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Preconception telomere length as a novel maternal biomarker to assess the risk of spina bifida in the offspring
BACKGROUND: Periconception interactions between maternal conditions and environmental and genetic factors are involved in the pathogenesis and prevention of neural tube defects (NTD), such as spina bifida. These factors have in common that they can impair the oxidative pathway, resulting in excessiv...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7432172/ https://www.ncbi.nlm.nih.gov/pubmed/32359029 http://dx.doi.org/10.1002/bdr2.1682 |
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author | Aoulad Fares, Damiat Schalekamp‐Timmermans, Sarah Nawrot, Tim S. Steegers‐Theunissen, Régine P. M. |
author_facet | Aoulad Fares, Damiat Schalekamp‐Timmermans, Sarah Nawrot, Tim S. Steegers‐Theunissen, Régine P. M. |
author_sort | Aoulad Fares, Damiat |
collection | PubMed |
description | BACKGROUND: Periconception interactions between maternal conditions and environmental and genetic factors are involved in the pathogenesis and prevention of neural tube defects (NTD), such as spina bifida. These factors have in common that they can impair the oxidative pathway, resulting in excessive (chronic) oxidative stress and inflammation. METHODS: Review of the literature concerning underlying mechanisms and biomarkers of aging particularly during reproduction. A number of molecular markers for biological aging have been identified, including telomere length (TL). Excessive telomere shortening is an index of senescence, causes genomic instability and is associated with a higher risk of age‐related diseases. Furthermore, TL shortening is associated with the similar environmental and lifestyle exposures associated with NTD risk. RESULTS: Embryonic mice deficient in the telomerase gene show shorter TL and failure of closure of the neural tube as the main defect, suggesting that this developmental process is among the most sensitive to telomere loss and chromosomal instability. CONCLUSIONS: From this background, we hypothesize that preconceptional long term exposure to harmful environmental and lifestyle risk factors accelerates a woman's aging process, which can be measured by TL, and thereby her underlying risk of NTD offspring. Alternatively, it might be that women with an increased NTD risk already exhibit a more advanced biological age before the onset of pregnancy compared to women of identical calendar age. |
format | Online Article Text |
id | pubmed-7432172 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-74321722020-08-20 Preconception telomere length as a novel maternal biomarker to assess the risk of spina bifida in the offspring Aoulad Fares, Damiat Schalekamp‐Timmermans, Sarah Nawrot, Tim S. Steegers‐Theunissen, Régine P. M. Birth Defects Res Hypothesis BACKGROUND: Periconception interactions between maternal conditions and environmental and genetic factors are involved in the pathogenesis and prevention of neural tube defects (NTD), such as spina bifida. These factors have in common that they can impair the oxidative pathway, resulting in excessive (chronic) oxidative stress and inflammation. METHODS: Review of the literature concerning underlying mechanisms and biomarkers of aging particularly during reproduction. A number of molecular markers for biological aging have been identified, including telomere length (TL). Excessive telomere shortening is an index of senescence, causes genomic instability and is associated with a higher risk of age‐related diseases. Furthermore, TL shortening is associated with the similar environmental and lifestyle exposures associated with NTD risk. RESULTS: Embryonic mice deficient in the telomerase gene show shorter TL and failure of closure of the neural tube as the main defect, suggesting that this developmental process is among the most sensitive to telomere loss and chromosomal instability. CONCLUSIONS: From this background, we hypothesize that preconceptional long term exposure to harmful environmental and lifestyle risk factors accelerates a woman's aging process, which can be measured by TL, and thereby her underlying risk of NTD offspring. Alternatively, it might be that women with an increased NTD risk already exhibit a more advanced biological age before the onset of pregnancy compared to women of identical calendar age. John Wiley & Sons, Inc. 2020-05-02 2020-05-15 /pmc/articles/PMC7432172/ /pubmed/32359029 http://dx.doi.org/10.1002/bdr2.1682 Text en © 2020 The Authors. Birth Defects Research published by Wiley Periodicals Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Hypothesis Aoulad Fares, Damiat Schalekamp‐Timmermans, Sarah Nawrot, Tim S. Steegers‐Theunissen, Régine P. M. Preconception telomere length as a novel maternal biomarker to assess the risk of spina bifida in the offspring |
title | Preconception telomere length as a novel maternal biomarker to assess the risk of spina bifida in the offspring |
title_full | Preconception telomere length as a novel maternal biomarker to assess the risk of spina bifida in the offspring |
title_fullStr | Preconception telomere length as a novel maternal biomarker to assess the risk of spina bifida in the offspring |
title_full_unstemmed | Preconception telomere length as a novel maternal biomarker to assess the risk of spina bifida in the offspring |
title_short | Preconception telomere length as a novel maternal biomarker to assess the risk of spina bifida in the offspring |
title_sort | preconception telomere length as a novel maternal biomarker to assess the risk of spina bifida in the offspring |
topic | Hypothesis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7432172/ https://www.ncbi.nlm.nih.gov/pubmed/32359029 http://dx.doi.org/10.1002/bdr2.1682 |
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