Unité de Pharmacoépidémiologie, UMR CERPOP, INSERM, Université de Toulouse, Toulouse, France.
Département d'Anatomie et Cytologie Pathologiques, IUCT-Oncopole, Toulouse, France.
Birth Defects Res. 2024 Nov;116(11):e2414. doi: 10.1002/bdr2.2414.
Congenital ocular anomalies (COA) are among the most common causes of visual impairment in children in high-income countries. The aim of the study is to describe the prevalence of the various COA recorded in European population-based registries of CA (EUROCAT) participating in the EUROmediCAT consortium.
Data from 19 EUROmediCAT registries and one healthcare database (EFEMERIS) were included in this descriptive epidemiological study. Cases of COA included live births, FD from 20 weeks gestational age (GA), and termination of pregnancy for fetal anomaly.
The prevalence of total COA was 3.47/10,000 births (95% CI [3.61-3.82]), ranging from 1.41 to 13.46/10,000 depending on the registry. Among COA cases, congenital lens anomalies were the most frequent anomalies (31%), of which over half were single ocular anomalies (presenting with only one ocular anomaly). An/microphthalmia was the second most frequent COA (24%) of which three-quarters were multiply malformed (associated to extraocular major anomalies). Among single COA cases, 58 were prenatally diagnosed (4%), of which, 58% were diagnosed in the second trimester. Known genetic causes of COA explained 2.5%-25% of COA depending on their class.
This is the first European study describing COA. The detailed prevalence data offered in this study could improve screening and early diagnosis of different classes of COA. As COA are rare, epidemiological surveillance of large populations and accurate clinical descriptions are essential.
先天性眼部异常(COA)是高收入国家儿童视力损害的最常见原因之一。本研究旨在描述参与 EUROmediCAT 联盟的欧洲基于人群的先天性白内障登记处(EUROCAT)记录的各种 COA 的患病率。
本描述性流行病学研究纳入了来自 19 个 EUROmediCAT 登记处和一个医疗保健数据库(EFEMERIS)的数据。COA 病例包括活产儿、从 20 孕周(GA)开始的 FD 以及因胎儿异常而终止妊娠。
总 COA 的患病率为 3.47/10000 例活产(95%CI [3.61-3.82]),根据登记处的不同,范围从 1.41 至 13.46/10000。在 COA 病例中,先天性晶状体异常是最常见的异常(31%),其中超过一半是单侧眼部异常(仅存在一种眼部异常)。无眼/小眼畸形是第二常见的 COA(24%),其中四分之三是多畸形(与眼外主要异常相关)。在单眼 COA 病例中,有 58 例(4%)在产前诊断,其中 58%在孕中期诊断。COA 的已知遗传病因取决于其类别,占 COA 的 2.5%-25%。
这是第一项描述 COA 的欧洲研究。本研究提供的详细患病率数据可以改善不同类型 COA 的筛查和早期诊断。由于 COA 很少见,因此对大量人群进行流行病学监测和准确的临床描述至关重要。