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1.
J Frailty Aging ; 9(2): 90-93, 2020.
Artículo en Inglés | MEDLINE | ID: mdl-32259182

RESUMEN

Previous studies proposed calf circumference cutoff values for predicting dual-energy X-ray absorptiometry (DXA)-derived low muscle mass. However, DXA-derived appendicular lean mass (aLM) includes non-skeletal muscle components such as the appendicular fat-free component of adipose tissue fat cells (aFFAT). The purpose of this study was to compare the calf circumference method of classification before (Model #1) and after (Model #2) eliminating the influence of FFAT in healthy Japanese adults (50 to 79 years; mean age 70 (SD 7) years). Model 1, and Model 2 for classifying low muscle mass had a sensitivity of 78% and 64%, specificity of 76% and 75%, positive predictive value of 31% and 28%, and negative predictive value of 96% and 93%, respectively. Appendicular fat-free component of adipose tissue has the potential to influence the ability of calf circumference to accurately classify individuals with low muscle mass. Consideration should be made when using this as a screening tool for low muscle mass.


Asunto(s)
Tejido Adiposo , Composición Corporal , Pierna/anatomía & histología , Músculo Esquelético/anatomía & histología , Sarcopenia/diagnóstico , Absorciometría de Fotón , Anciano , Humanos , Persona de Mediana Edad , Músculo Esquelético/diagnóstico por imagen , Prevalencia , Sensibilidad y Especificidad
2.
Br J Cancer ; 100(9): 1471-82, 2009 May 05.
Artículo en Inglés | MEDLINE | ID: mdl-19401703

RESUMEN

Neuroblastoma serves as a paradigm for utilising tumour genomic data for determining patient prognosis and treatment allocation. However, before the establishment of the International Neuroblastoma Risk Group (INRG) Task Force in 2004, international consensus on markers, methodology, and data interpretation did not exist, compromising the reliability of decisive genetic markers and inhibiting translational research efforts. The objectives of the INRG Biology Committee were to identify highly prognostic genetic aberrations to be included in the new INRG risk classification schema and to develop precise definitions, decisive biomarkers, and technique standardisation. The review of the INRG database (n=8800 patients) by the INRG Task Force finally enabled the identification of the most significant neuroblastoma biomarkers. In addition, the Biology Committee compared the standard operating procedures of different cooperative groups to arrive at international consensus for methodology, nomenclature, and future directions. Consensus was reached to include MYCN status, 11q23 allelic status, and ploidy in the INRG classification system on the basis of an evidence-based review of the INRG database. Standardised operating procedures for analysing these genetic factors were adopted, and criteria for proper nomenclature were developed. Neuroblastoma treatment planning is highly dependant on tumour cell genomic features, and it is likely that a comprehensive panel of DNA-based biomarkers will be used in future risk assignment algorithms applying genome-wide techniques. Consensus on methodology and interpretation is essential for uniform INRG classification and will greatly facilitate international and cooperative clinical and translational research studies.


Asunto(s)
Neuroblastoma/diagnóstico , Neuroblastoma/genética , Aberraciones Cromosómicas , Cromosomas Humanos Par 11 , Cromosomas Humanos Par 17 , Consenso , Amplificación de Genes , Marcadores Genéticos , Humanos , Cooperación Internacional , Proteína Proto-Oncogénica N-Myc , Neuroblastoma/epidemiología , Neuroblastoma/psicología , Neuroblastoma/terapia , Proteínas Nucleares/genética , Proteínas Oncogénicas/genética , Planificación de Atención al Paciente , Ploidias , Pronóstico , Biosíntesis de Proteínas , Medición de Riesgo , Factores de Riesgo , Análisis de Supervivencia
3.
Obstet Gynecol ; 63(3 Suppl): 78S-80S, 1984 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-6608072

RESUMEN

A case of postabortal hemorrhage in a patient with von Willebrand's disease was controlled by arteriographic embolization of the uterine branch of the internal iliac artery. Selective internal iliac artery embolization has been effectively used to control postpartum hemorrhage and hemorrhage resulting from pelvic malignancy. A discussion is presented for expanding the use of selective embolization for controlling uterine hemorrhage to patients suffering from postabortal bleeding as a means of controlling hemorrhage without sacrificing fertility.


