TY - JOUR
T1 - Arsenic methylation capacity and developmental delay in preschool children in Taiwan
AU - Hsieh, Ru-Lan
AU - Huang, Ya-Li
AU - Shiue, Horng Sheng
AU - Huang, Shiau Rung
AU - Lin, Ming I.
AU - Mu, Shu Chi
AU - Chung, Chi Jung
AU - Hsueh, Yu-Mei
N1 - Funding Information:
We appreciate the assistance from the doctors of Tseng-Chen Sung, Cheng Hui Lin, and Ling-Jen Wang of Department of Pediatrics, Shin Kong Wu Ho-Su Memorial Hospital in the recruitment of study subjects. The study was supported by grants from Shin Kong Wu Ho-Su Memorial Hospital, Taipei, Taiwan (SKH-TMU-99-03 and SKH-TMU-100-06) and from the National Science Council Taiwan (NSC 100-2314-B-038-026 ).
PY - 2014/7
Y1 - 2014/7
N2 - Environmental exposure to lead or mercury can cause neurodevelopmental damage. Arsenic is another neurotoxicant that can affect intellectual function in children. This study was designed to explore the difference of arsenic methylation capacity indices between with and without developmental delay in preschool children. We also aimed to identify whether blood levels of lead or mercury modify the effect of arsenic methylation capacity indices. A cross sectional study was conducted from August 2010 to March 2012. All participants recruited from the Shin Kong Wu Ho-Su Memorial Teaching Hospital. In all, 63 children with developmental delay and 35 children without developmental delay were recruited. Urinary arsenic species, including arsenite (AsIII), arsenate (AsV), monomethylarsonic acid (MMAV) and dimethylarsinic acid (DMAV) were measured with a high-performance liquid chromatography-linked hydride generator and atomic absorption spectrometry. Lead and mercury levels of red blood cells were measured by inductively coupled mass spectrometry. All participants underwent developmental assessments to confirm developmental delays, including evaluations of gross motor, fine motor, speech-language, cognition, social, and emotional domains. Urinary total arsenic and MMAV percentage were significantly positively associated and DMAV percentage was negatively associated with the risk of developmental delay in a dose-dependent manner after adjustment for blood lead or mercury levels and other risk factors. A multivariate regression analysis indicated that blood lead level and arsenic methylation capacity each independently contributed to the risk of developmental delay. This is the first study to show that arsenic methylation capacity is associated with developmental delay, even without obvious environmental arsenic exposure.
AB - Environmental exposure to lead or mercury can cause neurodevelopmental damage. Arsenic is another neurotoxicant that can affect intellectual function in children. This study was designed to explore the difference of arsenic methylation capacity indices between with and without developmental delay in preschool children. We also aimed to identify whether blood levels of lead or mercury modify the effect of arsenic methylation capacity indices. A cross sectional study was conducted from August 2010 to March 2012. All participants recruited from the Shin Kong Wu Ho-Su Memorial Teaching Hospital. In all, 63 children with developmental delay and 35 children without developmental delay were recruited. Urinary arsenic species, including arsenite (AsIII), arsenate (AsV), monomethylarsonic acid (MMAV) and dimethylarsinic acid (DMAV) were measured with a high-performance liquid chromatography-linked hydride generator and atomic absorption spectrometry. Lead and mercury levels of red blood cells were measured by inductively coupled mass spectrometry. All participants underwent developmental assessments to confirm developmental delays, including evaluations of gross motor, fine motor, speech-language, cognition, social, and emotional domains. Urinary total arsenic and MMAV percentage were significantly positively associated and DMAV percentage was negatively associated with the risk of developmental delay in a dose-dependent manner after adjustment for blood lead or mercury levels and other risk factors. A multivariate regression analysis indicated that blood lead level and arsenic methylation capacity each independently contributed to the risk of developmental delay. This is the first study to show that arsenic methylation capacity is associated with developmental delay, even without obvious environmental arsenic exposure.
KW - Arsenic
KW - Arsenic methylation capacity
KW - Developmental delay
KW - Lead
KW - Mercury
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U2 - 10.1016/j.ijheh.2014.02.004
DO - 10.1016/j.ijheh.2014.02.004
M3 - Article
C2 - 24698386
AN - SCOPUS:84902762441
SN - 1438-4639
VL - 217
SP - 678
EP - 686
JO - International Journal of Hygiene and Environmental Health
JF - International Journal of Hygiene and Environmental Health
IS - 6
ER -