Fan Zuqian, Weng Xunjin, Pan Zhijian, Fan Qiongying, Long Ju, Lin Guixian, Yang Qian, Sun Lei
Department of Clinical Laboratory, Qinzhou Maternal and Child Health Hospital, Guangxi.
Qinzhou Key Laboratory of Molecular and Cell Biology on Endemic Diseases, Qinzhou, Guangxi.
Medicine (Baltimore). 2021 Jun 25;100(25):e26331. doi: 10.1097/MD.0000000000026331.
Mosaicism can be observed in karyotype analyses of amniotic fluid cells. Differentiating between true mosaicism and pseudomosaicism and determining mosaic proportions can help avoid misjudgments by doctors and effectively reduce mental and physical harm to pregnant women. However, the detection of mosaicism and mosaic proportions via karyotype analysis and fluorescence in situ hybridization (FISH) is extremely complex. We have developed a novel approach, "segmental duplication quantitative fluorescent PCR" (SD-QF-PCR), to detect mosaicism and mosaic proportions.In this study, twenty control samples and fourteen mosaic samples were tested by first-line karyotype analysis; by second-line karyotype analysis, SD-QF-PCR and FISH were used to reassess fetal sex chromosome mosaicism and mosaic proportions.Detection of the 20 control samples by second-line karyotype analysis via FISH and SD-QF-PCR showed normal and consistent results. Among the 14 mosaic samples, the numbers of samples showing true mosaicism and pseudomosaicism detected by the three methods were 6 and 8, respectively.Our study demonstrates that SD-QF-PCR can be used as a complementary method to traditional cytogenetic analysis of amniotic fluid mosaics and has clinical application value.
在羊水细胞的核型分析中可观察到嵌合体现象。区分真嵌合体和假嵌合体并确定嵌合比例有助于避免医生误判,并有效减少对孕妇身心的伤害。然而,通过核型分析和荧光原位杂交(FISH)检测嵌合体和嵌合比例极其复杂。我们开发了一种新方法,即“节段重复定量荧光PCR”(SD-QF-PCR),用于检测嵌合体和嵌合比例。在本研究中,通过一线核型分析对20个对照样本和14个嵌合样本进行检测;通过二线核型分析,使用SD-QF-PCR和FISH重新评估胎儿性染色体嵌合体和嵌合比例。通过FISH和SD-QF-PCR对20个对照样本进行二线核型分析检测,结果正常且一致。在14个嵌合样本中,三种方法检测出的真嵌合体和假嵌合体样本数分别为6个和8个。我们的研究表明,SD-QF-PCR可作为羊水嵌合体传统细胞遗传学分析的补充方法,具有临床应用价值。