College of Public Health, University of South Florida, Tampa, FL, USA.
Division of Chronic Disease Research Across the Lifecourse, Department of Population Medicine, Harvard Medical School and Harvard Pilgrim Health Care Institute, Boston, MA, USA.
J Dev Orig Health Dis. 2023 Feb;14(1):88-95. doi: 10.1017/S2040174422000381. Epub 2022 Jul 8.
Exposure to maternal hyperglycemia has been associated with adverse metabolic outcomes in offspring. However, few studies have investigated the relationship between maternal hyperglycemia and offspring cortisol levels. We assessed associations of gestational diabetes mellitus (GDM) with cortisol biomarkers in two longitudinal prebirth cohorts: Project Viva included 928 mother-child pairs and Gen3G included 313 mother-child pairs. In Project Viva, GDM was diagnosed in N = 48 (5.2%) women using a two-step procedure (50 g glucose challenge test, if abnormal followed by 100 g oral glucose tolerance test [OGTT]), and in N = 29 (9.3%) women participating in Gen3G using one-step 75 g OGTT. In Project Viva, we measured cord blood glucocorticoids and child hair cortisol levels during mid-childhood (mean (SD) age: 7.8 (0.8) years) and early adolescence (mean (SD) age: 13.2 (0.9) years). In Gen3G, we measured hair cortisol at 5.4 (0.3) years. We used multivariable linear regression to examine associations of GDM with offspring cortisol, adjusting for child age and sex, maternal prepregnancy body mass index, education, and socioeconomic status. We additionally adjusted for child race/ethnicity in the cord blood analyses. In both Project Viva and Gen3G, we observed null associations of GDM and maternal glucose markers in pregnancy with cortisol biomarkers in cord blood at birth (β = 16.6 nmol/L, 95% CI -60.7, 94.0 in Project Viva) and in hair samples during childhood (β = -0.56 pg/mg, 95% CI -1.16, 0.04 in Project Viva; β = 0.09 pg/mg, 95% CI -0.38, 0.57 in Gen3G). Our findings do not support the hypothesis that maternal hyperglycemia is related to hypothalamic-pituitary-adrenal axis activity.
母体高血糖与后代不良代谢结局有关。然而,很少有研究调查母体高血糖与后代皮质醇水平之间的关系。我们评估了妊娠糖尿病(GDM)与两个纵向产前队列中皮质醇生物标志物的关系:Viva 项目包括 928 对母婴对,Gen3G 包括 313 对母婴对。在 Viva 项目中,通过两步程序(50g 葡萄糖挑战测试,如果异常,则进行 100g 口服葡萄糖耐量测试[OGTT])诊断了 N = 48(5.2%)名女性的 GDM,而在 Gen3G 中,通过一步 75g OGTT 诊断了 N = 29(9.3%)名女性的 GDM。在 Viva 项目中,我们测量了脐带血糖皮质激素和儿童头发皮质醇水平,在儿童中期(平均(SD)年龄:7.8(0.8)岁)和青少年早期(平均(SD)年龄:13.2(0.9)岁)。在 Gen3G 中,我们在 5.4(0.3)岁时测量了头发皮质醇。我们使用多变量线性回归来检查 GDM 与后代皮质醇的关系,调整了儿童年龄和性别、母亲孕前体重指数、教育程度和社会经济地位。我们还在脐带血分析中调整了儿童种族/民族。在 Viva 项目和 Gen3G 中,我们观察到 GDM 和妊娠期间母体葡萄糖标志物与出生时脐带血皮质醇生物标志物(Viva 项目中为 16.6nmol/L,95%CI-60.7,94.0)和儿童期头发样本中的皮质醇生物标志物(Viva 项目中为-0.56pg/mg,95%CI-1.16,0.04;Gen3G 中为 0.09pg/mg,95%CI-0.38,0.57)之间没有关联。我们的研究结果不支持母体高血糖与下丘脑-垂体-肾上腺轴活动有关的假设。