Chromosomal and Y-chromosome microdeletion analysis in 1,300 infertile males and the fertility outcome of patients with AZFc microdeletions.
Ummet AburSezgin GüneşRamazan AsciEngin AltundagOmer Salih AkarBulent AyasMediniye Karadag AlpaslanGonul OgurPublished in: Andrologia (2019)
The present study investigated the frequency of chromosome aberrations and AZF microdeletions in infertile patients with nonobstructive azoospermia (NOA) or severe oligozoospermia. Additionally, the effect of the AZFc microdeletions on the success of microdissection testicular sperm extraction (microTESE) and intracytoplasmic sperm injection (ICSI) methods were evaluated. Peripheral blood samples were received from 1,300 infertile men with NOA and severe oligozoospermia. Karyotyping and FISH analysis were performed according to standard methods. AZF microdeletions were analysed using multiplex polymerase chain reaction or GML Y-chromosome Microdeletion Detection System consisting of 14 markers. The chromosomal aberrations and the AZF microdeletions frequency among 1,300 infertile men were 10.6% and 4.0% respectively. Either ejaculated spermatozoa or microTESE was performed on only in 19 out of 26 patients with AZFc deletions. Of the 19 patients, four had severe oligozoospermia and 15 had NOA. In eight out of 15 NOA patients, testicular mature spermatozoa were obtained (53.3%) and then ICSI was applied to mature oocytes. After undergoing ICSI treatment, clinical pregnancy and live birth outcome rates were found to be 37.5% and 25% respectively. These results suggest that infertile patients with AZFc microdeletion could achieve successful fertilisation pregnancies with the help of assisted reproductive technology.
Keyphrases
- copy number
- end stage renal disease
- polycystic ovary syndrome
- ejection fraction
- pregnancy outcomes
- peripheral blood
- chronic kidney disease
- prognostic factors
- type diabetes
- dna methylation
- heart failure
- pregnant women
- preterm birth
- patient reported outcomes
- skeletal muscle
- mass spectrometry
- genome wide
- young adults
- middle aged
- gestational age
- left ventricular
- single cell
- quantum dots