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Mitochondrial oxidative DNA damage and exposure to particulate air pollution in mother-newborn pairs

BACKGROUND: Studies emphasize the importance of particulate matter (PM) in the formation of reactive oxygen species and inflammation. We hypothesized that PM exposure during different time windows in pregnancy influences mitochondrial 8-hydroxy-2′-deoxyguanosine (8-OHdG) levels, which is an establis...

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Autores principales: Grevendonk, Lotte, Janssen, Bram G., Vanpoucke, Charlotte, Lefebvre, Wouter, Hoxha, Mirjam, Bollati, Valentina, Nawrot, Tim S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4719654/
https://www.ncbi.nlm.nih.gov/pubmed/26792633
http://dx.doi.org/10.1186/s12940-016-0095-2
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author Grevendonk, Lotte
Janssen, Bram G.
Vanpoucke, Charlotte
Lefebvre, Wouter
Hoxha, Mirjam
Bollati, Valentina
Nawrot, Tim S.
author_facet Grevendonk, Lotte
Janssen, Bram G.
Vanpoucke, Charlotte
Lefebvre, Wouter
Hoxha, Mirjam
Bollati, Valentina
Nawrot, Tim S.
author_sort Grevendonk, Lotte
collection PubMed
description BACKGROUND: Studies emphasize the importance of particulate matter (PM) in the formation of reactive oxygen species and inflammation. We hypothesized that PM exposure during different time windows in pregnancy influences mitochondrial 8-hydroxy-2′-deoxyguanosine (8-OHdG) levels, which is an established biomarker for oxidative stress, in both maternal and foetal blood. METHODS: We investigated maternal (n = 224) and cord blood (n = 293) from mother-newborn pairs that were enrolled in the ENVIRONAGE birth cohort. We determined mitochondrial 8-OHdG by quantitative polymerase chain reaction (qPCR). Multivariable regression models were used to assess the association between mitochondrial 8-OHdG with PM(10) and PM(2.5) exposure over various time windows during pregnancy(.) RESULTS: In multivariable analysis, PM(10) exposure during the entire pregnancy was positively associated with levels of mitochondrial 8-OHdG in maternal blood. For an IQR increment in PM(10) exposure an increase of 18.3 % (95 % confidence interval (CI): 5.6 to 33.4 %, p = 0.004) in 8-OHdG was observed. PM(10) exposure during the last trimester of pregnancy was positively associated with levels of 8-OHdG (28.1, 95 % CI: 8.6 to 51.2 %, p = 0.004, for an IQR increment in PM(10)). In a similar way, PM(2.5) exposure was significantly associated with an increase of mitochondrial 8-OHdG levels in maternal blood during the entire pregnancy (13.9, 95 % CI: 0.4 to 29.4 %, p = 0.04 for an IQR increment in PM(2.5) exposure) and third trimester of pregnancy (28.1, 95 % CI: 3.6 to 58.4 %, p = 0.02 for an IQR increment in PM(2.5) exposure). In umbilical cord blood, 8-OHdG levels were significantly associated with PM(10) exposure during first and second trimester of pregnancy with respectively an increase of 23.0 % (95 % CI: 5.9 to 42.8 %, p = 0.007) and 16.6 % (95 % CI: 1.8 to 33.5 %, p = 0.03) for an IQR increment in PM(10) exposure. CONCLUSIONS: We found PM-associated increased mitochondrial oxidative DNA damage during pregnancy in both mothers and their newborns. Accordingly, our study showed that particulate air pollution exposure in early life plays a role in increasing systemic oxidative stress, at the level of the mitochondria, both in mother and foetus. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12940-016-0095-2) contains supplementary material, which is available to authorized users.
