Implication of Novel BMP15 and GDF9 Variants in Unexpected Poor Ovarian Response

• Published in: Reproductive sciences (Thousand Oaks, Calif.) Vol. 31; no. 3; pp. 840 - 850
• Main Authors: Mehdizadeh, Anahita, Soleimani, Mansoureh, Amjadi, Fatemehsadat, Sene, Azadeh Akbari, Sheikhha, Mohammad Hassan, Dehghani, Ali, Ashourzadeh, Sareh, Aali, Bibi Shahnaz, Dabiri, Shahriar, Zandieh, Zahra
• Format: Journal Article
• Language: English
• Published: Cham Springer International Publishing 01.03.2024
• Subjects: Bone Morphogenetic Protein 15 - genetics; Bone Morphogenetic Protein 15 - metabolism; Embryology; Female; Follicular Fluid - metabolism; Growth Differentiation Factor 9 - genetics; Growth Differentiation Factor 9 - metabolism; Humans; Medicine; Medicine & Public Health; Obstetrics/Perinatology/Midwifery; Oocytes - metabolism; Ovary - metabolism; Reproductive Genetics: Original Article; Reproductive Medicine; GDF9; Unexpected poor ovarian response; Sequencing; BMP15; POSEIDON criteria
• ISSN: 1933-7191; 1933-7205; 1933-7205
• DOI: 10.1007/s43032-023-01370-1

Unexpected poor ovarian response (UPOR) occurs when nine or fewer oocytes are retrieved from a young patient with normal ovarian reserve. Bone morphogenetic protein15 (BMP15) and growth differentiation factor 9 (GDF9) are two oocyte-specific factors with pivotal role in folliculogenesis. The aim of this study was to assess the relation between BMP15 and GDF9 variants with UPOR. Hundred women aged ≤ 39 with AMH ≥ 1.27 IU/ml participated as UPOR and normal ovarian responders (NOR) based on their oocyte number. Each group consisted of 50 patients. After genomic DNA extraction, the entire exonic regions of BMP15 and GDF9 were amplified and examined by direct sequencing. Western blotting was performed to determine the expression levels of BMP15 and GDF9 in follicular fluid. Additionally, in silico analysis was applied to predict the effect of discovered mutations. From four novel variants of BMP15 and GDF9 genes, silent mutations (c.744 T > C) and (c.99G > A) occurred in both groups, whereas missense variants: c.967-968insA and c.296A > G were found exclusively in UPORs. The latter variants caused reduction in protein expression. Moreover, the mutant allele (T) in a GDF9 polymorphism (C447T) found to be more in NOR individuals (58% NOR vs. 37% UPOR (OR = 2.3, CI 1.32–4.11, p  = 0.004). The novel missense mutations which were predicted as damaging, along with other mutations that happened in UPORs might result in ovarian resistance to stimulation. The mutant allele (T) in C447T polymorphism has a protective effect. It can be concluded that there is an association between BMP15 and GDF9 variants and follicular development and ovarian response.