Aksglaede Lise, Skakkebaek Niels E, Juul Anders
University Department of Growth and Reproduction, Rigshospitalet, University of Copenhagen, DK-2100 Copenhagen, Denmark.
J Clin Endocrinol Metab. 2008 Jan;93(1):169-76. doi: 10.1210/jc.2007-1426. Epub 2007 Oct 16.
Growth is a highly complex process regulated by the interaction between sex steroids and the GH IGF-axis. However, other factors such as sex chromosome-related genes play independent roles.
The aim of the study was to evaluate the role of abnormal chromosome constitution for longitudinal growth in relation to reproductive hormones, IGF-I, and IGF binding protein (IGFBP)-3.
The study was conducted at an outpatient clinic, Copenhagen University Hospital.
Participants included 86 47,XXY males, 14 46,XX-males, and nine 47,XYY.
Standing and sitting height, serum levels of reproductive hormones, IGF-I, and IGFBP-3 were measured.
In boys with 47,XXY and 47,XYY karyotypes, growth was accelerated already in childhood, compared with healthy boys. 46,XX-males were significantly shorter than healthy boys but matched the stature of healthy girls. In 47,XXY sitting height to height ratios were lower than expected, whereas body proportions in 46,XX-males and 47,XYY were normal. In all subjects serum levels of IGF-I and IGFBP-3 were within normal limits. The boys with 46,XX and 47,XXY karyotypes presented with low normal testosterone and elevated LH levels after puberty, whereas the sex hormone secretion of the 47,XYY boys remained normal.
We found accelerated growth in early childhood in boys with 47,XXY and 47,XYY karyotypes, whereas 46,XX-males were shorter than controls. These abnormal growth patterns were not reflected in circulating levels of IGF-I and IGFBP-3. The boys with 46,XX and 47,XXY karyotypes developed hypogonadism in puberty, but androgen secretion in 47,XYY boys remained normal. The abnormal stature of these patients may be a result of abnormal gene expression due to the underlying chromosome aberration resulting in excessive expression of growth-related genes.
生长是一个高度复杂的过程,受性类固醇与生长激素胰岛素样生长因子轴之间相互作用的调节。然而,其他因素,如与性染色体相关的基因也发挥着独立作用。
本研究旨在评估异常染色体构成在纵向生长方面相对于生殖激素、胰岛素样生长因子-I(IGF-I)和胰岛素样生长因子结合蛋白(IGFBP)-3的作用。
该研究在哥本哈根大学医院的门诊进行。
参与者包括86名47,XXY男性、14名46,XX男性和9名47,XYY男性。
测量身高、血清生殖激素水平、IGF-I和IGFBP-3。
与健康男孩相比,47,XXY和47,XYY核型的男孩在儿童期生长就已加速。46,XX男性明显比健康男孩矮,但身高与健康女孩相当。47,XXY的坐高与身高之比低于预期,而46,XX男性和47,XYY的身体比例正常。所有受试者的血清IGF-I和IGFBP-3水平均在正常范围内。46,XX和47,XXY核型的男孩在青春期后睾酮水平略低于正常范围而促黄体生成素(LH)水平升高,而47,XYY男孩的性激素分泌保持正常。
我们发现47,XXY和47,XYY核型的男孩在幼儿期生长加速,而46,XX男性比对照组矮。这些异常生长模式并未反映在IGF-I和IGFBP-3的循环水平上。46,XX和47,XXY核型的男孩在青春期出现性腺功能减退,但47,XYY男孩的雄激素分泌保持正常。这些患者的异常身高可能是由于潜在染色体畸变导致生长相关基因过度表达,进而引起基因表达异常所致。