Please wait a minute...
欢迎访问发育医学电子杂志,今天是
发育医学电子杂志  2023, Vol. 11 Issue (5): 338-345    DOI: 10.3969/j.issn.2095-5340.2023.05.003
  围产医学   论著 |产科 |
16 例无创产前检测8 号染色体异常病例的产前诊断结果及妊娠结局分析
于怡清 周希亚 蒋宇林 吕嬿 常家祯 郝娜 李萌萌 戚庆炜
(中国医学科学院北京协和医院 产科中心,北京 100730)
Analysis of prenatal diagnosis results and pregnancy outcomes of 16 cases with chromosome 8 abnormality detected by non-invasive prenatal testing
Yu Yiqing, Zhou Xiya, Jiang Yulin, et al
(Departmentof Obstetrics, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Beijing 100730, China)
下载:  PDF (887KB) 
输出:  BibTeX | EndNote (RIS)      
摘要 【摘要】 目的  探讨无创产前检测(non-invasive prenatal testing,NIPT)提示8 号染色体异常病例的产
前诊断、遗传学咨询和妊娠结局。 方法 2016 年4 月1 日至2022 年10 月31 日,在中国医学科学院
北京协和医院进行NIPT 检测的孕妇中,结果为8 号染色体异常且接受产前诊断的孕妇共16 例。所有
病例均接受羊膜腔穿刺术,进行羊水细胞染色体核型分析及染色体微阵列分析(chromosomal microarray
analysis,CMA),部分病例进行针对8 号染色体的未培养细胞的荧光原位杂交(fluorescence in situ
hybridization,FISH)。回顾性分析患者的临床资料、产前遗传学诊断结果和妊娠结局。 结果  ① 13 例
未提示其他染色体异常,为孤立性NIPT 8 号染色体异常组。其中1 例为胎儿8- 三体嵌合体,经咨询后
继续妊娠,后续超声检查未见异常,随访新生儿未见异常。其余12 例产前遗传学检测均未见异常,除
3 例失访之外,所有病例均继续妊娠,随访新生儿均未见异常。② 3 例同时提示其他染色体异常,为非
孤立性NIPT 8 号染色体异常组。其中1 例产前诊断结果为16- 三体嵌合体,超声发现胎儿心脏异常,
终止妊娠。其余2 例产前遗传学检测未见异常,1 例在孕29 周发现孕妇罹患左侧乳腺癌,行剖宫产终
止妊娠,随访新生儿未见异常;另1 例失访。 结论 对于NIPT 提示8 号染色体异常的病例,应进一
步行产前诊断,遗传学检测的方案建议包含染色体核型分析、CMA 和未培养细胞的FISH 分析。对于
产前诊断胎儿8- 三体嵌合体的病例,应进行详细的遗传咨询,如果超声检查未见异常,一般预后良好,
可以考虑继续妊娠。
服务
把本文推荐给朋友
加入引用管理器
E-mail Alert
RSS
作者相关文章
关键词:  无创产前检测  产前诊断  8- 三体嵌合体  染色体核型分析  染色体微阵列分析  荧光原位杂交分析  妊娠结局    
Abstract: 【Abstract】 Objective To explore the prenatal diagnosis, genetic counseling and pregnancy outcomes of patients with chromosome 8 abnormality detected by non-invasive prenatal testing (NIPT). Method From April 1, 2016 to October 31, 2022, among the pregnant women who underwent NIPT in Peking Union Medical College Hospital, 16 cases underwent prenatal diagnosis for chromosome 8 abnormality. All the 16cases underwent amniocentesis for prenatal chromosomal karyotyping and chromosomal microarray analysis(CMA). Fluorescence in situ hybridization (FISH) of uncultured cells on chromosome 8 was completed in some cases. Clinical data, prenatal genetic diagnosis results, and pregnancy outcomes were analyzed retrospectively. Result ① 13 cases without other chromosomal abnormality were considered as isolated NIPT chromosome 8 abnormality group (isolated group). One case was diagnosed as trisomy 8 mosaicism,and the pregnant woman decided to continue the pregnancy after counseling. No abnormality was found inprenatal ultrasound examination and postnatal neonatal follow-up. The other 12 cases were normal in theprenatal genetic testing and continued the pregnancy except three cases lost follow-up. No abnormality was found in neonates during follow-up. ② Three cases with other chromosomal abnormalities were considered asnon-isolated NIPT chromosome 8 abnormality group (non-isolated group). One case was diagnosed as trisomy16 mosaicism with fetal heart abnormality by ultrasound, and the pregnancy was terminated. The other twocases were normal in the prenatal genetic testing. One pregnant woman was diagnosed as left breast cancer at29 gestational weeks of pregnancy, who terminated the pregnancy via cesarean section, and no abnormalitywas found in the newborn during follow-up. One case lost follow-up. Conclusion Further prenatal diagnosis should be performed in cases with chromosome 8 abnormality detected by NIPT. The recommended genetic testing regimen includes chromosomal karyotyping, CMA and FISH analysis of uncultured cells. For cases diagnosed as trisomy 8 mosaicism, detailed genetic counseling should be performed. If no abnormality is detected by ultrasound, the prognosis of the fetus would be good in general, and the pregnancy could be considered to continue.
