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1.
Sleep Med ; 19: 116-22, 2016 03.
Artículo en Inglés | MEDLINE | ID: mdl-27198956

RESUMEN

OBJECTIVE: To examine the epidemiology of sleep problems and insomnia among the community older individuals in Hebei Province, China, and to investigate the potential sociodemographic and clinical correlates and medication use. METHODS: This cross-sectional study was conducted with community adults, aged 60 years or older, who resided in four major cities in Hebei province. Basic sociodemographic and clinical data were collected and analyzed. A total of 3176 older adults (1292 men, 70.2 ± 6.8 years; 1884 women, 68.8 ± 6.7 years) were interviewed. All of the participants were interviewed with a standardized questionnaire and underwent insomnia screening. RESULTS: The prevalence of insomnia was 37.75%. The most common type of sleep disturbance was difficulty maintaining sleep, followed by difficulty initiating sleep and early morning awakening. Never smoking, experiencing the loss of a parent, a history of coronary heart disease, and depression symptoms were independent risk factors for insomnia in men. Occasional drinking was an independent protective factor against insomnia in men. Older age, depression symptoms, a history of cerebral hemorrhage, hyperlipidemia, living without a spouse, and having mild cognitive impairment were independent risk factors for insomnia in women. Only 11.1% of the sample with insomnia were taking sleeping medications regularly. CONCLUSION: Insomnia is highly prevalent among the community older population in Hebei Province. The percentage of individuals regularly taking sleeping medication is low among those with insomnia. Individuals with complaints of insomnia frequently have poor physical and mental health and may need more medical attention. Comprehensive measures that involve psychosocial and personal behaviors should be implemented to alleviate insomnia in older individuals.


Asunto(s)
Envejecimiento , Ciudades , Trastornos del Inicio y del Mantenimiento del Sueño/epidemiología , Factores de Edad , Anciano , China/epidemiología , Estudios Transversales , Demografía , Femenino , Humanos , Masculino , Factores de Riesgo , Factores Sexuales , Encuestas y Cuestionarios
2.
Nat Genet ; 43(12): 1228-31, 2011 Oct 30.
Artículo en Inglés | MEDLINE | ID: mdl-22037552

RESUMEN

To identify susceptibility loci for schizophrenia, we performed a two-stage genome-wide association study (GWAS) of schizophrenia in the Han Chinese population (GWAS: 746 individuals with schizophrenia and 1,599 healthy controls; validation: 4,027 individuals with schizophrenia and 5,603 healthy controls). We identified two susceptibility loci for schizophrenia at 6p21-p22.1 (rs1233710 in an intron of ZKSCAN4, P(combined) = 4.76 × 10(-11), odds ratio (OR) = 0.79; rs1635 in an exon of NKAPL, P(combined) = 6.91 × 10(-12), OR = 0.78; rs2142731 in an intron of PGBD1, P(combined) = 5.14 × 10(-10), OR = 0.79) and 11p11.2 (rs11038167 near the 5' UTR of TSPAN18, P(combined) = 1.09 × 10(-11), OR = 1.29; rs11038172, P(combined) = 7.21 × 10(-10), OR = 1.25; rs835784, P(combined) = 2.73 × 10(-11), OR = 1.27). These results add to previous evidence of susceptibility loci for schizophrenia at 6p21-p22.1 in the Han Chinese population. We found that NKAPL and ZKSCAN4 were expressed in postnatal day 0 (P0) mouse brain. These findings may lead to new insights into the pathogenesis of schizophrenia.


Asunto(s)
Cromosomas Humanos Par 11 , Predisposición Genética a la Enfermedad , Polimorfismo de Nucleótido Simple , Esquizofrenia/genética , Adulto , Animales , Pueblo Asiatico , Encéfalo/metabolismo , Estudios de Casos y Controles , Cromosomas Humanos Par 6 , Proteínas Co-Represoras/genética , Proteínas de Unión al ADN/genética , Femenino , Frecuencia de los Genes , Sitios Genéticos , Estudio de Asociación del Genoma Completo , Humanos , Masculino , Ratones , Ratones Endogámicos ICR , Proteínas del Tejido Nervioso/genética , Proteínas Nucleares/genética , Análisis de Componente Principal , Sitios de Carácter Cuantitativo , Esquizofrenia/etnología , Tetraspaninas/genética , Transcripción Genética
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