Braun Lindsay M, Rodriguez Daniel A, Song Yan, Meyer Katie A, Lewis Cora E, Reis Jared P, Gordon-Larsen Penny
Department of City and Regional Planning, University of North Carolina at Chapel Hill.
Department of City and Regional Planning, University of California, Berkeley.
J Transp Health. 2016 Dec;3(4):426-439. doi: 10.1016/j.jth.2016.08.006. Epub 2016 Sep 13.
While many studies have found the built environment to be associated with walking, most have used cross-sectional research designs and few have examined more distal cardiometabolic outcomes. This study contributes longitudinal evidence based on changes in walking, body mass index (BMI), and cardiometabolic risk following residential relocation.
We examined 1,079 participants in the CARDIA study who moved residential locations between 2000 and 2006 (ages 32-46 in 2000, 49% white/51% black, 55% female). We created a walkability index from measures of population density, street connectivity, and food and physical activity resources, measured at participants' pre- and post-move residential locations. Outcomes measured before and after the move included walking, BMI, waist circumference, blood pressure, insulin resistance, triglycerides, cholesterol, atherogenic dyslipidemia, and C-reactive protein. Fixed effects (FE) models were used to estimate associations between within-person change in walkability and within-person change in each outcome. These estimates were compared to those from random effects (RE) models to assess the implications of unmeasured confounding.
In FE models, a one-SD increase in walkability was associated with a 0.81 mmHg decrease in systolic blood pressure [95% CI: (-1.55, -0.07)] and a 7.36 percent increase in C-reactive protein [95% CI: (0.60, 14.57)]. Although several significant associations were observed in the RE models, Hausman tests suggested that these estimates were biased for most outcomes. RE estimates were most commonly biased away from the null or in the opposite direction of effect as the FE estimates.
Greater walkability was associated with lower blood pressure and higher C-reactive protein in FE models, potentially reflecting competing health risks and benefits in dense, walkable environments. RE models tended to overstate or otherwise misrepresent the relationship between walkability and health. Approaches that base estimates on variation between individuals may be subject to bias from unmeasured confounding, such as residential self-selection.
虽然许多研究发现建筑环境与步行有关,但大多数研究采用的是横断面研究设计,很少有研究考察更远期的心脏代谢结局。本研究基于居住迁移后步行、体重指数(BMI)和心脏代谢风险的变化提供了纵向证据。
我们在CARDIA研究中考察了1079名在2000年至2006年间迁移居住地点的参与者(2000年年龄为32 - 46岁,49%为白人/51%为黑人,55%为女性)。我们根据在参与者迁移前后居住地点测量的人口密度、街道连通性以及食物和体育活动资源指标创建了一个步行适宜性指数。迁移前后测量的结局包括步行、BMI、腰围、血压、胰岛素抵抗、甘油三酯、胆固醇、致动脉粥样硬化血脂异常和C反应蛋白。使用固定效应(FE)模型来估计步行适宜性的个体内变化与每个结局的个体内变化之间的关联。将这些估计值与随机效应(RE)模型的估计值进行比较,以评估未测量混杂因素的影响。
在FE模型中,步行适宜性增加一个标准差与收缩压降低0.81 mmHg相关[95%置信区间:(-1.55,-0.07)],与C反应蛋白增加7.36%相关[95%置信区间:(0.60,14.57)]。虽然在RE模型中观察到了几个显著的关联,但豪斯曼检验表明,这些估计值对大多数结局存在偏差。RE估计值最常见的偏差是偏离零假设或与FE估计值的效应方向相反。
在FE模型中,更高的步行适宜性与更低的血压和更高的C反应蛋白相关,这可能反映了在密集、适宜步行的环境中存在相互竞争的健康风险和益处。RE模型倾向于夸大或以其他方式错误呈现步行适宜性与健康之间的关系。基于个体间差异进行估计的方法可能会受到未测量混杂因素(如居住自我选择)的偏差影响。