Tsoneva M, Krachunova M, Vulkova G
Eksp Med Morfol. 1978;17(3):145-8.
The authors examined comparatively the frequencies of genomic, counted and structural chromosomal aberrations and associations of acrocentric chromosomes (AAC) in lymphocytic cultures from 35 phenotipic healthy newborns and 15 clinically healthy persons over 60 years of age. Polyploidy was found in 0,16% of the cells in the newborns and in 0,47% of the cells of the adults (0,1 greater than P greater than 0,05). Aneuploidy was established in 0% of the cells of the newborns and in 5,7% of those of the adults (P less than 0,05). In the hyperploid karyotypes 1,3% of the cells of the adults the additional chromosomes were of group C and D. Structural aberrations were observed in 0,58% of the cells of the newborns and in 3,6% of those of the adults (P less than 0,05%. Chromosomal and chromatoid breaks with or without the presence of fragment predominated. Cells with AAC in the newborns were 61,7% against 81,4% in the adult persons (P less than 0,001). The number of the associating chromosomes increased with advancement of age--19,2% in the newborns and 31,9% in the adults (P less than 0,001). In the newborns 21,5% of the chromosomes from group G participated in associations and 17,7% of chromosomes from group D; in the adults both groups were equally engaged--31,3% of the chromosomes G and 32,4% of the chromosomes D.
作者比较研究了35名表型健康的新生儿和15名60岁以上临床健康者淋巴细胞培养物中的基因组、计数和结构染色体畸变以及近端着丝粒染色体(AAC)的关联。在新生儿细胞中发现多倍体的比例为0.16%,在成年人细胞中为0.47%(0.1>P>0.05)。在新生儿细胞中未发现非整倍体,在成年人细胞中为5.7%(P<0.05)。在成年人的超倍体核型中,1.3%的细胞中额外的染色体属于C组和D组。在新生儿细胞中观察到结构畸变的比例为0.58%,在成年人细胞中为3.6%(P<0.05%)。以有或无片段存在的染色体和染色单体断裂为主。新生儿中具有AAC的细胞为61.7%,成年人中为81.4%(P<0.001)。关联染色体的数量随着年龄的增长而增加——新生儿中为19.2%,成年人中为31.9%(P<0.001)。在新生儿中,G组21.5%的染色体参与了关联,D组为17.7%;在成年人中,两组参与关联的比例相同——G组染色体为31.3%,D组染色体为32.4%。