Imperial College London, London W12 0NN, United Kingdom.
Pediatr Res. 2011 Nov;70(5):507-12. doi: 10.1203/PDR.0b013e31822d7860.
Our investigation addresses the hypothesis that disruption of third trimester development by preterm birth alters multiple biological pathways affecting metabolic health in adult life. We compared healthy adult volunteers aged 18-27 y born at ≤ 33 wk gestation or at term. We used whole-body MRI, (1)H magnetic resonance spectroscopy (MRS) of liver and muscle, metabonomic profiling of blood and urine, and anthropometric and blood pressure measurements. Preterm subjects had greater (mean difference (95% CI)) total [2.21 L (0.3, 4.1), p = 0.03] and abdominal adipose tissue [internal 0.51 (0.1, 0.9), p = 0.007]; blood pressure [systolic 6.5 mm Hg (2.2, 10.8), p = 0.004; diastolic 5.9 (1.8, 10.1), p = 0.006]; and ectopic lipid (ratio (95% CI)), intrahepatocellular lipid (IHCL) 3.01 (1.78, 5.28) p < 0.001, and tibialis-intramyocellular lipid (T-IMCL) [1.31 (1.02, 1.69) p = 0.04]. In preterm, compared with term men, there was greater internal adipose tissue [mean (SD); men: preterm 4.0 (1.6), term 2.7 (1.1) liters; women: preterm 2.6 (0.9); term 2.6 (0.5); gender-gestation interaction p = 0.048] and significant differences in the urinary metabolome (elevated methylamines and acetyl-glycoproteins, lower hippurate). We have identified multiple premorbid biomarkers in ex-preterm young adults, which are most marked in men and indicative of risks to later wellbeing. These data offer insight into biological trajectories affected by preterm birth and/or neonatal care.
我们的研究旨在验证这样一个假设,即早产会破坏妊娠晚期的发育,从而改变多个影响成年后代谢健康的生物学途径。我们比较了 18-27 岁的健康成年志愿者,他们分别出生于≤33 孕周或足月。我们使用全身 MRI、肝脏和肌肉的(1)H 磁共振波谱(MRS)、血液和尿液的代谢组学分析以及人体测量学和血压测量。与足月出生的人相比,早产儿的总体(平均差异(95%CI))和腹部脂肪组织更大[2.21L(0.3,4.1),p=0.03];血压更高[收缩压 6.5mmHg(2.2,10.8),p=0.004;舒张压 5.9mmHg(1.8,10.1),p=0.006];异位脂质(比值(95%CI)),肝内细胞内脂质(IHCL)3.01(1.78,5.28),p<0.001,和胫骨肌内细胞内脂质(T-IMCL)[1.31(1.02,1.69),p=0.04]。与足月出生的男性相比,在早产儿中,内部脂肪组织更多[平均值(SD);男性:早产儿 4.0(1.6),足月 2.7(1.1)升;女性:早产儿 2.6(0.9);足月 2.6(0.5);性别-胎龄交互作用 p=0.048],尿液代谢组也存在显著差异(甲基胺和乙酰糖蛋白升高, hippurate 降低)。我们已经在年轻的前早产儿中发现了多种潜在的生物标志物,这些标志物在男性中最为明显,表明存在对以后健康的风险。这些数据提供了关于受早产和/或新生儿护理影响的生物学轨迹的深入了解。