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    <subfield code="a">AIT Diss. no.EV-10-05</subfield>
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    <subfield code="a">Sirilak Wongvijitsuk</subfield>
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    <subfield code="a">Low level occupational exposure to styrene and benzene :</subfield>
    <subfield code="b">its effects on DNA damage and DNA repair</subfield>
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    <subfield code="a">Pathum Thani, Thailand :</subfield>
    <subfield code="b">Asian Institute of Technology,</subfield>
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    <subfield code="a">Dissertation ;</subfield>
    <subfield code="v">no. EV-10-05</subfield>
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    <subfield code="a">A thesis proposal submitted in partial fulfillment of the requirements for the degree of Doctor of Technical science in Environmental Toxicology, Technology and Management Inter-University Program</subfield>
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    <subfield code="a">Thesis (Ph.D.) - Asian Institute of Technology - Chulabhorn Research Institute - Mahidol University, 2010</subfield>
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    <subfield code="a">The  present  study  aimed  to  evaluate  the  effects  of styrene  exposure  at  levels  below  the recommended standards of the Threshold Limit Value (TLV-TWA8) of 20 ppm (ACGIH, 2004)  in  reinforced  fiberglass  plastics  workers.  Study  subjects  comprised  50  exposed workers and 40 control subjects. The exposed workers were stratified by styrene exposure levels, i.e. group I (&lt;10 ppm), group II (10- 20 ppm), and group III (&gt; 20 ppm). The mean styrene  exposure  levels  of  exposed  workers  were  significantly  higher  than  those  of  the control workers. Respiratory particles increased significantly in factory workers (1.05&#xB1;0.17 mg/m3;  p&lt;  0.01)  compared  to  control  (0.36&#xB1;0.93  mg/m3).  Factory  workers  stratified  by job activity showed that there was a significant difference of exposure levels among study groups  (p&lt;0.01).  Respiratory  particle  level  in  trimming  workers  (1.79&#xB1;0.31mg/m3)  was significantly  higher  than  resin  laminator  workers  (0.54&#xB1;0.05  mg/m3).  Biomarkers  of exposure  to  styrene,  including  blood  styrene  and  the  urinary  metabolites,  mandelic  acid (MA) and phenylglyoxylic acid (PGA), were significantly increased with increasing levels of  styrene  exposure,  but  were  not  detected  in  the  control  group.  DNA  damage,  such  as DNA strand breaks, 8-hydroxydeoxyguanosine (8-OHdG), and DNA repair capacity, were used  as  biomarkers  of  early  biological  effects.  DNA  strand  breaks  and  8-OHdG/105  dG levels  in  peripheral  leukocytes  of  exposed  groups  were  significantly  higher  compared  to the   control   group   (P&lt;0.05).   In   addition,   DNA   repair   capacity,   determined   by   the cytogenetic  challenge  assay,  was  lower  in  all  exposed  groups  when  compared  to  the control   group   (P&lt;0.05).   The   expression   of   CYP2E1,   which   is   involved   in   styrene metabolism,  in  all  styrene  exposed  groups,  was  higher  than  that  of  the  control  group  at  a statistically  significant  level  (P&lt;0.05).  Levels  of  expression  of  the  DNA  repair  genes hOGG1  and  XRCC1  were  significantly  higher  in  all  exposed  groups  than  in  the  control group  (P  &lt;0.05).  In  addition  to  styrene  contamination  in  ambient  air,  a  trace  amount  of benzene  was  also  found,  but  the  correlation between benzene exposure and DNA damage or  DNA  repair  capacity  was  not  statistically  significant.  The  results  obtained  from  this study  indicate  an  increase  in  genotoxic  effects  and  thus  health  risk  from  occupational styrene exposure, even at levels below the recommended TLV-TWA8 of 20 ppm.  </subfield>
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    <subfield code="a">DNA damage</subfield>
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    <subfield code="a">DNA repair</subfield>
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    <subfield code="a">Mathuros Ruchirawat,</subfield>
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    <subfield code="a">Preeda Pakpian,</subfield>
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