Wu Xiaoqing, Su Linjuan, Shen Qingmei, Guo Qun, Li Ying, Xu Shiyi, Lin Na, Huang Hailong, Xu Liangpu
Department of Medical Genetic Diagnosis and Therapy Center, Fujian Maternity and Child Health Hospital, College of Clinical Medicine for Obstetrics and Gynecology and Pediatrics, Fujian Medical University, Fuzhou, China.
Fujian Provincial Key Laboratory for Prenatal Diagnosis and Birth Defect, Fuzhou, China.
Front Pediatr. 2022 Jun 6;10:918130. doi: 10.3389/fped.2022.918130. eCollection 2022.
Fetal gastrointestinal tract obstruction (GITO) is the most frequently encountered gastrointestinal defect in the prenatal period. This study aimed to investigate the genetic disorders and pregnancy outcomes of fetal GITO. We reviewed data from 70 pregnancies that were referred for invasive prenatal testing because of fetal GITO. According to the level of obstruction, they were classified into esophageal atresia/stenosis, duodenal atresia/stenosis, jejunal or ileal atresia/stenosis, or anal atresia. Traditional karyotyping was performed on all the 70 pregnancies, and chromosomal microarray analysis (CMA) was performed on 32 of them in parallel. Traditional karyotyping revealed twelve (17.1%) chromosomal abnormalities, including 11 cases of trisomy 21 (Down syndrome), and one case of a supernumerary marker chromosome related to Cat eye syndrome. According to the absence or presence of other ultrasound anomalies, they were categorized into isolated GITO ( = 36) and non-isolated GITO ( = 34). The rate of chromosomal abnormalities in the non-isolated GITO pregnancies was significantly higher than that in the isolated GITO pregnancies (29.4 vs. 5.5%, < 0.05); the survival rate in the isolated group was significantly higher than that in the non-isolated group (67.6 vs. 34.4%, < 0.05). Among the 32 cases where CMA was performed, an additional one (3.1%) copy number variant with clinical significance was noted in a fetus with normal karyotype. The microduplication on 7q12 was considered to be the genetic etiology of duodenal stenosis, although it was inherited from a phenotypically normal mother. Our study supports the strong association between Down syndrome and fetal GITO, especially duodenal stenosis. Our findings suggested that the risk of chromosomal abnormalities was increased when GITO was accompanied by other ultrasound anomalies; thus, chromosomal abnormalities and fetal anatomy should be carefully evaluated for pregnancy management of fetal GITO.
胎儿胃肠道梗阻(GITO)是产前最常见的胃肠道缺陷。本研究旨在调查胎儿GITO的遗传疾病和妊娠结局。我们回顾了70例因胎儿GITO而接受侵入性产前检测的妊娠数据。根据梗阻水平,将它们分为食管闭锁/狭窄、十二指肠闭锁/狭窄、空肠或回肠闭锁/狭窄或肛门闭锁。对所有70例妊娠进行了传统核型分析,并对其中32例同时进行了染色体微阵列分析(CMA)。传统核型分析发现12例(17.1%)染色体异常,包括11例21三体(唐氏综合征)和1例与猫眼综合征相关的额外标记染色体。根据是否存在其他超声异常,将它们分为孤立性GITO(n = 36)和非孤立性GITO(n = 34)。非孤立性GITO妊娠的染色体异常率显著高于孤立性GITO妊娠(29.4%对5.5%,P < 0.05);孤立组的存活率显著高于非孤立组(67.6%对34.4%,P < 0.05)。在进行CMA的32例病例中,在核型正常的胎儿中发现了另外1例(3.1%)具有临床意义的拷贝数变异。7q12的微重复被认为是十二指肠狭窄的遗传病因,尽管它是从表型正常的母亲遗传而来。我们的研究支持唐氏综合征与胎儿GITO尤其是十二指肠狭窄之间的强关联。我们的研究结果表明,当GITO伴有其他超声异常时,染色体异常的风险增加;因此,对于胎儿GITO的妊娠管理,应仔细评估染色体异常和胎儿解剖结构。