The DOI matches its Crossref record; 39 of the 43 references it cites were found in a registry or an index.
Mitochondrial oxidative DNA damage and exposure to particulate air pollution in mother-newborn pairs
Open accessAbstract
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 PM10 and PM2.5 exposure over various time windows during pregnancy. RESULTS: In multivariable analysis, PM10 exposure during the entire pregnancy was positively associated with levels of mitochondrial 8-OHdG in maternal blood. For an IQR increment in PM10 exposure an increase of 18.3 % (95 % confidence interval (CI): 5.6 to 33.4 %, p = 0.004) in 8-OHdG was observed. PM10 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 PM10). In a similar way, PM2.5 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 PM2.5 exposure) and third trimester of pregnancy (28.1, 95 % CI: 3.6 to 58.4 %, p = 0.02 for an IQR increment in PM2.5 exposure). In umbilical cord blood, 8-OHdG levels were significantly associated with PM10 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 PM10 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.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The cited source says what the claim attributes to it.
In the citing paper
“Grevendonk et al. [161] demonstrated PM2.5 exposure during pregnancy was positively associated with markers of mitochondrial DNA damage in maternal blood.”
From Air pollution and children’s health—a review of adverse effects associated with prenatal exposure from fine to ultrafine particulate matter (2021) · cites this paper as [161]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Toxic potential of materials at the nanolevel
Nel, A., Xia, T., Mädler, L., & Li, N. (2006) · Science · doi:10.1126/science.1114397 · Cited by 9,324 · cited 1×
“risk factor for the induction of inflammatory and oxidative stress responses [1–4], especially during the pregnancy period when increased levels of oxidative stress can be expected [5].”
BackgroundHellemans, J., Mortier, G., De Paepe, A., Speleman, F., & Vandesompele, J. (2007) · Genome Biology · doi:10.1186/gb-2007-8-2-r19 · Cited by 4,023 · cited 2×
“qBase software (Biogazelle, Zwijnaarde, BE) was used to normalize data and correct for run-to-run differences [22].”
MethodYakes, F. M., & Van Houten, B. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.2.514 · Cited by 1,854 · cited 1×
“be more extensive and persistent compared to nuclear DNA damage [30].”
Background8-Hydroxyguanine, an abundant form of oxidative DNA damage, causes G-T and A-C substitutions.
Cheng, K. C., Cahill, D. S., Kasai, H., Nishimura, S., & Loeb, L. A. (1992) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)48474-8 · Cited by 1,844 · cited 1×
“the most common one [7].”
Li, N., Xia, T., & Nel, A. E. (2008) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2008.01.028 · Cited by 949
Human mitochondrial DNA: roles of inherited and somatic mutations
Schon, E. A., DiMauro, S., & Hirano, M. (2012) · Nature Reviews Genetics · doi:10.1038/nrg3275 · Cited by 757 · cited 1×
“Besides metabolic disorders, the stochastic accumulation of mtDNA mutations encompasses the pathophysiological basis of disease processes including aging, neurodegenerative diseases, and cancer [38].”
BackgroundChuang, K.-J., Chan, C.-C., Su, T.-C., Lee, C.-T., & Tang, C.-S. (2007) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.200611-1627oc · Cited by 685 · cited 1×
“Consistent with our results, most of these studies observed a positive association between nuclear 8-OHdG levels in urine and PM exposure [14–16, 23–25] or tobacco smoke exposure [16, 26–29].”
ResultMitochondrial DNA Genetics and the Heteroplasmy Conundrum in Evolution and DiseasePreprint
Dc, W., & Chalkia, D. (2013) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a021220 · Cited by 680 · cited 1×
“If accumulation of 8-OHdG and somatic mtDNA mutations exceed a critical threshold, they can cause a biochemical defect in the mitochondrial respiratory chain and could result in a progressive decline of mitochondrial function [10, 34, 36].”
BackgroundLoft, S., Vistisen, K., Ewertz, M., Tjønneland, A., Overvad, K., & Poulsen, H. E. (1992) · Carcinogenesis · doi:10.1093/carcin/13.12.2241 · Cited by 643
Universal heteroplasmy of human mitochondrial DNA
Payne, B. A. I., Wilson, I., Yu‐Wai‐Man, P., Coxhead, J., Deehan, D. J., Horváth, R., Taylor, R. W., Samuels, D. C., Santibanez‐Koref, M., & Chinnery, P. F. (2012) · Human Molecular Genetics · doi:10.1093/hmg/dds435 · Cited by 396 · cited 2×
“Moreover, the mtDNA repair mechanisms work less efficiently resulting in a 5 to 15 times higher mutation rate compared with nDNA [6, 9].”
Background
Research works printed but not linked: 2
- de Souza-Pinto NC, Eide L, Hogue BA, Thybo T, Stevnsner T, Seeberg E, et al. Repair of 8-oxodeoxyguanosine lesions in mitochondrial dna depends on the oxoguanine dna glycosylase (OGG1) gene and 8-oxoguanine accumulates in the mitochondrial dna of OGG1-defective mice. Cancer Res. 2001;61(14):5378–81.