Key words:  Non-invasive prenatal testing    Prenatal diagnosis    Trisomy 8 mosaicism    Chromosomal karyotyping    Chromosomal microarray analysis    Fluorescence in situ hybridization    Pregnancy outcome
收稿日期:  2023-06-26                出版日期:  2023-09-30      发布日期:  2023-09-27      期的出版日期:  2023-09-30
基金资助: 中央高水平医院临床科研专项(2022-PUMCH-B-076)
通讯作者:  戚庆炜    E-mail:  qiqingwei@163.com
引用本文:    
于怡清 周希亚 蒋宇林 吕嬿 常家祯 郝娜 李萌萌 戚庆炜. 16 例无创产前检测8 号染色体异常病例的产前诊断结果及妊娠结局分析[J]. 发育医学电子杂志, 2023, 11(5): 338-345.
Yu Yiqing, Zhou Xiya, Jiang Yulin, et al. Analysis of prenatal diagnosis results and pregnancy outcomes of 16 cases with chromosome 8 abnormality detected by non-invasive prenatal testing. Journal of Developmental Medicine(Electronic Version), 2023, 11(5): 338-345.
链接本文:  
http://www.fyyxzz.com/CN/10.3969/j.issn.2095-5340.2023.05.003  或          http://www.fyyxzz.com/CN/Y2023/V11/I5/338
[1] 刘恒 郭婉茹 蒋天从 戚桂杰. 高龄孕妇产前诊断胎儿染色体异常结果特征分析[J]. 发育医学电子杂志, 2024, 12(5): 337-341,349.
[2] 吴正沐 王正权 王旻 谈雅静 李文. 时差成像胚胎培养系统观察精子DNA碎片化指数对卵胞浆内单精子显微注射的胚胎发育及临床结局的影响[J]. 发育医学电子杂志, 2024, 12(2): 130-135.
[3] 李丹 杨小倩 曹雪萍. 贫血孕妇血清铁及可溶性血清转铁蛋白受体检测对妊娠结局的预测价值[J]. 发育医学电子杂志, 2024, 12(1): 30-35.
[4] 王培 宛杨 吕嬿 戚庆炜. 染色体核型联合染色体微阵列分析序贯全外显子组测序在胎儿先天性心脏病产前诊断中的应用[J]. 发育医学电子杂志, 2023, 11(5): 331-337.
[5] 吕少广 刘芳 阴晓伟. 17p11.2 微重复致Potocki-Lupski 综合征1 例报道及四年随访结果[J]. 发育医学电子杂志, 2023, 11(4): 282-284,315.
[6] 曾贵红 邹伟洋 刘长娣 陈玉兰 温婷媚. 妊娠期特有并发症患者不同孕期脂代谢异质性及临床监测意义[J]. 发育医学电子杂志, 2023, 11(3): 174-180.
[7] 胡婷婷 汪伟伟 胡益祥 张颖 蔡艳萍 颜宏利. 卵胞浆内单精子显微注射治疗周期中促性腺激素用药对胚胎发育潜能的影响[J]. 发育医学电子杂志, 2023, 11(3): 168-173.
[8] 王磊 安邦权 黄盛文. 基于母体外周血胎儿游离DNA 的单基因病无创产前诊断研究进展[J]. 发育医学电子杂志, 2023, 11(1): 53-59.
