首页> 外文期刊>PLoS One >Association between GDF15, poverty and mortality in urban middle-aged African American and white adults
【24h】

Association between GDF15, poverty and mortality in urban middle-aged African American and white adults

机译:GDF15与城市中年非裔美国人和白人成年人的贫困和死亡率之间的关联

获取原文
获取外文期刊封面目录资料

摘要

Mortality disparities are influenced by race and poverty. There is limited information about whether poverty influences biologic markers of mortality risk. Emerging data suggests that growth differentiation factor 15 (GDF15) is associated with mortality; however, the interplay between GDF15, sociodemographic factors and mortality is not known. We sought to evaluate the interactions between GDF15 and sex, race and poverty status on mortality. Serum GDF15 was measured in 1036 African American and white middle-aged men and women above and below 125% of the Federal poverty status from the Healthy Aging in Neighborhoods of Diversity across the Life Span (HANDLS) study. Multivariable adjusted Cox regression models were used to assess the association between log-transformed GDF15 (logGDF15) and 12-year mortality outcomes (all-cause, cardiovascular- and cancer-specific outcomes) and interactions with sex, race and poverty status. Likelihood ratio tests were used to assess significance of the interaction terms. Median GDF15 was 655.2 pg/mL (IQR = 575.1). During 12.2 years of follow-up, 331 died of which 94 cardiovascular- and 87 were cancer-specific deaths. One unit of increase in logGDF15 was associated with a hazard ratio for all-cause mortality, cardiovascular- and cancer-specific mortality of 2.26 (95% confidence interval [CI], 1.94–2.64), 2.74 (95%CI, 2.06–3.63) and 1.41 (95%CI, 1.00–2.00), respectively. There was an interaction between logGDF15 and poverty status on all-cause mortality (p0.05). The GDF15×poverty status interaction term improved model calibration for all-cause mortality. Our study provides the first evidence that the effect of elevated GDF15 on all-cause mortality is modified by poverty status.
机译:死亡率差距受到种族和贫困的影响。有关贫困是否影响死亡率风险的生物学标志的信息有限。新兴数据表明,生长分化因子15(GDF15)与死亡率有关;但是,GDF15之间的相互作用是不知道的。我们试图评估GDF15与性别,种族和贫困地位对死亡率之间的互动。血清GDF15在1036名非裔美国人和白色中年男性和女性中测量,低于联邦扶贫125%的125%,来自寿命跨越的多样性邻近的健康老龄化(Handls)研究。多变量调整的Cox回归模型用于评估日志转化的GDF15(LOMGDF15)和12年死亡率结果(全因,心血管和癌症的结果)之间的关联和与性别,种族和贫困地位的相互作用。似然比测试用于评估相互作用术语的重要性。中位数GDF15为655.2 pg / ml(IQR = 575.1)。在12.2年的随访期间,331人死于其中94个心血管 - 87个是癌症的死亡。 LogGDF15的一个增加单位与2.26(95%置信区间[CI],1.94-2.64),2.74(95%CI,2.06-3.63的危险性的危险比分别为1.41(95%CI,1.00-2.00)。 LOGGDF15与全因死亡率的贫困状态之间存在相互作用(P <0.05)。 GDF15×贫困状态交互术语改进了全导致死亡率的模型校准。我们的研究提供了第一种证据,即GDF15升高的GDF15对所有原因死亡率的影响是通过扶贫改变的。

著录项

相似文献

  • 外文文献
  • 中文文献
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