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2013-2017 年美国基于人群的研究:唐氏综合征患儿的结构出生缺陷发生率。

Prevalence of structural birth defects among infants with Down syndrome, 2013-2017: A US population-based study.

机构信息

Center for Birth Defects Research and Prevention, Massachusetts Department of Public Health, Boston, Massachusetts, USA.

National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.

出版信息

Birth Defects Res. 2021 Jan 15;113(2):189-202. doi: 10.1002/bdr2.1854. Epub 2020 Dec 21.

Abstract

BACKGROUND

Down syndrome is the most common chromosomal disorder at birth and is often accompanied by structural birth defects. Current data on major structural defects in this population are limited.

METHODS

States and territorial population-based surveillance programs submitted data on identified cases of Down syndrome and identified structural birth defects during 2013-2017. We estimated prevalence by program type and maternal and infant characteristics. Among programs with active case ascertainment, we estimated the prevalence of birth defects by organ system and for specific defects by maternal age (<35, ≥35) and infant sex.

RESULTS

We identified 13,376 cases of Down syndrome. Prevalence among all programs was 12.7 per 10,000 live births. Among these children, 75% had at least one reported co-occurring birth defect diagnosis code. Among 6,210 cases identified by active programs, 66% had a cardiovascular defect with septal defects being the most common: atrial (32.5%), ventricular (20.6%), and atrioventricular (17.4%). Defect prevalence differed by infant sex more frequently than by maternal age. For example, atrioventricular septal defects were more common in female children (20.1% vs. 15.1%) while limb deficiencies were more prevalent in male children (0.4% vs. 0.1%).

CONCLUSIONS

Our study provides updated prevalence estimates for structural defects, including rare defects, among children with Down syndrome using one of the largest and most recent cohorts to date. These data may aid clinical care and surveillance.

摘要

背景

唐氏综合征是最常见的出生时染色体异常疾病,常伴有结构出生缺陷。目前该人群主要结构缺陷的数据有限。

方法

各州和地区基于人群的监测计划提交了 2013-2017 年间确定的唐氏综合征病例和确定的结构出生缺陷病例数据。我们根据方案类型和母婴特征估计患病率。在具有主动病例确定的方案中,我们按器官系统估计出生缺陷的患病率,并按母亲年龄(<35 岁、≥35 岁)和婴儿性别对特定缺陷进行估计。

结果

我们确定了 13376 例唐氏综合征病例。所有方案的患病率为每 10000 例活产 12.7 例。在这些儿童中,75%至少有一个报告的同时发生的出生缺陷诊断代码。在 6210 例由主动方案确定的病例中,66%有心血管缺陷,其中间隔缺损最常见:房间隔缺损(32.5%)、室间隔缺损(20.6%)和房室间隔缺损(17.4%)。缺陷的患病率比母亲年龄更频繁地因婴儿性别而异。例如,房室间隔缺损在女婴中更为常见(20.1% vs. 15.1%),而肢体缺陷在男婴中更为常见(0.4% vs. 0.1%)。

结论

我们的研究使用迄今为止最大和最新的队列之一,提供了唐氏综合征儿童结构缺陷(包括罕见缺陷)的最新患病率估计。这些数据可能有助于临床护理和监测。

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