Possible impact of phthalates on infant reproductive health

被引:162
作者
Lottrup, G
Andersson, AM
Leffers, H
Mortensen, GK
Toppari, J
Skakkebæek, NE
Main, KM
机构
[1] Rigshosp, Univ Dept Growth & Reprod, DK-2100 Copenhagen, Denmark
[2] Univ Turku, Dept Physiol & Pediat, Turku, Finland
来源
INTERNATIONAL JOURNAL OF ANDROLOGY | 2006年 / 29卷 / 01期
关键词
anogenital distance; breast milk; infant; male reproduction; phthalates; testicular dysgenesis syndrome; testosterone; virilization;
D O I
10.1111/j.1365-2605.2005.00642.x
中图分类号
R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
摘要
Phthalates adversely affect the male reproductive system in animals, inducing hypospadias, cryptorchidism, reduced testosterone production and decreased sperm counts. Phthalate effects are much more severe after in utero than adult exposure. Little is known about human health effects. This study discusses two recent studies on perinatal phthalate exposure, which indicated that human testicular development might be susceptible to phthalates. One study analysed phthalate monoesters in breast milk and reproductive hormone levels in infants. Five of six phthalates [monoethyl-(MEP), monobutyl- (MBP), monomethyl- (MMP), mono-2-ethylhexyl- (MEHP) and mono-isononyl phthalate (MiNP)] showed correlation with hormone levels in healthy boys, which were indicative of lower androgen activity and reduced Leydig cell function. MEP and MBP were positively correlated with serum sex hormone-binding globulin (SHBG) levels. MMP, MEP, MBP, MEHP and MiNP were positively correlated with the LH/testosterone ratio. Another study found a reduction of the anogenital index (AGI) in infant boys with increasing levels of MBP, MEP, monobenzyl- and mono-isobutyl phthalate in maternal urine samples during late-pregnancy. Boys with small AGI showed a high prevalence of cryptorchidism and small genital size. Taken together these studies suggest an antivirilizing effect of phthalates in infants. Most of these findings are in line with animal observations. However, the possible effects of MEP appear to be limited to humans. This may be due to differences in exposure routes (inhalation and dermal absorption which circumvents liver detoxification in addition to oral) and metabolism, or this association could be spurious. As phthalates are produced as bulk chemicals worldwide, these new findings raise concern about the safety of phthalate exposure for pregnant women and infants.
引用
收藏
页码:172 / 180
页数:9
相关论文
共 68 条
[31]  
Kavlock R, 2002, REPROD TOXICOL, V16, P529, DOI 10.1016/S0890-6238(02)00032-1
[32]  
Kavlock R, 2002, REPROD TOXICOL, V16, P489, DOI 10.1016/S0890-6238(02)00033-3
[33]  
KIRKOTHMER, 1996, KIRKOTHMER ENCY CHEM, V18, P991
[34]   Exposure in utero to di(n-butyl) phthalate alters the vimentin cytoskeleton of fetal rat sertoli cells and disrupts sertoli cell-gonocyte contact [J].
Kleymenova, E ;
Swanson, C ;
Boekelheide, K ;
Gaido, KW .
BIOLOGY OF REPRODUCTION, 2005, 73 (03) :482-490
[35]   Exposure of nursery school children and their parents and teachers to di-n-butylphthalate and butylbenzylphthalate [J].
Koch, HM ;
Preuss, R ;
Drexler, H ;
Angerer, J .
INTERNATIONAL ARCHIVES OF OCCUPATIONAL AND ENVIRONMENTAL HEALTH, 2005, 78 (03) :223-229
[36]   Di(2-ethylhexyl)phthalate (DEHP) metabolites in human urine and serum after a single oral dose of deuterium-labelled DEHP [J].
Koch, HM ;
Bolt, HM ;
Angerer, J .
ARCHIVES OF TOXICOLOGY, 2004, 78 (03) :123-130
[37]   Internal exposure of nursery-school children and their parents and teachers to di(2-ethylhexyl)phtha late (DEHP) [J].
Koch, HM ;
Drexler, H ;
Angerer, J .
INTERNATIONAL JOURNAL OF HYGIENE AND ENVIRONMENTAL HEALTH, 2004, 207 (01) :15-22
[38]   An estimation of the daily intake of di(2-ethylhexyl)phthalate (DEHP) and other phthalates in the general population [J].
Koch, HM ;
Drexler, H ;
Angerer, J .
INTERNATIONAL JOURNAL OF HYGIENE AND ENVIRONMENTAL HEALTH, 2003, 206 (02) :77-83
[39]   In utero exposure to di-(2-ethylhexyl)phthalate and duration of human pregnancy [J].
Latini, G ;
De Felice, C ;
Presta, G ;
Del Vecchio, A ;
Paris, I ;
Ruggieri, F ;
Mazzeo, P .
ENVIRONMENTAL HEALTH PERSPECTIVES, 2003, 111 (14) :1783-1785
[40]   Gene expression profiling following in utero exposure to phthalate esters reveals new gene targets in the etiology of testicular dysgenesis [J].
Liu, KJ ;
Lehmann, KP ;
Sar, M ;
Young, SS ;
Gaido, KW .
BIOLOGY OF REPRODUCTION, 2005, 73 (01) :180-192