Lenz P, Luetjens C M, Kamischke A, Kühnert B, Kennerknecht I, Nieschlag E
Institute of Reproductive Medicine and Institute of Human Genetics, Westphalian Wilhelms-University, Münster, Germany.
Hum Reprod. 2005 May;20(5):1248-55. doi: 10.1093/humrep/deh745. Epub 2005 Jan 21.
Gonosomal aneuploidies such as Klinefelter syndrome (47,XXY) are the most frequent chromosomal aberration in infertile men. Normally the chromosomal status of patients is detected by karyotyping of up to 20 metaphase spreads of lymphocyte nuclei, whereby low grade mosaicism may be overlooked. To test whether Klinefelter patients with 47,XXY karyotype or infertile men with 46,XY karyotype represent gonosomal mosaicisms, we performed meta- and interphase fluorescence in situ hybridization (FISH) on 45 men.
A total of 400 interphase and 40 metaphase lymphocyte nuclei per patient were scored after hybridization with DNA probes specific for chromosomes X and Y, and chromosome 9 as a control. On the basis of conventional karyotype, hormone levels and clinical appearance, patients were subdivided into 18 Klinefelter syndrome patients with 47,XXY (group I), 11 Klinefelter syndrome-like patients with normal karyotype, 46,XY (group II) and six non-Klinefelter-like infertile patients with normal 46,XY karyotype (group III). Ten normal men (group IV) served as controls. Testicular volume in the Klinefelter group I was smaller compared with group II (P = 0.016), group III (P < 0.001) and group IV (P < 0.001). In addition, testicular volumes in group II were lower compared with group III and group IV (P < 0.004). No significant differences between the aneuploidy rate analysed by FISH in interphase nuclei and metaphases were found in either single patients or groups. Patients with Klinefelter syndrome, 47,XXY (group I) or with symptoms similar to those in Klinefelter patients 46,XY (group II) showed a similar aneuploidy rate (group I 7.1 +/- 4.0% and group II 4.6 +/- 3.4%) and two 47,XXY patients with a high prevalence for normal 46,XY lymphocytes had sperm in their ejaculate. However, in general, no correlations between FISH mosaic status and serum hormone parameters, nor with ejaculate parameters were found.
The results suggest that 47,XXY patients with an increased incidence of XY cells (average of 4.2 +/- 2.3) may have a higher probability of germ cells as we found sperm only in the ejaculate of Klinefelter syndrome patients with mosaic 46,XY cells (6.0 and 7.0%). On the other hand, 46,XY patients with mosaic sex chromosome aneuploidies detected by FISH analysis more often show symptoms of hypogonadism phenotypically resembling Klinefelter syndrome.
性染色体非整倍体,如克兰费尔特综合征(47,XXY)是不育男性中最常见的染色体畸变。通常通过对多达20个淋巴细胞核中期分裂相进行核型分析来检测患者的染色体状态,由此可能会忽略低级别嵌合体。为了检测47,XXY核型的克兰费尔特患者或46,XY核型的不育男性是否代表性染色体嵌合体,我们对45名男性进行了中期和间期荧光原位杂交(FISH)。
用针对X和Y染色体以及作为对照的9号染色体的DNA探针杂交后,对每位患者的总共400个间期和40个中期淋巴细胞核进行评分。根据传统核型、激素水平和临床表现,将患者分为18例47,XXY的克兰费尔特综合征患者(I组)、11例核型正常的克兰费尔特综合征样患者(46,XY,II组)和6例核型正常的非克兰费尔特样不育患者(46,XY,III组)。10名正常男性(IV组)作为对照。I组克兰费尔特患者的睾丸体积比II组(P = 0.016)、III组(P < 0.001)和IV组(P < 0.001)小。此外,II组的睾丸体积比III组和IV组低(P < 0.004)。在单个患者或各组中,间期核和中期通过FISH分析的非整倍体率均未发现显著差异。47,XXY的克兰费尔特综合征患者(I组)或症状与46,XY的克兰费尔特患者相似的患者(II组)显示出相似的非整倍体率(I组7.1 +/- 4.0%,II组4.6 +/- 3.4%),并且两名46,XY淋巴细胞正常比例高的47,XXY患者精液中有精子。然而,总体而言,未发现FISH嵌合状态与血清激素参数之间以及与精液参数之间存在相关性。
结果表明,XY细胞发生率增加(平均为4.2 +/- 2.3)的47,XXY患者可能有更高的产生生殖细胞的概率,因为我们仅在具有46,XY嵌合细胞的克兰费尔特综合征患者(6.0%和7.0%)的精液中发现了精子。另一方面,通过FISH分析检测到的具有嵌合性染色体非整倍体的46,XY患者在表型上更常表现出性腺功能减退的症状,类似于克兰费尔特综合征。