Department of Preventive Medicine, College of Medicine, University of Tennessee Health Science Center, Memphis, TN, USA.
Medicinal Chemistry Core, Office of Research, University of Tennessee Health Science Center, Memphis, TN, USA; Department of Pharmaceutical Science, College of Pharmacy, University of Tennessee Health Science Center, Memphis, TN, USA.
Am J Clin Nutr. 2022 Nov;116(5):1343-1353. doi: 10.1093/ajcn/nqac244. Epub 2023 Feb 10.
Maternal prepregnancy obesity is an important risk factor for offspring obesity, which may partially operate through prenatal programming mechanisms.
The study aimed to systematically identify prenatal metabolomic profiles mediating the intergenerational transmission of obesity.
We included 450 African-American mother-child pairs from the Conditions Affecting Neurocognitive Development and Learning in Early Childhood (CANDLE) Study pregnancy cohort. LC-MS was used to conduct metabolomic profiling on maternal plasma samples of the second trimester. The childhood growth outcomes of interest included BMI trajectories from birth to age 4 y (rising-high-, moderate-, and low-BMI trajectories) as well as overweight/obesity (OWO) risk at age 4 y. Mediation analysis was conducted to identify metabolite mediators linking maternal OWO and childhood growth outcomes. The potential causal effects of maternal OWO on metabolite mediators were examined using the Mendelian randomization (MR) method.
Among the 880 metabolites detected in the maternal plasma during pregnancy, 14 and 11 metabolites significantly mediated the effects of maternal prepregnancy OWO on childhood BMI trajectories and the OWO risk at age 4 y, respectively, and 5 mediated both outcomes. The MR analysis suggested 6 of the 20 prenatal metabolite mediators might be causally influenced by maternal prepregnancy OWO, most of which are from the pathways related to the metabolism of amino acids (hydroxyasparagine, glutamate, and homocitrulline), sterols (campesterol), and nucleotides (N2,N2-dimethylguanosine).
Our study provides further evidence that prenatal metabolomic profiles might mediate the effect of maternal OWO on early childhood growth trajectories and OWO risk in offspring. The metabolic pathways, including identified metabolite mediators, might provide novel intervention targets for preventing the intrauterine development of obesity in the offspring of mothers with obesity.
母体孕前肥胖是后代肥胖的一个重要危险因素,这可能部分通过产前编程机制起作用。
本研究旨在系统识别介导肥胖代际传递的产前代谢组学特征。
我们纳入了来自条件影响神经认知发展和儿童早期学习(CANDLE)研究妊娠队列的 450 对非裔美国母子对。采用 LC-MS 对妊娠中期母亲血浆样本进行代谢组学分析。感兴趣的儿童生长结局包括从出生到 4 岁的 BMI 轨迹(上升高 BMI、中 BMI 和低 BMI 轨迹)以及 4 岁时超重/肥胖(OWO)的风险。采用中介分析来识别与母亲 OWO 和儿童生长结局相关的代谢物中介物。采用孟德尔随机化(MR)方法来检验母体 OWO 对代谢物中介物的潜在因果效应。
在妊娠期间母亲血浆中检测到的 880 种代谢物中,有 14 种和 11 种代谢物分别显著介导了母体孕前 OWO 对儿童 BMI 轨迹和 4 岁时 OWO 风险的影响,有 5 种代谢物同时介导了这两种结局。MR 分析表明,20 种产前代谢物中介物中的 6 种可能受到母体孕前 OWO 的因果影响,其中大多数来自与氨基酸(羟基天冬酰胺、谷氨酸和同型瓜氨酸)、甾醇(菜油甾醇)和核苷酸(N2,N2-二甲基鸟苷)代谢有关的途径。
本研究进一步证明了产前代谢组学特征可能介导母体 OWO 对后代早期儿童生长轨迹和 OWO 风险的影响。所鉴定的代谢物中介物的代谢途径可能为预防肥胖母亲后代宫内肥胖的发生提供新的干预靶点。