胚胎期后接触致畸原引起的出生缺陷和新生儿发病率

Q Medicine
Angela E. Scheuerle, Arthur S. Aylsworth
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引用次数: 7

摘要

药物妊娠暴露登记旨在评估药物暴露与不良后果,特别是先天性异常之间的时间关联。这些注册表记录了观察到的关联,这些关联可能与暴露有因果关系,也可能没有。大多数主要的先天性畸形(即结构性出生缺陷)是由于胚胎发育过程中的异常发育造成的。一个标准化的关注缺陷目录(通俗地称为“双酚A代码”)被用于公共卫生监督项目和妊娠暴露登记。然而,也有一些异常,引起显著的发病率和死亡率,孤立的第二或第三个月暴露可能具有显著的致病意义。目前还没有标准的缺陷清单,胎儿期暴露可能会有问题。方法采用六位数编码表确定胎儿期药物暴露可能导致的异常。结果有记录的妊娠早期发病机制的缺陷(如无脑畸形、异位)被排除在考虑之外,染色体和单基因疾病(如21三体、软骨发育不全)也被排除在外。剩下的缺陷包括以下几种:(1)已知或可能在胚胎期之后产生或表现的缺陷(例如,脑孔畸形、白内障);(2)发病机制尚不清楚或变化足够大,在任何胎龄暴露可能被认为是相关的(例如,畸形足,小头畸形);(3)包括某些异常生长成分的(例如,半增生)。“未明确”的缺陷(例如,“腿部异常”)默认包括在内,因为没有足够的信息来假设妊娠早期胚胎发生。结论总结了胎儿期接触致畸剂可能导致的11个器官系统类别的主要和次要异常。出生缺陷研究(A辑)(06):935 - 939,2016。©2016 Wiley期刊公司
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Birth defects and neonatal morbidity caused by teratogen exposure after the embryonic period

Background

Pharmaceutical pregnancy exposure registries seek to evaluate temporal associations between drug exposures and adverse outcomes, particularly congenital anomalies. These registries record observed associations that may or may not be causally-related to the exposure. Most major congenital malformations (i.e., structural birth defects) result from abnormal development during embryogenesis. A standardized catalog of defects of concern (colloquially the “BPA Codes”) is used both in public health surveillance programs and pregnancy exposure registries. There are, however, some anomalies that cause significant morbidity and mortality for which isolated second or third trimester exposures may be pathogenically significant. There currently exists no standardized list of defects for which exposure limited to the fetal period may be problematic.

Methods

The six-digit-code list was used to determine anomalies that might result from medication exposures limited to the fetal period.

Results

Defects with documented first trimester pathogenesis (e.g., anencephaly, heterotaxy) were eliminated from consideration, as were chromosomal and single gene disorders (e.g., trisomy 21, achondroplasia). The remaining defects include the following: (1) those that are known to or could reasonably originate or manifest after the embryonic period (e.g., porencephaly, cataracts); (2) those for which pathogenesis is unclear or variable enough that exposure at any gestational age might be considered relevant (e.g., club foot, microcephaly); and (3) those that include some component of abnormal growth (e.g., hemihyperplasia). “Unspecified” defects (e.g., “abnormality of the leg”) were included by default because there is insufficient information to assume first trimester embryogenesis.

Conclusion

The final result is a list of major and minor anomalies in 11 organ system categories that may be caused by teratogen exposure during the fetal period. Birth Defects Research (Part A) 106:935–939, 2016. © 2016 Wiley Periodicals, Inc.

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来源期刊
Birth defects research. Part A, Clinical and molecular teratology
Birth defects research. Part A, Clinical and molecular teratology 医药科学, 胎儿发育与产前诊断, 生殖系统/围生医学/新生儿
CiteScore
1.86
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