Endometriosis is a common benign disease in premenopausal women and causes chronic pelvic pain and infertility. This infertility may be due to pelvic adhesions and surgery but also because of poor oocyte quality. It is known that endometriosis is associated with an increase oxidative stress, wich induce chronic inflammation, deleterious effect for DNA, proteins and can caused cellular death. ROS markers found in follicular fluid or in serum are significatively higher in endometriosis women. The investigators want to dose a marker of apoptosis in infertile women and see if it's significatively higher in serum and in follicular fluid of patients with endometriosis compared to others infertility causes and if it's correlated to oocyte quality and IVF results. Real time PCR will be used to dose cell free DNA in serum and follicular fluid of patients undergoing IVF treatment (endometriosis and infertility due to tubal factor, male infertility or idiopathic cause). Then the investigators will compare cell free DNA rate with oocyte and embryo quality and with pregnancy outcomes in the different group.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
DIAGNOSTIC
Masking
SINGLE
Enrollment
114
10ml of blood will be sampled from patients before undergoing IVF treatment, the cell free DNA will be extracted and then quantified by a real time PCR. Another 10ml sample will be drawn the day of oocyte puncture for a new quantification of cell free DNA in plasma and cell free DNA will also be dose in follicular fluid of patients
CHU Amiens Picardie
Amiens, France
cell free DNA rate in serum in patients before they start IVF stimulation
cell free DNA in serum quantified by real time PCR in patients before they start IVF stimulation
Time frame: day 1
cell free DNA rate in follicular fluid the day of punction
cell free DNA in follicular fluid the day of punction
Time frame: day 1
number of oocytes reaching the metaphase II
number of oocytes reaching the metaphase II in both groups of patients
Time frame: 1 year
fragmentation rate
fragmentation rate
Time frame: 1 year
number of cells at day 2
number of cells at day 2
Time frame: day 2
number of cells at day 3
number of cells at day 3
Time frame: day 3
blastulation rate at day 5 of developement
blastulation rate at day 5 of developement
Time frame: day 5
number of clinical pregnancy in both groups
Time frame: 1 year
number of live birth in both groups
Time frame: 1 year
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