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        1 - The comparison of bacterial infection effects on semen parameters and assisted reproductive outcomes in infertile men
        Fatemeh Ghasemian Shahin Esmaeilnezhad Mohammad Javad Mehdipoor Moghaddam
        Semen analysis is one of the most important methods that reflects the fertility potential of men. Many factors lead to infertility in men, among which urogenital bacterial infections seem to play an effective role. Therefore, this study was planned to evaluate the frequ More
        Semen analysis is one of the most important methods that reflects the fertility potential of men. Many factors lead to infertility in men, among which urogenital bacterial infections seem to play an effective role. Therefore, this study was planned to evaluate the frequency of bacterial infection in men with different infertility factor. Then, the effect of bacteriospermia was studied on the basic semen parameters and assisted reproductive outcomes.In this study, 98 semen samples from infertile men with male-factor infertility were collected. The semen samples were analyzed based on World Health Organization (WHO) criteria and categorized to four groups with male factor infertility. About 0.5-1 mL samples were prepared and used to inject into oocytes. To evaluate bacterial infection, the remaining samples were transported to microbiological laboratory during 1 hour to culture using standard bacteriological techniques. The bacterial infections such as E. coli (12.24%) and Staphylococcus saprophyticus (28.57%) were detected in 40.81% of the cultured samples. The basic semen parameters such as concentration, progressive motility, viability (p<0.05), and normal morphology (p<0.01) of sperms were decreased in the samples with bacterial infections. The clinical pregnancy was also decreased in the bacteriospermia groups (p<0.05). In conclusion, the presence of bacteriospermia could influence basic semen parameters and assisted reproductive outcomes, subsequently. Manuscript profile
      • Open Access Article

        2 - Comparison of oocyte quality from normal mouse and mouse with polycystic ovarian syndrome following evaluation of GDF-9 gene
        Fatemeh Kousheh Fatemeh Ghasemian
        Introduction: Polycystic ovarian syndrome (PCOS) is one of the most common causes of infertility. One of assisted reproductive methods for PCOS patients is using of in-vitro maturation (IVM). Normal GDF-9 gene expression is one of the symptoms of good oocyte quality. Th More
        Introduction: Polycystic ovarian syndrome (PCOS) is one of the most common causes of infertility. One of assisted reproductive methods for PCOS patients is using of in-vitro maturation (IVM). Normal GDF-9 gene expression is one of the symptoms of good oocyte quality. This study examines the differences between quality of PCOS oocytes/follicles with normal oocytes/follicles during IVM.Materials and Methods: Induction of PCOS in NMRI mice (n=10) was performed by injection of 4mg/kg estradiol valerate dissolved in 0.2mg sesame oil once daily for 60 days. Oocytes and follicles were collected from control and PCOS groups, and cultured in the MEM-α medium supplemented with 10% FBS for 24-48 hrs. The evaluation of IVM rate and GDF-9 gene expression (Real-Time PCR method) was performed in different groups. Statistical analysis was performed using one-Way ANOVA test.Results: In the PCOS group, a significant decrease was observed in the number of primary follicles, preantral, antral, and corpus luteum. Increased cystic follicles and follicles with degenerated granulosa layer were also observed. 52% and 50% of PCOS oocytes and follicles was matured, respectively. In the control group, 83.33% of oocytes and 75% of follicles matured (P<0.05). GDF-9 gene expression was 1.00±0.08 and 1.24±0.2 in normal oocytes and follicles (P<0.01) and 0.66±0.02 and 0.37±0.02 in PCOS oocytes and follicles, respectively (P<0.001). Conclusion: Quality of PCOS oocytes, and especially, follicles (GDF-9 gene expression) was decreased following IVM. Therefore, using of PCOS oocytes was suggested for IVM Manuscript profile