McKeating Daniel R, Clifton Vicki L, Hurst Cameron P, Fisher Joshua J, Bennett William W, Perkins Anthony V
School of Medical Science, Griffith University, Gold Coast Campus, Parklands Drive, Southport, QLD, 4215, Australia.
Pregnancy and Development, Mater Research Institute-University of Queensland, Translational Research Institute, South Brisbane, Australia.
Biol Trace Elem Res. 2021 Jan;199(1):26-40. doi: 10.1007/s12011-020-02127-6. Epub 2020 Apr 1.
A normal pregnancy is essential to establishing a healthy start to life. Complications during have been associated with adverse perinatal outcomes and lifelong health problems. The ability to identify risk factors associated with pregnancy complications early in gestation is vitally important for preventing negative foetal outcomes. Maternal nutrition has been long considered vital to a healthy pregnancy, with micronutrients and trace elements heavily implicated in maternofoetal metabolism. This study proposed the use of elemental metabolomics to study multiple elements at 18 weeks gestation from blood plasma and urine to construct models that could predict outcomes such as small for gestational age (SGA) (n = 10), low placental weight (n = 18), and preterm birth (n = 13) from control samples (n = 87). Samples collected from the Lyell McEwin Hospital in Adelaide, South Australia, were measured for 27 plasma elements and 37 urine elements by inductively coupled plasma mass spectrometry. Exploratory analysis indicated an average selenium concentration 20 μg/L lower than established reference ranges across all groups, low zinc in preterm (0.64 μg/L, reference range 0.66-1.10 μg/L), and higher iodine in preterm and SGA gestations (preterm 102 μg/L, SGA 111 μg/L, reference range 40-92 μg/L). Using random forest algorithms with receiver operating characteristic curves, low placental weight was predicted with 86.7% accuracy using plasma, 78.6% prediction for SGA with urine, and 73.5% determination of preterm pregnancies. This study indicates that elemental metabolomic modelling could provide a means of early detection of at-risk pregnancies allowing for more targeted monitoring of mothers, with potential for early intervention strategies to be developed.
正常妊娠对于开启健康的人生起点至关重要。孕期并发症与不良围产期结局及终身健康问题相关。在妊娠早期识别与妊娠并发症相关的风险因素对于预防不良胎儿结局至关重要。长期以来,母体营养一直被认为对健康妊娠至关重要,微量营养素和微量元素在母胎代谢中起着重要作用。本研究提议使用元素代谢组学方法,在妊娠18周时从血浆和尿液中研究多种元素,以构建能够从对照样本(n = 87)中预测诸如小于胎龄儿(SGA)(n = 10)、低胎盘重量(n = 18)和早产(n = 13)等结局的模型。从南澳大利亚阿德莱德的莱尔·麦克尤恩医院收集的样本,通过电感耦合等离子体质谱法测定了27种血浆元素和37种尿液元素。探索性分析表明,所有组的平均硒浓度比既定参考范围低20μg/L,早产组锌含量低(0.64μg/L,参考范围0.66 - 1.10μg/L),早产和SGA妊娠组碘含量较高(早产组102μg/L,SGA组111μg/L,参考范围40 - 92μg/L)。使用具有受试者工作特征曲线的随机森林算法,使用血浆预测低胎盘重量的准确率为86.7%,使用尿液预测SGA的准确率为78.6%,确定早产妊娠的准确率为73.5%。本研究表明,元素代谢组学建模可为早期检测高危妊娠提供一种方法,从而对母亲进行更有针对性的监测,并有可能制定早期干预策略。