- Sorensen M, Autrup H, Hertel O, Wallin H, Knudsen LE, Loft S. Personal exposure to PM2.5 and biomarkers of DNA damage. Cancer Epidemiol Biomarkers Prev. 2003;12(3):191–6.
Cited by
Sorted by citations
Johnson, N. M., Hoffmann, A. R., Behlen, J. C., Lau, C., Pendleton, D., Harvey, N., Shore, R., Li, Y., Chen, J., Tian, Y., et al. (2021) · Environmental Health and Preventive Medicine · doi:10.1186/s12199-021-00995-5 · Cited by 339
Mechanisms of ultrafine particle-induced respiratory health effects
Leikauf, G. D., Kim, S., & Jang, A. (2020) · Experimental & Molecular Medicine · doi:10.1038/s12276-020-0394-0 · Cited by 345
Saenen, N. D., Martens, D. S., Neven, K. Y., Alfano, R., Bové, H., Janssen, B. G., Roels, H. A., Plusquin, M., Vrijens, K., & Nawrot, T. S. (2019) · Clinical Epigenetics · doi:10.1186/s13148-019-0688-z · Cited by 267
Self-citationPrenatal Air Pollution and Newborns' Predisposition to Accelerated Biological Aging
Martens, D. S., Cox, B., Janssen, B. G., Clemente, D. B. P., Gasparrini, A., Vanpoucke, C., Lefebvre, W., Roels, H. A., Plusquin, M., & Nawrot, T. S. (2017) · JAMA Pediatrics · doi:10.1001/jamapediatrics.2017.3024 · Cited by 241
Self-citationImpact of ambient PM2.5 on adverse birth outcome and potential molecular mechanism
Li, Z., Tang, Y., Song, X., Lazar, L., Li, Z., & Zhao, J. (2019) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2018.10.109 · Cited by 193
Bongaerts, E., Lecante, L. L., Bové, H., Roeffaers, M. B. J., Ameloot, M. M., Fowler, P., & Nawrot, T. S. (2022) · The Lancet Planetary Health · doi:10.1016/s2542-5196(22)00200-5 · Cited by 228
Self-citationEnvironmental Chemical Exposures and Mitochondrial Dysfunction: a Review of Recent Literature
Reddam, A., McLarnan, S. M., & Kupsco, A. J. (2022) · Current Environmental Health Reports · doi:10.1007/s40572-022-00371-7 · Cited by 192
“Studies have shown that increased prenatal exposure to particulate matter (PM) was associated with increased levels of mitochondrial urinary 8-OHdG in maternal and umbilical cord blood, suggesting oxidative stress within the mitochondria [94].”
Shukla, A., Bunkar, N., Kumar, R., Bhargava, A., Tiwari, R. R., Chaudhury, K., Goryacheva, I. Y., & Mishra, P. K. (2018) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2018.11.381 · Cited by 167
Soeur, J., Belaïdi, J.-P., Chollet, C., Denat, L., Dimitrov, A., Jones, C., Perez, P., Zanini, M., Zobiri, O., Mezzache, S., et al. (2017) · Journal of Dermatological Science · doi:10.1016/j.jdermsci.2017.01.007 · Cited by 131
Daiber, A., Kuntić, M., Hahad, O., Delogu, L. G., Rohrbach, S., Lisa, F. D., Schulz, R., & Münzel, T. F. (2020) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2020.108662 · Cited by 143
Saenen, N. D., Vrijens, K., Janssen, B. G., Roels, H. A., Neven, K. Y., Vanden Berghe, W., Gyselaers, W., Vanpoucke, C., Lefebvre, W., De Boever, P., et al. (2017) · Environmental Health Perspectives · doi:10.1289/ehp38 · Cited by 104
“…we reported that PM is associated with global methylation and gene-specific mitochondrial methylation in the placenta (Janssen et al. 2013; Janssen et al. 2015) and with mitochondrial oxidative DNA damage in cord blood and maternal blood (Grevendonk et al. 2016) in the ENVIRONAGE birth cohort.”
