Xuanyou Zhou, Naixin Xu, Xianling Cao, Weihui Shi, Shuyuan Li, Songchang Chen, Chenming Xu
Obstetrics and Gynecology Hospital, Institute of Reproduction and Development, Fudan University, Shanghai, China.
Departments of Obstetrics and Gynecology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Front Endocrinol (Lausanne). 2025 Jun 17;16:1609471. doi: 10.3389/fendo.2025.1609471. eCollection 2025.
The aim of the present study was to investigate whether the CGG repeat length and AGG interruption patterns on the FMR1 gene affect female fecundity.
A total of 266 infertile patients and 276 fertile controls were included in the study. All participants received FMR1 testing using triplet repeat primed PCR and capillary electrophoresis. The allele with the smaller number of CGG repeats was defined as "allele 1", and the allele with the larger number of CGG repeats was defined as "allele 2".
The mean number of CGG repeat length at allele 2 in the secondary infertility group was higher than that in the control group (33.1 ± 6.7 vs 30.9 ± 3.3, Bonferroni corrected p=0.003). The proportion of 35-44 CGG repeat at both FMR1 alleles showed a higher trend in the secondary infertility group as compared to the control group after adjusting for age, education, smoking status, cohort and the CGG repeats of the other FMR1 allele (aOR=7.812, 95% CI 0.884-69.001; p=0.064 for allele 1; aOR=3.657, 95% CI 2.193-6.098; p<0.001 for allele 2, respectively). Lower AMH levels were associated with increased CGG repeat length at allele 1 in infertile patients (Adjusted R = 0.178, p=0.003) after adjusting for age, education, smoking status, infertility type and the CGG repeats of FMR1 allele 2. However, no significant correlation was found between the number of CGG repeats at allele 2 and AMH levels (Adjusted R = 0.150, p=0.086). Although the difference was not statistically significant, there was a higher proportion of 3 AGG interruptions at both alleles in the secondary infertility group as compared to the control group (6.1% vs 0%, p=0.146 for allele 1, 30.6% vs 11.3%, p=0.099 for allele 2). Patients with 35-44 CGG repeat length showed a higher carrier rate of 3 AGG interruptions at both alleles (p<0.001 for both).
Overall, the high normal sized (35-44 CGG) repeat length at both FMR1 alleles may serve a promoting role in the development of secondary infertility in Asian women. In addition, the CGG repeat length at allele 1 appears to have a mild correlation with AMH levels in infertile patients.
本研究的目的是调查FMR1基因上的CGG重复长度和AGG中断模式是否会影响女性生育力。
本研究共纳入266例不孕患者和276例生育力正常的对照者。所有参与者均接受了使用三联体重复引物PCR和毛细管电泳的FMR1检测。CGG重复次数较少的等位基因定义为“等位基因1”,CGG重复次数较多的等位基因定义为“等位基因2”。
继发性不孕组中等位基因2的CGG重复长度平均数高于对照组(33.1±6.7对30.9±3.3,Bonferroni校正p=0.003)。在调整年龄、教育程度、吸烟状况、队列以及另一个FMR1等位基因的CGG重复次数后,继发性不孕组中两个FMR1等位基因上CGG重复次数为35-44的比例与对照组相比呈上升趋势(等位基因1的调整后比值比[aOR]=7.812,95%置信区间[CI]0.884-69.001;p=0.064;等位基因2的aOR=3.657,95%CI2.193-6.098;p<0.001)。在调整年龄、教育程度、吸烟状况、不孕类型以及FMR1等位基因2的CGG重复次数后,不孕患者中等位基因1的CGG重复长度增加与抗缪勒管激素(AMH)水平降低相关(调整后R=0.178,p=0.003)。然而,未发现等位基因2的CGG重复次数与AMH水平之间存在显著相关性(调整后R=0.150,p=0.086)。虽然差异无统计学意义,但继发性不孕组中两个等位基因上有3次AGG中断的比例高于对照组(等位基因1为6.1%对0%,p=0.146;等位基因2为30.6%对11.3%,p=0.099)。CGG重复长度为35-44的患者在两个等位基因上有3次AGG中断的携带率更高(两个均p<0.001)。
总体而言,FMR1基因两个等位基因上高正常大小(35-44个CGG)的重复长度可能对亚洲女性继发性不孕的发生起促进作用。此外,等位基因1的CGG重复长度与不孕患者的AMH水平似乎存在轻度相关性。