Schlüter Daniela K, Keogh Ruth H, Daniel Rhian M, Agbla Schadrac C, Taylor-Robinson David
From the Department of Public Health, Policy and Systems, University of Liverpool, Liverpool, United Kingdom.
Department of Medical Statistics and Centre for Statistical Methodology, London School of Hygiene and Tropical Medicine, London, United Kingdom.
Epidemiology. 2025 Mar 1;36(2):275-285. doi: 10.1097/EDE.0000000000001826. Epub 2021 Dec 31.
Children with cystic fibrosis (CF) from socioeconomically deprived areas have poorer growth, worse lung function, and shorter life expectancy than their less-deprived peers. While early growth is associated with lung function around age 6, it is unclear whether improving early growth in the most deprived children reduces inequalities in lung function.
We used data from the UK CF Registry, tracking children born 2000-2010 up to 2016. We extended the interventional disparity effects approach to the setting of a longitudinally measured mediator. Applying this approach, we estimated the association between socioeconomic deprivation (children in the least vs. most deprived population quintile; exposure) and lung function at first measurement (ages 6-8, outcome), and the role of early weight trajectories (ages 0-6) as mediators of this relationship. We adjusted for baseline confounding by sex, birthyear, and genotype and time-varying intermediate confounding by lung infection.
The study included 853 children, with 165 children from the least and 172 from the most deprived quintiles. The average lung function difference between the least and most deprived quintiles was 4.5% of predicted forced expiratory volume in 1 second (95% confidence interval: 1.1-7.9). If the distribution of early weight trajectories in the most deprived children matched that in the least deprived children, this difference would reduce to 4% (95% confidence interval: 0.57- 7.4).
Socioeconomic deprivation has a strong negative association with lung function for children with CF. We estimate that improving early weight trajectories in the most deprived children would only marginally reduce these inequalities.
来自社会经济贫困地区的囊性纤维化(CF)患儿,相比贫困程度较低地区的同龄人,生长发育较差、肺功能更差且预期寿命更短。虽然早期生长与6岁左右的肺功能相关,但尚不清楚改善最贫困儿童的早期生长是否能减少肺功能方面的不平等。
我们使用了英国CF注册中心的数据,追踪2000年至2010年出生的儿童至2016年。我们将干预差异效应方法扩展到纵向测量中介变量的情况。应用此方法,我们估计了社会经济贫困程度(最贫困与最不贫困人群五分之一分组中的儿童;暴露因素)与首次测量时(6至8岁,结局)的肺功能之间的关联,以及早期体重轨迹(0至6岁)作为这种关系中介变量的作用。我们对性别、出生年份和基因型等基线混杂因素以及肺部感染等随时间变化的中间混杂因素进行了调整。
该研究纳入了853名儿童,其中165名来自最不贫困五分之一分组,172名来自最贫困五分之一分组。最不贫困与最贫困五分之一分组之间的平均肺功能差异为预测第一秒用力呼气量的4.5%(95%置信区间:1.1 - 7.9)。如果最贫困儿童的早期体重轨迹分布与最不贫困儿童的分布相匹配,这种差异将降至4%(95%置信区间:0.57 - 7.4)。
社会经济贫困与CF患儿的肺功能呈强烈负相关。我们估计,改善最贫困儿童的早期体重轨迹只会略微减少这些不平等。