BackgroundSelf-citationAmbient air pollution and adverse birth outcomes: A review of underlying mechanisms
Fussell, J. C., Jauniaux, E. R. M., Smith, R. B., & Burton, G. J. (2023) · BJOG An International Journal of Obstetrics & Gynaecology · doi:10.1111/1471-0528.17727 · Cited by 102
“54 Studies that have sought to evaluate the involvement of oxidative stress by examining whether the OP of PM 2.5 modifies the relation between PM 2.5 mass concentrations/exposures and adverse birth outcomes have reported mixed re-sults, possibly indicative of different assays employed and birth…”
BackgroundInfluentialEnvironmental Air Pollutants Affecting Skin Functions with Systemic Implications
Bocheva, G., Slominski, R. M., & Slominski, A. T. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241310502 · Cited by 94
Ning, R., Li, Y., Du, Z., Li, T., Sun, Q., Lin, L., Xu, Q., Duan, J., & Sun, Z. (2021) · Redox Biology · doi:10.1016/j.redox.2021.102113 · Cited by 96
Meng, X., Zhang, Y., Yang, K., Yang, Y.-K., & Zhou, X. (2016) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph13080748 · Cited by 104
Klocke, C., Allen, J. L., Sobolewski, M., Mayer-Pröschel, M., Blum, J. L., Lauterstein, D., Zelikoff, J. T., & Cory-Slechta, D. A. (2017) · Toxicological Sciences · doi:10.1093/toxsci/kfx010 · Cited by 87
Cohort Profile: The ENVIRonmental influenceONearly AGEing (ENVIRONAGE): a birth cohort study
Janssen, B. G., Madlhoum, N., Gyselaers, W., Bijnens, E. M., Clemente, D. B. P., Cox, B., Hogervorst, J. G. F., Luyten, L. J., Martens, D. S., Peusens, M., et al. (2017) · International Journal of Epidemiology · doi:10.1093/ije/dyw269 · Cited by 113
Self-citationDiesel exhaust exposure, its multi-system effects, and the effect of new technology diesel exhaust
Reis, H., Reis, C., Sharip, A., Reis, W. P., Zhao, Y., Sinclair, R., & Beeson, W. L. (2018) · Environment International · doi:10.1016/j.envint.2018.02.042 · Cited by 80
Pre‐natal brain development as a target for urban air pollution
Sunyer, J., & Dadvand, P. (2019) · Basic & Clinical Pharmacology & Toxicology · doi:10.1111/bcpt.13226 · Cited by 83
Placental circadian pathway methylation and in utero exposure to fine particle air pollution
Nawrot, T. S., Saenen, N. D., Schenk, J., Janssen, B. G., Motta, V., Tarantini, L., Cox, B., Lefebvre, W., Vanpoucke, C., Maggioni, C., et al. (2018) · Environment International · doi:10.1016/j.envint.2018.02.034 · Cited by 77
Self-citationPrenatal fine particulate matter exposure, placental DNA methylation changes, and fetal growth
Zhao, Y., Wang, P., Zhou, Y., Xia, B., Zhu, Q., Ge, W., Li, J., Shi, H., Xiao, X., & Zhang, Y. (2020) · Environment International · doi:10.1016/j.envint.2020.106313 · Cited by 73
Impairment of mitochondrial function by particulate matter: Implications for the brain
Chew, S., Kołosowska, N., Saveleva, L., Malm, T., & Kanninen, K. M. (2020) · Neurochemistry International · doi:10.1016/j.neuint.2020.104694 · Cited by 77
Developmental programming of mitochondrial biology: a conceptual framework and review
Gyllenhammer, L. E., Entringer, S., Buß, C., & Wadhwa, P. D. (2020) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2019.2713 · Cited by 75
Liu, W., Zhang, M., Feng, J., Fan, A., Zhou, Y., & Xu, Y. (2017) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph14060592 · Cited by 63
Impact of Maternal Environment and Inflammation on Fetal Neurodevelopment
Lubrano, C., Parisi, F., & Cetin, I. (2024) · Antioxidants · doi:10.3390/antiox13040453 · Cited by 66
“Animal models showed that PM 2.5 (PM with diameter of 2.5 µ m or smaller) can cross the placenta and circulate in fetal blood, inducing oxidative stress and inflammatory responses in the growing fetus, thereby affecting fetal development [43,104,127–129].”
BackgroundInfluentialParticulate Matter, an Intrauterine Toxin Affecting Foetal Development and Beyond
Chen, H., Oliver, B. G. G., Pant, A., Olivera, A., Poronnik, P., Pollock, C. A., & Saad, S. (2021) · Antioxidants · doi:10.3390/antiox10050732 · Cited by 56
Effects of maternal exposure to ambient air pollution on newborn telomere length
Song, L., Zhang, B., Liu, B., Wu, M., Zhang, L., Wang, L., Xu, S., Cao, Z., & Wang, Y. (2019) · Environment International · doi:10.1016/j.envint.2019.04.064 · Cited by 53
Mitochondrial Function in Allergic Disease
Iyer, D., Mishra, N., & Agrawal, A. (2017) · Current Allergy and Asthma Reports · doi:10.1007/s11882-017-0695-0 · Cited by 63
Patterson, W. B., Glasson, J., Naik, N. C., Jones, R. B., Berger, P. K., Plows, J. F., Minor, H. A., Lurmann, F., Goran, M. I., & Alderete, T. L. (2021) · Environmental Health · doi:10.1186/s12940-021-00753-8 · Cited by 52
Tapia, V., Vasquez, B., Vu, B. N., Liu, Y., Steenland, K., & Gonzales, G. F. (2020) · Journal of Exposure Science & Environmental Epidemiology · doi:10.1038/s41370-020-0223-5 · Cited by 52
Sheffield, P. E., Speranza, R. J., Chiu, Y.-H. M., Hsu, H. L., Curtin, P. C. P., Renzetti, S., Pajak, A., Coull, B. A., Schwartz, J. D., Kloog, I., et al. (2018) · PLoS ONE · doi:10.1371/journal.pone.0195267 · Cited by 54
“[18] Exposure to ambient pollution in pregnancy can enhance systemic oxidative stress[19] and impact endocrine and immune system disruption[20] which in turn has implications for neuropsychological functioning in women during the perinatal period.”
