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Appendix D - Dossier (PDF) - Tera

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date: 20–JUL–2005<br />

5. Toxicity Substance ID: 71–43–2<br />

______________________________________________________________________________<br />

Type: other: effects on pregnancy<br />

Method: SUBJECTS<br />

The study population was recruited from female employees<br />

working for the Beijing Yanshan Petrochemical Corporation<br />

(BYPC), Peoples Republic of China. Eligible women were<br />

defined as non–drinking, non–smoking mothers who had a live<br />

single birth at the BYPC staff hospital between June 1995<br />

and June 1997. This resulted in recruitment of 302 reference<br />

(non–exposed) individuals and 240 benzene–exposed subjects<br />

(total: 542). Clinical and personal data were collected by<br />

interviewer–administered questionnaire. In general, pregnant<br />

employees stopped working at 28 weeks of gestation.<br />

<strong>Appendix</strong> D: Benzene SIDS <strong>Dossier</strong><br />

GESTATIONAL AGE<br />

The first date of the last menstrual period recorded at the<br />

first prenatal visit was used to estimate gestational age in<br />

days. The authors considered that prevailing social and<br />

administrative considerations within the Peoples Republic of<br />

China meant that this would be reliably noted by the<br />

participants.<br />

EXPOSURE ASSESSMENT<br />

The authors note that, in general, time–weighted average for<br />

benzene exposure in the<br />

BYPC facility was a range 0.017–0.191 ppm. Maternal<br />

occupational exposure to benzene was assessed qualitatively<br />

according to a woman’s workshop, job title and job activity.<br />

Air sample measurements for benzene, toluene, styrene,<br />

xylene and their derivatives were obtained from major<br />

workshops during the study period. The subjects were then<br />

classified into 3 groups based upon (1) no exposure to<br />

organic solvents; (2) exposure to benzene; and (3) exposure<br />

to other solvents (including styrene, toluene, xylene and<br />

their derivatives but not benzene). Note: only results for<br />

the benzene–exposed and non–benzene–exposed individuals were<br />

presented in this study report.<br />

GENOTYPING<br />

POLYMORPHISM OF CYP1A1<br />

Maternal genomic DNA was subject to 35 rounds of<br />

amplification using the polymerase chain reaction, followed<br />

by digestion of the products with HincII and agarose gel<br />

electrophoresis with ethidium bromide staining and<br />

visualisation under UV light. Homozygous wild–type<br />

individuals for cytochrome P450 1A1 (CYP1A1) show 139– and<br />

32–base pair (BP) fragments (BPF), while heterozygous<br />

subjects show 4 bands at 139, 120, 32 and 19 BP,<br />

respectively. Homozygous rare–allele individuals show only<br />

120–, 32– and 19 BP bands.<br />

POLYMORPHISM OF GSTT1<br />

Wild type homozygous glutathione S–transferase (GSTT1) was<br />

indicated by an amplified 457–BP product after PCR and<br />

agarose gel electrophoresis, while the null genotype was<br />

characterised by the absence of the 457–BP band.<br />

– 599/957 –

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