TY - JOUR
T1 - Prenatal metabolomic profiles mediate the effect of maternal obesity on early childhood growth trajectories and obesity risk
T2 - the Conditions Affecting Neurocognitive Development and Learning in Early Childhood (CANDLE) Study
AU - Hu, Zunsong
AU - Han, Luhang
AU - Liu, Jiawang
AU - Fowke, Jay H.
AU - Han, Joan C.
AU - Kakhniashvili, David
AU - Lewinn, Kaja Z.
AU - Bush, Nicole R.
AU - Alex Mason, W.
AU - Zhao, Qi
N1 - Publisher Copyright:
© 2022 The Author(s). Published by Oxford University Press on behalf of the American Society for Nutrition.
PY - 2022/11/1
Y1 - 2022/11/1
N2 - Background: Maternal prepregnancy obesity is an important risk factor for offspring obesity, which may partially operate through prenatal programming mechanisms. Objectives: The study aimed to systematically identify prenatal metabolomic profiles mediating the intergenerational transmission of obesity. Methods: 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. Results: 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). Conclusions: 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.
AB - Background: Maternal prepregnancy obesity is an important risk factor for offspring obesity, which may partially operate through prenatal programming mechanisms. Objectives: The study aimed to systematically identify prenatal metabolomic profiles mediating the intergenerational transmission of obesity. Methods: 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. Results: 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). Conclusions: 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.
KW - childhood obesity
KW - growth trajectory
KW - maternal obesity
KW - mediation
KW - metabolomics
UR - http://www.scopus.com/inward/record.url?scp=85144801339&partnerID=8YFLogxK
U2 - 10.1093/ajcn/nqac244
DO - 10.1093/ajcn/nqac244
M3 - Article
C2 - 36055779
AN - SCOPUS:85144801339
SN - 0002-9165
VL - 116
SP - 1343
EP - 1353
JO - American Journal of Clinical Nutrition
JF - American Journal of Clinical Nutrition
IS - 5
ER -