Reproductive Medicine Center, Third Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
BMC Med Genomics. 2023 Nov 1;16(1):273. doi: 10.1186/s12920-023-01715-4.
To determine the effect of different translocation characteristics on fertilization rate and blastocyst development in chromosomal translocation patients.
This retrospective cohort study was conducted at the Third Affiliated Hospital of Zhengzhou University From January 2017 to December 2022.All couples were diagnosed as reciprocal translocation or Robertsonian translocation by karyotype of peripheral blood lymphocytes test. After adjusting for confounding factors, the effect of chromosomal rearrangement characteristics, such as carrier sex, translocation type, chromosome length and break sites, on fertilization rate and embryo development were analysed separately using multiple linear regression.
In cases of Robertsonian translocation (RobT), the carrier sex plays an independent role in fertilization rate, and the male carriers was lower than that of female carriers (76.16% vs.86.26%, P = 0.009). In reciprocal translocation (RecT), the carrier sex, chromosome types and break sites had no influence on fertilization rate, blastocyst formation rate (P > 0.05). However, patients with human longer chromosomal (chromosomes 1-5) translocation have a lower available blastocyst formation rate (Group AB vs. Group CD: 41.49%vs.46.01%, P = 0.027). For male carriers, the translocation types was an independent factor affecting the fertilization rate, and the RobT was the negative one (B = - 0.075, P = 0 0.009). In female carriers, we did not observe this difference (P = 0.227).
In patients with chromosomal translocation, the fertilization rate may be influenced by carrier sex and translocation type, chromosomes 1-5 translocation may adversely affect the formation of available blastocysts. Break sites have no role in fertilization and blastocyst development.
探讨不同易位特征对染色体易位患者受精率和囊胚发育的影响。
本回顾性队列研究于 2017 年 1 月至 2022 年 12 月在郑州大学第三附属医院进行。所有夫妇均经外周血淋巴细胞核型检查诊断为相互易位或罗伯逊易位。调整混杂因素后,分别采用多元线性回归分析染色体重排特征(如携带者性别、易位类型、染色体长度和断裂点)对受精率和胚胎发育的影响。
在罗伯逊易位(RobT)病例中,携带者性别对受精率有独立作用,男性携带者的受精率低于女性携带者(76.16%比 86.26%,P=0.009)。在相互易位(RecT)中,携带者性别、染色体类型和断裂点对受精率、囊胚形成率无影响(P>0.05)。然而,人类较长染色体(1-5 号染色体)易位患者的可利用囊胚形成率较低(AB 组比 CD 组:41.49%比 46.01%,P=0.027)。对于男性携带者,易位类型是影响受精率的独立因素,RobT 为负相关(B=-0.075,P=0.009)。在女性携带者中,我们没有观察到这种差异(P=0.227)。
在染色体易位患者中,受精率可能受到携带者性别和易位类型的影响,1-5 号染色体易位可能对可利用囊胚的形成产生不利影响。断裂点对受精和囊胚发育没有作用。