...
首页> 外文期刊>BMJ Open >IFN production ability and healthy ageing: mixed model analysis of a 24?year longitudinal study in Japan
【24h】

IFN production ability and healthy ageing: mixed model analysis of a 24?year longitudinal study in Japan

机译:干扰素生产能力与健康老龄化:日本24年纵向研究的混合模型分析

获取原文
           

摘要

Objective To track changes in interferon (IFN) production in healthy individuals to shed light on the effect these changes have on the course of healthy ageing. Design Study is based on data that were collected over 24?years from a cohort of individuals whose IFN-α production was quantified as a part of their annual routine health check-up. Setting All individuals in this study underwent regular health check-ups at Louis Pasteur Center for Medical Research. Participants 295 healthy individuals (159 males and 136 females) without a history of cancer, autoimmune diseases and hepatitis C virus (HCV) whose IFN-α production was quantified more than five times within 24?years were selected. Finally, 29 males and 4 females whose IFN-α production was quantified more than 25 times were selected and their data were analysed using a mixed model. Main outcome measures HVJ stimulated IFN-α ?production was quantified. Healthy individual's periodical log transformed IFN-α values (y) were plotted versus age (x) and fitted to linear (y=mx+n) and quadratic formula (y=ax2+bx+c) expressions to reveal changes in the IFN-α ?production in these healthy individuals. Results The linear expression showed that log (IFN-α) had a slight tendency to decline (3% over 10?years). However, the quadratic formula analysis showed the quadratic expression to be more positive than negative (a concave U-shaped pattern) which means that individuals’ once declining IFN production recovered as they aged. Conclusions Although we observed a marginal decline in IFN-α ?production, we also observed that IFN production recovered even in individuals in their mid50s to early 60s. These results combined with our previous cross-sectional studies of patients with various diseases suggest that in healthy individuals, the impairment of IFN production is triggered more by the onset of disease (notwithstanding the cause) rather than by ageing.
机译:目的追踪健康个体中干扰素(IFN)产生的变化,以阐明这些变化对健康衰老过程的影响。设计研究的依据是24年来从一组人群中收集的数据,这些人群的IFN-α产生被量化为年度例行健康检查的一部分。设置本研究的所有个体均在Louis Pasteur医学研究中心进行定期健康检查。参加者295名健康人(男性159名,女性136名)没有癌症,自身免疫性疾病和丙型肝炎病毒(HCV)的病史,他们在24年内对IFN-α的产生进行了超过5次定量。最后,选择29例雄性和4例雌性,将其IFN-α产生定量超过25次,并使用混合模型分析其数据。量化HVJ刺激IFN-α产生的主要结局指标。绘制健康个体的定期对数转换的IFN-α值(y)对年龄(x)的图,并拟合线性(y = mx + n)和二次公式(y = ax 2 + bx + c)表达以揭示这些健康个体中IFN-α产生的变化。结果线性表达表明,log(IFN-α)略有下降趋势(10年内下降3%)。但是,二次方分析显示二次方的表达比负方的表达更积极(凹U形图案),这意味着随着年龄的增长,曾经下降的IFN产生量会恢复。结论尽管我们观察到IFN-α的产生量略有下降,但我们也观察到即使在50年代中期至60年代初的个体中,IFN的产生也得以恢复。这些结果与我们先前对各种疾病患者的横断面研究相结合,表明在健康个体中,IFN产生的损伤更多是由疾病的发作(尽管有病因)而不是衰老引起的。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号