Nagel Emily M, Peña Armando, Dreyfuss Jonathan M, Lock Eric F, Johnson Kelsey E, Lu Chang, Fields David A, Demerath Ellen W, Isganaitis Elvira
School of Public Health, University of Minnesota, Twin Cities.
Department of Pediatrics, University of Minnesota, Minneapolis.
JAMA Netw Open. 2024 Dec 2;7(12):e2450467. doi: 10.1001/jamanetworkopen.2024.50467.
Gestational diabetes (GD) is linked to health risks for the birthing parent and infant. The outcomes of GD on human milk composition are mostly unknown.
To determine associations between GD, the human milk metabolome, and infant growth and body composition.
DESIGN, SETTING, AND PARTICIPANTS: Cohort study using data from the Mothers and Infants Linked for Healthy Growth and the Maternal Milk, Metabolism, and the Microbiome studies at the University of Oklahoma and University of Minnesota, large prospective US cohorts with a high proportion of exclusive breastfeeding. Participants were mother-infant dyads recruited between October 2014 and August 2019 who planned to exclusively breastfeed for 3 or more months. Data were analyzed from July 2022 to August 2024.
GD diagnosed via oral glucose tolerance test.
The milk metabolome was assessed by untargeted liquid chromatography-gas chromatography-mass spectrometry at 1 month post partum. Infant growth (weight for length z score, length for age z score, and rapid weight gain) and body composition (percentage body fat and fat-free mass index) from 0 to 6 months were assessed. Linear regression analyses tested associations between GD and milk metabolites, with adjustment for covariates and potential confounders.
Among 348 dyads (53 with GD), 27 (51%) of the GD-exposed infants were female and 157 (53%) of nonexposed infants were male; 10 (19%) were Asian, 2 (4%) were Black or African American, and 37 (70%) were White. The mean (SD) age was higher in the GD group (with GD, 34.0 [4.3] years; without GD, 30.7 [4.1] years). In adjusted models, GD was associated with differential levels of 9 metabolites of 458 tested (FDR<0.05); 3 were higher (2-hydroxybutyric acid, 3-methylphenylacetic acid, and pregnanolone sulfate) and 6 were lower in women with GD (4-cresyl sulfate, cresol, glycine, P-cresol sulfate, phenylacetic acid, and stearoylcarnitine). Phenylacetic acid was associated with length for age z score (β = 0.27; SE, 0.13; 95% CI, 0.02 to 0.16), 2-hydroxybutryic acid with percentage body fat (β = -1.50; SE, 0.66; 95% CI, -2.79 to -4.82), and stearoylcarnitine with greater odds of rapid weight gain (odds ratio, 1.66; 95% CI, 1.23 to 2.25). GD was associated with greater length for age z scores (β = 0.48; SE, 0.22; 95% CI, 0.04 to 0.91).
In this observational cohort study, GD was associated with altered concentrations of several human milk metabolites. The associations between these metabolites and infant growth suggest that milk compositional differences in mothers with GD may beneficially moderate the growth and body composition of their infants.
妊娠期糖尿病(GD)与分娩者及婴儿的健康风险相关。GD对母乳成分的影响大多未知。
确定GD、母乳代谢组以及婴儿生长和身体成分之间的关联。
设计、背景和参与者:队列研究,使用来自俄克拉荷马大学和明尼苏达大学的“母婴健康成长关联研究”以及“母乳、代谢与微生物组研究”的数据,这是美国大型前瞻性队列研究,纯母乳喂养比例较高。参与者为2014年10月至2019年8月招募的母婴二元组,计划纯母乳喂养3个月或更长时间。数据于2022年7月至2024年8月进行分析。
通过口服葡萄糖耐量试验诊断的GD。
产后1个月采用非靶向液相色谱 - 气相色谱 - 质谱法评估母乳代谢组。评估0至6个月婴儿的生长情况(身长体重Z评分、年龄身长Z评分和快速体重增加)和身体成分(体脂百分比和去脂体重指数)。线性回归分析检验GD与母乳代谢物之间的关联,并对协变量和潜在混杂因素进行调整。
在348个二元组(53个患有GD)中,暴露于GD的婴儿中有27个(51%)为女性,未暴露的婴儿中有157个(53%)为男性;10个(19%)为亚洲人,2个(4%)为黑人或非裔美国人,37个(70%)为白人。GD组的平均(标准差)年龄较高(患有GD的为34.0 [4.3]岁;未患GD的为30.7 [4.1]岁)。在调整模型中,GD与458种检测代谢物中的9种代谢物水平差异相关(FDR<0.05);患有GD的女性中有3种代谢物水平较高(2 - 羟基丁酸、3 - 甲基苯乙酸和孕烷醇硫酸盐),6种代谢物水平较低(4 - 甲酚硫酸盐、甲酚、甘氨酸、对甲酚硫酸盐、苯乙酸和硬脂酰肉碱)。苯乙酸与年龄身长Z评分相关(β = 0.27;标准误,0.13;95%置信区间,0.02至0.16),2 - 羟基丁酸与体脂百分比相关(β = -1.50;标准误,0.66;95%置信区间,-2.79至-4.82),硬脂酰肉碱与快速体重增加几率较高相关(优势比,1.66;95%置信区间,1.23至2.25)。GD与年龄身长Z评分较高相关(β = 0.48;标准误,0.22;95%置信区间,0.04至0.91)。
在这项观察性队列研究中,GD与几种母乳代谢物浓度的改变相关。这些代谢物与婴儿生长之间的关联表明,患有GD的母亲的母乳成分差异可能对其婴儿的生长和身体成分产生有益的调节作用。