Department of Epidemiology, School of Public Health, Sun Yat-sen University, Guangzhou 510080, China.
Foshan Women and Children Hospital Affiliated to Southern Medical University, Foshan 528000, China.
Eur J Endocrinol. 2023 Jan 10;188(1). doi: 10.1093/ejendo/lvac019.
We aimed to investigate the associations between maternal fasting plasma glucose (FPG) levels and glycemic fluctuations during different trimesters and adverse birth outcomes among newborns.
This cohort study used data from 63 213 pregnant women and their offspring in Foshan city from November 2015 to January 2019. Associations between maternal FPG and glycemic fluctuations during different trimesters and adverse birth outcomes [congenital heart defect (CHD), macrosomia, small/large for gestational age (SGA/LGA), and preterm birth (PTB)] in newborns were estimated using mixed-effects logistic regression models.
A total of 45 516 participants accepted at least one FPG test throughout pregnancy, and 7852 of whom had glycemic trajectory data. In the adjusted model, higher maternal FPG throughout the pregnancy was associated with an increased risk of adverse birth outcomes (except for SGA). Each 1 mmol/L increase in maternal FPG during trimester 1 was associated with higher odds of CHD (OR = 1.14 (95% CI: 1.02, 1.26)). The same increase in maternal FPG during trimester 3 was associated with a higher risk of PTB (OR = 1.05 (95% CI: 1.01, 1.10)). Increment of maternal FPG during trimester 2 and trimester 3 was associated with a higher risk of macrosomia and LGA. Increase in FPG throughout the pregnancy was associated with slightly lower odds of SGA. Similar results were observed when analyzing the associations between glycemic fluctuations during different trimesters and adverse birth outcomes.
Our findings indicate higher maternal FPG levels during different trimesters were associated with different adverse birth outcomes, which suggests the importance of glycemic management throughout the pregnancy.
本研究旨在探讨孕妇不同孕期空腹血糖(FPG)水平及血糖波动与新生儿不良出生结局的关系。
本队列研究使用了 2015 年 11 月至 2019 年 1 月佛山市 63213 名孕妇及其后代的数据。采用混合效应逻辑回归模型,分析孕妇不同孕期 FPG 水平及血糖波动与新生儿不良出生结局(先天性心脏病(CHD)、巨大儿、胎儿大小与胎龄不符(SGA/LGA)及早产(PTB))的关系。
共有 45516 名参与者在整个孕期接受了至少一次 FPG 检测,其中 7852 名参与者有血糖轨迹数据。在调整后的模型中,整个孕期较高的 FPG 与不良出生结局的风险增加相关(除了 SGA)。孕期第 1 期 FPG 每增加 1mmol/L,患 CHD 的风险增加(OR=1.14(95%CI:1.02,1.26))。第 3 期 FPG 同样增加与 PTB 风险增加相关(OR=1.05(95%CI:1.01,1.10))。第 2 期和第 3 期 FPG 增加与巨大儿和 LGA 风险增加相关。整个孕期 FPG 增加与 SGA 风险降低相关。分析不同孕期血糖波动与不良出生结局的关系时,也观察到了类似的结果。
本研究结果表明,孕妇不同孕期 FPG 水平升高与不同的不良出生结局相关,这提示了整个孕期血糖管理的重要性。