Clinical relevance of partial AZFc deletions

被引:17
作者
de Vries, JWA [1 ]
Repping, S [1 ]
van Daalen, SKM [1 ]
Korver, CM [1 ]
Leschot, NJ [1 ]
van der Veen, F [1 ]
机构
[1] Acad Med Ctr, Ctr Reprod Med, Dept Obstet & Gynecol, NL-1105 AZ Amsterdam, Netherlands
关键词
microdeletions; AZFc; DAZ gene; spermatozoa; ICSI; male infertility;
D O I
10.1016/S0015-0282(02)04390-X
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective: To determine the number of DAZ gene clusters in the Y-bearing spermatozoa of patients who underwent intracytoplasmic sperm injection (ICSI) and to compare the outcome with the number of clusters found in the spermatozoa of normospermic men. Design: Prospective study. Setting: Academic hospital. Patient(s): Forty-seven patients with impaired spermatogenesis who were attending our clinic for ICSI and 56 semen donors. Intervention(s): Peripheral blood was drawn to obtain somatic DNA for polymerase chain reaction (PCR) analysis and leukocytes for karyotyping and FISH analysis. Three-color FISH was performed on the spermatozoa remaining after ICSI and on the spermatozoa of semen donors to determine the presence of the X and Y chromosome as well as the number of DAZ gene clusters. Main Outcome Measure(s): Number of DAZ gene clusters in Y-bearing spermatozoa. Result(s): Five patients had only one DAZ gene cluster, one patient had a complete AZFc deletion, and one patient had three clusters on average. One of the semen donors also showed three DAZ gene clusters in his Y-bearing spermatozoa. None of the semen donors had only one DAZ gene cluster. Conclusion(s): Besides complete AZFc deletions, partial deletions are also associated with impaired spermatogenesis. As a result, these partial deletions that are not recognized by routine PCR are reintroduced into the population by the ICSI technique.
引用
收藏
页码:1209 / 1214
页数:6
相关论文
共 20 条
[1]  
Causio F, 2000, J REPROD MED, V45, P591
[2]   Reduced copy number of DAZ genes in subfertile and infertile men [J].
de Vries, JWA ;
Hoffer, MJV ;
Repping, S ;
Hoovers, JMN ;
Leschot, NJ ;
van der Veen, F .
FERTILITY AND STERILITY, 2002, 77 (01) :68-75
[3]   Absence of deleted in azoospermia (DAZ) genes in spermatozoa of infertile men with somatic DAZ deletions [J].
de Vries, JWA ;
Repping, S ;
Oates, R ;
Carson, R ;
Leschot, NJ ;
van der Veen, F .
FERTILITY AND STERILITY, 2001, 75 (03) :476-479
[4]   Meiotic cell cycle requirement for a fly homologue of human Deleted in Azoospermia [J].
Eberhart, CG ;
Maines, JZ ;
Wasserman, SA .
NATURE, 1996, 381 (6585) :783-785
[5]  
Houston DW, 2000, DEVELOPMENT, V127, P447
[6]   Y chromosome microdeletions and germinal mosaicism in infertile males [J].
Le Bourhis, C ;
Siffroi, JP ;
McElreavey, K ;
Dadoune, JP .
MOLECULAR HUMAN REPRODUCTION, 2000, 6 (08) :688-693
[7]   Sperm deoxyribonucleic acid fragmentation is increased in poor-quality semen samples and correlates with failed fertilization in intracytoplasmic sperm injection [J].
Lopes, S ;
Sun, JG ;
Jurisicova, A ;
Meriano, J ;
Casper, RF .
FERTILITY AND STERILITY, 1998, 69 (03) :528-532
[8]   The role of Y chromosome deletions in male infertility [J].
Mallidis, KMC ;
Bhasin, S .
EUROPEAN JOURNAL OF ENDOCRINOLOGY, 2000, 142 (05) :418-430
[9]   RELIABILITY OF ANEUPLOIDY ESTIMATES IN HUMAN SPERM - RESULTS OF FLUORESCENCE IN-SITU HYBRIDIZATION STUDIES USING 2 DIFFERENT SCORING CRITERIA [J].
MARTIN, RH ;
RADEMAKER, A .
MOLECULAR REPRODUCTION AND DEVELOPMENT, 1995, 42 (01) :89-93
[10]  
Menke DB, 1997, AM J HUM GENET, V60, P237