BackgroundZhong, J., Allen, K. M., Rao, X., Ying, Z., Braunstein, Z., Kankanala, S., Xia, C. Q., Wang, X., Bramble, L. A., Wagner, J. G., et al. (2016) · Inhalation Toxicology · doi:10.1080/08958378.2016.1179373 · Cited by 47
“5 (Grevendonk et al., 2016; Rajagopalan & Brook, 2012; Sun et al., 2010; Xu et al., 2010; Xu et al., 2011) and cigarette smoking (Carnevali et al., 2003; Mons et al., 2016).”
BackgroundCellular mechanisms linking to outdoor and indoor air pollution damage during pregnancy
Chiarello, D. I., Ustáriz, J., Marı́n, R., Carrasco‐Wong, I., Farías, M., Giordano, A., Gallardo, F. S., Illanes, S. E., & Gutiérrez, J. (2023) · Frontiers in Endocrinology · doi:10.3389/fendo.2023.1084986 · Cited by 51
“(92) 293 mother-newborn pairs mixture PM2.”
BackgroundThe Impact of Oxidative Stress of Environmental Origin on the Onset of Placental Diseases
Ruano, C. S. M., Miralles, F., Méhats, C., & Vaiman, D. (2022) · Antioxidants · doi:10.3390/antiox11010106 · Cited by 47
Syama, K. P., Blais, E., & Kumarathasan, P. (2025) · Science of The Total Environment · doi:10.1016/j.scitotenv.2025.178999 · Cited by 39
Rehman, A., Kumari, R., Kamthan, A., Tiwari, R. R., Srivastava, R. K., van der Westhuizen, F. H., & Mishra, P. K. (2022) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2022.12.083 · Cited by 37
Association of ambient air pollutants and birth weight in Ningbo, 2015–2017
Li, Z., Yuan, X., Fu, J., Zhang, L., Hong, L., Hu, L., & Liu, L. (2019) · Environmental Pollution · doi:10.1016/j.envpol.2019.03.076 · Cited by 37
Maternal Particulate Matter Exposure Impairs Lung Health and Is Associated with Mitochondrial Damage
Wang, B., Chan, Y. L., Li, G., Ho, K., Anwer, A. G., Smith, B. J., Guo, H., Jalaludin, B. B., Herbert, C. A., Thomas, P. S., et al. (2021) · Antioxidants · doi:10.3390/antiox10071029 · Cited by 36
Scarpato, R., Testi, S., Colosimo, V., García‐Crespo, C., Micheli, C., Azzarà, A., Tozzi, M. G., & Ghirri, P. (2019) · Mutation Research/Reviews in Mutation Research · doi:10.1016/j.mrrev.2019.108295 · Cited by 36
Ye, Z., Lu, X., Deng, Y., Wang, X., Zheng, S., Ren, H., Zhang, M., Chen, T., Jose, P. A., Yang, J., et al. (2018) · Cellular Physiology and Biochemistry · doi:10.1159/000488418 · Cited by 34
“5 exposure leads to increased inflammation, enhanced production of reactive oxidative species (ROS), mitochondrial oxidative DNA damage and incident hypertension [37, 38].”
BackgroundXu, J., Liu, Y., Zhang, Q., Su, Z., Yan, T., Zhou, S., Wang, T., Wei, X., Chen, Z., Hu, G., et al. (2022) · Environmental Pollution · doi:10.1016/j.envpol.2021.118763 · Cited by 33
Yu, H.-R., Puthussery, J., Wang, Y., & Verma, V. (2021) · Atmospheric Chemistry and Physics · doi:10.5194/acp-2021-376-rc1
“…leading to a cascade of detrimental biological effects such as oxidation of DNA, lipids, and proteins (Rossner et al., 2008; Franco et al., 2008; Grevendonk et al., 2016), tissue injury (Feng et al., 2016; Gurgueira et al., 2002; Sun et al., 2020), and eventually cardiopulmonary impairment (Li…”
Neurodevelopmental toxicity induced by airborne particulate matter
Shang, M., Tang, M. X., & Xue, Y. (2022) · Journal of Applied Toxicology · doi:10.1002/jat.4382 · Cited by 30
“5 and PM10 during gestation has been shown to induce mitochondrial oxidative stress in human maternal blood and fetal umbilical cord blood when sampled at delivery (Grevendonk et al., 2016).”
BackgroundBiomarkers used in studying air pollution exposure during pregnancy and perinatal outcomes: a review
Desai, G. S., Chu, L., Guo, Y., Myneni, A. A., & Mu, L. (2017) · Biomarkers · doi:10.1080/1354750x.2017.1339294 · Cited by 29
Prenatal Exposure to Ambient Air Pollution and Epigenetic Aging at Birth in Newborns
Song, A., Feinberg, J. I., Bakulski, K. M., Croen, L., Fallin, M. D., Newschaffer, C. J., Hertz‐Picciotto, I., Schmidt, R. J., Ladd‐Acosta, C., & Volk, H. E. (2022) · Frontiers in Genetics · doi:10.3389/fgene.2022.929416 · Cited by 26
“Epidemiological and clinical studies have linked prenatal air pollution exposure to epigenetic alterations, inflammation, and oxidative stress (Janssen et al., 2013; Breton et al., 2016; Grevendonk et al., 2016; Saenen et al., 2016; Gruzieva et al., 2017; Breton et al., 2019).”
