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对来自纽约州染色体登记处的35000例新的产前细胞遗传学诊断数据中父亲年龄与47,+21情况的分析:无显著影响。

An analysis of paternal age and 47,+21 in 35,000 new prenatal cytogenetic diagnosis data from the New York State Chromosome Registry: no significant effect.

作者信息

Cross P K, Hook E B

机构信息

Bureau of Environmental Epidemiology and Occupational Health, New York State Department of Health, Albany 12237.

出版信息

Hum Genet. 1987 Dec;77(4):307-16. doi: 10.1007/BF00291415.

Abstract

In 35,680 fetuses of women who had prenatal cytogenetic diagnosis done upon amniotic fluid specimens obtained during 2nd trimester amniocentesis and in whom there was no increased cytogenetic risk except for age, there was no statistically significant evidence for an increase of 47,+21 at any paternal age after adjustment for maternal age. The ratio of observed-to-expected numbers in fathers less than 30 years old was 1.0 and in fathers 40 years or older was 0.9 when compared with numbers derived from maternal-age-specific rates in men 30-39 years old. The ratio was 1.1 for those younger than 34 years when compared with rates in fathers aged 34-39 years old. Only for men 55 years or older was there any, even suggestive, increase. The ratio was roughly 1.5 (9 observed to about 6 expected). This was not statistically significant, and moreover, the increase such as it was, was in men married to women 37-42 years old. Regression analyses using several additive parental age models introducing a parabolic function for paternal age, failed to reveal any paternal age contribution.

摘要

在35680例于孕中期羊水穿刺时采集羊水标本进行产前细胞遗传学诊断的孕妇所怀胎儿中,除年龄外无细胞遗传学风险增加因素,经调整母亲年龄后,未发现任何父亲年龄组中47,+21三体综合征发生率有统计学意义的增加。与30 - 39岁男性按母亲年龄分层的发生率相比,父亲年龄小于30岁者观察值与预期值之比为1.0,父亲年龄40岁及以上者为0.9。与父亲年龄34 - 39岁者的发生率相比,年龄小于34岁者的比值为1.1。仅父亲年龄55岁及以上者有任何增加,即便只是提示性的。该比值约为1.5(观察到9例,预期约6例)。这无统计学意义,此外,这种增加出现在与37 - 42岁女性结婚的男性中。使用几种引入父亲年龄抛物线函数的累加父母年龄模型进行回归分析,未发现父亲年龄有任何影响。

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