Denes Anna-Maria, Landin-Wilhelmsen Kerstin, Wettergren Yvonne, Bryman Inger, Hanson Charles
1 Department of Chemical and Biological Engineering, Chalmers University of Technology , Gothenburg, Sweden .
Genet Test Mol Biomarkers. 2015 Feb;19(2):82-7. doi: 10.1089/gtmb.2014.0240. Epub 2015 Jan 14.
In the normal population, loss of one of the sex chromosomes leading to monosomy (45,X) is a part of the aging process. In Turner syndrome (TS), the classic karyotype 45,X is found in up to 50% at birth, and others have a second cell line; mosaicism. The aim was to study if the chromosomal pattern in TS women changes over time. Fluorescence in situ hybridization was performed on buccal smear cells obtained twice, 10 years apart, from 42 women with TS aged 26-66 years (mean±standard deviation: 42.0±11.6). DNA probes specific for chromosomes X (DXZ1) and Y (DYZ3) were used and >100 cells were analyzed/patient. Nineteen women had monosomy (45,X) (<10% 46,XX), nine had 45,X/46,XX mosaicism, and 14 had iso, ring, or a marker chromosome at baseline. At 10 years, the percentage of diploid cells had increased in 29 of 42 women (69%), with an average increase of 5.7±13.0%. There was a positive correlation between age and % change in diploid 46,XX or 46,XY cells (r=0.38, p=0.023). This new finding might have relevance for the life expectancy in TS.
在正常人群中,性染色体之一的缺失导致单体型(45,X)是衰老过程的一部分。在特纳综合征(TS)中,出生时高达50%的患者具有经典核型45,X,其他患者则有第二种细胞系;即嵌合体。目的是研究TS女性的染色体模式是否随时间变化。对42名年龄在26 - 66岁(平均±标准差:42.0±11.6)的TS女性,在间隔10年的时间里两次采集的口腔黏膜涂片细胞上进行荧光原位杂交。使用针对X染色体(DXZ1)和Y染色体(DYZ3)的DNA探针,每位患者分析>100个细胞。19名女性为单体型(45,X)(<10%为46,XX),9名有45,X/46,XX嵌合体,14名在基线时有等臂染色体、环状染色体或标记染色体。10年后,42名女性中有29名(69%)的二倍体细胞百分比增加,平均增加5.7±13.0%。二倍体46,XX或46,XY细胞的百分比变化与年龄呈正相关(r = 0.38,p = 0.023)。这一新发现可能与TS患者的预期寿命有关。