Lardone María C, Parodi Daniela A, Ebensperger Mauricio, Peñaloza Paulina, Cornejo Valeria, Valdevenito Raúl, Pommer Ricardo, Castro Andrea
Institute of Maternal and Child Research, School of Medicine, University of Chile, Santiago, Chile.
Fertil Steril. 2007 Nov;88(5):1318-26. doi: 10.1016/j.fertnstert.2007.01.038. Epub 2007 Apr 9.
To determine the prevalence of AZFc subdeletions in infertile Chilean men with severe spermatogenic impairment.
Prospective analysis.
University infertility clinic.
PATIENT(S): Ninety-five secretory azo/oligozoospermic men without AZFc Y chromosome microdeletions: 71 whose testicular histology showed severe spermatogenic impairment and 24 who exhibited reduced testicular volume and elevated serum FSH levels. As controls, we studied 77 men (50 fertile and/or normozoospermic, and 27 with azoospermia and normal spermatogenesis).
INTERVENTION(S): Peripheral blood was drawn to obtain genomic DNA for polymerase chain reaction (PCR) digestion assays of DAZ-sequence nucleotide variants and for AZFc-STS PCR after a complete testicular characterization (biopsy, hormonal, and physical evaluation).
MAIN OUTCOME MEASURE(S): DAZ genes and AZFc subdeletion types.
RESULT(S): In cases we observed two "gr/gr" subdeletions (2.1%), one with absence of DAZ1/DAZ2 (g1/g2 subtype), and the other with absence of DAZ3/DAZ4 (r2/r4 subtype). Additionally, we found a g1/g3 subdeletion in a patient with Sertoli-cell-only syndrome. In controls, we observed two gr/gr subdeletions with absence of DAZ1/DAZ2 (2.6%) in a fertile/normozoospermic and in an obstructive azoospermic man.
CONCLUSION(S): AZFc subdeletions do not seem to cause severe impairment of spermatogenesis. Moreover, gr/gr-DAZ1/DAZ2 subdeletions do not appear to affect fertility in Chilean men.
确定患有严重生精功能障碍的智利不育男性中AZFc亚缺失的患病率。
前瞻性分析。
大学不育诊所。
95名分泌性无精子症/少精子症男性,无AZFc Y染色体微缺失:71名睾丸组织学显示严重生精功能障碍,24名睾丸体积减小且血清促卵泡激素(FSH)水平升高。作为对照,我们研究了77名男性(50名生育能力正常和/或精子正常的男性,以及27名无精子症但生精功能正常的男性)。
采集外周血以获取基因组DNA,用于DAZ序列核苷酸变异的聚合酶链反应(PCR)消化分析以及在完成睾丸全面特征分析(活检、激素和体格评估)后进行AZFc-STS PCR。
DAZ基因和AZFc亚缺失类型。
在病例组中,我们观察到两个“gr/gr”亚缺失(2.1%),一个缺失DAZ1/DAZ2(g1/g2亚型),另一个缺失DAZ3/DAZ4(r2/r4亚型)。此外,我们在一名唯支持细胞综合征患者中发现了一个g1/g3亚缺失。在对照组中,我们在一名生育能力正常/精子正常的男性和一名梗阻性无精子症男性中观察到两个缺失DAZ1/DAZ2的gr/gr亚缺失(2.6%)。
AZFc亚缺失似乎不会导致严重的生精功能障碍。此外,gr/gr-DAZ1/DAZ2亚缺失似乎不会影响智利男性的生育能力。