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Fig. 2 | BMC Pregnancy and Childbirth

Fig. 2

From: Investigation of the role of X chromosome inactivation and androgen receptor CAG repeat polymorphisms in patients with recurrent pregnancy loss: a prospective case–control study

Fig. 2

 A) Comparison of the XCI skew between the RPL and control groups. The XCI skew is significantly higher in patients with RPL than in the controls (mean ± standard deviation, 67.71 ± 10.50 vs. 64.22 ± 10.62, p = 0.011). XCI = X-chromosome inactivation; RPL = recurrent pregnancy loss

B) Comparison of the AR CAG repeat polymorphism between the RPL and control groups. The short allele (16.87 ± 2.39, vs. 17.77 ± 2.37, p = 0.003) and BAM (18.56 ± 1.97 vs. 19.34 ± 2.38, p = 0.005) were significantly shorter in patients with RPL than in controls. The difference in bioactive CAG repeats (XWBM) was more pronounced (18.46 ± 2.02 vs. 19.38 ± 2.53, p = 0.001). AR CAG = androgen receptor CAG; RPL = recurrent pregnancy loss; XWBM = X-weighted-biallelic-mean.

C) Percentage of women with XCI skew > 90, 85–90, and < 85 in the RPL and control groups. The prevalence of highly skewed XCI (≥ 85%) and extremely skewed XCI (≥ 90%) were not significantly different between the two groups. XCI = X-chromosome inactivation; RPL = recurrent pregnancy loss

D) Comparison of patients with RPL and controls according to CAG repeats. The median CAG repeat length of the control group was 19.50 or 19.72 calculated as BAM or XWBM, such that 20 was used as the cut-off value. The distribution was significantly different between the two groups (chi-square test, p-value = 0.000 for BAM, p-value = 0.000 for XWBM). RPL = recurrent pregnancy loss; XWBM = X-weighted biallelic mean; BAM = biallelic mean.

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