Guiney Hayley, Walker Robert, Broadbent Jonathan, Caspi Avshalom, Goodin Elizabeth, Kokaua Jesse, Moffitt Terrie E, Robertson Stephen, Theodore Reremoana, Poulton Richie, Endre Zoltan
Department of Psychology, Dunedin Multidisciplinary Health and Development Research Unit, University of Otago, Dunedin, New Zealand.
Department of Medicine, Otago Medical School, University of Otago, Dunedin, New Zealand.
Kidney Int Rep. 2022 Oct 11;8(1):51-63. doi: 10.1016/j.ekir.2022.10.005. eCollection 2023 Jan.
Understanding normative patterns of change in kidney function over the life course may allow targeting of early interventions to slow or prevent the onset of kidney disease, but knowledge about kidney functional change before middle age is limited. This study used prospective longitudinal data from a representative birth cohort to examine common patterns of change from young to midadulthood and to identify risk factors and outcomes associated with poorer trajectories.
We used group-based trajectory modeling in the Dunedin study birth cohort ( = 857) to identify the following: (i) common kidney function trajectories between the ages 32 and 45 years, (ii) early-life factors associated with those trajectories, (iii) modifiable physical and psychosocial factors across adulthood associated with differences in trajectory slope, and (iv) links between trajectories and kidney-related outcomes at age 45 years.
Three trajectory groups were identified and could be differentiated by age 32 years as follows: normal (58% of participants), low-normal (36%), and high-risk (6%) groups. Those from low socioeconomic backgrounds had higher odds of following a high-risk (vs. normal) trajectory. Modifiable factors (blood pressure, body mass index, inflammation, glycated hemoglobin, smoking, and socioeconomic status) across adulthood were associated with steeper age-related declines in kidney function, particularly among those in the low-normal and high-risk groups. Those in the low-normal and high-risk groups also had more adverse kidney-related outcomes at age 45 years.
The current findings could be used to inform the development of early interventions and point to socioeconomic conditions across the life course and health-related risk factors and behaviors in adulthood as kidney health promotion targets.
了解肾功能在生命过程中的正常变化模式,可能有助于确定早期干预措施,以减缓或预防肾脏疾病的发生,但中年之前肾脏功能变化的相关知识有限。本研究使用来自一个具有代表性出生队列的前瞻性纵向数据,来研究从青年到中年时期肾功能变化的常见模式,并确定与较差轨迹相关的风险因素和结果。
我们在达尼丁研究出生队列(n = 857)中使用基于组的轨迹模型来确定以下内容:(i)32岁至45岁之间的常见肾功能轨迹;(ii)与这些轨迹相关的早期生活因素;(iii)成年期可改变的身体和心理社会因素与轨迹斜率差异的关联;(iv)轨迹与45岁时肾脏相关结果之间的联系。
确定了三个轨迹组,到32岁时可区分如下:正常组(58%的参与者)、低正常组(36%)和高危组(6%)。社会经济背景较低的人遵循高危(相对于正常)轨迹的几率更高。成年期可改变的因素(血压、体重指数、炎症、糖化血红蛋白、吸烟和社会经济地位)与肾功能随年龄增长的下降幅度更大有关,尤其是在低正常组和高危组中。低正常组和高危组的人在45岁时也有更多不良的肾脏相关结果。
目前的研究结果可用于指导早期干预措施的制定,并指出生命过程中的社会经济状况以及成年期与健康相关的风险因素和行为,作为促进肾脏健康的目标。