BackgroundPremature births in Spain: Measuring the impact of air pollution using time series analyses
Arroyo, V., Linares, C., & Díaz, J. (2019) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2018.12.470 · Cited by 25
Nys, S. D., Duca, R. C., Nawrot, T. S., Hoet, P., MEERBEEK, B. V., LANDUYT, K. L. V., & Godderis, L. (2017) · Environment International · doi:10.1016/j.envint.2017.11.002 · Cited by 29
Self-citationLiu, J., Chen, Y., Liu, D., Ye, F., Sun, Q., Huang, Q., Dong, J., Pei, T., He, Y., & Zhang, Q. (2023) · Environmental Science and Pollution Research · doi:10.1007/s11356-023-26831-7 · Cited by 24
“One likely pathway manifested through inflammatory stress and endothelial function is the cardiovascular mechanisms (Brunst et al. 2018; Grevendonk et al. 2016; Rosa et al. 2017b; Kannan et al. 2006).”
BackgroundEffects of PM2.5 exposure during gestation on maternal gut microbiota and pregnancy outcomes
Liu, W., Zhou, Y., Li, Y., Qin, Y., Yu, L., Li, R., Chen, Y., & Xu, Y. (2020) · Chemosphere · doi:10.1016/j.chemosphere.2020.125879 · Cited by 24
Dagnino, S., & Macherone, A. (2018) · Springer eBooks · doi:10.1007/978-3-319-89321-1 · Cited by 24
Long-term impact of ambient air pollution on preterm birth in Xuzhou, China: a time series study
Li, S., Lei, P., Wu, X., Xu, G., Cheng, P., Hao, J., Huang, Z., Xu, M. R., Chen, S., Zhang, C., et al. (2021) · Environmental Science and Pollution Research · doi:10.1007/s11356-021-13621-2 · Cited by 26
“…stress, inflammation, leading to DNA damage and accumulation in fetal tissues, and changes in the viscosity of the blood and the release of proinflammatory cytokines, including IL-6, IL-8, IL-10, and TNF-α (Clemente et al. 2016; Grevendonk et al. 2016; Peters et al. 1997; Sun et al. 2015).”
BackgroundAl-Gubory, K. H. (2016) · Birth Defects Research Part C Embryo Today Reviews · doi:10.1002/bdrc.21142 · Cited by 21
Saenen, N. D., Provost, E. B., Cuypers, A., Kiciński, M., Pieters, N., Plusquin, M., Vrijens, K., Boever, P. D., & Nawrot, T. S. (2018) · Environment International · doi:10.1016/j.envint.2018.11.028 · Cited by 22
“Air pollution exposure can lead to increased oxidative stress and mtDNA damage (Grevendonk et al., 2016), with several lines of research suggesting that this damage is linked to age-related endothelial and vascular dysfunction (Mikhed et al., 2015; Forstermann, 2008).”
BackgroundSelf-citationPeng, C., Çayır, A., Sánchez-Guerra, M., Di, Q., Wilson, A., Zhong, J., Kosheleva, A., Trevisi, L., Colicino, E., Brennan, K. J. M., et al. (2017) · Epidemiology · doi:10.1097/ede.0000000000000717 · Cited by 19
You, Y., Park, S., Kwon, E., Kim, Y.-A., Hur, Y. M., Lee, G. I., Kim, S. M., Song, J. M., Kim, Y. J., Kim, Y. H., et al. (2024) · Environmental Science and Pollution Research · doi:10.1007/s11356-023-31774-0 · Cited by 19
“Several studies have linked in-utero PM exposure to mitochondrial oxidative dysfunction (Grevendonk et al. 2016; Brunst et al. 2018; Cosemans et al. 2022).”
BackgroundMandakh, Y., Oudin, A., Erlandsson, L., Isaxon, C., Hansson, S. R., Bröberg, K., & Malmqvist, E. (2021) · Frontiers in Toxicology · doi:10.3389/ftox.2021.659407 · Cited by 18
“As previously shown, exposure to ambient PM during pregnancy has been found to be associated with increased levels of mitochondrial 8-hydroxy 2-deoxyguanine, which is considered to be a marker of oxidative DNA damage (Grevendonk et al., 2016) which was found to be correlated with loss of mtDNA (Qian and Van Houten, 20…”
BackgroundCentral metabolism of functionally heterogeneous mesenchymal stromal cells
Barilani, M., Palorini, R., Votta, G., Piras, R., Buono, G., Grassi, M., Bollati, V., Chiaradonna, F., & Lazzari, L. (2019) · Scientific Reports · doi:10.1038/s41598-019-51937-9 · Cited by 17
Self-citationBai, Y., Casas, L., Scheers, H., Janssen, B., Nemery, B., & Nawrot, T. (2018) · Environment International · doi:10.1016/j.envint.2018.06.003 · Cited by 17
Self-citationWang, X.-T., Lin, Y., Ge, Y., Craig, E. A., Liu, X.-D., Miller, R. K., Thurston, S., Brunner, J., Barrett, E., O'Connor, T., et al. (2024) · Environmental Pollution · doi:10.1016/j.envpol.2024.124463 · Cited by 16
Does PM1 exposure during pregnancy impact the gut microbiota of mothers and neonates?
