Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 5 de 5
Filtrar
1.
Am J Cardiol ; 124(4): 618-626, 2019 08 15.
Artigo em Inglês | MEDLINE | ID: mdl-31303246

RESUMO

The aim of this study was to estimate the prevalence of the full spectrum of mental illness in adolescents (aged 11 to 17) and adults (aged 18 to 64) with congenital heart defects (CHDs) in the population-level Colorado Congenital Heart Disease Surveillance System. Further we sought to investigate whether severity of the defect, frequency of recent cardiac procedures or underlying genetic disorders influence these estimates. The cohort included patients in clinical care for CHDs between January 1, 2011 and December 31, 2013, identified across multiple healthcare systems and insurance claims. Of 2,192 adolescents with CHDs, 20% were diagnosed with a mental illness with the most prevalent categories being developmental disorders (8%), anxiety disorders (6%), attention, conduct, behavior, impulse control disorders (6%), and mood disorders (5%). Of 6,924 adults with CHDs, 33% were diagnosed with a mental illness with the most prevalent categories being mood disorders (13%), anxiety disorders (13%), and substance-related disorders (6%). Greater lesion complexity was associated with a higher likelihood of anxiety and developmental disorders in both adolescents and adults. Adolescents and adults who had ≥2 cardiac procedures in the 3-year surveillance period had a 3- and 4.5-fold higher likelihood of a mental illness diagnosis, respectively, compared with those who had fewer than 2 cardiac procedures. Finally, patients with a genetic syndrome were more likely to have a mental illness diagnosis. In conclusion, mental illness is a prevalent co-morbidity in the adolescent and adult population with CHDs, thus comprehensive care should include mental health care.


Assuntos
Cardiopatias Congênitas/epidemiologia , Transtornos Mentais/epidemiologia , Adolescente , Adulto , Transtornos de Ansiedade/epidemiologia , Transtornos de Deficit da Atenção e do Comportamento Disruptivo/epidemiologia , Criança , Colorado/epidemiologia , Síndrome de DiGeorge/epidemiologia , Síndrome de Down/epidemiologia , Feminino , Síndrome do Cromossomo X Frágil/epidemiologia , Disgenesia Gonadal/epidemiologia , Humanos , Masculino , Síndrome de Marfan/epidemiologia , Pessoa de Meia-Idade , Transtornos do Humor/epidemiologia , Síndrome de Prader-Willi/epidemiologia , Prevalência , Índice de Gravidade de Doença , Transtornos Relacionados ao Uso de Substâncias/epidemiologia , Adulto Jovem
2.
Am J Med Genet A ; 176(11): 2309-2317, 2018 11.
Artigo em Inglês | MEDLINE | ID: mdl-30216657

RESUMO

Dietary management is important to prevent severe obesity in individuals with Prader-Willi syndrome (PWS); however, few studies have examined dietary intake and quality in youth with PWS. Our objective was to estimate intake of essential nutrients and diet quality in youth with PWS compared to those without PWS. Three-day food records were used to estimate intake of energy, nutrients, nutrient-density, foods, and adherence to healthy eating guidelines. Data were presented as medians and interquartile ranges with Mann-Whitney U and Fisher's test used to compare between groups with p < .05 considered significant. Youth with (n = 23) and without (n = 23) PWS were similar in age and sex distribution. The PWS group had a lower energy intake (p ≤ .001), higher nutrient density (p = .003), and better adherence to guidelines (p = .007) compared to the control group. The proportion with nutrient intake from food below Estimated Average Requirement or Adequate Intake were similar between groups. Fiber, vitamin D, calcium, and potassium intake were below recommendations in 50% or more in both groups. The inclusion of supplement intake lowered the proportion below recommendations, except for fiber and potassium. Youth with PWS had a similar nutrient intake as those without PWS despite a lower energy intake, which could be attributed to higher diet quality. However, more than half of youth with PWS were at risk of inadequate fiber, vitamin D, calcium, and potassium intake. A greater emphasis on nutrient-dense foods would improve nutrient intake, but supplements may be warranted in youth with PWS who do not meet recommendations.


