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Modulation of CYP2E1 metabolic activity in a cohort of confirmed caffeine ingesting pregnant women with preterm offspring

BACKGROUND: To ascertain interactions of caffeine ingestion, food, medications, and environmental exposures during preterm human gestation, under informed consent, we studied a cohort of Mexican women with further preterm offspring born at ≤ 34 completed weeks. At birth, blood samples were taken fro...

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Autores principales: Alcorta-García, M. R., López-Villaseñor, C. N., Sánchez-Ferrer, G., Flores-Mendoza, H., Castorena-Torres, F., Aguilar-Torres, M. A., Sepúlveda-Treviño, C. M., Hernández-Hernández, J. A., López-Sánchez, R. C., Lara-Díaz, V. J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7261717/
https://www.ncbi.nlm.nih.gov/pubmed/32476096
http://dx.doi.org/10.1186/s40348-020-00096-3
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author Alcorta-García, M. R.
López-Villaseñor, C. N.
Sánchez-Ferrer, G.
Flores-Mendoza, H.
Castorena-Torres, F.
Aguilar-Torres, M. A.
Sepúlveda-Treviño, C. M.
Hernández-Hernández, J. A.
López-Sánchez, R. C.
Lara-Díaz, V. J.
author_facet Alcorta-García, M. R.
López-Villaseñor, C. N.
Sánchez-Ferrer, G.
Flores-Mendoza, H.
Castorena-Torres, F.
Aguilar-Torres, M. A.
Sepúlveda-Treviño, C. M.
Hernández-Hernández, J. A.
López-Sánchez, R. C.
Lara-Díaz, V. J.
author_sort Alcorta-García, M. R.
collection PubMed
description BACKGROUND: To ascertain interactions of caffeine ingestion, food, medications, and environmental exposures during preterm human gestation, under informed consent, we studied a cohort of Mexican women with further preterm offspring born at ≤ 34 completed weeks. At birth, blood samples were taken from mothers and umbilical cords to determine caffeine and metabolites concentrations and CYP1A2 (rs762551) and CYP2E1 (rs2031920, rs3813867) polymorphisms involved in caffeine metabolism. RESULTS: In 90 pregnant women who gave birth to 98 preterm neonates, self-informed caffeine ingestion rate was 97%, laboratory confirmed rate was 93 %. Theobromine was the predominant metabolite found. Consumption of acetaminophen correlated significantly with changes in caffeine metabolism (acetaminophen R(2) = 0.637, p = 0.01) due to activation of CYP2E1 alternate pathways. The main caffeine source was cola soft drinks. CONCLUSION: Environmental exposures, especially acetaminophen ingestion during human preterm pregnancy, can modulate CYP2E1 metabolic activity.
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spelling pubmed-72617172020-06-11 Modulation of CYP2E1 metabolic activity in a cohort of confirmed caffeine ingesting pregnant women with preterm offspring Alcorta-García, M. R. López-Villaseñor, C. N. Sánchez-Ferrer, G. Flores-Mendoza, H. Castorena-Torres, F. Aguilar-Torres, M. A. Sepúlveda-Treviño, C. M. Hernández-Hernández, J. A. López-Sánchez, R. C. Lara-Díaz, V. J. Mol Cell Pediatr Research BACKGROUND: To ascertain interactions of caffeine ingestion, food, medications, and environmental exposures during preterm human gestation, under informed consent, we studied a cohort of Mexican women with further preterm offspring born at ≤ 34 completed weeks. At birth, blood samples were taken from mothers and umbilical cords to determine caffeine and metabolites concentrations and CYP1A2 (rs762551) and CYP2E1 (rs2031920, rs3813867) polymorphisms involved in caffeine metabolism. RESULTS: In 90 pregnant women who gave birth to 98 preterm neonates, self-informed caffeine ingestion rate was 97%, laboratory confirmed rate was 93 %. Theobromine was the predominant metabolite found. Consumption of acetaminophen correlated significantly with changes in caffeine metabolism (acetaminophen R(2) = 0.637, p = 0.01) due to activation of CYP2E1 alternate pathways. The main caffeine source was cola soft drinks. CONCLUSION: Environmental exposures, especially acetaminophen ingestion during human preterm pregnancy, can modulate CYP2E1 metabolic activity. Springer Berlin Heidelberg 2020-06-01 /pmc/articles/PMC7261717/ /pubmed/32476096 http://dx.doi.org/10.1186/s40348-020-00096-3 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Research
Alcorta-García, M. R.
López-Villaseñor, C. N.
Sánchez-Ferrer, G.
Flores-Mendoza, H.
Castorena-Torres, F.
Aguilar-Torres, M. A.
Sepúlveda-Treviño, C. M.
Hernández-Hernández, J. A.
López-Sánchez, R. C.
Lara-Díaz, V. J.
Modulation of CYP2E1 metabolic activity in a cohort of confirmed caffeine ingesting pregnant women with preterm offspring
title Modulation of CYP2E1 metabolic activity in a cohort of confirmed caffeine ingesting pregnant women with preterm offspring
title_full Modulation of CYP2E1 metabolic activity in a cohort of confirmed caffeine ingesting pregnant women with preterm offspring
title_fullStr Modulation of CYP2E1 metabolic activity in a cohort of confirmed caffeine ingesting pregnant women with preterm offspring
title_full_unstemmed Modulation of CYP2E1 metabolic activity in a cohort of confirmed caffeine ingesting pregnant women with preterm offspring
title_short Modulation of CYP2E1 metabolic activity in a cohort of confirmed caffeine ingesting pregnant women with preterm offspring
title_sort modulation of cyp2e1 metabolic activity in a cohort of confirmed caffeine ingesting pregnant women with preterm offspring
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7261717/
https://www.ncbi.nlm.nih.gov/pubmed/32476096
http://dx.doi.org/10.1186/s40348-020-00096-3
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