Cao, Y., Zang, T., Qiu, T., Xu, Z., Chen, X., Fan, X., Zhang, Q., Huang, Y., Liu, J., Ni, W., et al. (2023) · Environmental Research · doi:10.1016/j.envres.2023.116304 · Cited by 15
Li, Z., Tian, F., Ban, H., Xia, S., Cheng, L., Ren, X., Lyu, Y., & Zheng, J. (2022) · Toxicology Letters · doi:10.1016/j.toxlet.2022.08.008 · Cited by 19
Li, Z., Fu, J., Zhou, L., Tang, Y., Hua, Q., Liu, L., & Zhao, J. (2019) · Environmental Pollution · doi:10.1016/j.envpol.2019.113266 · Cited by 19
Giovannini, N., Schwartz, L., Cipriani, S., Parazzini, F., Baini, I., Signorelli, V., & Cetin, I. (2017) · The Journal of Maternal-Fetal & Neonatal Medicine · doi:10.1080/14767058.2017.1293032 · Cited by 16
“PM10 exposure is also associated with systemic inflammation [24]: inhalation of particles”
BackgroundBongaerts, E., Nawrot, T. S., Wang, C., Ameloot, M. M., Bové, H., Roeffaers, M. B. J., Chavatte‐Palmer, P., Couturier‐Tarrade, A., & Cassee, F. R. (2023) · Particle and Fibre Toxicology · doi:10.1186/s12989-023-00531-z · Cited by 15
Self-citationLi, R.-Y., Li, S.-S., Pan, M.-M., Chen, H., Liu, X.-T., Chen, G.-B., Chen, R.-L., Yin, S., Hu, K., Mao, Z.-X., et al. (2021) · Chemosphere · doi:10.1016/j.chemosphere.2021.129907 · Cited by 15
Ambient Air Pollution and Congenital Heart Disease: Updated Evidence and Future Challenges
Gorini, F., & Tonacci, A. (2025) · Antioxidants · doi:10.3390/antiox14010048 · Cited by 11
Chu, M., Yang, J., Gong, C., Li, X., Wang, M., Han, B., Huo, Y., Wang, J., Bai, Z., & Zhang, Y. (2024) · Environmental Research · doi:10.1016/j.envres.2024.120136 · Cited by 16
Santos, J. X., Sampaio, P., Rasga, C., Martiniano, H., Faria, C., Café, C., Oliveira, A., Duque, F., Oliveira, G., Sousa, L., et al. (2023) · Environmental Research · doi:10.1016/j.envres.2023.115795 · Cited by 14
“…vulnerability to environmental toxins, and it has been suggested that PM 2.5 exposure during the first trimester promotes mitochondrial DNA damage at the placenta, leading to oxidative stress, and interfering with the barrier function of this structure (Grevendonk et al., 2016; Tapia et al., 2020).”
InfluentialValavanidis, A. (2019) · Springer eBooks · doi:10.1007/978-981-13-8413-4_13 · Cited by 16
Prenatal PM2.5 affects atopic dermatitis depending on maternal anxiety and gender: COCOA study
Kim, S., Yang, S., Lim, H., Lee, S., Park, M. J., Song, K., Choi, E. J., Oh, H. Y., Kim, H., Shin, Y., et al. (2021) · Clinical and Translational Allergy · doi:10.1002/clt2.12070 · Cited by 13
“5 and psychosocial stress during pregnancy are associated with oxidative stress.(10,11,27) Oxidative stress may influence AD pathogenesis.”
BackgroundCleemput, J. V., Poelaert, K. C., Laval, K., den Broeck, W. V., & Nauwynck, H. (2019) · Veterinary Microbiology · doi:10.1016/j.vetmic.2019.05.009 · Cited by 13
“Upon inhalation, these DEP cause oxidative stress with accompanying in fl ammatory processes and DNA damage (Grevendonk et al., 2016; Ito et al., 2000; Ma and Ma, 2002; Shukla et al., 2000; Zhao et al., 2009).”
Aging, longevity, and the role of environmental stressors: a focus on wildfire smoke and air quality
Scieszka, D. P., Bolt, A. M., McCormick, M. A., Brigman, J. L., & Campen, M. J. (2023) · Frontiers in Toxicology · doi:10.3389/ftox.2023.1267667 · Cited by 15
Huang, C., Liu, C., Chen, M., Tsao, P., Chen, C., Chou, H., & Chen, P. (2019) · Pediatrics & Neonatology · doi:10.1016/j.pedneo.2019.11.008 · Cited by 19
Detection of Mitochondrial Toxicity of Environmental Pollutants UsingCaenorhabditis elegans
Maurer, L. L., Luz, A. L., & Meyer, J. N. (2018) · Wiley eBooks · doi:10.1002/9781119329725.ch43 · Cited by 9
Manivannan, J., & Sundaresan, L. (2021) · Gene Reports · doi:10.1016/j.genrep.2021.101312 · Cited by 11
Wu, K., Hu, H., Ren, Z., Benmarhnia, T., Ren, M., He, S., Knibbs, L. D., Meng, X., Di, J., Huang, C., et al. (2021) · Environmental Research Letters · doi:10.1088/1748-9326/abf58c · Cited by 12
Oxidative Potential of Particulate Matter: A Prospective Measure to Assess PM Toxicity
Yadav, S., & Phuleria, H. C. (2019) · Energy, environment, and sustainability · doi:10.1007/978-981-15-0540-9_16 · Cited by 28
Song, J., Chen, Y. C., Wei, L., Ma, Y., Tian, N., Huang, S. Y., Dai, Y. M., Zhao, L. H., & Kong, Y. (2017) · BMJ Open · doi:10.1136/bmjopen-2017-015895 · Cited by 12
In Utero Exposure to Air Pollutants and Mitochondrial Heteroplasmy in Neonates.
