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  4. Prenatal perfluorooctanoic acid exposure and glutathione s-transferase T1/M1 genotypes and their association with atopic dermatitis at 2 years of age
 
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Prenatal perfluorooctanoic acid exposure and glutathione s-transferase T1/M1 genotypes and their association with atopic dermatitis at 2 years of age

Journal
PLoS ONE
Journal Volume
14
Journal Issue
1
Date Issued
2019
Author(s)
WU-SHIUN HSIEH  
Wang, I-Jen
PAU-CHUNG CHEN  
Yue Leon Guo  
Lin, Yen-Ju
Lin, Yen-Ju
Hsieh, Wu-Shiun  
Pau-Chung CHENChen, Pau-Chung
DOI
10.1371/journal.pone.0210708
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85060093811&doi=10.1371%2fjournal.pone.0210708&partnerID=40&md5=bb153c0de6411a3f1e3f7374d40ab847
https://scholars.lib.ntu.edu.tw/handle/123456789/415326
Abstract
Background Perfluoroalkyl substance (PFAS) exposure was found associated with atopic diseases. Atopic dermatitis (AD) is a childhood skin disorder. However, the effect of interaction between PFASs and glutathione S-transferase (GST) T1/M1 genotype on AD remains unclear. Objective To investigate the association between gene-environmental interaction and childhood AD using a birth cohort study. Methods From 2001 to 2005, 1,264 mother–newborn pairs were recruited from eight Taiwanese maternity hospitals. PFAS levels and Genotypes were analysed from cord blood. Information on children’s health status including AD occurrence was obtained via phone interviews at 6 months and 2 years. Cord plasma concentrations of nine PFASs were measured via ultra-high performance liquid chromatography/tandem mass spectrometry. GSTT1/M1 was genotyped (null/present) via polymerase chain reaction. Environment-gene interaction effects on AD were assessed using multiple logistic regression analysis. Results Overall, 839 mother–newborn pairs completed all measurements. The prevalence of ever having physician-diagnosed AD by 2 years of age was 5.4%. Among PFASs, perfluorooctanoic acid (PFOA) was positively associated with AD adjusted for potential confounders. After grouping PFOA levels into three groups: undetected, below and above the median in those with detected, children in above the median group who had the GSTT1-null, or GSTM1-null genotype exhibited a higher odds ratio for AD (OR [95%CI] = 3.45 [1.26–9.99] and 2.92 [1.12–7.91], respectively) as compared to the undetected group. Conclusions Our data demonstrated that in-utero PFOA exposure with GSTT1/M1 null genotype were associated with AD. Minimizing early-life PFAS exposure may help against AD development, especially in genetically susceptible individuals. ? 2019 Wen 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.
SDGs

[SDGs]SDG3

Other Subjects
glutathione transferase; perfluorooctanoic acid; fluorocarbon; glutathione S-transferase M1; glutathione S-transferase T1; octanoic acid derivative; perfluorooctanoic acid; adult; Article; atopic dermatitis; blood level; child; child health; clinical article; cohort analysis; concentration (parameter); confounding variable; controlled study; cordocentesis; disease association; female; follow up; gene; genetic association; genotype; genotype environment interaction; genotyping technique; GST gene; human; infant; liquid chromatography-mass spectrometry; longitudinal study; male; newborn; pathogenesis; polymerase chain reaction; prenatal exposure; preschool child; prevalence; Taiwan; Taiwanese; telephone interview; ultra performance liquid chromatography; atopic dermatitis; genetics; genotype; pregnancy; prenatal exposure; Caprylates; Cohort Studies; Dermatitis, Atopic; Female; Fluorocarbons; Genotype; Glutathione Transferase; Humans; Infant; Infant, Newborn; Male; Pregnancy; Prenatal Exposure Delayed Effects
Publisher
Public Library of Science
Type
journal article

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