Taesuwan Siraphat, McDougall Melissa Q, Malysheva Olga V, Bender Erica, Nevins Julie E H, Devapatla Srisatish, Vidavalur Ramesh, Caudill Marie A, Klatt Kevin C
Division of Nutritional Sciences, Cornell University, Ithaca, New York, USA.
Cluster of Agro Bio-Circular-Green Industry, Faculty of Agro-Industry, Chiang Mai University, Chiang Mai, Thailand.
FASEB J. 2021 Dec;35(12):e22063. doi: 10.1096/fj.202101401RR.
Pregnancy places a unique stress upon choline metabolism, requiring adaptations to support both maternal and fetal requirements. The impact of pregnancy and prenatal choline supplementation on choline and its metabolome in free-living, healthy adults is relatively uncharacterized. This study investigated the effect of prenatal choline supplementation on maternal and fetal biomarkers of choline metabolism among free-living pregnant persons consuming self-selected diets. Participants were randomized to supplemental choline (as choline chloride) intakes of 550 mg/d (500 mg/d d0-choline + 50 mg/d methyl-d9-choline; intervention) or 25 mg/d d9-choline (control) from gestational week (GW) 12-16 until Delivery. Fasting blood and 24-h urine samples were obtained at study Visit 1 (GW 12-16), Visit 2 (GW 20-24), and Visit 3 (GW 28-32). At Delivery, maternal and cord blood and placental tissue samples were collected. Participants randomized to 550 (vs. 25) mg supplemental choline/d achieved higher (p < .05) plasma concentrations of free choline, betaine, dimethylglycine, phosphatidylcholine (PC), and sphingomyelin at one or more study timepoint. Betaine was most responsive to prenatal choline supplementation with increases (p ≤ .001) in maternal plasma observed at Visit 2-Delivery (relative to Visit 1 and control), as well as in the placenta and cord plasma. Notably, greater plasma enrichments of d3-PC and LDL-C were observed in the intervention (vs. control) group, indicating enhanced PC synthesis through the de novo phosphatidylethanolamine N-methyltransferase pathway and lipid export. Overall, these data show that prenatal choline supplementation profoundly alters the choline metabolome, supporting pregnancy-related metabolic adaptations and revealing biomarkers for use in nutritional assessment and monitoring during pregnancy.
怀孕会给胆碱代谢带来独特的压力,需要进行适应性调整以满足母体和胎儿的需求。在自由生活的健康成年人中,怀孕和产前补充胆碱对胆碱及其代谢组的影响相对尚不明确。本研究调查了产前补充胆碱对自由选择饮食的孕妇及其胎儿胆碱代谢生物标志物的影响。参与者被随机分为两组,从妊娠第12 - 16周直至分娩,分别摄入550毫克/天的补充胆碱(以氯化胆碱形式,即500毫克/天的普通胆碱 + 50毫克/天的甲基 - d9 - 胆碱;干预组)或25毫克/天的d9 - 胆碱(对照组)。在研究的第1次访视(妊娠第12 - 16周)、第2次访视(妊娠第20 - 24周)和第3次访视(妊娠第28 - 32周)时采集空腹血液和24小时尿液样本。在分娩时,采集母体和脐带血以及胎盘组织样本。随机分配到补充550(对比25)毫克/天胆碱的参与者在一个或多个研究时间点的血浆中游离胆碱、甜菜碱、二甲基甘氨酸、磷脂酰胆碱(PC)和鞘磷脂浓度更高(p < 0.05)。甜菜碱对产前补充胆碱反应最为明显,在第2次访视至分娩期间(相对于第1次访视和对照组)母体血浆中甜菜碱增加(p ≤ 0.001),在胎盘和脐带血浆中也有增加。值得注意的是,干预组(对比对照组)血浆中d3 - PC和低密度脂蛋白胆固醇(LDL - C)的富集程度更高,表明通过从头合成磷脂酰乙醇胺N - 甲基转移酶途径增强了PC合成以及脂质输出。总体而言,这些数据表明产前补充胆碱会深刻改变胆碱代谢组,支持与怀孕相关的代谢适应,并揭示可用于孕期营养评估和监测的生物标志物。