Kovaleva N V, Tahmasebi-Hesari M, Verlinskaia D K
Tsitol Genet. 2010 Sep-Oct;44(5):47-53.
Advanced maternal age is a well-established factor of DS occurrence. However the majority of DS cases are born to young couples. Some studies suggested that the risk for Down syndrome may be related to an aging grandmother. We obtained data on grandmaternal ages in 243 families of DS and 330 families of healthy children born in 1990-1999. The data were analyzed according to two categories of maternal ages, <30 yr and > or =30 yr. We did not find systematic differences in grandparental age distribution between the studied groups. Specifically, in 102 young couples with DS, medians for both maternal and paternal grandmother's age appeared to be equal (26 yr). Similar figures were observed in 284 young controls (27 yr). There was no difference in age distribution between 141 older couples with DS and 104 control couples. Therefore we failed to support the suggestion that advanced age of the DS grandmother is responsible for meiotic disturbance in her daughter. Neither the hypothesis suggesting a significant contribution of parentally transmitted trisomy 21 to DS population rate has been confirmed.
高龄产妇是唐氏综合征发生的一个已被充分证实的因素。然而,大多数唐氏综合征病例是由年轻夫妇生育的。一些研究表明,唐氏综合征的风险可能与祖母年龄增大有关。我们获取了1990年至1999年出生的243个唐氏综合征家庭和330个健康儿童家庭中祖母年龄的数据。根据母亲年龄的两个类别,即<30岁和≥30岁,对数据进行了分析。我们没有在所研究的组之间发现祖父母年龄分布的系统性差异。具体而言,在102对患有唐氏综合征的年轻夫妇中,外祖母和祖母年龄的中位数似乎相等(26岁)。在284名年轻对照者中也观察到了类似的数据(27岁)。141对患有唐氏综合征的年长夫妇和104对对照夫妇之间的年龄分布没有差异。因此,我们无法支持这样的观点,即唐氏综合征患儿的祖母年龄增大是其女儿减数分裂紊乱的原因。认为父母遗传的21号染色体三体对唐氏综合征总体发生率有显著贡献的假设也未得到证实。