Cargando…
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...
Autores principales: | , , , , , , |
---|---|
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 |
_version_ | 1782410954998284288 |
---|---|
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. |
format | Online Article Text |
id | pubmed-4719654 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT grevendonklotte mitochondrialoxidativednadamageandexposuretoparticulateairpollutioninmothernewbornpairs AT janssenbramg mitochondrialoxidativednadamageandexposuretoparticulateairpollutioninmothernewbornpairs AT vanpouckecharlotte mitochondrialoxidativednadamageandexposuretoparticulateairpollutioninmothernewbornpairs AT lefebvrewouter mitochondrialoxidativednadamageandexposuretoparticulateairpollutioninmothernewbornpairs AT hoxhamirjam mitochondrialoxidativednadamageandexposuretoparticulateairpollutioninmothernewbornpairs AT bollativalentina mitochondrialoxidativednadamageandexposuretoparticulateairpollutioninmothernewbornpairs AT nawrottims mitochondrialoxidativednadamageandexposuretoparticulateairpollutioninmothernewbornpairs |