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. 2022 Dec 10;20(11):893–914. doi: 10.18502/ijrm.v20i11.12357

Table 3.

The results of meta-analysis, meta-regression, and publication bias of studies conducted on the prevalence / OR of gynecologic cancer in PCOS patients


Outcomes Number of observations #I2% &Publication bias £Pooled OR (95%CI), (95%PI) @Meta-regression
Endometrial cancer $ 6+3 > 50 0.015* 1Insufficient observations
PCOS $ 7+3 > 50 0.004*
NON-PCOS $ 6+3 > 50 0.039* $ 2.2 (1.03, 4.7)* (0.33, 9.5) 20.71 (0.10), 62.89%
Ovarian cancer 6 < 50 0.950
PCOS 7 > 50 0.764 Insufficient observations
NON-PCOS 5 > 50 0.051 1.3 (1.0, 1.8)* (0.74, 1.65) 1.0 (0.07), 0.00%
Breast cancer 7 < 50 0.452 1.0 (0.10), 0.00%
PCOS $ 8+4 > 50 0.015*
NON-PCOS 7 > 50 0.652 1.1 (0.87, 1.4) (0.89, 1.98) 0.98 (0.09), 23.98%
Overall $ 19+3 > 50 0.045* 0.99 (0.07), 82.46%
PCOS $ 22+10 > 50 0.000*
NON-PCOS $ 18+9 > 50 0.000* $ 1.4 (1.0, 1.9)* (0.57,4.5) 0.98 (0.09), 68.29%
# I-square (I2) was used to assess heterogeneity, & Beggs' test was run to assess publication bias, *Significant level was considered at p < 0.05, $ Trim and fill correction method was applied, £ To estimate pooled odds ratios (ORs), we applied the “Meta-prop” random effect method. The 95% prediction interval (95% PI) was estimated to evaluate clinical significance as compared to statistical significance for the pooled odds ratio, @ Exponential (beta regression coefficient) (Std. Err., I-squared residuals %): 1- age adjusted, 2- PCOS diagnostic criteria adjusted, PCOS: Polycystic ovary syndrome