Clinical Research Centre, Copenhagen University Hospital Amager and Hvidovre, Hvidovre, Denmark.
Department of Psychology and Neuroscience, Duke University, Durham, NC, USA.
J Child Psychol Psychiatry. 2019 Feb;60(2):199-208. doi: 10.1111/jcpp.12928. Epub 2018 May 9.
Childhood risk factors are associated with elevated inflammatory biomarkers in adulthood, but it is unknown whether these risk factors are associated with increased adult levels of the chronic inflammation marker soluble urokinase plasminogen activator receptor (suPAR). We aimed to test the hypothesis that childhood exposure to risk factors for adult disease is associated with elevated suPAR in adulthood and to compare suPAR with the oft-reported inflammatory biomarker C-reactive protein (CRP).
Prospective study of a population-representative 1972-1973 birth cohort; the Dunedin Multidisciplinary Health and Development Study observed participants to age 38 years. Main childhood predictors were poor health, socioeconomic disadvantage, adverse childhood experiences (ACEs), low IQ, and poor self-control. Main adult outcomes were adulthood inflammation measured as suPAR and high-sensitivity CRP (hsCRP).
Participants with available plasma samples at age 38 were included (N = 837, 50.5% male). suPAR (mean 2.40 ng/ml; SD 0.91) was positively correlated with hsCRP (r 0.15, p < .001). After controlling for sex, body mass index (BMI), and smoking, children who experienced more ACEs, lower IQ, or had poorer self-control showed elevated adult suPAR. When the five childhood risks were aggregated into a Cumulative Childhood Risk index, and controlling for sex, BMI, and smoking, Cumulative Childhood Risk was associated with higher suPAR (b 0.10; SE 0.03; p = .002). Cumulative Childhood Risk predicted elevated suPAR, after controlling for hsCRP (b 0.18; SE 0.03; p < .001).
Exposure to more childhood risk factors was associated with higher suPAR levels, independent of CRP. suPAR is a useful addition to studies connecting childhood risk to adult inflammatory burden.
儿童时期的风险因素与成年后炎症生物标志物水平升高有关,但尚不清楚这些风险因素是否与成年后慢性炎症标志物可溶性尿激酶型纤溶酶原激活物受体(suPAR)水平升高有关。我们旨在检验以下假设,即成年期疾病的儿童期危险因素暴露与成年后 suPAR 水平升高有关,并将 suPAR 与常报道的炎症生物标志物 C 反应蛋白(CRP)进行比较。
对具有代表性的 1972-1973 年出生队列进行前瞻性研究;达尼丁多学科健康与发展研究观察参与者至 38 岁。主要的儿童期预测因素包括健康状况不佳、社会经济劣势、不良的童年经历(ACEs)、低智商和自我控制能力差。主要的成年期结局是用 suPAR 和高敏 C 反应蛋白(hsCRP)来衡量的成年期炎症。
纳入了在 38 岁时有可用血浆样本的参与者(N=837,50.5%为男性)。suPAR(平均 2.40ng/ml;SD 0.91)与 hsCRP 呈正相关(r=0.15,p<0.001)。在控制了性别、体重指数(BMI)和吸烟因素后,经历更多 ACEs、智商较低或自我控制能力较差的儿童,其成年后 suPAR 水平升高。当将五种儿童时期的风险因素汇总为累积儿童期风险指数,并控制性别、BMI 和吸烟因素后,累积儿童期风险与较高的 suPAR 相关(b=0.10;SE=0.03;p=0.002)。在控制 hsCRP 后,累积儿童期风险预测了 suPAR 的升高(b=0.18;SE=0.03;p<0.001)。
暴露于更多的儿童期风险因素与 suPAR 水平升高有关,这与 CRP 无关。suPAR 是将儿童期风险与成年期炎症负担联系起来的研究的有用补充。