Metabolomics and fetal alcohol spectrum disorder

被引:6
作者
Goldberg, Erin M. [1 ]
Aliani, Michel [1 ,2 ,3 ,4 ]
机构
[1] Univ Manitoba, St Boniface Hosp, Dept Human Nutr Sci, Res Ctr, Winnipeg, MB R2H 2A6, Canada
[2] St Boniface Gen Hosp, Res Ctr, Dept Physiol, Winnipeg, MB R2H 2A6, Canada
[3] St Boniface Gen Hosp, Res Ctr, Dept Pathophysiol, Winnipeg, MB R2H 2A6, Canada
[4] St Boniface Gen Hosp, Res Ctr, Canadian Ctr Agri Food Res Hlth & Med CCARM, Winnipeg, MB R2H 2A6, Canada
关键词
metabolomics; fetal alcohol spectrum disorder; fetal alcohol syndrome; prenatal alcohol exposure; ethanol; ACID ETHYL-ESTERS; RESONANCE SPECTROSCOPY; MASS-SPECTROMETRY; PRENATAL EXPOSURE; BIOMARKERS; MECONIUM; ETHANOL; PREGNANCY; PLACENTA; MARKERS;
D O I
10.1139/bcb-2017-0080
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Fetal alcohol spectrum disorder (FASD) is a major public health issue that encompass an array of physical, neurological, and behavioral effects due to alcohol consumption during pregnancy. The classical biomarkers of FASD that are currently used lack sensitivity and specificity, and as such there is an opportunity through the use of novel metabolomics analysis to identify new biomarkers to identify those at risk for FASD, which could more effectively aid in early intervention. The focus of this minireview is to identify current work that is being done in the field of metabolomics in FASD in utero, and to highlight promising metabolites that could act as biomarkers in the future. We will conclude with suggestions for further research, as there is a large gap of knowledge in this particular area of metabolomics.
引用
收藏
页码:198 / 203
页数:6
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