TY - JOUR
T1 - Ambient particle components and newborn blood pressure in project viva
AU - Zanobetti, Antonella
AU - Coull, Brent A.
AU - Luttmann-Gibson, Heike
AU - Rossem, Lenie van
AU - Rifas-Shiman, Sheryl L.
AU - Kloog, Itai
AU - Schwartz, Joel D.
AU - Oken, Emily
AU - Bobb, Jennifer F.
AU - Koutrakis, Petros
AU - Gold, Diane R.
N1 - Publisher Copyright:
© 2020 The Authors.
PY - 2021/1/5
Y1 - 2021/1/5
N2 - BACKGROUND: Both elemental metals and particulate air pollution have been reported to influence adult blood pressure (BP). The aim of this study is to examine which elemental components of particle mass with diameter ≤2.5 Μm (PM2.5) are responsible for previously reported associations between PM2.5 and neonatal BP. METHODS AND RESULTS: We studied 1131 mother-infant pairs in Project Viva, a Boston-area prebirth cohort. We measured systolic BP (SBP) and diastolic BP (DBP) at a mean age of 30 hours. We calculated average exposures during the 2 to 7 days before birth for the PM2.5 components-aluminum, arsenic, bromine, sulfur, copper, iron, zinc, nickel, vanadium, titanium, magnesium, potassium, silicon, sodium, chlorine, calcium, and lead-measured at the Harvard supersite. Adjusting for covariates and PM2.5, we applied regression models to examine associations between PM2.5 components and median SBP and DBP, and used variable selection methods to select which components were more strongly associated with each BP outcome. We found consistent results with higher nickel associated with significantly higher SBP and DBP, and higher zinc associated with lower SBP and DBP. For an interquartile range increase in the log Z score (1.4) of nickel, we found a 1.78 mm Hg (95% CI, 0.72-2.84) increase in SBP and a 1.30 (95% CI, 0.54-2.06) increase in DBP. Increased zinc (interquartile range log Z score 1.2) was associated with decreased SBP (-1.29 mm Hg; 95% CI, -2.09 to -0.50) and DBP (-0.85 mm Hg; 95% CI: -1.42 to -0.29). CONCLUSIONS: Our findings suggest that prenatal exposures to particulate matter components, and particularly nickel, may increase newborn BP.
AB - BACKGROUND: Both elemental metals and particulate air pollution have been reported to influence adult blood pressure (BP). The aim of this study is to examine which elemental components of particle mass with diameter ≤2.5 Μm (PM2.5) are responsible for previously reported associations between PM2.5 and neonatal BP. METHODS AND RESULTS: We studied 1131 mother-infant pairs in Project Viva, a Boston-area prebirth cohort. We measured systolic BP (SBP) and diastolic BP (DBP) at a mean age of 30 hours. We calculated average exposures during the 2 to 7 days before birth for the PM2.5 components-aluminum, arsenic, bromine, sulfur, copper, iron, zinc, nickel, vanadium, titanium, magnesium, potassium, silicon, sodium, chlorine, calcium, and lead-measured at the Harvard supersite. Adjusting for covariates and PM2.5, we applied regression models to examine associations between PM2.5 components and median SBP and DBP, and used variable selection methods to select which components were more strongly associated with each BP outcome. We found consistent results with higher nickel associated with significantly higher SBP and DBP, and higher zinc associated with lower SBP and DBP. For an interquartile range increase in the log Z score (1.4) of nickel, we found a 1.78 mm Hg (95% CI, 0.72-2.84) increase in SBP and a 1.30 (95% CI, 0.54-2.06) increase in DBP. Increased zinc (interquartile range log Z score 1.2) was associated with decreased SBP (-1.29 mm Hg; 95% CI, -2.09 to -0.50) and DBP (-0.85 mm Hg; 95% CI: -1.42 to -0.29). CONCLUSIONS: Our findings suggest that prenatal exposures to particulate matter components, and particularly nickel, may increase newborn BP.
KW - Air pollution
KW - Child blood pressure
KW - Metals
KW - Pregnancy
UR - http://www.scopus.com/inward/record.url?scp=85099428380&partnerID=8YFLogxK
U2 - 10.1161/JAHA.120.016935
DO - 10.1161/JAHA.120.016935
M3 - Article
C2 - 33372530
AN - SCOPUS:85099428380
SN - 2047-9980
VL - 10
SP - 1
EP - 11
JO - Journal of the American Heart Association
JF - Journal of the American Heart Association
IS - 1
M1 - e016935
ER -