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德克萨斯州出生缺陷登记处的出生缺陷共现模式。

Birth defect co-occurrence patterns in the Texas Birth Defects Registry.

作者信息

Benjamin Renata H, Scheuerle Angela E, Scott Daryl A, Navarro Sanchez Maria Luisa, Langlois Peter H, Canfield Mark A, Northrup Hope, Schaaf Christian P, Ray Joseph W, McLean Scott D, Chen Han, Swartz Michael D, Lupo Philip J, Agopian A J

机构信息

Department of Epidemiology, Human Genetics and Environmental Sciences, UTHealth School of Public Health, Houston, TX, USA.

Department of Pediatrics, Division of Genetics and Metabolism, University of Texas Southwestern Medical Center, Dallas, TX, USA.

出版信息

Pediatr Res. 2022 Apr;91(5):1278-1285. doi: 10.1038/s41390-021-01629-w. Epub 2021 Jun 30.

Abstract

BACKGROUND

The population-level landscape of co-occurring birth defects among infants without a syndromic diagnosis is not well understood.

METHODS

We analyzed data from 40,771 infants with two or more major birth defects in the Texas Birth Defects Registry (TBDR; 1999-2014). We calculated adjusted observed-to-expected (O/E) ratios for all two, three, four, and five-way combinations of 138 major defects.

RESULTS

Among 530 patterns with the highest adjusted O/E ratios (top 5% of 10,595 patterns), 66% included only defects co-occurring within one organ system and 28% were suggestive of known patterns (e.g., midline developmental defects). Of the remaining patterns, the combination of defects with the highest O/E ratio (193.8) encompassed the diaphragm, spine, spleen, and heart defects. Fourteen patterns involved heart and spine defects with or without rib defects. Ten additional patterns primarily involved two hallmark components of VACTERL association (specifically, vertebral defects, anal atresia, cardiac defects, renal, or limb defects, but not tracheoesophageal fistula).

CONCLUSIONS

Our analyses provide a description of the birth defect co-occurrence patterns in a multi-ethnic, population-based sample, and revealed several patterns of interest. This work complements prior work that has suggested etiologic connections between select defects (e.g., diaphragmatic hernia and heart and spleen anomalies; heart and spine defects).

IMPACT

In this large-scale, population-based study of birth defect co-occurrence patterns, we found several birth defect combinations of potential interest that warrant further investigation: congenital diaphragmatic hernia, heart, spine, and spleen defects and scimitar syndrome with vertebral defects. The majority of patterns of co-occurring defects observed more frequently than expected involved multiple defects within the same system and combinations suggestive of known associations. Nearly all of the top patterns (beyond the same system and those suggestive of known associations) involved organ systems that are components of the VACTERL association, with heart, spine, and rib defect patterns being the most common.

摘要

背景

对于未进行综合征诊断的婴儿中同时出现的出生缺陷的人群层面情况,我们了解得并不充分。

方法

我们分析了德克萨斯州出生缺陷登记处(TBDR;1999 - 2014年)中40771名患有两种或更多种主要出生缺陷的婴儿的数据。我们计算了138种主要缺陷的所有两种、三种、四种和五种组合的调整后的观察值与预期值(O/E)比率。

结果

在调整后的O/E比率最高的530种模式中(占10595种模式的前5%),66%仅包括在一个器官系统内同时出现的缺陷,28%提示已知模式(例如中线发育缺陷)。在其余模式中,O/E比率最高的缺陷组合(193.8)包括膈肌、脊柱、脾脏和心脏缺陷。14种模式涉及心脏和脊柱缺陷,有或没有肋骨缺陷。另外10种模式主要涉及VACTERL综合征的两个标志性组成部分(具体为椎体缺陷、肛门闭锁、心脏缺陷、肾脏或肢体缺陷,但不包括气管食管瘘)。

结论

我们的分析描述了一个多民族、基于人群的样本中的出生缺陷共现模式,并揭示了几种有趣的模式。这项工作补充了之前表明特定缺陷之间病因联系的研究(例如膈疝与心脏和脾脏异常;心脏和脊柱缺陷)。

影响

在这项关于出生缺陷共现模式的大规模、基于人群的研究中,我们发现了几种可能值得进一步研究的潜在有趣的出生缺陷组合:先天性膈疝、心脏、脊柱和脾脏缺陷以及伴有椎体缺陷的弯刀综合征。观察到的共现缺陷模式中,大多数比预期更频繁出现的模式涉及同一系统内的多种缺陷以及提示已知关联的组合。几乎所有顶级模式(除了同一系统和提示已知关联的模式)都涉及作为VACTERL综合征组成部分的器官系统,其中心脏、脊柱和肋骨缺陷模式最为常见。

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