic evaluation of swallowing (FEES): (1) the amount and location of residue, (2) the presence of spontaneous clearing swallows, and (3) the effectiveness of clearing swallows. To determine inter-rater and test-retest reliability, 63 swallows from previously recorded FEES procedures were scored twice by 4 raters using (1) clinical judgment (none, mild, mild-moderate, moderate, moderate-severe, severe) and (2) BRACS. Concurrent validity was tested by correlating clinical judgment scores with BRACS scores. Internal consistency of the items in BRACS was examined. A factor analysis was performed to identify important factors that suggest grouping within the 12 location items in BRACS. RESULTS: BRACS showed excellent inter-rater reliability (intraclass correlation coefficient, ICC = 0.81), test-retest reliability (ICC: 0.82-0.92), high concurrent validity (Pearson's r = 0.76), and high internal consistency (Cronbach's α = 0.86). Factor analysis revealed 3 main latent factors for the 12 location items. CONCLUSION: BRACS is a valid and reliable tool that can rate the severity of residue.


Asunto(s)
Trastornos de Deglución/diagnóstico , Contenido Digestivo , Índice de Severidad de la Enfermedad , Anciano , Esofagoscopía , Femenino , Tecnología de Fibra Óptica , Grupos Focales , Alimentos , Humanos , Hipofaringe/fisiopatología , Masculino , Persona de Mediana Edad , Variaciones Dependientes del Observador , Reproducibilidad de los Resultados , Sensibilidad y Especificidad , Grabación en Video
3.
Dev Neuropsychol ; 30(1): 547-89, 2006.
Artículo en Inglés | MEDLINE | ID: mdl-16925475

RESUMEN

This article has 3 parts. The 1st part provides an overview of the family genetics, brain imaging, and treatment research in the University of Washington Multidisciplinary Learning Disabilities Center (UWLDC) over the past decade that points to a probable genetic basis for the unusual difficulty that individuals with dyslexia encounter in learning to read and spell. Phenotyping studies have found evidence that phonological, orthographic, and morphological word forms and their parts may contribute uniquely to this difficulty. At the same time, reviews of treatment studies in the UWLDC (which focused on children in Grades 4 to 6) and other research centers provide evidence for the plasticity of the brain in individuals with dyslexia. The 2nd part reports 4 sets of results that extend previously published findings based on group analyses to those based on analyses of individual brains and that support triple word form awareness and mapping theory: (a) distinct brain signatures for the phonological, morphological, and orthographic word forms; (b) crossover effects between phonological and morphological treatments and functional magentic resonance imaging (fMRI) tasks in response to instruction, suggestive of cross-word form computational and mapping processes; (c) crossover effects between behavioral measures of phonology or morphology and changes in fMRI activation following treatment; and (d) change in the relationship between structural MRI and functional magnetic resonance spectroscopy (fMRS) lactate activation in right and left inferior frontal gyri following treatment emphasizing the phonological, morphological, and orthographic word forms. In the 3rd part we discuss the next steps in this programmatic research to move beyond word form alone.


Asunto(s)
Mapeo Encefálico , Dislexia/fisiopatología , Reconocimiento Visual de Modelos/fisiología , Lectura , Estudios de Casos y Controles , Niño , Terapia Cognitivo-Conductual/métodos , Condicionamiento Operante/fisiología , Dislexia/genética , Dislexia/rehabilitación , Salud de la Familia , Femenino , Lateralidad Funcional , Humanos , Procesamiento de Imagen Asistido por Computador/métodos , Pruebas del Lenguaje/estadística & datos numéricos , Imagen por Resonancia Magnética/métodos , Masculino , Fenómenos Fisiológicos de la Nutrición , Oxígeno/sangre
4.
Pharmacotherapy ; 25(10): 1365-77, 2005 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-16185181

RESUMEN

Cardiovascular disease is the leading cause of death among adults in the United States, in Europe, and in much of Asia. Despite advances in primary prevention of coronary artery disease, including early detection and treatment of dyslipidemia, one half of all myocardial infarctions and strokes occur in patients with normal serum cholesterol levels. Observations like this prompt the search for new risk factors and improved identification of individuals at high risk. One proposed risk factor is an elevated level of C-reactive protein (CRP), a marker of inflammation independent of other risk factors. The CRP assay is desirable in terms of standardization and cost. The 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitors (statins) are indicated for the treatment of dyslipidemias, but data support their protective role against cardiovascular disease beyond their effects on lipids. Statins directly affect inflammatory markers, and nearly 2 dozen randomized studies have demonstrated statins' effects on CRP. Because information regarding the role of CRP in cardiovascular disease is compelling but sometimes contradictory and because the need to reduce CRP levels is unclear, the American Heart Association and the Centers for Disease Control and Prevention presented a panel statement on the topic. Ongoing trials will assist in determining the need to reduce CRP levels to lower cardiovascular risk. An understanding of these issues is important for improving the prediction of cardiovascular risk and for intervening to reduce this risk.


Asunto(s)
Proteína C-Reactiva/análisis , Inhibidores de Hidroximetilglutaril-CoA Reductasas/farmacología , Animales , Aterosclerosis/complicaciones , Atorvastatina , Enfermedades Cardiovasculares/sangre , Enfermedades Cardiovasculares/etiología , Ácidos Heptanoicos/farmacología , Humanos , Hipertensión/sangre , Síndrome Metabólico/sangre , Pravastatina/farmacología , Pirroles/farmacología , Factores de Riesgo , Simvastatina/farmacología
5.
J Child Neurol ; 19(3): 214-8, 2004 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-15119482

RESUMEN

Joubert syndrome is an autosomal recessive disorder characterized by hypotonia, ataxia, developmental delay, and a distinctive hindbrain malformation involving the cerebellum and brain stem, visualized radiographically on magnetic resonance imaging (MRI) as the "molar tooth sign." In postmortem brains from subjects with Joubert syndrome, there is an apparent absence of decussation of both corticospinal and superior cerebellar tracts, although the functional significance has not been elucidated. We sought to explore the cerebral and cerebellar activation pattern elicited by finger tapping in an adolescent with Joubert syndrome and in a normal control subject using functional MRI. In contrast to the typical highly lateralized activation seen in our control subject, the subject with Joubert syndrome demonstrated striking bilateral activation of the sensorimotor and cerebellar cortex. Although our functional MRI data do not indicate a clear absence of decussation, the abnormal activation pattern observed suggests altered brain functional organization in relation to anatomic differences. Malformation of the hindbrain could result in recruitment of alternative pathways, similar to what has been observed following ischemic injury to the developing or mature central nervous system.


Asunto(s)
Tronco Encefálico/anomalías , Cerebelo/anomalías , Cerebelo/fisiopatología , Corteza Cerebral/fisiopatología , Aberraciones Cromosómicas , Genes Recesivos/genética , Procesamiento de Imagen Asistido por Computador , Imagen por Resonancia Magnética , Actividad Motora/fisiología , Degeneraciones Espinocerebelosas/diagnóstico , Degeneraciones Espinocerebelosas/genética , Adolescente , Adulto , Mapeo Encefálico , Tronco Encefálico/fisiopatología , Niño , Dominancia Cerebral/genética , Dominancia Cerebral/fisiología , Femenino , Estudios de Seguimiento , Humanos , Corteza Motora/fisiopatología , Tractos Piramidales/anomalías , Tractos Piramidales/fisiopatología , Reclutamiento Neurofisiológico/fisiología , Valores de Referencia , Corteza Somatosensorial/fisiopatología , Síndrome
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