Artículo de revista
Androgen receptor gene CAG and GGN repeat polymorphisms in Chilean men with primary severe spermatogenic failure
Fecha
2010Registro en:
Journal of Andrology, Volumen 31, Issue 6, 2018, Pages 552-559
01963635
19394640
10.2164/jandrol.109.008821
Autor
Castro-Nallar, Eduardo
Bacallao, Ketty
Parada-Bustamante, Alexis
Lardone, María C.
López, Patricia V.
Madariaga, Marcia
Valdevenito, Raúl
Piottante, Antonio
Ebensperger, Mauricio
Castro, Andrea
Institución
Resumen
There is ample documentation supporting the fact that androgens are required for normal spermatogenesis. A minority of infertile men have abnormal testosterone blood levels or mild androgen receptor mutations. We investigated the androgen receptor CAG and GGN repeat lengths in Chilean men with spermatogenic impairment. We studied 117 secretory azoospermic/oligozoospermic men (93 idiopathic and 24 excryptorchidic), without Y-chromosome microdeletions, and 121 controls with normal spermatogenesis (42 obstructive and 79 normozoospermic men). Peripheral blood was drawn to obtain genomic DNA for polymerase chain reaction and automated sequencing of CAG and GGN repeats. Testicular characterization included hormonal studies, physical evaluation, and seminal and biopsy analysis. The CAG and GGN polymorphism distributions were similar among idiopathic men, excryptorchidic men, and controls and among the different types of spermatogenic impairment. However, the proportion of the CAG 21 allele wa