Dh. Kang et al., COPLANAR PCBS AND THE RELATIVE CONTRIBUTION OF COPLANAR PCBS, PCDDS, AND PCDFS TO THE TOTAL 2,3,7,8-TCDD TOXICITY EQUIVALENTS IN HUMAN SERUM, Chemosphere, 35(3), 1997, pp. 503-511
Coplanar PCBs in human serum were measured by high-resolution gas chro
matography/isotope-dilution high-resolution mass spectrometry in 46 pu
lp and paper mill workers and 16 community residents with no specific
known source of PCB exposure. The relative contribution of coplanar PC
Bs, PCDDs, and PCDFs to the total 2,3,7,8-TCDD toxicity equivalents (T
EQs) were compared using the toxic equivalency factors proposed by Saf
e [1] and the factors recently proposed by WHO [2]. The mean concentra
tions of PCB-126 and PCB-169 were higher in paper mill workers than in
community residents. However, these differences were not statisticall
y significant. Serum PCB-126, but not PCB-169, was correlated with bod
y mass index (Spearman's r=0.40, p=0.002). Serum PCB-169, but not PCB-
126, was correlated with age (Spearman's r=0.54, p=0.0001). Multiple l
inear regression analysis for log-transformed combined PCBs showed tha
t age (p=0.008). body mass index (p=0.031), and eating locally caught
fish (p=0.019) were statistically significant predictors. The majority
of the total TEQ in serum is due to PCDDs (63%), whereas PCDFs accoun
t for 21% and coplanar PCBs account for 15% when calculated using the
TEFs proposed by Safe. The percent contributions from PCDDs, PCDFs, an
d coplanar PCBs were 66%, 24%, and 10% respectively when calculated ba
sed on the TEFs proposed by WHO. Age, body mass index, and consumption
of locally caught fish are significant predictors for coplanar PCB le
vels in human serum. Serum PCDDs were the major contributors to the to
tal 2,3,7,8-TCDD equivalent toxicity in this study. (C) 1997 Elsevier
Science Ltd.