Prevalence of male subfertility ? Infertility is defined as
failure to conceive after one year of unprotected sexual intercourse .This
problem affects approximately
10%–15% of couples worldwide, and male-related factors are responsible
for half of this case . Several factors have been implicated in male
infertility such as Cause :1) hormonal
abnormalities, Cause :2 )
erectile dysfunction, Cause :3) infections, Cause :4 ) antisperm antibodies, Cause :5) exposure to chemical agents and radiations, Cause :6) testicular cancer, Cause :7) varicocele, Cause :8) genetic factors, and Cause :9) others .Thus, male
infertility is a multifactorial syndrome encompassing a wide variety of
disorders. However, in about 30%–50% of male cases, the etiology of infertility
is still unknown.
Sertoli cell-only syndrome
(SCOS), maturation arrest, and hypospermatogenesis à The main culprit is “Microdeletion of the
azoospermia factor (AZF) region located on the long arm of the Y chromosome (Yq11)”. This is considered the most common
genetic cause of male infertility .The AZF region is divided into three
nonoverlapping subregions called AZFa, AZFb, and AZFc,
all of which are required for normal spermatogenesis. Microdeletions in these
three regions are associated with various spermatogenetic alterations including
Sertoli cell-only syndrome
(SCOS), maturation arrest, and hypospermatogenesis.
Specifically, microdeletion of AZFa is relevant to complete SCOS and
azoospermia. The absence of AZFb is
associated with maturation arrest at meiosis, whereas microdeletion of AZFc
results in variable clinical and histologic phenotypes, ranging from oligozoospermia
to SCOS Extensive studies have been carried on Y microdeletions in
non-obstructive azoospermic and severely oligozoospermic patients, with a
reported incidence ranging from 3% to 28% Therefore, disruption of AZF can be
viewed as the most common molecularly diagnosable cause of spermatogenic
failure in the setting of non-obstructive azoospermia or severe oligozoospermia
Recently, the techniques of testicular sperm extraction (TESE) and
intracytoplasmic sperm injection (ICSI) have made it possible to help men with
azoospermia or severe oligozoospermia to achieve successful fertilizations and
pregnancies .However, Y microdeletions can be transmitted from
infertile fathers to their male offspring, who could also experience
infertility, through the procedure of ICSI. Thus, it is important to evaluate Y microdeletions in male
infertility before assisted reproduction in order to provide appropriate
information to patients.
Y chromosome microdeletions can be detected by using multiplex
polymerase chain reaction (PCR) in infertile men. Moreover, the relationship
between the levels of reproductive hormones and Y chromosome microdeletions has
to be analyzed.
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