C. Wohlfahrt-Veje, H. R. Andersen, I. M. Schmidt, L. Aksglaede, K. Sørensen, A. Juul, T. K. Jensen, P. Grandjean, N. E. Skakkebæk, K. M. Main
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We studied the offspring of these greenhouse workers, and evaluated the anthropometry, pubertal staging in the girls, and blood samples were drawn at 3 months of age (n = 90) and again once at school age (6-11 years, n = 83). No clinical and biochemical differences were found between the exposed and unexposed girls at 3 months of age. Mean onset of B2+ was 8.9 years (95% CI: 8.2; 9.7) in prenatally exposed girls, compared with 10.4 years (9.2; 17.6) in the unexposed (p = 0.05), and 10.0 (9.7-10.3) years in a Danish reference population (p = 0.001). Exposed girls had higher serum androstenedione levels (geometric means: 0.58 vs. 0.79 nmol/L, p = 0.046) and lower Anti-Müllerian Hormone (AMH) compared with the unexposed (geometric means: 16.4 vs. 21.3 pmol/L, p > 0.05) and the reference group (20.2 pmol/L, p = 0.012). Levels of testosterone, estradiol, prolactin, FSH, LH, SHBG, DHEAS, DHT, Inhibin A and Inhibin B did not differ between the groups. In conclusion, our findings suggest that prenatal exposure to currently approved pesticides may cause earlier breast development in girls. This association appeared not to be because of changes in gonadotropins, but rather to higher androgen levels, which indirectly may increase oestrogens through aromatization. In addition, lower serum AMH levels indicated a reduced pool of antral ovarian follicles. The long-term consequences of our findings with regard to establishment of future reproductive function still remain unknown.","PeriodicalId":13890,"journal":{"name":"International journal of andrology","volume":"35 3","pages":"273-282"},"PeriodicalIF":0.0000,"publicationDate":"2012-03-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1111/j.1365-2605.2011.01244.x","citationCount":"53","resultStr":"{\"title\":\"Early breast development in girls after prenatal exposure to non-persistent pesticides\",\"authors\":\"C. Wohlfahrt-Veje, H. R. Andersen, I. M. Schmidt, L. Aksglaede, K. Sørensen, A. Juul, T. K. Jensen, P. Grandjean, N. E. Skakkebæk, K. M. Main\",\"doi\":\"10.1111/j.1365-2605.2011.01244.x\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Contemporary American and European girls experience breast development at earlier ages compared with 15-20 years ago. 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Mean onset of B2+ was 8.9 years (95% CI: 8.2; 9.7) in prenatally exposed girls, compared with 10.4 years (9.2; 17.6) in the unexposed (p = 0.05), and 10.0 (9.7-10.3) years in a Danish reference population (p = 0.001). Exposed girls had higher serum androstenedione levels (geometric means: 0.58 vs. 0.79 nmol/L, p = 0.046) and lower Anti-Müllerian Hormone (AMH) compared with the unexposed (geometric means: 16.4 vs. 21.3 pmol/L, p > 0.05) and the reference group (20.2 pmol/L, p = 0.012). Levels of testosterone, estradiol, prolactin, FSH, LH, SHBG, DHEAS, DHT, Inhibin A and Inhibin B did not differ between the groups. In conclusion, our findings suggest that prenatal exposure to currently approved pesticides may cause earlier breast development in girls. This association appeared not to be because of changes in gonadotropins, but rather to higher androgen levels, which indirectly may increase oestrogens through aromatization. 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引用次数: 53
摘要
与15-20年前相比,当代美国和欧洲女孩乳房发育的年龄更早。单靠BMI的改变并不能解释这些变化。目前使用的几种农药具有内分泌干扰特性,可能干扰生殖发育,但人类数据很少。我们调查了母亲在怀孕前三个月在温室工作的女孩,以评估产前农药暴露对青春期的长期影响。母亲在产前被分为接触和未接触杀虫剂两类。我们研究了这些温室工人的后代,并评估了这些女孩的人体测量学、青春期发育阶段,并在3个月大时(n = 90)抽取了血液样本,在学龄期(6-11岁,n = 83)再次抽取了血液样本。在3个月大时,暴露组和未暴露组的女孩没有临床和生化差异。B2+的平均起病时间为8.9年(95% CI: 8.2;在产前暴露的女孩中为9.7岁,相比之下为10.4岁(9.2岁;未暴露人群为17.6岁(p = 0.05),丹麦参考人群为10.0(9.7-10.3)岁(p = 0.001)。与未暴露组(几何平均:16.4比21.3 pmol/L, p > 0.05)和对照组(20.2 pmol/L, p = 0.012)相比,暴露组女童血清雄烯二酮水平(几何平均:0.58比0.79 nmol/L, p = 0.046)较高,抗勒氏激素(AMH)较低。睾酮、雌二醇、催乳素、FSH、LH、SHBG、DHEAS、DHT、抑制素A和抑制素B的水平在两组之间没有差异。总之,我们的研究结果表明,产前暴露于目前批准的农药可能会导致女孩乳房发育提前。这种关联似乎不是由于促性腺激素的变化,而是由于更高的雄激素水平,这可能通过芳构化间接增加雌激素。此外,较低的血清AMH水平表明卵巢窦卵泡池减少。我们的发现对建立未来生殖功能的长期影响仍然未知。
Early breast development in girls after prenatal exposure to non-persistent pesticides
Contemporary American and European girls experience breast development at earlier ages compared with 15-20 years ago. Alterations in BMI alone cannot account for these changes. Several currently used pesticides possess endocrine disrupting properties and may interfere with reproductive development, but human data are sparse. We examined girls whose mothers worked in greenhouses in the first trimester of pregnancy to assess the long-term effects of prenatal pesticide exposure on puberty. Mothers were prenatally categorized as exposed or unexposed to pesticides. We studied the offspring of these greenhouse workers, and evaluated the anthropometry, pubertal staging in the girls, and blood samples were drawn at 3 months of age (n = 90) and again once at school age (6-11 years, n = 83). No clinical and biochemical differences were found between the exposed and unexposed girls at 3 months of age. Mean onset of B2+ was 8.9 years (95% CI: 8.2; 9.7) in prenatally exposed girls, compared with 10.4 years (9.2; 17.6) in the unexposed (p = 0.05), and 10.0 (9.7-10.3) years in a Danish reference population (p = 0.001). Exposed girls had higher serum androstenedione levels (geometric means: 0.58 vs. 0.79 nmol/L, p = 0.046) and lower Anti-Müllerian Hormone (AMH) compared with the unexposed (geometric means: 16.4 vs. 21.3 pmol/L, p > 0.05) and the reference group (20.2 pmol/L, p = 0.012). Levels of testosterone, estradiol, prolactin, FSH, LH, SHBG, DHEAS, DHT, Inhibin A and Inhibin B did not differ between the groups. In conclusion, our findings suggest that prenatal exposure to currently approved pesticides may cause earlier breast development in girls. This association appeared not to be because of changes in gonadotropins, but rather to higher androgen levels, which indirectly may increase oestrogens through aromatization. In addition, lower serum AMH levels indicated a reduced pool of antral ovarian follicles. The long-term consequences of our findings with regard to establishment of future reproductive function still remain unknown.