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Human placental microRNAs dysregulated by cadmium exposure predict neurobehavioral outcomes at birth

BACKGROUND: Prenatal cadmium (Cd) exposure has been implicated in both placental toxicity and adverse neurobehavioral outcomes. Placental microRNAs (miRNAs) may function to developmentally program adverse pregnancy and newborn health outcomes in response to gestational Cd exposure. METHODS: In a sub...

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Autores principales: Tehrani, Jesse M., Kennedy, Elizabeth, Tung, Pei Wen, Burt, Amber, Hermetz, Karen, Punshon, Tracy, Jackson, Brian P., Hao, Ke, Chen, Jia, Karagas, Margaret R., Koestler, Devin C., Lester, Barry, Marsit, Carmen J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9884320/
https://www.ncbi.nlm.nih.gov/pubmed/35906307
http://dx.doi.org/10.1038/s41390-022-02201-w
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author Tehrani, Jesse M.
Kennedy, Elizabeth
Tung, Pei Wen
Burt, Amber
Hermetz, Karen
Punshon, Tracy
Jackson, Brian P.
Hao, Ke
Chen, Jia
Karagas, Margaret R.
Koestler, Devin C.
Lester, Barry
Marsit, Carmen J.
author_facet Tehrani, Jesse M.
Kennedy, Elizabeth
Tung, Pei Wen
Burt, Amber
Hermetz, Karen
Punshon, Tracy
Jackson, Brian P.
Hao, Ke
Chen, Jia
Karagas, Margaret R.
Koestler, Devin C.
Lester, Barry
Marsit, Carmen J.
author_sort Tehrani, Jesse M.
collection PubMed
description BACKGROUND: Prenatal cadmium (Cd) exposure has been implicated in both placental toxicity and adverse neurobehavioral outcomes. Placental microRNAs (miRNAs) may function to developmentally program adverse pregnancy and newborn health outcomes in response to gestational Cd exposure. METHODS: In a subset of the Rhode Island Child Health Study (RICHS, n=115) and the New Hampshire Birth Cohort Study (NHBCS, =281), we used small RNA sequencing and trace metal analysis to identify Cd-associated expression of placental miRNAs using negative binomial generalized linear models. We predicted mRNAs targeted by Cd-associated miRNAs and relate them to neurobehavioral outcomes at birth through the integration of transcriptomic data and summary scores from the NICU Network Neurobehavioral Scale (NNNS). RESULTS: Placental Cd concentrations are significantly associated with the expression level of five placental miRNAs in NHBCS, with similar effect sizes in RICHS. These miRNA target genes overrepresented in nervous system development, and their expression is correlated with NNNS metrics suggestive of atypical neurobehavioral outcomes at birth. CONCLUSIONS: Gestational Cd exposure is associated with the expression of placental miRNAs. Predicted targets of these miRNAs are involved in nervous system development and may also regulate placental physiology, allowing their dysregulation to modify developmental programming of early life health outcomes.
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spelling pubmed-98843202023-04-29 Human placental microRNAs dysregulated by cadmium exposure predict neurobehavioral outcomes at birth Tehrani, Jesse M. Kennedy, Elizabeth Tung, Pei Wen Burt, Amber Hermetz, Karen Punshon, Tracy Jackson, Brian P. Hao, Ke Chen, Jia Karagas, Margaret R. Koestler, Devin C. Lester, Barry Marsit, Carmen J. Pediatr Res Article BACKGROUND: Prenatal cadmium (Cd) exposure has been implicated in both placental toxicity and adverse neurobehavioral outcomes. Placental microRNAs (miRNAs) may function to developmentally program adverse pregnancy and newborn health outcomes in response to gestational Cd exposure. METHODS: In a subset of the Rhode Island Child Health Study (RICHS, n=115) and the New Hampshire Birth Cohort Study (NHBCS, =281), we used small RNA sequencing and trace metal analysis to identify Cd-associated expression of placental miRNAs using negative binomial generalized linear models. We predicted mRNAs targeted by Cd-associated miRNAs and relate them to neurobehavioral outcomes at birth through the integration of transcriptomic data and summary scores from the NICU Network Neurobehavioral Scale (NNNS). RESULTS: Placental Cd concentrations are significantly associated with the expression level of five placental miRNAs in NHBCS, with similar effect sizes in RICHS. These miRNA target genes overrepresented in nervous system development, and their expression is correlated with NNNS metrics suggestive of atypical neurobehavioral outcomes at birth. CONCLUSIONS: Gestational Cd exposure is associated with the expression of placental miRNAs. Predicted targets of these miRNAs are involved in nervous system development and may also regulate placental physiology, allowing their dysregulation to modify developmental programming of early life health outcomes. 2023-04 2022-07-29 /pmc/articles/PMC9884320/ /pubmed/35906307 http://dx.doi.org/10.1038/s41390-022-02201-w Text en http://www.nature.com/authors/editorial_policies/license.html#termsUsers may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Tehrani, Jesse M.
Kennedy, Elizabeth
Tung, Pei Wen
Burt, Amber
Hermetz, Karen
Punshon, Tracy
Jackson, Brian P.
Hao, Ke
Chen, Jia
Karagas, Margaret R.
Koestler, Devin C.
Lester, Barry
Marsit, Carmen J.
Human placental microRNAs dysregulated by cadmium exposure predict neurobehavioral outcomes at birth
title Human placental microRNAs dysregulated by cadmium exposure predict neurobehavioral outcomes at birth
title_full Human placental microRNAs dysregulated by cadmium exposure predict neurobehavioral outcomes at birth
title_fullStr Human placental microRNAs dysregulated by cadmium exposure predict neurobehavioral outcomes at birth
title_full_unstemmed Human placental microRNAs dysregulated by cadmium exposure predict neurobehavioral outcomes at birth
title_short Human placental microRNAs dysregulated by cadmium exposure predict neurobehavioral outcomes at birth
title_sort human placental micrornas dysregulated by cadmium exposure predict neurobehavioral outcomes at birth
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9884320/
https://www.ncbi.nlm.nih.gov/pubmed/35906307
http://dx.doi.org/10.1038/s41390-022-02201-w
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