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spelling pubmed-47196542016-01-21 Mitochondrial oxidative DNA damage and exposure to particulate air pollution in mother-newborn pairs Grevendonk, Lotte Janssen, Bram G. Vanpoucke, Charlotte Lefebvre, Wouter Hoxha, Mirjam Bollati, Valentina Nawrot, Tim S. Environ Health Research BACKGROUND: Studies emphasize the importance of particulate matter (PM) in the formation of reactive oxygen species and inflammation. We hypothesized that PM exposure during different time windows in pregnancy influences mitochondrial 8-hydroxy-2′-deoxyguanosine (8-OHdG) levels, which is an established biomarker for oxidative stress, in both maternal and foetal blood. METHODS: We investigated maternal (n = 224) and cord blood (n = 293) from mother-newborn pairs that were enrolled in the ENVIRONAGE birth cohort. We determined mitochondrial 8-OHdG by quantitative polymerase chain reaction (qPCR). Multivariable regression models were used to assess the association between mitochondrial 8-OHdG with PM(10) and PM(2.5) exposure over various time windows during pregnancy(.) RESULTS: In multivariable analysis, PM(10) exposure during the entire pregnancy was positively associated with levels of mitochondrial 8-OHdG in maternal blood. For an IQR increment in PM(10) exposure an increase of 18.3 % (95 % confidence interval (CI): 5.6 to 33.4 %, p = 0.004) in 8-OHdG was observed. PM(10) exposure during the last trimester of pregnancy was positively associated with levels of 8-OHdG (28.1, 95 % CI: 8.6 to 51.2 %, p = 0.004, for an IQR increment in PM(10)). In a similar way, PM(2.5) exposure was significantly associated with an increase of mitochondrial 8-OHdG levels in maternal blood during the entire pregnancy (13.9, 95 % CI: 0.4 to 29.4 %, p = 0.04 for an IQR increment in PM(2.5) exposure) and third trimester of pregnancy (28.1, 95 % CI: 3.6 to 58.4 %, p = 0.02 for an IQR increment in PM(2.5) exposure). In umbilical cord blood, 8-OHdG levels were significantly associated with PM(10) exposure during first and second trimester of pregnancy with respectively an increase of 23.0 % (95 % CI: 5.9 to 42.8 %, p = 0.007) and 16.6 % (95 % CI: 1.8 to 33.5 %, p = 0.03) for an IQR increment in PM(10) exposure. CONCLUSIONS: We found PM-associated increased mitochondrial oxidative DNA damage during pregnancy in both mothers and their newborns. Accordingly, our study showed that particulate air pollution exposure in early life plays a role in increasing systemic oxidative stress, at the level of the mitochondria, both in mother and foetus. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12940-016-0095-2) contains supplementary material, which is available to authorized users. BioMed Central 2016-01-20 /pmc/articles/PMC4719654/ /pubmed/26792633 http://dx.doi.org/10.1186/s12940-016-0095-2 Text en © Grevendonk et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Grevendonk, Lotte
Janssen, Bram G.
Vanpoucke, Charlotte
Lefebvre, Wouter
Hoxha, Mirjam
Bollati, Valentina
Nawrot, Tim S.
Mitochondrial oxidative DNA damage and exposure to particulate air pollution in mother-newborn pairs
title Mitochondrial oxidative DNA damage and exposure to particulate air pollution in mother-newborn pairs
title_full Mitochondrial oxidative DNA damage and exposure to particulate air pollution in mother-newborn pairs
title_fullStr Mitochondrial oxidative DNA damage and exposure to particulate air pollution in mother-newborn pairs
title_full_unstemmed Mitochondrial oxidative DNA damage and exposure to particulate air pollution in mother-newborn pairs
title_short Mitochondrial oxidative DNA damage and exposure to particulate air pollution in mother-newborn pairs
title_sort mitochondrial oxidative dna damage and exposure to particulate air pollution in mother-newborn pairs
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4719654/
https://www.ncbi.nlm.nih.gov/pubmed/26792633
http://dx.doi.org/10.1186/s12940-016-0095-2
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