TY - JOUR
T1 - Attention deficit/hyperactivity disorder and urinary nonylphenol levels
T2 - A case-control study in taiwanese children
AU - Yu, Ching Jung
AU - Du, Jung Chieh
AU - Chiou, Hsien Chih
AU - Yang, Shang Han
AU - Liao, Kai Wei
AU - Yang, Winnie
AU - Chung, Ming Yi
AU - Chien, Ling Chu
AU - Hwang, Betau
AU - Chen, Mei Lien
N1 - Publisher Copyright:
© 2016 Yu et al.This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
PY - 2016/2
Y1 - 2016/2
N2 - Objective: Nonylphenol (NP) belongs to the family of endocrine disruptors, and it is widely used in industrial applications and is ubiquitous in daily foods. Animal studies have suggested that NP exposure might promote motor hyperactivity, likely by causing deficits in dopaminergic neurons. However, research assessing NP exposure and epidemiology studies on human populations are limited. The aim of this study was to explore the association between child NP exposure and ADHD while considering particular covariants, such as lead levels and dopamine-related gene variations. Methods: A case-control study was conducted on patients with clinically diagnosed ADHD; the Swan son, Nolan and Pelham, Fourth Revision (SNAP-IV) questionnaire was used to identify normal controls aged 4-15 years. Participants were examined for urinary NP concentrations, blood lead levels, and select single-nucleotide polymorphisms of two dopamine-related genes (D4 dopamine receptor, DRD4, and dopamine transporter, DAT1). Socio-demo-graphic variables, maternal lifestyle factors during pregnancy and family medical history were obtained using a questionnaire. Results: A total of 97 children with doctor-diagnosed ADHD and 110 normal controls were enrolled. The blood lead levels in both groups were similar (1.57±0.73 vs. 1.73±0.77 pg/dL, p = 0.15). No significant difference in urinary NP concentration was found between the children with ADHD and the control subjects (4.52±3.22 pg/g cr. vs. 4.64±2.95 pg/g cr., p = 0.43). ADHD was significantly more prevalent among males in this study (male to female ratio: 5:1 for the ADHD group and 1.3:1 for the control group, p
AB - Objective: Nonylphenol (NP) belongs to the family of endocrine disruptors, and it is widely used in industrial applications and is ubiquitous in daily foods. Animal studies have suggested that NP exposure might promote motor hyperactivity, likely by causing deficits in dopaminergic neurons. However, research assessing NP exposure and epidemiology studies on human populations are limited. The aim of this study was to explore the association between child NP exposure and ADHD while considering particular covariants, such as lead levels and dopamine-related gene variations. Methods: A case-control study was conducted on patients with clinically diagnosed ADHD; the Swan son, Nolan and Pelham, Fourth Revision (SNAP-IV) questionnaire was used to identify normal controls aged 4-15 years. Participants were examined for urinary NP concentrations, blood lead levels, and select single-nucleotide polymorphisms of two dopamine-related genes (D4 dopamine receptor, DRD4, and dopamine transporter, DAT1). Socio-demo-graphic variables, maternal lifestyle factors during pregnancy and family medical history were obtained using a questionnaire. Results: A total of 97 children with doctor-diagnosed ADHD and 110 normal controls were enrolled. The blood lead levels in both groups were similar (1.57±0.73 vs. 1.73±0.77 pg/dL, p = 0.15). No significant difference in urinary NP concentration was found between the children with ADHD and the control subjects (4.52±3.22 pg/g cr. vs. 4.64±2.95 pg/g cr., p = 0.43). ADHD was significantly more prevalent among males in this study (male to female ratio: 5:1 for the ADHD group and 1.3:1 for the control group, p
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U2 - 10.1371/journal.pone.0149558
DO - 10.1371/journal.pone.0149558
M3 - Article
C2 - 26890918
AN - SCOPUS:84960540690
SN - 1932-6203
VL - 11
JO - PLoS ONE
JF - PLoS ONE
IS - 2
M1 - e0149558
ER -