Asunto(s)
Aborto Inducido/efectos adversos , Embolización Terapéutica , Hemorragia Uterina/terapia , Adulto , Angiografía , Femenino , Humanos , Embarazo , Hemorragia Uterina/diagnóstico por imagen , Hemorragia Uterina/etiología , Útero/irrigación sanguínea , Enfermedades de von Willebrand/complicaciones
4.
Eur J Pharmacol ; 31(1): 110-4, 1975 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-1126371

RESUMEN

Unanesthetized rats were injected i.v. either with commercial regular insulin, or the diluting fluid of the commercial insulin solution used, or with 0.9 percent NaCl, and placed in individual cages containing no food. Water intake was measured for 2 hr. Injection of the hyposmolar diluting fluid containing glycerol and phenol slightly, but significantly, enhanced the water intake. Insulin in doses from 0.05 to 43.0 U/kg induced an additional drinking response, while 0.02 U/kg had no effect. A linear log dose--response for insulin-induced drinking was obtained between 0.05 and 21.0 U/kg. Small doses of insulin, thus, undoubtly, enhance water intake. Insulin could play a minor role in body water honeostasis in mammals.


Asunto(s)
Conducta de Ingestión de Líquido/efectos de los fármacos , Insulina/farmacología , Animales , Soluciones Hipertónicas , Masculino , Vehículos Farmacéuticos , Ratas , Estimulación Química , Factores de Tiempo
5.
Psychiatr Serv ; 47(10): 1123-5, 1996 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-8890345

RESUMEN

At a maximum-security forensic hospital over a three-year period, 79 patients (35 percent of all patients) were involved in 157 staff injuries. Staff members' average postinjury absence from work was 85 days, at a cost equivalent to about 2 percent of the hospital's budget. Nursing staff, particularly psychiatric technicians, had the highest injury rate. Male staff were about twice as likely to be injured as female staff. More injuries occurred on the second shift. Patients who injured staff were younger than those who did not. Florid psychotic behavior, nonpsychotic agitation, and the recent use of restraints were the most common prodromal signs.


Asunto(s)
Accidentes de Trabajo/economía , Internamiento Obligatorio del Enfermo Mental/economía , Medidas de Seguridad/economía , Violencia/economía , Heridas y Lesiones/economía , Absentismo , Adulto , Presupuestos , Connecticut , Costos y Análisis de Costo , Femenino , Hospitales Psiquiátricos/economía , Humanos , Masculino , Persona de Mediana Edad , Trastornos Psicóticos/economía , Trastornos Psicóticos/rehabilitación , Gestión de Riesgos/economía
6.
Ethn Dis ; 7(3): 259-70, 1997.
Artículo en Inglés | MEDLINE | ID: mdl-9467709

RESUMEN

OBJECTIVE: This study examined the relationship of serum creatine kinase (CK) levels with aggressive behavior as a function of psychosis and ethnicity in a sample of violent forensic patients. DESIGN: CK levels were determined on admission in a sample of 195 males consecutively admitted to a forensic hospital. The patients' aggressive behavior during their hospital stay was monitored using the Overt Aggression Scale (OAS). All data for this study was archival and gathered from hospital records. METHODS: Multivariate analysis of variance was used to examine whether African-American and Caucasian patients differed in serum CK levels and severity, frequency, and type (verbal vs physical) of aggression. T-tests were performed to compare ethnic groups in terms of age, weight, height, systolic and diastolic blood pressure. All patients who had been in restraints, had been administered intramuscular medications, had a history of drug or alcohol abuse, and were classified as schizophrenic were compared using chi-square analysis. For each of these variables further comparisons were made of CK levels between African-American and Caucasian patients. RESULTS: Mean serum CK in African-American patients was 64% higher than in Caucasians. African Americans displayed significantly greater physical aggression than Caucasian patients. In addition, African-American patients with a diagnosis of schizophrenia had significantly higher CK levels than African Americans with other diagnoses, with no significant differences related to schizophrenia noted within the Caucasian group. No significant differences in aggressive behavior related to schizophrenia were found in African-American patients. CONCLUSIONS: This study confirms the findings of previous reports which observed higher CK levels in African Americans than in Caucasians. It is also proposed that a confluence of physiologic and psychosocial factors may affect biological marker presentation, particularly as manifest in CK differences between ethnic groups.


