Department of Reproductive Medicine, Affiliated Hospital of Shandong Second Medical University, Weifang, Shandong, China.
Reprod Health. 2024 Sep 5;21(1):130. doi: 10.1186/s12978-024-01854-6.
This work aimed to investigate the potential correlation between chromosomal polymorphisms and various reproductive abnormalities.
We examined 21,916 patients affected by infertility who sought care at the Department of Reproductive Medicine, Affiliated Hospital of Shandong Second Medical University between January 2018 and December 2022. A total of 2227 individuals identified as chromosomal polymorphism carriers constituted the polymorphism group, and 2245 individuals with normal chromosome karyotypes were randomly selected to form a control group. Clinical manifestations, histories of spontaneous miscarriage, abnormal reproductive developments, fetal abnormalities, and male sperm quality anomalies were statistically compared between these two groups.
Of the 21,916 patients analyzed, 2227 displayed chromosomal polymorphism, representing a 10.16% detection rate. Amongst the male patients, 1622 out of 10,827 exhibited polymorphisms (14.98%), whereas 605 out of 11,089 females showed polymorphisms (5.46%). Female carriers in the polymorphism group, showed statistically significant increased rates of spontaneous abortion (29.75% vs. 18.54%), fetal anomalies (1.32% vs. 0.81%), and uterine abnormalities compared with the control group (1.32% vs. 0.81%). Male carriers in the polymorphism group had higher rates of spontaneous abortion in partners (22.87% vs. 10.37%), fetal anomalies (1.97% vs. 0.25%), compromised sperm quality (41.74% vs. 7.18%), testicular underdevelopment (2.28% vs. 0.92%), and hypogonadotropic hypogonadism (0.62% vs. 0.37%) compared with the control group.
Chromosomal polymorphisms may have a certain negative effect on reproductive irregularities, including spontaneous abortions, fetal anomalies, and reduced sperm quality in males. Their clinical effects deserve further investigation.
本研究旨在探讨染色体多态性与各种生殖异常之间的潜在相关性。
我们对 2018 年 1 月至 2022 年 12 月在山东第二医科大学附属医院生殖医学科就诊的 21916 例不孕患者进行了检查。共有 2227 名被鉴定为染色体多态性携带者的个体组成多态性组,随机选择 2245 名染色体核型正常的个体组成对照组。对两组患者的临床表现、自然流产史、生殖发育异常、胎儿异常和男性精子质量异常进行统计学比较。
在分析的 21916 例患者中,2227 例显示染色体多态性,检出率为 10.16%。在男性患者中,10827 例中有 1622 例(14.98%)表现出多态性,而 11089 例女性中有 605 例(5.46%)表现出多态性。多态性组女性携带者自然流产率(29.75%比 18.54%)、胎儿异常率(1.32%比 0.81%)和子宫异常率明显高于对照组(1.32%比 0.81%)。多态性组男性携带者配偶自然流产率(22.87%比 10.37%)、胎儿异常率(1.97%比 0.25%)、精子质量受损率(41.74%比 7.18%)、睾丸发育不良率(2.28%比 0.92%)和低促性腺激素性性腺功能减退症发生率(0.62%比 0.37%)均明显高于对照组。
染色体多态性可能对生殖异常有一定的负面影响,包括自然流产、胎儿异常和男性精子质量下降。其临床影响值得进一步研究。