Androgen receptor gene CAG and GGN repeat polymorphisms in Chilean men with primary severe spermatogenic failure
Author
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Castro-Nallar, Eduardo
Author
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Bacallao, Ketty
Author
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Parada-Bustamante, Alexis
Author
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Lardone, María C.
Author
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López, Patricia V.
Author
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Madariaga, Marcia
Author
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Valdevenito, Raúl
Author
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Piottante, Antonio
Author
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Ebensperger, Mauricio
Author
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Castro, Andrea
Admission date
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2019-03-11T13:00:43Z
Available date
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2019-03-11T13:00:43Z
Publication date
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2010
Cita de ítem
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Journal of Andrology, Volumen 31, Issue 6, 2018, Pages 552-559
Identifier
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01963635
Identifier
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19394640
Identifier
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10.2164/jandrol.109.008821
Identifier
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https://repositorio.uchile.cl/handle/2250/165123
Abstract
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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