Oocyte-Secreted Serum Biomarkers GDF9 and BMP15 in Women with Endometriosis

• Published in: Reproductive sciences (Thousand Oaks, Calif.) Vol. 30; no. 5; pp. 1521 - 1527
• Main Authors: Shamsa, Aiat, Gilchrist, Robert B., Robertson, David M., Rodgers, Rachael J., Donoghoe, Mark W., Ledger, William L., Abbott, Jason A., Riepsamen, Angelique H.
• Format: Journal Article
• Language: English
• Published: Cham Springer International Publishing 01.05.2023
• Subjects: Biomarkers - metabolism; Bone Morphogenetic Protein 15 - metabolism; Case-Control Studies; Embryology; Endometriosis - diagnosis; Endometriosis - metabolism; Female; Growth Differentiation Factor 9 - metabolism; Humans; Medicine; Medicine & Public Health; Obstetrics/Perinatology/Midwifery; Oocytes - metabolism; Reproductive Biology: Original; Reproductive Biology: Original Article; Reproductive Medicine; GDF9; Oocyte-secreted factors; Endometriosis; Biomarker; BMP15
• DOI: 10.1007/s43032-022-01107-6
• ISSN: 1933-7191

Oocyte-secreted growth differentiation factor 9 (GDF9) and bone morphogenetic protein 15 (BMP15) are critical paracrine regulators of female fertility. Recent studies demonstrated that serum concentrations are associated with the number of oocytes retrieved during IVF, and therefore potential clinical use as biomarkers. However, it is unknown if the presence of endometriosis affects serum GDF9 or BMP15. An exploratory case–control study was prospectively performed on 60 women who underwent laparoscopy between April 2017 and August 2018 at two hospitals. GDF9 and BMP15 were measured by validated immunoassays in pre-operative serum samples. Data were analysed relative to laparoscopic assessment of endometriosis and staging. There were 35 women with confirmed laparoscopic diagnosis of endometriosis and 25 controls with no evidence of endometriosis at laparoscopy. GDF9 was detectable in 40% of controls and 48% of cases. There was no difference in median GDF9 concentrations between controls (20.0 pg/ml, range 20.0–2504 pg/ml) and cases (20.0 pg/ml, range 20.0–2963 pg/ml). BMP15 was detectable in 48% of controls and 58% of cases, with no difference in median concentrations between controls (26.5 pg/ml, range 24.0–1499 pg/ml) and cases (24.0 pg/ml, range 24.0–796 pg/ml). Furthermore, there were no significant differences in the proportion of detectable samples or concentrations of GDF9 or BMP15 with differing severities of endometriosis. In conclusion, serum concentrations of oocyte-secreted factors, GDF9 and BMP15 did not differ between control patients and patients with endometriosis. For clinical application in reproductive medicine, GDF9 and BMP15 serum biomarker quantitation is unlikely to be aberrant in the presence of endometriosis.