Asunto(s)
Agresión , Población Negra , Creatina Quinasa/sangre , Trastornos Mentales/etnología , Violencia/etnología , Población Blanca , Adolescente , Adulto , Anciano , Análisis de Varianza , Connecticut , Psiquiatría Forense/estadística & datos numéricos , Hospitalización , Humanos , Masculino , Trastornos Mentales/enzimología , Trastornos Mentales/genética , Análisis Multivariante , Reproducibilidad de los Resultados , Estudios Retrospectivos
7.
Child Abuse Negl ; 23(1): 1-14, 1999 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-10075189

RESUMEN

OBJECTIVE: This paper describes the development and preliminary validation of a prescriptive home danger and safety precaution instrument containing 14 epidemiological categories to be used in the design and evaluation of family-tailored injury prevention and safety interventions. METHOD: The HIDSP-2 evolved from application and revision of the previous home danger and safety precaution recognition and observation instruments. As part of this process, the suitability of the HIDSP-2 for use in a broad-based trial was evaluated with 29 low income parents exhibiting individual learning needs. Inter-rater reliability and stability of scores were examined. Internal consistency was examined for total dangers and precautions and for those categories in which there were sufficient items to do so. RESULTS: Administrative time was reduced while continuing usefulness in the identification and remediation of dangers and implementation of precautions was demonstrated. Stability of observation was high. Alphas as a measure of internal consistency was satisfactory for total danger and precautions separately; however, those for most individual categories were low. There was significant reduction in the number of dangers identified initially and significant improvement in the safety precautions implemented. CONCLUSIONS: The HIDSP-2 can assist healthcare, education, disability, and child protective service workers in the development of home safety plans for remediating home dangers and implementing precautions. While we see this instrument as eminently suitable for use in broad-based interventions and in epidemiological studies, further research must continue to examine the psychometric characteristics of the individual danger and precaution categories.


Asunto(s)
Prevención de Accidentes , Accidentes Domésticos/prevención & control , Maltrato a los Niños/prevención & control , Artículos Domésticos , Humanos , Lactante , Psicometría , Reproducibilidad de los Resultados
8.
J Speech Lang Hear Res ; 40(5): 990-1001, 1997 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-9328871

RESUMEN

Language impairments have been hypothesized to have a genetic component. Previous studies of the familial aggregation of language impairments have relied on a retrospective approach based on parental/self-reported history of language development. This study examined familial aggregation prospectively, by investigating language acquisition and cognitive development in the younger siblings and offspring of individuals with well-defined language impairments. It was predicted that children with a positive family history for language impairments would be more likely to show delays in language acquisition than would age- and gender-matched controls. Similar delays were not expected in nonlinguistic domains, such as conceptual, gestural, or general cognitive development. Ten children with a positive family history and 10 age- and gender-matched controls were tested. Analyses of linguistic and cognitive assessments at 16 to 26 months confirmed the predictions. Children with a family history of language impairments had lower receptive and expressive language scores than controls, with 50% of them scoring at least 1.5 SD below the mean for their age. At the same time, performance on a number of tasks that did not rely on language abilities did not differ as a function of family history. These results indicate that children with a positive family history for language impairments are at risk for language delay; the results also support a familial component to language impairments.


Asunto(s)
Trastornos del Lenguaje/genética , Trastornos del Habla/genética , Orden de Nacimiento , Preescolar , Cognición , Formación de Concepto , Femenino , Gestos , Humanos , Conducta Imitativa , Lactante , Trastornos del Lenguaje/diagnóstico , Pruebas del Lenguaje , Masculino , Estudios Prospectivos , Trastornos del Habla/diagnóstico , Medición de la Producción del Habla , Tacto
9.
J Learn Disabil ; 34(6): 492-502, 2001.
Artículo en Inglés | MEDLINE | ID: mdl-15503564

RESUMEN

Recent behavioral genetic research has shown that genetic propensities are associated with individual differences in experiences, and thus, what may appear to be environmental effects can reflect genetic influence. This study examines passive genotype-environment correlations (GECs) for language-related abilities by comparing environment-child language associations in adoptive and nonadoptive families. The results provide evidence for the genetic mediation of the association between home environmental variables, such as the provision of toys and games, maternal involvement, and degree of intellectual/cultural orientation with children's language-related abilities. Developmental changes in passive GECs are considered, and the implications for typical and atypical learners are discussed.


Asunto(s)
Dislexia/genética , Genotipo , Trastornos del Desarrollo del Lenguaje/genética , Discapacidades para el Aprendizaje/genética , Medio Social , Adopción , Niño , Preescolar , Colorado , Dislexia/diagnóstico , Humanos , Inteligencia/genética , Trastornos del Desarrollo del Lenguaje/diagnóstico , Discapacidades para el Aprendizaje/diagnóstico , Estudios Longitudinales , Relaciones Madre-Hijo , Fenotipo , Estadística como Asunto
10.
J Am Acad Psychiatry Law ; 27(3): 426-44, 1999.
Artículo en Inglés | MEDLINE | ID: mdl-10509942