Cosemans, C., Wang, C.-R., Martens, D., Janssen, B., Vanpoucke, C., Lefebvre, W., Smeets, K., Nawrot, T., & Plusquin, M. (2022) · Environmental Science and Technology · doi:10.1021/acs.est.2c02556 · Cited by 9
Self-citationPrenatal Exposure to Fine Particulate Matter Components and Autism Risk in Childhood
Cloutier, M., Yu, C., Talarico, R., Hawken, S., Chen, H., Weichenthal, S., Cakmak, S., Hebbern, C., Gunz, A. C., van Donkelaar, A., et al. (2025) · JAMA Network Open · doi:10.1001/jamanetworkopen.2025.38882 · Cited by 8
Chen, S., Yu, W., Shen, Y., Lu, L., Meng, X., & Liu, J. (2025) · Asian Biomedicine · doi:10.2478/abm-2025-0002 · Cited by 8
Raheel, H., Sinharoy, S. S., Díaz-Artiga, A., Garg, S. S., Pillarisetti, A., Balakrishnan, K., Chiang, M., Lovvorn, A. E., Kirby, M. A., Ramakrishnan, U., et al. (2024) · Environment International · doi:10.1016/j.envint.2024.109211 · Cited by 8
Kumar, S. H., Acharyya, S., Chouksey, A., Soni, N., Nazeer, N., & Mishra, P. K. (2024) · Reproductive Toxicology · doi:10.1016/j.reprotox.2024.108675 · Cited by 9
The telomere-mitochondrial axis of aging in newborns
Stukken, C. V. D., Nawrot, T. S., Alfano, R., Wang, C., Langie, S. A. S., Plusquin, M., Janssen, B. G., & Martens, D. S. (2022) · Aging · doi:10.18632/aging.203897 · Cited by 22
Self-citationYu, Y.-Y., Fan, W., Ni, J.-Y., Gao, X., Li, W., Zheng, J.-Q., Zhang, H., Chen, J., Liu, Q., Lin, Z., et al. (2025) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2025.139598 · Cited by 6
Erlandsson, L., Hirschmugl, B., Hansson, E., Merčnik, M. H., Wadsack, C., & Hansson, S. R. (2025) · Journal of Environmental Science · doi:10.1016/j.jes.2025.03.043 · Cited by 6
Ward, G., Watts, M. P. C., & Hansson, S. R. (2025) · Pregnancy Hypertension · doi:10.1016/j.preghy.2025.101204 · Cited by 10
Liu, L., Yang, J., Ye, Z.-L., Tian, C., Huang, X., Zhang, H., & Mo, X.-H. (2022) · Frontiers in Environmental Science · doi:10.3389/fenvs.2022.747286 · Cited by 3
“The characteristic indexes were selected and detected from the aspects of oxidative stress, the level of inflammatory factors, and the intercellular communication between gap junctions (Bekki et al., 2016; Grevendonk et al., 2016).”
BackgroundCoumans, J. V. F., & Al‐Jaaidi, S. (2023) · Environmental Research Health · doi:10.1088/2752-5309/acdd18 · Cited by 4
King, C. (2025) · Global Public Health · doi:10.1080/17441692.2025.2492234 · Cited by 4
“…via the olfactory nerve, where they instigate immune dysfunction via glial cells of the central nervous system, leading to oxidative DNA damage (Grevendonk et al., 2016), lipid peroxidation (Ambroz et al., 2016; Bernardi et al., 2021), and pathological white matter changes (Allen et al., 2017;…”
Chiu, Y.-H. M., Coull, B. A., Wilson, A., Hsu, H. L., Xhani, N., Nentin, F., Deli, B. C., Schwartz, J. D., Colicino, E., Wright, R. O., et al. (2024) · Journal of Exposure Science & Environmental Epidemiology · doi:10.1038/s41370-024-00726-2 · Cited by 6
“Exposure to ambient AP during pregnancy may further increase systemic oxidative stress [12, 13] and disrupt immune and endocrine system [14], which may have implications for women ’ s perinatal neuropsychological functioning [15].”
Kahroba, H., Krauskopf, J., Briedé, J. J., Nawrot, T. S., & de Kok, T. M. C. M. (2025) · Environmental Health · doi:10.1186/s12940-025-01238-8 · Cited by 3
“Air pollutants can inflict a range of cellular injuries by inducing the endoplasmic reticulum (ER) stress, promoting the accumulation of misfolded proteins [45] and causing DNA damage that can initiate repair mechanisms, enforce cell cycle arrest, or trigger apoptosis [46, 47].”