Assuntos
Dieta , Ingestão de Alimentos , Síndrome de Prader-Willi/epidemiologia , Adolescente , Bebidas , Estudos de Casos e Controles , Criança , Dieta Saudável , Suplementos Nutricionais , Ingestão de Energia , Feminino , Humanos , Masculino , Micronutrientes , Nutrientes
4.
Curr Opin Pulm Med ; 16(6): 568-73, 2010 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-20814307

RESUMO

PURPOSE OF REVIEW: Although several studies in the last years have evaluated obesity, obstructive sleep apnea (OSAS), and excessive daytime sleepiness (EDS) in patients with Prader-Willi syndrome (PWS), their pathophysiologies and interactions and the role of treatment with growth hormone are not completely understood. The present review analyzes the contributing role of obesity, OSAS, and sleep structure abnormalities in determining the EDS and the role of specific treatment in improving the clinical outcome. RECENT FINDINGS: The studies on sleep structure of PWS patients show abnormalities of rapid eye movement (REM) sleep and a decrease in non-REM sleep instability, corroborating the hypothesis of the presence of a primary disorder of vigilance and the similarities with narcolepsy. These sleep alterations might also be linked to the action of mediators of inflammation (i.e. adiponectin or cytokines) determined by obesity. Obesity and hypothalamic dysfunction could be responsible for the primary abnormalities of ventilation during sleep that, in turn, might contribute to EDS. Although EDS seems to resemble narcolepsy, PWS patients do not present the other typical symptoms of narcolepsy. SUMMARY: The most consistent hypothesis for linking the three different symptoms of PWS is a primary central hypothalamic dysfunction. Further research is needed to evaluate the contribution of the upper airway resistance syndrome in the pathogenesis of EDS, the role of the alterations of sleep microstructure, the relationships between PWS and narcoleptic phenotype, the involvement of orexin/hypocretin, and the effects of drugs acting on REM sleep and/or wakefulness.


Assuntos
Distúrbios do Sono por Sonolência Excessiva/fisiopatologia , Obesidade/fisiopatologia , Síndrome de Prader-Willi/fisiopatologia , Apneia Obstrutiva do Sono/fisiopatologia , Comorbidade , Distúrbios do Sono por Sonolência Excessiva/epidemiologia , Distúrbios do Sono por Sonolência Excessiva/etiologia , Humanos , Hipotálamo/fisiopatologia , Obesidade/epidemiologia , Síndrome de Prader-Willi/complicações , Síndrome de Prader-Willi/epidemiologia , Apneia Obstrutiva do Sono/epidemiologia
5.
J Autism Dev Disord ; 38(9): 1642-53, 2008 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-18311513

RESUMO

Prader-Willi syndrome (PWS) is a neurodevelopmental disorder characterized by hyperphagia and food preoccupations. Although dysfunction of the hypothalamus likely has a critical role in hyperphagia, it is only one of several regions involved in the regulation of eating. The purpose of this research was to examine food-related neural circuitry using functional magnetic resonance imaging in individuals with PWS and matched controls. Individuals with PWS showed increased activation in neural circuitry known to mediate hunger and motivation (hypothalamus, OFC) in response to high- versus low-calorie foods and in comparison to controls. This suggests neural circuitry for PWS is abnormally activated during hunger, particularly for high-calorie foods, and may mediate abnormally strong hunger states, therefore playing a significant role in PWS-induced hyperphagia.


Assuntos
Ingestão de Energia , Alimentos , Rede Nervosa/fisiopatologia , Obesidade/epidemiologia , Síndrome de Prader-Willi/epidemiologia , Síndrome de Prader-Willi/fisiopatologia , Adolescente , Adulto , Criança , Humanos , Hipotálamo/fisiopatologia , Cariotipagem , Imageamento por Ressonância Magnética , Masculino , Córtex Pré-Frontal/fisiopatologia
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA