Carothers A D, Filippi G
Medical Research Council, Western General Hospital, Edinburgh, UK.
Hum Genet. 1988 Dec;81(1):71-5. doi: 10.1007/BF00283733.
Data on 151 non-mosaic 47,XXY males from Sardinia, previously reported by Filippi (1986), were analysed for associations with parental ages at birth, sib order and sex ratio among siblings. The results confirm those of the earlier Scottish-based studies in that: (1) there was a significant increase in risk of 47,XXY livebirths at advanced parental ages; (2) maternal age, and maternal age alone, was sufficient to explain the effect; (3) there were no independent effects of paternal age or sib order once maternal age had been taken into account; (4) there was no evidence of any distortion of the sex ratio among siblings. Estimates of relative risk at different maternal ages were compatible with those from the Scottish studies, and pooled estimates are therefore derived. They suggest, for example, that the risk at maternal age 40 years is 2-3 times that at age 30 years. In 33 cases, the parental origin of the supernumerary X chromosome was determined by analysing the segregation of genetic markers. The mean parental ages of 19 'maternal' cases were significantly raised above those of controls, whereas those of 14 'paternal' cases were slightly, and marginally significantly, reduced. The conclusions were essentially unaffected by whether the Sardinian population, the siblings of cases or a group of 94 unrelated Sardinian males were used as controls.
菲利皮(1986年)之前报告的来自撒丁岛的151名非嵌合型47,XXY男性的数据,被用于分析与父母生育年龄、出生顺序以及兄弟姐妹间性别比的关联。结果证实了早期基于苏格兰的研究结果,即:(1)父母年龄较大时,47,XXY活产的风险显著增加;(2)仅母亲年龄就足以解释这种影响;(3)考虑母亲年龄后,父亲年龄或出生顺序没有独立影响;(4)没有证据表明兄弟姐妹间的性别比存在任何扭曲。不同母亲年龄的相对风险估计与苏格兰研究的结果相符,因此得出合并估计值。例如,这些估计值表明,母亲年龄40岁时的风险是30岁时的2至3倍。在33例中,通过分析遗传标记的分离情况确定了额外X染色体的亲本来源。19例“母源”病例的父母平均年龄显著高于对照组,而14例“父源”病例的父母平均年龄略有降低,且在边缘上具有显著差异。无论使用撒丁岛人群、病例的兄弟姐妹还是94名无关的撒丁岛男性组成的群体作为对照,结论基本不受影响。