Foresta C, Caretta N, Palego P, Ferlin A, Zuccarello D, Lenzi A, Selice R
Department of Molecular Medicine, Section of Clinical Pathology and Center for Human Reproduction Pathology, University of Padova, Padova, Italy.
Int J Androl. 2012 Oct;35(5):720-5. doi: 10.1111/j.1365-2605.2012.01269.x. Epub 2012 Apr 10.
Various epidemiological studies in relatively large cohorts of patients with Klinefelter syndrome (KS) described the increased morbidity and mortality in these subjects. Our aim was to study the structure and function of arteries in different districts to investigate in these subjects possible alterations. A total of 92 patients having non-mosaic KS, diagnosed in Centre for Human Reproduction Pathology at the University of Padova, and 50 age-matched healthy male controls were studied. Klinefelter syndrome subjects and controls evaluation included complete medical history, physical examination, measurement of concentrations of the reproductive hormones, lipidic and glycidic metabolism, AR function and sensitivity, ultrasound examinations (diameters, carotid intima-media thickness and brachial flow-mediated dilation) of brachial, common carotid and common femoral artery and abdominal aorta. Klinefelter syndrome patients showed significantly reduced artery diameters in all districts evaluated. On the contrary no statistically significant difference was found in cIMT and brachial FMD values between KS patients and controls. Furthermore, we found no statistically significant correlation of artery diameters with reproductive hormones, metabolic parameters, anthropometric measures and weighted CAG repeats. To our knowledge, this is the first study finding a reduced artery diameter in several districts in KS patients compared with that of normal male subjects and overlapping to that of female subjects. We have not an explanation for this phenomenon, even if a possible involvement of genes controlling the development of vascular system might be hypothesized, and further research is required to verify this hypothesis.
在相对较大队列的克兰费尔特综合征(KS)患者中进行的各种流行病学研究表明,这些患者的发病率和死亡率有所增加。我们的目的是研究不同区域动脉的结构和功能,以调查这些患者可能存在的改变。对在帕多瓦大学人类生殖病理学中心诊断出的92例非嵌合型KS患者以及50例年龄匹配的健康男性对照进行了研究。对克兰费尔特综合征患者和对照的评估包括完整的病史、体格检查、生殖激素浓度测量、脂质和糖代谢、AR功能和敏感性、肱动脉、颈总动脉、股总动脉和腹主动脉的超声检查(直径、颈动脉内膜中层厚度和肱动脉血流介导的扩张)。克兰费尔特综合征患者在所有评估区域的动脉直径均显著减小。相反,KS患者与对照之间的颈动脉内膜中层厚度(cIMT)和肱动脉血流介导的扩张(FMD)值未发现统计学上的显著差异。此外,我们发现动脉直径与生殖激素、代谢参数、人体测量指标和加权CAG重复序列之间无统计学上的显著相关性。据我们所知,这是第一项发现KS患者与正常男性受试者相比,多个区域动脉直径减小且与女性受试者的动脉直径减小情况重叠的研究。即使可以假设控制血管系统发育的基因可能参与其中,但我们对这一现象尚无解释,需要进一步研究来验证这一假设。