Aneuploidy in human sperm: a review of the frequency and distribution of aneuploidy, effects of donor age and lifestyle factors

被引:123
作者
Shi, Q
Martin, RH
机构
[1] Alberta Childrens Prov Gen Hosp, Dept Genet, Calgary, AB T2T 5C7, Canada
[2] Univ Calgary, Fac Med, Dept Med Genet, Calgary, AB, Canada
来源
CYTOGENETICS AND CELL GENETICS | 2000年 / 90卷 / 3-4期
关键词
D O I
10.1159/000056773
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Application of fluorescence in situ hybridization (FISH) analysis has opened the way for comprehensive studies on numerical chromosome abnormalities in human sperm. During the last decade, more than five million sperm from approximately 500 normal men were analyzed by a number of laboratories from around the world by this approach. Except for chromosome 19 which has been analyzed in only one study, all other chromosomes have been examined by two or more studies with considerable differences in disomy frequency for an individual chromosome among studies. The mean disomy frequency is 0.15 % for each of the autosomes and 0.26 % for the sex chromosomes. Most chromosomes analyzed have an equal distribution of disomy with the exception of chromosomes 14, 21, 22 and the sex chromosomes, which display significantly higher disomy frequencies. Slight but significant increases in disomy frequency with advancing paternal age were observed for some chromosomes, in particular for the sex chromosomes. Some lifestyle factors such as smoking, alcohol drinking and caffeine consumption have been investigated and no consistent association between disomy frequency and any type of lifestyle factors has been established. The question of whether different geographic and ethnic groups of men have inherent differences in frequency of disomic sperm has been investigated by two studies with conflicting results. Copyright (C) 2000 S. Karger AG, Basel.
引用
收藏
页码:219 / 226
页数:8
相关论文
共 94 条
[1]  
Abruzzo MA, 1996, HUM GENET, V97, P819
[2]   The effects of age and abnormal sperm count on the nondisjunction of spermatozoa [J].
Asada, H ;
Sueoka, K ;
Hashiba, T ;
Kuroshima, M ;
Kobayashi, N ;
Yoshimura, Y .
JOURNAL OF ASSISTED REPRODUCTION AND GENETICS, 2000, 17 (01) :51-59
[3]   CHROMOSOME SEGREGATION INTO THE SPERMATOZOA OF 2 MEN HETEROZYGOUS FOR DIFFERENT RECIPROCAL TRANSLOCATIONS [J].
BALKAN, W ;
MARTIN, RH .
HUMAN GENETICS, 1983, 63 (04) :345-348
[4]  
Baumgartner A, 1999, ENVIRON MOL MUTAGEN, V33, P49, DOI 10.1002/(SICI)1098-2280(1999)33:1<49::AID-EM6>3.0.CO
[5]  
2-F
[6]   ESTIMATES OF ANEUPLOIDY USING MULTICOLOR FLUORESCENCE IN-SITU HYBRIDIZATION ON HUMAN SPERM [J].
BISCHOFF, FZ ;
NGUYEN, DD ;
BURT, KJ ;
SHAFFER, LG .
CYTOGENETICS AND CELL GENETICS, 1994, 66 (04) :237-243
[7]   Chromosome 21 disomy in the spermatozoa of the fathers of children with trisomy 21, in a population with a high prevalence of Down syndrome:: Increased incidence in cases of paternal origin [J].
Blanco, J ;
Gabau, E ;
Gómez, D ;
Baena, N ;
Guitart, M ;
Egozcue, J ;
Vidal, F .
AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 63 (04) :1067-1072
[8]  
Blanco J, 1996, HUM REPROD, V11, P722
[9]   Increased incidence of disomic sperm nuclei in a 47,XYY male assessed by fluorescent in situ hybridization (FISH) [J].
Blanco, J ;
Rubio, C ;
Simon, C ;
Egozcue, J ;
Vidal, F .
HUMAN GENETICS, 1997, 99 (03) :413-416
[10]   FISH on sperm heads allows the analysis of chromosome segregation and interchromosomal effects in carriers of structural rearrangements: results in a translocation carrier, t(5;8)(q33;q13) [J].
Blanco, J ;
Egozcue, J ;
Clusellas, N ;
Vidal, F .
CYTOGENETICS AND CELL GENETICS, 1998, 83 (3-4) :275-280