PMID- 27796806 OWN - NLM STAT- MEDLINE DCOM- 20170317 LR - 20181113 IS - 1573-7330 (Electronic) IS - 1058-0468 (Print) IS - 1058-0468 (Linking) VI - 34 IP - 1 DP - 2017 Jan TI - Correlation analysis between ultrasound findings and abnormal karyotypes in the embryos from early pregnancy loss after in vitro fertilization-embryo transfer. PG - 43-50 LID - 10.1007/s10815-016-0821-2 [doi] AB - PURPOSE: The purpose of the study is to evaluate the correlation between ultrasound findings and abnormal karyotypes in early pregnancy losses (EPLs) after in vitro fertilization-embryo transfer (IVF-ET). METHODS: This retrospective analysis assessed 2172 cases of EPL after IVF-ET occurring between January 2008 and December 2013. The cases were examined via transvaginal ultrasonography (TVS). Embryonic tissue karyotyping following miscarriage was performed using a comparative genomic hybridization (CGH) analysis with fluorescence in situ hybridization (FISH). The correlations between the ultrasound findings and the karyotypes were evaluated. RESULTS: Six categories of ultrasound findings were observed: normal ultrasound, empty sac, yolk sac only, small gestational sac, small embryonic pole, and early symmetrical arrested growth. The overall rate of abnormal karyotypes was 44.9 % (976/2172), and the rate of abnormal karyotypes associated with a normal ultrasound, empty sac, yolk sac only, small gestational sac, small embryonic pole, and early symmetrical arrested growth was 49.5 % (218/440), 28.1 % (138/491), 43.4 % (197/454), 50.0 % (43/86), 49.8 % (155/311), and 57.7 % (225/390), respectively. Compared with the other groups, the prevalence of chromosomal abnormalities was significantly higher in the early symmetrical arrested growth group but was markedly lower in the empty sac group in all cases and when cases of 46,XX were excluded (p < 0.05). Trisomy 16 was the most common chromosomal abnormality in the yolk sac only, small embryonic pole and early symmetrical arrested growth groups. In the empty sac, small gestational sac and normal ultrasound groups, monosomy X was the most frequent abnormality. CONCLUSIONS: Chromosomal anomalies may be associated with specific types of ultrasound findings in EPLs after IVF-ET. FAU - Li, Xihong AU - Li X AD - Reproductive and Genetic Hospital of CITIC-Xiangya, No. 84, Xiangya road, Changsha city, Hunan, 410078, China. FAU - Ouyang, Yan AU - Ouyang Y AD - Reproductive and Genetic Hospital of CITIC-Xiangya, No. 84, Xiangya road, Changsha city, Hunan, 410078, China. AD - Institute of Reproductive and Stem Cell Engineering, Central South University, No. 84, Xiangya road, Changsha city, Hunan, 410078, China. FAU - Yi, Yan AU - Yi Y AD - Institute of Reproductive and Stem Cell Engineering, Central South University, No. 84, Xiangya road, Changsha city, Hunan, 410078, China. FAU - Tan, Yueqiu AU - Tan Y AD - Reproductive and Genetic Hospital of CITIC-Xiangya, No. 84, Xiangya road, Changsha city, Hunan, 410078, China. tanyueqiu@csu.edu.cn. AD - Institute of Reproductive and Stem Cell Engineering, Central South University, No. 84, Xiangya road, Changsha city, Hunan, 410078, China. tanyueqiu@csu.edu.cn. FAU - Lu, Guangxiu AU - Lu G AD - Reproductive and Genetic Hospital of CITIC-Xiangya, No. 84, Xiangya road, Changsha city, Hunan, 410078, China. guangxiulu@163.com. LA - eng PT - Journal Article DEP - 20161028 PL - Netherlands TA - J Assist Reprod Genet JT - Journal of assisted reproduction and genetics JID - 9206495 SB - IM MH - Abnormal Karyotype MH - Abortion, Spontaneous/diagnostic imaging/*genetics/pathology MH - Adult MH - Chromosome Aberrations MH - Comparative Genomic Hybridization MH - Embryo Transfer/*adverse effects MH - Female MH - Fertilization in Vitro/*adverse effects MH - Humans MH - In Situ Hybridization, Fluorescence MH - Pregnancy MH - Pregnancy Trimester, First MH - *Ultrasonography, Prenatal PMC - PMC5330976 OTO - NOTNLM OT - Early pregnancy loss OT - In vitro fertilization-embryo transfer OT - Karyotype OT - Transvaginal ultrasonography OT - Ultrasound findings COIS- FUNDING: This study was supported by the National Natural Science (No. 81471432), State Key Development Program for Basic Research of China (No.2012CB944901) and the Scientific Research Foundation of Reproductive and Genetic Hospital of Citic-Xiangya. CONFLICT OF INTEREST: The authors declare that they have no conflict of interest. EDAT- 2016/11/01 06:00 MHDA- 2017/03/18 06:00 PMCR- 2018/01/01 CRDT- 2016/11/01 06:00 PHST- 2016/06/28 00:00 [received] PHST- 2016/09/22 00:00 [accepted] PHST- 2016/11/01 06:00 [pubmed] PHST- 2017/03/18 06:00 [medline] PHST- 2016/11/01 06:00 [entrez] PHST- 2018/01/01 00:00 [pmc-release] AID - 10.1007/s10815-016-0821-2 [pii] AID - 821 [pii] AID - 10.1007/s10815-016-0821-2 [doi] PST - ppublish SO - J Assist Reprod Genet. 2017 Jan;34(1):43-50. doi: 10.1007/s10815-016-0821-2. Epub 2016 Oct 28.