Short term air pollution exposure during pregnancy and associations with maternal immune markers

被引:0
|
作者
Yount, C. S. [1 ]
Scheible, K. [2 ]
Thurston, S. W. [3 ]
Qiu, X. [3 ]
Ge, Y. [4 ,5 ]
Hopke, P. K. [1 ,6 ]
Lin, Y. [4 ,5 ]
Miller, R. K. [7 ,8 ]
Murphy, S. K. [2 ]
Brunner, J. [7 ]
Barrett, E. [1 ,7 ,9 ]
O'Connor, T. G. [7 ,10 ,11 ]
Zhang, J. [4 ,5 ]
Rich, D. Q. [1 ,8 ]
机构
[1] Univ Rochester, Med Ctr, Dept Publ Hlth Sci, Rochester, NY 14642 USA
[2] Univ Rochester, Med Ctr, Dept Pediat, Rochester, NY USA
[3] Univ Rochester, Med Ctr, Dept Biostat & Computat Biol, Rochester, NY USA
[4] Duke Univ, Nicholas Sch Environm, Durham, NC USA
[5] Duke Univ, Duke Global Hlth Inst, Durham, NC USA
[6] Clarkson Univ, Ctr Air & Aquat Resources Engn & Sci, Potsdam, NY USA
[7] Univ Rochester, Med Ctr, Dept Obstet & Gynecol, Rochester, NY USA
[8] Univ Rochester, Med Ctr, Dept Environm Med, Rochester, NY USA
[9] Rutgers State Univ, Sch Publ Hlth, Dept Biostat & Epidemiol, Piscataway, NJ USA
[10] Univ Rochester, Dept Psychol, Rochester, NY USA
[11] Univ Rochester, Sch Med & Dent, Dept Psychiat, Rochester, NY USA
基金
美国国家卫生研究院;
关键词
Air pollution; Pregnancy; Immune markers; Immune activation; SYSTEM; INFLAMMATION; BIRTH; MECHANISMS; CYTOKINES; TH1;
D O I
10.1016/j.envres.2024.119639
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
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 mu g/ m3) and NO2 (7.82 ppb) 0-6 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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页数:14
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