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Association between prenatal particulate air pollution exposure and telomere length in cord blood: Effect modification by fetal sex.
Rosa, Maria José; Hsu, Hsiao-Hsien Leon; Just, Allan C; Brennan, Kasey J; Bloomquist, Tessa; Kloog, Itai; Pantic, Ivan; Mercado García, Adriana; Wilson, Ander; Coull, Brent A; Wright, Robert O; Téllez Rojo, Martha María; Baccarelli, Andrea A; Wright, Rosalind J.
Afiliação
  • Rosa MJ; Department of Environmental Medicine and Public Health, Icahn School of Medicine at Mount Sinai, New York, NY, USA. Electronic address: maria.rosa@mssm.edu.
  • Hsu HL; Department of Environmental Medicine and Public Health, Icahn School of Medicine at Mount Sinai, New York, NY, USA. Electronic address: leon.hsu@mssm.edu.
  • Just AC; Department of Environmental Medicine and Public Health, Icahn School of Medicine at Mount Sinai, New York, NY, USA. Electronic address: allan.just@mssm.edu.
  • Brennan KJ; Department of Environmental Health Sciences, Columbia University Mailman School of Public Health, New York, NY, USA. Electronic address: kb2891@cumc.columbia.edu.
  • Bloomquist T; Department of Environmental Health Sciences, Columbia University Mailman School of Public Health, New York, NY, USA. Electronic address: tb2715@cumc.columbia.edu.
  • Kloog I; Department of Geography and Environmental Development, Ben-Gurion University of the Negev, P.O.B. 653, Beer Sheva, Israel. Electronic address: ikloog@bgu.ac.il.
  • Pantic I; Department of Developmental Neurobiology, National Institute of Perinatology, Mexico City, Mexico.
  • Mercado García A; Center for Nutrition and Health Research, National Institute of Public Health, Ministry of Health, Cuernavaca, Morelos, Mexico. Electronic address: adrianam@insp.mx.
  • Wilson A; Department of Statistics, Colorado State University, Fort Collins, CO, USA. Electronic address: ander.wilson@colostate.edu.
  • Coull BA; Department of Environmental Health, Harvard T.H. Chan School of Public Health, Boston, MA, USA. Electronic address: bcoull@hsph.harvard.edu.
  • Wright RO; Department of Environmental Medicine and Public Health, Icahn School of Medicine at Mount Sinai, New York, NY, USA; Institute for Exposomic Research, Icahn School of Medicine at Mount Sinai, New York, NY, USA. Electronic address: robert.wright@mssm.edu.
  • Téllez Rojo MM; Center for Nutrition and Health Research, National Institute of Public Health, Ministry of Health, Cuernavaca, Morelos, Mexico. Electronic address: mmtellez@insp.mx.
  • Baccarelli AA; Department of Environmental Health Sciences, Columbia University Mailman School of Public Health, New York, NY, USA. Electronic address: ab4303@cumc.columbia.edu.
  • Wright RJ; Department of Environmental Medicine and Public Health, Icahn School of Medicine at Mount Sinai, New York, NY, USA; Institute for Exposomic Research, Icahn School of Medicine at Mount Sinai, New York, NY, USA; Kravis Children's Hospital, Department of Pediatrics, Icahn School of Medicine at Mount Si
Environ Res ; 172: 495-501, 2019 05.
Article em En | MEDLINE | ID: mdl-30852452
INTRODUCTION: In utero particulate matter exposure produces oxidative stress that impacts cellular processes that include telomere biology. Newborn telomere length is likely critical to an individual's telomere biology; reduction in this initial telomere setting may signal increased susceptibility to adverse outcomes later in life. We examined associations between prenatal particulate matter with diameter ≤2.5 µm (PM2.5) and relative leukocyte telomere length (LTL) measured in cord blood using a data-driven approach to characterize sensitive windows of prenatal PM2.5 effects and explore sex differences. METHODS: Women who were residents of Mexico City and affiliated with the Mexican Social Security System were recruited during pregnancy (n = 423 for analyses). Mothers' prenatal exposure to PM2.5 was estimated based on residence during pregnancy using a validated satellite-based spatio-temporally resolved prediction model. Leukocyte DNA was extracted from cord blood obtained at delivery. Duplex quantitative polymerase chain reaction was used to compare the relative amplification of the telomere repeat copy number to single gene (albumin) copy number. A distributed lag model incorporating weekly averages for PM2.5 over gestation was used in order to explore sensitive windows. Sex-specific associations were examined using Bayesian distributed lag interaction models. RESULTS: In models that included child's sex, mother's age at delivery, prenatal environmental tobacco smoke exposure, pre-pregnancy BMI, gestational age, birth season and assay batch, we found significant associations between higher PM2.5 exposure during early pregnancy (4-9 weeks) and shorter LTL in cord blood. We also identified two more windows at 14-19 and 34-36 weeks in which increased PM2.5 exposure was associated with longer LTL. In stratified analyses, the mean and cumulative associations between PM2.5 and shortened LTL were stronger in girls when compared to boys. CONCLUSIONS: Increased PM2.5 during specific prenatal windows was associated with shorter LTL and longer LTL. PM2.5 was more strongly associated with shortened LTL in girls when compared to boys. Understanding sex and temporal differences in response to air pollution may provide unique insight into mechanisms.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Telômero / Exposição Materna / Poluentes Atmosféricos / Poluição do Ar Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Child / Female / Humans / Male / Newborn / Pregnancy País/Região como assunto: Mexico Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Telômero / Exposição Materna / Poluentes Atmosféricos / Poluição do Ar Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Child / Female / Humans / Male / Newborn / Pregnancy País/Região como assunto: Mexico Idioma: En Ano de publicação: 2019 Tipo de documento: Article