[9] 陈廖粤 马巍 袁正伟. 血清标志物、彩色多普勒超声及两者 联合筛查神经管缺陷的研究进展[J]. 发育医学电子杂志, 2022, 10(6): 470-476.
[10] 吕嬿 戚庆炜 蒋宇林 周希亚 郭琦 郝娜 常家桢 刘俊涛. 高龄孕妇胎儿染色体非整倍体产前筛查和产前诊断的卫生经济学分析[J]. 发育医学电子杂志, 2022, 10(5): 321-329.
[11] 邹旷妮 姜春蓉 张素蓉. 孕中期子宫动脉多普勒超声血流参数联合血清学指标预测不良妊娠结局的价值[J]. 发育医学电子杂志, 2022, 10(3): 189-195.
[12] 刘宇 肖冰 刘慧丽 徐燕 韩连书. 1 例Meckel 综合征3 型胎儿的分子病因诊断[J]. 发育医学电子杂志, 2021, 9(6): 460-462.
[13] 卢雪景 梁建梅 申林林 白娅琴 秦丽欣 高金霞 王亚凡. 低分子肝素联合小剂量阿司匹林对复发性流产患者血栓前状态、肝功能及免疫功能的影响[J]. 发育医学电子杂志, 2021, 9(3): 214-219.
[14] 葛海燕 乔彦霞 张明 刘伟娜. 新生儿期杜氏进行性肌营养不良1 例[J]. 发育医学电子杂志, 2021, 9(3): 238-240.
[15] 刘丽欣 周希亚. 巨细胞病毒感染的产前诊断、治疗及管理[J]. 发育医学电子杂志, 2021, 9(3): 176-181,205.
[1] Society of Neonatologist, Chinese Medical Doctor Association. Consensus recommendations on the prevention and early management of respiratory distress syndrome in preterm infants[J]. Journal of Developmental Medicine(Electronic Version), 2017, 5(3): 129 -131 .
[2] Professional Committee of Respiratory, Society of Neonatologist, Chinese Medical Doctor Association. Clinical application recommendations for heated humidified high flow nasal cannula[J]. Journal of Developmental Medicine(Electronic Version), 2017, 5(3): 132 -135 .
[3] YAN Jun, ZHU Xing-wang, SHI Yuan. Application progress of noninvasive ventilate technique for premature infants[J]. Journal of Developmental Medicine(Electronic Version), 2017, 5(3): 136 -140 .
[4] GU Min-fang, YANG Chuan-zhong. Progress of intrapartum resuscitation for premature infants[J]. Journal of Developmental Medicine(Electronic Version), 2017, 5(3): 141 -145 .
[5] LIU Shu-hua, SHEN Yue-bo, LIU Cui-qing, MA Li. The efficacy of pulmonary surfactant for pulmonary function in premature tension pneumothorax[J]. Journal of Developmental Medicine(Electronic Version), 2017, 5(3): 146 -151 .
[6] GAO Xiao-hui, MAO Jian. Clinical features of non-oliguric hyperkalemia in extremely low birth weight infants[J]. Journal of Developmental Medicine(Electronic Version), 2017, 5(3): 152 -158 .
[7] XIA Yao-fang, YANG Juan , TIAN Bao-li, et al. Value of amplitude-integrated electroencephalography in monitoring acute period of neonatal bilirubin encephalopathy and prognostic assessment[J]. Journal of Developmental Medicine(Electronic Version), 2017, 5(3): 159 -163 .
[8] WANG Li-rong, SUN Xiao-yan, ZHU Ruo-xin, et al. Epidemiological investigation and analysis of women aged 40-55 years old with osteoporosis in Gansu province[J]. Journal of Developmental Medicine(Electronic Version), 2017, 5(3): 164 -167 .
[9] CHEN Ru-yue, SHEN Yun-yan, CHEN Qing , et al. Five cases about Henoch-Schönlein purpura complicated with central nervous system injury in children and literatures review[J]. Journal of Developmental Medicine(Electronic Version), 2017, 5(3): 168 -171 .
[10] ZHANG Ai-run, FANG Xiao-yi. Lung function testing of bronchopulmonary dysplasia for infants and children[J]. Journal of Developmental Medicine(Electronic Version), 2017, 5(3): 172 -176 .
Viewed
Full text


Abstract

Cited

  Shared   
  Discussed