Malini Suttur S, Ramachandra Nallur B
Human Genetics Laboratory, Department of Studies in Zoology, University of Mysore, Manasagangotri, Mysore 570 006, India.
BMC Med Genet. 2006 Jan 14;7:4. doi: 10.1186/1471-2350-7-4.
Down syndrome (DS) is the most common chromosomal anomaly associated with mental retardation. This is due to the occurrence of free trisomy 21 (92-95%), mosaic trisomy 21 (2-4%) and translocation (3-4%). Advanced maternal age is a well documented risk factor for maternal meiotic nondisjunction. In India three children with DS are born every hour and more DS children are given birth to by young age mothers than by advanced age mothers. Therefore, detailed analysis of the families with DS is needed to find out other possible causative factors for nondisjunction.
We investigated 69 families of cytogenetically confirmed DS children and constructed pedigrees of these families. We also studied 200 randomly selected families belonging to different religions as controls. Statistical analysis was carried out using logistic regression.
Out of the 69 DS cases studied, 67 were free trisomy 21, two cases were mosaic trisomy 21 and there were none with translocation. The number of DS births was greater for the young age mothers compared with the advanced age mothers. It has also been recorded that young age mothers (18 to 29 years) born to their mothers at the age 30 years and above produced as high as 91.3% of children with DS. The logistic regression of case- control study of DS children revealed that the odds ratio of age of grandmother was significant when all the four variables were used once at a time. However, the effect of age of mother and father was smaller than the effect of age of maternal grandmother. Therefore, for every year of advancement of age of the maternal grandmother, the risk (odds) of birth of DS baby increases by 30%.
Besides the known risk factors, mother's age, father's age, the age of the maternal grandmother at the time of birth of the mother is a risk factor for the occurrence of Down syndrome.
唐氏综合征(DS)是与智力发育迟缓相关的最常见染色体异常疾病。这是由于21号染色体游离三体(92 - 95%)、21号染色体嵌合三体(2 - 4%)和易位(3 - 4%)的发生。高龄产妇是已被充分证明的母亲减数分裂不分离的危险因素。在印度,每小时有三名唐氏综合征患儿出生,并且与高龄母亲相比,年轻母亲生育的唐氏综合征患儿更多。因此,需要对唐氏综合征家庭进行详细分析,以找出不分离的其他可能致病因素。
我们调查了69个经细胞遗传学确诊的唐氏综合征患儿家庭,并构建了这些家庭的系谱。我们还研究了200个随机选择的来自不同宗教的家庭作为对照。使用逻辑回归进行统计分析。
在所研究的69例唐氏综合征病例中,67例为21号染色体游离三体,2例为21号染色体嵌合三体,无易位病例。与高龄母亲相比,年轻母亲生育的唐氏综合征患儿数量更多。还记录到,母亲在30岁及以上时生育的18至29岁年轻母亲所生的唐氏综合征患儿高达91.3%。对唐氏综合征患儿病例对照研究的逻辑回归显示,当一次使用所有四个变量时,外祖母年龄的优势比具有显著性。然而,母亲和父亲年龄的影响小于外祖母年龄的影响。因此,外祖母年龄每增加一岁,生出唐氏综合征患儿的风险(几率)增加30%。
除了已知的危险因素,母亲年龄、父亲年龄外,母亲出生时外祖母的年龄也是唐氏综合征发生的一个危险因素。