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. 2015 Mar 6;123(7):730–736. doi: 10.1289/ehp.1308005

Table 2.

Infant blood concentrations for PCB-153 and p,p’-DDE prenatal and postnatal exposure, estimated through pharmacokinetic modeling (ng/g lipid).

Study n Prenatal PCB-153 < LODn (%) Postnatal PCB-153 n Prenatal p,p’-DDE < LODn (%) Postnatal p,p’-DDE
Mean ± SD Median Mean ± SD Median Mean ± SD Median Mean ± SD Median
Duisburga 215 63.6 ± 45.9 56.7 0d 126.1 ± 98.8 108.7 215 141.4 ± 205.1 95.2 0d 255.3 ± 287.6 178.1
ELFEb 35 92.6 ± 41.9 83.3 0 301.1 ± 133.0 268.1 0 NA NA NA NA NA
FLEHS Ic 129 54.0 ± 38.4 41.3 6 (4.5)d 66.5 ± 69.6 47.1 130 214.7 ± 244.5 145.6 0d 272.6 ± 412.9 150.6
GRDc 321 184.7 ± 72.9 176.7 0 280.4 ± 152.0 252.4 0 NA NA NA NA NA
HUMISb 399 36.4 ± 17.1 33.1 0d 104.7 ± 52.2 96.8 399 63.4 ± 94.8 42.1 0d 177.3 ± 236.9 123.1
Michalovcec 880 164.4 ± 219.2 111.2 2 (0.2) 292.4 ± 425.4 175.3 880 540.5 ± 459.0 413.5 6 (0.7) 954.3 ± 1032.8 619.6
PELAGIEc 168 43.0 ± 31.5 32.1 0d 48.3 ± 55.9 26.2 168 73.5 ± 74.4 53.9 28 (16.4)d 75.7 ± 99.8 36.6
NA, not available. aPrenatal and postnatal concentrations estimated from maternal blood concentrations. bPrenatal and postnatal concentrations estimated from breast milk concentrations. cPrenatal and postnatal concentrations estimated from cord blood concentrations. dProvided LOQ instead of LOD.