RESUMEN

Forensic patients with schizophrenia who fail to adhere to prescribed antipsychotic medication risk recidivism, which continues to be a serious concern. It affects all stages of trial proceedings and impacts on the treaters' liability. Although much remains unchanged since the authors reviewed the subject in 1986, significant advances have occurred. A patient's insight can be assessed with greater precision. Risks posed by past noncompliance, substance abuse, and a dysphoric response to medication are more clearly documented. Clinical and laboratory methods for assessing compliance have improved. Major advances in the effective amelioration of adverse effects can be applied to promote adherence. New augmentation strategies enable adequate treatment at lower doses. The development of atypical antipsychotic agents makes compliance easier to achieve and maintain. Other advances apply to the containment of relapse when it does occur. This review organizes the literature documenting these trends for use in both treatment and consultation.


Asunto(s)
Antipsicóticos/administración & dosificación , Psiquiatría Forense/métodos , Cooperación del Paciente , Esquizofrenia/tratamiento farmacológico , Antipsicóticos/efectos adversos , Humanos , Cooperación del Paciente/psicología , Medición de Riesgo/métodos , Esquizofrenia/diagnóstico , Psicología del Esquizofrénico
11.
Psychol Rep ; 73(3 Pt 2): 1105-6, 1993 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-8115561

RESUMEN

Analysis of hemoglobin, mean corpuscular volume, mean corpuscular hemoglobin concentration, and red blood-cell count for a group of 46 black and 59 white male forensic patients showed significant hematological differences between the groups, with white patients demonstrating higher mean values for all four measures.


Asunto(s)
Agresión/fisiología , Negro o Afroamericano/psicología , Recuento de Eritrocitos , Índices de Eritrocitos , Hemoglobinometría , Población Blanca/psicología , Adulto , Agresión/psicología , Psicología Criminal , Jerarquia Social , Humanos , Masculino , Violencia
12.
Psychol Rep ; 74(2): 622, 1994 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-8197299

RESUMEN

Analysis of serum cholesterol levels of 106 male forensic patients showed significant differences in frequency of aggression, with low cholesterol levels predominant among those more frequently violent.


Asunto(s)
Agresión/psicología , Colesterol/sangre , Psiquiatría Forense , Humanos , Masculino , Trastornos Mentales/sangre , Violencia
13.
Oncogene ; 29(6): 865-75, 2010 Feb 11.
Artículo en Inglés | MEDLINE | ID: mdl-19901960

RESUMEN

Imbalances in chromosome 11q occur in approximately 30% of primary neuroblastoma and are associated with poor outcome. It has been suggested that 11q loss constitutes a distinct clinico-genetic neuroblastoma subgroup by affecting expression levels of corresponding genes. This study analysed the relationship of 11q loss, clinical phenotype and global transcriptomic profiles in four clinico-genetic subgroups (11q alteration/favourable outcome, n=7; 11q alteration/unfavourable outcome, n=14; no 11q alteration/favourable outcome, n=81; no 11q alteration/unfavourable outcome, n=8; tumours with MYCN amplification and/or 1p loss were excluded). Unsupervised and supervised comparisons of gene expression profiles consistently showed significantly different mRNA patterns between favourable and unfavourable neuroblastomas, both in the subgroups with and without 11q loss. In contrast, favourable tumours with and without 11q loss showed highly similar transcriptomic profiles. Disproportionate downregulation of 11q genes was observed only in unfavourable tumours with 11q loss. The diverging molecular profiles were neither caused by considerable differences in the size of the deleted regions nor by differential methylation patterns of 11q genes. Together, this study shows that neuroblastoma with 11q loss comprises two biological subgroups that differ both in their clinical phenotype and gene expression patterns, indicating that 11q loss is not a primary determinant of neuroblastoma tumour behaviour.


Asunto(s)
Deleción Cromosómica , Cromosomas Humanos Par 11/genética , Biología Computacional , Perfilación de la Expresión Génica , Genómica , Neuroblastoma/diagnóstico , Neuroblastoma/genética , Preescolar , Cromosomas Humanos Par 11/metabolismo , Regulación Neoplásica de la Expresión Génica , Humanos , Metilación , Neuroblastoma/metabolismo , Neuroblastoma/patología , Pronóstico , Regiones Promotoras Genéticas/genética
16.
Int J Psychoanal ; 47(2): 269-73, 1966.
Artículo en Inglés | MEDLINE | ID: mdl-6007177
19.
Psyche (Stuttg) ; 26(4): 249-64, 1972 Apr.
Artículo en Alemán | MEDLINE | ID: mdl-5024893
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