Sandra India Aldana, Lauren Petrick, Megan M. Niedzwiecki, Damaskini Valvi, Allan C. Just, Iván Gutiérrez-Avila, Itai Kloog, Dinesh K. Barupal, Martha María Téllez-Rojo, Robert O. Wright, Andrea A. Baccarelli, Haotian Wu, Elena Colicino
{"title":"妊娠期是环境空气污染暴露对产妇产后代谢组的易感期","authors":"Sandra India Aldana, Lauren Petrick, Megan M. Niedzwiecki, Damaskini Valvi, Allan C. Just, Iván Gutiérrez-Avila, Itai Kloog, Dinesh K. Barupal, Martha María Téllez-Rojo, Robert O. Wright, Andrea A. Baccarelli, Haotian Wu, Elena Colicino","doi":"10.1021/acs.est.4c10717","DOIUrl":null,"url":null,"abstract":"Pregnancy is a potential critical window to air pollution exposure for long-term maternal metabolic effects. However, little is known about potential early metabolic mechanisms linking air pollution to maternal metabolic health. We included 544 pregnant Mexican women with both ambient PM<sub>2.5</sub> levels during pregnancy and untargeted serum metabolomics to examine associations between pregnancy PM<sub>2.5</sub> exposure (overall and monthly) and postpartum metabolites, implementing FDR-adjusted robust linear regression controlling for covariates. Pathway enrichment analyses (in Reactome and MetaboAnalyst) and effect modification by fetal sex and folic acid supplementation were also evaluated. Higher PM<sub>2.5</sub> exposure levels throughout pregnancy were associated with higher bile acids and amino acids, dysregulated glycerophospholipids, or lower fatty acyl levels (FDR < 0.05), among other metabolites. Potential critical windows of susceptibility to monthly PM<sub>2.5</sub> on metabolites were observed in early to midpregnancy (FDR < 0.005). Main findings were consistent by strata of fetal sex and folic acid supplementation. Metabolic pathways corresponding to positive PM<sub>2.5</sub>-metabolite associations indicated enriched bile acid, dietary lipid, and transmembrane transport metabolism, whereas for negative PM<sub>2.5</sub>-metabolite associations, we identified altered pathways involving adipogenesis, incretin peptide hormone, GLP-1, PPAR-alpha, and fatty acid receptors (FDR < 0.05). PM<sub>2.5</sub> exposures during pregnancy, especially in early gestation, altered maternal postpartum lipids as well as amino acid metabolism.","PeriodicalId":36,"journal":{"name":"环境科学与技术","volume":"87 1","pages":""},"PeriodicalIF":11.3000,"publicationDate":"2025-03-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Pregnancy as a Susceptible Period to Ambient Air Pollution Exposure on the Maternal Postpartum Metabolome\",\"authors\":\"Sandra India Aldana, Lauren Petrick, Megan M. Niedzwiecki, Damaskini Valvi, Allan C. Just, Iván Gutiérrez-Avila, Itai Kloog, Dinesh K. Barupal, Martha María Téllez-Rojo, Robert O. Wright, Andrea A. Baccarelli, Haotian Wu, Elena Colicino\",\"doi\":\"10.1021/acs.est.4c10717\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Pregnancy is a potential critical window to air pollution exposure for long-term maternal metabolic effects. However, little is known about potential early metabolic mechanisms linking air pollution to maternal metabolic health. We included 544 pregnant Mexican women with both ambient PM<sub>2.5</sub> levels during pregnancy and untargeted serum metabolomics to examine associations between pregnancy PM<sub>2.5</sub> exposure (overall and monthly) and postpartum metabolites, implementing FDR-adjusted robust linear regression controlling for covariates. Pathway enrichment analyses (in Reactome and MetaboAnalyst) and effect modification by fetal sex and folic acid supplementation were also evaluated. Higher PM<sub>2.5</sub> exposure levels throughout pregnancy were associated with higher bile acids and amino acids, dysregulated glycerophospholipids, or lower fatty acyl levels (FDR < 0.05), among other metabolites. Potential critical windows of susceptibility to monthly PM<sub>2.5</sub> on metabolites were observed in early to midpregnancy (FDR < 0.005). Main findings were consistent by strata of fetal sex and folic acid supplementation. Metabolic pathways corresponding to positive PM<sub>2.5</sub>-metabolite associations indicated enriched bile acid, dietary lipid, and transmembrane transport metabolism, whereas for negative PM<sub>2.5</sub>-metabolite associations, we identified altered pathways involving adipogenesis, incretin peptide hormone, GLP-1, PPAR-alpha, and fatty acid receptors (FDR < 0.05). 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Pregnancy as a Susceptible Period to Ambient Air Pollution Exposure on the Maternal Postpartum Metabolome
Pregnancy is a potential critical window to air pollution exposure for long-term maternal metabolic effects. However, little is known about potential early metabolic mechanisms linking air pollution to maternal metabolic health. We included 544 pregnant Mexican women with both ambient PM2.5 levels during pregnancy and untargeted serum metabolomics to examine associations between pregnancy PM2.5 exposure (overall and monthly) and postpartum metabolites, implementing FDR-adjusted robust linear regression controlling for covariates. Pathway enrichment analyses (in Reactome and MetaboAnalyst) and effect modification by fetal sex and folic acid supplementation were also evaluated. Higher PM2.5 exposure levels throughout pregnancy were associated with higher bile acids and amino acids, dysregulated glycerophospholipids, or lower fatty acyl levels (FDR < 0.05), among other metabolites. Potential critical windows of susceptibility to monthly PM2.5 on metabolites were observed in early to midpregnancy (FDR < 0.005). Main findings were consistent by strata of fetal sex and folic acid supplementation. Metabolic pathways corresponding to positive PM2.5-metabolite associations indicated enriched bile acid, dietary lipid, and transmembrane transport metabolism, whereas for negative PM2.5-metabolite associations, we identified altered pathways involving adipogenesis, incretin peptide hormone, GLP-1, PPAR-alpha, and fatty acid receptors (FDR < 0.05). PM2.5 exposures during pregnancy, especially in early gestation, altered maternal postpartum lipids as well as amino acid metabolism.
期刊介绍:
Environmental Science & Technology (ES&T) is a co-sponsored academic and technical magazine by the Hubei Provincial Environmental Protection Bureau and the Hubei Provincial Academy of Environmental Sciences.
Environmental Science & Technology (ES&T) holds the status of Chinese core journals, scientific papers source journals of China, Chinese Science Citation Database source journals, and Chinese Academic Journal Comprehensive Evaluation Database source journals. This publication focuses on the academic field of environmental protection, featuring articles related to environmental protection and technical advancements.