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Y chromosome microdeletions in infertile men with cryptorchidism
Tanja Kunej1, Branko Zorn, Borut Peterlin
1Division of Medical Genetics, Department of Obstetrics and Gynecology, University Medical Center, Ljubljana, Slovenia.
Objective:
To determine whether cryptorchidism associated with azoospermia or oligozoospermia may be due to microdeletions of the Y chromosome.
Design:
Controlled clinical study.
Settings:
Division of Medical Genetics and the Andrology Centre, Department of Obstetrics and Gynecology, University Medical Center, Ljubljana.
Patient(S):
Ninety men from infertile couples (36 azoospermics, 35 oligozoospermics, and 19 normozoospermics) with a medical history of cryptorchidism. Nineteen excryptorchid patients with cryptorchidism and Y chromosome microdeletions among 3099 patients from 14 publications.
Intervention(S):
Collection of semen and blood samples.
Main Outcome Measure(S):
Medical history, testicular volume, sperm characteristics, serum FSH levels, testicular histology, presence or absence of Y chromosome microdeletions, including all known Y chromosome genes/gene families in the azoospermia factor (AZF) region.
Result(S):
Deletions of the Y chromosome were found in 2 out of 71 cryptorchid patients with azoospermia or oligozoospermia (2.8%). The literature review showed that the incidence of microdeletions in infertile patients with cryptorchidism is lower in comparison with the general population of infertile men (4.9% vs. 8.1%), and that the frequency of cryptorchidism in patients with Y chromosome deletions (6 out of 103, 5.8%) is significantly lower in comparison to infertile patients without deletions (178 out of 1141, 15.6%).
Conclusion(S):
No causal relation exists between Y chromosome microdeletions and cryptorchidism.