Prevalence of fetal exposure to environmental toxins as determined by meconium analysis

被引:128
作者
Ostrea, EM
Morales, V
Ngoumgna, E
Prescilla, R
Tan, E
Hernandez, E
Ramirez, GB
Cifra, HL
Manlapaz, ML
机构
[1] Wayne State Univ, Hutzel Hosp, Dept Pediat, Detroit, MI 48201 USA
[2] Philippine Childrens Med Ctr, Manila, Philippines
[3] Philippine Gen Hosp, Manila, Philippines
[4] St Lukes Hosp, Manila, Philippines
[5] FIRST Integrated Hosp, Manila, Philippines
[6] Univ Santo Tomas, Manila, Philippines
关键词
meconium; drugs; environmental pollutants; Neonate; pesticide; heavy metals; lead; mercury;
D O I
10.1016/S0161-813X(02)00077-3
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Objective: The primary objective was to determine whether environmental pollutants, specifically lead (Pb), cadmium (Cd), mercury (Hg), arsenic (As) and organochlorine and organophosphate pesticides can be detected in meconium. Study design: Prospective, cohort study. Infants were randomly recruited from the nurseries of five hospitals in Manila, Philippines. Their stools (meconium) were collected and analyzed for heavy metals by atomic absorption spectrophotometry and for pesticides by gas chromatography/mass spectrometry (GCMS). Results: A total of 426 infants were studied. The exposure rate (based on meconium analysis) and the median concentration of the pollutants in the positive samples were as follows: lead (26.5%; 35.77 mug/ml), cadmium (8.5%; 13.37 mug/ml), mercury (83.9%; 3.17 ng/ml), chlordane (12.7%; 22.48 mug/ml), chlorpyrifos (11.0%; 8.26 mug/ml), diazinon (34.3%; 12.96 mug/ml), DDT (26.5%; 12.56 mug/ml), lindane (73.5%; 2.0 mug/ml), malathion (53.0; 6.80 mug/ml), parathion (32.0%; 2.30 mug/ml) and pentachlorphenol (16.1%; 90.00 mug/ml). Some maternal and neonatal factors that were significantly associated with the presence of environmental toxins in meconium included multigravidity, multiparity, multiple gestation, meconium stained fluid, smoking, gestational age, low birth weight and infant gender Conclusion: Meconium analysis is a new and sensitive tool to detect fetal exposure to environmental toxins and its clinical use awaits further investigation. (C) 2002 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:329 / 339
页数:11
相关论文
共 79 条
[1]   EXPOSURE TO AN ORGANOPHOSPHATE (DFP) DURING A DEFINED PERIOD IN NEONATAL LIFE INDUCES PERMANENT CHANGES IN BRAIN MUSCARINIC RECEPTORS AND BEHAVIOR IN ADULT MICE [J].
AHLBOM, J ;
FREDRIKSSON, A ;
ERIKSSON, P .
BRAIN RESEARCH, 1995, 677 (01) :13-19
[2]   Analysis of nonsteroidal antiinflammatory drugs in meconium and its relation to persistent pulmonary hypertension of the newborn [J].
Alano, MA ;
Ngougmna, E ;
Ostrea, EM ;
Konduri, GG .
PEDIATRICS, 2001, 107 (03) :519-523
[3]   PERINATAL METHYLMERCURY POISONING IN IRAQ [J].
AMINZAKI, L ;
ELHASSANI, S ;
MAJEED, MA ;
CLARKSON, TW ;
DOHERTY, RA ;
GREENWOOD, MR ;
GIOVANOLIJAKUBCZAK, T .
AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1976, 130 (10) :1070-1076
[4]   PRENATAL LEAD-EXPOSURE IN RELATION TO GESTATIONAL-AGE AND BIRTH-WEIGHT - A REVIEW OF EPIDEMIOLOGIC STUDIES [J].
ANDREWS, KW ;
SAVITZ, DA ;
HERTZPICCIOTTO, I .
AMERICAN JOURNAL OF INDUSTRIAL MEDICINE, 1994, 26 (01) :13-32
[5]  
BAILEY CH, 1991, ANN NY ACAD SCI, V627, P181
[6]   CLINICAL AND EPIDEMIOLOGICAL ASPECTS OF METHYLMERCURY POISONING [J].
BAKIR, F ;
TIKRITI, S ;
RUSTAM, H ;
ALDAMLUJI, SF ;
SHIHRISTANI, H .
POSTGRADUATE MEDICAL JOURNAL, 1980, 56 (651) :1-10
[7]   Gestational exposure to methylmercury alters the developmental pattern of trk-like immunoreactivity in the rat brain and results in cortical dysmorphology [J].
Barone, S ;
Haykal-Coates, N ;
Parran, DK ;
Tilson, HA .
DEVELOPMENTAL BRAIN RESEARCH, 1998, 109 (01) :13-31
[8]   Ethyl linoleate in meconium: A biomarker for prenatal ethanol exposure [J].
Bearer, CF ;
Lee, S ;
Salvator, AE ;
Minnes, S ;
Swick, A ;
Yamashita, T ;
Singer, LT .
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 1999, 23 (03) :487-493
[9]   LONGITUDINAL ANALYSES OF PRENATAL AND POSTNATAL LEAD-EXPOSURE AND EARLY COGNITIVE-DEVELOPMENT [J].
BELLINGER, D ;
LEVITON, A ;
WATERNAUX, C ;
NEEDLEMAN, H ;
RABINOWITZ, M .
NEW ENGLAND JOURNAL OF MEDICINE, 1987, 316 (17) :1037-1043
[10]  
BOYLE CA, 1994, PEDIATRICS, V93, P399