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Short term air pollution exposure during pregnancy and associations with maternal immune markers.
Yount, C S; Scheible, K; Thurston, S W; Qiu, X; Ge, Y; Hopke, P K; Lin, Y; Miller, R K; Murphy, S K; Brunner, J; Barrett, E; O'Connor, T G; Zhang, J; Rich, D Q.
Afiliação
  • Yount CS; Department of Public Health Sciences, University of Rochester Medical Center, Rochester, New York, USA.
  • Scheible K; Department of Pediatrics, University of Rochester Medical Center, Rochester, New York, USA.
  • Thurston SW; Department of Biostatistics and Computational Biology, University of Rochester Medical Center, Rochester, New York, USA.
  • Qiu X; Department of Biostatistics and Computational Biology, University of Rochester Medical Center, Rochester, New York, USA.
  • Ge Y; Nicholas School of the Environment & Duke Global Health Institute, Duke University, Durham, North Carolina, USA.
  • Hopke PK; Department of Public Health Sciences, University of Rochester Medical Center, Rochester, New York, USA; Center for Air and Aquatic Resources Engineering and Sciences, Clarkson University, Potsdam, New York, USA.
  • Lin Y; Nicholas School of the Environment & Duke Global Health Institute, Duke University, Durham, North Carolina, USA.
  • Miller RK; Department of Obstetrics and Gynecology, University of Rochester Medical Center, Rochester, New York, USA; Department of Environmental Medicine, University of Rochester Medical Center, Rochester, New York, USA.
  • Murphy SK; Department of Pediatrics, University of Rochester Medical Center, Rochester, New York, USA.
  • Brunner J; Department of Obstetrics and Gynecology, University of Rochester Medical Center, Rochester, New York, USA.
  • Barrett E; Department of Public Health Sciences, University of Rochester Medical Center, Rochester, New York, USA; Department of Obstetrics and Gynecology, University of Rochester Medical Center, Rochester, New York, USA; Department of Biostatistics and Epidemiology, Rutgers University School of Public Health,
  • O'Connor TG; Department of Obstetrics and Gynecology, University of Rochester Medical Center, Rochester, New York, USA; Department of Psychology, University of Rochester, Rochester, New York, USA; Department of Psychiatry, University of Rochester School of Medicine and Dentistry, Rochester, New York, USA; Depart
  • Zhang J; Nicholas School of the Environment & Duke Global Health Institute, Duke University, Durham, North Carolina, USA.
  • Rich DQ; Department of Public Health Sciences, University of Rochester Medical Center, Rochester, New York, USA; Department of Environmental Medicine, University of Rochester Medical Center, Rochester, New York, USA; Department of Medicine, University of Rochester School of Medicine and Dentistry, Rochester,
Environ Res ; : 119639, 2024 Jul 19.
Article em En | MEDLINE | ID: mdl-39034020
ABSTRACT

BACKGROUND:

Air pollution exposure during pregnancy has been associated with numerous adverse pregnancy, birth, and child health outcomes. One proposed mechanism underlying these associations is maternal immune activation and dysregulation. We examined associations between PM2.5 and NO2 exposure during pregnancy and immune markers within immune function groups (TH1, TH2, TH17, Innate/Early Activation, Regulatory, Homeostatic, and Proinflammatory), and examined whether those associations changed across pregnancy.

METHODS:

In a pregnancy cohort study (n=290) in Rochester, New York, we measured immune markers (using Luminex) in maternal plasma up to 3 times during pregnancy. We estimated ambient PM2.5 and NO2 concentrations at participants' home addresses using a spatial-temporal model. Using mixed effects models, we estimated changes in immune marker concentrations associated with interquartile range increases in PM2.5 (2.88 µg/m3) and NO2 (7.82 ppb) 0 to 6 days before blood collection, and assessed whether associations were different in early, mid, and late pregnancy.

RESULTS:

Increased NO2 concentrations were associated with higher maternal immune markers, with associations observed across TH1, TH2, TH17, Regulatory, and Homeostatic groups of immune markers. Furthermore, the largest increases in immune markers associated with each 7.82 ppb increase in NO2 concentration were in late pregnancy (e.g., IL-23 = 0.26 pg/ml, 95% CI= 0.07, 0.46) compared to early pregnancy (e.g., IL-23 = 0.08 pg/ml, 95% CI= -0.11, 0.26).

CONCLUSIONS:

Results were suggestive of NO2-related immune activation. Increases in effect sizes from early to mid to late pregnancy may be due to changes in immune function over the course of pregnancy. These findings provide a basis for immune activation as a mechanism for previously observed associations between air pollution exposure during pregnancy and reduced birthweight, fetal growth restriction, and pregnancy complications.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Environ Res Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Environ Res Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos