Wang Linda X, Filipp Stephanie L, Urbina Elaine M, Gurka Matthew J, DeBoer Mark D
1 Department of Pediatrics, University of Virginia , Charlottesville, Virginia.
2 Department of Health Outcomes and Policy, College of Medicine, University of Florida , Gainesville, Florida.
Metab Syndr Relat Disord. 2018 Jun;16(5):208-214. doi: 10.1089/met.2017.0160. Epub 2018 Mar 27.
Childhood metabolic syndrome (MetS) is associated with insulin resistance and increased risk for later development of type 2 diabetes (T2DM) and cardiovascular disease (CVD). In using MetS severity z-scores, our objective was to assess longitudinal associations in MetS severity, fasting insulin levels as a sign of insulin resistance and risk for T2DM, and uric acid levels as a biomarker of oxidative stress leading to CVD.
We used linear regression to analyze longitudinal data from 285 white and black participants from the Bogalusa Heart Study evaluated at baseline at ages 5-19 and as young adults after a mean of 12.0 years follow-up. We assessed correlations between childhood MetS severity and young-adult MetS severity, fasting insulin, and uric acid levels, both overall and by sex- and racial subgroups.
Overall, childhood MetS z-scores were positively associated with young-adult MetS z-scores (r = 0.52), insulin (r = 0.34), and uric acid (r = 0.28) (all P < 0.001). These associations were consistent across all sex- and racial subgroups, except for young adult uric acid in white males in which childhood MetS-z was not associated (r = 0.15, P = 0.243). There was a strong cross-sectional association of young-adult MetS z-scores with insulin (r = 0.70) and uric acid (r = 0.57) (both P < 0.001), which was consistent for all sex- and racial subgroups.
These positive longitudinal correlations between childhood MetS z-scores and markers of later insulin resistance and oxidative stress suggest long-term durability of risk for CVD and T2DM. This suggests potential for MetS severity to serve as an indicator to monitor for future risk of T2DM and CVD.
儿童代谢综合征(MetS)与胰岛素抵抗相关,且会增加日后患2型糖尿病(T2DM)和心血管疾病(CVD)的风险。我们使用MetS严重程度z评分,目的是评估MetS严重程度、作为胰岛素抵抗标志的空腹胰岛素水平及T2DM风险,以及作为导致CVD的氧化应激生物标志物的尿酸水平之间的纵向关联。
我们使用线性回归分析来自博加卢萨心脏研究的285名白人和黑人参与者的纵向数据,这些参与者在5至19岁时进行了基线评估,并在平均12.0年的随访后作为年轻人进行了评估。我们评估了儿童期MetS严重程度与青年期MetS严重程度、空腹胰岛素和尿酸水平之间的相关性,包括总体相关性以及按性别和种族亚组的相关性。
总体而言,儿童期MetS z评分与青年期MetS z评分(r = 0.52)、胰岛素(r = 0.34)和尿酸(r = 0.28)呈正相关(均P < 0.001)。除白人男性青年期尿酸外,这些关联在所有性别和种族亚组中均一致,在白人男性中儿童期MetS - z与青年期尿酸无关联(r = 0.15,P = 0.243)。青年期MetS z评分与胰岛素(r = 0.70)和尿酸(r = 0.57)存在很强的横断面关联(均P < 0.001),这在所有性别和种族亚组中均一致。
儿童期MetS z评分与后期胰岛素抵抗和氧化应激标志物之间的这些正纵向相关性表明CVD和T2DM风险具有长期持续性。这表明MetS严重程度有可能作为监测T2DM和CVD未来风险的指标。