Department of Medicine, Feinberg School of Medicine, Northwestern University, Chicago, Illinois 60611, USA.
Pediatrics. 2010 Dec;126(6):e1545-52. doi: 10.1542/peds.2009-2257. Epub 2010 Nov 15.
The goal was to describe the temporal pattern of neonatal plasma glucose levels and associations with maternal glucose levels, cord serum C-peptide levels, and neonatal size and adiposity.
A total of 17,094 mothers and infants were included in the Hyperglycemia and Adverse Pregnancy Outcome Study (15 centers in 9 countries). Mothers underwent a 75-g, 2-hour, oral glucose tolerance test (OGTT) at 24 to 32 weeks of gestation. Cord blood and neonatal blood samples were collected. Biochemical neonatal hypoglycemia was defined as glucose levels of <10th percentile (2.2 mmol/L). Clinically identified hypoglycemia was ascertained through medical record review and associations were assessed.
Plasma glucose concentrations were stable during the first 5 hours after birth. Maternal glucose levels were weakly positively associated with biochemical neonatal hypoglycemia (odds ratios: 1.07-1.14 for 1-SD higher OGTT glucose levels). Frequency of neonatal hypoglycemia was higher with higher cord C-peptide levels (odds ratio: 11.6 for highest versus lowest C-peptide category). Larger and/or fatter infants were more likely to have hypoglycemia (P < .001), and infants with hypoglycemia tended to have a higher frequency of cord C-peptide levels of >90th percentile.
Mean neonatal plasma glucose concentrations varied little in the first 5 hours after birth, which suggests normal postnatal adjustment. Biochemical and clinical hypoglycemia were weakly related to maternal OGTT glucose measurements but were strongly associated with elevated cord serum C-peptide levels. Larger and/or fatter infants were more likely to develop hypoglycemia and hyperinsulinemia. These relationships suggest physiologic relationships between maternal glycemia and fetal insulin production.
描述新生儿血浆葡萄糖水平的时间模式,并探讨其与母体血糖水平、脐血清 C 肽水平以及新生儿大小和肥胖的关系。
共有 17094 名母亲及其婴儿纳入高血糖与不良妊娠结局研究(9 个国家的 15 个中心)。母亲在妊娠 24 至 32 周时进行 75g、2 小时口服葡萄糖耐量试验(OGTT)。采集脐血和新生儿血样。生化新生儿低血糖定义为血糖水平<第 10 百分位数(2.2mmol/L)。通过病历回顾确定临床诊断的低血糖,并评估其相关性。
新生儿出生后 5 小时内血糖浓度稳定。母体血糖水平与生化新生儿低血糖呈弱正相关(OGTT 血糖水平每升高 1 个标准差,比值比为 1.07-1.14)。脐血 C 肽水平越高,新生儿低血糖的发生率越高(最高与最低 C 肽类别相比,比值比为 11.6)。较大和/或较胖的婴儿发生低血糖的可能性更高(P<.001),且低血糖婴儿的脐血 C 肽水平>第 90 百分位数的频率更高。
新生儿出生后 5 小时内平均血浆葡萄糖浓度变化不大,提示正常的产后调节。生化和临床低血糖与母体 OGTT 血糖测量值呈弱相关,但与脐血清 C 肽水平升高密切相关。较大和/或较胖的婴儿更有可能发生低血糖和高胰岛素血症。这些关系提示母体血糖与胎儿胰岛素产生之间存在生理关系。