Self-citationImpacts of PM 2.5 on stillbirth and the potential mechanism: a narrative review
Li, Z., Liu, R., & Zhang, E. (2025) · Reviews on Environmental Health · doi:10.1515/reveh-2025-0090 · Cited by 2
From exposure to outcomes: How air pollutants impact maternal and foetal health
Parikh, G., & Patel, B. M. (2025) · Reproductive Toxicology · doi:10.1016/j.reprotox.2025.109080 · Cited by 3
The association of prenatal ambient air pollution with placental epigenetic gestational age at birth
He, Z., Song, A., Schrott, R., Feinberg, J. I., Bakulski, K. M., Benke, K. S., Croen, L., Hertz‐Picciotto, I., Schmidt, R. J., Lyall, K., et al. (2025) · Environmental Epidemiology · doi:10.1097/ee9.0000000000000384 · Cited by 4
“12 13–15 Air pollution particles can pass placenta and translocate directly toward fetus, 16,17 which induces inflammation, 18,19 oxidative/nitrosative stress, 13,14 and epigenetic alterations.”
Hautekiet, P., Nawrot, T. S., Martens, D. S., Bijnens, E. M., Keersmaecker, S. C. J. D., der Heyden, J. V., Clercq, E. M. D., & Saenen, N. D. (2025) · Environmental Research · doi:10.1016/j.envres.2025.121525 · Cited by 4
Self-citationZhang, K., Tian, L., Sun, Q., Lv, J., Ding, R., Yu, Y., Yang, L., & Duan, J. (2024) · Environmental Toxicology and Pharmacology · doi:10.1016/j.etap.2024.104585 · Cited by 4
Preliminary Study of Air Pollution and Adverse Pregnancy Outcomes: A Mendelian Randomization Study
Shan, C., Chen, L., Mo, H.-Y., Chen, X., Chen, H., Tao, F., & Gao, H. (2024) · Atmosphere · doi:10.3390/atmos15111285 · Cited by 3
Xu, R., Zhang, Y., Gao, Y., Jia, S., Choi, S., Xu, Y., & Gong, J. (2024) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2024.135018 · Cited by 5
Effect Of Atmospheric Particulate Matter On The Functional State Of Mitochondria
Kondratyeva, E. V., & Vitkina, T. (2023) · Russian Open Medical Journal · doi:10.15275/rusomj.2023.0106 · Cited by 3
“This phenomenon can be observed in cells exposed to pollutants or in people living in a highly polluted environment [42-44].”
Background
Metadata
- Authors
- Grevendonk, L., Janssen, B. G., Vanpoucke, C., Lefebvre, W., Hoxha, M., Bollati, V., & Nawrot, T. S.
- Affiliations
- University of Milan (IT)
- Hasselt University (BE)
- Flemish Institute for Technological Research (BE)
- Corresponding author
- Nawrot, Tim S.
- Venue
- Environmental Health
- Published
- 2016-01-20
- Volume
- 15
- Issue
- 1
- Pages
- 10-10
- ISSN
- 1476-069X (ISSN-L)
- PMC
- PMC4719654
- OpenAlex
- W2286090902
- Cited by
- 145
- References
- 43
- Citations by year
- 2026: 6 · 2025: 17 · 2024: 13 · 2023: 16 · 2022: 16 · 2021: 28 · 2020: 8 · 2019: 13 · 2018: 12 · 2017: 12 · 2016: 4
- FWCI
- 8.59
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- cc-by
- Locations
- Environmental Health (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Lirias (KU Leuven) (submittedVersion, cc-by)
- Archivio Istituzionale della Ricerca (Universita Degli Studi Di Milano) (submittedVersion, other-oa)
- Document Server@UHasselt (UHasselt) (submittedVersion, cc-by)
- Funders
- EU Programme “Ideas” (ERC-2011-StG 282413)
- EU Program “Ideas” (ERC-2012-StG 310898)
- Flemish Scientific Fund (FWO) (N1516112/G.0.873.11.N.10)
- Topics
- Physical Sciences › Environmental Science › Health, Toxicology and Mutagenesis › Air Quality and Health Impacts
- Physical Sciences › Environmental Science › Health, Toxicology and Mutagenesis › Health, Environment, Cognitive Aging
- Physical Sciences › Environmental Science › Health, Toxicology and Mutagenesis › Indoor Air Quality and Microbial Exposure
- Keywords
- particulate matter, PM10, PM2.5, prenatal air pollution exposure, 8-hydroxy-2'-deoxyguanosine, oxidative stress, maternal blood, umbilical cord blood, pregnancy trimesters, ENVIRONAGE birth cohort, prenatal exposure, birth cohort studies, biomarkers of exposure, inflammation, reactive oxygen species
- MeSH terms
- Adult, Air Pollutants, DNA, Mitochondrial, Environmental Exposure, Female, Fetal Blood, Humans, Infant, Newborn, Placenta, Pregnancy, Cohort Studies, Maternal Exposure, Particulate Matter, Young Adult
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review