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1.
Zhonghua Yu Fang Yi Xue Za Zhi ; 53(5): 540-544, 2019 May 06.
Artículo en Zh | MEDLINE | ID: mdl-31091617

RESUMEN

The hazard ratio and median survival time are the routine indicators in survival analysis. We briefly introduced the relationship between hazard ratio and median survival time and the role of proportional hazard assumption. We compared 110 pairs of hazard ratio and median survival time ratio in 58 articles and demonstrated the reasons for the difference by examples. The results showed that the hazard ratio estimated by the Cox regression model is unreasonable and not equivalent to median survival time ratio when the proportional hazard assumption is not met. Therefore, before performing the Cox regression model, the proportional hazard assumption should be tested first. If proportional hazard assumption is met, Cox regression model can be used; if proportional hazard assumption is not met, restricted mean survival times is suggested.


Asunto(s)
Modelos de Riesgos Proporcionales , Tasa de Supervivencia , Humanos , Reproducibilidad de los Resultados , Análisis de Supervivencia
2.
Zhonghua Liu Xing Bing Xue Za Zhi ; 41(1): 31-35, 2020 Jan 10.
Artículo en Zh | MEDLINE | ID: mdl-32062939

RESUMEN

Objective: To understand the relationship between visual impairment and risk of all-cause mortality in the elderly aged 65 years and older in 8 longevity areas in China. Methods: The data of the elderly aged 65 years and older in the project in 2012 were obtained from Healthy Aging and Biomarkers Cohort Study, a sub-cohort of the Chinese Longitudinal Healthy Longevity Survey, including physical measurement and survival status, and a follow-up for survival outcomes were conducted in 2014 and 2017 respectively. Cox proportional hazard regression model was used to analyze the influence of visual impairment on mortality. Gender and age specific analysis was conducted. Results: A total of 1 736 elderly adults were included. A total of 943 deaths occurred during the 5-year follow-up period with a 5-year mortality rate of 54.3%. The 5-year mortality rate was 76.7% in the group with visual impairment, and 47.6% in the group without visual impairment (P<0.001). After adjusting for demographic information, life style and some disease factors, the risk of 5-year mortality in the group with visual impairment group was 1.30 times higher than that in the group without visual impairment (HR=1.30, 95%CI: 1.09-1.55). In the females, the risk for mortality in the group with visual impairment was 1.48 times higher than that in the group without visual impairment (HR=1.48, 95%CI:1.20-1.84). However, vision status was not associated with the risk for mortality in males (HR=1.02, 95%CI: 0.72-1.43). The risk for mortality in the group with visual impairment was 1.39 times higher than that in the group without visual impairment in the elderly aged over 90 years (HR=1.39, 95%CI: 1.13-1.70). Vision status was not associated with mortality risk in the elderly aged 65-79 years and 80-89 years (HR=1.37, 95%CI: 0.61-3.07; HR=0.95, 95%CI: 0.61-1.48). Conclusion: In the elderly people in China, visual impairment is a risk factor for mortality.


Asunto(s)
Longevidad , Trastornos de la Visión , Adulto , Anciano , Anciano de 80 o más Años , China/epidemiología , Estudios de Cohortes , Femenino , Humanos , Estudios Longitudinales , Masculino , Modelos de Riesgos Proporcionales , Factores de Riesgo , Trastornos de la Visión/mortalidad
5.
6.
Artículo en Zh | MEDLINE | ID: mdl-21207686

RESUMEN

AIM: To explore the effects of acute and chronic hypoxia on brain mitochondrial transcription activity in vitro of rats. METHODS: Animal grouping: Wistar rats were randomized into acute hypoxic group (AH), chronic hypoxic group (CH) and the control. Mitochondrial transcription activity in vitro was measured in each group respectively as well as mitochondrial F0F1-ATPase activity, and effects of environmental ATP concentration on mitochondrial transcription activity in vitro was observed. RESULTS: Brain mitochondrial transcription activity and F0F1-ATPase activity were marked depressed in AH while partly reversed in CH, and they were linearly related. Mitochondrial transcription activity in vitro was affected by ATP concentration diphasely. CONCLUSION: Acute hypoxia may impair brain mitochondria energy metabolism by way of depressing mitochondrial transcription and then partially recover during chronic hypoxia. And mitochondrial transcription in vitro might be precisely regulated by ATP concentration.


Asunto(s)
Encéfalo/metabolismo , Hipoxia , Mitocondrias/metabolismo , ATPasas de Translocación de Protón Mitocondriales/metabolismo , Animales , Masculino , Ratas , Ratas Wistar , Transcripción Genética
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