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DOI 10.1007/s10815-016-0835-9

Медицинская библиотека · Journal of assisted reproduction and genetics · 2016

The carriers of the A/G-G/G allelic combination of the c.2039 A>G and c.-29 G>A FSH receptor polymorphisms retrieve the highest number of oocytes in IVF/ICSI cycles.

Allegra Adolfo, Marino Angelo, Raimondo Stefania, Maiorana Antonio, Gullo Salvatore, Scaglione Piero, Volpes Aldo, Alessandro Riccardo

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Аннотация

PURPOSE: The objective of this study was the elucidation of the possible role of the single-nucleotide polymorphisms (SNP) at position -29 and 2039 of the FSH receptor gene (FSHR) as independent predictive markers of ovarian response. Indeed, the tailoring of reproductive treatments is crucial for both maximizing the success of IVF patients and obtaining a reduction in hypo- or hyper-response rates.

METHODS

This prospective, observational study analyzed the association of -29 and 2039 FSHR polymorphisms with the number of retrieved oocytes in 140 patients attending an IVF/ICSI cycle for severe male factors (≤5,000,000 spermatozoa/mL) or tubal factors at the ANDROS Day Surgery Clinic, Palermo, Italy.

RESULTS

The results of this study demonstrate that the genetic combination of A/G for polymorphism c.2039 A>G with G/G for polymorphism c.-29 G>A is significantly associated with the highest number of collected oocytes (p = 0.03). This association was significant even after controlling for the effect of other clinical variables.

CONCLUSIONS

The A/G-G/G allelic variant, identified as an independent variable, if confirmed in a larger number of patients, could be considered as a new genetic biomarker, which could increase the efficacy of prediction models for ovarian stimulation.

Для цитирования: Allegra Adolfo, Marino Angelo, Raimondo Stefania, Maiorana Antonio, Gullo Salvatore, Scaglione Piero, Volpes Aldo, Alessandro Riccardo. The carriers of the A/G-G/G allelic combination of the c.2039 A>G and c.-29 G>A FSH receptor polymorphisms retrieve the highest number of oocytes in IVF/ICSI cycles.. Journal of assisted reproduction and genetics. 2016. DOI: 10.1007/s10815-016-0835-9.

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