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产前地塞米松用于先天性肾上腺皮质增生症:现代医学矿井中的一只伦理金丝雀

Prenatal Dexamethasone for Congenital Adrenal Hyperplasia: An Ethics Canary in the Modern Medical Mine.

作者信息

Dreger Alice, Feder Ellen K, Tamar-Mattis Anne

出版信息

J Bioeth Inq. 2012 Sep;9(3):277-294. doi: 10.1007/s11673-012-9384-9. Epub 2012 Jul 31.

DOI:10.1007/s11673-012-9384-9
PMID:22904609
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3416978/
Abstract

Following extensive examination of published and unpublished materials, we provide a history of the use of dexamethasone in pregnant women at risk of carrying a female fetus affected by congenital adrenal hyperplasia (CAH). This intervention has been aimed at preventing development of ambiguous genitalia, the urogenital sinus, tomboyism, and lesbianism. We map out ethical problems in this history, including: misleading promotion to physicians and CAH-affected families; de facto experimentation without the necessary protections of approved research; troubling parallels to the history of prenatal use of diethylstilbestrol (DES); and the use of medicine and public monies to attempt prevention of benign behavioral sex variations. Critical attention is directed at recent investigations by the U.S. Food and Drug Administration (FDA) and Office of Human Research Protections (OHRP); we argue that the weak and unsupported conclusions of these investigations indicate major gaps in the systems meant to protect subjects of high-risk medical research.

摘要

在广泛查阅已发表和未发表的资料后,我们呈现了地塞米松在怀有受先天性肾上腺皮质增生症(CAH)影响的女胎风险孕妇中的使用历史。这种干预旨在预防生殖器模糊、泌尿生殖窦、男子气以及女同性恋倾向的发展。我们梳理了这段历史中的伦理问题,包括:对医生和受CAH影响家庭的误导性宣传;在没有经批准研究的必要保护措施的情况下进行事实上的实验;与己烯雌酚(DES)产前使用历史令人不安的相似之处;以及使用药物和公共资金试图预防良性行为性别差异。批判性关注指向美国食品药品监督管理局(FDA)和人类研究保护办公室(OHRP)最近的调查;我们认为这些调查得出的薄弱且无根据的结论表明,旨在保护高风险医学研究受试者的系统存在重大漏洞。

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Trophoblast Retrieval and Isolation From the Cervix for Noninvasive, First Trimester, Fetal Gender Determination in a Carrier of Congenital Adrenal Hyperplasia.从宫颈获取和分离滋养层细胞用于先天性肾上腺皮质增生症携带者孕早期无创胎儿性别鉴定
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本文引用的文献

1
Prenatal treatment of congenital adrenal hyperplasia-not standard of care.先天性肾上腺皮质增生症的产前治疗——并非标准治疗方法。
J Genet Couns. 2012 Oct;21(5):615-24. doi: 10.1007/s10897-012-9508-8. Epub 2012 May 26.
2
Cognitive outcome of offspring from dexamethasone-treated pregnancies at risk for congenital adrenal hyperplasia due to 21-hydroxylase deficiency.由于 21-羟化酶缺乏导致先天性肾上腺皮质增生症风险的地塞米松治疗妊娠的后代的认知结果。
Eur J Endocrinol. 2012 Jul;167(1):103-10. doi: 10.1530/EJE-11-0789. Epub 2012 May 1.
3
Prenatal dexamethasone treatment of children at risk for congenital adrenal hyperplasia: the Swedish experience and standpoint.先天性肾上腺皮质增生症高危儿童的产前地塞米松治疗:瑞典的经验与立场。
J Clin Endocrinol Metab. 2012 Jun;97(6):1881-3. doi: 10.1210/jc.2012-1222.
4
Noninvasive fetal sex determination using cell-free fetal DNA: a systematic review and meta-analysis.使用游离胎儿 DNA 进行非侵入性胎儿性别鉴定:系统评价和荟萃分析。
JAMA. 2011 Aug 10;306(6):627-36. doi: 10.1001/jama.2011.1114.
5
Long range outcome of prenatal treatment.产前治疗的远期结局。
Adv Exp Med Biol. 2011;707:33-5. doi: 10.1007/978-1-4419-8002-1_7.
6
The long-term effects of in utero exposures--the DES story.子宫内暴露的长期影响——己烯雌酚的故事。
N Engl J Med. 2011 Jun 2;364(22):2083-4. doi: 10.1056/NEJMp1104409. Epub 2011 Apr 20.
7
Glucocorticoids in pregnancy.孕期糖皮质激素。
Curr Pharm Biotechnol. 2011 May;12(5):750-7. doi: 10.2174/138920111795470868.
8
Review of Outcome Information in 46,XX Patients with Congenital Adrenal Hyperplasia Assigned/Reared Male: What Does It Say about Gender Assignment?对46,XX型先天性肾上腺皮质增生症被指定为男性/按男性养育患者的结局信息回顾:这对性别指定意味着什么?
Int J Pediatr Endocrinol. 2010;2010:982025. doi: 10.1155/2010/982025. Epub 2010 Dec 21.
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Long-term outcome of prenatal dexamethasone treatment of 21-hydroxylase deficiency.产前地塞米松治疗21-羟化酶缺乏症的长期预后。
Endocr Dev. 2011;20:96-105. doi: 10.1159/000321228. Epub 2010 Dec 16.
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