Pan Yun, Chen Changshui, Li Haibo
The Central Laboratory of Birth Defects Prevention and Control, The Affiliated Women and Children's Hospital of Ningbo University, Ningbo, China.
Ningbo Key Laboratory for the Prevention and Treatment of Embryogenic Diseases, The Affiliated Women and Children's Hospital of Ningbo University, Ningbo, China.
Birth Defects Res. 2025 Jun;117(6):e2489. doi: 10.1002/bdr2.2489.
The aim of this study was to investigate the underlying factors contributing to gender-based disparities in the prevalence of trisomy 21 (Downs's syndrome) and trisomy 18 (Edwards's syndrome).
Overall, 551 cases of trisomy 21 (T21) and 154 cases of trisomy 18 (T18) diagnosed through amniotic fluid karyotyping and chromosomal microarray analysis (CMA) between 2005 and 2023 at the Affiliated Women and Children's Hospital of Ningbo University. The study population consisted of fetuses at 19-23 gestational weeks across various maternal age groups. A control group comprising 662,453 newborns from the same institution between 2011 and 2018 was established for sex ratio comparison. Parental origin of diploids in T21 and T18 cases was determined using quantitative fluorescence-polymerase chain reaction (QF-PCR) analysis. Statistical significance of gender bias was evaluated using chi-squared tests, with a threshold of p < 0.05 considered statistically significant.
The study revealed distinct sex ratio patterns across different maternal age groups. The control group exhibited a sex ratio of 1.06 (male:female), while the overall sex ratio for T21 cases was significantly elevated at 1.32. Notably, the highest sex ratio (1.84) was observed in T21 cases among women aged 20-25 years, with a progressive decline in sex ratio corresponding to increasing maternal age. The sex ratio of newborns born to women aged ≥ 35 years approximated that of the control. In contrast, T18 cases demonstrated an overall female predominance, with a sex ratio of 0.67, reaching its lowest value (0.56) in the 25-30 years maternal age group. Regarding the parent origin of diploids, maternal meiosis errors accounted for > 90% of cases in both T21 and T18. However, a higher prevalence of paternal origin was observed in younger women (≤ 35 years). Male fetuses of paternal diploid origin of T21 were 2.5 times more than female fetuses.
In our sample of over 500,000 births, between 2005 and 2023 in Ningbo, China, fetuses with T21 were more likely to be males while fetuses with T18 were more likely to be females. However, this gender bias exhibited a significant age-dependent pattern, being predominantly observed in women under 35 years of age. Specifically, in T21 cases of paternal origin among women ≤ 35 years, the frequency of nondisjunction involving Y-chromosome-bearing sperm was 2.5-fold higher than that involving X-chromosome-bearing sperm.
本研究旨在调查导致21三体综合征(唐氏综合征)和18三体综合征(爱德华兹综合征)患病率存在性别差异的潜在因素。
总体而言,2005年至2023年期间,在宁波大学附属妇女儿童医院通过羊水核型分析和染色体微阵列分析(CMA)诊断出551例21三体(T21)和154例18三体(T18)病例。研究对象包括不同母亲年龄组妊娠19 - 23周的胎儿。设立了一个对照组,由2011年至2018年来自同一机构的662453名新生儿组成,用于性别比比较。使用定量荧光聚合酶链反应(QF-PCR)分析确定T21和T18病例中二倍体的亲本来源。使用卡方检验评估性别偏差的统计学意义,以p < 0.05为具有统计学显著性的阈值。
研究揭示了不同母亲年龄组的性别比模式不同。对照组的性别比为1.06(男:女),而T21病例的总体性别比显著升高至1.32。值得注意的是,在20 - 25岁女性的T21病例中观察到最高性别比(1.84),随着母亲年龄增加,性别比逐渐下降。35岁及以上女性所生新生儿的性别比接近对照组。相比之下,T18病例总体上以女性为主,性别比为0.67,在母亲年龄25 - 30岁组中达到最低值(0.56)。关于二倍体的亲本来源,T21和T18病例中母源减数分裂错误均占90%以上。然而,在年轻女性(≤35岁)中观察到父源的患病率较高。T21父源二倍体的男性胎儿是女性胎儿的2.5倍。
在我们对2005年至2023年中国宁波超过50万例出生病例的样本中,T21胎儿更可能为男性,而T18胎儿更可能为女性。然而,这种性别偏差呈现出显著的年龄依赖性模式,主要在35岁以下女性中观察到。具体而言,在≤35岁女性的T21父源病例中,涉及携带Y染色体精子的不分离频率比涉及携带X染色体精子的高2.5倍。