Department of Endocrinology, Shandong Provincial Hospital affiliated to Shandong University, Institute of Endocrinology and Metabolism, Shandong Academy of Clinical Medicine, Shandong Clinical Medical Center of Endocrinology and Metabolism, Jinan, Shandong 250021, China.
Department of Endocrinology, Shandong Provincial Hospital affiliated to Shandong University, Institute of Endocrinology and Metabolism, Shandong Academy of Clinical Medicine, Shandong Clinical Medical Center of Endocrinology and Metabolism, Jinan, Shandong 250021, China; Department of Biological Sciences, The University of Texas at Dallas, 800 W. Campbell Road, Richardson, TX 75080, USA.
Life Sci. 2019 Jul 1;228:215-220. doi: 10.1016/j.lfs.2019.04.033. Epub 2019 Apr 16.
Small-for-gestational-age (SGA) fetus is an important public health issue because of its high mortality and long-term effects on health. Maternal hyperuricemia is associated with diverse adverse pregnant outcomes and neonatal disturbance. We aimed to evaluate whether maternal hyper-uric acid (HUA) is associated with the risk of SGA fetus and to explore whether it can modify the association between maternal hyper-blood pressure (HBP) and SGA fetus.
We performed a population-based cross-section retrospective study, a total of 6715 pregnant females were recruited. Multiple logistic regression analysis was performed to identify risk factors significantly correlated with SGA fetus, and then studied the effect of maternal HUA on the association between maternal HBP and SGA fetus.
We collected 537 SGA fetuses among 6715 pregnant females. Maternal HUA was an independent risk factor for SGA delivery (odds ratio (OR), 2.737; 95% confidence interval (CI), 2.110-3.551). A dose-response association between maternal uric acid and SGA delivery was found among normotensive and hypertensive group. Compared with those whose uric acid was lower than 270 μmo/L with normal-blood pressure (NBP), the risk for SGA delivery in those whose uric acid was higher than 370 μmo/L with stage 2 or 3 hypertension increased 12.695-fold.
Our results suggest that maternal HUA could increase the risk of neonatal SGA, and maternal HUA could be superimposed upon pre-existing maternal HBP and increase the risk for SGA fetus.
胎儿小于胎龄(SGA)是一个重要的公共卫生问题,因为其具有较高的死亡率和对健康的长期影响。母体高尿酸血症与多种不良妊娠结局和新生儿紊乱有关。我们旨在评估母体高尿酸血症(HUA)是否与 SGA 胎儿的风险相关,并探讨其是否可以改变母体高血压(HBP)与 SGA 胎儿之间的关联。
我们进行了一项基于人群的横断面回顾性研究,共招募了 6715 名孕妇。采用多因素逻辑回归分析确定与 SGA 胎儿显著相关的危险因素,然后研究母体 HUA 对母体 HBP 与 SGA 胎儿之间关联的影响。
我们从 6715 名孕妇中收集了 537 例 SGA 胎儿。母体 HUA 是 SGA 分娩的独立危险因素(比值比(OR),2.737;95%置信区间(CI),2.110-3.551)。在正常血压和高血压组中均发现母体尿酸与 SGA 分娩之间存在剂量-反应关系。与正常血压(NBP)下尿酸低于 270μmol/L 的孕妇相比,2 或 3 期高血压下尿酸高于 370μmol/L 的孕妇发生 SGA 分娩的风险增加了 12.695 倍。
我们的研究结果表明,母体 HUA 可增加新生儿 SGA 的风险,且母体 HUA 可叠加于母体 HBP 之上,增加 SGA 胎儿的风险。