Frequency of XY sperm increases with age in fathers of boys with Klinefelter syndrome

被引:88
作者
Lowe, X
Eskenazi, B
Nelson, DO
Kidd, S
Alme, A
Wyrobek, AJ
机构
[1] Lawrence Livermore Natl Lab, Biol & Biotechnol Res Program, Livermore, CA 94550 USA
[2] Univ Calif Berkeley, Sch Publ Hlth, Berkeley, CA 94720 USA
关键词
D O I
10.1086/323763
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
With increasing availability of drugs for impotence and advanced reproductive technologies for the treatment of subfertility, more men are fathering children at advanced ages. We conducted a study of the chromosomal content of sperm of healthy men aged 24-57 years to (a) determine whether father's age was associated with increasing frequencies of aneuploid sperm including XY, disomy X, disomy Y, disomy 21, and sperm diploidy, and (b) examine the association between the frequencies of disomy 21 and sex-chromosomal aneuploidies. The study group consisted of 38 fathers of boys with Klinefelter syndrome (47, XXY) recruited nationwide, and sperm aneuploidy was assessed using multicolor X-Y-21 sperm FISH (10,000 sperm per donor). Paternal age was significantly correlated with the sex ratio of sperm (Y/X; P=.006) and with the frequency of XY sperm (P=.02), with a clear trend with age by decades (P<.006). Compared with fathers in their 20s (who had an average frequency of 7.5 XY sperm per 10,000), the frequencies of XY sperm were 10% higher among fathers in their 30s, 31% higher among those in their 40s, and 160% higher among those in their 50s (95% CI 69%-300%). However, there was no evidence for age effects on frequencies of sperm carrying nullisomy sex; disomies X, Y, or 21; or meiosis I or II diploidies. The frequencies of disomy 21 sperm were significantly associated with sex-chromosomal aneuploidy (P=.04)-in particular, with disomy X (P=.004), but disomy 21 sperm did not preferentially carry either sex chromosome. These findings suggest that older fathers produce higher frequencies of XY sperm, which may place them at higher risk of fathering boys with Klinefelter syndrome, and that age effects on sperm aneuploidy are chromosome specific.
引用
收藏
页码:1046 / 1054
页数:9
相关论文
共 61 条
[1]   HUMAN CHROMOSOME-21 - GENOME MAPPING AND EXPLORATION, CIRCA 1993 [J].
ANTONARAKIS, SE .
TRENDS IN GENETICS, 1993, 9 (04) :142-148
[2]  
Baumgartner A, 1999, ENVIRON MOL MUTAGEN, V33, P49, DOI 10.1002/(SICI)1098-2280(1999)33:1<49::AID-EM6>3.0.CO
[3]  
2-F
[4]  
Bishop J, 1997, AM J EPIDEMIOL, V145, P134
[5]  
Bishop JB, 1996, ENVIRON MOL MUTAGEN, V28, P159
[6]  
Blanco J, 1996, HUM REPROD, V11, P722
[7]  
Bolognesi C, 1997, CANCER EPIDEM BIOMAR, V6, P249
[8]  
BORDSON BL, 1991, FERTIL STERIL, V56, P397
[9]   Age-dependent inclusion of sex chromosomes in lymphocyte micronuclei of man [J].
Catalán, J ;
Autio, K ;
Kuosma, E ;
Norppa, H .
AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 63 (05) :1464-1472
[10]  
CREASY MR, 1978, LANCET, V1, P716