11
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Air pollution exposure is linked with methylation of immunoregulatory genes, altered immune cell profiles, and increased blood pressure in children

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Ambient air pollution exposure is associated with cardiovascular dysregulation and immune system alterations, yet no study has investigated both simultaneously in children. Understanding the multifaceted impacts may provide early clues for clinical intervention prior to actual disease presentation. We therefore determined the associations between exposure to multiple air pollutants and both immunological outcomes (methylation and protein expression of immune cell types associated with immune regulation) and cardiovascular outcomes (blood pressure) in a cohort of school-aged children (6–8 years; n = 221) living in a city with known elevated pollution levels. Exposure to fine particular matter (PM 2.5), carbon monoxide (CO), and ozone (O 3) was linked to altered methylation of most CpG sites for genes Foxp3, IL-4, IL-10 and IFN-g, all involved in immune regulation (e.g. higher PM 2.5 exposure 1 month prior to the study visit was independently associated with methylation of the IL-4 CpG24 site (est = 0.16; P = 0.0095). Also, immune T helper cell types (Th1, Th2 and Th17) were associated with short-term exposure to PM 2.5, O 3 and CO (e.g. Th1 cells associated with PM 2.5 at 30 days: est = − 0.34, P < 0.0001). Both B cells (est = − 0.19) and CD4+ cells (est = 0.16) were associated with 1 day NO2 exposure (P ≤ 0.031), whereas CD4+ and CD8+ cells were associated with chronic exposure to PAH 456, NOx and/or NO 2 ( P ≤ 0.038 for all). Finally, diastolic BP (DBP) was inversely associated with long-term exposures to both CO and PAH 456, and both systolic and pulse pressure were associated with short-term NO 2 and chronic NOx exposure. Our findings demonstrate links between air pollution exposure and methylation of immunoregulatory genes, immune cell profiles and blood pressure, suggesting that even at a young age, the immune and cardiovascular systems are negatively impacted by exposure to air pollution.

          Related collections

          Most cited references59

          • Record: found
          • Abstract: found
          • Article: not found

          Particulate matter air pollution and cardiovascular disease: An update to the scientific statement from the American Heart Association.

          In 2004, the first American Heart Association scientific statement on "Air Pollution and Cardiovascular Disease" concluded that exposure to particulate matter (PM) air pollution contributes to cardiovascular morbidity and mortality. In the interim, numerous studies have expanded our understanding of this association and further elucidated the physiological and molecular mechanisms involved. The main objective of this updated American Heart Association scientific statement is to provide a comprehensive review of the new evidence linking PM exposure with cardiovascular disease, with a specific focus on highlighting the clinical implications for researchers and healthcare providers. The writing group also sought to provide expert consensus opinions on many aspects of the current state of science and updated suggestions for areas of future research. On the basis of the findings of this review, several new conclusions were reached, including the following: Exposure to PM <2.5 microm in diameter (PM(2.5)) over a few hours to weeks can trigger cardiovascular disease-related mortality and nonfatal events; longer-term exposure (eg, a few years) increases the risk for cardiovascular mortality to an even greater extent than exposures over a few days and reduces life expectancy within more highly exposed segments of the population by several months to a few years; reductions in PM levels are associated with decreases in cardiovascular mortality within a time frame as short as a few years; and many credible pathological mechanisms have been elucidated that lend biological plausibility to these findings. It is the opinion of the writing group that the overall evidence is consistent with a causal relationship between PM(2.5) exposure and cardiovascular morbidity and mortality. This body of evidence has grown and been strengthened substantially since the first American Heart Association scientific statement was published. Finally, PM(2.5) exposure is deemed a modifiable factor that contributes to cardiovascular morbidity and mortality.
            Bookmark
            • Record: found
            • Abstract: not found
            • Article: not found

            2019 ACC/AHA Guideline on the Primary Prevention of Cardiovascular Disease: Executive Summary

              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Mass Cytometry: Single Cells, Many Features.

              Technology development in biological research often aims to either increase the number of cellular features that can be surveyed simultaneously or enhance the resolution at which such observations are possible. For decades, flow cytometry has balanced these goals to fill a critical need by enabling the measurement of multiple features in single cells, commonly to examine complex or hierarchical cellular systems. Recently, a format for flow cytometry has been developed that leverages the precision of mass spectrometry. This fusion of the two technologies, termed mass cytometry, provides measurement of over 40 simultaneous cellular parameters at single-cell resolution, significantly augmenting the ability of cytometry to evaluate complex cellular systems and processes. In this Primer, we review the current state of mass cytometry, providing an overview of the instrumentation, its present capabilities, and methods of data analysis, as well as thoughts on future developments and applications.
                Bookmark

                Author and article information

                Contributors
                knadeau@stanford.edu
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                18 February 2021
                18 February 2021
                2021
                : 11
                : 4067
                Affiliations
                [1 ]GRID grid.168010.e, ISNI 0000000419368956, Sean N. Parker Center for Allergy and Asthma Research at Stanford University, ; Stanford, CA 94305 USA
                [2 ]GRID grid.5596.f, ISNI 0000 0001 0668 7884, Department of Cardiovascular Sciences, , University of Leuven, ; Leuven, Belgium
                [3 ]GRID grid.168010.e, ISNI 0000000419368956, Department of Medicine, , Stanford University, ; Stanford, CA 94305 USA
                [4 ]GRID grid.168010.e, ISNI 0000000419368956, Quantitative Sciences Unit, , Stanford University, ; Stanford, CA 94305 USA
                [5 ]GRID grid.47840.3f, ISNI 0000 0001 2181 7878, School of Public Health, , University of California, Berkeley, ; Berkeley, CA 94720 USA
                [6 ]GRID grid.427236.6, ISNI 0000 0001 0294 3035, Sonoma Technology, Inc., ; Petaluma, CA 94954 USA
                [7 ]GRID grid.266102.1, ISNI 0000 0001 2297 6811, Department of Medicine, , University of California, ; San Francisco, CA 94143 USA
                [8 ]GRID grid.168010.e, ISNI 0000000419368956, Stanford Cardiovascular Institute, , Stanford University, ; Stanford, CA 94305 USA
                [9 ]GRID grid.168010.e, ISNI 0000000419368956, Division of Pulmonary and Critical Care Medicine, Department of Medicine, , Sean N. Parker Center for Allergy and Asthma Research at Stanford University, Stanford University, Stanford University School of Medicine, ; 269 Campus Drive, CCSR 3215, MC 5366, Stanford, CA 94305-5101 USA
                Article
                83577
                10.1038/s41598-021-83577-3
                7893154
                33603036
                46f1c4b3-4fe9-4a75-aa9d-b84e92929284
                © The Author(s) 2021

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 12 June 2020
                : 5 January 2021
                Funding
                Funded by: Sean N. Parker Center for Allergy and Asthma Research, Stanford
                Categories
                Article
                Custom metadata
                © The Author(s) 2021

                Uncategorized
                immunology,environmental sciences,natural hazards,cardiology,medical research,risk factors

                Comments

                Comment on this article